SCHEMBL7953584

SCHEMBL7953584

CCC(=O)c1cc(C)c(C)cc1C

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSP90AB1 P08238 1/20 0.45
ALDH1A1 P00352 2/20 0.45
HSD17B10 Q99714 2/20 0.43
ALOX15 P16050 1/20 0.43
GAA P10253 1/20 0.42
HMGCR P04035 1/20 0.42
SMN1; SMN2 Q16637 2/20 0.41
ATM Q13315 1/20 0.41
MAPT P10636 5/20 0.41
LMNA P02545 3/20 0.41
RAB9A P51151 2/20 0.41
KDM4E B2RXH2 1/20 0.40
UBE2N P61088 1/20 0.40
MEN1 O00255 1/20 0.40
CYP3A4 P08684 1/20 0.40
PTGS1 P23219 1/20 0.40
DRD3 P35462 1/20 0.40
KMT2A Q03164 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.39
POLB P06746 2/20 0.38

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
SCHEMBL28048673 0.85 HSP90AB1 (0.50) HSP90AB1ALDH1A1HSD17B10ALOX15HMGCR
SCHEMBL15543252 0.85 ALDH1A1 (0.42) HSP90AB1ALDH1A1HSD17B10ALOX15GAA
SCHEMBL4841923 0.82 HMGCR (0.58) HSP90AB1ALDH1A1HSD17B10ALOX15HMGCR
SCHEMBL23544604 0.82 HPGD (0.53) ALDH1A1HSD17B10ALOX15GAASMN1; SMN2
SCHEMBL13284210 0.82 HSP90AB1 (0.52) HSP90AB1ALDH1A1HSD17B10ALOX15HMGCR
SCHEMBL11328772 0.81 GAA (0.42) ALDH1A1HSD17B10ALOX15GAASMN1; SMN2
SCHEMBL23520996 0.80 ALDH1A1 (0.56) HSP90AB1ALDH1A1HSD17B10ALOX15HMGCR
SCHEMBL10518482 0.80 HSP90AB1 (0.41) HSP90AB1ALDH1A1HSD17B10GAAHMGCR
SCHEMBL15543162 0.80 BAZ2B (0.44) HSP90AB1ALDH1A1HSD17B10GAAHMGCR
SCHEMBL9720571 0.80 HMGCR (0.56) ALDH1A1HMGCRSMN1; SMN2RAB9AKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2018089904-A1 HETEROCYCLIC MODULATORS OF LIPID SYNTHESIS 3-V BIOSCIENCES, INC. (US) 2018-05-17 WO disclosed
CN-103657631-A Catalyst and method for producing carboxylic acid and/or carboxylic anhydride in the presence of the catalyst MITSUBISHI GAS CHEMICAL CO 2014-03-26 CN disclosed
CN-101632925-B Catalyst and process for producing carboxylic acid and/or carboxylic acid anhydride using the same MITSUBISHI GAS CHEMICAL CO 2014-02-26 CN disclosed
WO-2001096277-A1 METHOD FOR PRODUCING 2,3,4,6-TETRAMETHYL MANDELIC ACID AND 2,3,4,6-TETRAMETHYL MANDELIC ACID ACETATE BAYER AKTIENGESELLSCHAFT (DE) 2001-12-20 WO disclosed
US-5103022-A Reacting dl-2-methyl-1-(4-trifluoromethylphenyl)-3-pyrrolidino -1-propanone with l-acetylphenylglycine to form corresponding diastereomeric salt, deposition, isolation of l-2-methyl-1-(4-trifluoromethylphenyl)-3-pyrrolidino-1-propanone NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1992-04-07 US disclosed
US-5057535-A Muscle relaxants NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1991-10-15 US disclosed
EP-0200942-A2 New derivatives of an aminoketone NIPPON KAYAKU KABUSHIKI KAISHA (JP) 1986-11-12 EP disclosed
US-4182730-A Process for the preparation of substituted dihydrocinnamaldehydes via novel β-chlorocinnamaldehydes GIVAUDAN CORPORATION (US) 1980-01-08 US disclosed