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psx:substance/diphenidine/claim/f42573ee-2e3a-4cdc-9b48-0b2c570fe106

claim2026-05-03recordsupported

feeds · downstream

Closure of psx:substance/diphenidine/claim/f42573ee-2e3a-4cdc-9b48-0b2c570fe106: 40 upstream, 82 downstream.

psx:substance/diphenidine/claim/f42573ee-2e3a-4cdc-9b48-0b2c570fe106
├─ used  src/doi:10.1002/dta.1946  Diphenidine, a new psychoactive substance: metabolic fate elucidated with rat urine and human liver preparations and detectability in urine using GC-MS, LC-MSn, and LC-HR-MSn
  ├─ informed_by  claim/f9d9028f-8735-4de9-8def-d0c903d04a06  Claim in pharmacokinetic-detail — supported
    ├─ used  src/doi:10.1371/journal.pone.0157021  Pharmacological Investigations of the Dissociative 'Legal Highs' Diphenidine, Methoxphenidine and Analogues
    ├─ used  src/url:79103079b3858529  WHO ECDD 43rd Meeting: Critical Review Report on Diphenidine
    ├─ used  src/doi:10.1007/164_2018_148  1,2-Diarylethylamine- and Ketamine-Based New Psychoactive Substances
    ├─ used  src/doi:10.1002/dta.1689  Preparation and characterization of the 'research chemical' diphenidine, its pyrrolidine analogue, and their 2,2-diphenylethyl isomers
    ├─ used  src/doi:10.3390/brainsci8040063  Mechanistic Insights into the Stimulant Properties of Novel Psychoactive Substances (NPS) and Their Discrimination by the Dopamine Transporter-In Silico and In Vitro Exploration of Dissociative Diarylethylamines
    ├─ used  src/doi:10.3109/15563650.2015.1033630  Intoxications by the dissociative new psychoactive substances diphenidine and methoxphenidine
    ├─ used  src/doi:10.1111/1556-4029.13355  A Case of Nonfatal Intoxication Associated with the Recreational use of Diphenidine
    ├─ used  src/url:fa9f1dd5951ccff4  ACMD Review of the Evidence on the Use and Harms of Diphenidine
    ├─ used  src/doi:10.3109/15563650.2014.974264  Acute toxicity associated with the recreational use of the novel dissociative psychoactive substance methoxphenidine
    ├─ used  src/doi:10.1007/s11419-014-0240-y  A large amount of new designer drug diphenidine coexisting with a synthetic cannabinoid 5-fluoro-AB-PINACA found in a dubious herbal product
    ├─ used  src/url:50e9b3a16f12af2d  Canada Gazette: Regulations Amending the Food and Drug Regulations (Parts G and J - Lefetamine, AH-7921, MT-45 and W-18)
    ├─ used  src/doi:10.1007/s11419-015-0300-y  Semiquantitation of diphenidine in tissue sections obtained from a human cadaver in a poisoning case by direct MALDI-QTOF mass spectrometry
    ├─ used  src/doi:10.1016/j.forsciint.2016.08.013  An overview of emerging and new psychoactive substances in the United Kingdom
    ├─ used  src/doi:10.1107/S2056989025001288
    ├─ used  src/doi:10.1016/j.jpba.2025.116728  Guilty by dissociation: Part C: Enantiomeric separation of diphenidine-derived new psychoactive substances (NPS) by polar organic chiral HPLC
    ├─ used  src/doi:10.1021/acs.jmedchem.5c02700  Bioisostere-Driven Discovery of SePP: A Selenium-Containing Polypharmacological Agent Relevant to Fragile X Syndrome
    ├─ used  src/pmid:27744478  Guilty by dissociation-development of gas chromatography-mass spectrometry (GC-MS) and other rapid screening methods for the analysis of 13 diphenidine-derived new psychoactive substances (NPSs)
    ├─ used  src/doi:10.1016/j.legalmed.2015.07.011  Identification and quantification of metabolites of AB-CHMINACA in a urine specimen of an abuser
    ├─ used  src/doi:10.1093/jat/bkv006  First Reported Fatalities Associated with the 'Research Chemical' 2-Methoxydiphenidine
    ├─ derived_from  gen/59503530-65c1-4b66-869a-e09370ab5433  Generation — pipeline-v5
    ├─ generated_by  pub/05944e28-bc80-4463-b985-c0213e60e1bc  Publication — backfill
      ├─ used  search/19705dbf-ceac-4eb2-9ee1-16d7c457397a  Searched PubChem for "Diphenidine"
      ├─ used  search/df0605c7-78da-4182-ae2d-8bc0dd2cd768  Searched PubMed for "Diphenidine NMDA receptor pharmacology"
      ├─ used  search/9503461f-e60a-4993-865e-8b30e89a3e95  Searched PubMed for "Diphenidine toxicology case report adverse effects"
      ├─ used  search/dc3561c6-6261-443a-95f7-56cced66f70d  Searched OpenAlex for "Diphenidine dissociative drug"
      ├─ used  search/2d58be8e-b2b9-45fb-b4b2-62fef81b2934  Searched ClinicalTrials.gov for "Diphenidine"
      ├─ used  search/fad43954-639c-4e6d-9a9d-e51ddbd474c1  Searched PubMed for "PMID 27314670"
