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 SCHEMBL28191470 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL10900199 | 1.00 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL29044849 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL40840 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL793200 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL11706156 | 1.00 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL9188686 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL10620300 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL20563836 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL9792262 | 1.00 | CA4 (0.50) | — |
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 1681 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122079836-A | Method for synthesizing aromatic carbon decasulfur-containing compound from isoprene | — | 2026-05-26 | — | — | CN | claimed |
| CN-122079823-A | Method for synthesizing amidino cobalt complex promoted by acetate | — | 2026-05-26 | — | — | CN | claimed |
| CN-116813686-B | Asymmetric synthesis method and application of 7-oxo-resorcinol lactone | 欣凯医药化工中间体（上海）有限公司 | 2026-05-15 | — | — | CN | claimed |
| US-20260068255-A1 | SEMICONDUCTOR STRUCTURE WITH SIDEWALL-FREE DIPOLE METAL FEATURE AND METHOD FOR MANUFACTURING THE SAME | TAIWAN SEMICONDUCTOR MANUFACTURING COMPANY, LTD. (TW) | 2026-03-05 | — | — | US | claimed |
| US-20260027096-A1 | PHD INHIBITORS | UNIV OXFORD INNOVATION LTD (GB) | 2026-01-29 | — | — | US | claimed |
| EP-4680573-A1 | METHOD FOR PRODUCING A CERIUM-GADOLINIUM OXIDE POWDER, IN PARTICULAR INTENDED FOR THE PRODUCTION OF AN ELECTROLYTE | SAINT-GOBAIN CENTRE DE RECHERCHES ET D'ETUDES EUROPEEN (FR) | 2026-01-21 | — | — | EP | claimed |
| EP-4655288-A1 | PHD INHIBITORS | Oxford University Innovation Limited (GB) | 2025-12-03 | — | — | EP | claimed |
| CN-116768824-B | Imide azole heterocyclic compound and application thereof | 华南农业大学 | 2025-06-10 | — | — | CN | claimed |
| CN-115696892-B | Cobalt niobium sulfide/niobium carbide composite wave-absorbing material, and preparation method and application thereof | 南通先进通信技术研究院有限公司 | 2025-05-27 | — | — | CN | claimed |
| CN-120015496-A | Preparation method and production equipment of heteroatom doped magnetic carbon material | 山西路桥建设集团有限公司 | 2025-05-16 | — | — | CN | claimed |
| EP-0697210-B1 | Use of a manganese, zinc and/or cobalt salt in a two-steps dyeing process based on an ondole or indoline compound | OREAL (FR) | 1996-09-25 | — | — | EP | claimed |
| CN-1122708-A | Chinese herbal medicine extract with complex enzyme | CHENG YUNWEN (CN) | 1996-05-22 | — | — | CN | claimed |
| CN-1027442-C | Long-acting complete-element compound fertilizer | LIU CHENGCAI (CN) | 1995-01-18 | — | — | CN | claimed |
| CN-1086507-A | A kind of long-lasting complete-nutrition composite fertilizer | LIU CHENGCAI (CN) | 1994-05-11 | — | — | CN | claimed |
| CN-1060098-A | Differentiate the printing liquid making method of true or false mark of printed matter | WU ZHENG (CN) | 1992-04-08 | — | — | CN | claimed |
| US-4997979-A | Carbonylation, cobalt catalyst | RHONE-POULENC CHIMIE (FR) | 1991-03-05 | — | — | US | claimed |
| US-4450298-A | Vapor phase catalytic hydrolysis of benzal chloride or its halogen- or trifluoromethyl-substitute to form benzaldehyde or substitute | CENTRAL GLASS COMPANY, LIMITED (JP) | 1984-05-22 | — | — | US | claimed |
| EP-0090926-A1 | A soluble magnesium hydride reagent | Conoco Phillips Company (US) | 1983-10-12 | — | — | EP | claimed |
| US-4129587-A | ACRYLONITRILE WITH ORGANIC PHOSPHINITES OR PHOSPHONITES AS CATALYSTS | IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) | 1978-12-12 | — | — | US | claimed |
| US-3991097-A | BORON HYDRIDE OR METAL BOROHYDRIDES AS REDUCING AGENT, LEWIS ACID | HOECHST AKTIENGESELLSCHAFT (DT) | 1976-11-09 | — | — | US | claimed |