Hydrochloric Acid

Hydrochloric Acid

SCHEMBL5054649

CN(C)C(=N)C(C)(C)N=NC(C)(C)C(=N)N(C)C.Cl.Cl

nearest known ligand 0.48

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 5)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.48
CYP3A4 P08684 1/20 0.48
MAPT P10636 1/20 0.48
CYP2D6 P10635 1/20 0.48
HTT P42858 1/20 0.33

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 SCHEMBL10778726 1.00 ALDH1A1 (0.48) ALDH1A1CYP3A4MAPTCYP2D6HTT
SCHEMBL7999819 0.97 ALDH1A1 (0.43) ALDH1A1CYP3A4MAPTCYP2D6
Hydrochloric Acid SCHEMBL10872431 0.72 ALDH1A1 (0.42) ALDH1A1CYP3A4MAPTCYP2D6
Hydrochloric Acid SCHEMBL10872435 0.72 ALDH1A1 (0.42) ALDH1A1CYP3A4MAPTCYP2D6
SCHEMBL1106487 0.72
SCHEMBL18804388 0.67
Hydrochloric Acid SCHEMBL23478926 0.65 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6HTT
Hydrochloric Acid SCHEMBL34438 0.65 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6HTT
SCHEMBL18647232 0.65
Hydrochloric Acid SCHEMBL276014 0.65 ALDH1A1 (1.00) ALDH1A1CYP3A4MAPTCYP2D6HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1472291-B1 ORGANIC-INORGANIC NANOCOMPOSITE AND PREPARATION THEREOF LG CHEMICAL LTD (KR) 2008-09-17 EP disclosed
US-7115683-B2 Polymerizing monomers in the presence of an emulsifier and a layered silicate salt ion-exchanged with a cationic initiator and a dithiocarboxylate cationic chain transfer agent having a quaternary ammonium group LG CHEM, LTD. (KR) 2006-10-03 US disclosed
US-20040259998-A1 Adding monomers, an initiator, and an emulsifier to an ion-exchanged layered silicate salt that is prepared by adding a cationic initiator and a cationic chain transfer agent to a layered silicate compound to cause polymerization LG CHEM, LTD. (KR) 2004-12-23 US disclosed
EP-1472291-A1 ORGANIC-INORGANIC NANOCOMPOSITE AND PREPARATION THEREOF LG Chem, Ltd. (KR) 2004-11-03 EP disclosed
WO-2003066686-A1 ORGANIC-INORGANIC NANOCOMPOSITE AND PREPARATION THEREOF LG CHEM, LTD. (KR) 2003-08-14 WO disclosed
US-4644042-A USING WATER SOLUBLE FREE RADICAL POLYMERIZATION CATALYST NITTO BOSEKI CO., LTD. (JP) 1987-02-17 US disclosed
EP-0196588-A2 Process for the preparation of copolymers of N-substituted secondary monoallylamines or salts thereof NITTO BOSEKI CO., LTD. (JP) 1986-10-08 EP disclosed
EP-0173963-A2 Polymers of n-substituted secondary monoallylamines and their salts and process for producing the same NITTO BOSEKI CO., LTD. (JP) 1986-03-12 EP disclosed