Hydrochloric Acid

Hydrochloric Acid

SCHEMBL29565629

Cl.OCc1ccc(O)c(CO)c1

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
ADRB2 known ✓ P07550 5/20 0.46
GABRA1 known ✓ P14867 1/20 0.45
GABRB2 known ✓ P47870 1/20 0.45
GAA known ✓ P10253 2/20 0.41
TTR known ✓ P02766 1/20 0.41
CA2 known ✓ P00918 1/20 0.41
EGFR known ✓ P00533 1/20 0.39
ADRA2A known ✓ P08913 1/20 0.39
DRD2 known ✓ P14416 1/20 0.39
DRD1 known ✓ P21728 1/20 0.39
DRD4 known ✓ P21917 1/20 0.39
SLC6A2 known ✓ P23975 1/20 0.39
DRD3 known ✓ P35462 1/20 0.39
SLC6A3 known ✓ Q01959 1/20 0.39
PKM P14618 1/20 0.53
KLF10 Q13118 1/20 0.50
KDM4E B2RXH2 3/20 0.43
CASP6 P55212 1/20 0.43
BACE1 P56817 2/20 0.42
MAPT P10636 3/20 0.41

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
SCHEMBL29942487 0.98 PKM (0.55) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL1604304 0.98 PKM (0.55) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL209075 0.86 CA1 (0.58) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL5373052 0.82 BACE1 (0.63) PKMKLF10GABRA1GABRB2KDM4E
SCHEMBL16021957 0.82 BACE1 (0.48) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL10450798 0.82 KDM4E (0.65) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL20313914 0.82 MAPT (0.55) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL8495480 0.82 TRPA1 (0.61) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL13761123 0.81 PKM (0.46) PKMKLF10ADRB2GABRA1GABRB2
SCHEMBL14242913 0.80 IGF1R (0.59) PKMKLF10ADRB2KDM4EBACE1

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
CN-118546066-A Preparation method and application of levosalbutamol hydrochloride impurity 常州亚邦制药有限公司 2024-08-27 CN disclosed
CN-114539077-B Synthesis method of levosalbutamol hydrochloride 南京恒道医药科技股份有限公司 2023-12-08 CN disclosed
CN-115109026-A Preparation method of levalbuterol intermediate and hydrochloride with high ee value 北京云鹏鹏程医药科技有限公司 2022-09-27 CN disclosed
CN-114539077-A Synthesis method of levalbuterol hydrochloride 南京恒道医药科技有限公司 2022-05-27 CN disclosed