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 | |
|---|---|---|---|---|
| SCHEMBL1771685 | 0.96 | CCR1 (0.71) | — | |
| SCHEMBL9611 | 0.96 | — | — | |
| SCHEMBL30421349 | 0.96 | — | — | |
| Hydrochloric Acid SCHEMBL15145084 | 0.94 | CCR1 (0.60) | — | |
| Iodide SCHEMBL8148528 | 0.93 | — | — | |
| Bromide SCHEMBL5437785 | 0.93 | — | — | |
| Hydrogen Sulfide SCHEMBL20214420 | 0.93 | — | — | |
| Ammonia Solution, Strong SCHEMBL18983640 | 0.93 | — | — | |
| SCHEMBL31058624 | 0.93 | — | — | |
| SCHEMBL184761 | 0.93 | — | — |
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 134 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119100907-A | Synthetic method of chloroethylene and polyvinyl chloride | 厦门中科易工化学科技有限公司 | 2024-12-10 | — | — | CN | claimed |
| CN-122010156-A | Method for preparing high-purity calcium fluoride and calcium sulfate by recycling fluorine-containing mixed acid | 南京格洛特环境工程股份有限公司 | 2026-05-12 | — | — | CN | disclosed |
| US-20260015743-A1 | MEDIATED HYDROGEN ANODE FOR USE IN REDUCTIVE ELECTROSYNTHESIS | WISCONSIN ALUMNI RES FOUND (US) | 2026-01-15 | — | — | US | disclosed |
| EP-4596563-A2 | ELECTROCHEMICAL BIOSENSOR COMPRISING TRANSITION METAL COMPLEX OR OXIDATION-REDUCTION POLYMER | i-Sens, Inc. (KR) | 2025-08-06 | — | — | EP | disclosed |
| US-20250244282-A1 | ELECTROCHEMICAL BIOSENSOR COMPRISING TRANSITION METAL COMPLEX OR OXIDATION-REDUCTION POLYMER | I SENS INC (KR) | 2025-07-31 | — | — | US | disclosed |
| CN-119100907-A | Synthetic method of chloroethylene and polyvinyl chloride | 厦门中科易工化学科技有限公司 | 2024-12-10 | — | — | CN | disclosed |
| CN-119053609-A | Crystal form of lubidine and preparation method thereof | 上海皓元医药股份有限公司 | 2024-11-29 | — | — | CN | disclosed |
| US-20240366629-A1 | Porphyrin Complexes as Antidotes for Carbon Monoxide Exposure and Methods of Use for Same | UNIV CALIFORNIA (US) | 2024-11-07 | — | — | US | disclosed |
| US-20240368777-A1 | ELECTROCHEMICAL REDUCTIVE COUPLING OF PHENOL DERIVATIVES | NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT | 2024-11-07 | — | — | US | disclosed |
| EP-4395773-A1 | PORPHYRIN COMPLEXES AS ANTIDOTES FOR CARBON MONOXIDE EXPOSURE AND METHODS OF USE FOR SAME | The Regents of the University of California (US) | 2024-07-10 | — | — | EP | disclosed |
| EP-0087326-B1 | SUBSTITUTED PYRIMIDIN-2-ONES AND THE SALTS THEREOF | NYCOMED AS (NO) | 1987-05-13 | — | — | EP | disclosed |
| US-4539324-A | ANTICANCER AGENTS | NYEGAARD & CO. A/S (NO) | 1985-09-03 | — | — | US | disclosed |
| EP-0124561-A1 | PROCESS FOR PRODUCING OLIGONUCLEOSIDE PHOSPHONATES. | KOSTER HUBERT | 1984-11-14 | — | — | EP | disclosed |
| US-4472583-A | AND CORRESPONDING ISOCYANATE; UREA, THIOUREA, GUANIDINE INTERMEDIATES; FUNGICIDES, BACTERICIDES | THE DOW CHEMICAL COMPANY (US) | 1984-09-18 | — | — | US | disclosed |
| WO-1984001778-A1 | PROCESS FOR PRODUCING OLIGONUCLEOSIDE PHOSPHONATES | KOESTER HUBERT (DE) | 1984-05-10 | — | — | WO | disclosed |
| EP-0087326-A1 | Substituted pyrimidin-2-ones and the salts thereof | NYCOMED AS (NO) | 1983-08-31 | — | — | EP | disclosed |
| US-4331669-A | Fungicidal pyridyl arylureas, compositions containing them and method of controlling fungi and bacteria | DOW CHEMICAL COMPANY LIMITED, ENGLAND (GB) | 1982-05-25 | — | — | US | disclosed |
| US-4066435-A | BENZYL TRIALKYL PHOSPHONIUM HALIDE | MONSANTO COMPANY (US) | 1978-01-03 | — | — | US | disclosed |
| US-4053501-A | PLANT GROWTH REGULATORS | MONSANTO COMPANY (US) | 1977-10-11 | — | — | US | disclosed |
| US-4045501-A | DEHYDROBROMINATING CHLOROMETHYL(1-BROMOETHYL) BENZENES WITH AN AMINE ACCEPTOR | EASTMAN KODAK COMPANY (US) | 1977-08-30 | — | — | US | disclosed |