Hydrochloric Acid

Hydrochloric Acid

SCHEMBL314296

Cc1ccccc1N1CCNCC1.Cl.Cl

nearest known ligand 0.96

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
ADRB1 known ✓ P08588 5/20 0.96
HTR7 known ✓ P34969 3/20 0.71
HTR3A known ✓ P46098 9/20 0.68
HTR1A known ✓ P08908 8/20 0.68
HTR6 known ✓ P50406 2/20 0.58
HTR3E known ✓ A5X5Y0 1/20 0.58
HTR3B known ✓ O95264 1/20 0.58
DRD2 known ✓ P14416 1/20 0.58
DRD3 known ✓ P35462 1/20 0.58
HTR3D known ✓ Q70Z44 1/20 0.58
HTR3C known ✓ Q8WXA8 1/20 0.58
SIGMAR1 known ✓ Q99720 1/20 0.58
ADRB2 known ✓ P07550 1/20 0.55
HRH2 known ✓ P25021 1/20 0.55
HTR1B known ✓ P28222 1/20 0.55
HTR2A known ✓ P28223 1/20 0.55
HTR2C known ✓ P28335 1/20 0.55
SLC6A4 known ✓ P31645 1/20 0.55
HRH1 known ✓ P35367 1/20 0.55
HTR5A known ✓ P47898 1/20 0.55

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 SCHEMBL30182987 1.00 ADRB1 (0.96) ADRB1HTR7HTR3AHTR1ACYP1A2
Hydrochloric Acid SCHEMBL615080 1.00 ADRB1 (0.96) ADRB1HTR7HTR3AHTR1ACYP1A2
Hydrochloric Acid SCHEMBL615079 1.00 ADRB1 (0.96) ADRB1HTR7HTR3AHTR1ACYP1A2
SCHEMBL2209183 0.98 ADRB1 (1.00) ADRB1HTR7HTR3AHTR1ACYP1A2
SCHEMBL4896 0.98 ADRB1 (1.00) ADRB1HTR7HTR3AHTR1ACYP1A2
SCHEMBL29432760 0.98 ADRB1 (1.00) ADRB1HTR7HTR3AHTR1ACYP1A2
Bromide SCHEMBL10672999 0.96 ADRB1 (0.96) ADRB1HTR7HTR3AHTR1ACYP1A2
Hydrochloric Acid SCHEMBL18043576 0.93 ADRB1 (0.83) ADRB1HTR7HTR3AHTR1ACYP1A2
SCHEMBL409069 0.91 ADRB1 (0.86) ADRB1HTR7HTR3AHTR1ACYP1A2
Bicarbonate SCHEMBL11622663 0.89 ADRB1 (0.83) ADRB1HTR7HTR3AHTR1ACYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105198803-A Phenyl-alkyl piperazines with TNF modulating activity SANOFI AVENTIS 2015-12-30 CN claimed
CN-102123995-A Phenyl-alkyl piperazines with TNF modulating activity SANOFI AVENTIS 2011-07-13 CN claimed
EP-0091511-A2 1-(3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl)-4-(substituted)-piperazines and -piperidines, a process for the preparation thereof, pharmaceutical compositions containing the same and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1983-10-19 EP claimed
EP-3292102-B1 ISOINDOLINONES, PROCESSES FOR THE PRODUCTION OF CHIRAL DERIVATIVES THEREOF AND USE THEREOF UNIV DEGLI STUDI DI SALERNO (IT) 2021-09-08 EP disclosed
EP-3575294-A1 5-[(PIPERAZIN-1-YL)-3-OXO-PROPYL]-IMIDAZOLIDINE-2,4-DIONE DERIVATIVES AS ADAMTS INHIBITORS FOR THE TREATMENT OF OSTEOARTHRITIS Les Laboratoires Servier (FR) 2019-12-04 EP disclosed
EP-3292102-A1 ISOINDOLINONES, PROCESSES FOR THE PRODUCTION OF CHIRAL DERIVATIVES THEREOF AND USE THEREOF Universitá Degli Studi Salerno (IT) 2018-03-14 EP disclosed
WO-2016178140-A1 ISOINDOLINONES, PROCESSES FOR THE PRODUCTION OF CHIRAL DERIVATIVES THEREOF AND USE THEREOF UNIVERSITA' DEGLI STUDI DI SALERNO (IT) 2016-11-10 WO disclosed
CN-105198803-A Phenyl-alkyl piperazines with TNF modulating activity SANOFI AVENTIS 2015-12-30 CN disclosed
CN-104080784-A Benzamide derivatives as modulators of the follicle stimulating hormone MERCK PATENT GMBH 2014-10-01 CN disclosed
CN-103328449-A Novel tetrahydroquinoline derivatives HOFFMANN LA ROCHE 2013-09-25 CN disclosed
EP-2234992-B1 PIPERAZINE DERIVATIVES AND THEIR USE AS LEPTIN RECEPTOR MODULATORS ASTRAZENECA AB (SE) 2012-02-22 EP disclosed
EP-0064704-B1 4-AMINOMETHYL-5-ACYL-1,3-DIHYDRO-2H-IMIDAZOL-2-ONES MERRELL DOW PHARMACEUTICALS INC. (US) 1986-04-16 EP disclosed
US-4559403-A FOR TREATMENT OF CEREBRAL AND CARDIAC ISCHEMIAS HOFFMANN-LA ROCHE INC. (US) 1985-12-17 US disclosed
US-4544657-A ANTISCHEMIC AGENTS HOFFMANN-LA ROCHE INC. (US) 1985-10-01 US disclosed
US-4536578-A ANTIHALLUCINOGENS, HYPOTENSIVE AGENTS HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1985-08-20 US disclosed
EP-0126480-A1 Substituted isoquinoline derivatives, method for their preparation, and pharmaceutical compositions containing these compounds F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1984-11-28 EP disclosed
US-4381393-A 4-Aminomethyl-5-acyl-1,3-dihydro-2H-imidazol-2-ones MERRELL DOW PHARMACEUTICALS INC. (US) 1983-04-26 US disclosed
EP-0064704-A1 4-Aminomethyl-5-acyl-1,3-dihydro-2H-imidazol-2-ones MERRELL DOW PHARMACEUTICALS INC. (US) 1982-11-17 EP disclosed
US-4140775-A HYPOTENSIVE AGENTS THE UPJOHN COMPANY (US) 1979-02-20 US disclosed
US-3948898-A HYPOTENSIVES, SEDATIVES, ANTIARRHYTHMICS, BRADYCARDIACS BOEHRINGER INGELHEIM GMBH (DT) 1976-04-06 US disclosed