Hydrochloric Acid

Hydrochloric Acid

SCHEMBL358299

CCC(C)(C)N.Cl

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

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.

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL3633234 1.00
Hydrochloric Acid SCHEMBL5429217 1.00
Hydrochloric Acid SCHEMBL15112570 1.00 TSHR (0.46)
Hydrochloric Acid SCHEMBL4979563 0.96
Hydrochloric Acid SCHEMBL6360430 0.96
Hydrochloric Acid SCHEMBL6010481 0.96
SCHEMBL1725 0.95
Hydrochloric Acid SCHEMBL6010478 0.92 TSHR (0.40)
Bromide SCHEMBL1566230 0.91
SCHEMBL15821668 0.91

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 419 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119976882-A Method for synthesizing hierarchical pore molecular sieve 中国石油大学(华东) 2025-05-13 CN claimed
EP-4473070-A1 CERIA-BASED SLURRY COMPOSITIONS FOR SELECTIVE AND NONSELECTIVE CMP OF SILICON OXIDE, SILICON NITRIDE, AND POLYSILICON CMC Materials LLC (US) 2024-12-11 EP claimed
EP-4473071-A1 CERIA-BASED SLURRY COMPOSITIONS FOR SELECTIVE AND NONSELECTIVE CMP OF SILICON OXIDE, SILICON NITRIDE, AND POLYSILICON CMC Materials LLC (US) 2024-12-11 EP claimed
EP-4396409-A1 USE OF MODIFIED LIGNIN AS A WET END STRENGTH ADDITIVE Ecolab USA Inc. (US) 2024-07-10 EP claimed
CN-117916423-A Novel compositions and methods for papermaking 埃科莱布美国股份有限公司 2024-04-19 CN claimed
WO-2024080933-A1 A METHOD OF SEPARATING PROTEIN FRACTIONS AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2024-04-18 WO claimed
EP-4315482-A1 HALOGEN COMPLEXING AGENTS BOUND TO THE CATHODE SURFACE IN A STATIC ZINC HALIDE BATTERY EOS Energy Technology Holdings, LLC (US) 2024-02-07 EP claimed
CN-117296189-A Halogen complexing agent combined with cathode surface in static zinc halide battery EOS能源技术控股有限责任公司 2023-12-26 CN claimed
CN-117120563-A Self-stopping polishing composition and method for high topography selectivity CMC材料有限责任公司 2023-11-24 CN claimed
EP-4277935-A1 RUBBER VULCANIZATION PROCESSES EMPLOYING A EUTECTIC MIXTURE BRIDGESTONE CORPORATION (JP) 2023-11-22 EP claimed
EP-2341886-A1 ANTIMICROBIAL N-CHLORINATED COMPOSITIONS NovaBay Pharmaceuticals, Inc. (US) 2011-07-13 EP claimed
WO-2010054269-A1 ANTIMICROBIAL N-CHLORINATED COMPOSITIONS NOVABAY PHARMACEUTICALS, INC. (US) 2010-05-14 WO claimed
EP-0683163-B1 Process for producing glycidyl acrylate or glycidyl methacrylate MITSUBISHI GAS CHEMICAL CO (JP) 2000-03-01 EP claimed
US-5750739-A Process for producing glycidyl ester of acrylic acid or methacrylic acid MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1998-05-12 US claimed
US-5543522-A Process for preparing an ambient temperature molten salt using thionyl chloride MITSUBISHI CHEMICAL CORPORATION (JP) 1996-08-06 US claimed
US-5527927-A CATALYTIC TRANSESTERIFICATION OF GLYCIDOL AND METHYL METHACRYLATE MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1996-06-18 US claimed
EP-0683163-A1 Process for producing glycidyl acrylate or glycidyl methacrylate MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 1995-11-22 EP claimed
US-5232497-A With quaternary ammonium alkyl substituted salts THE WESTERN COMPANY OF NORTH AMERICA (US) 1993-08-03 US claimed
EP-0082814-B1 MICROORGANISMS OF THE GENUS PSEUDOMONAS AND METHOD FOR THE DECOMPOSITION OF COMPOUNDS CONTAINING METHYL GROUPS IN AQUEOUS SOLUTIONS CIBA-GEIGY AG (CH) 1987-03-04 EP claimed
US-4490471-A PURIFICATION CIBA-GEIGY CORPORATION (US) 1984-12-25 US claimed