Hydrochloric Acid

Hydrochloric Acid

SCHEMBL1268973

CN1C=CC=CC1.Cl

nearest known ligand 0.00

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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
SCHEMBL190345 0.97
Bromide SCHEMBL27702312 0.94
SCHEMBL30661008 0.94
Water SCHEMBL7537804 0.94
Iodide SCHEMBL7099467 0.94
SCHEMBL28812505 0.94
Iodide SCHEMBL27309520 0.92
Bromide SCHEMBL27671123 0.92
SCHEMBL28458457 0.87
SCHEMBL27375739 0.87

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-222724341-U Continuous reaction device for 1-methyl pyridine chloride 安徽国星生物化学有限公司 2025-04-08 CN claimed
CN-119059875-A Chloromethane tail gas recovery process 安徽国星生物化学有限公司 2024-12-03 CN claimed
CN-119019225-A Application of ionic liquid in preparation of electronic grade isopropanol and preparation method thereof 山东海科创新研究院有限公司 2024-11-26 CN claimed
CN-118558241-A Methyl chloride recycling device and method in synthesis of 1-methyl pyridine chloride 安徽国星生物化学有限公司 2024-08-30 CN claimed
CN-117816240-A Preparation method of catalyst for synthesizing 1-methyl pyridine chloride 安徽国星生物化学有限公司 2024-04-05 CN claimed
CN-117658764-A Method for preparing 1, 2-dichloroethane 中国科学院大连化学物理研究所 2024-03-08 CN claimed
CN-117482760-A Cellulose-based nanofiltration membrane and preparation method and application thereof 浙江大学绍兴研究院 2024-02-02 CN claimed
CN-115448872-B Process for preparing paraquat by homogeneous catalytic oxidation of purple crystals 安徽国星生物化学有限公司 2023-12-26 CN claimed
CN-116622168-A Low-surface free energy culture dish and preparation method thereof 深圳市碳源生物科技有限公司 2023-08-22 CN claimed
CN-115557884-A Process for synthesizing 1-methylpyridine chloride by high-temperature method 安徽国星生物化学有限公司 2023-01-03 CN claimed
CN-115448872-A Process for preparing paraquat by homogeneous catalytic oxidation of amethyst 安徽国星生物化学有限公司 2022-12-09 CN claimed
CN-115403513-A Continuous synthesis process of N-methylpyridine chloride 安徽国星生物化学有限公司 2022-11-29 CN claimed
CN-217856087-U N-picoline chloride apparatus for producing 安徽国星生物化学有限公司 2022-11-22 CN claimed
CN-115090246-A Purification treatment device and method for N-methylpyridine chloride 安徽国星生物化学有限公司 2022-09-23 CN claimed
CN-114806869-A Culture dish and application thereof in preparing cell film 深圳市碳源生物科技有限公司 2022-07-29 CN claimed
CN-109503693-B Process for synthesizing Aramchol by using cholic acid as raw material 合肥工业大学 2021-04-06 CN claimed
US-20260118757-A1 RADIATION-SENSITIVE RESIST COMPOSITION AND PATTERN FORMATION METHOD USING THE SAME SAMSUNG ELECTRONICS CO., LTD. (KR) 2026-04-30 US disclosed
CN-117816240-B Preparation method of catalyst for synthesizing 1-methyl pyridine chloride 安徽国星生物化学有限公司 2026-02-13 CN disclosed
US-20080221172-A1 Use of Quaternary Pyridinium Compounds for Vasoprotection and/or Hepatoprotection TRIGENDO SP. Z O.O. 2008-09-11 US disclosed
WO-2008104920-A1 THE USE OF QUATERNARY PYRIDINIUM COMPOUNDS FOR VASOPROTECTION AND/OR HEPATOPROTECTION TRIGENDO SP. Z O.O. (PL) 2008-09-04 WO disclosed