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 SCHEMBL7765960 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL4264797 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL1836320 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL11064222 | 0.82 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL10701120 | 0.82 | CA4 (0.50) | — | |
| SCHEMBL3693356 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL10681574 | 0.82 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL14635381 | 0.82 | — | — | |
| Hydrochloric Acid SCHEMBL15638259 | 0.82 | CA4 (0.50) | — | |
| Hydrochloric Acid SCHEMBL2965880 | 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 334 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116103692-B | PdCu@UiO-S@PDMS core-shell structure composite catalyst and preparation method and application thereof | 中国科学院合肥物质科学研究院 | 2025-05-30 | — | — | CN | claimed |
| CN-120037972-A | Application of supported palladium catalyst in hydrogen production from formic acid | 青岛展能新材料科技有限公司 | 2025-05-27 | — | — | CN | claimed |
| CN-119701913-A | Pd-based mobile catalyst and preparation method and application thereof | 北京理工大学 | 2025-03-28 | — | — | CN | claimed |
| CN-119282129-A | Size-controllable palladium nanoparticle and preparation method and application thereof | 聊城大学 | 2025-01-10 | — | — | CN | claimed |
| CN-116081572-B | Palladium-based hydride and preparation method and application thereof | 南京理工大学 | 2024-12-13 | — | — | CN | claimed |
| CN-118996446-A | Preparation method and application of composite PdS self-supporting electrode material | 浙江工业大学 | 2024-11-22 | — | — | CN | claimed |
| CN-118875305-A | Preparation method of PdZr two-dimensional ultrathin metal alkene material and application of PdZr two-dimensional ultrathin metal alkene material to anode of anion exchange membrane fuel cell | 南通大学 | 2024-11-01 | — | — | CN | claimed |
| CN-118122367-A | Supported noble metal catalyst, preparation method thereof and application thereof in gas phase method synthesis of dimethyl carbonate and co-production of methyl formate | 中国科学院大连化学物理研究所 | 2024-06-04 | — | — | CN | claimed |
| CN-118079971-A | High-heat-conductivity heterogeneous catalyst for preparing methyl formate by CO esterification and preparation method and application thereof | 中国科学院福建物质结构研究所 | 2024-05-28 | — | — | CN | claimed |
| CN-117960058-A | Two types of preparation methods and applications of metal aerogel | 温州大学 | 2024-05-03 | — | — | CN | claimed |
| US-5731457-A | Vinyl acetate process utilizing a palladium-gold-copper catalyst | HOECHST CELANESE CORPORATION (US) | 1998-03-24 | — | — | US | claimed |
| EP-0526334-B1 | Electroless palladium plating composition | OKUNO CHEM IND CO (JP) | 1998-01-21 | — | — | EP | claimed |
| WO-1997036678-A1 | A METHOD OF PREPARING A VINYL ACETATE CATALYST EMPLOYING AN ALKALI METAL BORATE | HOECHST CELANESE CORPORATION (US) | 1997-10-09 | — | — | WO | claimed |
| EP-0557722-B1 | Process for producing 2,6-dimethylnaphthalene | MITSUBISHI GAS CHEMICAL CO (JP) | 1996-11-13 | — | — | EP | claimed |
| US-5321178-A | Cyclization dehydrogenation of 2-methyl-1-(p-tolyl) butane or butene using catalyst of palladium component and alkali or alkaline earth component supprted on alumina | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 1994-06-14 | — | — | US | claimed |
| US-5292361-A | Hypophosphite, ammonia or alkylamine, polyethyleneimine, aliphatic alkylamine | OKUNO CHEMICAL INDUSTRIES CO., LTD. (JP) | 1994-03-08 | — | — | US | claimed |
| EP-0557722-A2 | Process for producing 2,6-dimethylnaphthalene | MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) | 1993-09-01 | — | — | EP | claimed |
| EP-0526334-A2 | Electroless palladium plating composition | OKUNO CHEMICAL INDUSTRIES CO. LTD (JP) | 1993-02-03 | — | — | EP | claimed |
| US-4233242-A | SILICA OR PALLADIUM COMPOUND AS CATALYST | SHOWA DENKO KABUSHIKI KAISHA (JP) | 1980-11-11 | — | — | US | claimed |
| US-4118426-A | REACTING AN EPOXIDE WITH AN ALCOHOL OR PHENOL, PALLADIUM AND COPPER SALTS CATALYST | WESTERN KENTUCKY UNIVERSITY (US) | 1978-10-03 | — | — | US | claimed |