Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL6288403

CC(=O)O.O=S(=O)(O)C(F)(F)F.[Sc]

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Trifluoromethanesulfonic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.50
L3MBTL1 Q9Y468 1/20 0.50
FFAR3 O14843 1/20 0.41
LCK P06239 1/20 0.41
FYN P06241 1/20 0.41
CA1 P00915 2/20 0.33
CA2 P00918 2/20 0.33
CA7 P43166 1/20 0.33
CA13 Q8N1Q1 1/20 0.33
MAPK1 P28482 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
TSHR P16473 1/20 0.32
TDP1 Q9NUW8 1/20 0.32

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 SCHEMBL1698310 0.97 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL17318233 0.97 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL10796158 0.97 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL1663542 0.97 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL17508492 0.94 ALDH1A1 (0.50) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL261406 0.92 ALDH1A1 (0.48) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL5093696 0.92 ALDH1A1 (0.48) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL7647499 0.88 ALDH1A1 (0.48) ALDH1A1L3MBTL1CA1CA2CA7
Trifluoromethanesulfonic Acid SCHEMBL2167128 0.87 ALDH1A1 (0.44) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL8369202 0.84 ALDH1A1 (0.47) ALDH1A1L3MBTL1CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6916963-B2 Process using water tolerant Lewis acids in catalytic hydration of alkylene oxides to alkylene glycols SAUDI BASIC INDUSTRIES CORPORATION (SA) 2005-07-12 US claimed
US-20050014980-A1 Process using water tolerant lewis acids in catalytic hydration of alkylene oxides to alkylene glycols SAUDI BASIC INDUSTRIES CORPORATION 2005-01-20 US claimed
US-6916963-B2 Process using water tolerant Lewis acids in catalytic hydration of alkylene oxides to alkylene glycols SAUDI BASIC INDUSTRIES CORPORATION (SA) 2005-07-12 US disclosed
US-6916963-B2 Process using water tolerant Lewis acids in catalytic hydration of alkylene oxides to alkylene glycols SAUDI BASIC INDUSTRIES CORPORATION (SA) 2005-07-12 US disclosed
US-20050014980-A1 Process using water tolerant lewis acids in catalytic hydration of alkylene oxides to alkylene glycols SAUDI BASIC INDUSTRIES CORPORATION 2005-01-20 US disclosed
US-20050014980-A1 Process using water tolerant lewis acids in catalytic hydration of alkylene oxides to alkylene glycols SAUDI BASIC INDUSTRIES CORPORATION 2005-01-20 US disclosed