SCHEMBL5791802

SCHEMBL5791802

COc1ccc(CC(=O)C(=O)O)cc1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTBP2 P56545 1/20 0.64
HTT P42858 1/20 0.61
LDHA P00338 1/20 0.56
SMN1; SMN2 Q16637 2/20 0.56
USP2 O75604 1/20 0.56
TP53 P04637 1/20 0.56
KDM4E B2RXH2 1/20 0.56
POLB P06746 1/20 0.56
NPC1 O15118 1/20 0.54
F2 P00734 2/20 0.52
ALDH1A1 P00352 2/20 0.51
PTGS1 P23219 1/20 0.51
AKR1C3 P42330 1/20 0.51
AKR1C2 P52895 1/20 0.51
MAPT P10636 1/20 0.51
RAB9A P51151 1/20 0.51
CYP3A4 P08684 1/20 0.51
CYP2C19 P33261 1/20 0.51
PLG P00747 1/20 0.50
PRSS1 P07477 1/20 0.50

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
SCHEMBL240822 0.83 KDM4E (0.74) CTBP2HTTLDHASMN1; SMN2USP2
SCHEMBL4643470 0.82 HTT (0.59) CTBP2HTTLDHASMN1; SMN2USP2
SCHEMBL14813139 0.82 HTT (0.59) CTBP2HTTLDHASMN1; SMN2USP2
SCHEMBL7642020 0.82 HTT (0.65) CTBP2HTTSMN1; SMN2USP2TP53
SCHEMBL10640045 0.82 HTT (0.63) CTBP2HTTLDHASMN1; SMN2USP2
Hydrochloric Acid SCHEMBL2022863 0.82 KDM4E (0.72) CTBP2HTTLDHASMN1; SMN2USP2
SCHEMBL5969736 0.82 HTT (0.63) CTBP2HTTLDHASMN1; SMN2USP2
SCHEMBL27952524 0.82 KDM4E (0.72) CTBP2HTTLDHASMN1; SMN2USP2
Hydrogen Sulfide SCHEMBL29062416 0.82 KDM4E (0.72) CTBP2HTTLDHASMN1; SMN2USP2
4-Hydroxyphenylpyruvic Acid SCHEMBL8363620 0.81 TAS2R14 (0.56) CTBP2HTTSMN1; SMN2POLBNPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3619214-B1 GAMMA-SPIROKETAL-GAMMA-LACTONES AND PHARMACEUTICAL COMPOSITION CONTAINING SAME AND PROCESS FOR PREPARATION THEREOF COUNCIL SCIENT IND RES (IN) 2024-11-06 EP claimed
EP-3630776-B1 FURO[2,3-B]PYRAN-2-ONE COMPOUNDS AND PROCESS FOR PREPARATION THEREOF COUNCIL SCIENT IND RES (IN) 2023-05-17 EP claimed
EP-0912467-B1 ASYMMETRIC HYDROGENATION METHOD OF A KETONIC COMPOUND AND DERIVATIVE RHODIA CHIMIE SA (FR) 2002-04-24 EP claimed
WO-2023031246-A1 SUBSTITUTED THIOPHENE COMPOUNDS AS D-DOPACHROME TAUTOMERASE INHIBITORS RIJKSUNIVERSITEIT GRONINGEN (NL) 2023-03-09 WO disclosed
US-9310681-B2 Negative resist composition and patterning process using same SHIN-ETSU CHEMICAL CO., LTD. (JP) 2016-04-12 US disclosed
US-9310681-B2 Negative resist composition and patterning process using same SHIN-ETSU CHEMICAL CO., LTD. (JP) 2016-04-12 US disclosed
US-9310681-B2 Negative resist composition and patterning process using same SHIN-ETSU CHEMICAL CO., LTD. (JP) 2016-04-12 US disclosed
US-20150198883-A1 NEGATIVE RESIST COMPOSITION AND PATTERNING PROCESS USING SAME SHIN-ETSU CHEMICAL CO., LTD. (JP) 2015-07-16 US disclosed
US-20150198883-A1 NEGATIVE RESIST COMPOSITION AND PATTERNING PROCESS USING SAME SHIN-ETSU CHEMICAL CO., LTD. (JP) 2015-07-16 US disclosed
US-20150198883-A1 NEGATIVE RESIST COMPOSITION AND PATTERNING PROCESS USING SAME SHIN-ETSU CHEMICAL CO., LTD. (JP) 2015-07-16 US disclosed
EP-2574667-A1 Enzyme variants Technische Universität Graz (AT) 2013-04-03 EP disclosed
EP-0295890-B1 PROCESS OF PREPARING OPTICALLY ACTIVE ALCOHOL Takasago International Corporation (JP) 1992-09-16 EP disclosed
US-5066815-A Asymmetric hydrogenation of ketone, ruthenium-phosphine catalyst TAKASAGO INTERNATIONAL CORPORATION (JP) 1991-11-19 US disclosed
US-5028738-A Process for producing 2-oxo-3-aromatic carboxylic acid derivatives SAGAMI CHEMICAL RESEARCH CENTER (JP) 1991-07-02 US disclosed
US-4992544-A Intermediates for b-lactam antibiotics and b-lactamase inhibitor UNIVERSITY OF NOTRE DAME DU LAC (US) 1991-02-12 US disclosed
EP-0407588-A1 PROCESS FOR PRODUCING 2-OXO-3-AROMATIC CARBOXYLIC ACID DERIVATIVES SAGAMI CHEMICAL RESEARCH CENTER (JP) 1991-01-16 EP disclosed
EP-0386243-A1 PLATINUM (II) COMPLEXES SAGAMI CHEMICAL RESEARCH CENTER (JP) 1990-09-12 EP disclosed
US-4849345-A L-phenylalanine dehydrogenase and use thereof SAGAMI CHEMICAL RESEARCH CENTER (JP) 1989-07-18 US disclosed
EP-0295890-A2 Process of preparing optically active alcohol Takasago International Corporation (JP) 1988-12-21 EP disclosed
EP-0206460-A2 L-phenylalanine dehydrogenase and use thereof SAGAMI CHEMICAL RESEARCH CENTER (JP) 1986-12-30 EP disclosed