Known targets — ChEMBL curated mechanism
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 15)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| Trifluoromethanesulfonic Acid SCHEMBL5960768 | 1.00 | CA1 (0.44) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL6683175 | 1.00 | CA1 (0.44) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL6744412 | 0.96 | CA1 (0.41) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL18835233 | 0.96 | CA1 (0.41) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL5960808 | 0.96 | CA1 (0.41) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL5795370 | 0.96 | CA1 (0.41) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL25285896 | 0.92 | CA1 (0.44) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL25287606 | 0.92 | CA1 (0.44) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL25301943 | 0.92 | CA1 (0.44) | CA1CA2CA7CA13GPR3 | |
| Trifluoromethanesulfonic Acid SCHEMBL23430060 | 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 2464 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122079748-A | Guaazulene triarylmethane, synthesis method and application thereof in preparation of antibacterial products | — | 2026-05-26 | — | — | CN | claimed |
| CN-117440957-B | Process for the production of biotin intermediates | DSM IP ASSETS B.V. (NL) | 2026-05-26 | — | — | CN | claimed |
| CN-122059808-A | Method for selectively synthesizing isopentenyl phenol compounds | 兰州石化职业技术大学 | 2026-05-19 | — | — | 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 |
| CN-122010969-A | Aminated 20 (S) -10, 11-difluoro methylenedioxy camptothecin derivative, and preparation method and application thereof | 浙江工业大学 | 2026-05-12 | — | — | CN | claimed |
| EP-4724512-A1 | METHOD FOR SYNTHESISING A GLYCEROL POLYESTER AND GLYCEROL POLYESTER OBTAINED THEREBY | COMPAGNIE GENERALE DES ETABLISSEMENTS MICHELIN (FR) | 2026-04-15 | — | — | EP | claimed |
| EP-4015592-B1 | CURABLE CONDENSATION COMPOUNDS ON THE BASIS OF ALKOXY-FUNCTIONAL POLYSILOXANES | EVONIK OPERATIONS GMBH (DE) | 2026-03-18 | — | — | EP | claimed |
| EP-4685150-A1 | METHOD FOR PRODUCING AMIDE GROUP-CONTAINING COMPOUND USING N-CARBOXYAMINO ACID ANHYDRIDE | CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) | 2026-01-28 | — | — | EP | claimed |
| US-20250368599-A1 | PROCESS FOR THE PREPARATION OF CYCLOHOMOGERANATES | BASF SE (DE) | 2025-12-04 | — | — | US | claimed |
| US-12460081-B2 | Curable condensation compounds based on alkoxy-functional polysiloxanes | EVONIK OPERATIONS GMBH (DE) | 2025-11-04 | — | — | US | claimed |
| WO-2003085071-A1 | PREPARATION OF LEVULINIC ACID ESTERS AND FORMIC ACID ESTERS FROM BIOMASS AND OLEFINS | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 2003-10-16 | — | — | WO | claimed |
| US-6608232-B1 | Acylating an aromatic compound in presence of zeolite or friedel crafts catalyst, reduction to a carbinol and cata-lytic etherification | Chimie, Rhodia (FR) | 2003-08-19 | — | — | US | claimed |
| US-20030109724-A1 | Manufacture of 3-methyl-tetrahydrofuran from alpha-methylene-gamma-butyrolactone in a two step process | INVISTA NORTH AMERICA S.A.R.L. | 2003-06-12 | — | — | US | claimed |
| US-20030065198-A1 | By hydrogenation | INVISTA NORTH AMERICA S.A.R.L. | 2003-04-03 | — | — | US | claimed |
| US-6348631-B1 | REACTING AROMATIC COMPOUND WITH ACYLATING OR SULFONYLATING AGENT IN PRESENCE OF FRIEDEL-CRAFTS CATALYST, WHEREIN ACYLATION OR SULFONYLATION REACTION IS CARRIED OUT IN LIQUID PHASE UNDER MICROWAVE IRRADIATION | RHODIA CHIMIE (FR) | 2002-02-19 | — | — | US | claimed |
| US-20020010374-A1 | Continuous process for the preparation of polytrimethylene ether glycol | DUPONT INDUSTRIAL BIOSCIENCES USA, LLC | 2002-01-24 | — | — | US | claimed |
| EP-0877726-B1 | AROMATIC COMPOUND ACYLATION METHOD | RHODIA CHIMIE SA (FR) | 2001-12-12 | — | — | EP | claimed |
| WO-2001000552-A9 | SELECTIVE ALKANOL ALKOXYLATIONS PROCESS | UNION CARBIDE CHEM PLASTIC (US) | 2001-06-21 | — | — | WO | claimed |
| WO-2001000552-A1 | SELECTIVE ALKANOL ALKOXYLATIONS PROCESS | UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) | 2001-01-04 | — | — | WO | claimed |
| CN-1249737-A | Method for acylation or sulphonation of aromatic compound | RHODIA CHIMIE SA (FR) | 2000-04-05 | — | — | CN | claimed |