Amphetamine

Amphetamine

SCHEMBL6251827

CC(N)Cc1ccccc1.O=C(O)C(O)C(O)C(=O)O

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2SLC6A3

The experimentally established mechanism targets of Amphetamine. 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 2/20 0.70
SLC6A3 known ✓ Q01959 1/20 0.70
TAAR1 Q96RJ0 4/20 0.70
SLC6A4 P31645 3/20 0.70
MAOA P21397 1/20 0.70
SIGMAR1 Q99720 1/20 0.70
CYP2A6 P11509 1/20 0.70
ADORA2A P29274 1/20 0.70
ADORA1 P30542 1/20 0.70
ALPI P09923 1/20 0.58
PKM P14618 1/20 0.58
PTGS1 P23219 1/20 0.58
XIAP P98170 1/20 0.58
SLC7A5 Q01650 1/20 0.58
SLC1A3 P43003 2/20 0.53
SLC1A2 P43004 2/20 0.53
SLC1A1 P43005 2/20 0.53
CYP1A2 P05177 1/20 0.52
LAP3 P28838 2/20 0.50
TRPA1 O75762 1/20 0.50

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
Levamfetamine SCHEMBL1320449 1.00 TAAR1 (0.70) TAAR1SLC6A4SLC6A2MAOASLC6A3
Dextroamphetamine SCHEMBL6251824 1.00 TAAR1 (0.70) TAAR1SLC6A4SLC6A2MAOASLC6A3
Dextroamphetamine SCHEMBL31637552 1.00 TAAR1 (0.70) TAAR1SLC6A4SLC6A2MAOASLC6A3
Dextroamphetamine SCHEMBL8505954 0.93 TAAR1 (0.61) TAAR1SLC6A4SLC6A2MAOASLC6A3
Mucic Acid SCHEMBL578987 0.93 TAAR1 (0.66) TAAR1SLC6A4SLC6A2MAOASLC6A3
Mucic Acid SCHEMBL28326693 0.93 TAAR1 (0.66) TAAR1SLC6A4SLC6A2MAOASLC6A3
Mucic Acid SCHEMBL578988 0.93 TAAR1 (0.66) TAAR1SLC6A4SLC6A2MAOASLC6A3
Amphetamine SCHEMBL29127738 0.89 TAAR1 (0.76) TAAR1SLC6A4SLC6A2MAOASLC6A3
Amphetamine SCHEMBL157108 0.86 TAAR1 (0.79) TAAR1SLC6A4SLC6A2MAOASLC6A3
Amphetamine SCHEMBL8589685 0.86 TAAR1 (0.79) TAAR1SLC6A4SLC6A2MAOASLC6A3

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 14 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3717452-B1 PROCESS FOR PREPARING ACYLATED AMPHETAMINE DERIVATIVES SpecGx LLC (US) 2024-06-05 EP claimed
EP-3717452-A1 PROCESS FOR PREPARING ACYLATED AMPHETAMINE DERIVATIVES SpecGx LLC (US) 2020-10-07 EP claimed
CN-101426496-A Use of cholesterol lowering agents and/or H3Treatment of non-alcoholic fatty liver disease with receptor antagonists/inverse agonists SCHERING CORP (US) 2009-05-06 CN claimed
US-20250368601-A1 PROCESS FOR THE PREPARATION OF LISDEXAMFETAMINE VERANOVA L P (US) 2025-12-04 US disclosed
US-20250090554-A1 A METHOD OF TREATING DEPRESSION BY IMMUNE MODULATION MYND LIFE SCIENCES INC (CA) 2025-03-20 US disclosed
EP-3717452-B1 PROCESS FOR PREPARING ACYLATED AMPHETAMINE DERIVATIVES SpecGx LLC (US) 2024-06-05 EP disclosed
WO-2024089666-A1 PROCESS FOR THE PREPARATION OF LISDEXAMFETAMINE MACFARLAN SMITH LIMITED (GB) 2024-05-02 WO disclosed
US-10927068-B2 Process for preparing acylated amphetamine derivatives SpecGx LLC (US) 2021-02-23 US disclosed
EP-3717452-A1 PROCESS FOR PREPARING ACYLATED AMPHETAMINE DERIVATIVES SpecGx LLC (US) 2020-10-07 EP disclosed
US-20190161435-A1 PROCESS FOR PREPARING ACYLATED AMPHETAMINE DERIVATIVES SpecGx LLC 2019-05-30 US disclosed
CN-101426496-A Use of cholesterol lowering agents and/or H3Treatment of non-alcoholic fatty liver disease with receptor antagonists/inverse agonists SCHERING CORP (US) 2009-05-06 CN disclosed
EP-1442006-B1 PREPARATION OF AMPHETAMINES FROM PHENYLPROPANOLAMINES BOEHRINGER INGELHEIM CHEMICALS (US) 2005-08-24 EP disclosed
US-6399828-B1 ACYLATION OF PHENYLPROPANOLAMINE; CATALYTIC HYDROGENATION BOEHRINGER INGELHEIM CHEMICALS, INC. 2002-06-04 US disclosed
US-4203986-A TRANQUILIZERS, SEDATIVES, ANTITUSSIVE AGNETS METABIO-JOULLIE (FR) 1980-05-20 US 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 (3 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-10927068-B2 Process for preparing acylated amphetamine derivatives COMT, DOT1L, AASDHPPT SLC6A2 169/4885SLC6A3 66/4885TAAR1 483/4885
US-20250368601-A1 PROCESS FOR THE PREPARATION OF LISDEXAMFETAMINE PHYKPL, DLST, COMT SLC6A2 63/4885SLC6A3 19/4885TAAR1 786/4885
US-20190161435-A1 PROCESS FOR PREPARING ACYLATED AMPHETAMINE DERIVATIVES COMT, DOT1L, AASDHPPT SLC6A2 169/4885SLC6A3 66/4885TAAR1 483/4885

“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.