      ├─ used  search/b8c46406-c0fe-42c5-81fe-6e87b3c8e15b  Searched PubMed for "PMID 26811026"
      ├─ used  search/5671d1d6-d0a0-48d4-8fcd-630dcf5e5fba  Searched PubMed for "diphenidine new psychoactive substance forensic detection analytical"
      ├─ used  search/2d3272ec-fe1c-49fe-84d9-03b494326ff2  Searched PubMed Central for "PMC4912077 full text Wallach 2016 diphenidine pharmacology"
      ├─ used  search/dae9ed4a-4a02-4380-aff0-5464e968041a  Searched PubMed for "PMID 29642450 Sahai 2018 DPH DAT dopamine"
      ├─ used  search/e43b63ca-aa6a-4a56-9fea-f24140534878  Searched WebSearch for "WHO ECDD 43rd expert committee diphenidine critical review schedule II 2021"
      ├─ used  search/205592c3-c7b3-4e37-90ee-8866aa99c145  Searched WebSearch for "diphenidine Searle patent 1989 history discovery"
      ├─ used  search/e54b3d0f-b400-4fb6-97c4-8a7a1ff5130c  Searched WebSearch for "diphenidine legal status scheduling UK US Canada Australia"
      ├─ used  search/480a4da9-33af-4445-837a-c4a66031b491  Searched CrossRef DOI verification for "DOI 10.1007/s11419-015-0300-y and related diphenidine Forensic Toxicology papers"
      ├─ used  search/6aa2dd59-cca1-4418-8f72-7c5445911ace  Searched GOV.UK ACMD for "ACMD review diphenidine use and harms"
      ├─ used  search/63e24208-9627-4db9-b0a0-a216ceeda508  Searched Canada Gazette for "diphenidine DEP Canada scheduling"
      └─ used  search/67508e55-a495-48b1-af65-1676b21147da  Searched WebSearch for "diphenidine EU Germany scheduling narcotic"
├─ informed_by  section/pharmacokinetic-detail.full@1
  ├─ used  version/1  Revision 1
  ├─ used  claim/7bd10fba-d106-4fdb-aafc-7dc667af321c  Claim in summary — not_supported  working
  ├─ used  claim/bda743c0-46c7-4333-9033-238ad388378a  Claim in pharmacology — supported
  ├─ used  claim/0885541f-1db0-47ad-9498-b25fd7d7ec48  Claim in pharmacology — supported
  ├─ used  claim/6049c433-4495-4715-9640-472d901efe64  Claim in safety — supported
  ├─ used  claim/ff35e1ac-7d7c-4c7d-a758-891fc981bbac  Claim in safety — supported
  ├─ used  claim/d53948f3-2ae9-43f8-9548-39aa910e972c  Claim in pharmacokinetic-detail — supported
  ├─ used  claim/75223cd8-e1b0-4aef-a131-d578df1b7a4e  Claim in pharmacokinetic-detail — inconclusive  working
    ├─ derived_from  issue/notice@c090e106affa  Issued notice
    ├─ derived_from  issue/info_card@bea672264454  Issued info_card
    ├─ derived_from  issue/emergency@ba304cf8bf8d  Issued emergency
    ├─ derived_from  issue/info_card@8177e6b20c60  Issued info_card
    ├─ informed_by  section/summary.full@1
    ├─ informed_by  section/pharmacology.full@1
    ├─ informed_by  section/safety.full@1
      ├─ used  claim/d2abafb8-67b9-44c4-9a42-4f5082aa4409  Claim in summary — supported
      ├─ used  claim/0ec01321-5d86-493d-b534-ddf914979435  Claim in summary — supported
      ├─ used  claim/c12aa8aa-edef-4d6f-a1ff-b0c4cf5a60f9  Claim in summary — supported
      ├─ used  claim/76e7cdd9-332d-471f-a9d4-96a09cab6e62  Claim in pharmacology — supported
      ├─ used  claim/c4d10ecf-1ec3-4b8c-80e5-32a0045507b8  Claim in pharmacology — supported
      ├─ used  claim/b35ee2d7-7678-47a0-b7dc-8beed19dd146  Claim in pharmacology — supported
      ├─ used  claim/ce82fad0-0308-4aef-a17d-10dbf3a560a1  Claim in pharmacology — inconclusive  working
      ├─ used  claim/38d08f29-8938-4dad-baba-ba96857944b4  Claim in receptor-pharmacology — supported
      ├─ used  claim/df2cbe65-2c53-475a-ae7e-a74c1de9d202  Claim in neuroscience — supported
      ├─ used  claim/bb19a220-10a0-44b2-92bd-4d5e696421c0  Claim in safety — supported
      ├─ used  claim/56046ab1-3442-4b78-90bb-a1e195b0d062  Claim in safety — supported
      ├─ used  claim/1c42e237-bb50-4566-b1d2-dcf6ea4b42f0  Claim in history — inconclusive  working
      ├─ used  claim/d588d727-8163-4ccd-9054-ff8e5c00e10f  Claim in history — supported
      ├─ used  claim/71d2682c-6d9a-4b98-8442-b1b3efb6c4f0  Claim in chemistry — inconclusive  working
      ├─ used  claim/bdbdf749-a6dd-4ae1-a7cc-0c5cc8f27116  Claim in receptor-pharmacology — supported
      ├─ used  claim/919b52c7-afd3-484f-a717-952c721dcd4a  Claim in comparative-pharmacology — supported
      ├─ used  claim/9dc4a998-2e15-4beb-b0d6-9e556b61ea2d  Claim in effects-overview — supported
      ├─ used  claim/f802e9ca-4b59-4ff7-b096-d5517653f4ec  Claim in summary — inconclusive  working
      ├─ used  claim/d4f2d866-d0b2-4fc1-b7d5-bb0989ac3685  Claim in history — inconclusive  working
