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 | |
|---|---|---|---|---|
| SCHEMBL6842 | 0.96 | — | — | |
| SCHEMBL14690989 | 0.96 | — | — | |
| SCHEMBL4735385 | 0.96 | CYP19A1 (0.57) | — | |
| Chloromethane SCHEMBL27600897 | 0.94 | CYP19A1 (0.52) | — | |
| Hydrochloric Acid SCHEMBL25275623 | 0.93 | — | — | |
| SCHEMBL29843433 | 0.93 | — | — | |
| Ammonia Solution, Strong SCHEMBL28661135 | 0.90 | — | — | |
| Benzene SCHEMBL29047908 | 0.90 | TSHR (0.53) | — | |
| Bromomethane SCHEMBL9741255 | 0.87 | — | — | |
| Cyanide SCHEMBL27759767 | 0.87 | — | — |
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 1644 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-120004697-A | Preparation method of OrgVO material and application of OrgVO material as secondary battery anode material | 同济大学 | 2025-05-16 | — | — | CN | claimed |
| CN-118688366-B | Kit for extracting free testosterone in serum, extraction method and detection method | 杭州佰辰医疗器械有限公司 | 2024-12-20 | — | — | CN | claimed |
| CN-119144004-A | M-HOF material, preparation method thereof and application thereof in hydroxide ion identification | 兰州大学 | 2024-12-17 | — | — | CN | claimed |
| CN-118688366-A | Kit for extracting free testosterone in serum, extraction method and detection method | 杭州佰辰医疗器械有限公司 | 2024-09-24 | — | — | CN | claimed |
| CN-118580178-A | Method for synthesizing C-4 alkylpyridine by taking alcohol as alkylating reagent | 陕西师范大学 | 2024-09-03 | — | — | CN | claimed |
| CN-118204105-B | Preparation method of desulfurization catalyst | 烟台百川汇通科技有限公司 | 2024-07-16 | — | — | CN | claimed |
| CN-116532084-B | Nd-doped Bi2WO6Preparation and application of nanoflower-biomass porous carbon material | 北京知投家知识产权运营有限公司 | 2024-06-21 | — | — | CN | claimed |
| CN-118204105-A | Preparation method of desulfurization catalyst | 烟台百川汇通科技有限公司 | 2024-06-18 | — | — | CN | claimed |
| CN-118063783-A | For CO2/N2Preparation method of metal organic framework material for mixed gas separation | 辽宁大学 | 2024-05-24 | — | — | CN | claimed |
| CN-117551023-A | Preparation method and application of N-thio-phenyl phthalimide compound | 太原理工大学 | 2024-02-13 | — | — | CN | claimed |
| CN-107501173-A | A kind of method for synthesizing 4 alkanamine yl pyridines in a mild condition | 武汉桀升生物科技有限公司 | 2017-12-22 | — | — | CN | claimed |
| CN-103483244-A | Preparation method of 2-(pyridine-4-yl) acetonitrile | WYLTON JINGLIN ELECTRONIC MATERIAL CO LTD | 2014-01-01 | — | — | CN | claimed |
| CN-103360306-A | Method for synthesizing 4-chloro-pyridine | SHANGHAI SYNCHES CO LTD | 2013-10-23 | — | — | CN | claimed |
| CN-101260128-B | Method for synthesizing trichlorosucrosepentaacetate | UNIV JILIANG CHINA | 2011-04-27 | — | — | CN | claimed |
| CN-101302193-B | Entironment-friendly preparation of sorafenib intermediate | SHANGHAI HWASUN LIFE SCIENCE CO LTD | 2010-06-23 | — | — | CN | claimed |
| CN-101302193-A | Entironment-friendly preparation of sorafenib intermediate | SHANGHAI HWASUN LIFE SCIENCE C (CN) | 2008-11-12 | — | — | CN | claimed |
| CN-101260128-A | Method for synthesizing trichlorosucrosepentaacetate | UNIV JILIANG CHINA (CN) | 2008-09-10 | — | — | CN | claimed |
| EP-0982308-B1 | Derivatives of the 8H-(2,3-b)-pyrrolizine-8-one, process for their preparation and pharmaceutical compositions containing them | SERVIER LAB (FR) | 2003-02-26 | — | — | EP | claimed |
| US-4873364-A | THERMAL DECOMPOSITION OF THE CORRESPONDING UREA IN THE PRESENCE OF A TERTIARY AMINE HYDROHALIDE | ARCO CHEMICAL TECHNOLOGY, INC. (US) | 1989-10-10 | — | — | US | claimed |
| EP-0324543-A2 | Antiarrhythmic agents | Pfizer Limited (GB) | 1989-07-19 | — | — | EP | claimed |