Hydrochloric Acid

Hydrochloric Acid

SCHEMBL703118

COC(=O)[C@@H](N)Cc1c[nH]cn1.Cl.Cl

nearest known ligand 0.38

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 4)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 1/20 0.31
ALDH1A1 P00352 1/20 0.38
LTA4H P09960 2/20 0.31
KIF11 P52732 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 SCHEMBL940526 1.00 ALDH1A1 (0.38) ALDH1A1PTGS2LTA4HKIF11
Hydrochloric Acid SCHEMBL9081237 1.00 ALDH1A1 (0.38) ALDH1A1PTGS2LTA4HKIF11
Hydrochloric Acid SCHEMBL1375315 1.00 ALDH1A1 (0.38) ALDH1A1PTGS2LTA4HKIF11
Hydrochloric Acid SCHEMBL4389612 1.00 ALDH1A1 (0.38) ALDH1A1PTGS2LTA4HKIF11
Hydrochloric Acid SCHEMBL852606 1.00 ALDH1A1 (0.38) ALDH1A1PTGS2LTA4HKIF11
SCHEMBL3846863 0.98 ALDH1A1 (0.36) ALDH1A1PTGS2LTA4HKIF11
SCHEMBL262238 0.98 ALDH1A1 (0.36) ALDH1A1PTGS2LTA4HKIF11
SCHEMBL833709 0.98 ALDH1A1 (0.36) ALDH1A1PTGS2LTA4HKIF11
Selenium SCHEMBL30525936 0.97 ALDH1A1 (0.35) ALDH1A1PTGS2LTA4HKIF11
Histidine SCHEMBL27511748 0.94 SLC7A5 (0.38) ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120511435-B Lithium ion battery diaphragm based on composite coating and preparation method and application thereof Shanxi Housheng New Material Technology Co.,Ltd. (CN) 2026-05-26 CN claimed
CN-115343261-B Application of supermolecular gel in selective identification of sialic acid and sialic acid sugar chains 中国科学院大连化学物理研究所 2025-05-06 CN claimed
CN-119708124-A Liquid phase synthesis method of bursin tripeptide 厦门胜泽泰医药科技有限公司 2025-03-28 CN claimed
CN-118126117-A Synthesis method of copper peptide 深圳市维琪科技股份有限公司 2024-06-04 CN claimed
CN-117903078-A Amide derivative containing 3, 4-dichloro isothiazole, preparation method and application thereof 南开大学 2024-04-19 CN claimed
CN-116987289-A Preparation method and application of Bola type supermolecule copper ion antibacterial hydrogel 沈阳药科大学 2023-11-03 CN claimed
CN-115343261-A Application of supramolecular gel in selective recognition of sialic acid and sialic acid sugar chain 中国科学院大连化学物理研究所 2022-11-15 CN claimed
CN-114230260-A Manganese tailing slag concrete and preparation method thereof 广西旭阳环保建材有限公司 2022-03-25 CN claimed
WO-2017075242-A1 METAL-CONTAINING IONIC LIQUIDS AND METHODS OF PREPARING AND USING SAME THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) 2017-05-04 WO claimed
US-20080076831-A1 Hemorrhoid reliever and method of use GOETZ BERNARD 2008-03-27 US claimed
WO-2002022120-A1 PAIN RELIEVER AND METHOD OF USE MEDICAL MERCHANDISING, INC. (US) 2002-03-21 WO claimed
US-6350879-B1 ENZYME INHIBITORS COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2002-02-26 US claimed
US-6197823-B1 Pain reliever and method of use MEDICAL MERCHANDISING, INC. 2001-03-06 US claimed
JP-5294961-A None JP disclosed
JP-61176573-A None JP disclosed
CN-120511435-B Lithium ion battery diaphragm based on composite coating and preparation method and application thereof Shanxi Housheng New Material Technology Co.,Ltd. (CN) 2026-05-26 CN disclosed
US-4204991-A Sarcosine1 dehydroalanine8 angiotensin II derivatives G. D. SEARLE & CO. (US) 1980-05-27 US disclosed
US-4048305-A PHENYLALANINE, HISTIDINE DR. L. ZAMBELETTI S.P.A. (IT) 1977-09-13 US disclosed
US-3959248-A TRIPEPTIDES; ANTIDEPRESSANTS MERCK & CO., INC. (US) 1976-05-25 US disclosed
US-3934027-A 18β-Glycyrrhetinic acid amides useful as antiulcer agents PFIZER INC. (US) 1976-01-20 US disclosed