generation run 2026-05-08
70 min completedmodel pipeline-v5plan not recordedrun/b9562ed2…Selection
Verification
- record
- seen / partial
- working
The model's own caveats
- sparse_evidence
- structural_inference
- safety_data_unverified
Reproduce
- inputs
- 29 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
18 searches — query, source, results, what was kept and why
| # | source | query | seen | kept | rationale |
|---|---|---|---|---|---|
| 1 | PubChem | U-47700 | 1 | 1 | Primary chemical identity verification |
| 2 | PubMed | U-47700 forensic postmortem blood concentration fatality | 7 | 7 | All provide key postmortem toxicology data for U-47700 |
| 3 | ClinicalTrials.gov · absence | U-47700 | 0 | 0 | Expected — U-47700 is a Schedule I controlled substance with no approved therapeutic use |
| 4 | PubMed | U-47700 overdose death case report toxicology | 5 | 5 | Direct case reports and forensic series on U-47700 fatalities |
| 5 | PubMed | U-47700 opioid pharmacology receptor binding | 5 | 5 | All directly relevant to U-47700 pharmacology and receptor binding |
| 6 | OpenAlex | U-47700 synthetic opioid pharmacology toxicology | 10 | 3 | Highly cited reviews with substantive U-47700 coverage |
| 7 | Web | U-47700 Ki binding affinity mu opioid receptor nM radioligand | 10 | 1 | Key pharmacological data points |
| 8 | PubMed | U-47700 analytical method detection urine blood screening | 5 | 4 | All provide validated analytical methods and metabolic data |
| 9 | Web | U-47700 DEA Schedule I emergency scheduling 2016 Federal Register | 10 | 3 | Primary regulatory documentation |
| 10 | UNODC | U-47700 substance details | 1 | 1 | Verified chemical identity and international scheduling |
| 11 | ClinicalTrials.gov · absence | U-47700 | 0 | 0 | Confirms absence of clinical trial program |
| 12 | Web | U-47700 legal status UK Canada Australia New Zealand | 10 | 3 | International scheduling documentation |
| 13 | PubMed | U-47700 pharmacodynamics pharmacokinetics rat Ki binding | 1 | 1 | Primary quantitative PK/PD source with binding affinity data |
| 14 | Web | U-47700 Szmuszkovicz Upjohn patent 1978 | 10 | 1 | Primary discovery documentation |
| 15 | Web | U-47700 CYP3A4 CYP2B6 FMO3 metabolism N-demethylation human liver microsomes | 10 | 2 | CYP enzyme identification for metabolism section |
| 16 | PubMed | U-47700 synthesis Upjohn benzamide opioid history 1970s | 1 | 1 | Definitive review paper; covers >40 year history |
| 17 | Web | U-47700 Prince death opioid toxicology 2016 | 10 | 1 | Significant public health event linked to U-47700 |
| 18 | CDC MMWR | U-47700 deaths fentanyl analogs 10 states 2016 | 1 | 1 | Key epidemiological data source |
158 claims by section — every cited sentence, checked against its source
safety46 · 2 ok
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
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Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
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A multi-drug fatality combining 3-fluorophenmetrazine, U-47700, amitriptyline, methamphetamine, and two designer benzodiazepines (flubromazolam, delorazepam).supported
Polydrug fatality case involving flubromazolam and delorazepam among other NPS. Cause of death: multiple drug toxicity. bkx060
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
Benzodiazepines: Multiple fatal cases document co-ingestion of designer benzodiazepines (flubromazolam, diclazepam) and classical benzodiazepines (alprazolam) with U-47700. Benzodiazepines augment respiratory depression through GABAergic potentiation of brainstem depression. This combination is documented as directly lethal.supported
Polydrug fatality case involving flubromazolam and delorazepam among other NPS. Cause of death: multiple drug toxicity. bkx060
Claim in safety — inconclusiveinconclusiveworking →
Claim in safety — inconclusiveinconclusiveworking →
pharmacology24 · 1 ok
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
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Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — not_supportednot supportedworking →
Full MOR agonism has been confirmed by GTPγS functional assay, where U-47700 produces maximal stimulation comparable to reference MOR agonists (DAMGO, fentanyl)partially supported
Morphine used as reference: butyrylfentanyl, U-47700, and MT-45 have nM affinities at MOR-1, less potent than morphine at MOR, much weaker at DOR and KOR. Morphine MOR potency reference in GTPγS assay. j.neuropharm.2017.08.016
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
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Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
Claim in pharmacology — inconclusiveinconclusiveworking →
history22 · 0 ok
Claim in history — inconclusiveinconclusiveworking →
Claim in history — inconclusiveinconclusiveworking →
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Claim in history — inconclusiveinconclusiveworking →
Claim in history — inconclusiveinconclusiveworking →
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pharmacokinetic-detail16 · 0 ok
Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →
Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →
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Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →
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Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →
Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →
Claim in pharmacokinetic-detail — inconclusiveinconclusiveworking →
receptor-pharmacology12 · 0 ok
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
Claim in receptor-pharmacology — inconclusiveinconclusiveworking →
summary12 · 1 ok
Claim in summary — inconclusiveinconclusiveworking →
Claim in summary — inconclusiveinconclusiveworking →
Claim in summary — inconclusiveinconclusiveworking →
Claim in summary — inconclusiveinconclusiveworking →
Claim in summary — inconclusiveinconclusiveworking →
Claim in summary — inconclusiveinconclusiveworking →
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Claim in summary — inconclusiveinconclusiveworking →
It functions as a full MOR agonist through canonical Gαi/o signaling, confirmed by GTPγS functional assays and complete reversal of all effects by naloxone.partially supported
Morphine used as reference: butyrylfentanyl, U-47700, and MT-45 have nM affinities at MOR-1, less potent than morphine at MOR, much weaker at DOR and KOR. Morphine MOR potency reference in GTPγS assay. j.neuropharm.2017.08.016
Claim in summary — inconclusiveinconclusiveworking →
Claim in summary — inconclusiveinconclusiveworking →
chemistry10 · 0 ok
Claim in chemistry — inconclusiveinconclusiveworking →
Claim in chemistry — inconclusiveinconclusiveworking →
Claim in chemistry — inconclusiveinconclusiveworking →
Claim in chemistry — inconclusiveinconclusiveworking →
Claim in chemistry — inconclusiveinconclusiveworking →
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Claim in chemistry — inconclusiveinconclusiveworking →
Claim in chemistry — inconclusiveinconclusiveworking →
Claim in chemistry — inconclusiveinconclusiveworking →
comparative-pharmacology8 · 0 ok
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
Claim in comparative-pharmacology — inconclusiveinconclusiveworking →
neuroscience6 · 0 ok
Claim in neuroscience — inconclusiveinconclusiveworking →
Claim in neuroscience — inconclusiveinconclusiveworking →
Claim in neuroscience — inconclusiveinconclusiveworking →
Claim in neuroscience — inconclusiveinconclusiveworking →
Claim in neuroscience — inconclusiveinconclusiveworking →
Claim in neuroscience — inconclusiveinconclusiveworking →