SCHEMBL6549790

SCHEMBL6549790

CC(=O)C[S+](C)C1CCCCC1.Cc1ccc(S(=O)(=O)[O-])cc1

nearest known ligand 0.41

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 19)

geneUniProtsupporting neighboursconfidence
ADORA3 P0DMS8 1/20 0.41
ALDH1A1 P00352 8/20 0.40
TSHR P16473 2/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2C9 P11712 1/20 0.40
POLB P06746 3/20 0.40
HSD17B10 Q99714 2/20 0.38
HTT P42858 1/20 0.38
GAA P10253 1/20 0.38
KCNH2 Q12809 1/20 0.38
ACHE P22303 1/20 0.38
KMT2A Q03164 1/20 0.37
TP53 P04637 1/20 0.37
LMNA P02545 2/20 0.37
EPHX2 P34913 1/20 0.37
AKR1C3 P42330 1/20 0.36
ENPP3 O14638 1/20 0.36
ENPP1 P22413 1/20 0.36
ENPP2 Q13822 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
SCHEMBL6550691 0.87 ADORA3 (0.40) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6735792 0.87 ALDH1A1 (0.43) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6728663 0.87 ALDH1A1 (0.43) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6726338 0.86 ALDH1A1 (0.39) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6550779 0.86 TSHR (0.41) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6549432 0.85 ADORA3 (0.38) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6550369 0.83 CCR1 (0.37) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6550976 0.82 ADORA3 (0.36) ADORA3ALDH1A1TSHRCYP3A4CYP2C9
SCHEMBL6551324 0.81 ALDH1A1 (0.38) ADORA3ALDH1A1TSHRCYP2C9HTT
SCHEMBL6551138 0.78 ALDH1A1 (0.42) ALDH1A1CYP3A4CYP2C9POLBGAA

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