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psx:substance/nep/search/1215c7da-3d1c-4a0f-9c71-4555a9f0fdbb

search2026-04-26recordliterature_search

derived from · upstream

none recorded

feeds · downstream

Closure of psx:substance/nep/search/1215c7da-3d1c-4a0f-9c71-4555a9f0fdbb: 44 upstream, 102 downstream.

psx:substance/nep/search/1215c7da-3d1c-4a0f-9c71-4555a9f0fdbb
  ├─ used  search/2e7d4e04-714c-42b3-9fe7-661cc3451eb3  Searched PubChem for "NEP N-Ethylpentedrone / 2-(ethylamino)-1-phenylpentan-1-one"
  ├─ used  search/1876c0e7-4ba9-4593-87a6-0572f8d18413  Searched PubMed for "NEP N-Ethylpentedrone cathinone pharmacology"
  ├─ used  search/16158c00-e066-4acb-a823-ef5ed9a3ffdc  Searched PubMed for "N-Ethylpentedrone stimulant synthetic cathinone"
  ├─ used  search/4930b71e-c7a4-4280-ab73-4201e8dbb09c  Searched PubMed for "N-ethylpentedrone forensic detection mass spectrometry"
  ├─ used  search/5a0ce40a-3cf9-4200-b8bc-653465e3bcc2  Searched PubMed for "Daziani NEP hepatocyte metabolism authentic urine metabolites"
  ├─ used  search/1f7052bb-9e8c-45a3-be85-32e7ddef3deb  Searched OpenAlex for "N-ethylpentedrone synthetic cathinone"
  ├─ used  search/2ce9478b-1c5e-4f0a-aeed-8f48c1d1b20a  Searched PubMed for "Simmler Liechti cathinone pharmacological characterization designer beta-keto"
  ├─ used  search/f1d84af9-f89a-4f4b-87ac-d6d40a0604c6  Searched PubMed for "PMID lookup for Gatch 2025, Massano 2024, Kolaczynska 2021"
  ├─ used  search/0edc335c-6013-4d25-827e-4a5f5a333727  Searched WebSearch + WebFetch for "N-ethylpentedrone NEP legal status controlled substance UK US EU scheduling"
  ├─ used  search/37cb56f4-7fa0-414c-92d9-7e5b72b8b5b1  Searched WebFetch
  ├─ used  search/e4d22f84-c2d1-4fb3-86b3-b6455564aa79  Searched ClinicalTrials.gov for "N-ethylpentedrone synthetic cathinone"
  ├─ used  search/6083861e-8049-426e-8d16-aa58a9b6825c  Searched PubMed for "N-ethyl-pentedrone aggression social behavior mice withdrawal repeated administration"
  ├─ used  search/9d7a5f38-5e0c-4173-b074-be620465d252  Searched PubMed for "pentedrone cathinone reward dopamine self-administration conditioned place preference"
  ├─ used  search/97a55d01-2420-4a8a-80f2-e0f512cd06cc  Searched PubChem REST API
  ├─ used  search/aa4cf5bb-984c-4bdf-913d-df5a954f3aad  Searched WebSearch for "NEP N-ethylpentedrone DEA scheduling Federal Analog Act US"
  ├─ used  search/d561350e-9ad6-40d2-a2e8-5640c992779d  Searched WebSearch for "N-ethylpentedrone UK Psychoactive Substances Act EU EUDA initial report 2025"
  ├─ used  search/a28ee5d2-6c41-4c3a-a51b-e6d2410ef752  Searched PubMed for "NPS deaths cathinone Poland forensic 2024"
  ├─ used  search/1ffc7304-1f92-4b6b-984d-55817ca82c1a  Searched Crossref via verify_doi for "DOI verification for key papers"
    ├─ used  src/url:99b110234253d97e  N-Ethylpentedrone PubChem Entry (CID 205593)
    ├─ used  src/doi:10.1093/jat/bkac092  Synthetic Cathinones in Belgium: Two Case Reports with Different Outcomes Observed in the Emergency Room
    ├─ used  src/url:980a9e743d118ad6  EUDA initial report on the new psychoactive substance N-ethylnorpentedrone (NEP)
    ├─ used  src/doi:10.1016/j.pbb.2025.174100  Locomotor stimulant and drug discrimination effects of five synthetic cathinones in rodents
    ├─ used  src/doi:10.1016/j.neuropharm.2013.11.008  Monoamine transporter and receptor interaction profiles of a new series of designer cathinones
    ├─ used  src/doi:10.3390/ijms22158277  The Pharmacological Profile of Second Generation Pyrovalerone Cathinones and Related Cathinone Derivative.
    ├─ used  src/doi:10.1016/j.forsciint.2024.112030  Synthetic cathinones in drug-facilitated sexual assault: A case report involving N-ethylpentedrone
    ├─ used  src/doi:10.1016/j.pnpbp.2022.110562  Repeated administration of N-ethyl-pentedrone induces increased aggression and impairs social exploration after withdrawal in mice
    ├─ used  src/doi:10.1093/jat/bkab119  Toxicological Analysis of Cases of Mixed Poisonings with Synthetic Cathinones and Other Drugs of Abuse.
    ├─ used  src/url:3c0a926a9003c891  Schedules of Controlled Substances: Placement of N-Ethylhexedrone, alpha-Pyrrolidinohexanophenone, 4-Methyl-alpha-ethylaminopentiophenone, 4′-Methyl-alpha-pyrrolidinohexiophenone, alpha-Pyrrolidinoheptaphenone, and 4′-Chloro-alpha-pyrrolidinovalerophenone in Schedule I
    ├─ used  src/doi:10.1007/7854_2016_41  Structure-Activity Relationships of Synthetic Cathinones.
    ├─ used  src/doi:10.1016/j.jpba.2026.117474  First enantioselective determination of N-ethylpentedrone and its major phase-1 metabolites using supercritical fluid chromatography coupled with tandem mass spectrometry and its application to human oral fluid and urine samples.
    ├─ used  src/doi:10.1007/s00216-022-04440-6  Synthesis of emerging cathinones and validation of a SPE GC-MS method for their simultaneous quantification in blood.
    ├─ used  src/doi:10.1111/j.1476-5381.2012.02145.x  Pharmacological characterization of designer cathinones in vitro
    ├─ used  src/doi:10.1007/s00204-020-02693-7  Designer drugs: mechanism of action and adverse effects
    ├─ used  src/doi:10.1016/j.neuropharm.2023.109827  Structure-activity relationships for locomotor stimulant effects and monoamine transporter interactions of substituted amphetamines and cathinones.
    ├─ used  src/doi:10.1016/j.jpba.2025.117170  Comparison of authentic urine N-ethylpentedrone metabolites to predicted in silico and in vitro human hepatocyte metabolism.
    ├─ used  src/doi:10.1016/j.jpba.2024.115994  Metabolic profile of N-ethylhexedrone, N-ethylpentedrone, and 4-chloromethcathinone in urine samples by UHPLC-QTOF-HRMS.
    ├─ used  src/doi:10.1002/dta.70047  Analytical Challenges in Detecting NPS in Anti-Doping: A Proof-of-Concept Involving Pentedrone Metabolite
    ├─ used  src/doi:10.1177/00045632251331404  Underreporting of synthetic cathinone poisoning with clinical immunoassays: An experimental and observational study.
    ├─ used  src/doi:10.1016/j.neuropharm.2021.108475  Role of amino terminal substitutions in the pharmacological, rewarding and psychostimulant profiles of novel synthetic cathinones.
    ├─ used  src/doi:10.1016/j.forsciint.2024.112204  New psychoactive substances - 96 cases of deaths related to their use based on forensic toxicological practice.
    ├─ used  src/doi:10.1111/adb.12299  The new stimulant designer compound pentedrone exhibits rewarding properties and affects dopaminergic activity.
    ├─ used  src/doi:10.2147/sar.s37257  Emerging drugs of abuse: current perspectives on substituted cathinones
    ├─ used  src/doi:10.1016/j.taap.2015.12.019  The combination of ethanol with mephedrone increases the signs of neurotoxicity and impairs neurogenesis and learning in adolescent CD-1 mice.
    └─ generated_by  pub/368957df-e308-43f2-8685-469d3d632881  Publication — backfill
├─ used  gen/ec7550e5-cb90-4737-9ea9-ffaf73e0b688  Generation — pipeline-v5
  ├─ derived_from  version/1  Revision 1
    ├─ derived_from  issue/notice@3f4c880461bf  Issued notice
    ├─ derived_from  issue/info_card@f7337863d805  Issued info_card
    ├─ derived_from  issue/emergency@58d3299a8754  Issued emergency
    ├─ derived_from  issue/info_card@b28e5806fbb9  Issued info_card
      ├─ used  claim/91586a95-22e0-457e-b0ff-246f4e679e3a  Claim in summary — supported
      ├─ used  claim/75084afb-c9d6-45f2-8933-44578f76e942  Claim in summary — supported
      ├─ used  claim/2f01591d-debe-4d1f-a6a6-5910a60215b0  Claim in history — supported
      ├─ used  claim/592848b4-a152-4e46-ac26-77fc3d31e225  Claim in neuroscience — supported
      ├─ used  claim/8e3fadf1-4f22-488c-8311-2630a92ce17c  Claim in pharmacology — supported
      ├─ used  claim/aeb45d6a-8bb9-4114-be88-632b3e550558  Claim in pharmacology — inconclusive  working
      ├─ used  claim/6a045d19-ee28-4cf5-b75c-feddac521e52  Claim in clinical-evidence — inconclusive  working
      ├─ used  claim/cc63e573-9256-467b-be9f-9823c3954115  Claim in safety — supported
      ├─ used  claim/7bd88152-0aaa-4602-b0d6-bee8ae665d26  Claim in safety — supported
      ├─ used  claim/eb0d5afb-5e11-421b-b5a7-198bd779d57f  Claim in safety — supported
