Hydrochloric Acid

Hydrochloric Acid

SCHEMBL409480

Cl.NC(=O)c1ccc(Cl)cc1

nearest known ligand 0.60

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 20)

geneUniProtsupporting neighboursconfidence
CA2 known ✓ P00918 2/20 0.54
PARP1 known ✓ P09874 2/20 0.52
MAP4K4 O95819 4/20 0.60
CES2 O00748 2/20 0.59
CES1 P23141 2/20 0.59
LMNA P02545 2/20 0.58
TSHR P16473 2/20 0.56
ALOX15 P16050 1/20 0.56
CA1 P00915 2/20 0.54
MAPT P10636 2/20 0.54
L3MBTL1 Q9Y468 2/20 0.54
ALDH1A1 P00352 2/20 0.54
KDM4E B2RXH2 1/20 0.54
POLB P06746 1/20 0.52
CYP3A4 P08684 1/20 0.52
CYP2C19 P33261 1/20 0.52
RECQL P46063 1/20 0.52
BLM P54132 1/20 0.52
PMP22 Q01453 1/20 0.52
HSD17B10 Q99714 1/20 0.52

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 SCHEMBL28021646 1.00 MAP4K4 (0.60) MAP4K4CES2CES1LMNATSHR
Hydrochloric Acid SCHEMBL3772040 1.00 MAP4K4 (0.60) MAP4K4CES2CES1LMNATSHR
SCHEMBL29959902 0.97 MAP4K4 (0.62) MAP4K4CES2CES1LMNATSHR
SCHEMBL77931 0.97 MAP4K4 (0.62) MAP4K4CES2CES1LMNATSHR
Bromide SCHEMBL28799121 0.95 MAP4K4 (0.60) MAP4K4CES2CES1LMNATSHR
Iodide SCHEMBL19056893 0.95 MAP4K4 (0.60) MAP4K4CES2CES1LMNATSHR
Nitrogen SCHEMBL27780715 0.92 MAP4K4 (0.58) MAP4K4CES2CES1LMNATSHR
SCHEMBL2689662 0.90 MAP4K4 (0.72) MAP4K4CES2CES1LMNATSHR
Benzamide SCHEMBL9812910 0.88 PARP1 (0.73) MAP4K4CES2CES1TSHRALOX15
4-Chloroaniline SCHEMBL11600778 0.88 PARP10 (0.61) MAP4K4CES2CES1LMNATSHR