      ├─ used  claim/b64bf998-459e-47fa-8f2f-48265f783ce1  Claim in history — inconclusive  working
      ├─ used  claim/03c006d9-0be0-4b9a-a567-f159310f5027  Claim in chemistry — inconclusive  working
      ├─ used  claim/db153ab3-c661-420b-a538-c07137f8b704  Claim in summary — inconclusive  working
      ├─ used  claim/3afea31b-acd4-40d9-b59d-11d9d11e3abc  Claim in pharmacology — supported
      ├─ used  claim/f9ec3b61-29d2-4c2e-a49e-3092a5f9e5ca  Claim in comparative-pharmacology — supported
      ├─ used  claim/a758b149-3212-436e-9c00-e38e6a7dc597  Claim in summary — supported
      ├─ used  claim/3d725ada-653f-4ee2-8eb0-105e7f7a0d4b  Claim in pharmacology — supported
      ├─ used  claim/706da3a5-e635-486a-b01f-0c4d16bd0a09  Claim in neuroscience — supported
      ├─ used  claim/3bc554c9-7cd3-46d5-8b0f-6eb0fd6a0487  Claim in safety — supported
      ├─ used  claim/b53ecd75-9665-4eb7-8170-c4409561f154  Claim in receptor-pharmacology — supported
      ├─ used  claim/367ba716-17d9-458a-b24a-dcf7681e4415  Claim in receptor-pharmacology — supported
      ├─ used  claim/b4ffc47c-c5ef-4504-9958-6604562af9a5  Claim in comparative-pharmacology — supported
      ├─ used  claim/9f88c981-4298-42e2-836b-894fda6998e0  Claim in neuroscience — supported
      ├─ used  claim/5968e2da-6f83-419e-92ea-b632d0066b9e  Claim in neuroscience — supported
      ├─ used  claim/781a308f-15e8-4177-9050-a617019791bf  Claim in summary — inconclusive  working
      ├─ used  claim/1d7c389a-5b22-4fc1-a5f3-79d320aaedde  Claim in summary — supported
      ├─ used  claim/12f896e7-7a45-4e5f-97df-d2e4e23c494d  Claim in history — partially_supported
      ├─ used  claim/7323549b-703b-4d05-b688-65a8bb16ab50  Claim in safety — supported
      ├─ used  claim/30f406c1-4a98-4bdc-9bcb-e96756db63f8  Claim in safety — supported
      ├─ used  claim/31a46bcf-667f-4068-88ef-bca4f942c142  Claim in safety — supported
      ├─ used  claim/e8f502bb-2701-4db8-aa1d-ba8af72afb41  Claim in safety — inconclusive  working
      ├─ used  claim/dfe0c9d9-5a6c-47a8-b15c-2792cdc34430  Claim in safety — inconclusive  working
      ├─ used  claim/9507bbec-fbdf-44f6-9b8e-2f3bb587091f  Claim in safety — supported
      ├─ used  claim/7623bedb-9d3a-4344-bee6-fec2e683a28b  Claim in clinical-evidence — supported
      ├─ used  claim/83b05274-23d4-462d-81d9-f3cac6053905  Claim in neuroscience — supported
      ├─ used  claim/619349fc-43f4-436a-86f3-df492a40256f  Claim in effects-overview — supported
      ├─ used  claim/4324adf6-08d9-4112-9d5f-0059749c7da1  Claim in summary — inconclusive  working
      ├─ used  claim/52bf81c4-d288-4381-94c7-90f12d9f5845  Claim in pharmacology — supported
      ├─ used  claim/0f898978-b8ea-4ae4-a269-d75dbdbd9390  Claim in clinical-evidence — supported
      ├─ used  claim/a44b2ce9-ccd7-4c5b-b557-2e973450e79e  Claim in safety — supported
      ├─ used  claim/acf899a8-7abd-42fc-8c02-4d2d3a1bb477  Claim in safety — supported
      ├─ used  claim/3b397ccc-66bf-4c40-930e-7178adbd1c48  Claim in safety — inconclusive  working
      ├─ used  claim/4e384953-6618-4259-be5e-116007488d95  Claim in safety — supported
      ├─ used  claim/1ccac05b-0e92-425c-9ca3-0527febe0074  Claim in safety — supported
      ├─ used  claim/39c74621-ec39-4f84-a295-c3c873e8a2fd  Claim in clinical-evidence — inconclusive  working
      ├─ used  claim/6fba7534-bca2-44b8-adfa-c91402361d26  Claim in effects-overview — inconclusive  working
      ├─ used  claim/66d3139d-e388-4561-8177-ecc4fb4e62de  Claim in history — supported
      ├─ used  claim/d0811c3e-3414-4d80-98ca-09f96ae88b9b  Claim in history — inconclusive  working
      ├─ used  claim/d48de068-939a-496f-bb3e-b7129307ba14  Claim in safety — inconclusive  working
      ├─ used  claim/9ceafd3c-30b7-4156-b997-def47d13d9cc  Claim in history — inconclusive  working
      ├─ used  claim/9fe20d4d-0714-474a-85b9-df1272587e2e  Claim in history — inconclusive  working
      ├─ used  claim/6306b073-4f97-4dfb-b079-3a337d053e9a  Claim in chemistry — supported
      ├─ used  claim/b8e27802-9c74-4f8e-addf-d067ad4656e3  Claim in chemistry — supported
      ├─ used  claim/8f4d9f3c-4603-4eac-ae6f-d4e5b369b36b  Claim in neuroscience — supported
      ├─ used  claim/b005954c-add4-4f53-868a-e8fafc9f8592  Claim in pharmacology — supported
      ├─ used  claim/91cd3447-d9a0-4e9e-ad13-62aae434d3a7  Claim in safety — supported
      └─ used  claim/7c966247-980d-46b8-9381-f1a933ea77b2  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