      ├─ used  claim/fe358b03-c1c4-42ee-ba7a-d7ed550401f3  Claim in safety — supported
      ├─ used  claim/405b5e9f-dffe-4aae-ab9e-61d67de565d9  Claim in safety — supported
      ├─ used  claim/d3be5ba4-5337-4edf-ad82-4abbeaaf7195  Claim in safety — inconclusive  working
      ├─ used  claim/51da0ade-715f-4acd-9554-6e9c9d1013af  Claim in safety — supported
      ├─ used  claim/3f15c771-6bdb-4590-bcd3-1a2eb4f1c50f  Claim in safety — supported
      ├─ used  claim/06a4db62-bf2e-4778-8d04-3aa8937fe896  Claim in safety — supported
      ├─ used  claim/2cbe333e-e75d-4656-9bcc-5fc1ceed7b2c  Claim in safety — supported
      ├─ used  claim/5ef3b809-0228-47fd-b391-f5816bac7ea0  Claim in safety — supported
      ├─ used  claim/3f330345-1b64-4870-a3bf-e7af5ce3e212  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/05b09961-987f-484a-b3f3-a90127d42da4  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/dea85e7a-2b58-4e5d-81d0-0e0511631a46  Claim in clinical-evidence — supported
      ├─ used  claim/e4031c13-bb37-4e8e-aed6-2471ee7098d5  Claim in summary — supported
      ├─ used  claim/003d9f38-a8ff-4b43-b6c2-24137a0719a4  Claim in clinical-evidence — supported
      ├─ used  claim/e9be05b1-0b74-4cd9-95e1-cb24cde08b95  Claim in comparative-pharmacology — supported
      ├─ used  claim/feea2cb4-e170-4e9a-aeda-a6f4424fcf33  Claim in comparative-pharmacology — supported
      ├─ used  claim/53f40a85-1b65-4c25-bf63-7c8d0aa5b783  Claim in summary — supported
      ├─ used  claim/bb1ad99d-ed95-4228-a11c-90f53ad81c97  Claim in pharmacology — supported
      ├─ used  claim/d7f0cfe2-5829-4444-b6ff-b01282afcb3b  Claim in receptor-pharmacology — supported
      ├─ used  claim/288c0513-7640-4999-b9ab-408ad0947021  Claim in summary — supported
      ├─ used  claim/eb87d664-80d9-48f7-b17e-e5bc7b8418a2  Claim in pharmacology — supported
      ├─ used  claim/8ca967d7-eab9-4d34-a0d1-942e060d4428  Claim in chemistry — supported
      ├─ used  claim/4162e20a-4546-4e2a-9505-1b560e6b17b4  Claim in receptor-pharmacology — supported
      ├─ used  claim/588d524a-0d3a-4f04-8357-03b4012c2e54  Claim in receptor-pharmacology — supported
      ├─ used  claim/6de42a6d-7e62-4cb6-968a-01325c3c3df3  Claim in history — supported
      ├─ used  claim/7a6177f2-dfce-49fe-a6fd-4afd65ee64d9  Claim in summary — supported
      ├─ used  claim/adb4d8e0-5661-4444-b8d8-a181a0dde896  Claim in history — supported
      ├─ used  claim/bb583b39-28a7-4314-b172-bb6f4e264c5b  Claim in safety — inconclusive  working
      ├─ used  claim/d3a8895b-3eb1-4c82-8a56-83d240d0f599  Claim in history — not_supported  working
      ├─ used  claim/ae548c2a-8c87-4c81-9e03-cfb851c8e50f  Claim in chemistry — not_supported  working
      ├─ used  claim/3f01af74-1dd6-4ebe-a07f-8efaf32a0f1a  Claim in clinical-evidence — supported
      ├─ used  claim/96f5f344-cf35-47c5-a5c5-9c5573ac8e76  Claim in clinical-evidence — supported
      ├─ used  claim/3de5ca1b-9bd3-4d22-a281-046e69317e93  Claim in comparative-pharmacology — supported
      ├─ used  claim/e77b7653-2b82-4a41-9acd-d15ceb3a24b9  Claim in effects-overview — not_supported  working
      ├─ used  claim/86551c78-3368-4b55-ae1a-b2cf0cbba5d2  Claim in summary — supported
      ├─ used  claim/102f4d19-9758-4c60-87ad-e5153702482b  Claim in clinical-evidence — supported
      ├─ used  claim/0bf5246c-c31d-4674-a3b5-fcb0a6b29c64  Claim in clinical-evidence — supported
      ├─ used  claim/042f0b9e-f3cb-4459-a1f0-94d993c68446  Claim in neuroscience — supported
      ├─ used  claim/30950e07-cc74-4631-b86e-fda8eac161ee  Claim in neuroscience — supported
      ├─ used  claim/a801463f-36c0-4037-b8db-d57a72ee0250  Claim in neuroscience — supported
      ├─ used  claim/8e0005a1-7567-4359-a280-4d19fc1a9e51  Claim in neuroscience — partially_supported
      ├─ used  claim/8438409d-c9c8-4f43-b46d-af5377cbb0f0  Claim in neuroscience — supported
      ├─ used  claim/0a21114f-b5f0-4d99-ab5c-0267758ac51c  Claim in neuroscience — supported
      ├─ used  claim/49244c96-fd0d-41b9-aea1-1dd4b5ab3691  Claim in safety — supported
      ├─ used  claim/d6044bf0-003a-4f25-9e81-f68119c88785  Claim in safety — supported
      ├─ used  claim/7ea0298b-e65f-4a5e-96cf-df77dce05f15  Claim in safety — supported
      ├─ used  claim/12f93337-c946-4ab2-8166-c0ffff031ee8  Claim in safety — supported
      ├─ used  claim/f67bc3e1-341d-451c-adfa-ea3811cbd9fd  Claim in history — supported
      ├─ used  claim/ca50697c-3687-4222-b0bf-95694ea71ffe  Claim in clinical-evidence — supported
      ├─ used  claim/33619686-9014-41df-836f-c55f6327a68e  Claim in safety — supported
      ├─ used  claim/be66200a-ee67-4d84-a0f5-d048c7001738  Claim in history — not_supported  working
      ├─ used  claim/6ec80b9b-cb7c-47cc-9062-861fbc976db3  Claim in clinical-evidence — supported
      ├─ used  claim/416cde1d-b347-4293-a302-d735d6661d3b  Claim in chemistry — supported
      ├─ used  claim/47d55f7d-d66e-47ad-8581-e417d621101b  Claim in receptor-pharmacology — supported
      ├─ used  claim/6c3578d0-0d92-4463-874a-5550c3341558  Claim in chemistry — supported
      ├─ used  claim/d5e164d9-e4c6-4c5e-9dbd-17e50d0c5433  Claim in chemistry — supported
      ├─ used  claim/91bcbb50-8485-45b5-96bc-3762944635ff  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/14d9e416-fb96-4480-8a95-ace6312bbf1e  Claim in pharmacology — supported
      ├─ used  claim/ac1b6ba0-db27-4d8e-9b1e-a7c13436865d  Claim in safety — inconclusive  working
      ├─ used  claim/82316b28-efd1-40cc-99ce-3150a9067b10  Claim in comparative-pharmacology — supported
      ├─ used  claim/3b361b44-5646-47da-8cd5-33d090c4ffb0  Claim in comparative-pharmacology — inconclusive  working
      ├─ used  claim/88fd57c9-df58-42af-8a1b-312a492c12ac  Claim in pharmacology — supported
      ├─ used  claim/8ecab559-db82-4c1a-86ad-b819e8817035  Claim in safety — supported
      ├─ used  claim/bc322e9b-15f4-43e3-b704-c407ce4a1fe4  Claim in neuroscience — supported
      ├─ used  claim/6d818554-bff1-491a-9aec-a02fc5e30170  Claim in pharmacology — supported
      ├─ used  claim/84e34586-dff9-4f63-9077-5fb5a47e7ef0  Claim in receptor-pharmacology — supported
      ├─ used  claim/4e3ec900-0b95-4a76-ab37-4637a8979fd6  Claim in pharmacology — supported
      ├─ used  claim/602ad08e-de6b-4ebf-958e-9df982e198ae  Claim in safety — supported
      ├─ used  claim/7dbc7424-dab4-4b84-b33b-8b9a21630a23  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/da0d4684-7527-40f9-834a-a25cb6982ccf  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/eddf474e-c5eb-481b-9187-9f1de4d13274  Claim in pharmacology — supported
      ├─ used  claim/600487b0-974a-4400-bf4f-39b5b75ac960  Claim in pharmacology — supported
      ├─ used  claim/7dc75cf1-0c2a-4a44-8e1a-ad6aaa529ef9  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/f8dc6df2-cf8b-4b73-b2cd-bf67c9cf77ea  Claim in pharmacokinetic-detail — supported
      ├─ used  claim/7b144d05-ea13-4317-a2b6-b4351cf45797  Claim in clinical-evidence — supported
      ├─ used  claim/06927e5d-354f-4abf-bbce-571720142622  Claim in pharmacology — supported
      ├─ used  claim/3aa18dc8-6d21-4961-bcc8-6199c399b163  Claim in pharmacology — supported
      ├─ used  claim/44a19a8d-f576-47c4-8e6e-e9aa487cbba9  Claim in clinical-evidence — supported
      ├─ used  claim/afb0c1c6-ce76-4078-840e-12442b3e1a01  Claim in safety — supported
      ├─ used  claim/ac444b36-b9f0-43a1-8cf7-c5da89821749  Claim in safety — supported
      ├─ used  claim/4de1fced-8986-4b29-b126-2c8c3ca57697  Claim in clinical-evidence — partially_supported
      ├─ used  claim/373a5e8d-534b-4a5a-b5c4-22303562e321  Claim in comparative-pharmacology — supported
      ├─ used  claim/a43ec9e9-ed0e-4e6c-8b7d-349a441508a4  Claim in safety — supported
      ├─ used  claim/e32a1f42-c000-4bef-ac41-aed7be7b8cf0  Claim in safety — supported
      ├─ used  claim/601426b3-928a-4aec-a3ff-1befb4e0baf6  Claim in neuroscience — supported
      ├─ used  claim/8b3aa222-f374-4096-b8e6-a653a6fd66db  Claim in safety — supported
      └─ used  claim/75e3245f-2e38-46f6-91a4-637e6878fff3  Claim in safety — supported
… closure truncated at 200 nodes

