Hydrochloric Acid

Hydrochloric Acid

SCHEMBL18304151

COc1c(O)ccc2c1CC1c3c(cc4c(c3-2)OCO4)CCN1C.Cl

nearest known ligand 0.79

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
HTR2A known ✓ P28223 2/20 0.79
HTR2C known ✓ P28335 2/20 0.79
HTR2B known ✓ P41595 2/20 0.79
DRD2 known ✓ P14416 5/20 0.70
BCHE known ✓ P06276 2/20 0.66
ACHE known ✓ P22303 2/20 0.66
ADRA1A known ✓ P35348 3/20 0.61
ADRA1D known ✓ P25100 2/20 0.61
ADRA1B known ✓ P35368 2/20 0.61
GAA known ✓ P10253 1/20 0.61
DRD1 known ✓ P21728 2/20 0.55
ADRB1 known ✓ P08588 1/20 0.55
ADRA2A known ✓ P08913 1/20 0.55
ADRA2B known ✓ P18089 1/20 0.55
ADRA2C known ✓ P18825 1/20 0.55
DRD4 known ✓ P21917 1/20 0.55
HRH2 known ✓ P25021 1/20 0.55
HTR1D known ✓ P28221 1/20 0.55
HTR1B known ✓ P28222 1/20 0.55
SLC6A4 known ✓ P31645 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
Crebanine SCHEMBL30690403 0.89 HTR2A (1.00) HTR2AHTR2CHTR2BKDM4ELMNA
Crebanine SCHEMBL25472585 0.89 HTR2A (1.00) HTR2AHTR2CHTR2BKDM4ELMNA
SCHEMBL32690248 0.87 KDM4E (1.00) HTR2AHTR2CHTR2BKDM4ELMNA
SCHEMBL11249690 0.83 DRD2 (0.76) HTR2AHTR2CHTR2BKDM4ELMNA
Stephanine SCHEMBL27780270 0.82 DRD2 (1.00) HTR2AHTR2CHTR2BKDM4ELMNA
Stephanine SCHEMBL29543045 0.82 DRD2 (1.00) HTR2AHTR2CHTR2BKDM4ELMNA
Stephanine SCHEMBL25472587 0.82 DRD2 (1.00) HTR2AHTR2CHTR2BKDM4ELMNA
Cassythicine SCHEMBL31029807 0.81 KDM4E (0.84) HTR2AHTR2CHTR2BKDM4ELMNA
Cassythicine SCHEMBL30883018 0.81 KDM4E (0.84) HTR2AHTR2CHTR2BKDM4ELMNA
Isolaureline SCHEMBL29761843 0.79 BCHE (1.00) HTR2AHTR2CHTR2BKDM4ELMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20180098933-A1 COMPOSITION FOR TREATMENT OF HAIR LOSS AND REGROWTH STIMULATION NINA ELYA LTD. (IL) 2018-04-12 US disclosed
WO-2016199147-A1 A COMPOSITION FOR TREATMENT OF HAIR LOSS AND REGROWTH STIMULATION NINA ELYA LTD. (IL) 2016-12-15 WO disclosed