2016 with DOI

0 strong · 11 moderate · 9 weak

Compilations

12026-05-03T16:09:45.376Z

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

Decisions

46last ruled 2026-06-04

0 awaiting a ruling

Issued documents

42026-10-19T20:31:33.908Z

notice · info card · emergency

Searches

171 with no results

queries and counts on the build

Claims checked

7554 supported

54 supported · 21 not

Correspondence

0received

consent field ships in Phase 4

Edges

246

derivations recorded for this entity

Complete over 20 sources, 1 compilation, and 46 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/diphenidine/archive

2Build

one panel per compilation run

generation run 2026-05-03

65 min completedmodel pipeline-v5plan not recordedrun/1248f320…

Selection

results seen72
selected by the model43
consumed as sources20

Verification

claims checked75
supported53
partially supported1
not supported1
inconclusive20
  • record
  • seen / partial
  • working

The model's own caveats

  • sparse_evidence
  • dependence_values_unverified

Reproduce

inputs
20 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
17 searches — query, source, results, what was kept and why
17 searches for this run
#sourcequeryseenkeptrationale
1PubChemDiphenidine11Primary chemical identity source; fills missing fields in seed data (formula, weight, SMILES, InChIKey, CID)
2ClinicalTrials.gov · absenceDiphenidine00N/A - no trials registered
3PubMeddiphenidine new psychoactive substance forensic detection analytical33Analytical characterization papers for diphenidine
4PubMedDiphenidine toxicology case report adverse effects11References a fatal case involving diphenidine - need to find the primary 2015 Forensic Toxicol paper
5PubMedPMID 2681102611Only published study on diphenidine metabolism; critical for pharmacokinetics section
6OpenAlexDiphenidine dissociative drug104High-citation papers that cover diphenidine; Helander and Wallach are substance-specific
7PubMedDiphenidine NMDA receptor pharmacology109All directly relevant to diphenidine pharmacology, toxicology, or characterization
8PubMedPMID 2731467011Primary pharmacology paper for diphenidine
9WebSearchdiphenidine Searle patent 1989 history discovery94History and patent information for diphenidine
10PubMed CentralPMC4912077 full text Wallach 2016 diphenidine pharmacology15Critical quantitative pharmacology data
11PubMedPMID 29642450 Sahai 2018 DPH DAT dopamine11Important mechanistic data distinguishing DPH from MXP at DAT
12WebSearchWHO ECDD 43rd expert committee diphenidine critical review schedule II 202192International scheduling status confirmed
13WebSearchdiphenidine legal status scheduling UK US Canada Australia103Legal status data
14CrossRef DOI verificationDOI 10.1007/s11419-015-0300-y and related diphenidine Forensic Toxicology papers44Key Japan case papers and comprehensive review on diphenidine
15Canada Gazettediphenidine DEP Canada scheduling11Canadian legal scheduling confirmation
16WebSearchdiphenidine EU Germany scheduling narcotic92EU/Germany legal status data
17GOV.UK ACMDACMD review diphenidine use and harms11Authoritative UK government toxicological review
75 claims by section — every cited sentence, checked against its source
safety19 · 15 ok
  • Claim in safety — inconclusiveinconclusiveworking →

  • The best-characterized acute toxicity data come from the Swedish STRIDA case series (n = 17 cases, 14 confirmed diphenidine-positive):supported

    Case series of 17 patients: 14 diphenidine-positive, 3 MXP-positive. 15563650.2015.1033630

  • Median hospitalization was 2 days (range 1–3)supported

    Hospitalization 1-3 days. 15563650.2015.1033630

  • A single Italian case additionally documented miotic pupils (atypical for NMDA dissociatives), increased body temperature, and increased respiratory rate, though co-ingestion of methylphenidate and diclazepam confounded the presentation.supported

    Tachycardia, miotic pupils, elevated temperature and respiratory rate. Co-detected methylphenidate and diclazepam. 1556-4029.13355

  • A fatal case in Japan involved diphenidine alongside AB-CHMINACA and 5-fluoro-AMB; tissue distribution was mapped by MALDI-QTOF mass spectrometrysupported

    References an autopsy case (Forensic Toxicol 33:45-53, 2015) where death was caused by AB-CHMINACA, 5-fluoro-AMB and diphenidine combined. j.legalmed.2015.07.011

  • Three deaths attributed primarily to methoxphenidine also showed diphenidine and hydroxy-diphenidine in post-mortem blood, though it was unclear whether diphenidine arose from MXP biotransformation or separate intake.supported

    Three MXP-related deaths. Diphenidine and hydroxy-diphenidine also detected in post-mortem samples (uncertain if metabolite of MXP or separate compound). bkv006

  • Severe agitation and confusionsupported

    Common presentations: anxiety (65%), altered mental status (65%). 15563650.2015.1033630

  • Severe agitation and confusionsupported

    30-year-old male found confused, agitated, unable to communicate. 1556-4029.13355

  • Claim in safety — inconclusiveinconclusiveworking →

  • Inability to communicatesupported

    30-year-old male found confused, agitated, unable to communicate. 1556-4029.13355

  • Diphenidine's demonstrated increase in nucleus accumbens dopamine efflux engages the mesolimbic reward pathway and provides a mechanistic basis for potential addictive liabilitysupported

    DPH increased DA efflux via DAT binding (autoradiography and voltammetry). DPH suggested to have addictive liability unlike MXP. brainsci8040063

  • Diclazepam (a designer benzodiazepine) was co-detected in the Italian case report, and ethanol was among co-detected substances in the STRIDA series.supported

    Co-detected methylphenidate and diclazepam. 1556-4029.13355

  • Claim in safety — inconclusiveinconclusiveworking →

  • Claim in safety — inconclusiveinconclusiveworking →

  • Diphenidine's SERT IC₅₀ exceeds 10 μM, indicating negligible serotonin reuptake inhibitionsupported

    DPH and 2-MXP are relatively selective NMDAR antagonists with weak off-target effects on dopamine and norepinephrine reuptake. journal.pone.0157021

  • Diphenidine is metabolized by CYP1A2, CYP2B6, CYP2C9, CYP3A4, and CYP2D6supported