indented by distance from this node, not by parentage

1Provenance card

the boundary, as counts

Sources

2522 with DOI

1 strong · 18 moderate · 6 weak

Compilations

12026-04-26T19:45:03.334Z

pipeline-v5 · prompt hash not recorded — run predates 2026-09

Decisions

44last ruled 2026-06-04

0 awaiting a ruling

Issued documents

42026-10-19T20:33:18.417Z

notice · info card · emergency

Searches

191 with no results

queries and counts on the build

Claims checked

9686 supported

86 supported · 10 not

Correspondence

0received

consent field ships in Phase 4

Edges

293

derivations recorded for this entity

Complete over 25 sources, 1 compilation, and 44 decisions.Not here: the private journal (never).Working material — drafts, discards, unsupported claims — is listed below and readable on the working page.Cite: psychedex.org/substances/nep/archive

2Build

one panel per compilation run

generation run 2026-04-26

69 min completedmodel pipeline-v5plan not recordedrun/86eea338…

Selection

results seen70
selected by the model32
consumed as sources25

Verification

claims checked96
supported84
partially supported2
not supported4
inconclusive6
  • record
  • seen / partial
  • working

The model's own caveats

  • sparse_evidence
  • no_clinical_guidelines

Reproduce

inputs
25 source keys (listed under Sources)
plan
not recorded — template version, prompt hash and git SHA are written from 2026-09 onward
model
pipeline-v5
streams
none — agent transcripts are persisted from 2026-09 onward
19 searches — query, source, results, what was kept and why
19 searches for this run
#sourcequeryseenkeptrationale
1WebSearch + WebFetchN-ethylpentedrone NEP legal status controlled substance UK US EU scheduling102Provides legal status overview for key jurisdictions
2PubMedN-Ethylpentedrone stimulant synthetic cathinone74All contain NEP-specific data
3PubMedNEP N-Ethylpentedrone cathinone pharmacology22Both directly concern NEP; selected for metabolic and analytical data
4OpenAlexN-ethylpentedrone synthetic cathinone101Duart-Castells 2021 is landmark paper for cathinone pharmacology with terminal substitution SAR
5PubMedSimmler Liechti cathinone pharmacological characterization designer beta-keto22Pentedrone (NEP's parent compound) characterized as non-releasing NE/DA reuptake inhibitor — key structural analog data
6PubChemNEP N-Ethylpentedrone / 2-(ethylamino)-1-phenylpentan-1-one11Only result; confirms seed data chemical identity
7WebFetch—10Inaccessible in text form; web search metadata used instead
8PubMedN-ethylpentedrone forensic detection mass spectrometry41New result about pentedrone metabolite detection in anti-doping samples
9PubMedDaziani NEP hepatocyte metabolism authentic urine metabolites11Key paper for NEP metabolic pathway data
10PubMedPMID lookup for Gatch 2025, Massano 2024, Kolaczynska 202133Key pharmacological and dosing data confirmed
11PubMedcathinone amphetamine SAR locomotor transporter substitution N-ethyl 202411SAR data directly relevant to understanding how NEP's N-ethyl group affects its pharmacological profile
12Crossref via verify_doiDOI verification for key papers22DOI verification for api_verified status
13PubMedN-ethyl-pentedrone aggression social behavior mice withdrawal repeated administration11Only published animal study of repeated NEP administration; crucial for dependence/withdrawal characterization
14PubChem REST API—13Primary source for all chemical identity data
15PubMedpentedrone cathinone reward dopamine self-administration conditioned place preference11Closest structural analog study (pentedrone) on reward/dopamine effects - informs NEP abuse potential
16PubMedNPS deaths cathinone Poland forensic 202431Toxicity/fatality context for synthetic cathinone class including NEP
17WebSearchNEP N-ethylpentedrone DEA scheduling Federal Analog Act US103Establishes US legal status as unscheduled but DEA-monitored
18WebSearchN-ethylpentedrone UK Psychoactive Substances Act EU EUDA initial report 2025103Completes legal status across key jurisdictions
19ClinicalTrials.gov · absenceN-ethylpentedrone synthetic cathinone00Confirms no registered trials; gap to flag in output
96 claims by section — every cited sentence, checked against its source
safety26 · 23 ok
  • In mice, withdrawal from repeated NEP administration produces increased aggressive behavior, persistently impaired social exploration, and abolition of the anxiolytic effect observed during acute exposuresupported

