SCHEMBL4444134

SCHEMBL4444134

COc1ccc(Cl)cc1.[MgH2]

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.65
CA2 P00918 2/20 0.65
CA7 P43166 2/20 0.65
CA9 Q16790 2/20 0.65
CA12 O43570 1/20 0.65
CA14 Q9ULX7 1/20 0.65
HPGD P15428 1/20 0.64
ACHE P22303 1/20 0.52
TDP1 Q9NUW8 3/20 0.50
MAPK1 P28482 2/20 0.50
NPC1 O15118 2/20 0.50
RAB9A P51151 2/20 0.50
AHR P35869 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
MAOB P27338 2/20 0.48
PTGS2 P35354 2/20 0.48
MAOA P21397 1/20 0.48
NFE2L2 Q16236 1/20 0.48
KDM4E B2RXH2 1/20 0.48
GAA P10253 1/20 0.48

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
SCHEMBL154527 0.97
SCHEMBL2226770 0.97
Chloromethane SCHEMBL9703019 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
Hydrochloric Acid SCHEMBL11293911 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
SCHEMBL29069477 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
SCHEMBL28525728 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
Iodide SCHEMBL5695908 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
Water SCHEMBL9443323 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
Water SCHEMBL28888589 0.94 CA1 (0.65) CA1CA2CA7CA9CA12
Ammonia Solution, Strong SCHEMBL4259791 0.94 CA1 (0.65) CA1CA2CA7CA9CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108178724-A The preparation method of compound 四川大学 2018-06-19 CN claimed
CN-106397320-A A synthetic method of a hexahydro cis dimethyl bridged-ring compound 和鼎(南京)医药技术有限公司 2017-02-15 CN claimed
CN-1289190-C Process for preparing aryl compounds BAYER AG (DE) 2006-12-13 CN claimed
CN-1466487-A Process for preparing aryl compounds 2004-01-07 CN claimed
CN-113999232-B MAT2A inhibitors 南京正大天晴制药有限公司 2025-01-07 CN disclosed
CN-110590778-B 3, 10 di-p-methoxyphenyl 6, 12 diaza tetracubane compound, synthetic method and pharmaceutical composition 华北理工大学 2022-02-08 CN disclosed
CN-108178724-B Process for the preparation of compounds 四川大学 2020-09-11 CN disclosed
CN-110590778-A 3, 10 di-p-methoxyphenyl 6, 12 diaza tetracubane compound, synthetic method and application thereof, and pharmaceutical composition 华北理工大学 2019-12-20 CN disclosed
CN-108178724-A The preparation method of compound 四川大学 2018-06-19 CN disclosed
CN-106397320-A A synthetic method of a hexahydro cis dimethyl bridged-ring compound 和鼎(南京)医药技术有限公司 2017-02-15 CN disclosed
CN-102666504-B Compounds as lysophosphatidic acid receptor antagonists AMIRA PHARMACEUTICALS, INC. (US) 2016-06-01 CN disclosed
EP-0895992-B1 Copper complexes of optically active bisoxazolines as enantioselective catalysts in cyclopropanation reactions SUMITOMO CHEMICAL CO (JP) 2009-06-10 EP disclosed
CN-1250524-C Method for preparing 2-cyanobiphenyl derivatives HUAHAI PHARMACEUTICAL CO LTD Z (CN) 2006-04-12 CN disclosed
CN-1528740-A Method for preparing 2-cyanobiphenyl derivatives 浙江华海药业股份有限公司 2004-09-15 CN disclosed
CN-1466487-A Process for preparing aryl compounds 2004-01-07 CN disclosed
US-6410741-B1 INSECTICIDES SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-06-25 US disclosed
US-6072081-A Optically active bisoxazoline compounds, production and use thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2000-06-06 US disclosed
EP-0895992-A2 Copper complexes of optically active bisoxazolines as enantioselective catalysts in cyclopropanation reactions SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1999-02-10 EP disclosed
CN-1087092-A Novel 7 beta-substituted-4-aza-5 alpha-androstan-3-ones as 5 alpha-reductase inhibitors MERCK & CO INC (US) 1994-05-25 CN disclosed
EP-0465123-A2 New intermediates in the synthesis of 17beta-acyl-3-carboxy-androsta-3,5-dienes MERCK & CO. INC. (US) 1992-01-08 EP disclosed