SCHEMBL272604

SCHEMBL272604

NC(Cc1ccccc1)c1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 2/20 0.61
SLC6A2 P23975 3/20 0.56
TAAR1 Q96RJ0 2/20 0.56
SLC6A4 P31645 2/20 0.56
SLC6A3 Q01959 2/20 0.56
MAOA P21397 1/20 0.56
SIGMAR1 Q99720 1/20 0.56
CYP2A6 P11509 1/20 0.56
ADORA2A P29274 1/20 0.56
ADORA1 P30542 1/20 0.56
GRIN2D O15399 1/20 0.53
GRIN3B O60391 1/20 0.53
GRIN1 Q05586 1/20 0.53
GRIN2A Q12879 1/20 0.53
GRIN2B Q13224 1/20 0.53
GRIN2C Q14957 1/20 0.53
GRIN3A Q8TCU5 1/20 0.53
CYP2D6 P10635 2/20 0.52
ANPEP P15144 1/20 0.52
CYP1A2 P05177 2/20 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
SCHEMBL468022 1.00 EPHX1 (0.61) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL3451169 1.00 EPHX1 (0.61) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
Hydrochloric Acid SCHEMBL28839661 0.98 EPHX1 (0.58) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL8422879 0.89 SLC6A2 (0.57) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL28893947 0.89 SLC6A2 (0.56) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL17463566 0.87 EPHX1 (0.52) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL9323047 0.87 EPHX1 (0.52) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL17887234 0.87 ACP3 (0.51) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL9322166 0.87 MAOB (0.50) EPHX1SLC6A2TAAR1SLC6A4SLC6A3
SCHEMBL3289611 0.85 SLC6A4 (0.52) EPHX1SLC6A2TAAR1SLC6A4SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120192526-A High-colloid thick oil viscosity reducer and preparation method thereof 中石化石油工程技术服务股份有限公司 2025-06-24 CN claimed
US-20250145472-A1 METHOD FOR GENERATING CARBON DIOXIDE KOBE GAKUIN EDUCATIONAL FOUNDATION (JP) 2025-05-08 US claimed
US-20250057959-A1 PHOSPHANE GOLD(I)-N-HETEROCYCLIC CARBENE COMPLEXES FOR TREATING CANCER KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2025-02-20 US claimed
EP-4480568-A1 METHOD FOR GENERATING CARBON DIOXIDE Kobe Gakuin Educational Foundation (JP) 2024-12-25 EP claimed
WO-2023153506-A1 METHOD FOR GENERATING CARBON DIOXIDE 学校法人神戸学院 2023-08-17 WO claimed
CN-107573228-A A kind of preparation method of the carboxylic acid of 2 oxo of optical voidness, three ring [2.2.1.0] heptane 7 沈阳欧利康化学科技有限公司 2018-01-12 CN claimed
US-20170112829-A1 USE OF COMPOUNDS BINDING TO THE SIGMA RECEPTOR LIGANDS FOR THE TREATMENT OF NEUROPATHIC PAIN DEVELOPING AS A CONSEQUENCE OF CHEMOTHERAPY LABORATORIOS DEL DR. ESTEVE, S.A. (ES) 2017-04-27 US claimed
EP-2705028-A1 PROCESS FOR THE PREPARATION OF A RIVAROXABAN AND INTERMEDIATES FORMED IN SAID PROCESS Egis Gyógyszergyár Nyilvánosan Müködö Részvény-Társaság (HU) 2014-03-12 EP claimed
CN-101184737-B 1-(imidazolin-2-yl)amino-1,2-diphenylethane compounds for combating animal pests BASF SE 2012-12-26 CN claimed
WO-2012153155-A1 PROCESS FOR THE PREPARATION OF A RIVAROXABAN AND INTERMEDIATES FORMED IN SAID PROCESS EGIS GYÓGYSZERGYÁR NYILVÃNOSAN MÜKÖDÖ RÉSZVÉNY-TÁRSASÁG (HU) 2012-11-15 WO claimed
EP-0086324-B1 PROCESS FOR PREPARING ASCORBIC ACID F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1988-09-21 EP claimed
EP-0092194-B1 METHOD OF OBTAINING OPTICALLY ACTIVE HALF ESTERS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1987-07-08 EP claimed
EP-0093511-B1 METHOD FOR PRODUCING AND OPTICALLY ACTIVE 2,2-DIMETHYLCYCLOPROPANECARBOXYLIC ACID SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1986-09-24 EP claimed
EP-0163094-A2 Preparation of optically-active alpha-substituted phenylacetic acids E.I. DU PONT DE NEMOURS AND COMPANY (US) 1985-12-04 EP claimed
US-4542235-A Method for producing an optically active 2,2-dimethylcyclopropanecarboxylic acid SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1985-09-17 US claimed
EP-0093511-A1 Method for producing and optically active 2,2-dimethylcyclopropanecarboxylic acid SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1983-11-09 EP claimed
EP-0082523-A2 Intermediates for the preparation of 4-phenyl-1,3-benzodiazepins and methods for preparing the intermediates HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1983-06-29 EP claimed
US-4297282-A REACTING AN A-METHYL-B-ACYLTHIOPROPIONIC ACID WITH AN OPTICALLY ACTIVE ARYLALKYL PRIMARY AMINE; CRYSTALLIZATION SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1981-10-27 US claimed
US-3970700-A Racemization of optically active amines SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1976-07-20 US claimed
US-3954870-A RANEY NICKEL CATALYST SUMITOMO CHEMICAL COMPANY, LIMITED (JA) 1976-05-04 US claimed