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 SCHEMBL27333994 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL28627688 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL27962955 | 0.95 | — | — | |
| SCHEMBL9614403 | 0.94 | HIF1A (0.56) | — | |
| SCHEMBL26047 | 0.94 | — | — | |
| Methane SCHEMBL18191054 | 0.89 | HIF1A (0.50) | — | |
| Iodide SCHEMBL19272496 | 0.89 | — | — | |
| SCHEMBL13671434 | 0.89 | HIF1A (0.67) | — | |
| Piperazine SCHEMBL22158351 | 0.89 | HIF1A (0.67) | — | |
| SCHEMBL4273750 | 0.89 | — | — |
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 51 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-119859216-A | Polar functionalized conjugated diene polymer and preparation method thereof | 东华大学 | 2025-04-22 | — | — | CN | claimed |
| CN-109320559-B | Nickel-palladium metal complex, preparation method and application thereof, product and application thereof | 东华大学 | 2020-10-30 | — | — | CN | claimed |
| EP-2178943-A1 | METHOD FOR THE PRODUCTION OF THIOPHENE OLIGOMERS | Bayer Technology Services GmbH (DE) | 2010-04-28 | — | — | EP | claimed |
| EP-2176314-A2 | PROCESS FOR THE PREPARATION OF POLY- AND OLIGOTHIOPHENES ON AN INDUSTRIAL SCALE | Bayer Technology Services GmbH (DE) | 2010-04-21 | — | — | EP | claimed |
| EP-2167565-A1 | PROCESS FOR SYNTHESIZING OLIGO/POLYTHIOPHENES BY A 'ONE-POT' SYNTHESIS ROUTE | Bayer Technology Services GmbH (DE) | 2010-03-31 | — | — | EP | claimed |
| WO-2009021639-A1 | METHOD FOR THE PRODUCTION OF THIOPHENE OLIGOMERS | BAYER TECHNOLOGY SERVICES GMBH (DE) | 2009-02-19 | — | — | WO | claimed |
| WO-2009015810-A2 | PROCESS FOR THE PREPARATION OF POLY- AND OLIGOTHIOPHENES ON AN INDUSTRIAL SCALE | BAYER TECHNOLOGY SERVICES GMBH (DE) | 2009-02-05 | — | — | WO | claimed |
| WO-2009007012-A1 | PROCESS FOR SYNTHESIZING OLIGO/POLYTHIOPHENES BY A 'ONE-POT' SYNTHESIS ROUTE | BAYER TECHNOLOGY SERVICES GMBH (DE) | 2009-01-15 | — | — | WO | claimed |
| CN-119859216-A | Polar functionalized conjugated diene polymer and preparation method thereof | 东华大学 | 2025-04-22 | — | — | CN | disclosed |
| US-20250019565-A1 | POLYCYCLOCARBONATE COMPOUNDS AND POLYMERS AND COMPOSITIONS FORMED THEREFROM | SWIMC LLC (US) | 2025-01-16 | — | — | US | disclosed |
| US-12077676-B2 | Polycyclocarbonate compounds and polymers and compositions formed therefrom | SWIMC LLC (US) | 2024-09-03 | — | — | US | disclosed |
| CN-112135830-B | Oxo-substituted compounds | 住友制药株式会社 | 2024-06-14 | — | — | CN | disclosed |
| US-11746096-B2 | Polycyclocarbonate compounds and polymers formed therefrom | SWIMC LLC (US) | 2023-09-05 | — | — | US | disclosed |
| CN-109320559-B | Nickel-palladium metal complex, preparation method and application thereof, product and application thereof | 东华大学 | 2020-10-30 | — | — | CN | disclosed |
| CN-1046501-C | Novel thiourea complexes and process for preparing nitroarylimino heterocycles | ALCON LAB INC (US) | 1999-11-17 | — | — | CN | disclosed |
| CN-1220261-A | Novel process for preparation of clonidine derivatives | ALCON LAB INC (US) | 1999-06-23 | — | — | CN | disclosed |
| CN-1123026-A | Novel process for preparing clonidine derivatives | ALCON LAB INC (US) | 1996-05-22 | — | — | CN | disclosed |
| EP-0178581-B1 | Use of 2-[(2-bromo-6-fluorophenyl)imino]imidazolidine as a sedative | BOEHRINGER INGELHEIM VETMEDICA GMBH (DE) | 1992-01-22 | — | — | EP | disclosed |
| US-4624960-A | 2-112-BROMO-6-FLUOROPHENYLIMINOIMIDAZOLIDINE | BOEHRINGER INGELHEIM VETMEDICA GMBH (DE) | 1986-11-25 | — | — | US | disclosed |
| EP-0178581-A2 | Use of 2-[(2-bromo-6-fluorophenyl)imino]imidazolidine as a sedative | BOEHRINGER INGELHEIM VETMEDICA GMBH (DE) | 1986-04-23 | — | — | EP | disclosed |