Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL1698310

CC(=O)O.CC(=O)O.CC(=O)O.CC(=O)O.O=S(=O)(O)C(F)(F)F

nearest known ligand 0.52

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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 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.52
L3MBTL1 Q9Y468 1/20 0.52
FFAR3 O14843 1/20 0.44
LCK P06239 1/20 0.44
FYN P06241 1/20 0.44
CA1 P00915 2/20 0.35
CA2 P00918 2/20 0.35
CA7 P43166 1/20 0.35
CA13 Q8N1Q1 1/20 0.35
MAPK1 P28482 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
TSHR P16473 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
F2 P00734 2/20 0.31
PRSS1 P07477 2/20 0.31
PRSS2 P07478 2/20 0.31
PRSS3 P35030 2/20 0.31

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 SCHEMBL17318233 1.00 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL1663542 1.00 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL10796158 1.00 ALDH1A1 (0.52) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL6288403 0.97 ALDH1A1 (0.50) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL17508492 0.97 ALDH1A1 (0.50) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL5093696 0.94 ALDH1A1 (0.48) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL261406 0.94 ALDH1A1 (0.48) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL7647499 0.90 ALDH1A1 (0.48) ALDH1A1L3MBTL1CA1CA2CA7
Trifluoromethanesulfonic Acid SCHEMBL2167128 0.89 ALDH1A1 (0.44) ALDH1A1L3MBTL1FFAR3LCKFYN
Trifluoromethanesulfonic Acid SCHEMBL28053484 0.85 ALDH1A1 (0.43) 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 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2569071-B1 METHOD FOR THE DIRECT ELUTION OF REACTIVE [18F]FLUORIDE FROM AN ANION EXCHANGE RESIN IN AN ORGANIC MEDIUM SUITABLE FOR RADIOLABELLING WITHOUT ANY EVAPORATION STEP BY THE USE OF ALKALIMETAL AND ALKALINE EARTH METAL CRYPTATES UNIV MUENCHEN TECH (DE) 2015-07-08 EP disclosed
EP-2569071-A1 METHOD FOR THE DIRECT ELUTION OF REACTIVE [18F]FLUORIDE FROM AN ANION EXCHANGE RESIN IN AN ORGANIC MEDIUM SUITABLE FOR RADIOLABELLING WITHOUT ANY EVAPORATION STEP BY THE USE OF ALKALIMETAL AND ALKALINE EARTH METAL CRYPTATES Technische Universität München (DE) 2013-03-20 EP disclosed
WO-2011141410-A1 METHOD FOR THE DIRECT ELUTION OF REACTIVE [18F]FLUORIDE FROM AN ANION EXCHANGE RESIN IN AN ORGANIC MEDIUM SUITABLE FOR RADIOLABELLING WITHOUT ANY EVAPORATION STEP BY THE USE OF ALKALIMETAL AND ALKALINE EARTH METAL CRYPTATES Technische Universität München (DE) 2011-11-17 WO disclosed