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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL6881991 | 1.00 | — | — | |
| SCHEMBL2105399 | 0.64 | — | — | |
| SCHEMBL19036807 | 0.61 | — | — | |
| SCHEMBL20850257 | 0.58 | — | — | |
| Hydrochloric Acid SCHEMBL29087542 | 0.57 | — | — | |
| SCHEMBL22627194 | 0.56 | — | — | |
| SCHEMBL115308 | 0.55 | — | — | |
| Trimethylammonium SCHEMBL11045756 | 0.54 | — | — | |
| Trimethylammonium SCHEMBL11755984 | 0.54 | — | — | |
| Trimethylammonium SCHEMBL17005746 | 0.54 | — | — |
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 135 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-2951140-B1 | PROCESS FOR THE PREPARATION OF 1-CHLORO-3,3,3-TRIFLUOROPROPENE USING A PHASE TRANSFER CATALYST | HONEYWELL INT INC (US) | 2018-01-10 | — | — | EP | claimed |
| EP-2951140-A1 | PROCESS FOR THE PREPARATION OF 1-CHLORO-3,3,3-TRIFLUOROPROPENE USING A PHASE TRANSFER CATALYST | Honeywell International Inc. (US) | 2015-12-09 | — | — | EP | claimed |
| US-8907146-B2 | Process for the preparation of 1-chloro-3,3,3-trifluoropropene using a phase transfer catalyst | HONEYWELL INTERNATIONAL INC. (US) | 2014-12-09 | — | — | US | claimed |
| US-20140221704-A1 | PROCESS FOR THE PREPARATION OF 1-CHLORO-3,3,3-TRIFLUOROPROPENE USING A PHASE TRANSFER CATALYST | HONEYWELL INTERNATIONAL INC. (US) | 2014-08-07 | — | — | US | claimed |
| WO-2014121171-A1 | PROCESS FOR THE PREPARATION OF 1-CHLORO-3,3,3-TRIFLUOROPROPENE USING A PHASE TRANSFER CATALYST | HONEYWELL INTERNATIONAL INC. (US) | 2014-08-07 | — | — | WO | claimed |
| EP-1430011-B1 | PROCESS FOR PRODUCING FLUOROOLEFINS | HONEYWELL INT INC (US) | 2014-07-23 | — | — | EP | claimed |
| US-6548719-B1 | Such as 1,1,1,3,3-pentafluoropropene via dehydrohalogenation in the presence of a phase transfer catalyst and alkali metal hydroxide | HONEYWELL INTERNATIONAL | 2003-04-15 | — | — | US | claimed |
| US-20030060670-A1 | PROCESS FOR PRODUCING FLUOROOLEFINS | HONEYWELL INTERNATIONAL INC. | 2003-03-27 | — | — | US | claimed |
| EP-3309139-B1 | PROCESS FOR THE PREPARATION OF 2,3,3,3-TRIFLUOROPROPENE | MEXICHEM FLUOR SA DE CV (MX) | 2023-12-06 | — | — | EP | disclosed |
| US-11731925-B2 | Process for producing halogenated olefins | THE CHEMOURS COMPANY FC, LLC (US) | 2023-08-22 | — | — | US | disclosed |
| EP-3872058-B1 | PROCESS FOR THE PREPARATION OF 2,3,3,3 TETRAHYDROFLUOROPROPENE | MEXICHEM FLUOR SA DE CV (MX) | 2023-08-16 | — | — | EP | disclosed |
| EP-3872059-B1 | PROCESS FOR THE PREPARATION OF 2,3,3,3 TETRAHYDROFLUOROPROPENE | MEXICHEM FLUOR SA DE CV (MX) | 2023-08-16 | — | — | EP | disclosed |
| EP-4215515-A1 | METHOD FOR PRODUCING TETRAFLUOROPROPENES | Honeywell International Inc. (US) | 2023-07-26 | — | — | EP | disclosed |
| US-20220220050-A1 | PROCESS FOR THE PREPARATION OF 2,3,3,3-TETRAFLUOROPROPENE | MEXICHEM AMANCO HOLDING S.A. DE C.V. (MX) | 2022-07-14 | — | — | US | disclosed |
| WO-2002046149-A2 | 2-THIO-5-AMINO SUBSTITUTED BENZOQUINONES, THEIR MANUFACTURE AND THEIR USE IN RUBBER | FLEXSYS AMERICA L.P. (US) | 2002-06-13 | — | — | WO | disclosed |
| EP-1068177-A1 | PREPARATION OF QUINONEIMINES FROM HYDROXYPHENYLAMINES USING A HYPOCHLORITE AS AN OXIDATION AGENT | FLEXSYS AMERICA L.P. (US) | 2001-01-17 | — | — | EP | disclosed |
| US-6114554-A | Preparation of quinonediimines from phenylenediamines using a hypochlorite as an oxidation agent | FLEXSYS AMERICA L.P. (US) | 2000-09-05 | — | — | US | disclosed |
| US-6072061-A | Preparation of quinoneimines from hydroxyphenylamines using a hypochlorite as an oxidation agent | FLEXSYS AMERICA L.P. (US) | 2000-06-06 | — | — | US | disclosed |
| US-6025508-A | HIGH YIELDS BY USING SUPPORTED METAL CATALYSTS WHICH CAN BE FILTERED FROM REACTION SOLVENTS AND REUSED | FLEXSYS AMERICA L.P. (US) | 2000-02-15 | — | — | US | disclosed |
| WO-1999052860-A1 | PREPARATION OF QUINONEIMINES FROM HYDROXYPHENYLAMINES USING A HYPOCHLORITE AS AN OXIDATION AGENT | FLEXSYS AMERICA L.P. (NL) | 1999-10-21 | — | — | WO | disclosed |