SCHEMBL2886387

SCHEMBL2886387

C=CC(OC(=O)O)c1ccccc1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 1/20 0.43
CYP2D6 P10635 1/20 0.40
SRC P12931 1/20 0.40
HCAR2 Q8TDS4 1/20 0.40
LMNA P02545 4/20 0.39
MAPK1 P28482 1/20 0.39
KMT2A Q03164 1/20 0.38
CES2 O00748 2/20 0.38
CES1 P23141 2/20 0.38
AKT1 P31749 1/20 0.38
ALDH1A1 P00352 1/20 0.37
CYP3A4 P08684 1/20 0.37
ESR1 P03372 1/20 0.37
ESR2 Q92731 1/20 0.37
TDP1 Q9NUW8 1/20 0.36
L3MBTL1 Q9Y468 1/20 0.36
HPGD P15428 1/20 0.36
HDAC3 O15379 1/20 0.35
HDAC4 P56524 1/20 0.35
HDAC1 Q13547 1/20 0.35

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
SCHEMBL2886386 0.88 CYP2C19 (0.43) CYP2C19CYP2D6SRCHCAR2LMNA
SCHEMBL3828726 0.85 CYP2D6 (0.44) CYP2C19CYP2D6SRCHCAR2LMNA
SCHEMBL299987 0.85 THRB (0.41) CYP2C19CYP2D6SRCHCAR2LMNA
SCHEMBL11216512 0.85 CYP2D6 (0.42) CYP2C19CYP2D6SRCHCAR2LMNA
SCHEMBL61038 0.85 CYP3A4 (0.50) CYP2C19CYP2D6SRCHCAR2LMNA
SCHEMBL28701229 0.83 ALDH1A1 (0.41) LMNAKMT2ACES2CES1ALDH1A1
SCHEMBL28450136 0.83 CYP2C19 (0.45) CYP2C19LMNAKMT2ACES2CES1
SCHEMBL29190248 0.83 TSHR (0.52) CYP2C19LMNAKMT2ACES2CES1
SCHEMBL5837445 0.83 KMT2A (0.47) CYP2C19CYP2D6HCAR2LMNAMAPK1
SCHEMBL14011311 0.82 HCAR2 (0.42) CYP2C19CYP2D6SRCHCAR2LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4889894-A Compatible polymer mixtures ROHM GMBH (DE) 1989-12-26 US claimed
CN-103814052-A Polymerizable composition containing (meth) acrylate monomer having thioether linkage PPG IND OHIO INC 2014-05-21 CN disclosed
US-7824899-B2 Preparation of enantiomerically enriched amines and amides by enzymatic resolution using a sulfonylacetic acid ester as acyl donor EVONIK DEGUSSA GMBH (DE) 2010-11-02 US disclosed
EP-1870475-B1 Process for the preparation of optically active amines and amides employing a hydrolase and sulfonyl acetic acid ester as the acyl donor EVONIK DEGUSSA GMBH (DE) 2008-12-10 EP disclosed
US-20070298471-A1 PROCESS FOR THE PREPARATION OF ENANTIOMERICALLY ENRICHED AMINES AND AMIDES BY ENZYMATIC RESOLUTION DEGUSSA GMBH (DE) 2007-12-27 US disclosed
EP-1870475-A1 Process for the preparation of optically active amines and amides employing a hydrolase and sulfonyl acetic acid ester as the acyl donor Evonik Degussa GmbH (DE) 2007-12-26 EP disclosed
EP-0268168-B1 COMPATIBLE POLYMER BLENDS RÖHM GMBH (DE) 1992-12-16 EP disclosed
US-5023123-A Molding materials ROHM GMBH (DE) 1991-06-11 US disclosed
US-4889894-A Compatible polymer mixtures ROHM GMBH (DE) 1989-12-26 US disclosed
EP-0268168-A2 Compatible polymer blends RÖHM GMBH (DE) 1988-05-25 EP disclosed
EP-0257419-A1 Process for the preparation of antibacterial 7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-ene derivatives HOECHST AKTIENGESELLSCHAFT (DE) 1988-03-02 EP disclosed
US-4330665-A Process for the preparation of aromatic polycarbonates BAYER AKTIENGESELLSCHAFT (DE) 1982-05-18 US disclosed