    CYP1A2, CYP2B6, CYP2C9, CYP3A4 form initial metabolites; CYP2D6 also involved. dta.1946

  • Pre-existing hypertension, cardiac arrhythmia, or structural heart disease constitute relative contraindications given the 76% hypertension rate and 47% tachycardia rate observed in hospitalized diphenidine casessupported

    Common presentations: hypertension (76%), tachycardia (47%). 15563650.2015.1033630

  • Diphenidine's NMDA antagonism produces hallucinations, delusions, and paranoia and disrupts sensorimotor gating (PPI), consistent with psychotomimetic potentialsupported

    DPH inhibited PPI with ED50 9.5 mg/kg in rats. journal.pone.0157021

  • Diphenidine undergoes extensive hepatic metabolism via multiple CYP enzymessupported

    CYP1A2, CYP2B6, CYP2C9, CYP3A4 form initial metabolites; CYP2D6 also involved. Metabolites detectable in rat urine at common user doses. dta.1946

pharmacology10 · 9 ok
  • Diphenidine functions as an uncompetitive (channel-blocking) NMDA receptor antagonistsupported

    DPH and 2-MXP are relatively selective NMDAR antagonists with weak off-target effects on dopamine and norepinephrine reuptake. journal.pone.0157021

  • Diphenidine functions as an uncompetitive (channel-blocking) NMDA receptor antagonistsupported

    DPH at 30 μM reduced NMDA-fEPSPs similarly to ketamine in rat hippocampal slices. dta.1689

  • A 2026 structure-activity relationship study explicitly characterizes diphenidine as "a prototypical 1,2-diarylethylamine that functions as an uncompetitive N-methyl-D-aspartate receptor (NMDAR) antagonist and monoamine reuptake inhibitor".supported

    Diphenidine as prototypical 1,2-diarylethylamine - uncompetitive NMDAR antagonist and monoamine reuptake inhibitor. acs.jmedchem.5c02700

  • At the NMDA receptor phencyclidine binding site, diphenidine displays a Kᵢ of 18.2 ± 2.2 nM — approximately 18-fold more potent than ketamine (~324 nM) at the same sitesupported

    Binding studies at 46 CNS receptors for DPH, 2-MXP and analogues. DPH and 2-MXP are relatively selective NMDAR antagonists. journal.pone.0157021

  • Beyond NMDA antagonism, diphenidine weakly inhibits monoamine reuptake: DAT IC₅₀ = 1.99 μM, NET IC₅₀ = 9.25 μM, and SERT IC₅₀ > 10 μM (effectively inactive)supported

    DPH and 2-MXP are relatively selective NMDAR antagonists with weak off-target effects on dopamine and norepinephrine reuptake. journal.pone.0157021

  • Autoradiography and fast cyclic voltammetry demonstrate that diphenidine increases dopamine efflux in rat nucleus accumbens slices through its DAT interaction, whereas the structurally related methoxphenidine does not produce this effectsupported

    DPH increased DA efflux via DAT binding (autoradiography and voltammetry); MXP had no significant effect on DAT. brainsci8040063

  • Claim in pharmacology — inconclusiveinconclusiveworking →

  • The metabolic fate of diphenidine has been elucidated using rat urine and pooled human liver microsomes (pHLM) and cytosol (pHLC)supported

    Metabolites identified in rat and human liver preparations. dta.1946

  • The enzymes CYP1A2, CYP2B6, CYP2C9, CYP3A4, and CYP2D6 are all capable of forming the initial metabolites (hydroxy-aryl, hydroxy-piperidine, bis-hydroxy-piperidine).supported

    CYP1A2, CYP2B6, CYP2C9, CYP3A4 form initial metabolites (hydroxy-aryl, hydroxy-piperidine, bis-hydroxy-piperidine); CYP2D6 also involved. dta.1946

  • Biofluid concentrations from a single analytically confirmed non-fatal intoxication case (30-year-old male, Italy) provide the only published human concentration data: plasma 308 ng/mL and urine 631 ng/mL at emergency department presentationsupported

    30-year-old male found confused, agitated, unable to communicate. DPH plasma 308 ng/mL, urine 631 ng/mL. 1556-4029.13355

summary10 · 5 ok
  • Its binding affinity at the NMDA phencyclidine site (Kᵢ = 18.2 ± 2.2 nM) exceeds that of ketamine (~324 nM) but remains below that of phencyclidinesupported

    Binding studies at 46 CNS receptors for DPH, 2-MXP and analogues. DPH and 2-MXP are relatively selective NMDAR antagonists with weak off-target effects on dopamine and norepinephrine reuptake. journal.pone.0157021

  • Claim in summary — not_supportednot supportedworking →

  • Claim in summary — inconclusiveinconclusiveworking →

  • Claim in summary — inconclusiveinconclusiveworking →

  • Binding and selectivity data across 46 CNS receptor sites were published the following yearsupported

    Binding studies at 46 CNS receptors for DPH, 2-MXP and analogues. journal.pone.0157021

  • Diphenidine blocks the open NMDA receptor ion channel at the phencyclidine binding site (Kᵢ = 18.2 nM), with secondary weak inhibition of dopamine reuptake (IC₅₀ = 1.99 μM) and negligible serotonin transporter activity (IC₅₀ > 10 μM)supported

    DPH and 2-MXP are relatively selective NMDAR antagonists with weak off-target effects on dopamine and norepinephrine reuptake. journal.pone.0157021

  • Unlike the structurally related methoxphenidine, diphenidine increases dopamine efflux in the nucleus accumbens — a functional difference with implications for reinforcement potential.supported

    DPH increased DA efflux via DAT binding (autoradiography and voltammetry); MXP had no significant effect on DAT. DPH suggested to have addictive liability unlike MXP. brainsci8040063

