SCHEMBL1967290

SCHEMBL1967290

CC(N)COCc1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TACR1 P25103 6/20 0.59
TSHR P16473 1/20 0.56
SLC6A2 P23975 2/20 0.54
TAAR1 Q96RJ0 2/20 0.54
MAOA P21397 1/20 0.54
SLC6A4 P31645 1/20 0.54
SLC6A3 Q01959 1/20 0.54
SIGMAR1 Q99720 1/20 0.54
CYP2A6 P11509 1/20 0.54
ADORA2A P29274 1/20 0.54
ADORA1 P30542 1/20 0.54
CA1 P00915 4/20 0.52
CA2 P00918 2/20 0.52
CA7 P43166 2/20 0.52
CA9 Q16790 2/20 0.52
SLC1A1 P43005 1/20 0.51
KMT2A Q03164 1/20 0.49
IDO1 P14902 1/20 0.46

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
SCHEMBL507258 1.00 TACR1 (0.59) TACR1TSHRSLC6A2TAAR1MAOA
SCHEMBL3553258 1.00 TACR1 (0.59) TACR1TSHRSLC6A2TAAR1MAOA
Trifluoroacetic Acid SCHEMBL23390351 0.85 SLC1A1 (0.51) TACR1SLC6A2TAAR1MAOASLC6A4
Trifluoroacetic Acid SCHEMBL23390354 0.85 SLC1A1 (0.51) TACR1SLC6A2TAAR1MAOASLC6A4
SCHEMBL7421010 0.84 TACR1 (0.66) TACR1TSHRCA1CA2CA7
SCHEMBL7332866 0.84 TACR1 (0.66) TACR1TSHRCA1CA2CA7
SCHEMBL9677926 0.84 TACR1 (0.66) TACR1TSHRCA1CA2CA7
SCHEMBL22013212 0.83 TACR1 (0.63) TACR1TSHRCA1CA2CA7
SCHEMBL7095981 0.83 TACR1 (0.75) TACR1TSHRCA1CA2CA7
SCHEMBL18394417 0.83 TACR1 (0.63) TACR1TSHRCA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020193636-A1 Benzaldehyde reacted with a primary amine to give an imine, which is hydrogenated with hydrogen in the presence of a catalyst and a water miscible solvent BASF AKTIENGESELLCHAFT (DE) 2002-12-19 US claimed
US-6476268-B1 Preparation of N-benzylamines BASF AKTIENGESELLSCHAFT (DE) 2002-11-05 US claimed
EP-1247799-A2 Process for the preparation of N-benzylamines BASF AKTIENGESELLSCHAFT (DE) 2002-10-09 EP claimed
CN-121779431-A Synthesis method of key intermediate of ebastine 山东盛安贝新材料有限公司 2026-04-03 CN disclosed
US-12195446-B2 Heteroaryl compounds and their use as therapeutic drugs DONG-A SOCIO HOLDINGS CO., LTD. (KR) 2025-01-14 US disclosed
US-20240294565-A1 UNNATURAL CONFIGURATION NUCLEOTIDE PRODRUG COMPOUNDS LIGAND PHARMACEUTICALS INCORPORATED 2024-09-05 US disclosed
CN-111527090-B Pyrazolo-pyrrolo-pyrimidine-dione derivatives as P2X3 inhibitors 拜耳公司 2023-05-26 CN disclosed
US-20230020092-A1 COMPOSITIONS FOR DELIVERY OF ANTISENSE COMPOUNDS ENTRADA THERAPEUTICS, INC. 2023-01-19 US disclosed
US-20230002353-A1 HETEROARYL COMPOUNDS AND THEIR USE AS THERAPEUTIC DRUGS DONG A SOCIO HOLDINGS CO LTD (KR) 2023-01-05 US disclosed
WO-2022245584-A1 UNNATURAL CONFIGURATION NUCLEOTIDE PRODRUG COMPOUNDS LIGAND PHARMACEUTICALS INCORPORATED (US) 2022-11-24 WO disclosed
CN-109863160-B Nucleoside phosphate compound and preparation method and application thereof 四川科伦博泰生物医药股份有限公司 2022-06-07 CN disclosed
EP-2223929-A1 GAMBOGIC GLYCOSIDE DERIVATIVES AND ANALOGS, THE PREPARATION AND THE APPLICATION THEREOF Liaoning Lifeng Scientific&Technology Development Company Ltd. (CN) 2010-09-01 EP disclosed
US-7288562-B2 Fluoro and sulphonylamino containing 3,6-disubstituted azabicyclo (3.1.0) hexane derivatives as muscarinic receptor antagonists RANBAXY LABORATORIES LIMITED (IN) 2007-10-30 US disclosed
EP-1846469-A1 A POLYUREA COMPOUND Nuplex Resins B.V. (NL) 2007-10-24 EP disclosed
WO-2006075000-A1 A POLYUREA COMPOUND NUPLEX RESINS B.V. (NL) 2006-07-20 WO disclosed
US-20020193636-A1 Benzaldehyde reacted with a primary amine to give an imine, which is hydrogenated with hydrogen in the presence of a catalyst and a water miscible solvent BASF AKTIENGESELLCHAFT (DE) 2002-12-19 US disclosed
US-6476268-B1 Preparation of N-benzylamines BASF AKTIENGESELLSCHAFT (DE) 2002-11-05 US disclosed
EP-1247799-A2 Process for the preparation of N-benzylamines BASF AKTIENGESELLSCHAFT (DE) 2002-10-09 EP disclosed
EP-0877815-A1 METHOD OF PRODUCING OPTICALLY ACTIVE AMINES BAYER AG (DE) 1998-11-18 EP disclosed
WO-1997028271-A1 METHOD OF PRODUCING OPTICALLY ACTIVE AMINES BAYER AKTIENGESELLSCHAFT (DE) 1997-08-07 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 (5 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-12195446-B2 Heteroaryl compounds and their use as therapeutic drugs MERTK, ERBB2, SRC TACR1 801/4885TSHR 1878/4885SLC6A2 1378/4885
US-20230020092-A1 COMPOSITIONS FOR DELIVERY OF ANTISENSE COMPOUNDS HNRNPAB, SNRPE, HNRNPA2B1 TACR1 3300/4885TSHR 2244/4885SLC6A2 1820/4885
US-20020193636-A1 Benzaldehyde reacted with a primary amine to give an imine, which is hydrogenated with hydrogen in the presence of a catalyst and a water miscible solvent HNMT, INMT, H1-2 TACR1 3372/4885TSHR 3777/4885SLC6A2 1541/4885
US-20230002353-A1 HETEROARYL COMPOUNDS AND THEIR USE AS THERAPEUTIC DRUGS MERTK, ERBB2, SRC TACR1 801/4885TSHR 1878/4885SLC6A2 1378/4885
US-20240294565-A1 UNNATURAL CONFIGURATION NUCLEOTIDE PRODRUG COMPOUNDS PNP, NUDT1, ENTPD5 TACR1 1886/4885TSHR 3979/4885SLC6A2 822/4885

“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.