    Acute: anxiolytic effects. Withdrawal: increased aggression, persistently impaired social exploration. j.pnpbp.2022.110562

  • The most detailed acute toxicity data derive from the Belgian case report: a male patient developed severe agitation, delusions of persecution, tachycardia, mydriasis, and fever following intranasal NEP administration, progressing to rhabdomyolysis, acute renal failure, metabolic acidosis, and coma requiring ICU admission and mechanical ventilation for three dayssupported

    male patient snorted NEP, admitted with severe agitation, delusions of persecution, tachycardia, mydriasis, fever; developed renal failure, rhabdomyolysis, metabolic acidosis, coma. Intubated 3 days. bkac092

  • Complete recovery was achieved with supportive care.supported

    Recovery complete. bkac092

  • In mice, NEP produces slight hyperthermia at 10 mg/kg (i.p.) and reduced weight gain with repeated dosing.supported

    Acute: slight hyperthermia. Withdrawal: reduced weight gain. j.pnpbp.2022.110562

  • Tachycardia is confirmed in clinical case reportssupported

    admitted with severe agitation, delusions of persecution, tachycardia, mydriasis, fever. bkac092

  • Rhabdomyolysis and acute renal failure are documented as NEP-attributable sequelae in a single case reportsupported

    developed renal failure, rhabdomyolysis, metabolic acidosis, coma. bkac092

  • Fever is documented in the clinical case, and slight hyperthermia occurs in mice at 10 mg/kg.supported

    admitted with severe agitation, delusions of persecution, tachycardia, mydriasis, fever. bkac092

  • Fever is documented in the clinical case, and slight hyperthermia occurs in mice at 10 mg/kg.supported

    Acute: anxiolytic effects, reduced social exploration, slight hyperthermia. j.pnpbp.2022.110562

  • NEP was detected in blood samples from 26 fatal and 2 non-fatal poisoning cases in Polandsupported

    26 fatal and 2 non-fatal cases with synthetic cathinones in Poland. NEP among most commonly detected. bkab119

  • In a broader forensic series of 96 NPS-related fatalities, synthetic cathinones were detected in 67% of cases, with alcohol co-detected in 27 cases (blood alcohol 0.6–3.6‰).supported

    96 NPS-related fatalities from forensic practice 2010-2023. Synthetic cathinones in 67% of cases. Ethanol co-detected in 27 cases (0.6-3.6‰). j.forsciint.2024.112204

  • Management is supportive, extrapolated from cocaine and amphetamine overdose protocolssupported

    No specific antidote; management extrapolated from cocaine/amphetamines. sar.s37257

  • Claim in safety — inconclusiveinconclusiveworking →

  • Acute psychological adverse effects documented in case reports include severe agitation, delusions of persecution, and paranoiasupported

    admitted with severe agitation, delusions of persecution. bkac092

  • In the overdose context described by Deville et al., the patient exhibited persecutory delusions before progressing to coma.supported

    admitted with severe agitation, delusions of persecution... coma. bkac092

  • Repeated NEP administration in mice (twice daily for 5 days) produces robust striatal ΔFosB accumulation — the most reliable molecular marker of addiction vulnerability — alongside decreased striatal dopamine and elevated corticosterone during withdrawalsupported

    repeatedly (twice/day, 5 days). Withdrawal: elevated corticosterone, decreased striatal dopamine. Robust ΔFosB increase in striatum suggests high dependence risk. j.pnpbp.2022.110562

  • The structural precursor pentedrone maintains self-administration in rats at 0.3 mg/kg/infusion and produces conditioned place preference at 3–10 mg/kg.supported

    self-administration (0.3 mg/kg/infusion) in rodents. Conditioned place preference (3, 10 mg/kg). adb.12299

  • Claim in safety — inconclusiveinconclusiveworking →

  • DAT-predominant cathinones carry the highest addiction liability among the three cathinone pharmacological groupssupported

    Dopaminergic drugs highly addictive; toxicity includes prolonged stimulation, insomnia, agitation, psychosis. s00204-020-02693-7

  • Claim in safety — inconclusiveinconclusiveworking →

  • Approximately 95% of synthetic cathinone users co-use alcoholsupported

    ~95% of cathinone consumers combine with alcohol. j.taap.2015.12.019

  • In adolescent mice, the ethanol-mephedrone combination potentiates neurotoxicity approximately 2-fold compared to either substance alonesupported

    Mephedrone + ethanol combination in mice: 2-fold increase in neurotoxicity markers. j.taap.2015.12.019

  • In the forensic series reported by Rojek et al., alcohol was co-detected in 27 of 96 NPS-related fatalities (blood alcohol 0.6–3.6‰)supported

    Ethanol co-detected in 27 cases (0.6-3.6‰). j.forsciint.2024.112204

  • NEP's CYP metabolism profile has not been characterizedsupported

    20 metabolites identified via hepatocyte incubation; 18 confirmed in authentic human urine. Major pathways: N-deethylation, carbonyl reduction. j.jpba.2025.117170

  • Cardiovascular disease (hypertension, coronary artery disease, arrhythmias, structural heart disease) represents an absolute contraindication given the confirmed tachycardia and expected noradrenergic-mediated cardiovascular stresssupported

    admitted with severe agitation, delusions of persecution, tachycardia, mydriasis, fever. bkac092

  • Renal impairment constitutes a relative contraindication in light of the documented rhabdomyolysis and acute renal failure.supported

    developed renal failure, rhabdomyolysis, metabolic acidosis, coma. bkac092

  • Psychotic disorders and bipolar disorder represent relative contraindications, as dopaminergic stimulation may precipitate or exacerbate psychotic episodes — a risk supported by the persecutory delusions documented in the overdose casesupported

    admitted with severe agitation, delusions of persecution. bkac092

clinical-evidence12 · 11 ok
  • The only controlled human administration of NEP appears in Massano et al., where volunteers received 20–40 mg intranasally or orally as part of a metabolic profiling studysupported

    Human volunteers administered 20-40 mg NEP intranasally or orally. j.jpba.2024.115994

  • Claim in clinical-evidence — inconclusiveinconclusiveworking →

  • Pieprzyca et al. identified NEP among the most frequently detected synthetic cathinones in blood samples from a series of 26 fatal and 2 non-fatal poisoning casessupported

    26 fatal and 2 non-fatal cases with synthetic cathinones in Poland. NEP among most commonly detected. bkab119