  • Claim in summary — inconclusiveinconclusiveworking →

  • Claim in summary — inconclusiveinconclusiveworking →

  • Acute toxicity includes hypertension (76% of hospitalized cases), tachycardia, and severe agitation requiring sedationsupported

    Common presentations: hypertension (76%), tachycardia (47%), anxiety (65%), altered mental status (65%). Treatment: benzodiazepines and/or propofol in 50%. 15563650.2015.1033630

history9 · 3 ok
  • The Swedish STRIDA project identified 14 analytically confirmed diphenidine intoxications by 2015, and a fatal case involving diphenidine in a multi-drug poisoning was reported in Japanpartially supported

    Case series of 17 patients: 14 diphenidine-positive, 3 MXP-positive. 15563650.2015.1033630

  • Claim in history — inconclusiveinconclusiveworking →

  • Searle & Co. filed European patent EP346791A1, titled "Preparation of 1,2-diarylethylamines for treatment of neurotoxic injury"supported

    References 1989 Searle Company patent as original source. 15563650.2014.974264

  • Claim in history — inconclusiveinconclusiveworking →

  • Claim in history — inconclusiveinconclusiveworking →

  • Claim in history — inconclusiveinconclusiveworking →

  • Claim in history — inconclusiveinconclusiveworking →

  • A comprehensive pharmacological investigation followed in 2016, profiling diphenidine across 46 CNS receptor sites and establishing its binding affinity and selectivity data.supported

    Binding studies at 46 CNS receptors for DPH, 2-MXP and analogues. journal.pone.0157021

  • Claim in history — inconclusiveinconclusiveworking →

neuroscience6 · 6 ok
  • PPI disruption in rats (ED₅₀ = 9.5 mg/kg) directly operationalizes the sensorimotor gating deficits central to this framework.supported

    DPH inhibited PPI with ED50 9.5 mg/kg in rats. journal.pone.0157021

  • Does nucleus accumbens dopamine efflux translate to human addiction liability? The mechanistic signal exists but no human dependence cases have been published.supported

    DPH increased DA efflux via DAT binding. DPH suggested to have addictive liability unlike MXP. brainsci8040063

  • Diphenidine's high NMDA affinity (Kᵢ = 18.2 nM) predicts potent disruption of these circuits, consistent with the prominent dissociation and hallucinations observed in clinical cases.supported

    Common presentations: altered mental status (65%), anxiety (65%). 15563650.2015.1033630

  • Diphenidine's demonstrated increase in dopamine efflux within the nucleus accumbens engages the mesolimbic reward pathway (ventral tegmental area → nucleus accumbens)supported

    DPH increased DA efflux via DAT binding (autoradiography and voltammetry). DPH suggested to have addictive liability unlike MXP. brainsci8040063

  • The dopamine efflux data position diphenidine within the incentive salience framework, where mesolimbic dopamine mediates "wanting" (motivational drive to consume) rather than "liking" (hedonic pleasure)supported

    DPH increased DA efflux via DAT binding. DPH suggested to have addictive liability unlike MXP. brainsci8040063

  • What is the enantioselective neuropharmacology? S-ketamine and R-ketamine show divergent neural effects. Diphenidine is used as a racemate, and the individual enantiomers have never been tested in any neural preparation.supported

    Real-life samples of DPH and 2-MXP confirmed to be sold as racemic products. j.jpba.2025.116728

chemistry4 · 2 ok
  • Claim in chemistry — inconclusiveinconclusiveworking →

  • Claim in chemistry — inconclusiveinconclusiveworking →

  • Analytical confirmation from real-world market samples demonstrates that diphenidine is sold as a racemic mixturesupported

    Real-life samples of DPH and 2-MXP confirmed to be sold as racemic products. j.jpba.2025.116728

  • Chiral HPLC methods capable of separating the enantiomers have been developed for forensic applicationssupported

    Chiral HPLC separation of 32 diphenidine-derived NPS. Real-life samples of DPH and 2-MXP confirmed to be sold as racemic products. Enantiomer elution order reversal observed between different CSP types. j.jpba.2025.116728

pharmacokinetic-detail4 · 3 ok
  • The metabolic pathway of diphenidine has been characterized using rat urine, pooled human liver microsomes (pHLM), and pooled human liver cytosol (pHLC).supported

    Metabolites identified in rat and human liver preparations. dta.1946

  • The involvement of multiple CYP isoforms in generating the same initial metabolites suggests that no single enzyme is the rate-limiting step in diphenidine clearance, which may reduce the significance of CYP polymorphism-related variabilitysupported

    CYP1A2, CYP2B6, CYP2C9, CYP3A4 form initial metabolites; CYP2D6 also involved. dta.1946

  • Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →

  • Validated GC-MS screening methods for 13 diphenidine-derived NPS have been publishedsupported

    GC-MS and rapid screening methods for 13 diphenidine-derived NPS encountered in casework. Validated screening and quantification method. pmid:27744478

receptor-pharmacology4 · 4 ok
  • The negligible SERT activity (IC₅₀ > 10 μM) distinguishes diphenidine from serotonergically active dissociatives such as methoxetamine and suggests low serotonin syndrome risk in the context of monoamine-mediated interactions.supported

    DPH and 2-MXP are relatively selective NMDAR antagonists with weak off-target effects on dopamine and norepinephrine reuptake. journal.pone.0157021

  • Binding studies across 46 CNS receptor sites using rat forebrain preparations provide the most comprehensive receptor pharmacology dataset for diphenidine.supported

    Binding studies at 46 CNS receptors for DPH, 2-MXP and analogues. journal.pone.0157021

  • Beyond transporter binding, autoradiography using [¹²⁵I]RTI-121 displacement in rat striatal sections and fast cyclic voltammetry in nucleus accumbens slices demonstrate that diphenidine increases evoked dopamine effluxsupported

