SCHEMBL6549549

SCHEMBL6549549

CCC(=O)C[S+](CC)CC.Cc1ccc(S(=O)(=O)[O-])cc1

nearest known ligand 0.39

Known targets — ChEMBL curated mechanism

CHRM1CHRM2CHRM3CHRM4CHRM5SLC6A2dacAdacBdacCftsImrcAmrcBmrdA

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
ALDH1A1 P00352 7/20 0.39
LMNA P02545 3/20 0.38
CYP3A4 P08684 2/20 0.38
CYP2D6 P10635 1/20 0.38
MAPK1 P28482 1/20 0.38
THPO P40225 1/20 0.38
TSHR P16473 2/20 0.37
GAA P10253 2/20 0.37
KMT2A Q03164 3/20 0.36
CYP2C9 P11712 3/20 0.36
MEN1 O00255 2/20 0.36
CA1 P00915 2/20 0.36
CA2 P00918 2/20 0.36
MMP1 P03956 1/20 0.36
MMP2 P08253 1/20 0.36
MMP9 P14780 1/20 0.36
MMP8 P22894 1/20 0.36
MMP13 P45452 1/20 0.36
CYP2C19 P33261 1/20 0.36
HSD11B1 P28845 1/20 0.36

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
SCHEMBL6551160 0.88 ALDH1A1 (0.37) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6549313 0.86 ALDH1A1 (0.40) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6551304 0.86 ALDH1A1 (0.40) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6551166 0.85 ALDH1A1 (0.41) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6551402 0.85 ALDH1A1 (0.41) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6549220 0.84 ALDH1A1 (0.41) ALDH1A1LMNACYP2D6TSHRKMT2A
SCHEMBL6551150 0.83 ALDH1A1 (0.43) ALDH1A1LMNACYP2D6TSHRKMT2A
SCHEMBL926758 0.83 GAA (0.48) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6551144 0.82 NPC1 (0.37) ALDH1A1LMNACYP3A4CYP2D6MAPK1
SCHEMBL6551397 0.82 ALDH1A1 (0.41) ALDH1A1LMNACYP3A4CYP2D6MAPK1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1167349-B1 Chemical amplifying type positive resist composition SUMITOMO CHEMICAL CO (JP) 2004-12-01 EP disclosed
US-20040224251-A1 Positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-11-11 US disclosed
US-6548220-B2 Containing acid generator SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2003-04-15 US disclosed
US-20020015913-A1 Chemical amplifying type positive resist composition and sulfonium salt SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-02-07 US disclosed
EP-1167349-A1 Chemical amplifying type positive resist composition and sulfonium salt SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-01-02 EP disclosed