  • Rojek et al. analyzed 96 NPS-related fatalities from 2010–2023, finding synthetic cathinones in 67% of casessupported

    96 NPS-related fatalities from forensic practice 2010-2023. Synthetic cathinones in 67% of cases. j.forsciint.2024.112204

  • In drug discrimination assays, NEP fully substituted for both cocaine (10 mg/kg) and methamphetamine (1 mg/kg) discriminative stimulus cues in rats.supported

    NEP fully substituted for cocaine and methamphetamine discriminative cues. j.pbb.2025.174100

  • Espinosa-Velasco et al. investigated acute and repeated NEP exposure in male OF1 mice (i.p. 1, 3, 10 mg/kg, twice daily for 5 days)supported

    Male OF1 mice treated acutely (1,3,10 mg/kg i.p.) and repeatedly (twice/day, 5 days) with NEPD. j.pnpbp.2022.110562

  • Neurochemically, withdrawal was associated with increased plasma corticosterone, decreased striatal dopamine, and robust long-lasting ΔFosB accumulation in the striatum.supported

    Withdrawal: elevated corticosterone, decreased striatal dopamine. Robust ΔFosB increase in striatum suggests high dependence risk. j.pnpbp.2022.110562

  • Deville et al. reported a male patient presenting to the emergency department following intranasal NEP use with severe agitation, delusions of persecution, tachycardia, mydriasis, and feversupported

    male patient snorted NEP, admitted with severe agitation, delusions of persecution, tachycardia, mydriasis, fever. bkac092

  • Drevin et al. reported NEP detection in the plasma and urine of a 36-year-old male victim of drug-facilitated sexual assault, confirmed by LC-HRMSsupported

    NEPD detected in plasma and urine of 36-year-old male victim of DFSA via LC-HRMS. j.forsciint.2024.112030

  • The authors note that NEP's limited entactogenic properties relative to methylone or mephedrone position it as more relevant to chemsex contexts than to classical DFSA scenarios, though the case demonstrates the potential for non-consensual administration.supported

    only small minority of users report entactogenic effects. NEPD more suitable for chemsex than DFSA context. j.forsciint.2024.112030

  • The study provides pioneering blood concentration data for NEP in poisoning contexts.supported

    Presents pioneering blood concentration data for NEP. bkab119

  • Alcohol was co-detected in 27 cases (blood alcohol 0.6–3.6‰), and co-use with opioids and benzodiazepines was common.partially supported

    Ethanol co-detected in 27 cases (0.6-3.6‰). 37 NPS and 9 metabolites detected. j.forsciint.2024.112204

pharmacology12 · 11 ok
  • Pentedrone (N-methylpentedrone) — differs from NEP only by a single methyl-to-ethyl substitution at the terminal amine. Simmler et al. characterized pentedrone as a non-releasing NE and DA uptake inhibitor in HEK-293 cells expressing human monoamine transporters.supported

    Pentedrone (NEP's parent compound) characterized as non-releasing NE and DA uptake inhibitor at human transporters. j.neuropharm.2013.11.008

  • N-Ethylhexedrone (NEH) — one additional α-chain carbon relative to NEP. Kolaczynska et al. reported DAT IC₅₀ = 0.17 µM and NET IC₅₀ = 0.18 µM in human transporter-expressing HEK-293 cells, with no SERT activity at concentrations below 10 µM (DAT/SERT selectivity ratio = 264–356). No compounds in the series induced monoamine efflux.supported

    NEH shows DAT IC50=0.17µM, NET IC50=0.18µM, >10µM at SERT. DAT/SERT ratio=264-356 for NEH. None induce monoamine efflux. ijms22158277

  • Within the three-group pharmacological classification of designer cathinones established by Simmler et al. — (1) non-selective monoamine uptake inhibitors (cocaine-like), (2) preferential DA/NE releasers (amphetamine-like), and (3) highly potent selective DAT/NET inhibitors without releasing activity (pyrovalerone-like) — NEP falls into Group 3 by structural and functional analogysupported

    Landmark paper: pharmacological classification of cathinones into three groups based on DAT/SERT selectivity and releasing vs inhibiting mechanism. Pyrovalerone and MDPV identified as highly potent selective DAT/NET transporter inhibitors without releasing activity. j.1476-5381.2012.02145.x

  • This classification predicts strong dopaminergic stimulant effects and elevated addiction liability relative to SERT-active cathinones.supported

    Dopaminergic drugs highly addictive; toxicity includes prolonged stimulation, insomnia, agitation, psychosis. s00204-020-02693-7

  • Fitzgerald et al. demonstrated that N-ethyl substitution on cathinone backbones augments relative SERT potency compared to N-methyl while reducing NET/DAT releasing effects — consistent with NEP's non-releasing NDRI profile.supported

    Para-chloro substitution or increased N-alkyl chain length augmented SERT potency. Combined para-chloro + N-ethyl substitutions reduced releasing at NET/DAT. j.neuropharm.2023.109827

  • Daziani et al. identified the primary metabolic pathways of NEP in human urine and hepatocyte incubations: N-deethylation constitutes the dominant route, with carbonyl reduction as a secondary pathwaysupported

    Major pathways: N-deethylation, carbonyl reduction, and their combination. j.jpba.2025.117170

  • Massano et al. confirmed the urinary metabolic profile following administration of 20–40 mg NEP (intranasal or oral) to human volunteers, identifying key metabolites via UHPLC-QTOF-HRMS.supported

    Human volunteers administered 20-40 mg NEP intranasally or orally. Phase-I and glucuronide (phase-II) metabolites identified. j.jpba.2024.115994

  • The Belgian case report by Deville et al. documents blood NEP concentrations exceeding 2,000 ng/mL with no measurable decline over a 17-hour observation window following intranasal administration — the only published quantitative plasma persistence datasupported

    Blood NEP >2000 ng/mL with no decrease over 17h — consistent with long half-life. bkac092

  • NEP shares the metabolite 2-amino-1-phenylpentan-1-ol with pentedrone and α-PVP, creating analytical challenges for anti-doping testingsupported

    Metabolite 2-amino-1-phenylpentan-1-ol identified in anti-doping sample; shared by pentedrone, α-PVP, and NEP. Highlights analytical challenges with NPS in doping control. dta.70047

  • Standard clinical immunoassays (EMIT-type amphetamine and MDMA screens) show poor cross-reactivity with synthetic cathinones including NEP, producing frequent false negativessupported

    SCs can produce false positives on MDMA and amphetamine immunoassays but may be missed by standard screening. 00045632251331404

  • Confirmatory identification requires LC-MS/MS or UHPLC-QTOF-HRMS methodology.supported

    Metabolic profile of N-ethylhexedrone, N-ethylpentedrone, and 4-chloromethcathinone in urine samples by UHPLC-QTOF-HRMS. j.jpba.2024.115994

  • Claim in pharmacology — inconclusiveinconclusiveworking →

neuroscience9 · 9 ok
  • Espinosa-Velasco et al. demonstrated that repeated NEP administration (1, 3, or 10 mg/kg i.p., twice daily for 5 days) in mice produces robust and long-lasting ΔFosB accumulation in the striatum. ΔFosB is a truncated splice variant of the FosB transcription factor that accumulates with chronic drug exposure and persists for weeks after cessationsupported

    Male OF1 mice treated acutely (1,3,10 mg/kg i.p.) and repeatedly (twice/day, 5 days) with NEPD. Robust ΔFosB increase in striatum suggests high dependence risk. j.pnpbp.2022.110562

  • The same study documented decreased striatal dopamine during withdrawal from repeated NEP administrationsupported

    Withdrawal: decreased striatal dopamine. j.pnpbp.2022.110562

  • Plasma corticosterone was elevated during NEP withdrawal in mice, indicating hypothalamic-pituitary-adrenal (HPA) axis activationsupported

