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 16)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | DNM1 | Q05193 | 3/20 | 0.45 |
| ▸ | CA12 | O43570 | 2/20 | 0.43 |
| ▸ | CA1 | P00915 | 2/20 | 0.43 |
| ▸ | CA9 | Q16790 | 2/20 | 0.43 |
| ▸ | TSHR | P16473 | 2/20 | 0.43 |
| ▸ | LMNA | P02545 | 1/20 | 0.43 |
| ▸ | MAPT | P10636 | 1/20 | 0.41 |
| ▸ | KDM5A | P29375 | 3/20 | 0.40 |
| ▸ | THRB | P10828 | 1/20 | 0.40 |
| ▸ | PHF8 | Q9UPP1 | 2/20 | 0.38 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.38 |
| ▸ | ALDH2 | P05091 | 1/20 | 0.38 |
| ▸ | KDM4C | Q9H3R0 | 1/20 | 0.38 |
| ▸ | MEN1 | O00255 | 1/20 | 0.37 |
| ▸ | KMT2A | Q03164 | 1/20 | 0.37 |
| ▸ | NPSR1 | Q6W5P4 | 1/20 | 0.37 |
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 | |
|---|---|---|---|---|
| Hydrochloric Acid SCHEMBL27642008 | 1.00 | DNM1 (0.45) | DNM1CA12CA1CA9TSHR | |
| Hydrochloric Acid SCHEMBL15068365 | 1.00 | DNM1 (0.45) | DNM1CA12CA1CA9TSHR | |
| Bromide SCHEMBL8369863 | 0.96 | DNM1 (0.43) | DNM1CA12CA1CA9TSHR | |
| Methane SCHEMBL14889208 | 0.96 | DNM1 (0.43) | DNM1CA12CA1CA9TSHR | |
| Hydrochloric Acid SCHEMBL28504354 | 0.96 | DNM1 (0.43) | DNM1CA12CA1CA9TSHR | |
| SCHEMBL27566038 | 0.96 | TSHR (0.46) | DNM1CA12CA1CA9TSHR | |
| SCHEMBL896 | 0.96 | TSHR (0.46) | DNM1CA12CA1CA9TSHR | |
| SCHEMBL3904839 | 0.96 | TSHR (0.46) | DNM1CA12CA1CA9TSHR | |
| Hydrochloric Acid SCHEMBL8540929 | 0.93 | DNM1 (0.41) | DNM1CA12CA1CA9TSHR | |
| Hydrochloric Acid SCHEMBL11442180 | 0.93 | DNM1 (0.41) | DNM1CA12CA1CA9TSHR |
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 1194 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250216403-A1 | CHEMILUMINESCENT SUBSTRATE SOLUTION AND CHEMILUMINESCENCE DETECTION METHOD | SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (CN) | 2025-07-03 | — | — | US | claimed |
| EP-4579239-A1 | CHEMILUMINESCENT SUBSTRATE SOLUTION AND CHEMILUMINESCENCE DETECTION METHOD | Shenzhen Mindray Bio-Medical Electronics Co., Ltd. (CN) | 2025-07-02 | — | — | EP | claimed |
| EP-4565694-A1 | EXTRACTION-LESS REVERSE PHASE (RP) CHROMATOGRAPHY FOR MRNA PURITY ASSESSMENT | ModernaTX, Inc. (US) | 2025-06-11 | — | — | EP | claimed |
| US-20250092440-A1 | EXTRACTION-LESS REVERSE PHASE (RP) CHROMATOGRAPHY OF MRNA ENCAPSULATED IN LIPID NANOPARTICLES FOR MRNA PURITY ASSESSMENT | MODERNATX, INC. (US) | 2025-03-20 | — | — | US | claimed |
| CN-119409726-A | Efficient preparation method of antioxidant 168 | 湖北兴发化工集团股份有限公司 | 2025-02-11 | — | — | CN | claimed |
| CN-119219233-A | Nitrate removal method for salt-separating mother liquor of chemical high-salt wastewater | 北京恒其德生科技有限公司 | 2024-12-31 | — | — | CN | claimed |
| CN-116284193-B | Method for separating cholic acid and deoxycholic acid | 浙江大学 | 2024-11-08 | — | — | CN | claimed |
| CN-118874463-A | Load type Pt2Cluster catalyst and preparation method and application thereof | 北京结力能源科技有限公司 | 2024-11-01 | — | — | CN | claimed |
| EP-4381059-A1 | EXTRACTION-LESS REVERSE PHASE (RP) CHROMATOGRAPHY OF MRNA ENCAPSULATED IN LIPID NANOPARTICLES FOR MRNA PURITY ASSESSMENT | ModernaTX, Inc. (US) | 2024-06-12 | — | — | EP | claimed |
| CN-118005953-A | High-viscoelasticity double-network carboxymethyl chitosan gel and preparation method and application thereof | 苏州浩微生物医疗科技有限公司 | 2024-05-10 | — | — | CN | claimed |
| EP-0461597-A2 | Method for preparing monohalogenosilanes | Shin-Etsu Chemical Co., Ltd. (JP) | 1991-12-18 | — | — | EP | claimed |
| EP-0194059-B1 | PROCESS FOR PRODUCTION OF ADIPONITRILE | THE STANDARD OIL COMPANY (US) | 1989-09-20 | — | — | EP | claimed |
| US-4681968-A | Method of producing adiponitrile | THE STANDARD OIL COMPANY (US) | 1987-07-21 | — | — | US | claimed |
| EP-0213215-A1 | Chlorosilane disproportionation catalyst and method for producing a silane compound by means of the catalyst | DENKI KAGAKU KOGYO KABUSHIKI KAISHA (JP) | 1987-03-11 | — | — | EP | claimed |
| EP-0194059-A1 | Process for production of adiponitrile | THE STANDARD OIL COMPANY (US) | 1986-09-10 | — | — | EP | claimed |
| EP-0025829-B1 | PROCESS FOR THE PREPARATION OF ALKYL CHLORIDES | BASF Aktiengesellschaft (DE) | 1982-12-22 | — | — | EP | claimed |
| EP-0025829-A1 | Process for the preparation of alkyl chlorides | BASF Aktiengesellschaft (DE) | 1981-04-01 | — | — | EP | claimed |
| US-4246091-A | COATING A SULFONATED FLUORO POLYMER WITH AN AMINE SALT TO INCREASE THE ION SELECTIVE PERMEABILITY | KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JP) | 1981-01-20 | — | — | US | claimed |
| US-4063879-A | CROSSLINKING CATALYST | BASF AKTIENGESELLSCHAFT (DT) | 1977-12-20 | — | — | US | claimed |
| US-4042605-A | Process for the production of 1,4-diaminoanthraquinone-2,3-dinitrile | BASF AKTIENGESELLSCHAFT (DT) | 1977-08-16 | — | — | US | claimed |