Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8481908

Cl.Cl.N=C(N)Nc1nc(CSCCN)cs1

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 20)

geneUniProtsupporting neighboursconfidence
HRH2 known ✓ P25021 3/20 0.34
CA2 known ✓ P00918 2/20 0.34
MAOA known ✓ P21397 2/20 0.34
MAOB known ✓ P27338 3/20 0.34
KCNH2 known ✓ Q12809 1/20 0.32
GAA known ✓ P10253 1/20 0.31
AOC3 Q16853 12/20 0.38
KMT2A Q03164 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
SLC22A2 O15244 2/20 0.34
CA12 O43570 2/20 0.34
SLC22A3 O75751 2/20 0.34
CA1 P00915 2/20 0.34
LMNA P02545 2/20 0.34
TSHR P16473 2/20 0.34
CA4 P22748 2/20 0.34
CA6 P23280 2/20 0.34
CA5A P35218 2/20 0.34
CA7 P43166 2/20 0.34
BLM P54132 2/20 0.34

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 SCHEMBL10934527 1.00 AOC3 (0.38) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
SCHEMBL8487525 0.99 AOC3 (0.39) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
Hydrochloric Acid SCHEMBL11259470 0.92 AOC3 (0.36) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
SCHEMBL11002732 0.90 AOC3 (0.37) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
Hydrochloric Acid SCHEMBL10439042 0.88 HRH2 (0.39) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
Hydrochloric Acid SCHEMBL11236238 0.88 HRH2 (0.39) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
SCHEMBL8411573 0.86 KMT2A (0.35) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
SCHEMBL10587291 0.86 HRH2 (0.39) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
Hydrochloric Acid SCHEMBL10586317 0.85 HRH2 (0.37) AOC3KMT2ASMN1; SMN2HRH2SLC22A2
Hydrochloric Acid SCHEMBL10390042 0.84 HRH2 (0.38) AOC3KMT2ASMN1; SMN2HRH2SLC22A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6005115-A HISTAMINE H.SUB.2-RECEPTOR ANTAGONIST, USEFUL IN THERAPY AS AN ACID SECRETION INHIBITOR FERRER INTERNACIONAL, S.A. (ES) 1999-12-21 US claimed
EP-0738721-A1 FORMS A AND B OF N-[[[2-[[[2-[(DIAMINOMETHYLEN)AMINO]-4-THIAZOLYL]METHYL]THIO]ETHYL]AMINO]METHYLEN]-4-BROMOBENZENOSULPHONAMIDE FERRER INTERNACIONAL, S.A. (ES) 1996-10-23 EP claimed
US-6005115-A HISTAMINE H.SUB.2-RECEPTOR ANTAGONIST, USEFUL IN THERAPY AS AN ACID SECRETION INHIBITOR FERRER INTERNACIONAL, S.A. (ES) 1999-12-21 US disclosed
EP-0738721-A1 FORMS A AND B OF N-[[[2-[[[2-[(DIAMINOMETHYLEN)AMINO]-4-THIAZOLYL]METHYL]THIO]ETHYL]AMINO]METHYLEN]-4-BROMOBENZENOSULPHONAMIDE FERRER INTERNACIONAL, S.A. (ES) 1996-10-23 EP disclosed
US-5120746-A Inhibit gastric acid secretion TOYAMA CHEMICAL CO., LTD. (JP) 1992-06-09 US disclosed
US-4923882-A Novel amine derivatives, salts thereof and an anti-ulcer agent containing the same TOYAMA CHEMICAL CO., LTD. (JP) 1990-05-08 US disclosed
EP-0159012-B1 SULFONAMIDINES, A PROCESS FOR PREPARING THEM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM FERRER INTERNACIONAL, S.A. (ES) 1989-02-01 EP disclosed
US-4742055-A ANTISECRETORY, ANTIULCER RORER PHARMACEUTICAL CORPORATION (US) 1988-05-03 US disclosed
US-4728655-A ANTIULCER, H2-ANTAGONISTS FERRER INTERNACIONAL S.A. (ES) 1988-03-01 US disclosed
US-4649145-A ANTISECRETORY, ANTIULCER, HISTAMINE H-2 ANTAGONIST HOECHST UK LIMITED (GB) 1987-03-10 US disclosed
US-4643849-A ANTIULCER, ANTISECRETORY AGENTS TOYAMA CHEMICAL CO., LTD. (JP) 1987-02-17 US disclosed
US-4359466-A Guanidine compounds SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1982-11-16 US disclosed
US-4347370-A HISTAMINE H-2 ANTAGONISTS, INHIBIT GASTRIC ACID SECRETION IMPERIAL CHEMICAL INDUSTRIES LTD. (GB) 1982-08-31 US disclosed
US-4309435-A HISTAMINE ANTAGONISTS IMPERIAL CHEMICAL INDUSTRIES LTD. (GB) 1982-01-05 US disclosed
EP-0039989-A1 Pyrimidone derivatives, processes for their preparation and pharmaceutical compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1981-11-18 EP disclosed
EP-0028117-A1 Guanidine compounds, process for preparing them and compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1981-05-06 EP disclosed
US-4262126-A INHIBIT SECRETION OF GASTRIC JUICE IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1981-04-14 US disclosed
EP-0015138-A1 Pyrimidone derivatives, processes for their preparation and pharmaceutical compositions containing them SMITH KLINE & FRENCH LABORATORIES LIMITED (GB) 1980-09-03 EP disclosed
EP-0010418-A1 Antisecretory guanidine derivatives, processes for their manufacture and pharmaceutical compositions containing them IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1980-04-30 EP disclosed
US-4165378-A ANTISECRETORY, ANTIHISTAMINE ICI AMERICAS INC. (US) 1979-08-21 US disclosed