    DPH increased DA efflux via DAT binding (autoradiography and voltammetry). brainsci8040063

  • Computational molecular dynamics simulations support differential binding poses at the transporter as the mechanistic basis for this distinction.supported

    Computational modeling supports DPH-DAT interaction. brainsci8040063

clinical-evidence3 · 2 ok
  • A single analytically confirmed non-fatal intoxication in a 30-year-old male presented with tachycardia, miotic pupils (atypical for NMDA dissociatives; mydriasis is more common), increased body temperature, and increased respiratory ratesupported

    Tachycardia, miotic pupils, elevated temperature and respiratory rate. DPH plasma 308 ng/mL, urine 631 ng/mL. 1556-4029.13355

  • The Swedish STRIDA project (a national clinical-toxicological surveillance system for NPS) identified 17 cases involving diphenidine or its analogue methoxphenidine, of which 14 were analytically confirmed as diphenidine-positivesupported

    Case series of 17 patients: 14 diphenidine-positive, 3 MXP-positive. 15563650.2015.1033630

  • Claim in clinical-evidence — inconclusiveinconclusiveworking →

comparative-pharmacology3 · 3 ok
  • Prepulse inhibition (PPI) of the acoustic startle reflex — a standard behavioural assay for dissociative potency — provides in vivo confirmation of the binding data:supported

    DPH inhibited PPI with ED50 9.5 mg/kg in rats. journal.pone.0157021

  • In rat hippocampal slices, diphenidine at 30 μM reduced NMDA-mediated field excitatory postsynaptic potentials (fEPSPs) to a similar extent as ketamine at the same concentration, confirming functional NMDA channel blockade in neural tissue.supported

    DPH at 30 μM reduced NMDA-fEPSPs similarly to ketamine in rat hippocampal slices. dta.1689

  • Diphenidine increases evoked dopamine efflux in rat nucleus accumbens; MXP does notsupported

    DPH increased DA efflux via DAT binding (autoradiography and voltammetry); MXP had no significant effect on DAT. brainsci8040063

effects-overview3 · 2 ok
  • Claim in effects-overview — inconclusiveinconclusiveworking →

  • Compared to ketamine, diphenidine occupies a similar functional space but with higher receptor potency (Kᵢ ~18 nM vs ~324 nM) that does not translate linearly to equipotent dosessupported

    Binding studies at 46 CNS receptors for DPH, 2-MXP and analogues. DPH and 2-MXP are relatively selective NMDAR antagonists. journal.pone.0157021

  • The subjective character is reported as "heavier" and more amnestic than ketamine, with a cardiovascular burden (76% hypertension in clinical cases) that exceeds what is typical for ketamine at recreational doses.supported

    Common presentations: hypertension (76%), tachycardia (47%), anxiety (65%), altered mental status (65%). 15563650.2015.1033630

