SCHEMBL7026181

SCHEMBL7026181

CC(=O)O[C@H](C)C=Cc1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 3/20 0.48
GLA P06280 1/20 0.48
CYP1A2 P05177 3/20 0.47
ALDH1A1 P00352 2/20 0.42
CYP2C9 P11712 2/20 0.42
HDAC3 O15379 1/20 0.42
TNKS O95271 1/20 0.42
HDAC4 P56524 1/20 0.42
HDAC1 Q13547 1/20 0.42
HCAR2 Q8TDS4 1/20 0.42
HDAC7 Q8WUI4 1/20 0.42
HDAC2 Q92769 1/20 0.42
HDAC10 Q969S8 1/20 0.42
HDAC11 Q96DB2 1/20 0.42
HDAC8 Q9BY41 1/20 0.42
TNKS2 Q9H2K2 1/20 0.42
HDAC6 Q9UBN7 1/20 0.42
HDAC9 Q9UKV0 1/20 0.42
HDAC5 Q9UQL6 1/20 0.42
PLIN1 O60240 1/20 0.42

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
SCHEMBL7028151 1.00 TDP1 (0.48) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL12738779 1.00 TDP1 (0.48) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL7022280 1.00 TDP1 (0.48) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL7022285 1.00 TDP1 (0.48) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL7017483 1.00 TDP1 (0.48) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL21055708 0.87 CYP1A2 (0.49) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL21055707 0.87 CYP1A2 (0.49) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL7194535 0.87 CYP1A2 (0.49) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL7097856 0.85 TDP1 (0.52) TDP1GLACYP1A2ALDH1A1CYP2C9
SCHEMBL1199677 0.85 TDP1 (0.52) TDP1GLACYP1A2ALDH1A1CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0872467-B1 Process for the production of chiral unsaturated alcohols in high optical purity EASTMAN CHEM CO (US) 2003-01-22 EP disclosed
US-5886214-A CATALYTIC ASYMMETRIC HYDROGENATION OF ENOL ESTERS BEARING A VINYLLIC OR AN ACETYLENIC SUBSTITUENT BY USING A CHIRAL RHODIUM(I) HYDROGENATION CATALYST PREPARED FROM A SUITABLE RHODIUM SALT AND AN OPTICALLY PURE PHOSPHINE LIGAND EASTMAN CHEMICAL COMPANY (US) 1999-03-23 US disclosed
EP-0872467-A1 Process for the production of chiral unsaturated alcohols in high optical purity EASTMAN CHEMICAL COMPANY (US) 1998-10-21 EP disclosed