Known targets — ChEMBL curated mechanism
ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
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.
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 SCHEMBL19915225 | 1.00 | CA1 (0.44) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL25301943 | 1.00 | CA1 (0.44) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL796767 | 0.96 | CA1 (0.41) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL28741583 | 0.96 | CA1 (0.41) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL28993864 | 0.96 | CA1 (0.41) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL28670856 | 0.96 | CA1 (0.41) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL29808804 | 0.93 | GPR3 (0.39) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL25285896 | 0.92 | CA1 (0.44) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL23430060 | 0.92 | CA1 (0.44) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL25292878 | 0.92 | CA1 (0.44) | — |
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 7157 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 |
|---|---|---|---|---|---|---|---|
| EP-4748882-A1 | NON-HALOGENATED HIGHLY FLAME RETARDANT COMPOSITE THERMOPLASTIC RESIN COMPOSITIONS CONTAINING RECYCLED RESINS AND MOLDED ARTICLES MADE THEREFROM | Hanwha TotalEnergies Petrochemical Co., Ltd. (KR) | 2026-05-27 | — | — | EP | claimed |
| CN-122091675-A | High-voltage polymer-based solid-state battery based on thermodynamic and kinetic regulation and control | — | 2026-05-26 | — | — | CN | claimed |
| CN-122080424-A | Tetraphenyl ethylene chiral metal cage complex based on chiral Pt metal coordination and preparation method and application thereof | — | 2026-05-26 | — | — | CN | claimed |
| CN-122091533-A | Preparation method of high-entropy sodium ferrous sulfate/carbon composite positive electrode material and application of high-entropy sodium ferrous sulfate/carbon composite positive electrode material in high-temperature sodium ion battery | — | 2026-05-26 | — | — | CN | claimed |
| CN-122091749-A | Flame-retardant high-stability liquid electrolyte additive, electrolyte, and preparation and application thereof | — | 2026-05-26 | — | — | CN | claimed |
| CN-122091800-A | High-adhesiveness wide-temperature-range aqueous zinc ion battery hydrogel electrolyte and preparation method and application thereof | — | 2026-05-26 | — | — | CN | claimed |
| CN-122079825-A | Synthesis method of nickel amidinate complex promoted by triflate | — | 2026-05-26 | — | — | CN | claimed |
| CN-122080523-A | Halogen-free high flame retardant composite thermoplastic resin composition containing recycled resin and molded article made therefrom | — | 2026-05-26 | — | — | CN | claimed |
| CN-117051441-B | Aluminum-containing heavy water-based electrolyte and preparation method and application thereof | CENTRAL SOUTH UNIVERSITY (CN) | 2026-05-26 | — | — | CN | claimed |
| CN-122091726-A | Double-salt flame-retardant gel polymer electrolyte, in-situ preparation method and battery | — | 2026-05-26 | — | — | CN | claimed |
| US-5097078-A | Using hydrogen peroxide | RHONE-POULENC CHIMIE (FR) | 1992-03-17 | — | — | US | claimed |
| CN-1053324-A | Produce the battery of secondary battery | UNIV OF CALIFONIA (US) | 1991-07-24 | — | — | CN | claimed |
| WO-1991006132-A1 | CELL FOR MAKING SECONDARY BATTERIES | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 1991-05-02 | — | — | WO | claimed |
| EP-0317572-A4 | METHOD OF PREPARING MERACETYL OXAZOLINES. | GEN HOSPITAL CORP (US) | 1989-11-23 | — | — | EP | claimed |
| EP-0317572-A1 | METHOD OF PREPARING PERACETYL OXAZOLINES | THE GENERAL HOSPITAL CORPORATION (US) | 1989-05-31 | — | — | EP | claimed |
| US-4785084-A | REACTION WITH TRIFLUOROMETHANESULFONIC ACID TO FORM PERACETYL OXAZOLINE | THE GENERAL HOSPITAL CORPORATION (US) | 1988-11-15 | — | — | US | claimed |
| WO-1988000951-A1 | METHOD OF PREPARING MERACETYL OXAZOLINES | THE GENERAL HOSPITAL CORPORATION (US) | 1988-02-11 | — | — | WO | claimed |
| US-4639364-A | WATER SOLUBLE SALT OF TRIFLUOROMETHANE COMPOUND | MALLINCKRODT, INC. (US) | 1987-01-27 | — | — | US | claimed |
| EP-0178184-A1 | Preparation of aromatic carbonyl compounds | RAYCHEM CORPORATION (a Delaware corporation) (US) | 1986-04-16 | — | — | EP | claimed |
| US-4153595-A | ADMIXTURE WITH ALKALINE EARTH OR ALKALI METAL SALTS OF HALOGENATED METHANESULFONIC ACIDS | GENERAL ELECTRIC COMPANY (US) | 1979-05-08 | — | — | US | claimed |