(S)-P-Hydroxyamphetamine

(S)-P-Hydroxyamphetamine

SCHEMBL256809

C[C@H](N)Cc1ccc(O)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3

The experimentally established mechanism targets of (S)-P-Hydroxyamphetamine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 5/20 1.00
SLC6A2 P23975 5/20 1.00
SLC6A3 Q01959 3/20 0.61
SLC6A4 P31645 3/20 0.60
MAOA P21397 2/20 0.60
SIGMAR1 Q99720 1/20 0.60
CYP2A6 P11509 1/20 0.60
ADORA2A P29274 1/20 0.60
ADORA1 P30542 1/20 0.60
ESR1 P03372 1/20 0.59
ESR2 Q92731 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
Hydroxyamphetamine SCHEMBL125440 1.00 TAAR1 (1.00) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL125442 1.00 TAAR1 (1.00) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL219712 0.98 TAAR1 (0.95) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL221649 0.98 TAAR1 (1.00) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL28160718 0.98 TAAR1 (1.00) TAAR1SLC6A2SLC6A3SLC6A4MAOA
(S)-P-Hydroxyamphetamine SCHEMBL9707065 0.98 TAAR1 (1.00) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL219710 0.98 TAAR1 (0.95) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL11539011 0.98 TAAR1 (0.95) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL221291 0.98 TAAR1 (0.95) TAAR1SLC6A2SLC6A3SLC6A4MAOA
Hydroxyamphetamine SCHEMBL221647 0.98 TAAR1 (1.00) TAAR1SLC6A2SLC6A3SLC6A4MAOA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112939900-B Preparation method of buvaracetam intermediate 广东东阳光药业股份有限公司 2024-01-16 CN claimed
CN-112939900-A Preparation method of brivaracetam intermediate 广东东阳光药业有限公司 2021-06-11 CN claimed
CN-101829598-B Preparation method of acetylated glycosyl thiourea derivative and application thereof in isoquinoline acid synthesis NANJING UNIVERSITY OF TECHNOLOGY 2011-12-28 CN claimed
CN-102153520-A Chiral 2- aryl substituted 1,3-oxazoline compounds and preparation method thereof UNIV SHANGHAI 2011-08-17 CN claimed
CN-101829598-A Preparation method of acetylated glycosyl thiourea derivative and application thereof in isoquinoline acid synthesis NANJING UNIVERSITY OF TECHNOLOGY 2010-09-15 CN claimed
CN-112939900-B Preparation method of buvaracetam intermediate 广东东阳光药业股份有限公司 2024-01-16 CN disclosed
CN-112500308-B Golden amide alcohol ester and fluorinated derivative thereof, and preparation method and application thereof 澳门科技大学 2023-10-03 CN disclosed
EP-2611771-B1 SUBSTITUTED HETEROARYL- AND ARYLALKYNYL BENZENE DERIVATIVES AS ACC-INHIBITORS FOR THE TREATMENT OF METABOLIC DISEASES BOEHRINGER INGELHEIM INT (DE) 2016-11-23 EP disclosed
US-9315792-B2 Nitrilases, nucleic acids encoding them and methods for making and using them BASF ENZYMES LLC (US) 2016-04-19 US disclosed
US-20150125928-A1 NITRILASES, NUCLEIC ACIDS ENCODING THEM AND METHODS FOR MAKING AND USING THEM BASF ENZYMES LLC 2015-05-07 US disclosed
US-8835472-B2 Compounds, pharmaceutical compositions and uses thereof BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2014-09-16 US disclosed
US-8835472-B2 Compounds, pharmaceutical compositions and uses thereof BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2014-09-16 US disclosed
US-7217728-B2 Diaminopropionic acid derivatives HOFFMANN-LA ROCHE INC. (US) 2007-05-15 US disclosed
US-7217728-B2 Diaminopropionic acid derivatives HOFFMANN-LA ROCHE INC. (US) 2007-05-15 US disclosed
US-20070066586-A1 ANILINE DERIVATIVES AJINOMOTO CO., INC. (JP) 2007-03-22 US disclosed
CN-1088912-A The 4-amino-3-hydroxycarboxylic acid derivatives SANDOZ LTD (CH) 1994-07-06 CN disclosed
US-5017619-A Anitdiabetic HOFFMANN-LA ROCHE INC. (US) 1991-05-21 US disclosed
EP-0198412-B1 PHENETHANOL AMINE DERIVATIVES F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1989-03-22 EP disclosed
EP-0198412-A1 Phenethanol amine derivatives F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1986-10-22 EP disclosed
US-4156010-A TREATMENT OF GLAUCOMA MERCK & CO., INC. (US) 1979-05-22 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 (1 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-20070066586-A1 ANILINE DERIVATIVES SERPINB1, ACE, REN TAAR1 1799/4885SLC6A2 435/4885SLC6A3 540/4885

“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.