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 SCHEMBL383054 | 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 1066 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-122059785-A | Method for preparing 1, 1-disubstituted alkene by rhodium-catalyzed decarboxylation cracking | 华南理工大学 | 2026-05-19 | — | — | CN | claimed |
| CN-120115192-A | Rhodium-tungsten opposite site MOF-based catalyst, preparation and application | 南京工业大学 | 2025-06-10 | — | — | CN | 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-116606197-B | Method and product for preparing aldehyde by Fischer-Tropsch oil hydroformylation reaction | 国家能源集团宁夏煤业有限责任公司 | 2025-05-06 | — | — | CN | claimed |
| CN-116556044-B | High-entropy hydrotalcite modified carbon fiber photo-thermal conversion material and preparation method thereof | 武汉科技大学 | 2025-02-28 | — | — | CN | claimed |
| CN-119456022-A | Carbide-promoted noble metal-based catalyst and preparation method and application thereof | 大连理工大学 | 2025-02-18 | — | — | CN | claimed |
| CN-119462333-A | Synthetic method of isomerism tridecanol | 国家能源集团宁夏煤业有限责任公司 | 2025-02-18 | — | — | CN | claimed |
| CN-119371275-A | Synthesis method of diene coordinated rhodium tetrafluoroborate | 中国船舶集团有限公司第七一八研究所 | 2025-01-28 | — | — | CN | claimed |
| CN-119368212-A | Metal-based two-dimensional/two-dimensional heterojunction catalyst and preparation method thereof | 丰田自动车株式会社 | 2025-01-28 | — | — | CN | claimed |
| CN-119263964-A | Composition and method for preparing high-carbon aldehyde by two-phase hydroformylation | 中国石油天然气股份有限公司 | 2025-01-07 | — | — | CN | claimed |
| EP-1138791-B1 | Process for the recovery and refining of rhodium | CHIMET S P A (IT) | 2004-09-15 | — | — | EP | claimed |
| US-6596245-B2 | Process for the recovery and refining of rhodium | CHIMET S.P.A. (IT) | 2003-07-22 | — | — | US | claimed |
| WO-2002048039-A1 | CATALYSTS AND THE HYDROFORMYLATION OF OLEFINS | VICTORIA LINK LIMITED (NZ) | 2002-06-20 | — | — | WO | claimed |
| US-20010025548-A1 | Process for the recovery and refining of rhodium | CHIMET S.P.A. (IT) | 2001-10-04 | — | — | US | claimed |
| EP-1138791-A1 | Process for the recovery and refining of rhodium | Chimet S.p.A. (IT) | 2001-10-04 | — | — | EP | claimed |
| CN-1120468-A | Multi dentate heterodesmic Rh catalyst and its prepn. method | CHINESE ACAD INST CHEMISTRY (CN) | 1996-04-17 | — | — | CN | claimed |
| CN-1008884-B | RHODIUM ON CARBON CATALYST | AMOCO CORP (US) | 1990-07-25 | — | — | CN | claimed |
| EP-0114612-B1 | RACEMIC AND OPTICALLY ACTIF 3-HYDROXY-ALPHA-CYCLOCITRAL, THEIR ACETALS AND OPTICALLY ACTIF 3-OXO-ALPHA-CYCLOCITRALACETALS, AND ALSO THE PREPARATION AND USE OF THESE COMPOUNDS | BASF Aktiengesellschaft (DE) | 1988-03-23 | — | — | EP | claimed |
| CN-86106590-A | Be stated from the rhodium catalyst on the carbon | — | 1987-04-22 | — | — | CN | claimed |
| US-4115417-A | ENANTIOSELECTIVITY | HOFFMANN-LA ROCHE INC. (US) | 1978-09-19 | — | — | US | claimed |