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 7)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SIGMAR1 known ✓ | Q99720 | 4/20 | 0.65 |
| ▸ | HRH3 known ✓ | Q9Y5N1 | 1/20 | 0.62 |
| ▸ | CHRNA7 known ✓ | P36544 | 1/20 | 0.55 |
| ▸ | TAAR1 | Q96RJ0 | 6/20 | 0.95 |
| ▸ | AOC3 | Q16853 | 3/20 | 0.64 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.54 |
| ▸ | TSHR | P16473 | 1/20 | 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 | |
|---|---|---|---|---|
| SCHEMBL168948 | 0.97 | TAAR1 (1.00) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| SCHEMBL22863888 | 0.97 | TAAR1 (1.00) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Ethylene SCHEMBL27562091 | 0.95 | TAAR1 (0.86) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Bromide SCHEMBL29033194 | 0.95 | TAAR1 (0.95) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Bromide SCHEMBL3881997 | 0.95 | TAAR1 (0.95) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Water SCHEMBL9747156 | 0.95 | TAAR1 (0.95) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Methyl Alcohol SCHEMBL9781334 | 0.93 | TAAR1 (0.91) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Methyl Alcohol SCHEMBL28673594 | 0.91 | TAAR1 (0.86) | TAAR1SIGMAR1AOC3HRH3CHRNA7 | |
| Hydrochloric Acid SCHEMBL5091388 | 0.86 | SIGMAR1 (0.80) | TAAR1SIGMAR1AOC3 | |
| Tetrylammonium SCHEMBL29892551 | 0.85 | TAAR1 (0.76) | TAAR1SIGMAR1AOC3HRH3CHRNA7 |
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 120 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-116948512-B | Thermal transfer paper and preparation method thereof | 湖南肆玖科技股份有限公司 | 2025-04-18 | — | — | CN | claimed |
| CN-119528769-A | Production process of methyl cyanamide formate | 安徽东至广信农化有限公司 | 2025-02-28 | — | — | CN | claimed |
| CN-116948512-A | Thermal transfer paper and preparation method thereof | 湖南肆玖科技有限公司 | 2023-10-27 | — | — | CN | claimed |
| CN-116285456-A | Printable lettering film and preparation method thereof | 湖南肆玖科技有限公司 | 2023-06-23 | — | — | CN | claimed |
| CN-111777505-B | Preparation method of 3-chloropropionyl chloride | 宿迁市科莱博生物化学有限公司 | 2022-12-23 | — | — | CN | claimed |
| CN-112739440-A | Eutectic extract formation and purification | 纳图瑞克斯有限公司 | 2021-04-30 | — | — | CN | claimed |
| CN-111777505-A | Preparation method of 3-chloropropionyl chloride | 宿迁市科莱博生物化学有限公司 | 2020-10-16 | — | — | CN | claimed |
| US-20200131431-A1 | CHEMICAL ADDITIVES AND SURFACTANT COMBINATIONS FOR FAVORABLE WETTABILITY ALTERATION AND IMPROVED HYDROCARBON RECOVERY FACTORS | ALCHEMY SCIENCES INC (US) | 2020-04-30 | — | — | US | claimed |
| CN-105061753-B | Preparation method of solar light-gathering resin | 深圳市三十一科技有限公司 | 2020-04-10 | — | — | CN | claimed |
| EP-3041889-B1 | A METHOD FOR REGENERATION OF SPENT ION EXCHANGE RESINS | RELIANCE INDUSTRIES LTD (IN) | 2019-03-20 | — | — | EP | claimed |
| EP-3041889-A2 | A METHOD FOR REGENERATION OF SPENT ION EXCHANGE RESINS | Reliance Industries Limited (IN) | 2016-07-13 | — | — | EP | claimed |
| CN-105694385-A | Master batch capable of enhancing properties and melt strength of condensation polymer and preparation method thereof | 上海富元塑胶科技有限公司 | 2016-06-22 | — | — | CN | claimed |
| CN-105237776-A | Synthetic method for super-soft hydrophilic polyester silicone oil and epoxy active polyester intermediate thereof | GUANGZHOU YANGUANG CHEMICAL INDUSTRY CO LTD | 2016-01-13 | — | — | CN | claimed |
| CN-102775364-A | Preparation method of cross linking agent triallyl isocyanurate | UNIV HEFEI TECHNOLOGY | 2012-11-14 | — | — | CN | claimed |
| CN-100469768-C | Preparation method of hydrated sodium phenolate trichloropyridine | QUZHOU HENGSHUN CHEMICAL INDUS (CN) | 2009-03-18 | — | — | CN | claimed |
| CN-101058450-A | Synergistic biocidal mixtures | HERCULES INC (US) | 2007-10-24 | — | — | CN | claimed |
| CN-101045705-A | Preparation method of hydrated sodium phenolate trichloropyridine | HENGSHUN CHEMICAL INDUSTRY CO (CN) | 2007-10-03 | — | — | CN | claimed |
| CN-1325388-C | Synergistic biocidal mixtures | HERCULES INC (US) | 2007-07-11 | — | — | CN | claimed |
| CN-1678534-A | Synergistic biocidal mixtures | HERCULES INC (US) | 2005-10-05 | — | — | CN | claimed |
| CN-1368522-A | Ultralow-temp quick-drying three-component atomic filler powder and its preparing process | LI JIANBAO (CN) | 2002-09-11 | — | — | CN | claimed |