SCHEMBL7004872

SCHEMBL7004872

COC(=O)C(N)Cc1csc2ccccc12.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.52

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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 18)

geneUniProtsupporting neighboursconfidence
F10 known ✓ P00742 1/20 0.37
TP53 P04637 2/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
RXFP1 Q9HBX9 1/20 0.47
DPP4 P27487 2/20 0.43
DPP8 Q6V1X1 2/20 0.43
DPP9 Q86TI2 2/20 0.43
CA1 P00915 2/20 0.41
CA2 P00918 2/20 0.41
OPRD1 P41143 1/20 0.41
CA12 O43570 1/20 0.39
CA4 P22748 1/20 0.39
CA9 Q16790 1/20 0.39
TACR1 P25103 1/20 0.39
CTSL P07711 1/20 0.38
CTSS P25774 1/20 0.38
CTSK P43235 1/20 0.38
CYP2A6 P11509 2/20 0.37

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
SCHEMBL3743962 0.87 DPP4 (0.49) TP53SMN1; SMN2RXFP1DPP4DPP8
SCHEMBL2536966 0.87 DPP4 (0.49) TP53SMN1; SMN2RXFP1DPP4DPP8
SCHEMBL2536963 0.87 DPP4 (0.49) TP53SMN1; SMN2RXFP1DPP4DPP8
Hydrochloric Acid SCHEMBL3743959 0.85 DPP4 (0.48) TP53SMN1; SMN2RXFP1DPP4DPP8
Hydrochloric Acid SCHEMBL3743965 0.85 DPP4 (0.48) TP53SMN1; SMN2RXFP1DPP4DPP8
SCHEMBL7011991 0.78 OPRD1 (0.51) TP53SMN1; SMN2RXFP1DPP4DPP8
SCHEMBL4902378 0.78 OPRD1 (0.51) TP53SMN1; SMN2RXFP1DPP4DPP8
Hydrochloric Acid SCHEMBL4902375 0.77 OPRD1 (0.50) TP53SMN1; SMN2RXFP1DPP4DPP8
Hydrochloric Acid SCHEMBL7008761 0.77 OPRD1 (0.50) TP53SMN1; SMN2RXFP1DPP4DPP8
SCHEMBL24709579 0.73 CYP2A6 (0.53) TP53SMN1; SMN2RXFP1DPP4DPP8

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-0285671-B1 PYRIDINE DERIVATIVES ASAHI CHEMICAL IND (JP) 2003-09-03 EP disclosed
US-5126448-A Anxiolytic agents, learning enhancement ASAHI KASEI KOGYO K.K. (JP) 1992-06-30 US disclosed
EP-0285671-A1 PYRIDINE DERIVATIVES Asahi Kasei Kabushiki Kaisha (JP) 1988-10-12 EP disclosed