SCHEMBL7211832

SCHEMBL7211832

CC=CC(=O)NC(C)CS(=O)(=O)[O-].[Na+]

nearest known ligand 0.36

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 14)

geneUniProtsupporting neighboursconfidence
ACACB O00763 1/20 0.36
TAAR1 Q96RJ0 1/20 0.33
ALDH1A1 P00352 4/20 0.32
GAA P10253 1/20 0.32
CYP1A2 P05177 1/20 0.31
CYP3A4 P08684 1/20 0.31
CYP2C9 P11712 1/20 0.31
MAPK1 P28482 1/20 0.31
CYP2C19 P33261 1/20 0.31
TSHR P16473 1/20 0.31
L3MBTL1 Q9Y468 2/20 0.30
TP53 P04637 1/20 0.30
TAS1R3 Q7RTX0 1/20 0.30
TAS1R1 Q7RTX1 1/20 0.30

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
SCHEMBL7211824 1.00 ACACB (0.36) ACACBTAAR1ALDH1A1GAACYP1A2
SCHEMBL3685622 0.84 TSHR (0.48) ACACBALDH1A1MAPK1CYP2C19TSHR
SCHEMBL8961250 0.82 ACACB (0.38) ACACBTAAR1ALDH1A1GAACYP1A2
SCHEMBL8961255 0.82 ACACB (0.38) ACACBTAAR1ALDH1A1GAACYP1A2
Potassium Ion SCHEMBL9616732 0.81 TSHR (0.48) ACACBALDH1A1MAPK1CYP2C19TSHR
SCHEMBL20450459 0.74 TAS1R3 (0.47) ACACBTAAR1ALDH1A1GAATSHR
SCHEMBL20586386 0.71 CNR2 (0.45) ACACBTAAR1ALDH1A1GAACYP1A2
SCHEMBL27602907 0.70 TGFBR1 (0.44)
SCHEMBL27651780 0.69 ACACB (0.39) ACACBTAAR1ALDH1A1GAACYP1A2
SCHEMBL9578217 0.69 POLB (0.43) L3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0558612-B1 POLYMER BLENDS FOR AQUEOUS DISPERSIONS HAVING IMPROVED FREEZE-THAW STABILITY EASTMAN CHEM CO (US) 1996-01-10 EP claimed
US-5268412-A Sulfonate group containing poly(amide)esters EASTMAN KODAK COMPANY (US) 1993-12-07 US claimed
EP-0558612-A1 POLYMER BLENDS FOR AQUEOUS DISPERSIONS HAVING IMPROVED FREEZE-THAW STABILITY. EASTMAN KODAK CO (US) 1993-09-08 EP claimed
WO-1992009657-A1 POLYMER BLENDS FOR AQUEOUS DISPERSIONS HAVING IMPROVED FREEZE-THAW STABILITY EASTMAN KODAK COMPANY (US) 1992-06-11 WO claimed
US-6548571-B1 Mixing ink, colorant and latex generated by addition poymerization of A-olefin and sodium- or potassium vinylsulfonate XEROX CORPORATION 2003-04-15 US disclosed
EP-0558612-B1 POLYMER BLENDS FOR AQUEOUS DISPERSIONS HAVING IMPROVED FREEZE-THAW STABILITY EASTMAN CHEM CO (US) 1996-01-10 EP disclosed
US-5268412-A Sulfonate group containing poly(amide)esters EASTMAN KODAK COMPANY (US) 1993-12-07 US disclosed