Known targets — ChEMBL curated mechanism
ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Hydrochloric 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 | |
|---|---|---|---|---|
| Iodide SCHEMBL7633138 | 0.89 | — | — | |
| Tetrafluoroethylene SCHEMBL11716843 | 0.68 | — | — | |
| Tetrafluoroethylene SCHEMBL821995 | 0.60 | — | — | |
| Hydrochloric Acid SCHEMBL28037891 | 0.60 | — | — | |
| SCHEMBL6832083 | 0.60 | — | — | |
| Hydrochloric Acid SCHEMBL28138067 | 0.60 | — | — | |
| Tetrafluoroethylene SCHEMBL15536 | 0.60 | — | — | |
| Hydrochloric Acid SCHEMBL11722996 | 0.59 | — | — | |
| SCHEMBL1115626 | 0.58 | — | — | |
| SCHEMBL82518 | 0.58 | — | — |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-115819662-B | Fluorine-containing epoxy resin and preparation method thereof | 四川轻化工大学 | 2023-09-12 | — | — | CN | claimed |
| CN-115819662-A | Novel fluorine-containing epoxy resin and preparation method thereof | 四川轻化工大学 | 2023-03-21 | — | — | CN | claimed |
| US-12612419-B2 | Method for producing fluorine-containing (cyclo)alkenyl zinc halide compound | DAIKIN INDUSTRIES, LTD. (JP) | 2026-04-28 | — | — | US | disclosed |
| WO-2025124066-A1 | PREPARATION METHOD AND PRODUCTION SYSTEM FOR HEXAFLUOROBUTADIENE | 中化蓝天电子材料(杭州)有限公司 | 2025-06-19 | — | — | WO | disclosed |
| CN-116393092-B | Method for separating and purifying hexafluorobutadiene and efficient adsorbent for separating and purifying hexafluorobutadiene | 福州绿航环保技术服务有限公司 | 2024-07-12 | — | — | CN | disclosed |
| CN-115819662-B | Fluorine-containing epoxy resin and preparation method thereof | 四川轻化工大学 | 2023-09-12 | — | — | CN | disclosed |
| CN-116393092-A | Method for separating and purifying hexafluorobutadiene and efficient adsorbent for separating and purifying hexafluorobutadiene | 福州绿航环保技术服务有限公司 | 2023-07-07 | — | — | CN | disclosed |
| CN-115819662-A | Novel fluorine-containing epoxy resin and preparation method thereof | 四川轻化工大学 | 2023-03-21 | — | — | CN | disclosed |
| US-20220324883-A1 | METHOD FOR PRODUCING FLUORINE-CONTAINING (CYCLO)ALKENYL ZINC HALIDE COMPOUND | DAIKIN INDUSTRIES, LTD. (JP) | 2022-10-13 | — | — | US | disclosed |
| CN-114901667-A | Process for producing fluorine-containing (cyclo) alkenyl halide zinc compound | 大金工业株式会社 | 2022-08-12 | — | — | CN | disclosed |
| WO-2021132011-A1 | METHOD FOR PRODUCING FLUORINE-CONTAINING (CYCLO)ALKENYL ZINC HALIDE COMPOUND | ダイキン工業株式会社 | 2021-07-01 | — | — | WO | disclosed |
| CN-102627534-A | Compounds including indene and difluoroethylene bridge bond, preparation method thereof and application thereof | JIANGSU HECHENG DISPLAY TECH | 2012-08-08 | — | — | CN | disclosed |
| CN-101525267-A | Method for preparing hexachlorobutadiene | UNIV HENAN TECHNOLOGY | 2009-09-09 | — | — | CN | disclosed |
| CN-101255090-A | Synthesis of alpha, beta, beta-trifluorostyrene via in-situ for mation or trifluorovinyl metal halide | BALLARD POWER SYSTEMS (CA) | 2008-09-03 | — | — | CN | disclosed |
| CN-100381409-C | Synthesis of alpha, beta-trifluorostyrene by in situ formation of trifluorovinyl metal halide | BALLARD POWER SYSTEMS (CA) | 2008-04-16 | — | — | CN | disclosed |
| CN-1829673-A | Synthesis of alpha, beta-trifluorostyrene by in situ formation of trifluorovinyl metal halide | BALLARD POWER SYSTEMS (CA) | 2006-09-06 | — | — | CN | disclosed |
| EP-1463697-A2 | SYNTHESIS OF ALFA,BETA,BETA-TRIFLUOROSTYRENE VIA IN-SITU FORMATION OF TRIFLUOROVINYL METAL HALIDE | BALLARD POWER SYSTEMS INC. (CA) | 2004-10-06 | — | — | EP | disclosed |
| US-6653515-B2 | One pot process comprising reacting tetrafluoroethylene with bases, metal halides and optionally amines to form trifluorovinyl metal complexes, then arylating in the presence of catalysts to form trifluorophenylethylene | BALLARD POWER SYSTEMS INC. (CA) | 2003-11-25 | — | — | US | disclosed |
| US-20030144439-A1 | Synthesis of alpha, beta, beta-trifluorostyrene via in-situ formation of trifluorovinyl metal halide | BALLARD POWER SYSTEMS INC. (CA) | 2003-07-31 | — | — | US | disclosed |
| WO-2003051801-A2 | SYNTHESIS OF ALPHA, BETA, BETA-TRIFLUOROSTYRENE VIA IN-SITU FORMATION OF TRIFLUOROVINYL METAL HALIDE | BALLARD POWER SYSTEMS INC. (CA) | 2003-06-26 | — | — | WO | disclosed |