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 SCHEMBL7047186 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL212093 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL4367150 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL441937 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL8911044 | 1.00 | CA4 (0.33) | — | |
| Hydrochloric Acid SCHEMBL5353097 | 1.00 | — | — | |
| Water SCHEMBL7586756 | 0.87 | — | — | |
| Hydrochloric Acid SCHEMBL9303767 | 0.87 | — | — | |
| Hydrochloric Acid SCHEMBL5583383 | 0.87 | — | — | |
| Hydrochloric Acid SCHEMBL106288 | 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 752 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122032631-A | Catalyst for catalytic cracking of alkane and method for catalytic cracking of alkane | 中国石油化工股份有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-122032634-A | Composite molecular sieve and preparation method and application thereof | 中国石油化工股份有限公司 | 2026-05-15 | — | — | CN | claimed |
| US-20250198996-A1 | EXTENDED LIVE CELL BARCODING APPROACH FOR MULTIPLEXED MASS CYTOMETRY | BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) | 2025-06-19 | — | — | US | claimed |
| CN-120115163-A | Three-functional amorphous/crystalline Rh (OH)3/NiMoO4Preparation method and application of heterojunction electrolyzed water catalyst | 昆明理工大学 | 2025-06-10 | — | — | CN | claimed |
| CN-119571376-A | Preparation method for preparing single-atom electrocatalyst on surface of current collector in situ | 苏州行则兴氢能源科技有限公司 | 2025-03-07 | — | — | CN | claimed |
| CN-119465275-A | Three-dimensional net Rh/Ni (OH)2Preparation method and application of nanowire composite material | 江苏大学 | 2025-02-18 | — | — | CN | claimed |
| EP-3464173-B1 | CATALYST FOR LOW TEMPERATURE ETHANOL STEAM REFORMING AND RELATED PROCESS | KT KINETICS TECH S P A (IT) | 2024-08-07 | — | — | EP | claimed |
| CN-117947461-A | Preparation method, structure and application of non-noble metal oxide modified ultra-fine noble metal nano particles synthesized by low-temperature heat treatment | 大连理工大学 | 2024-04-30 | — | — | CN | claimed |
| CN-117797812-A | Rhodium-ruthenium bimetallic catalyst and preparation method and application thereof | 天津大学 | 2024-04-02 | — | — | CN | claimed |
| CN-117800821-A | Method and catalyst for preparing chiral alpha-aryl propanal through asymmetric hydroformylation | 青岛科技大学 | 2024-04-02 | — | — | CN | claimed |
| US-20110263916-A1 | CARBOHYDRATES UPGRADING AND HYDROTREATING TO HYDROCARBONS | CONOCOPHILLIPS COMPANY (US) | 2011-10-27 | — | — | US | claimed |
| US-20090282730-A1 | METHOD AND COMPOSITION FOR IMPROVING FUEL COMBUSTION | CARROLL & ASSOCIATES LLC | 2009-11-19 | — | — | US | claimed |
| EP-2093275-A2 | Method and composition for improving fuel combustion | Carroll & Associates LLC (US) | 2009-08-26 | — | — | EP | claimed |
| EP-1461402-B1 | METHOD AND COMPOSITION FOR IMPROVING FUEL COMBUSTION | CARROLL ASSOCIATES LLC (US) | 2009-05-27 | — | — | EP | claimed |
| US-7503944-B2 | Method and composition for improving fuel combustion | CARROLL & ASSOCIATES LLC | 2009-03-17 | — | — | US | claimed |
| CN-101172987-A | Method for producing 3-(triphenylphosphine )-carbonyl hydrogenation Rh | CHINA PETROLEUM CHEM CO LTD (CN) | 2008-05-07 | — | — | CN | claimed |
| US-6987200-B2 | Process for producing catalysts comprising nanosize metal particles on a porous support, in particular for the gas-phase oxidation of ethylene and acetic acid to give vinyl acetate | CELANESE CHEMICALS EUROPE GMBH (DE) | 2006-01-17 | — | — | US | claimed |
| EP-0621250-B1 | Process for the codimerisation of dienes and olefins | INST FRANCAIS DU PETROLE (FR) | 2000-01-05 | — | — | EP | claimed |
| US-5476956-A | Catalytic system comprising a rhodium compound and a quaternary nitrogen or phosphorus salt | INSTITUT FRANCAIS DU PETROLE (FR) | 1995-12-19 | — | — | US | claimed |
| US-4085145-A | Process for manufacturing carbonyl compounds by oxidation with molecular oxygen of olefinic compounds in liquid phase in the presence of soluble bimetallic catalysts | INSTITUT FRANCAIS DU PETROLE (FR) | 1978-04-18 | — | — | US | claimed |