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 SCHEMBL10786924 | 1.00 | ALDH1A1 (0.50) | — | |
| SCHEMBL132037 | 0.96 | — | — | |
| Bromide SCHEMBL460261 | 0.92 | — | — | |
| Iodide SCHEMBL19205926 | 0.92 | — | — | |
| Ammonia Solution, Strong SCHEMBL14629934 | 0.92 | — | — | |
| Alcohol SCHEMBL28625012 | 0.84 | — | — | |
| SCHEMBL10425474 | 0.82 | TSHR (0.45) | — | |
| Hydrochloric Acid SCHEMBL759783 | 0.82 | — | — | |
| SCHEMBL14302146 | 0.79 | — | — | |
| Urea SCHEMBL1179739 | 0.79 | — | — |
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 258 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-4317208-B1 | AMINATION METHOD FOR POLYSTYRENE RESIN, AND METHOD FOR IMMOBILIZING ENZYME USING AMINATED RESIN | ASYMCHEM LAB TIANJIN CO LTD (CN) | 2026-02-25 | — | — | EP | claimed |
| 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-119842405-A | Silicon wafer chemical polishing solution with high etching rate and high flatness and application thereof | 湖北兴福电子材料股份有限公司 | 2025-04-18 | — | — | CN | claimed |
| CN-119350563-B | Polymer capable of being assembled with protein and hydrophobic small molecule medicine and preparation method thereof | 至微(深圳)医学科技有限公司 | 2025-04-04 | — | — | CN | claimed |
| CN-119350563-A | Polymer capable of being assembled with protein and hydrophobic small molecule medicine and preparation method thereof | 至微(深圳)医学科技有限公司 | 2025-01-24 | — | — | CN | claimed |
| CN-119119388-A | Colloidal gold-labeled hydrogel polymer nanoparticle and application thereof in SARS-CoV-2 virus detection | 华中农业大学 | 2024-12-13 | — | — | CN | claimed |
| CN-118374097-B | Polypropylene composite material for 5G radome and preparation method thereof | 江苏久耀新材料科技有限公司 | 2024-11-12 | — | — | CN | claimed |
| CN-118558049-B | Filtering material for water treatment and preparation method thereof | 北京鹏发环保水处理股份有限公司 | 2024-10-25 | — | — | CN | claimed |
| CN-116284978-B | Fluorescent microsphere and preparation method and application thereof | 厦门为正生物科技股份有限公司 | 2024-09-20 | — | — | CN | claimed |
| CN-118558049-A | Filtering material for water treatment and preparation method thereof | 北京鹏发环保水处理股份有限公司 | 2024-08-30 | — | — | CN | claimed |
| CN-112266352-B | Piperlongumine derivative and preparation method and application thereof | 绍兴文理学院 | 2022-02-08 | — | — | CN | claimed |
| CN-113402683-A | Core-shell structure gold nanoparticle and preparation method and application thereof | 齐鲁工业大学 | 2021-09-17 | — | — | CN | claimed |
| CN-112707977-B | Method for amination of polystyrene-based resin, and method for immobilizing enzyme on aminated resin | 凯莱英医药集团（天津）股份有限公司 | 2021-07-02 | — | — | CN | claimed |
| CN-112707977-A | Method for amination of polystyrene-based resin, and method for immobilizing enzyme on aminated resin | 凯莱英医药集团（天津）股份有限公司 | 2021-04-27 | — | — | CN | claimed |
| CN-112266352-A | Piperlongumine derivative and preparation method and application thereof | 绍兴文理学院 | 2021-01-26 | — | — | CN | claimed |
| EP-1948611-A2 | PROCESS FOR THE PREPARATION OF A LEUKOTRIENE ANTAGONIST AND INTERMEDIATES THEREOF | ESTEVE QUIMICA, S.A. (ES) | 2008-07-30 | — | — | EP | claimed |
| WO-2007051828-A2 | PROCESS FOR THE PREPARATION OF A LEUKOTRIENE ANTAGONIST AND INTERMEDIATES THEREOF | ESTEVE QUÍMICA, S. A. (ES) | 2007-05-10 | — | — | WO | claimed |
| US-4713423-A | USING AQUEOUS HYPOCHLORITE SOLUTION AND PHASE TRANSFER CATALYST | MOHANRAJ SUBRAMANIAM (US) | 1987-12-15 | — | — | US | claimed |
| EP-0160218-B1 | PROCESS FOR PREPARING C8 -C24 ALKYLBENZENE SULFONYLAZIDES | MERCK & CO. INC. (US) | 1987-10-21 | — | — | EP | claimed |
| EP-0160218-A1 | Process for preparing C8 -C24 alkylbenzene sulfonylazides | MERCK & CO. INC. (US) | 1985-11-06 | — | — | EP | claimed |