Benzphetamine

Benzphetamine

SCHEMBL678807

CC(Cc1ccccc1)N(C)Cc1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC18A2SLC6A2

The experimentally established mechanism targets of Benzphetamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 1/20 1.00
ADRA2B P18089 2/20 1.00
ADRA2C P18825 2/20 1.00
ADRA1A P35348 2/20 1.00
OPRK1 P41145 2/20 1.00
HTR2A P28223 1/20 1.00
SLC6A4 P31645 1/20 1.00
SLC6A3 Q01959 1/20 1.00
KCNH2 Q12809 1/20 1.00
SIGMAR1 Q99720 5/20 0.67
MAOB P27338 6/20 0.62
MAOA P21397 4/20 0.62
TSHR P16473 3/20 0.62
CYP1A2 P05177 2/20 0.62
CYP2D6 P10635 2/20 0.62
ADRA2A P08913 1/20 0.62
SNCA P37840 1/20 0.62
PKM P14618 1/20 0.62
MAPK1 P28482 1/20 0.61
KDM4E B2RXH2 1/20 0.61

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Benzphetamine SCHEMBL19285634 1.00 ADRA2B (1.00) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL49120 1.00 ADRA2B (1.00) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL6272098 0.98 ADRA2B (0.96) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL265137 0.98 ADRA2B (0.96) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL260091 0.98 ADRA2B (0.96) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL28360250 0.98 ADRA2B (0.96) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL4329836 0.96 ADRA2B (0.92) ADRA2BADRA2CADRA1AOPRK1SLC6A2
Benzphetamine SCHEMBL15388333 0.93 ADRA2B (0.86) ADRA2BADRA2CADRA1AOPRK1SLC6A2
SCHEMBL12648381 0.83 SLC6A2 (0.71) ADRA2BADRA2CADRA1AOPRK1SLC6A2
SCHEMBL15003030 0.83 ADRA2B (0.71) ADRA2BADRA2CADRA1AOPRK1SLC6A2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 107 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4444283-A1 SPECIALIZED COMBINATIONS FOR MENTAL DISORDERS OR MENTAL ENHANCEMENT Tactogen Inc. (US) 2024-10-16 EP claimed
WO-2023107715-A1 SPECIALIZED COMBINATIONS FOR MENTAL DISORDERS OR MENTAL ENHANCEMENT TACTOGEN INC (US) 2023-06-15 WO claimed
EP-4683622-A1 NON-DISTILLATIVE PROCESS FOR MANUFACTURING HIGH PURITY AMPHETAMINES Pharmapotheca A, Inc. (US) 2026-01-28 EP disclosed
US-12534428-B2 Non-distillative process for manufacturing high purity amphetamines Pharmapotheca A, Inc. (US) 2026-01-27 US disclosed
US-20250213502-A1 Amphetamine Controlled Release, Prodrug, and Abuse-deterrent Dosage Forms Pharmapotheca A, Inc. 2025-07-03 US disclosed
US-12208068-B2 Amphetamine controlled release, prodrug, and abuse-deterrent dosage forms Pharmapotheca A Inc. (US) 2025-01-28 US disclosed
EP-4444283-A1 SPECIALIZED COMBINATIONS FOR MENTAL DISORDERS OR MENTAL ENHANCEMENT Tactogen Inc. (US) 2024-10-16 EP disclosed
US-20240286993-A1 Non-distillative Process for Manufacturing High Purity Amphetamines Pharmapotheca A, Inc. 2024-08-29 US disclosed
WO-2024175957-A1 NON-DISTILLATIVE PROCESS FOR MANUFACTURING HIGH PURITY AMPHETAMINES Pharmapotheca A, Inc. (US) 2024-08-29 WO disclosed
US-20230321010-A1 Amphetamine Controlled Release, Prodrug, and Abuse-deterrent Dosage Forms CHEMAPOTHECA, LLC (US) 2023-10-12 US disclosed
US-11717498-B2 Methods of treatment using amphetamine controlled release, prodrug, and abuse deterrent dosage forms Pharmapotheca A, Inc. (US) 2023-08-08 US disclosed
US-20070129444-A1 Novel weight reduction composition and uses thereof MALLINCKRODT INC. 2007-06-07 US disclosed
US-20070112017-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS BRAINCELLS, INC. (US) 2007-05-17 US disclosed
WO-2007053596-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS BRAINCELLS, INC. (US) 2007-05-10 WO disclosed
WO-2007047978-A2 MODULATION OF NEUROGENESIS BY PDE INHIBITION BRAINCELLS, INC. (US) 2007-04-26 WO disclosed
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION BRAINCELLS, INC. (US) 2007-04-05 US disclosed
WO-2007025177-A2 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 WO disclosed
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 US disclosed
WO-2006060099-A1 CRYSTALLIZATION METHOD FOR BENZPHETAMINE MALLINCKRODT INC. (US) 2006-06-08 WO disclosed
WO-2006057778-A2 PROCESS FOR THE PURIFICATION OF BENZPHETAMINE HYDROCHLORIDE MALLINCKRODT INC. (US) 2006-06-01 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (10 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11717498-B2 Methods of treatment using amphetamine controlled release, prodrug, and abuse deterrent dosage forms SLC6A3, SLC6A2, CES2 SLC6A2 2/4885ADRA2B 72/4885ADRA2C 80/4885
US-20070112017-A1 GABA RECEPTOR MEDIATED MODULATION OF NEUROGENESIS GABRB2, GAP43, GABRB1 SLC6A2 330/4885ADRA2B 518/4885ADRA2C 571/4885
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION DCX, BDNF, NTRK2 SLC6A2 2832/4885ADRA2B 3274/4885ADRA2C 3410/4885
US-20240286993-A1 Non-distillative Process for Manufacturing High Purity Amphetamines AASDHPPT, AADAT, SLC6A3 SLC6A2 30/4885ADRA2B 1011/4885ADRA2C 868/4885
US-20230321010-A1 Amphetamine Controlled Release, Prodrug, and Abuse-deterrent Dosage Forms SLC6A3, CES2, SLC6A2 SLC6A2 3/4885ADRA2B 95/4885ADRA2C 111/4885
US-12534428-B2 Non-distillative process for manufacturing high purity amphetamines SMS, SRMS, SRM SLC6A2 12/4885ADRA2B 390/4885ADRA2C 157/4885
US-12208068-B2 Amphetamine controlled release, prodrug, and abuse-deterrent dosage forms SLC6A3, CES2, SLC6A2 SLC6A2 3/4885ADRA2B 95/4885ADRA2C 111/4885
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION CHRNB2, CHAT, CHRNB4 SLC6A2 1348/4885ADRA2B 374/4885ADRA2C 301/4885
US-20070129444-A1 Novel weight reduction composition and uses thereof HCRTR1, GPR119, HCRTR2 SLC6A2 163/4885ADRA2B 171/4885ADRA2C 200/4885
US-20250213502-A1 Amphetamine Controlled Release, Prodrug, and Abuse-deterrent Dosage Forms SLC6A3, CES2, SLC6A2 SLC6A2 3/4885ADRA2B 111/4885ADRA2C 122/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.