SCHEMBL7401882

SCHEMBL7401882

O=C(O)CC1=CCCc2ccccc21

nearest known ligand 0.59

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
SIGMAR1 Q99720 1/20 0.45
SRD5A1 P18405 1/20 0.44
SRD5A2 P31213 1/20 0.44
AKR1B1 P15121 4/20 0.43
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41
LMNA P02545 1/20 0.41
HPGD P15428 1/20 0.41
NOTUM Q6P988 1/20 0.41

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
SCHEMBL2674626 0.88 SIGMAR1 (0.43) SIGMAR1SRD5A1SRD5A2KDM4EALDH1A1
SCHEMBL28294184 0.85 ALDH1A1 (0.43) SIGMAR1SRD5A1SRD5A2KDM4EALDH1A1
SCHEMBL27821528 0.85 NOTUM (0.42) SIGMAR1SRD5A1SRD5A2KDM4EALDH1A1
SCHEMBL13090339 0.84 SIGMAR1 (0.47) SIGMAR1SRD5A1SRD5A2AKR1B1ALDH1A1
SCHEMBL7825602 0.83 SIGMAR1 (0.49) SIGMAR1SRD5A1SRD5A2KDM4EALDH1A1
SCHEMBL1520645 0.82 HTR6 (0.47) AKR1B1KDM4ELMNA
SCHEMBL30486873 0.82 HTR6 (0.47) AKR1B1KDM4ELMNA
SCHEMBL7403188 0.82 KDM4E (0.47) KDM4EALDH1A1HPGDNOTUM
Hydrochloric Acid SCHEMBL30279689 0.81 HTR6 (0.46) AKR1B1KDM4ELMNA
SCHEMBL3451418 0.80 AKR1B1 (0.56) AKR1B1

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
EP-2730918-B1 MATRIX FOR MALDI MASS SPECTROMETRY AND MALDI MASS SPECTROMETRY METHOD UNIV KYUSHU NAT UNIV CORP (JP) 2016-09-14 EP disclosed
WO-2014109712-A1 PALLADIUM-CATALYZED ASYMMETRIC (HETERO)ARYLATION AND VINYLATION OF KETONE ENOLATES TO PRODUCE TERTIARY STEREOCENTERS AT ALPHA(α)-POSITION NANAYNG TECHNOLOGICAL UNIVERSITY (SG) 2014-07-17 WO disclosed
US-20140151548-A1 MATRIX FOR MALDI MASS SPECTROMETRY AND MALDIMASS SPECTROMETRY METHOD KYUSHU UNIVERSITY, NATIONAL UNIVERSITY CORPORATION (JP) 2014-06-05 US disclosed
EP-2730918-A1 MATRIX FOR MALDI MASS SPECTROMETRY Kyushu University National University Corporation (JP) 2014-05-14 EP disclosed
US-6133446-A Heterocyclic compounds for the treatment of CNS and cardiovascular disorders PHARMACIA & UPJOHN COMPANY (US) 2000-10-17 US disclosed
CN-1046507-C Heterocyclic compounds for the treatment of central nervous system and cardiovascular diseases UPJOHN CO (US) 1999-11-17 CN disclosed
US-5877317-A Heterocyclic compounds for the treatment of CNS and cardiovascular disorders PHARMACIA & UPJOHN COMPANY (US) 1999-03-02 US disclosed
CN-1139431-A Heterocyclic compounds for the treatment of central nervous system and cardiovascular diseases PHARMACIA & UPJOHN CO LLC (US) 1997-01-01 CN disclosed
EP-0737189-A1 HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF CNS AND CARDIOVASCULAR DISORDERS PHARMACIA & UPJOHN COMPANY (US) 1996-10-16 EP disclosed
WO-1995018118-A1 HETEROCYCLIC COMPOUNDS FOR THE TREATMENT OF CNS AND CARDIOVASCULAR DISORDERS THE UPJOHN COMPANY (US) 1995-07-06 WO disclosed
EP-0287987-A1 Analgesic and antiinflammatory pharmaceutical compositions containing a naphthyl-acetic acid derivative L.B.S. S.r.l. LABORATORIO BIOCHIMICO SPERIMENTALE (IT) 1988-10-26 EP disclosed
EP-0287987-A1 Analgesic and antiinflammatory pharmaceutical compositions containing a naphthyl-acetic acid derivative L.B.S. S.r.l. LABORATORIO BIOCHIMICO SPERIMENTALE (IT) 1988-10-26 EP disclosed