Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8089171

Cc1ccccc1CN1CCc2sccc2C1.Cl

nearest known ligand 0.97

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
▸ DRD1 known ✓ P21728 2/20 0.69
▸ DRD4 known ✓ P21917 2/20 0.69
▸ DRD3 known ✓ P35462 2/20 0.69
▸ ADRA2A known ✓ P08913 1/20 0.69
▸ ADRB3 known ✓ P13945 1/20 0.69
▸ ADRA2B known ✓ P18089 1/20 0.69
▸ ADRA2C known ✓ P18825 1/20 0.69
▸ HRH2 known ✓ P25021 1/20 0.69
▸ ADRA1A known ✓ P35348 1/20 0.69
▸ OPRM1 known ✓ P35372 1/20 0.69
▸ OPRK1 known ✓ P41145 1/20 0.69
▸ HTR2B known ✓ P41595 1/20 0.69
▸ KCNH2 known ✓ Q12809 1/20 0.69
▸ SIGMAR1 known ✓ Q99720 1/20 0.69
▸ ACHE known ✓ P22303 1/20 0.46
▸ DRD2 known ✓ P14416 1/20 0.41
▸ CYP2C19 P33261 2/20 0.97
▸ MAPK1 P28482 3/20 0.71
▸ KDM4E B2RXH2 2/20 0.71
▸ TSHR P16473 1/20 0.71

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
SCHEMBL10623569 0.99 CYP2C19 (1.00) CYP2C19MAPK1KDM4ETSHRRECQL
SCHEMBL11544083 0.85 CYP2C19 (0.76) CYP2C19MAPK1KDM4ETSHRRECQL
Ticlopidine SCHEMBL33596 0.83 KDM4E (1.00) CYP2C19MAPK1KDM4ETSHRRECQL
Ticlopidine SCHEMBL29580621 0.83 KDM4E (1.00) CYP2C19MAPK1KDM4ETSHRRECQL
SCHEMBL11548022 0.83 ALDH1A1 (0.72) CYP2C19MAPK1KDM4ETSHRRECQL
SCHEMBL9570465 0.82 ALDH1A1 (0.71) CYP2C19MAPK1KDM4ETSHRRECQL
Ticlopidine SCHEMBL29379997 0.82 ALDH1A1 (1.00) CYP2C19MAPK1KDM4ETSHRRECQL
Ticlopidine SCHEMBL4204 0.82 ALDH1A1 (1.00) CYP2C19MAPK1KDM4ETSHRRECQL
SCHEMBL10625312 0.82 ALDH1A1 (0.71) CYP2C19MAPK1KDM4ETSHRRECQL
SCHEMBL10625318 0.81 CYP2C19 (0.70) CYP2C19MAPK1KDM4ETSHRRECQL

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6043368-A Method of making thieno-pyridine derivatives POLI INDUSTRIA CHIMICA, S.P.A. (IT) 2000-03-28 — — US disclosed
EP-0829482-A2 Method of making thieno-pyridine derivatives Poli Industria Chimica S.p.A. (IT) 1998-03-18 — — EP disclosed
US-4051141-A ANTIINFLAMMATORY, VASODILATOR, ANTICOAGULANTS CENTRE D'ETUDES POUR L'INDUSTRIE PHARMACEUTIQUE (FR) 1977-09-27 — — US disclosed
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