SCHEMBL5486543

SCHEMBL5486543

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

nearest known ligand 0.37

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 5)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.37
ALDH1A1 P00352 1/20 0.37
TSHR P16473 1/20 0.37
KMT2A Q03164 1/20 0.37
TSSK1B Q9BXA7 1/20 0.31

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
SCHEMBL29021353 0.80 MEN1 (0.35) MEN1ALDH1A1TSHRKMT2ATSSK1B
SCHEMBL364400 0.78
SCHEMBL28527739 0.77 MEN1 (0.37) MEN1ALDH1A1TSHRKMT2ATSSK1B
SCHEMBL126355 0.75 MEN1 (0.33) MEN1ALDH1A1TSHRKMT2A
SCHEMBL28348853 0.74 TP53 (0.40) MEN1ALDH1A1TSHRKMT2A
Sulfuric Acid SCHEMBL28159484 0.74 ALDH1A1 (0.47) MEN1ALDH1A1TSHRKMT2ATSSK1B
SCHEMBL11018854 0.72 MEN1 (0.33) MEN1ALDH1A1TSHRKMT2A
Potassium Ion SCHEMBL3298233 0.71
SCHEMBL9001606 0.71 ALDH1A1 (0.35) MEN1ALDH1A1TSHRKMT2ATSSK1B
Sulfuric Acid SCHEMBL20975176 0.71 TP53 (0.40) MEN1ALDH1A1TSHRKMT2A

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
US-7189798-B2 Composition containing mixture of dihydroxybutane sulfonates EASTMAN CHEMICAL COMPANY (US) 2007-03-13 US disclosed
EP-1425311-A4 CYCLODEXTRIN SULFONATES, GUEST INCLUSION COMPLEXES, METHODS OF MAKING THE SAME AND RELATED MATERIALS EASTMAN CHEM CO (US) 2004-12-01 EP disclosed
EP-1425311-A2 CYCLODEXTRIN SULFONATES, GUEST INCLUSION COMPLEXES, METHODS OF MAKING THE SAME AND RELATED MATERIALS EASTMAN CHEMICAL COMPANY (US) 2004-06-09 EP disclosed
US-20040054164-A1 Cyclodextrin sulfonates, guest inclusion complexes, methods of making the same and related materials EASTMAN CHEMICAL COMPANY (US) 2004-03-18 US disclosed
US-6610671-B2 Cyclodextrin derivatives for use in cosmetics, pharmacolog, cosmetic, or nutrients EASTMAN CHEMICAL COMPANY 2003-08-26 US disclosed
US-20020128468-A1 Cyclodextrin sulfonates, guest inclusion complexes methods of making the same and related materials BUCHANAN CHARLES M (US) 2002-09-12 US disclosed
WO-2002055562-A2 CYCLODEXTRIN SULFONATES, GUEST INCLUSION COMPLEXES, METHODS OF MAKING THE SAME AND RELATED MATERIALS EASTMAN CHEM CO (US) 2002-07-18 WO disclosed