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.
Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | HRH3 known ✓ | Q9Y5N1 | 1/20 | 0.62 |
| ▸ | CHRM2 known ✓ | P08172 | 1/20 | 0.54 |
| ▸ | HTR1A known ✓ | P08908 | 1/20 | 0.54 |
| ▸ | ADRA2A known ✓ | P08913 | 1/20 | 0.54 |
| ▸ | CHRM1 known ✓ | P11229 | 1/20 | 0.54 |
| ▸ | DRD1 known ✓ | P21728 | 1/20 | 0.54 |
| ▸ | SLC6A2 known ✓ | P23975 | 1/20 | 0.54 |
| ▸ | SLC6A4 known ✓ | P31645 | 1/20 | 0.54 |
| ▸ | ADRA1A known ✓ | P35348 | 1/20 | 0.54 |
| ▸ | OPRM1 known ✓ | P35372 | 1/20 | 0.54 |
| ▸ | DRD3 known ✓ | P35462 | 1/20 | 0.54 |
| ▸ | SLC6A3 known ✓ | Q01959 | 1/20 | 0.54 |
| ▸ | KCNH2 known ✓ | Q12809 | 1/20 | 0.54 |
| ▸ | BCHE known ✓ | P06276 | 1/20 | 0.53 |
| ▸ | MAOB known ✓ | P27338 | 2/20 | 0.51 |
| ▸ | CNR2 | P34972 | 1/20 | 0.61 |
| ▸ | KDM4E | B2RXH2 | 1/20 | 0.60 |
| ▸ | TSHR | P16473 | 3/20 | 0.58 |
| ▸ | MAPK1 | P28482 | 1/20 | 0.58 |
| ▸ | ALDH1A1 | P00352 | 2/20 | 0.54 |
Click a target to see other patent compounds predicted against it — the reverse direction, in place.
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 | |
|---|---|---|---|---|
| SCHEMBL81248 | 0.97 | HRH3 (0.65) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Bromide SCHEMBL11663269 | 0.95 | HRH3 (0.62) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Water SCHEMBL5507580 | 0.95 | HRH3 (0.62) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Iodide SCHEMBL21693881 | 0.95 | HRH3 (0.62) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Fluoride SCHEMBL11307410 | 0.95 | HRH3 (0.62) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Hydrochloric Acid SCHEMBL11608574 | 0.95 | KDM4E (0.66) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Chloromethane SCHEMBL27279684 | 0.93 | HRH3 (0.60) | HRH3CNR2KDM4ETSHRMAPK1 | |
| SCHEMBL8064154 | 0.93 | HRH3 (0.60) | HRH3CNR2KDM4ETSHRMAPK1 | |
| Ethylene SCHEMBL28212464 | 0.93 | HRH3 (0.60) | HRH3CNR2KDM4ETSHRMAPK1 | |
| SCHEMBL375111 | 0.92 | KDM4E (0.68) | HRH3CNR2KDM4ETSHRMAPK1 |
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 127 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-118144394-B | Release film and preparation method and application thereof | 博益鑫成高分子材料股份有限公司 | 2024-07-09 | — | — | CN | claimed |
| CN-118144394-A | Release film and preparation method and application thereof | 博益鑫成高分子材料股份有限公司 | 2024-06-07 | — | — | CN | claimed |
| CN-110028652-A | A kind of high purity epoxy resins and preparation method thereof containing biphenyl structural | 上海华谊树脂有限公司 | 2019-07-19 | — | — | CN | claimed |
| CN-109651596-A | A kind of epoxy resin and preparation method thereof containing naphthalene ring | 上海华谊树脂有限公司 | 2019-04-19 | — | — | CN | claimed |
| CN-108101799-A | A kind of high-efficient production technology of glycine | 严世佳 | 2018-06-01 | — | — | CN | claimed |
| CN-104650311-B | Self-dispersion type UV curable urethane acrylates aqueous copolymer and preparation method and its manufactured aqueous emulsion | 中科院广州化学有限公司 | 2017-12-26 | — | — | CN | claimed |
| CN-105218401-B | The method that continuity method synthesizes benzene acetonitrile | 河北诚信有限责任公司 | 2017-08-11 | — | — | CN | claimed |
| US-20160122450-A1 | SYNTHESIS OF A SUBSTITUTED FURAN | AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) | 2016-05-05 | — | — | US | claimed |
| CN-105218401-A | The method of continuous processing synthesis benzyl cyanide | Hebei chengxin co ltd | 2016-01-06 | — | — | CN | claimed |
| US-9226941-B2 | Two-component cleaning and disinfecting system | UNION GAS CAPITAL PARTNERS, LLC | 2016-01-05 | — | — | US | claimed |
| US-20150320797-A1 | TWO-COMPONENT CLEANING AND DISINFECTING SYSTEM | UNION GAS CAPITAL PARTNERS, LLC | 2015-11-12 | — | — | US | claimed |
| CN-104650311-A | Self-dispersing UV photo-curing urethane acrylate aqueous copolymer, preparation method of aqueous copolymer and aqueous emulsion prepared from aqueous copolymer | CAS GUANGZHOU CHEMISTRY CO LTD | 2015-05-27 | — | — | CN | claimed |
| CN-104478831-A | Preparation method of triglycidyl-meta-aminophenol epoxy resin | SHANGHAI HUAYI RESINS CO LTD | 2015-04-01 | — | — | CN | claimed |
| EP-1981988-A2 | ANTISEPTIC COMPOSITIONS AND METHODS OF USING SAME | Do-Coop Technologies Ltd (IL) | 2008-10-22 | — | — | EP | claimed |
| WO-2007077562-A2 | ANTISEPTIC COMPOSITIONS AND METHODS OF USING SAME | DO-COOP TECHNOLOGIES LTD. (IL) | 2007-07-12 | — | — | WO | claimed |
| US-20020168423-A1 | High strength liquid antiseptic | WURZBURGER STEPHEN RAY (US) | 2002-11-14 | — | — | US | claimed |
| CN-122074095-A | Catalyst and method for hydrogen production by proton reduction | 瑞内尔公司 | 2026-05-22 | — | — | CN | disclosed |
| CN-119954677-A | Cyclopropionamide substituted benzamide derivative and preparation method and application thereof | 山东省联合农药工业有限公司 | 2025-05-09 | — | — | CN | disclosed |
| US-4116866-A | REACTION PRODUCT OF CASTOR-FATTY PROPYLAMIDO BENZYL DIALKYL AMMONIUM COMPOUND AND SMECTITE CLAY | N L INDUSTRIES, INC. (US) | 1978-09-26 | — | — | US | disclosed |
| US-3984605-A | Heat sensitive recording material containing decolorizing agent | MITSUBISHI PAPER MILLS, LTD. (JA) | 1976-10-05 | — | — | US | disclosed |
Patent text — is the patent's own abstract consistent with the prediction?
For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20160122450-A1 | SYNTHESIS OF A SUBSTITUTED FURAN | DCXR, PFAS, FUT6 | HRH3 2244/4885CHRM2 4205/4885HTR1A 3408/4885 |
| US-20020168423-A1 | High strength liquid antiseptic | CUTA, LIPA, POLR1C | HRH3 367/4885CHRM2 3147/4885HTR1A 4543/4885 |
“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.