SCHEMBL9767835

SCHEMBL9767835

O=C(C=Cc1cccs1)Nc1ccccc1C(=O)[O-].[Na+]

nearest known ligand 0.66

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 10/20 0.66
SMN1; SMN2 Q16637 9/20 0.66
NPC1 O15118 8/20 0.66
MAPT P10636 7/20 0.54
MEN1 O00255 7/20 0.54
KMT2A Q03164 7/20 0.54
KDM4E B2RXH2 5/20 0.54
LMNA P02545 4/20 0.54
HTT P42858 3/20 0.54
PSMD14 O00487 1/20 0.54
TP53 P04637 1/20 0.54
GLA P06280 1/20 0.54
ALDH1A1 P00352 8/20 0.53
MAPK1 P28482 1/20 0.52
CYP1A2 P05177 1/20 0.52
CYP2D6 P10635 1/20 0.52
GAA P10253 1/20 0.52
ABCG2 Q9UNQ0 1/20 0.50
ALPL P05186 1/20 0.50
ALPI P09923 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
SCHEMBL9768214 0.97 RAB9A (0.66) RAB9ASMN1; SMN2NPC1MAPTMEN1
Potassium Ion SCHEMBL9767821 0.97 RAB9A (0.66) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL9767854 0.86 RAB9A (0.69) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL13854028 0.86 RAB9A (0.69) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL9768217 0.85 RAB9A (0.67) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL9767841 0.83 SMN1; SMN2 (0.68) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL27752033 0.80 RAB9A (0.71) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL27752039 0.80 RAB9A (0.71) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL9767935 0.79 SMN1; SMN2 (0.62) RAB9ASMN1; SMN2NPC1MAPTMEN1
SCHEMBL9767800 0.79 ALDH1A1 (0.67) RAB9ASMN1; SMN2NPC1MAPTMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5006548-A Hyaluronidase inhibitors, antiallergens, immunomodulators SAWAI PHARMACEUTICAL CO., LTD. (JP) 1991-04-09 US disclosed
EP-0153850-B1 ACRYLAMIDOBENZOIC ACID DERIVATIVES AND THEIR USE SAWAI PHARMACEUTICAL CO., LTD. (JP) 1989-09-13 EP disclosed