Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL63150

O=S(=O)([O-])C(F)(F)F.O=S(=O)([O-])C(F)(F)F.O=S(=O)([O-])C(F)(F)F.[Yb+3]

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.44
CA2 P00918 2/20 0.44
CA7 P43166 1/20 0.44
CA13 Q8N1Q1 1/20 0.44
GPR3 P46089 2/20 0.42
ACHE P22303 2/20 0.33
KCNH2 Q12809 6/20 0.31
MEN1 O00255 1/20 0.31
ALDH1A1 P00352 1/20 0.31
TSHR P16473 1/20 0.31
KMT2A Q03164 1/20 0.31
F2 P00734 1/20 0.30
PRSS1 P07477 1/20 0.30
PRSS2 P07478 1/20 0.30
PRSS3 P35030 1/20 0.30

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 SCHEMBL6682798 1.00 CA1 (0.44) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL15569459 0.96 CA1 (0.41) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL6086977 0.96 CA1 (0.41) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL336135 0.96 CA1 (0.41) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL25287606 0.92 CA1 (0.44) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL23430060 0.92 CA1 (0.44) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL25292546 0.92 GPR3 (0.48) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL25292878 0.92 CA1 (0.44) CA1CA2CA7CA13GPR3
Trifluoromethanesulfonic Acid SCHEMBL20570425 0.92
Trifluoromethanesulfonic Acid SCHEMBL18788979 0.92 CA1 (0.44) CA1CA2CA7CA13GPR3

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

Appears in 4925 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117440957-B Process for the production of biotin intermediates DSM IP ASSETS B.V. (NL) 2026-05-26 CN claimed
CN-122079748-A Guaazulene triarylmethane, synthesis method and application thereof in preparation of antibacterial products 2026-05-26 CN claimed
WO-2026101069-A1 DEGRADABLE LOW-DIELECTRIC ECO-FRIENDLY EPOXY-BASED THERMOSETTING RESIN 숙명여자대학교산학협력단 2026-05-15 WO claimed
WO-2026099776-A1 A PROCESS FOR THE PREPARATION OF PACLITAXEL FRESENIUS KABI ONCOLOGY LTD. (IN) 2026-05-15 WO claimed
CN-122036496-A Preparation method for co-production of acetyl chloride and phosphorous acid, and product and application thereof 南通江山农药化工股份有限公司 2026-05-15 CN claimed
CN-122010956-A Chiral 1, 4-diazabicyclo [3.1.1] heptane derivatives, synthesis and application thereof 浙江师范大学 2026-05-12 CN claimed
US-20260090547-A1 BIO-INSECTICIDES FROM WASTE BIOMASS UNIVERSITY OF DELAWARE (US) 2026-04-02 US claimed
EP-4709483-A1 NEW 5H-PYRROLO[3,2-B:5,4-C']DIPYRIDINE DERIVATIVES AND 6,7,8,9-TETRAHYDRO-5H-PYRROLO[3,2-B:5,4-C']DIPYRIDINE USEFUL IN THE TREATMENT OF CANCER Institut Regional du Cancer de Montpellier (FR) 2026-03-18 EP claimed
CN-121574135-A Method for synthesizing 7-oxa-2-azabicyclo [3.3.1] non-3-alkene-1-alcohol by rare earth catalysis 北京化工大学 2026-02-27 CN claimed
EP-4688909-A1 POLYESTER ELASTOMERS FROM DI-CARBOXYLIC ACID OR TRI-CARBOXYLIC ACID, MONO-CARBOXYLIC ACID, AND POLYOL FOR COSMETIC AND PERSONAL CARE APPLICATIONS Momentive Performance Materials Inc. (US) 2026-02-11 EP claimed
WO-2000053313-A2 LANTHANIDE CATALYSTS FOR SYNTHESIS OF COMPOUNDS AND COMBINATORIAL LIBRARIES ARQULE, INC. (US) 2000-09-14 WO claimed
EP-1000937-A1 PROCESS FOR PRODUCING 4-ALKOXYCARBONYL-2-OXAZOLIDINONE COMPOUNDS UBE INDUSTRIES LIMITED (JP) 2000-05-17 EP claimed
WO-2000018724-A1 (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(n+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY MONSANTO COMPANY (US) 2000-04-06 WO claimed
EP-0742194-B1 Process for the preparation of substituted phenols RHONE POULENC NUTRITION ANIMAL (FR) 1999-08-04 EP claimed
EP-0658552-B1 Process for the preparation of alpha-tocopherol derivatives EISAI CO LTD (JP) 1999-03-31 EP claimed
US-5756695-A MONOSIALOGANGLISIDE LUDWIG INSTITUTE FOR CANCER RESEARCH (US) 1998-05-26 US claimed
US-5744617-A ALKYLATION OF PHENOLS WITH BUTADIENE DERIVATIVE RHONE-POULENC NUTRITION ANIMALE (FR) 1998-04-28 US claimed
US-5728901-A PERFLUOROALKYL SULFONATES, FLUOROSULFONATES, HEXAFLUOROPHOSPHATES, NITRATES AIR PRODUCTS AND CHEMICALS, INC. (US) 1998-03-17 US claimed
US-5532387-A CYCLIZATION OF TRIMETHYLHYDROQUINONE AND AN ALKENYL ALCOHOL, REUSABLE CATALYST, IIIB FLUOROSULFONATE, NITRATE, SULFATE, OR FLUOROALKYLSULFONATE EISAI CO., LTD. (JP) 1996-07-02 US claimed
EP-0658552-A1 Process for the preparation of alpha-tocopherol derivatives Eisai Co., Ltd. (JP) 1995-06-21 EP claimed