Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9250962

COc1ccc(CCN2CCC(C(=O)c3ccc(NS(C)(=O)=O)cc3)CC2)cc1.Cl

nearest known ligand 0.62

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 2/20 0.62
HTR2A known ✓ P28223 3/20 0.55
HTR2C known ✓ P28335 3/20 0.55
HTR7 known ✓ P34969 3/20 0.55
HTR6 known ✓ P50406 2/20 0.55
GAA known ✓ P10253 1/20 0.50
HRH2 known ✓ P25021 1/20 0.49
HRH1 known ✓ P35367 1/20 0.49
HTR1A known ✓ P08908 1/20 0.49
HTR1D known ✓ P28221 1/20 0.49
HTR2B known ✓ P41595 1/20 0.49
GLA known ✓ P06280 1/20 0.48
POLB P06746 3/20 0.62
KDM4E B2RXH2 1/20 0.62
CYP2C19 P33261 2/20 0.60
CYP3A4 P08684 1/20 0.60
CYP2D6 P10635 1/20 0.60
LMNA P02545 1/20 0.55
TSHR P16473 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55

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
SCHEMBL9175462 0.99 KCNH2 (0.61) POLBKCNH2KDM4ECYP2C19CYP3A4
Hydrochloric Acid SCHEMBL9448751 0.88 KCNH2 (0.64) POLBKCNH2KDM4ECYP2C19CYP3A4
Hydrochloric Acid SCHEMBL9172595 0.88 KCNH2 (0.69) POLBKCNH2KDM4ECYP2C19CYP3A4
SCHEMBL9444458 0.88 KCNH2 (0.67) POLBKCNH2KDM4ECYP2C19CYP3A4
SCHEMBL9444435 0.88 KCNH2 (0.64) POLBKCNH2KDM4ECYP2C19CYP3A4
Hydrochloric Acid SCHEMBL9444430 0.87 KCNH2 (0.59) POLBKCNH2KDM4ECYP2C19CYP3A4
SCHEMBL9174047 0.87 HTR2A (0.74) POLBKCNH2KDM4ECYP2C19CYP3A4
SCHEMBL9444393 0.87 KCNH2 (0.63) POLBKCNH2KDM4ECYP2C19CYP3A4
SCHEMBL9172253 0.86 HTR2A (0.70) POLBKCNH2KDM4ECYP2C19CYP3A4
SCHEMBL9444495 0.86 KCNH2 (0.58) POLBKCNH2KDM4ECYP2C19CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0320983-B1 Piperidinyl compounds MERRELL DOW PHARMA (US) 1995-06-28 EP disclosed
US-5286866-A Piperidinyl compounds MERRELL DOW PHARMACEUTICALS INC. (US) 1994-02-15 US disclosed
US-5166211-A Method of using 1,4-disubstituted piperidinyl compounds in the treatment of coronary vasospasons and variant angina MERRELL DOW PHARMACEUTICALS INC. (US) 1992-11-24 US disclosed
US-5093341-A N-ARALKYL PIPERIDINE DERIVATIVES USEFUL AS ANTITHROMBOLYTIC AGENTS MERRELL DOW PHARMACEUTICALS INC. (US) 1992-03-03 US disclosed