    Withdrawal: elevated corticosterone. j.pnpbp.2022.110562

  • Acute NEP administration produced dose-dependent locomotor stimulation, anxiolytic effects, reduced social exploration, slight hyperthermia (at 10 mg/kg), and reduced weight gain in micepartially supported

    Acute: anxiolytic effects, reduced social exploration, slight hyperthermia. Withdrawal: increased aggression, persistently impaired social exploration, increased locomotor activity, reduced weight gain. j.pnpbp.2022.110562

  • During withdrawal, the anxiolytic effect was abolished, social exploration remained impaired, aggressive behavior increased, and locomotor activity was elevated — a behavioral profile consistent with dopaminergic sensitization and noradrenergic dysregulation.supported

    Withdrawal: increased aggression, persistently impaired social exploration, increased locomotor activity. j.pnpbp.2022.110562

  • In the Espinosa-Velasco data, the increased locomotor activity during withdrawal from repeated NEP likely reflects locomotor sensitizationsupported

    Withdrawal: increased locomotor activity. j.pnpbp.2022.110562

  • Does NEP's prolonged plasma persistence (>17 hours at >2,000 ng/mL in one case) reflect slow metabolism, extensive tissue distribution, or continued absorption? This question is critical for overdose management.supported

    Blood NEP >2000 ng/mL with no decrease over 17h — consistent with long half-life. bkac092

  • By blocking dopamine reuptake at presynaptic DAT terminals, NEP prolongs dopaminergic signaling in the NAc, producing the euphoric and motivational effects characteristic of psychostimulants.supported

    Cathinones/stimulants: primarily interact with monoamine transporters. Dopaminergic drugs highly addictive. s00204-020-02693-7

  • By blocking dopamine reuptake at presynaptic DAT terminals, NEP prolongs dopaminergic signaling in the NAc, producing the euphoric and motivational effects characteristic of psychostimulants.supported

    Mechanism: catecholamine release/reuptake inhibition. Desired effects: increased energy, empathy, libido. sar.s37257

pharmacokinetic-detail7 · 7 ok
  • Massano et al. administered 20–40 mg NEP intranasally or orally to human volunteers for metabolic profiling purposes; pharmacokinetic parameters (Tmax, Cmax, AUC) were not reported as study endpointssupported

    Human volunteers administered 20-40 mg NEP intranasally or orally. Phase-I and glucuronide (phase-II) metabolites identified. j.jpba.2024.115994

  • Urinary metabolites are detectable by UHPLC-QTOF-HRMS following doses of 20–40 mgsupported

    Human volunteers administered 20-40 mg NEP intranasally or orally. Phase-I and glucuronide (phase-II) metabolites identified. Urine collected 0-5h post-administration. j.jpba.2024.115994

  • These pathways were characterized in both authentic human urine samples and in vitro human hepatocyte incubations, with good concordance between the two systems. In silico metabolite prediction also demonstrated agreement with experimental findings.supported

    20 metabolites identified via hepatocyte incubation; 18 confirmed in authentic human urine. j.jpba.2025.117170

  • These pathways were characterized in both authentic human urine samples and in vitro human hepatocyte incubations, with good concordance between the two systems. In silico metabolite prediction also demonstrated agreement with experimental findings.supported

    20 metabolites identified via hepatocyte incubation; 18 confirmed in authentic human urine. j.jpba.2025.117170

  • The sole published plasma persistence data derive from a case of severe intoxication: blood NEP concentrations exceeded 2,000 ng/mL with no measurable decrease over 17 hours of monitoring following intranasal administrationsupported

    Blood NEP >2000 ng/mL with no decrease over 17h — consistent with long half-life. bkac092

  • Enantioselective analysis of NEP and metabolites in oral fluid and urine has been demonstrated using SFC-MS/MS.supported

    SFC-MS/MS method for enantioselective separation and detection of NEP and major phase-1 metabolites in human oral fluid and urine. j.jpba.2026.117474

  • <div class="compact-kv"> <table> <tbody> <tr><td>Oral bioavailability</td><td>Not determined</td></tr> <tr><td>Tmax</td><td>Not determined</td></tr> <tr><td>Elimination half-life</td><td>Not determined (>17 h implied by case data)</td></tr> <tr><td>Volume of distribution</td><td>Not determined</td></tr> <tr><td>Protein binding</td><td>Not determined</td></tr> <tr><td>Primary metabolism</td><td>N-deethylation, carbonyl reduction</td></tr> <tr><td>CYP enzymes</td><td>Not characterized (CYP2D6, CYP3A4 suspected)</td></tr> <tr><td>Active metabolites</td><td>Not determined</td></tr> </tbody> </table> </div>supported

    Blood NEP >2000 ng/mL with no decrease over 17h — consistent with long half-life. bkac092

summary7 · 7 ok
  • Case data suggest a prolonged pharmacokinetic profile, with plasma concentrations exceeding 2,000 ng/mL showing no decline over 17 hours following intranasal administration.supported

    Blood NEP >2000 ng/mL with no decrease over 17h — consistent with long half-life. bkac092

  • A DEA-commissioned behavioral study classified NEP as producing psychostimulant effects with abuse liability comparable to cocaine and methamphetaminesupported

    NEP fully substituted for cocaine and methamphetamine discriminative cues. Suggests high abuse liability similar to cocaine/methamphetamine. j.pbb.2025.174100

  • NEP is presumed to act as a non-releasing norepinephrine-dopamine reuptake inhibitor (NDRI) based on structural analogy with pentedrone and N-ethylhexedrone (DAT IC₅₀ = 0.17 µM, NET IC₅₀ = 0.18 µM, negligible SERT activity)supported

    Pentedrone (NEP's parent compound) characterized as non-releasing NE and DA uptake inhibitor at human transporters. j.neuropharm.2013.11.008

  • NEP is presumed to act as a non-releasing norepinephrine-dopamine reuptake inhibitor (NDRI) based on structural analogy with pentedrone and N-ethylhexedrone (DAT IC₅₀ = 0.17 µM, NET IC₅₀ = 0.18 µM, negligible SERT activity)supported

    NEH (N-ethylhexedrone, one-carbon homolog of NEP) shows DAT IC50=0.17µM, NET IC50=0.18µM, >10µM at SERT. None induce monoamine efflux. ijms22158277

  • The resulting pharmacological profile predicts cocaine-like sympathomimetic stimulation — tachycardia, mydriasis, psychomotor activation, appetite suppression — with minimal entactogenic or serotonergic charactersupported

    only small minority of users report entactogenic effects. j.forsciint.2024.112030

  • A single case report documents rhabdomyolysis, acute renal failure, metabolic acidosis, and coma as sole-substance sequelae of intranasal NEPsupported

    male patient snorted NEP... developed renal failure, rhabdomyolysis, metabolic acidosis, coma. bkac092

  • Repeated administration in mice produces robust striatal ΔFosB accumulation and decreased dopamine during withdrawal — molecular signatures predicting high dependence liabilitysupported

    Robust ΔFosB increase in striatum suggests high dependence risk. Withdrawal: decreased striatal dopamine. j.pnpbp.2022.110562

comparative-pharmacology6 · 5 ok
  • In drug discrimination assays, NEP fully substituted for both cocaine (10 mg/kg) and methamphetamine (1 mg/kg) discriminative stimulus cues in rats, confirming functional overlap with both reference stimulants.supported

    NEP fully substituted for cocaine and methamphetamine discriminative cues. Suggests high abuse liability similar to cocaine/methamphetamine. j.pbb.2025.174100

  • The structural precursor pentedrone maintains responding in self-administration paradigms and produces conditioned place preference at 3 and 10 mg/kg in ratssupported

    Pentedrone (NEP parent compound) shows rewarding properties in conditioned place preference (3, 10 mg/kg) and self-administration (0.3 mg/kg/infusion) in rodents. adb.12299

