Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL5433012

Cc1ccc([S+](c2ccc(C)cc2)c2ccc(Oc3ccc([S+](c4ccc(C)cc4)c4ccc(C)cc4)cc3)cc2)cc1.O=S(=O)([O-])C(F)(F)F.O=S(=O)([O-])C(F)(F)F

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.46
HTT P42858 4/20 0.46
TDP1 Q9NUW8 2/20 0.42
L3MBTL1 Q9Y468 1/20 0.42
KCNH2 Q12809 2/20 0.41
FFAR1 O14842 1/20 0.40
PTPN1 P18031 1/20 0.40
TEAD4 Q15561 1/20 0.39
GPR3 P46089 1/20 0.38
ALDH1A1 P00352 4/20 0.38
POLB P06746 2/20 0.38
MAPT P10636 1/20 0.38
PTGS1 P23219 1/20 0.38
MMP2 P08253 1/20 0.37
MMP9 P14780 1/20 0.37
AR P10275 1/20 0.37
CA1 P00915 1/20 0.37
CA2 P00918 1/20 0.37
CA9 Q16790 1/20 0.37
BCHE P06276 1/20 0.37

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
Trifluoromethanesulfonic Acid SCHEMBL4643748 0.92 HTT (0.40) SMN1; SMN2HTTTDP1L3MBTL1KCNH2
Trifluoromethanesulfonic Acid SCHEMBL36224 0.90 GPR3 (0.44) SMN1; SMN2KCNH2FFAR1GPR3ALDH1A1
Trifluoromethanesulfonic Acid SCHEMBL2901812 0.89 ACHE (0.47) KCNH2ALDH1A1MAPTBCHEACHE
Trifluoromethanesulfonic Acid SCHEMBL8862157 0.86 BCHE (0.40) SMN1; SMN2HTTKCNH2GPR3ALDH1A1
Trifluoromethanesulfonic Acid SCHEMBL5427818 0.85 SOS1 (0.43) SMN1; SMN2HTTFFAR1PTPN1GPR3
Trifluoromethanesulfonic Acid SCHEMBL5436738 0.84 ALDH1A1 (0.45) SMN1; SMN2HTTPTPN1ALDH1A1MAPT
Trifluoromethanesulfonic Acid SCHEMBL51417 0.84 SOS1 (0.46) SMN1; SMN2HTTFFAR1PTPN1GPR3
Trifluoromethanesulfonic Acid SCHEMBL31720833 0.84 KCNH2 (0.43) SMN1; SMN2HTTKCNH2GPR3ALDH1A1
Trifluoromethanesulfonic Acid SCHEMBL2324715 0.84 KCNH2 (0.43) SMN1; SMN2HTTKCNH2GPR3ALDH1A1
Trifluoromethanesulfonic Acid SCHEMBL9135540 0.83 ACHE (0.45) L3MBTL1KCNH2GPR3ALDH1A1CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070072120-A1 Method for producing resin for chemically amplified positive resist SUMITOMO SEIKA CHEMICALS CO., LTD. (JP) 2007-03-29 US disclosed
US-7144674-B2 Positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-12-05 US disclosed
US-7129014-B2 Positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-10-31 US disclosed
US-20060073411-A1 Chemically amplified resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2006-04-06 US disclosed
US-6893792-B2 Positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2005-05-17 US disclosed
US-20040191674-A1 Chemical amplification resist composition SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-09-30 US disclosed
US-6762007-B2 A BLENDS COMPRISING A PARTIALLY ETHERIFIED POLYHYDROXYSTYRENE-P AND A PARTIALLY ESTERIFIED POLYHYDROXYSTYRENE-P WITH PIVALIC ACID, AN ACID GENERATORS; PHOTOLITHOGRAPHY ACTIVATED BY HIGH-ENERGY ULTRAVIOLET RAY SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2004-07-13 US disclosed
US-20030236351-A1 Positive resist composition SUMITOMO CHEMICAL COMPANY, LIMITIED (JP) 2003-12-25 US disclosed
US-20030194639-A1 Positive resist composition FORTINET, INC. 2003-10-16 US disclosed
US-20030180663-A1 Chemical amplification type positive resist composition SUMITOMO CHEMICAL COMPANY (JP) 2003-09-25 US disclosed