SCHEMBL6677158

SCHEMBL6677158

O=C(CC(c1ccccc1)S(=O)(=O)[O-])c1ccccc1O.[Na+]

nearest known ligand 0.44

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
CA12 known ✓ O43570 1/20 0.41
CA1 known ✓ P00915 1/20 0.41
CA2 known ✓ P00918 1/20 0.41
CA4 known ✓ P22748 1/20 0.41
NFKB1 P19838 1/20 0.44
NFKB2 Q00653 1/20 0.44
RELA Q04206 1/20 0.44
KDM4E B2RXH2 8/20 0.42
ALDH1A1 P00352 8/20 0.42
HPGD P15428 6/20 0.42
TDP1 Q9NUW8 3/20 0.41
HIF1A Q16665 1/20 0.41
SMN1; SMN2 Q16637 4/20 0.41
HMGB1 P09429 1/20 0.41
CA6 P23280 1/20 0.41
CA7 P43166 1/20 0.41
CA9 Q16790 1/20 0.41
NAPRT Q6XQN6 1/20 0.41
CA14 Q9ULX7 1/20 0.41
LMNA P02545 4/20 0.40

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
SCHEMBL6674306 0.85 SRC (0.46) NFKB1NFKB2RELAKDM4EALDH1A1
SCHEMBL6677164 0.84 SRC (0.45) NFKB1NFKB2RELAKDM4EALDH1A1
SCHEMBL6673822 0.81 ALDH1A1 (0.51) KDM4EALDH1A1HPGDTDP1SMN1; SMN2
SCHEMBL6674606 0.75 NPC1 (0.57) KDM4EALDH1A1TDP1SMN1; SMN2LMNA
SCHEMBL6680581 0.75 PDPK1 (0.52) KDM4EALDH1A1TDP1SMN1; SMN2LMNA
SCHEMBL6677052 0.74 PDE4A (0.45) KDM4EALDH1A1TDP1SMN1; SMN2LMNA
SCHEMBL6675659 0.74 HTT (0.49) NFKB1NFKB2RELAKDM4EALDH1A1
SCHEMBL15649525 0.73 HPGD (0.53) NFKB1NFKB2RELAKDM4EALDH1A1
SCHEMBL7253269 0.72 ALDH1A1 (0.65) KDM4EALDH1A1TDP1SMN1; SMN2LMNA
SCHEMBL9067586 0.71 KDM4E (0.73) NFKB1NFKB2RELAKDM4EALDH1A1

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
EP-1204636-B1 3-OXOPROPANE-1-SULPHONIC ACIDS AND SULPHONATES DSM IP ASSETS BV (NL) 2004-10-27 EP disclosed
US-6639103-B1 Enantiomerically enriched forms; resolving amino functiona-lized enantiomers DSM N.V. (NL) 2003-10-28 US disclosed