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 53 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2367822-B1 TRICYCLIC AZAINDOLES MERCK PATENT GMBH (DE) 2016-10-05 EP claimed
CN-104744306-A P-chloroaniline isocyanate preparation method HUNAN LIJIE BIOCHEMICAL CO LTD 2015-07-01 CN claimed
US-8853391-B2 Tricyclic azaindoles MERCK PATENT GMBH (DE) 2014-10-07 US claimed
CN-103910650-A Preparation method for 4-chlorophenylhydrazine hydrochloride TIANJIN QIDONG CHEMICAL PLANT 2014-07-09 CN claimed
CN-102993056-A Preparation method of chlorhexidine compound GANSU RES INST OF CHEMICAL INDUSTRY 2013-03-27 CN claimed
CN-102993044-A Preparation method of 4-chlorophenylhydrazine hydrochloride TIANJIN SHI TIANCHUAN HUAGONG CO LTD 2013-03-27 CN claimed
US-20120022060-A1 Tricyclic Azaindoles MERCK PATENT GMBH (DE) 2012-01-26 US claimed
EP-2367822-A1 TRICYCLIC AZAINDOLES Merck Patent GmbH (DE) 2011-09-28 EP claimed
CN-101565839-B Cyanogen to cyanogen-free alkali environment-friendly galvanizing brightener WUHAN FENGFAN ELECTROPLATING TECHNOLOGY CO LTD 2011-04-06 CN claimed
CN-101555609-B An environment-protective alkali galvanization composition brightener for transformation from cyanide to non-cyanide WUHAN FENGFAN ELECTROPLATING TECHNOLOGY CO LTD 2010-08-04 CN claimed
WO-2010080253-A1 TRICYCLIC AZAINDOLES MERCK PATENT GMBH (DE) 2010-07-15 WO claimed
CN-101565839-A Cyanogen to cyanogen-free alkali environment-friendly galvanizing brightener WUHAN FENGZHENG ELECTROPLATING (CN) 2009-10-28 CN claimed
CN-101555609-A An environment-protective composition brightener for transformation between alkali non-cyanide galvanization and alkali cyanide galvanization WUHAN FENGFAN ELECTROPLATING T (CN) 2009-10-14 CN claimed
EP-1897881-A2 Compounds useful for the treatment of obesity, type II diabetes and CNS disorders Biovitrum AB (publ) (SE) 2008-03-12 EP claimed
CN-101081845-A Substituted sulphone and sulphonamide compounds useful for the treatment of obesity, type II diabetes and cns disorders BIOVITRUM AB (SE) 2007-12-05 CN claimed
CN-1662521-A Novel compounds useful for the treatment of obesity, type II diabetes and CNS disorders BIOVITRUM AB (SE) 2005-08-31 CN claimed
EP-1513828-A1 NEW COMPOUNDS USEFUL FOR THE TREATMENT OF OBESITY, TYPE II DIABETES AND CNS DISORDERS Biovitrum AB (SE) 2005-03-16 EP claimed
US-20040024210-A1 New compounds PROXIMAGEN NEUROSCIENCE PLC (GB) 2004-02-05 US claimed
WO-2004000828-A1 NEW COMPOUNDS USEFUL FOR THE TREATMENT OF OBESITY, TYPE II DIABETES AND CNS DISORDERS BIOVITRUM AB (SE) 2003-12-31 WO claimed
US-12559461-B2 Antibiotic adjuvant compounds UNIVERSITY OF NOTRE DAME DU LAC (US) 2026-02-24 US disclosed
US-20230286922-A1 ANTIBIOTIC ADJUVANT COMPOUNDS UNIVERSITY OF NOTRE DAME DU LAC (US) 2023-09-14 US disclosed
CN-115038451-A Multimodal compositions and methods of treatment 阿奎斯蒂弗医疗股份有限公司 2022-09-09 CN disclosed
CN-115003279-A Prodrug compositions and methods of treatment 阿奎斯蒂弗医疗股份有限公司 2022-09-02 CN disclosed
EP-3187492-A1 PYRIMIDINONE DERIVATIVE HAVING AUTOTAXIN-INHIBITORY ACTIVITY The University of Tokyo (JP) 2017-07-05 EP disclosed
EP-2367822-B1 TRICYCLIC AZAINDOLES MERCK PATENT GMBH (DE) 2016-10-05 EP disclosed
CN-105461724-A Nitrogen-containing bridged ring compound having insect disinfestation activity, preparation and uses thereof UNIV EAST CHINA SCIENCE & TECH 2016-04-06 CN disclosed
CN-104744306-A P-chloroaniline isocyanate preparation method HUNAN LIJIE BIOCHEMICAL CO LTD 2015-07-01 CN disclosed
US-8853391-B2 Tricyclic azaindoles MERCK PATENT GMBH (DE) 2014-10-07 US disclosed
US-8796180-B2 Aminoquinazoline compounds for combating invertebrate pests BASF SE (DE) 2014-08-05 US disclosed
CN-103910650-A Preparation method for 4-chlorophenylhydrazine hydrochloride TIANJIN QIDONG CHEMICAL PLANT 2014-07-09 CN disclosed
CN-103848752-A Novel synthesis process of P-chlorophenylhydrazine hydrochloride UNIV NANJING SCIENCE & TECH 2014-06-11 CN disclosed
CN-102993056-A Preparation method of chlorhexidine compound GANSU RES INST OF CHEMICAL INDUSTRY 2013-03-27 CN disclosed
