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 SCHEMBL9619496 | 1.00 | TSHR (0.46) | — | |
| Hydrochloric Acid SCHEMBL9619502 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL28196669 | 1.00 | — | — | |
| Bromide SCHEMBL28223442 | 0.96 | — | — | |
| SCHEMBL29823 | 0.96 | — | — | |
| SCHEMBL7775400 | 0.96 | — | — | |
| SCHEMBL25174990 | 0.92 | — | — | |
| Fluoride SCHEMBL18173294 | 0.92 | — | — | |
| Iodide SCHEMBL3466919 | 0.92 | — | — | |
| SCHEMBL3974702 | 0.92 | TSHR (0.46) | — |
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 598 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20230167144-A1 | PREPARATION AND ITS APPLICATION OF A CYANIDE-BRIDGED METAL ORGANIC COMPOUND WITH INTRAMOLECULAR MAGNETIC TRANSFORMATION | Hubei Jingmen Industrial Technology Research Institute Co., Ltd. (CN) | 2023-06-01 | — | — | US | claimed |
| CN-108997420-B | Synthesis method of triphenyl-n- (colchicine amido) butyl phosphonium chloride compound and application of triphenyl-n- (colchicine amido) butyl phosphonium chloride compound in antitumor drugs | 湖北大学 | 2020-11-13 | — | — | CN | claimed |
| CN-109880062-A | A kind of cross-linkable solidifying material and its continuous production method | 广东博兴新材料科技有限公司 | 2019-06-14 | — | — | CN | claimed |
| CN-106085317-B | Epoxy resin-matrix plastic packaging material, preparation method containing fluorescent powder and raising LED white chip fall the application of Bin rate | 天津德高化成光电科技有限责任公司 | 2019-05-14 | — | — | CN | claimed |
| CN-109675533-A | A kind of graphene film and its application that removing heavy metals are removed in cosmetics | 汕头市特丝多丽化妆品有限公司 | 2019-04-26 | — | — | CN | claimed |
| CN-109280186-A | For solidifying the method and composition on the surface of uncured polysulfide rubber | 波音公司 | 2019-01-29 | — | — | CN | claimed |
| CN-105294643-B | Ethylene oxide and carbon dioxide prepare the catalyst and its method of ethylene carbonate | 中国石油化工股份有限公司 | 2018-07-13 | — | — | CN | claimed |
| CN-108147956-A | A kind of method for mixing naphthols selective oxidation and preparing 1,4- naphthoquinones | 中国科学院成都有机化学有限公司 | 2018-06-12 | — | — | CN | claimed |
| CN-106927497-B | Raw powder's production technology containing nano yttrium oxide | 镧明新材料科技（上海）有限公司 | 2018-05-18 | — | — | CN | claimed |
| CN-107837824-A | Purposes of the catalyst of load quaternary alkylphosphonium salt and metal chloride in acetylene hydrochlorination | 天津大学 | 2018-03-27 | — | — | CN | claimed |
| CN-1178921-C | Preparation of sulfonamides | - | 2004-12-08 | — | — | CN | claimed |
| EP-1430011-A1 | PROCESS FOR PRODUCING FLUOROOLEFINS | Honeywell International Inc. (US) | 2004-06-23 | — | — | EP | claimed |
| CN-1425007-A | Preparation of sulfonamides | HOFFMANN LA ROCHE (CH) | 2003-06-18 | — | — | CN | claimed |
| WO-2003027051-A1 | PROCESS FOR PRODUCING FLUOROOLEFINS | HONEYWELL INTERNATIONAL INC. (US) | 2003-04-03 | — | — | WO | claimed |
| CN-1070162-C | Catalytic composition and a process of olefins | INST FRANCAIS DU PETROLE (FR) | 2001-08-29 | — | — | CN | claimed |
| CN-1035823-C | Process for preparing latent catalysts for curing epoxy resins | DOW CHEMICAL CO (US) | 1997-09-10 | — | — | CN | claimed |
| CN-1106023-A | Catalytic composition and a process of olefins | INST FRANCAIS DU PETROLE (FR) | 1995-08-02 | — | — | CN | claimed |
| CN-1056699-A | Latent catalysts and cure-inhibited epoxy resin compositions and laminates made therefrom | DOW CHEMICAL CO (US) | 1991-12-04 | — | — | CN | claimed |
| EP-0402048-A1 | Improved process for preparing benzenesulfonate salts | E.I. DU PONT DE NEMOURS AND COMPANY (US) | 1990-12-12 | — | — | EP | claimed |
| EP-0179685-B1 | PROCESS FOR THE PREPARATION OF TERTIARY, OPTIONALLY HALOGENATED ALLYLIC ESTERS | RHONE-POULENC SANTE (FR) | 1988-09-28 | — | — | EP | claimed |