  • Gatch et al. directly compared locomotor stimulant effects of NEP against four other synthetic cathinones in micesupported

    DEA-identified cathinones including NEP tested in mice/rats. Rank order potency: 4-MEAP > NEP > N-ethylheptedrone > 4-methylpentedrone. j.pbb.2025.174100

  • Only a small minority of users report mild MDMA-like effectssupported

    only small minority of users report entactogenic effects. j.forsciint.2024.112030

  • This pharmacological distinction has practical implications: NEP produces a dopaminergic stimulant experience that is mechanistically more comparable to cocaine than to mephedrone.supported

    Pyrovalerone and MDPV identified as highly potent selective DAT/NET transporter inhibitors without releasing activity. j.1476-5381.2012.02145.x

  • Claim in comparative-pharmacology — inconclusiveinconclusiveworking →

history6 · 4 ok
  • NEP has also appeared in chemsex settings, where its stimulant profile without entactogenic properties positions it distinctly among synthetic cathinones.supported

    NEPD more suitable for chemsex than DFSA context. Only small minority of users report entactogenic effects. j.forsciint.2024.112030

  • By 2022, NEP had emerged among the most frequently detected synthetic cathinones in fatal poisoning cases in Poland, where a forensic toxicological analysis identified it in blood samples from 26 fatal and 2 non-fatal casessupported

    26 fatal and 2 non-fatal cases with synthetic cathinones in Poland. NEP among most commonly detected. bkab119

  • Case reports from 2023–2024 documented severe ICU-level toxicity in Belgium and use in a drug-facilitated sexual assault context in Francesupported

    Intubated 3 days. Blood NEP >2000 ng/mL with no decrease over 17h — consistent with long half-life. Recovery complete. bkac092

  • Case reports from 2023–2024 documented severe ICU-level toxicity in Belgium and use in a drug-facilitated sexual assault context in Francesupported

    NEPD detected in plasma and urine of 36-year-old male victim of DFSA via LC-HRMS. j.forsciint.2024.112030

  • Claim in history — not_supportednot supportedworking →

  • Claim in history — not_supportednot supportedworking →

chemistry5 · 4 ok
  • Structure-activity relationship analyses identify the size of the N-alkyl substituent and the α-chain length as the principal determinants of transporter selectivity and releasing vs. inhibiting mechanism in this series.supported

    Key structural features: nature of terminal amine, size of alpha-substituent, stereochemistry. These features determine whether compound acts as releasing agent or reuptake inhibitor, and transporter selectivity. 7854_2016_41

  • Structure-activity relationship analyses identify the size of the N-alkyl substituent and the α-chain length as the principal determinants of transporter selectivity and releasing vs. inhibiting mechanism in this series.supported

    Extension of alkyl chain enhances NET/DAT inhibition potency. ijms22158277

  • Cathinone derivatives including NEP exhibit chemical and stereochemical instability, particularly at elevated pHsupported

    Demonstrates stereochemical instability at high pH. j.jpba.2026.117474

  • An SFC-MS/MS method provides efficient chiral separation of both enantiomers and their polar metabolites in oral fluid and urine matricessupported

    SFC-MS/MS method for enantioselective separation and detection of NEP and major phase-1 metabolites in human oral fluid and urine. j.jpba.2026.117474

  • Claim in chemistry — not_supportednot supportedworking →

receptor-pharmacology5 · 5 ok
  • NEP's position between pentedrone and NEH in α-chain length, combined with its shared N-ethyl substituent with NEH, predicts a DAT/NET inhibition profile of comparable or slightly lower potency than NEH (IC₅₀ values in the low-to-sub-micromolar range) with negligible SERT activity.supported

    NEH shows DAT IC50=0.17µM, NET IC50=0.18µM, >10µM at SERT. Extension of alkyl chain enhances NET/DAT inhibition potency. ijms22158277

  • NEP's position between pentedrone and NEH in α-chain length, combined with its shared N-ethyl substituent with NEH, predicts a DAT/NET inhibition profile of comparable or slightly lower potency than NEH (IC₅₀ values in the low-to-sub-micromolar range) with negligible SERT activity.supported

    Pentedrone (NEP's parent compound) characterized as non-releasing NE and DA uptake inhibitor at human transporters. j.neuropharm.2013.11.008

  • Glennon and Dukat identified terminal amine size and α-substituent chain length as the principal SAR determinants for cathinone transporter selectivitysupported

    Key structural features: nature of terminal amine, size of alpha-substituent. These features determine whether compound acts as releasing agent or reuptake inhibitor, and transporter selectivity. 7854_2016_41

  • Extension of the N-alkyl chain from methyl to ethyl tends to augment SERT potency relative to DAT/NET while reducing releasing efficacy, shifting the compound toward a pure uptake inhibitor profilesupported

    Para-chloro substitution or increased N-alkyl chain length augmented SERT potency. Combined para-chloro + N-ethyl substitutions reduced releasing at NET/DAT. j.neuropharm.2023.109827

  • Kolaczynska et al. demonstrated that both N-ethyl substitution and longer α-chains enhance DAT/NET inhibition potency in the cathinone series.supported

    Extension of alkyl chain enhances NET/DAT inhibition potency. ijms22158277

effects-overview1 · 0 ok
  • Claim in effects-overview — not_supportednot supportedworking →

