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 SCHEMBL28405765 | 1.00 | — | — | |
| Methane SCHEMBL28716732 | 0.95 | — | — | |
| SCHEMBL455299 | 0.95 | — | — | |
| Iodide SCHEMBL28566891 | 0.90 | — | — | |
| Phosphine SCHEMBL17491850 | 0.90 | — | — | |
| SCHEMBL11140190 | 0.90 | — | — | |
| Methane SCHEMBL28567348 | 0.90 | — | — | |
| Bromide SCHEMBL2059867 | 0.90 | — | — | |
| Hydrochloric Acid SCHEMBL28395120 | 0.84 | — | — | |
| Chloromethane SCHEMBL6054127 | 0.82 | — | — |
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 1320 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122036738-A | Chiral indolone spirochroman compound, and synthetic method and application thereof | 成都大学 | 2026-05-15 | — | — | CN | claimed |
| CN-122036792-A | Preparation of diphenyl ether biphosphine ligand and application of diphenyl ether biphosphine ligand in carbonyl esterification reaction | 深圳职业技术大学 | 2026-05-15 | — | — | CN | claimed |
| US-12398089-B2 | Method for preparing organic carboxylic ester by using combined catalyst of aryl bidentate phosphine ligand | NANJING CHENGZHI CLEAN ENERGY CO. LTD. (CN) | 2025-08-26 | — | — | US | claimed |
| CN-116410118-B | Preparation method of beta-lactam compound | 中国科学技术大学 | 2025-06-24 | — | — | CN | claimed |
| CN-120001402-A | Mesoporous carbon nitride supported palladium diatomic photocatalyst and preparation method and application thereof | 南京林业大学 | 2025-05-16 | — | — | CN | claimed |
| CN-115894556-B | Synthesis method of beta-fluoroallylphosphine | 南通大学 | 2025-04-29 | — | — | CN | claimed |
| CN-119409657-B | Preparation method for synthesizing isatoic anhydride by using carbon dioxide | 湖南工程学院 | 2025-04-18 | — | — | CN | claimed |
| US-12275752-B2 | Class of phosphine nitrogen ligand with multiple chiral centers and its synthesis method and application | SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) | 2025-04-15 | — | — | US | claimed |
| CN-115957823-B | Ethylene carbonylation catalyst and application thereof | 上海浦景化工技术股份有限公司 | 2025-04-08 | — | — | CN | claimed |
| CN-119488956-A | Sulfonic acid resin-based Pd catalyst, preparation method thereof and application thereof in olefin hydroesterification reaction | 中国石油化工股份有限公司 | 2025-02-21 | — | — | CN | claimed |
| CN-1153769-C | Process for production of purine derivatives and intermediates therefor | ŵ��ҩƷ��˾ | 2004-06-16 | — | — | CN | claimed |
| US-6749990-B2 | UNSATURATED HALOGENATED HYDROCARBON AS PHOTORESIST MONOMER, FOR EXAMPLE 3,3,4,4,5,5,6,6,6-NONAFLUORO-1-HEXENE; ETCHING RESISTANCE, HEAT RESISTANCE AND ADHESIVENESS, AND IS DEVELOPABLE IN AQUEOUS TETRAMETHYLAMMONIUM HYDROXIDE | HYNIX SEMICONDUCTOR INC. (KR) | 2004-06-15 | — | — | US | claimed |
| US-6602649-B2 | Photolithography; using ultraviolet radiation | HYNIX SEMICONDUCTOR INC (KR) | 2003-08-05 | — | — | US | claimed |
| CN-1106393-C | Optically active beta-aryl substitution-2(5H)-ketofuran and its synthesis process | SHANGHAI INST ORGANIC CHEM (CN) | 2003-04-23 | — | — | CN | claimed |
| US-20030017404-A1 | Chemical amplification photoresist monomers, polymers therefrom and photoresist compositions containing the same | HYNIX SEMICONDUCTOR INC. (KR) | 2003-01-23 | — | — | US | claimed |
| US-6426314-B1 | Hydrogen scavengers | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA | 2002-07-30 | — | — | US | claimed |
| WO-2002015216-A1 | HYDROGEN SCAVENGERS | THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) | 2002-02-21 | — | — | WO | claimed |
| US-20020015912-A1 | Photoresist monomers, polymers thereof and photoresist compositions containing the same | HYNIX SEMICONDUCTOR INC. (KR) | 2002-02-07 | — | — | US | claimed |
| CN-1299816-A | Optically active beta-aryl substitution-2(5H)-ketofuran and its synthesis process | SHANGHAI INST ORGANIC CHEM (CN) | 2001-06-20 | — | — | CN | claimed |
| US-3996130-A | Method of purifying crude petroleum and primary refining products | NAMETKIN NIKOLAI SERGEEVICH | 1976-12-07 | — | — | US | claimed |