Hydrochloric Acid

Hydrochloric Acid

SCHEMBL3672319

Cl.Cl.Nc1ccc(N)cc1.Nc1ccc(N)cc1

nearest known ligand 0.89

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
ACHE known ✓ P22303 1/20 0.57
MAOA known ✓ P21397 1/20 0.47
MAOB known ✓ P27338 1/20 0.47
MEN1 O00255 2/20 0.89
MAPT P10636 2/20 0.89
KMT2A Q03164 2/20 0.89
CYP3A4 P08684 8/20 0.67
TDP1 Q9NUW8 8/20 0.67
ALDH1A1 P00352 7/20 0.67
TP53 P04637 2/20 0.67
MAPK1 P28482 4/20 0.57
ALOX15 P16050 3/20 0.57
HSD17B10 Q99714 2/20 0.57
CA3 P07451 1/20 0.57
THRB P10828 1/20 0.57
CA6 P23280 1/20 0.57
CASP1 P29466 1/20 0.57
HIF1A Q16665 1/20 0.57
CA14 Q9ULX7 1/20 0.57
TSHR P16473 4/20 0.54

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 SCHEMBL378591 1.00 MEN1 (0.89) MEN1MAPTKMT2ACYP3A4TDP1
Hydrochloric Acid SCHEMBL135990 1.00
Hydrochloric Acid SCHEMBL4949584 1.00 MEN1 (0.89) MEN1MAPTKMT2ACYP3A4TDP1
Hydrochloric Acid SCHEMBL28945243 0.95 MEN1 (0.80) MEN1MAPTKMT2ACYP3A4TDP1
Hydrochloric Acid SCHEMBL21523285 0.95 MEN1 (0.80) MEN1MAPTKMT2ACYP3A4TDP1
Hydrochloric Acid SCHEMBL10638088 0.95 MEN1 (0.80) MEN1MAPTKMT2ACYP3A4TDP1
Hydrochloric Acid SCHEMBL7371349 0.95 MEN1 (0.80) MEN1MAPTKMT2ACYP3A4TDP1
SCHEMBL27981 0.94
SCHEMBL320609 0.94 MEN1 (1.00) MEN1MAPTKMT2ACYP3A4TDP1
Methylamine SCHEMBL27939730 0.91 MAPT (0.73) MEN1MAPTKMT2ACYP3A4TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122011311-A Preparation method of metal nanocluster confined covalent organic framework composite material 西北工业大学 2026-05-12 CN disclosed
CN-119060606-A Radiation-resistant color development paint and preparation method and application thereof 海洋化工研究院有限公司 2024-12-03 CN disclosed
CN-118978653-A Metal nanoparticle domain-limited porous organic framework composite material and preparation method thereof 西北工业大学 2024-11-19 CN disclosed
CN-103703056-B Aramid copolymers 纳幕尔杜邦公司 2016-10-12 CN disclosed
WO-2010121714-A1 COMPLEXES BETWEEN PHOSPHOLIPIDS AND PROTEIN VIMENTIN, AND IN VITRO METHODS FOR THE DETECTION OF ANTIBODIES AGAINST THESE COMPLEXES DIAMETRA S.R.L. (IT) 2010-10-28 WO disclosed
EP-1766008-A1 PHAGE SCREENING ASSAY Moredun Research Institute (GB) 2007-03-28 EP disclosed
WO-2006005943-A1 PHAGE SCREENING ASSAY MOREDUN RESEARCH INSTITUTE (GB) 2006-01-19 WO disclosed
US-6537546-B2 Process for macromolecularizing phenolic compounds etc. and use thereof SDS BIOTECH K.K. (JP) 2003-03-25 US disclosed
US-20010007762-A1 Process for macromolecularizing phenolic compounds etc. and use thereof ECHIGO TAKASHI (JP) 2001-07-12 US disclosed
US-6190891-B1 Process for producing high-molecular-weight phenolic compounds with myrothecium SHOWA DENKO K.K. (JP) 2001-02-20 US disclosed
EP-0919628-A1 PROCESS FOR PRODUCING HIGH-MOLECULAR-WEIGHT COMPOUNDS OF PHENOLIC COMPOUNDS, ETC. AND USE THEREOF SHOWA DENKO KABUSHIKI KAISHA (JP) 1999-06-02 EP disclosed