3Sources

25 consumed · sorted by year · feeds = sections resting on it

Sources
yearsourcetierstatusfeeds
2026Analytical Challenges in Detecting NPS in Anti-Doping: A Proof-of-Concept Involving Pentedrone MetaboliteKwiatkowska D, Peta B, Grucza K, et al. · Drug testing and analysisdoi:10.1002/dta.70047moderateconsumed1 section
2026Comparison of authentic urine N-ethylpentedrone metabolites to predicted in silico and in vitro human hepatocyte metabolism.Daziani G, Taoussi O, Berardinelli D, Bambagiotti G, Huestis MA, Busardò FP, Carlier J · Journal of pharmaceutical and biomedical analysisdoi:10.1016/j.jpba.2025.117170moderateconsumed3 sections
2026First enantioselective determination of N-ethylpentedrone and its major phase-1 metabolites using supercritical fluid chromatography coupled with tandem mass spectrometry and its application to human oral fluid and urine samples.Jorbenadze S, Tchelidze A, Sprega G, Tkemaladze V, Dolidze G, Minutillo A, Farré M, Poyatos L, Papaseit E, Basile G, Farkas T, Busardo FP, Chankvetadze B · Journal of pharmaceutical and biomedical analysisdoi:10.1016/j.jpba.2026.117474moderateconsumed2 sections
2025EUDA initial report on the new psychoactive substance N-ethylnorpentedrone (NEP)European Union Drugs Agency (EUDA)url:980a9e743d118ad6weakconsumedcited only
2025Locomotor stimulant and drug discrimination effects of five synthetic cathinones in rodentsGatch MB, Hill RD, Shetty RA, et al. · Pharmacology, biochemistry, and behaviordoi:10.1016/j.pbb.2025.174100moderateconsumed3 sections
2025Underreporting of synthetic cathinone poisoning with clinical immunoassays: An experimental and observational study.Willeman T, Laudet M, Revol B, Boudin C, Eysseric-Guerin H, Scolan V, Stanke-Labesque F · Annals of clinical biochemistrydoi:10.1177/00045632251331404moderateconsumed1 section
2024Metabolic profile of N-ethylhexedrone, N-ethylpentedrone, and 4-chloromethcathinone in urine samples by UHPLC-QTOF-HRMS.Massano M, Nuñez-Montero M, Papaseit E, Hladun O, Pérez-Mañá C, Ventura M, Marchei E, Alladio E, Gerace E, Pichini S, Farré M, Salomone A · Journal of pharmaceutical and biomedical analysisdoi:10.1016/j.jpba.2024.115994moderateconsumed3 sections
2024N-Ethylpentedrone PubChem Entry (CID 205593)National Center for Biotechnology Information (NCBI)url:99b110234253d97eweakconsumedcited only
2024New psychoactive substances - 96 cases of deaths related to their use based on forensic toxicological practice.Rojek S, Maciów-Głąb M, Romańczuk A, Kula K, Synowiec K, Kłys M · Forensic science internationaldoi:10.1016/j.forsciint.2024.112204moderateconsumed2 sections
2024Structure-activity relationships for locomotor stimulant effects and monoamine transporter interactions of substituted amphetamines and cathinones.Fitzgerald LR, Gannon BM, Walther D, Landavazo A, Hiranita T, Blough BE, Baumann MH, Fantegrossi WE · Neuropharmacologydoi:10.1016/j.neuropharm.2023.109827moderateconsumed2 sections
2024Synthetic cathinones in drug-facilitated sexual assault: A case report involving N-ethylpentedroneDrevin G, Gaulier JM, Hakim F, et al. · Forensic science internationaldoi:10.1016/j.forsciint.2024.112030weakconsumed7 sections
2023Synthetic Cathinones in Belgium: Two Case Reports with Different Outcomes Observed in the Emergency RoomDeville M, Fedorowicz R, Grandjean F, Simon M, Charlier C · Journal of analytical toxicologydoi:10.1093/jat/bkac092weakconsumed7 sections
2023Toxicological Analysis of Cases of Mixed Poisonings with Synthetic Cathinones and Other Drugs of Abuse.Pieprzyca E, Skowronek R, Czekaj P · Journal of Analytical Toxicologydoi:10.1093/jat/bkab119weakconsumed3 sections
2022Repeated administration of N-ethyl-pentedrone induces increased aggression and impairs social exploration after withdrawal in miceEspinosa-Velasco M, Reguilón MD, Bellot M, et al. · Progress in neuro-psychopharmacology & biological psychiatrydoi:10.1016/j.pnpbp.2022.110562moderateconsumed4 sections
2022Schedules of Controlled Substances: Placement of N-Ethylhexedrone, alpha-Pyrrolidinohexanophenone, 4-Methyl-alpha-ethylaminopentiophenone, 4′-Methyl-alpha-pyrrolidinohexiophenone, alpha-Pyrrolidinoheptaphenone, and 4′-Chloro-alpha-pyrrolidinovalerophenone in Schedule IDrug Enforcement Administration (DEA)url:3c0a926a9003c891weakconsumedcited only
2022Synthesis of emerging cathinones and validation of a SPE GC-MS method for their simultaneous quantification in blood.Júlio S, Ferro RA, Santos S, Alexandre A, Caldeira MJ · Analytical and Bioanalytical Chemistrydoi:10.1007/s00216-022-04440-6moderateconsumedcited only
2021Role of amino terminal substitutions in the pharmacological, rewarding and psychostimulant profiles of novel synthetic cathinones.Duart-Castells L, Nadal-Gratacós N, Muralter M, Puster B, Berzosa X, Estrada-Tejedor R, Niello M, Bhat S, Pubill D, Camarasa J, Sitte HH, Escubedo E, López-Arnau R · Neuropharmacologydoi:10.1016/j.neuropharm.2021.108475moderateconsumedcited only
2021The Pharmacological Profile of Second Generation Pyrovalerone Cathinones and Related Cathinone Derivative.Kolaczynska KE, Thomann J, Hoener MC, Liechti ME · International journal of molecular sciencesdoi:10.3390/ijms22158277moderateconsumed4 sections
2020Designer drugs: mechanism of action and adverse effectsLuethi D, Liechti ME · Archives of Toxicologydoi:10.1007/s00204-020-02693-7strongconsumed3 sections
2017Structure-Activity Relationships of Synthetic Cathinones.Glennon RA, Dukat M · Current topics in behavioral neurosciencesdoi:10.1007/7854_2016_41moderateconsumed2 sections
2017The new stimulant designer compound pentedrone exhibits rewarding properties and affects dopaminergic activity.Hwang JY, Kim JS, Oh JH, Hong SI, Ma SX, Jung YH, Ko YH, Lee SY, Kim HC, Jang CG · Addiction biologydoi:10.1111/adb.12299moderateconsumed2 sections
2016The combination of ethanol with mephedrone increases the signs of neurotoxicity and impairs neurogenesis and learning in adolescent CD-1 mice.Ciudad-Roberts A, Duart-Castells L, Camarasa J, Pubill D, Escubedo E · Toxicology and applied pharmacologydoi:10.1016/j.taap.2015.12.019moderateconsumed1 section
2014Emerging drugs of abuse: current perspectives on substituted cathinonesDebruyne D, Loilier M, Cesbron A, Le Boisselier R, Bourgine J · Substance Abuse and Rehabilitationdoi:10.2147/sar.s37257moderateconsumed2 sections
2014Monoamine transporter and receptor interaction profiles of a new series of designer cathinonesSimmler LD, Rickli A, Hoener MC, Liechti ME · Neuropharmacologydoi:10.1016/j.neuropharm.2013.11.008moderateconsumed3 sections
2012Pharmacological characterization of designer cathinones in vitroSimmler LD, Buser TA, Donzelli M, et al. · British Journal of Pharmacologydoi:10.1111/j.1476-5381.2012.02145.xmoderateconsumed3 sections
—Searched ClinicalTrials.gov for "N-ethylpentedrone synthetic cathinone" — no resultsabsenceno results—

4Docket

one filing per activity — decisions, correspondence, reports

  1. 0012026-04-26revisionRevision 1

    Initial LLM generation (v5 pipeline, wiki)

    psx:substance/nep/version/1
  2. 0022026-06-04proposal42 value proposals approved together

    one review action inferred from a shared reviewer and instant — the graph records one activity per proposal

    42 items in this filing

    • dose_tier · light
    • dose_tier · common
    • dose_tier · strong
    • dose_tier · heavy
    • timeline · insufflated · onset
    • timeline · insufflated · come_up
    • timeline · insufflated · peak
    • timeline · insufflated · plateau
    • timeline · insufflated · resolution
    • timeline · insufflated · afterglow
    • timeline · oral · onset
    • timeline · oral · come_up
    • timeline · oral · peak
    • timeline · oral · plateau
    • timeline · oral · resolution
    • timeline · oral · afterglow
    • toxicity
    • dependence · full
    • withdrawal
    • tolerance
    • dosage · insufflated
    • dosage · oral
    • duration · insufflated · onset
    • duration · insufflated · come_up
    • duration · insufflated · peak
    • duration · insufflated · offset
    • duration · insufflated · total
    • duration · insufflated · aftereffects
    • duration · oral · onset
    • duration · oral · come_up
    • duration · oral · peak
    • duration · oral · offset
    • duration · oral · total
    • duration · oral · aftereffects
    • contraindication · cardiovascular
    • contraindication · renal
    • contraindication · psychiatric
    • contraindication · psychiatric
    • contraindication · neurological
    • contraindication · pregnancy_breastfeeding
    • contraindication · other
    psx:substance/nep/proposal/dose_tier/e4fb04cf-595b-477a-9f83-121e1e5909d4
  3. 0032026-06-04publicationPublication — backfill

5Issued documents

what the notice, info card and emergency page said, by hash

Issued documents
documentcontent hashissuedfrom versionsuperseded
info_cardb28e5806fbb9bece2b96c59d…2026-10-19 20:33Revision 1current
emergency58d3299a8754d788e3d74c0e…2026-09-04 04:31Revision 1current
info_cardf7337863d805ea32396b8d59…2026-09-04 04:31Revision 1superseded2026-10-19
notice3f4c880461bf91f680f3c15d…2026-09-04 04:31Revision 1current