Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
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 SCHEMBL29105899 | 1.00 | ALDH1A1 (0.47) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL27930703 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL28684804 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL27549329 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL6288311 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL295 | 0.96 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL39465 | 0.96 | ALDH1A1 (0.50) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL3507077 | 0.96 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL3950101 | 0.96 | — | — | |
| Trifluoromethanesulfonic Acid SCHEMBL25292879 | 0.92 | — | — |
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 214 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-6417382-B1 | — | — | None | — | — | US | claimed |
| CN-114981253-B | Process and intermediates for preparing chroman compounds and methods therefor | 印度鲁宾有限公司 | 2024-06-18 | — | — | CN | claimed |
| CN-112830887-A | Preparation method of N-phenyl bis (trifluoromethanesulfonyl) imide | 中船重工（邯郸）派瑞特种气体有限公司 | 2021-05-25 | — | — | CN | claimed |
| CN-109331868-A | A kind of phenylglycine class bifunctional catalysis' agent and its preparation method and application | 广东工业大学 | 2019-02-15 | — | — | CN | claimed |
| EP-3156395-B1 | METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND | UBE INDUSTRIES (JP) | 2019-01-09 | — | — | EP | claimed |
| US-20170121288-A1 | METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND | UBE INDUSTRIES, LTD. (JP) | 2017-05-04 | — | — | US | claimed |
| EP-3156395-A1 | METHOD FOR PRODUCING HETEROAROMATIC SULFONAMIDE COMPOUND | UBE Industries, Ltd. (JP) | 2017-04-19 | — | — | EP | claimed |
| US-20050014980-A1 | Process using water tolerant lewis acids in catalytic hydration of alkylene oxides to alkylene glycols | SAUDI BASIC INDUSTRIES CORPORATION | 2005-01-20 | — | — | US | claimed |
| WO-2005000879-A1 | CYCLOSPORIN DERIVATIVES FOR THE TREATMENT OF IMMUNE DISORDERS | ENANTA PHARMACEUTICALS, INC. (US) | 2005-01-06 | — | — | WO | claimed |
| US-20040266669-A1 | Cyclosporin derivatives for the treatment of immune disorders | ENANTA PHARMACEUTICALS, INC. | 2004-12-30 | — | — | US | claimed |
| US-6417382-B2 | REACTING 4-((3-(PHENOXYMETHYL)PHENOXYMETHYL)BENZONITRILE WITH AN ALKALI METAL HEXAALKYLDISILAZANE AND TREATING THE RESULTING COMPOUND WITH A CARBONATE OR HALOFORMATE, FORMING A PROTIC ACID SALT, ISOLATING THE SALT AND TREATING WITH BASE | BOEHRINGER INGELHEIM PHARMA KG (DE) | 2002-07-09 | — | — | US | claimed |
| US-20010009958-A1 | Process for preparing aryl-iminomethyl-carbamino acid esters | BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) | 2001-07-26 | — | — | US | claimed |
| EP-0437567-B1 | PHENYL-GLYCINE DERIVATIVES | CHINOIN GYOGYSZER ES VEGYESZET (HU) | 1994-12-07 | — | — | EP | claimed |
| US-6417382-B1 | — | — | None | — | — | US | disclosed |
| EP-4720172-A1 | SIDE-CHAIN FUNCTIONALIZED POLYNORBORNENES AS IONOMERS AND AS MEMBRANE MATERIALS FOR ALKALINE ELECTROLYSIS OF WATER, AND FUEL CELL | Forschungszentrum Jülich GmbH (DE) | 2026-04-08 | — | — | EP | disclosed |
| US-12565514-B2 | Nucleic acid containing perfluoroalkyl group, and method for its production | AGC Inc. (JP) | 2026-03-03 | — | — | US | disclosed |
| US-5030697-A | Polymer-bound dyes, process for their production and use | BAYER AKTIENGESELLSCHAFT (DE) | 1991-07-09 | — | — | US | disclosed |
| WO-1991001968-A1 | PHENYL-GLYCINE DERIVATIVES | CHINOIN GYÓGYSZER ÉS VEGYÉSZETI TERMÉKEK GYÁRA RT (HU) | 1991-02-21 | — | — | WO | disclosed |
| WO-1991001969-A1 | PHENYL-GLYCINE DERIVATIVES | CHINOIN GYÓGYSZER ÉS VEGYÉSZETI TERMÉKEK GYÁRA RT (HU) | 1991-02-21 | — | — | WO | disclosed |
| EP-0352856-A1 | Process of selective oligomerization of olefins and new catalyst for such a process | Enichem Anic S.r.l. (IT) | 1990-01-31 | — | — | EP | disclosed |