SCHEMBL6549683

SCHEMBL6549683

CCCCCC(=O)C[S+]1CCCCC1.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 4/20 0.39
LMNA P02545 3/20 0.38
CYP2C9 P11712 2/20 0.38
TSHR P16473 2/20 0.38
KCNH2 Q12809 2/20 0.38
CYP2D6 P10635 2/20 0.38
CYP2C19 P33261 1/20 0.38
HTT P42858 1/20 0.38
HIF1A Q16665 1/20 0.38
ALB P02768 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
RAB9A P51151 1/20 0.36
KMT2A Q03164 1/20 0.36
MCHR1 Q99705 1/20 0.36
NR1I2 O75469 1/20 0.35
HSD17B10 Q99714 1/20 0.35
CA1 P00915 1/20 0.34
CA2 P00918 1/20 0.34
CYP3A4 P08684 1/20 0.34
MAPK1 P28482 1/20 0.34

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
SCHEMBL6549225 0.99 ALDH1A1 (0.40) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6549842 0.99 ALDH1A1 (0.39) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6550375 0.98 ALDH1A1 (0.41) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6550445 0.96 ALDH1A1 (0.38) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6550664 0.95 ALDH1A1 (0.39) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6551056 0.91 ALDH1A1 (0.37) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6549461 0.90 LMNA (0.37) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6723253 0.88 ALDH1A1 (0.37) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6726210 0.88 ALDH1A1 (0.37) ALDH1A1LMNACYP2C9TSHRKCNH2
SCHEMBL6726465 0.88 ALDH1A1 (0.38) ALDH1A1LMNACYP2C9TSHRKCNH2

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