Hydrochloric Acid

Hydrochloric Acid

SCHEMBL9138402

C[C@H](NCCc1ccccc1)[C@H](O)c1ccccc1.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
SLC6A2 known ✓ P23975 3/20 0.69
OPRM1 known ✓ P35372 3/20 0.69
ADRB3 known ✓ P13945 3/20 0.69
SLC6A4 known ✓ P31645 2/20 0.69
SIGMAR1 known ✓ Q99720 1/20 0.69
ADRB1 known ✓ P08588 4/20 0.67
ADRA1A known ✓ P35348 4/20 0.67
ADRB2 known ✓ P07550 3/20 0.67
OPRK1 known ✓ P41145 2/20 0.67
SLC6A3 known ✓ Q01959 2/20 0.67
ADRA1D known ✓ P25100 1/20 0.57
ADRA1B known ✓ P35368 1/20 0.57
ADRA2C known ✓ P18825 2/20 0.55
HTR2A known ✓ P28223 2/20 0.55
HTR1A known ✓ P08908 1/20 0.55
ADRA2A known ✓ P08913 1/20 0.55
ADRA2B known ✓ P18089 1/20 0.55
DRD3 known ✓ P35462 1/20 0.55
HTR2B known ✓ P41595 1/20 0.55
KCNH2 known ✓ Q12809 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
SCHEMBL5076478 0.98 LMNA (0.69) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL7381182 0.89 SIGMAR1 (0.57) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL3580767 0.88 ADRB1 (0.64) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL3580761 0.88 ADRB1 (0.64) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL3580764 0.88 ADRB1 (0.64) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL3581431 0.84 ADRB3 (0.62) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL3581425 0.84 ADRB3 (0.62) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL3581428 0.84 ADRB3 (0.62) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL5079112 0.83 HIF1A (0.62) LMNASLC6A2OPRM1HIF1AADRB3
SCHEMBL5076518 0.83 HIF1A (0.62) LMNASLC6A2OPRM1HIF1AADRB3

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
US-RE35128-E Method for the preparation of erythro vicinyl amino-alcohols DUPHAR INTERNATIONAL RESEARCH B.V. (NL) 1995-12-19 US disclosed
US-5189219-A Reacting hydroxyl-protected cyanohydrin with grignard reagent, then with primary amine, reducing, deprotecting DUPHAR INTERNATIONAL RESEARCH B.V. (NL) 1993-02-23 US disclosed
EP-0492719-A1 Method for the preparation of erythro vicinal amino-alcohols DUPHAR INTERNATIONAL RESEARCH B.V (NL) 1992-07-01 EP disclosed