Hydrochloric Acid

Hydrochloric Acid

SCHEMBL8984092

Cl.Nc1c2c(nc3ccccc13)CCCC2=O

nearest known ligand 0.80

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 8/20 0.63
BCHE known ✓ P06276 6/20 0.63
GLA known ✓ P06280 3/20 0.58
GAA known ✓ P10253 2/20 0.58
KCNH2 known ✓ Q12809 3/20 0.56
CHRM2 known ✓ P08172 2/20 0.56
ADRA2A known ✓ P08913 2/20 0.56
CHRM1 known ✓ P11229 2/20 0.56
SLC6A2 known ✓ P23975 2/20 0.56
OPRM1 known ✓ P35372 2/20 0.56
CACNB4 known ✓ O00305 1/20 0.56
CACNA1A known ✓ O00555 1/20 0.56
CACNA1G known ✓ O43497 1/20 0.56
CACNG3 known ✓ O60359 1/20 0.56
CACNA1F known ✓ O60840 1/20 0.56
CACNA1H known ✓ O95180 1/20 0.56
CACNB3 known ✓ P54284 1/20 0.56
CACNA2D1 known ✓ P54289 1/20 0.56
CACNG7 known ✓ P62955 1/20 0.56
CACNA1B known ✓ Q00975 1/20 0.56

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
SCHEMBL4495989 0.98 KDM4E (0.82) KDM4EACHEBCHEHSD17B10ALDH1A1
SCHEMBL9875563 0.89 KDM4E (0.68) KDM4EACHEBCHEHSD17B10ALDH1A1
SCHEMBL9874322 0.81 ACHE (0.60) KDM4EACHEBCHEHSD17B10ALDH1A1
SCHEMBL9685408 0.79 ACHE (0.61) KDM4EACHEBCHEHSD17B10ALDH1A1
SCHEMBL8791193 0.79 KDM4E (0.57) KDM4EACHEBCHEHSD17B10ALDH1A1
SCHEMBL10847043 0.78 ACHE (0.62) KDM4EACHEBCHEGRIN1GRIN2A
SCHEMBL9873371 0.78 ACHE (0.68) KDM4EACHEBCHECHRM1GRIN1
SCHEMBL9876043 0.78 ACHE (0.63) KDM4EACHEBCHECHRM1GRIN1
SCHEMBL9874848 0.78 ACHE (0.64) KDM4EACHEBCHEHSD17B10ALDH1A1
SCHEMBL10848027 0.78 ACHE (0.66) KDM4EACHEBCHEALDH1A1APP

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-0449172-B1 A method of reducing a carbonyl containing acridine HOECHST ROUSSEL PHARMA (US) 1996-06-05 EP disclosed
EP-0449172-A1 A method of reducing a carbonyl containing acridine HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1991-10-02 EP disclosed
US-5053513-A Catalytic hydrogenation using noble metal catalyst, lithium hydroxide, solvent HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1991-10-01 US disclosed