Hydrochloric Acid

Hydrochloric Acid

SCHEMBL276013

CC(C)(/N=N/C(C)(C)C(=N)N)C(=N)N.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

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.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 1.00
CYP3A4 P08684 1/20 1.00
MAPT P10636 1/20 1.00
CYP2D6 P10635 1/20 1.00
NOS1 P29475 1/20 0.35
HTT P42858 1/20 0.31

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.

Compoundsimilaritytop predictedshared targets
Hydrochloric Acid SCHEMBL276014 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL738578 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL23508 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL1525615 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL954633 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL23478926 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL34438 1.00 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6NOS1
Hydrochloric Acid SCHEMBL1362721 0.97 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPTCYP2D6NOS1
SCHEMBL246819 0.97 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPTCYP2D6NOS1
SCHEMBL246818 0.97 ALDH1A1 (0.94) ALDH1A1CYP3A4MAPTCYP2D6NOS1

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

Appears in 3203 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250316753-A1 BATTERY CELL AND PREPARATION METHOD THEREFOR, BATTERY AND ELECTRICAL APPARATUS CONTEMPORARY AMPEREX TECHNOLOGY CO., LIMITED (CN) 2025-10-09 US claimed
EP-4621906-A1 BATTERY CELL AND PREPARATION METHOD THEREFOR, BATTERY AND ELECTRIC APPARATUS Contemporary Amperex Technology Co., Limited (CN) 2025-09-24 EP claimed
US-12384953-B1 Strongly adsorbed hyper-branched filtrate reducer for water-based drilling fluid with resistance to 240° C. and saturated salinity, preparation method therefor and use thereof CHINA UNIVERSITY OF PETROLEUM (EAST CHINA) (CN) 2025-08-12 US claimed
WO-2025082044-A1 COPOLYMER AND PREPARATION METHOD THEREFOR, AND FRACTURING FLUID 中国石油集团渤海钻探工程有限公司 2025-04-24 WO claimed
WO-2025065965-A1 PERFLUOROALKYL-SUBSTITUTED ALLYL QUATERNARY AMMONIUM SALT AND PREPARATION METHOD THEREFOR, COPOLYMER AS WELL AS PREPARATION METHOD THEREFOR AND USE THEREOF, AND WASTEWATER TREATMENT METHOD 中国石油天然气股份有限公司 2025-04-03 WO claimed
US-12220685-B2 Solid-phase extraction material, and preparation method and use thereof NANJING UNIVERSITY (CN) 2025-02-11 US claimed
US-20250038254-A1 ELECTROCHEMICAL APPARATUS AND ELECTRONIC APPARATUS INCLUDING SAME NINGDE AMPEREX TECHNOLOGY LIMITED (CN) 2025-01-30 US claimed
WO-2025016066-A1 ADHESIVE FOR SILICON-BASED NEGATIVE ELECTRODE ACTIVE MATERIAL, AND PREPARATION METHOD AND USE 华为技术有限公司 2025-01-23 WO claimed
WO-2024255789-A1 MULTI-COMPONENT COPOLYMER AND PREPARATION METHOD THEREFOR AND USE THEREOF 中国石油天然气集团有限公司 2024-12-19 WO claimed
WO-2024239155-A1 BATTERY CELL AND PREPARATION METHOD THEREFOR, BATTERY AND ELECTRIC APPARATUS 宁德时代新能源科技股份有限公司 2024-11-28 WO claimed
US-5283306-A Diallyldimethylammonium chloride copolymerized with dimethylaminoethyl(meth)acrylate that has been quaternized NALCO CHEMICAL COMPANY (US) 1994-02-01 US claimed
EP-0528182-A1 Process for preparing water soluble polymer gels DIATEC ENVIRONMENTAL (US) 1993-02-24 EP claimed
US-5037906-A Cooled to produce cold syrup or slurry continuous or batch controlled polymerization absorbing heat of reaction AMERICAN CYANAMID (US) 1991-08-06 US claimed
US-5006590-A Process for the preparation of dispersion of water-soluble cationic polymer KYORITSU YUKI CO., LTD. (JP) 1991-04-09 US claimed
US-4951921-A WATER SOLUBLE POLYMERS FOR SUBTERRANEAN WELLBORES PHILLIPS PETROLEUM COMPANY (US) 1990-08-28 US claimed
EP-0364175-A2 Process for the preparation of water-soluble cationic polymer HYMO CORPORATION (JP) 1990-04-18 EP claimed
EP-0136649-B1 PROCESS FOR THE PREPARATION OF CATIONIC VINYL ESTER BASED POLYMER LATICES AND THEIR USE AS FORMALDEHYDE-FREE BINDERS. National Starch and Chemical Corporation (US) 1989-11-15 EP claimed
EP-0296331-A2 High solids process for the production of water soluble polymers by exothermic polymerization CYTEC TECHNOLOGY CORP. (US) 1988-12-28 EP claimed
EP-0136649-A2 Process for the preparation of cationic vinyl ester based polymer latices and their use as formaldehyde-free binders. National Starch and Chemical Corporation (US) 1985-04-10 EP claimed
US-4489192-A QUATERNARY AMMONIUM MONOMER NATIONAL STARCH AND CHEMICAL CORPORATION (US) 1984-12-18 US claimed