SCHEMBL336332

SCHEMBL336332

O=C1[CH]SCC1

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL5505223 0.82
SCHEMBL12816642 0.80
SCHEMBL3191508 0.77
SCHEMBL2346875 0.71
SCHEMBL5160170 0.66
SCHEMBL12817083 0.61
SCHEMBL16797719 0.59
SCHEMBL5433560 0.57
SCHEMBL1032769 0.56
SCHEMBL1593092 0.56

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2018170067-A1 SMALL MOLECULE SENSITIZATION OF BAX ACTIVATION FOR INDUCTION OF CELL DEATH DANA-FARBER CANCER INSTITUTE, INC. (US) 2018-09-20 WO claimed
US-9688645-B2 Macrocyclic urea and sulfamide derivatives as inhibitors of TAFIa SANOFI (FR) 2017-06-27 US claimed
US-20160251324-A1 MACROCYCLIC UREA AND SULFAMIDE DERIVATIVES AS INHIBITORS OF TAFIA SANOFI-AVENTIS (FR) 2016-09-01 US claimed
EP-2226319-B1 Process for the preparation of 2-(2-aminopyrimidin-4-yl)-1H-indol-5-carbonic acid derivatives SANOFI SA (FR) 2016-03-16 EP claimed
EP-2240486-B1 TRIAZOLIUM SALTS AS PAR1 INHIBITORS, THEIR MANUFACTURE AND THEIR APPLICATION AS MEDICINE SANOFI SA (FR) 2015-09-09 EP claimed
EP-2520568-B1 Spirocyclic nitriles as inhibitors of protease SANOFI SA (FR) 2015-09-09 EP claimed
EP-2104497-B1 SULFAMIDE DERIVATIVES AS TAFIA INHIBITORS SANOFI SA (FR) 2015-02-25 EP claimed
EP-2558465-B1 TRICYCLIC PYRIDYL-VINYL-PYROLES AS PAR1 INHIBITORS SANOFI SA (FR) 2014-12-17 EP claimed
US-8871798-B2 Tricyclic pyridyl-vinyl pyrroles as PAR1 inhibitors SANOFI (FR) 2014-10-28 US claimed
US-8853206-B2 Triazolium salts as PAR1 inhibitors, production thereof, and use as medicaments SANOFI (FR) 2014-10-07 US claimed
WO-2006077013-A1 TETRAHYDROFURANE DERIVATIVES FOR USE AS INHIBITORS OF MATRIX METALLOPROTEINASES SANOFI-AVENTIS (DE) 2006-07-27 WO claimed
EP-1670766-A1 BICYCLIC IMINO ACID DERIVATIVES USED AS INHIBITORS OF MATRIX-METALLOPROTEINASES Sanofi-Aventis Deutschland GmbH (DE) 2006-06-21 EP claimed
WO-2006002764-A1 4-TRIFLUOROMETHOXYPHENOXYBENZOL-4'-SULFONIC ACIDS, METHOD FOR THE PRODUCTION AND USE THEREOF IN MEDICAMENTS SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2006-01-12 WO claimed
EP-1585728-A1 IMINO ACID DERIVATIVES FOR USE AS INHIBITORS OF MATRIX METALLOPROTEINASES Aventis Pharma Deutschland GmbH (DE) 2005-10-19 EP claimed
WO-2005073236-A2 THIENO-IMINO ACID DERIVATIVES FOR USE AS MATRIX METALLOPROTEINASE INHIBITORS SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2005-08-11 WO claimed
US-20050080127-A1 Bicyclic imino acid derivatives as inhibitors of matrix metalloproteinases AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-04-14 US claimed
WO-2005030728-A1 BICYCLIC IMINO ACID DERIVATIVES USED AS INHIBITORS OF MATRIX-METALLOPROTEINASES SANOFI-AVENTIS DEUTSCHLAND GMBH (DE) 2005-04-07 WO claimed
US-20050004166-A1 Imino acid derivatives as inhibitors of matrix metalloproteinases AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2005-01-06 US claimed
WO-2004060874-A1 IMINO ACID DERIVATIVES FOR USE AS INHIBITORS OF MATRIX METALLOPROTEINASES AVENTIS PHARMA DEUTSCHLAND GMBH (DE) 2004-07-22 WO claimed
US-6646010-B2 Enzyme inhibitors such as N(3-benzyloxycarbonylamino-2-hydroxy -4-phenylbutyl)-N-isoamylamine, used for prophylaxis of viral diseases and infections; lymphadenopathy associated virus G. D. SEARLE & CO. 2003-11-11 US claimed