Levamfetamine

Levamfetamine

SCHEMBL2636

C[C@@H](N)Cc1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC18A2SLC6A2SLC6A3

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
SLC6A2 known ✓ P23975 4/20 1.00
SLC6A3 known ✓ Q01959 2/20 1.00
TAAR1 Q96RJ0 4/20 1.00
SLC6A4 P31645 3/20 1.00
MAOA P21397 1/20 1.00
SIGMAR1 Q99720 1/20 1.00
CYP2A6 P11509 1/20 1.00
ADORA2A P29274 1/20 1.00
ADORA1 P30542 1/20 1.00
CYP2D6 P10635 1/20 0.67
EPHX1 P07099 1/20 0.64
PNMT P11086 1/20 0.59

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
Amphetamine SCHEMBL8858 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL1560962 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL13747797 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL13747801 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Dextroamphetamine SCHEMBL8859 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL15094242 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Levamfetamine SCHEMBL9673275 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL13746679 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL910141 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA
Amphetamine SCHEMBL4781164 1.00 SLC6A2 (1.00) SLC6A2TAAR1SLC6A4SLC6A3MAOA

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

Appears in 2933 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260027043-A1 EXTENDED RELEASE AMPHETAMINE TABLETS TRIS PHARMA INC (US) 2026-01-29 US claimed
EP-4683622-A1 NON-DISTILLATIVE PROCESS FOR MANUFACTURING HIGH PURITY AMPHETAMINES Pharmapotheca A, Inc. (US) 2026-01-28 EP claimed
US-12534428-B2 Non-distillative process for manufacturing high purity amphetamines Pharmapotheca A, Inc. (US) 2026-01-27 US claimed
US-20250352466-A1 EXTENDED RELEASE AMPHETAMINE TABLETS TRIS PHARMA INC (US) 2025-11-20 US claimed
US-12458592-B1 Extended release amphetamine tablets TRIS PHARMA, INC. (US) 2025-11-04 US claimed
US-20250320178-A1 AMPHETAMINE CARBAMATE COMPOUNDS AND METHODS NOVEN PHARMACEUTICALS, INC. (US) 2025-10-16 US claimed
EP-4594294-A1 DOPAMINE D3/D2 RECEPTOR PARTIAL AGONISTS FOR THE TREATMENT OF NEUROPSYCHIATRIC DISORDERS The United States of America, as represented by the Secretary, Department of Health and Human Services (US) 2025-08-06 EP claimed
US-20250206698-A1 Process for Making Lisdexamfetamine Dimesylate Pharmapotheca A, Inc. 2025-06-26 US claimed
US-20250064747-A1 EXTENDED RELEASE AMPHETAMINE TABLETS TRIS PHARMA, INC. (US) 2025-02-27 US claimed
US-20250025432-A1 METHODS FOR IMPROVING DRIVING BEHAVIOR TRIS PHARMA INC (US) 2025-01-23 US claimed
EP-0987332-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE AMINO COMPOUNDS Kaneka Corporation (JP) 2000-03-22 EP claimed
EP-0977572-A1 USE OF NK-1 RECEPTOR ANTAGONISTS FOR TREATING EATING DISORDERS MERCK SHARP & DOHME LTD. (GB) 2000-02-09 EP claimed
WO-1998047513-A1 USE OF NK-1 RECEPTOR ANTAGONISTS FOR TREATING EATING DISORDERS MERCK SHARP & DOHME LIMITED (GB) 1998-10-29 WO claimed
EP-0110955-B1 BRAIN-SPECIFIC DRUG DELIVERY UNIV FLORIDA (US) 1995-08-23 EP claimed
US-5440062-A One-(substituted)amino-7-(substituted)imino-1,3,5-cycloheptatriene-metal complexes as catalysts MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1995-08-08 US claimed
EP-0174342-B1 BRAIN-SPECIFIC ANALOGUES OF CENTRALLY ACTING AMINES UNIVERSITY OF FLORIDA (US) 1989-12-20 EP claimed
WO-1989010916-A1 ENANTIOSELECTIVE ADDITION OF HYDROCARBONS TO ALPHA,BETA-UNSATURATED CARBONYL COMPOUNDS MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 1989-11-16 WO claimed
EP-0222425-A2 Brain-specific drug delivery UNIVERSITY OF FLORIDA (US) 1987-05-20 EP claimed
EP-0218300-A2 Brain-specific drug delivery UNIVERSITY OF FLORIDA (US) 1987-04-15 EP claimed
US-4479932-A DIHYDROPYRIDINE PYRIDINIUM SALT REDOX CARRIER UNIVERSITY OF FLORIDA (US) 1984-10-30 US claimed