CN-102993044-A Preparation method of 4-chlorophenylhydrazine hydrochloride TIANJIN SHI TIANCHUAN HUAGONG CO LTD 2013-03-27 CN disclosed
CN-101928246-B N-[(1-aryl-3-substituted phenyl-pyrazol-4-yl) methenyl]-2-hydroxyl benzoyl hydrazine compound or pharmaceutically acceptable salts and preparation method thereof UNIV TIANJIN TECHNOLOGY 2013-02-27 CN disclosed
EP-2480537-A1 AMINOQUINAZOLINE COMPOUNDS FOR COMBATING INVERTEBRATE PESTS BASF SE (DE) 2012-08-01 EP disclosed
US-20120178622-A1 Aminoquinazoline Compounds for Combating Invertebrate Pests BASF SE (DE) 2012-07-12 US disclosed
US-20120022060-A1 Tricyclic Azaindoles MERCK PATENT GMBH (DE) 2012-01-26 US disclosed
CN-101565839-B Cyanogen to cyanogen-free alkali environment-friendly galvanizing brightener WUHAN FENGFAN ELECTROPLATING TECHNOLOGY CO LTD 2011-04-06 CN disclosed
WO-2011036074-A1 AMINOQUINAZOLINE COMPOUNDS FOR COMBATING INVERTEBRATE PESTS BASF SE (DE) 2011-03-31 WO disclosed
CN-101928246-A N-[(1-aryl-3-substituted phenyl-pyrazol-4-yl) methenyl]-2-hydroxyl benzoyl hydrazine compound or pharmaceutically acceptable salts and preparation method thereof UNIV TIANJIN TECHNOLOGY 2010-12-29 CN disclosed
CN-101555609-B An environment-protective alkali galvanization composition brightener for transformation from cyanide to non-cyanide WUHAN FENGFAN ELECTROPLATING TECHNOLOGY CO LTD 2010-08-04 CN disclosed
CN-101624371-A 4-carbostyril and 4H-1,4-benzothiazine derivatives and preparation method and application thereof UNIV CHINA PHARMA 2010-01-13 CN disclosed
CN-101565839-A Cyanogen to cyanogen-free alkali environment-friendly galvanizing brightener WUHAN FENGZHENG ELECTROPLATING (CN) 2009-10-28 CN disclosed
CN-101555609-A An environment-protective composition brightener for transformation between alkali non-cyanide galvanization and alkali cyanide galvanization WUHAN FENGFAN ELECTROPLATING T (CN) 2009-10-14 CN disclosed
EP-1897881-A2 Compounds useful for the treatment of obesity, type II diabetes and CNS disorders Biovitrum AB (publ) (SE) 2008-03-12 EP disclosed
CN-101081845-A Substituted sulphone and sulphonamide compounds useful for the treatment of obesity, type II diabetes and cns disorders BIOVITRUM AB (SE) 2007-12-05 CN disclosed
CN-1907982-A New compounds useful for the treatment of obesity,type II diabetes and CNS disorders BIOVITRUM AB (SE) 2007-02-07 CN disclosed
CN-1662521-A Novel compounds useful for the treatment of obesity, type II diabetes and CNS disorders BIOVITRUM AB (SE) 2005-08-31 CN disclosed
EP-1513828-A1 NEW COMPOUNDS USEFUL FOR THE TREATMENT OF OBESITY, TYPE II DIABETES AND CNS DISORDERS Biovitrum AB (SE) 2005-03-16 EP disclosed
US-20040024210-A1 New compounds PROXIMAGEN NEUROSCIENCE PLC (GB) 2004-02-05 US disclosed
WO-2004000828-A1 NEW COMPOUNDS USEFUL FOR THE TREATMENT OF OBESITY, TYPE II DIABETES AND CNS DISORDERS BIOVITRUM AB (SE) 2003-12-31 WO disclosed
CN-1038248-C Diguanide derivatives, process of preparation thereof and disinfetants containing them OTSUKA CHEMCIAL CO LTD (JP) 1998-05-06 CN disclosed
CN-1065453-A Biguanide derivative, its manufacture method and the Herb of Common violet that contains this derivative OTSUKA CHEMICAL CO LTD (JP) 1992-10-21 CN disclosed
CN-1065453-A Biguanide derivative, its manufacture method and the Herb of Common violet that contains this derivative OTSUKA CHEMICAL CO LTD (JP) 1992-10-21 CN disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20230286922-A1 ANTIBIOTIC ADJUVANT COMPOUNDS MYD88, TLR5, TLR8 CA2 4387/4885PARP1 3913/4885MAP4K4 2094/4885
US-20040024210-A1 New compounds SULT1E1, SULT2A1, SULT1A1 CA2 1228/4885PARP1 4152/4885MAP4K4 3061/4885
US-20120022060-A1 Tricyclic Azaindoles AZI2, DCK, PPP2CA CA2 4497/4885PARP1 845/4885MAP4K4 203/4885
US-12559461-B2 Antibiotic adjuvant compounds MYD88, TLR5, TLR4 CA2 4031/4885PARP1 4393/4885MAP4K4 2938/4885
US-20120178622-A1 Aminoquinazoline Compounds for Combating Invertebrate Pests AAAS, ATL3, H1-3 CA2 3458/4885PARP1 1559/4885MAP4K4 1614/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.