SCHEMBL5244036

SCHEMBL5244036

CC1CCC(C(C)C)C(O)(c2ccccc2)C1

nearest known ligand 0.43

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
NPSR1 Q6W5P4 3/20 0.43
MAPT P10636 2/20 0.43
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
LMNA P02545 1/20 0.41
HTT P42858 1/20 0.41
ATM Q13315 1/20 0.41
OPRL1 P41146 2/20 0.38
OPRM1 P35372 1/20 0.38
CCR2 P41597 1/20 0.38
MAPK1 P28482 1/20 0.38
RECQL P46063 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.37
CHRNA7 P36544 1/20 0.37

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
SCHEMBL12484267 1.00 NPSR1 (0.43) NPSR1MAPTMEN1KMT2ALMNA
SCHEMBL337275 0.80 CCR2 (0.36) NPSR1MAPTMEN1KMT2ACCR2
SCHEMBL4668738 0.78 CHRM2 (0.45) NPSR1MAPTMEN1KMT2ALMNA
SCHEMBL11437597 0.76 CCR2 (0.34) OPRL1CCR2
SCHEMBL597190 0.75 CCR2 (0.33) CCR2
SCHEMBL27997618 0.73 CYP2A6 (0.38) LMNA
SCHEMBL4753780 0.73 CCR2 (0.35) LMNACCR2
SCHEMBL5605712 0.71 CCR2 (0.36) LMNACCR2MAPK1
SCHEMBL4647450 0.71 KCNA5 (0.33) MEN1KMT2ALMNACHRNA7
SCHEMBL25428324 0.71 CHRNB2 (0.34) CCR2

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 18 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105622937-A Polyetherimide compositions and methods for the manufacture and use thereof SABIC INNOVATIVE PLASTICS IP BV 2016-06-01 CN disclosed
CN-103748133-B Polycarbonate compositions and for the preparation of with use its method SABIC INNOVATIVE PLASTICS IP B.V. (NL) 2015-09-16 CN disclosed
CN-103764722-A Polyetherimide compositions and methods of making and using the same SABIC INNOVATIVE PLASTICS IP 2014-04-30 CN disclosed
CN-103748133-A Polycarbonate compositions and methods for the manufacture and use thereof SABIC INNOVATIVE PLASTICS IP 2014-04-23 CN disclosed
CN-103748129-A Polyepoxides and epoxy resins and methods for the manufacture and use thereof SABIC INNOVATIVE PLASTICS IP 2014-04-23 CN disclosed
CN-103732652-A Polysulfone compositions and methods for the manufacture and use thereof SABIC INNOVATIVE PLASTICS IP 2014-04-16 CN disclosed
WO-2013118118-A1 ALPHA-HYDROGEN SUBSTITUTED NITROXYLS AND DERIVATIVES THEREOF AS CATALYSTS TECHNION RESEARCH AND DEVELOPMENT FOUNDATION LTD. (IL) 2013-08-15 WO disclosed
EP-1828089-A2 PROCESS FOR PREPARING BISPHENOLS General Electric Company (US) 2007-09-05 EP disclosed
WO-2006065570-A2 PROCESS FOR PREPARING BISPHENOLS GENERAL ELECTRIC COMPANY (US) 2006-06-22 WO disclosed
CN-1678657-A Bis-hydroxyphenyl menthane polyesters and polyester/polycarbonates and methods of making the same GEN ELECTRIC (US) 2005-10-05 CN disclosed
EP-1519976-A1 BIS-HYDROXYPHENYL MENTHANE POLYESTERS AND POLYESTER/POLYCARBONATES AND METHODS FOR MAKING SAME GENERAL ELECTRIC COMPANY (US) 2005-04-06 EP disclosed
WO-2004005367-A1 BIS-HYDROXYPHENYL MENTHANE POLYESTERS AND POLYESTER/POLYCARBONATES AND METHODS FOR MAKING SAME GENERAL ELECTRIC COMPANY (US) 2004-01-15 WO disclosed
EP-0751934-B1 SUBSTITUTED AZETIDINONE COMPOUNDS USEFUL AS HYPOCHOLESTEROLEMIC AGENTS SCHERING CORP (US) 1999-08-25 EP disclosed
EP-0751934-A1 SUBSTITUTED AZETIDINONE COMPOUNDS USEFUL AS HYPOCHOLESTEROLEMIC AGENTS SCHERING CORPORATION (US) 1997-01-08 EP disclosed
WO-1995026334-A1 SUBSTITUTED AZETIDINONE COMPOUNDS USEFUL AS HYPOCHOLESTEROLEMIC AGENTS SCHERING CORPORATION (US) 1995-10-05 WO disclosed
EP-0342904-A2 2-Hydroxy-3-(4-methoxyphenyl)-3-(2-aminophenylthio)propionic acid, 8'-phenylmenthyl ester, especially for diltiazem MARION LABORATORIES, INC. (a Delaware corporation) (US) 1989-11-23 EP disclosed
EP-0303562-A1 Process for the preparation of E/Z mixtures of 2-(bicyclo[3.3.0]octan-3-ylidene) acetic-acid derivatives with a major proportion of E or Z isomer SCHERING AKTIENGESELLSCHAFT (DE) 1989-02-15 EP disclosed
US-4187152-A Extractive distillation for separating ketones and/or alcohols from phenol and/or cresol ALLIED CHEMICAL CORPORATION (US) 1980-02-05 US disclosed