Trifluoromethanesulfonic Acid

Trifluoromethanesulfonic Acid

SCHEMBL160986

O=S(=O)([O-])C(F)(F)F.[Cu+].c1ccccc1

nearest known ligand 0.48

Full drug profile on Sugi Atlas →

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
GPR3 P46089 2/20 0.48
PTPN1 P18031 1/20 0.38
CA1 P00915 2/20 0.37
CA2 P00918 2/20 0.37
CA7 P43166 1/20 0.37
CA13 Q8N1Q1 1/20 0.37
KCNH2 Q12809 9/20 0.36
ACHE P22303 6/20 0.36
CA5A P35218 1/20 0.33
CA9 Q16790 1/20 0.33

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 SCHEMBL29642024 1.00 GPR3 (0.48) GPR3PTPN1CA1CA2CA7
Trifluoromethanesulfonic Acid SCHEMBL596729 0.93 GPR3 (0.48) GPR3PTPN1CA1CA2CA7
Trifluoromethanesulfonic Acid SCHEMBL10579458 0.93 GPR3 (0.48) GPR3PTPN1CA1CA2CA7
Trifluoromethanesulfonic Acid SCHEMBL25292546 0.89 GPR3 (0.48) GPR3PTPN1CA1CA2CA7
Trifluoromethanesulfonic Acid SCHEMBL164548 0.89
Trifluoromethanesulfonic Acid SCHEMBL6478953 0.89 CA1 (0.44) GPR3CA1CA2CA7CA13
Trifluoromethanesulfonic Acid SCHEMBL16829697 0.86 CA1 (0.41) GPR3CA1CA2CA7CA13
Trifluoromethanesulfonic Acid SCHEMBL25255863 0.82 CA1 (0.44) GPR3CA1CA2CA7CA13
Trifluoromethanesulfonic Acid SCHEMBL23430060 0.82 CA1 (0.44) GPR3CA1CA2CA7CA13
Trifluoromethanesulfonic Acid SCHEMBL25301943 0.82 CA1 (0.44) GPR3PTPN1CA1CA2CA7

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 770 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115716805-B Asymmetric catalytic synthesis method of chiral pyrazolone derivative containing propargyl alcohol structural fragment 重庆医科大学 2024-05-07 CN claimed
EP-3956321-B1 PROCESS FOR PREPARING AXITINIB, PROCESS FOR PURIFYING THE INTERMEDIATE 2-((3-IODO-1H-INDAZOL-6-YL)THIO)-N-METHYLBENZAMIDE, PROCESS FOR PURIFYING AXITINIB VIA THE AXITINIB HCL SALT, SOLID FORM OF THE AXITINIB HCL SALT SYNTHON BV (NL) 2024-03-20 EP claimed
CN-113444057-B Single chiral arm aminophenol sulfonamide ligand and application thereof in asymmetric catalysis 重庆医科大学 2023-06-20 CN claimed
US-20220389310-A1 LUMINESCENT MATERIALS AND METHODS THEREOF UNIVERSITY OF WASHINGTON (US) 2022-12-08 US claimed
CN-113214069-B Chiral 10-propargyl anthrone compound and synthetic method thereof 华中师范大学 2022-07-08 CN claimed
EP-3956321-A1 PROCESS FOR PREPARING AXITINIB, PROCESS FOR PURIFYING THE INTERMEDIATE 2-((3-IODO-1H-INDAZOL-6-YL)THIO)-N-METHYLBENZAMIDE, PROCESS FOR PURIFYING AXITINIB VIA THE AXITINIB HCL SALT, SOLID FORM OF THE AXITINIB HCL SALT Synthon B.V. (NL) 2022-02-23 EP claimed
WO-2021062035-A1 LUMINESCENT MATERIALS AND METHODS THEREOF UNIVERSITY OF WASHINGTON (US) 2021-04-01 WO claimed
WO-2020212253-A1 PROCESS FOR PREPARING AXITINIB, PROCESS FOR PURIFYING THE INTERMEDIATE 2-((3-IODO-1H-INDAZOL-6-YL)THIO)-N-METHYLBENZAMIDE, PROCESS FOR PURIFYING AXITINIB VIA THE AXITINIB HCL SALT, SOLID FORM OF THE AXITINIB HCL SALT SYNTHON B.V. (NL) 2020-10-22 WO claimed
EP-2460789-B1 METHOD FOR PRODUCING BIARYL COMPOUND SUMITOMO CHEMICAL CO (JP) 2017-04-19 EP claimed
EP-2855419-B1 NEW INDANYLOXYPHENYLCYCLOPROPANECARB OXYLIC ACIDS BOEHRINGER INGELHEIM INT (DE) 2017-03-01 EP claimed
US-8633182-B2 Indanyloxyphenylcyclopropanecarboxylic acids BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2014-01-21 US claimed
US-20130324514-A1 INDANYLOXYPHENYLCYCLOPROPANECARBOXYLIC ACIDS BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2013-12-05 US claimed
EP-2460789-A1 METHOD FOR PRODUCING BIARYL COMPOUND Sumitomo Chemical Company, Limited (JP) 2012-06-06 EP claimed
US-20120123154-A1 METHOD FOR PRODUCING BIARYL COMPOUND SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-05-17 US claimed
EP-2245020-A2 THIAZOLYLIDINE UREA AND AMIDE DERIVATIVES AND METHODS OF USE THEREOF Abbott Laboratories (US) 2010-11-03 EP claimed
WO-2009086163-A2 THIAZOLYLIDINE UREA AND AMIDE DERIVATIVES AND METHODS OF USE THEREOF ABBOTT LABORATORIES (US) 2009-07-09 WO claimed
US-20090163470-A1 THIAZOLYLIDINE UREA AND AMIDE DERIVATIVES AND METHODS OF USE THEREOF ABBOTT LABORATORIES (US) 2009-06-25 US claimed
US-4948904-A REACTING HYDROXYPHTHALIC ANHYDRIDE WITH BROMOPHTHALIC OR FLUOROPHTHALIC ANHYDRIDE IN PRESENCE OF COPPER CATALYST OCCIDENTAL CHEMICAL CORPORATION (US) 1990-08-14 US claimed
US-4946985-A REACTING A HALOPHTHALIC ANHYDRIDE WITH WATER AND ALKALI METAL COMPOUND; COPPER CATALYST OCCIDENTAL CHEMICAL CORPORATION (US) 1990-08-07 US claimed
US-4689427-A Hydroquinone derivatives useful in the production of vitamin E HOFFMANN-LA ROCHE INC. (US) 1987-08-25 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20090163470-A1 THIAZOLYLIDINE UREA AND AMIDE DERIVATIVES AND METHODS OF USE THEREOF NMUR1, NMUR2, PAM GPR3 302/4885PTPN1 1725/4885CA1 1235/4885
US-20130324514-A1 INDANYLOXYPHENYLCYCLOPROPANECARBOXYLIC ACIDS GPR119, GPR65, INSR GPR3 22/4885PTPN1 2123/4885CA1 3467/4885
US-20120123154-A1 METHOD FOR PRODUCING BIARYL COMPOUND AKR7A2, AOC2, CBR1 GPR3 2107/4885PTPN1 4606/4885CA1 1446/4885
US-20220389310-A1 LUMINESCENT MATERIALS AND METHODS THEREOF TYR, GSTA2, CYBA GPR3 2806/4885PTPN1 4329/4885CA1 2776/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.