Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9438773

CN1CCN(C(c2ccc(Cl)cc2)c2ccccc2Br)CC1.Cl.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
▸ CHRM2 known ✓ P08172 3/20 0.67
▸ ADRA2A known ✓ P08913 3/20 0.67
▸ CHRM1 known ✓ P11229 3/20 0.67
▸ DRD1 known ✓ P21728 3/20 0.67
▸ DRD3 known ✓ P35462 3/20 0.67
▸ SLC6A3 known ✓ Q01959 3/20 0.67
▸ KCNH2 known ✓ Q12809 3/20 0.67
▸ HTR1A known ✓ P08908 2/20 0.67
▸ SLC6A2 known ✓ P23975 2/20 0.67
▸ SLC6A4 known ✓ P31645 2/20 0.67
▸ ADRA1A known ✓ P35348 2/20 0.67
▸ HRH3 known ✓ Q9Y5N1 1/20 0.67
▸ OPRM1 known ✓ P35372 3/20 0.60
▸ CHRM4 known ✓ P08173 1/20 0.51
▸ CHRM5 known ✓ P08912 1/20 0.51
▸ CHRM3 known ✓ P20309 1/20 0.51
▸ ADRA1D known ✓ P25100 1/20 0.51
▸ HTR2A known ✓ P28223 1/20 0.51
▸ HTR2C known ✓ P28335 1/20 0.51
▸ HRH1 known ✓ P35367 1/20 0.51

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
SCHEMBL9439159 0.99 CHRM2 (0.68) CYP2D6TSHRCYP2C19TDP1CHRM2
Chlorcyclizine SCHEMBL321657 0.82 CYP2D6 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2
Chlorcyclizine SCHEMBL13724147 0.81 KCNH2 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2
Chlorcyclizine SCHEMBL4383 0.81 KCNH2 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2
Chlorcyclizine SCHEMBL16769331 0.81 KCNH2 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2
Chlorcyclizine SCHEMBL12157065 0.81 KCNH2 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2
SCHEMBL2056217 0.80 CHRM2 (0.86) CYP2D6TSHRCYP2C19TDP1CHRM2
SCHEMBL10673353 0.77 CHRM2 (0.66) CYP2D6TSHRCYP2C19TDP1CHRM2
Homochlorcyclizine SCHEMBL1977999 0.77 SMN1; SMN2 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2
Homochlorcyclizine SCHEMBL122573 0.77 SMN1; SMN2 (1.00) CYP2D6TSHRCYP2C19TDP1CHRM2

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
US-5364843-A Chlorophenyl methoxybenzyl-4-allylpiperazine dihydrochloride BURROUGHS WELLCOME CO. (US) 1994-11-15 — — US claimed
US-5124330-A (E)-ethyl 3-(4-chloro-α-(4-methyl-1-piperazinyl)benzyl)cinnamate used for potentiating the effects of antitumor agents and combating multiple drug resistance BURROUGHS WELLCOME COMPANY (US) 1992-06-23 — — US claimed
US-5364843-A Chlorophenyl methoxybenzyl-4-allylpiperazine dihydrochloride BURROUGHS WELLCOME CO. (US) 1994-11-15 — — US disclosed
EP-0409406-B1 ARYL-SUBSTITUTED AMINE DERIVATIVES USEFUL IN CANCER THERAPY THE WELLCOME FOUNDATION LIMITED (GB) 1993-09-08 — — EP disclosed
US-5124330-A (E)-ethyl 3-(4-chloro-α-(4-methyl-1-piperazinyl)benzyl)cinnamate used for potentiating the effects of antitumor agents and combating multiple drug resistance BURROUGHS WELLCOME COMPANY (US) 1992-06-23 — — US disclosed
EP-0487502-A2 Pharmaceutically active aryl-substituted amine derivatives THE WELLCOME FOUNDATION LIMITED (GB) 1992-05-27 — — EP disclosed
EP-0409406-A2 Aryl-substituted amine derivatives useful in cancer therapy THE WELLCOME FOUNDATION LIMITED (GB) 1991-01-23 — — EP disclosed
WO-1990015599-A1 MEDICAMENTS USEFUL IN CANCER THERAPY AND HAVING ANTIHISTAMINIC PROPERTIES THE WELLCOME FOUNDATION LIMITED (GB) 1990-12-27 — — WO disclosed
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