Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9504062

COc1cc(C2Sc3ccccc3N(CCCN(C)C)C(=O)C2OC(C)=O)cc(OC)c1OC.Cl

nearest known ligand 0.69

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
KCNH2 known ✓ Q12809 3/20 0.69
CACNA1S known ✓ Q13698 8/20 0.67
ADRA1A known ✓ P35348 2/20 0.67
CACNA1F known ✓ O60840 1/20 0.67
HRH2 known ✓ P25021 1/20 0.67
SCN1A known ✓ P35498 1/20 0.67
SCN4A known ✓ P35499 1/20 0.67
SCN7A known ✓ Q01118 1/20 0.67
CACNA1D known ✓ Q01668 1/20 0.67
CACNA1C known ✓ Q13936 1/20 0.67
SCN5A known ✓ Q14524 1/20 0.67
SCN9A known ✓ Q15858 1/20 0.67
GHSR known ✓ Q92847 1/20 0.67
SCN2A known ✓ Q99250 1/20 0.67
SCN3A known ✓ Q9NY46 1/20 0.67
SCN11A known ✓ Q9UI33 1/20 0.67
SCN8A known ✓ Q9UQD0 1/20 0.67
SCN10A known ✓ Q9Y5Y9 1/20 0.67
CHRM2 known ✓ P08172 1/20 0.42
HTR1A known ✓ P08908 1/20 0.42

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
Oxalic Acid SCHEMBL10578735 0.92 CACNA1S (0.72) LMNACYP3A4KCNH2ABCB11MEN1
Hydrochloric Acid SCHEMBL9505009 0.88 CYP3A4 (0.75) LMNACYP3A4KCNH2ABCB11MEN1
Hydrochloric Acid SCHEMBL9504966 0.87 CACNA1S (0.51) LMNACYP3A4KCNH2ABCB11MEN1
Hydrochloric Acid SCHEMBL9505932 0.85 LMNA (0.74) LMNACYP3A4KCNH2ABCB11MEN1
Diltiazem SCHEMBL6531617 0.81 CYP3A4 (1.00) LMNACYP3A4KCNH2ABCB11MEN1
Diltiazem SCHEMBL2365380 0.81 CYP3A4 (1.00) LMNACYP3A4KCNH2ABCB11MEN1
Diltiazem SCHEMBL10831293 0.81 CYP3A4 (1.00) LMNACYP3A4KCNH2ABCB11MEN1
Diltiazem SCHEMBL30490635 0.81 CYP3A4 (1.00) LMNACYP3A4KCNH2ABCB11MEN1
Diltiazem SCHEMBL20394103 0.81 CYP3A4 (1.00) LMNACYP3A4KCNH2ABCB11MEN1
Diltiazem SCHEMBL15457 0.81 CYP3A4 (1.00) LMNACYP3A4KCNH2ABCB11MEN1

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
EP-0279425-B1 USE OF BENZOTHIAZEPINE DERIVATIVES, IN PARTICULAR DILTIAZEM, IN THE MANUFACTURE OF MEDICAMENTS TO PROTECT LYMPHOCYTES GÖDECKE AKTIENGESELLSCHAFT (DE) 1993-08-04 EP disclosed
US-4861770-A Use of benzothiazepine derivatives as lymphocyte protectors GOEDECKE AKTIENGESELLSCHAFT (DE) 1989-08-29 US disclosed
EP-0279425-A2 Use of benzothiazepine derivatives, in particular diltiazem, in the manufacture of medicaments to protect lymphocytes GÖDECKE AKTIENGESELLSCHAFT (DE) 1988-08-24 EP disclosed