3Sources

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

Sources
yearsourcetierstatusfeeds
2026Bioisostere-Driven Discovery of SePP: A Selenium-Containing Polypharmacological Agent Relevant to Fragile X SyndromeWallach J, Cameron S, Dybek M, Stanley B, Orme C, Riad N, Kavanagh P, Brandt SD, Knapp A, Gamrat J, Jauhola-Straight R, Adejare A, Rogier AJ, Tyagi R, Canal CE · Journal of Medicinal Chemistrydoi:10.1021/acs.jmedchem.5c02700moderateconsumed1 section
2025Guilty by dissociation: Part C: Enantiomeric separation of diphenidine-derived new psychoactive substances (NPS) by polar organic chiral HPLCEuerby MR, Barrett BS, Costello A, Farkas T, Sallenger MA, Sutcliffe OB · Journal of Pharmaceutical and Biomedical Analysisdoi:10.1016/j.jpba.2025.116728moderateconsumed2 sections
2025Synthesis and crystal structures of five fluorinated diphenidine derivativesMewis RE, Hulme MC, Marron J, Langley SK, Sutcliffe OB, Benjamin SL · Acta Crystallographica Section Edoi:10.1107/s2056989025001288moderateconsumedcited only
2023ACMD Review of the Evidence on the Use and Harms of DiphenidineAdvisory Council on the Misuse of Drugs (ACMD)url:fa9f1dd5951ccff4weakconsumedcited only
2020WHO ECDD 43rd Meeting: Critical Review Report on DiphenidineWHO Expert Committee on Drug Dependenceurl:79103079b3858529weakconsumedcited only
20181,2-Diarylethylamine- and Ketamine-Based New Psychoactive SubstancesWallach J, Brandt SD · Handbook of Experimental Pharmacologydoi:10.1007/164_2018_148moderateconsumed3 sections
2018Mechanistic Insights into the Stimulant Properties of Novel Psychoactive Substances (NPS) and Their Discrimination by the Dopamine Transporter-In Silico and In Vitro Exploration of Dissociative DiarylethylaminesSahai MA, Davidson C, Dutta N, Opacka-Juffry J · Brain Sciencesdoi:10.3390/brainsci8040063moderateconsumed6 sections
2017A Case of Nonfatal Intoxication Associated with the Recreational use of DiphenidineGerace E, Bovetto E, Corcia DD, Vincenti M, Salomone A · Journal of Forensic Sciencesdoi:10.1111/1556-4029.13355weakconsumed5 sections
2016An overview of emerging and new psychoactive substances in the United KingdomBeharry S, Gibbons S · Forensic Science Internationaldoi:10.1016/j.forsciint.2016.08.013moderateconsumed1 section
2016Canada Gazette: Regulations Amending the Food and Drug Regulations (Parts G and J - Lefetamine, AH-7921, MT-45 and W-18)Health Canadaurl:50e9b3a16f12af2dweakconsumedcited only
2016Diphenidine, a new psychoactive substance: metabolic fate elucidated with rat urine and human liver preparations and detectability in urine using GC-MS, LC-MSn, and LC-HR-MSnWink CS, Michely JA, Jacobsen-Bauer A, Zapp J, Maurer HH · Drug Testing and Analysisdoi:10.1002/dta.1946moderateconsumed4 sections
2016Guilty by dissociation-development of gas chromatography-mass spectrometry (GC-MS) and other rapid screening methods for the analysis of 13 diphenidine-derived new psychoactive substances (NPSs)Geyer PM, Hulme MC, Irving JP, Thompson PD, Ashton RN, Lee RJ, Johnson L, Marron J, Banks CE, Sutcliffe OB · Analytical and Bioanalytical Chemistrypmid:27744478moderateconsumed1 section
2016Identification and quantification of metabolites of AB-CHMINACA in a urine specimen of an abuserWurita A, Hasegawa K, Minakata K, Gonmori K, Nozawa H, Yamagishi I, Suzuki O, Watanabe K · Legal Medicine (Tokyo)doi:10.1016/j.legalmed.2015.07.011weakconsumed1 section
2016Pharmacological Investigations of the Dissociative 'Legal Highs' Diphenidine, Methoxphenidine and AnaloguesWallach J, Kang H, Colestock T, Morris H, Bortolotto ZA, Collingridge GL, Lodge D, Halberstadt AL, Brandt SD, Adejare A · PLoS ONEdoi:10.1371/journal.pone.0157021moderateconsumed9 sections
2015First Reported Fatalities Associated with the 'Research Chemical' 2-MethoxydiphenidineElliott SP, Brandt SD, Wallach J, Morris H, Kavanagh PV · Journal of Analytical Toxicologydoi:10.1093/jat/bkv006weakconsumed1 section
2015Intoxications by the dissociative new psychoactive substances diphenidine and methoxphenidineHelander A, Beck O, Bäckberg M · Clinical Toxicologydoi:10.3109/15563650.2015.1033630weakconsumed6 sections
2015Preparation and characterization of the 'research chemical' diphenidine, its pyrrolidine analogue, and their 2,2-diphenylethyl isomersWallach J, Kavanagh PV, McLaughlin G, Morris N, Power JD, Elliott SP, Mercier MS, Lodge D, Morris H, Dempster NM, Brandt SD · Drug Testing and Analysisdoi:10.1002/dta.1689moderateconsumed3 sections
2015Semiquantitation of diphenidine in tissue sections obtained from a human cadaver in a poisoning case by direct MALDI-QTOF mass spectrometryMinakata K, Yamagishi I, Nozawa H, Hasegawa K, Gonmori K, Suzuki M, Wurita A, Suzuki O, Watanabe K · Forensic Toxicologydoi:10.1007/s11419-015-0300-yweakconsumed2 sections
2014A large amount of new designer drug diphenidine coexisting with a synthetic cannabinoid 5-fluoro-AB-PINACA found in a dubious herbal productWurita A, Hasegawa K, Minakata K, Watanabe K, Suzuki O · Forensic Toxicologydoi:10.1007/s11419-014-0240-ymoderateconsumed1 section
2014Acute toxicity associated with the recreational use of the novel dissociative psychoactive substance methoxphenidineHofer KE, Degrandi C, Müller DM, Zürrer-Härdi U, Wahl S, Rauber-Lüthy C, Ceschi A · Clinical Toxicologydoi:10.3109/15563650.2014.974264weakconsumed1 section
—Searched ClinicalTrials.gov for "Diphenidine" — no resultsabsenceno results—

4Docket

one filing per activity — decisions, correspondence, reports

  1. 0012026-05-03revisionRevision 1

    Initial LLM generation (v5 pipeline, wiki)

    psx:substance/diphenidine/version/1
  2. 0022026-06-04proposal44 value proposals approved together

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

    44 items in this filing

    • dose_tier · light
    • dose_tier · common
    • dose_tier · strong
    • dose_tier · heavy
    • timeline · oral · onset
    • timeline · oral · come_up
    • timeline · oral · peak
    • timeline · oral · plateau
    • timeline · oral · resolution
    • timeline · oral · afterglow
    • timeline · rectal · onset
    • timeline · rectal · come_up
    • timeline · rectal · peak
    • timeline · rectal · plateau
    • timeline · rectal · resolution
    • timeline · rectal · afterglow
    • timeline · smoked · onset
    • timeline · smoked · come_up
    • timeline · smoked · peak
    • timeline · smoked · resolution
    • timeline · smoked · afterglow
    • toxicity
    • dependence · full
    • withdrawal
    • tolerance
    • dosage · oral
    • dosage · rectal
    • dosage · smoked
    • duration · oral · onset
    • duration · oral · total
    • duration · oral · aftereffects
    • duration · rectal · onset
    • duration · rectal · total
    • duration · smoked · onset
    • duration · smoked · peak
    • duration · smoked · total
    • contraindication · cardiovascular
    • contraindication · cardiovascular
    • contraindication · psychiatric
    • contraindication · psychiatric
    • contraindication · renal
    • contraindication · hepatic
    • contraindication · pregnancy_breastfeeding
    psx:substance/diphenidine/proposal/dose_tier/741bee51-b0f1-40e3-a6a6-c804011e5afd
  3. 0032026-06-04publicationPublication — backfill

5Issued documents

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

Issued documents
documentcontent hashissuedfrom versionsuperseded
info_card8177e6b20c60304dcda7a76f…2026-10-19 20:31Revision 1current
emergencyba304cf8bf8de5b4ec66cb2b…2026-09-04 04:29Revision 1current
info_cardbea672264454863d3050d043…2026-09-04 04:29Revision 1superseded2026-10-19
noticec090e106affaf8958ae0c2cb…2026-09-04 04:29Revision 1current