Hydrochloric Acid

Hydrochloric Acid

SCHEMBL7694248

CC(C)C(=O)O.Cl.O.OC(CCCN1CCC(C(O)(c2ccccc2)c2ccccc2)CC1)c1ccccc1

nearest known ligand 0.74

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
▸ HRH1 known ✓ P35367 7/20 0.74
▸ DRD3 known ✓ P35462 3/20 0.74
▸ DRD2 known ✓ P14416 2/20 0.74
▸ KCNH2 known ✓ Q12809 5/20 0.73
▸ HTR2A known ✓ P28223 2/20 0.73
▸ HTR2B known ✓ P41595 2/20 0.73
▸ PDE4A known ✓ P27815 1/20 0.73
▸ PDE3A known ✓ Q14432 1/20 0.73
▸ CACNA1F known ✓ O60840 1/20 0.72
▸ EGFR known ✓ P00533 1/20 0.72
▸ CHRM2 known ✓ P08172 1/20 0.72
▸ HTR1A known ✓ P08908 1/20 0.72
▸ ADRA2A known ✓ P08913 1/20 0.72
▸ GAA known ✓ P10253 1/20 0.72
▸ CHRM1 known ✓ P11229 1/20 0.72
▸ ADRB3 known ✓ P13945 1/20 0.72
▸ ADRA2C known ✓ P18825 1/20 0.72
▸ DRD1 known ✓ P21728 1/20 0.72
▸ SLC6A2 known ✓ P23975 1/20 0.72
▸ HRH2 known ✓ P25021 1/20 0.72

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 SCHEMBL2985731 0.99 HRH1 (0.76) HRH1LMNADRD3DRD2ALOX15
SCHEMBL3431215 0.98 KCNH2 (0.76) HRH1LMNADRD3DRD2ALOX15
SCHEMBL18590352 0.90 KCNH2 (0.84) HRH1LMNADRD3DRD2ALOX15
SCHEMBL9076527 0.90 KCNH2 (0.84) HRH1LMNADRD3DRD2ALOX15
SCHEMBL14507814 0.90 KCNH2 (0.84) HRH1LMNADRD3DRD2ALOX15
SCHEMBL11396565 0.90 KCNH2 (0.74) HRH1LMNADRD3DRD2ALOX15
SCHEMBL6327395 0.89 KCNH2 (0.77) HRH1LMNADRD3DRD2ALOX15
SCHEMBL6452301 0.89 HRH1 (0.64) HRH1LMNADRD3DRD2ALOX15
Methane SCHEMBL14121758 0.88 KCNH2 (0.75) HRH1LMNADRD3DRD2ALOX15
SCHEMBL13516821 0.87 KCNH2 (0.83) HRH1LMNADRD3DRD2ALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-2002316978-A ANTIHISTAMINIC PIPERIDINE DERIVATIVE HAVING THE FORM IV AND METHOD FOR PRODUCING THE SAME DERIVATIVE AVENTIS PHARMACEUTICALS INC 2002-10-31 — — JP disclosed
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