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TargetBeta-galactosidase
LigandBDBM50118923
Substrate/Competitorn/a
Meas. Tech.ChEBML_305098
IC50 18000000000±n/a nM
Citation Ogawa, SFunayama, SOkazaki, KIshizuka, FSakata, YDoi, F Synthesis of 5a-carba-hexopyranoses and hexopyranosylamines, as well as 5a,5a'-dicarbadisaccharides, from 3,8-dioxatricyclo[4.2.1.0(2,4)]nonan-9-ol: glycosidase inhibitory activity of N-substituted 5a-carba-beta-gluco- and beta-galactopyranosylamines, and derivatives thereof. Bioorg Med Chem Lett14:5183-8 (2004) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Beta-galactosidase
Name:Beta-galactosidase
Synonyms:β-galactosidase | BGAL_BOVIN | Beta-galactosidase/Glucosylceramidase | GLB1
Type:Protein
Mol. Mass.:73420.88
Organism:Bos taurus (Bovine)
Description:n/a
Residue:653
Sequence:
MPGVVRLLALLLVPLLLGSARGLHNATQRTFQIDYRRNRFLKDGQPFRYISGSIHYFRVP
RFYWKDRLLKMKMAGLNAIQTYVAWNFHELQPGRYNFSGDHDVEHFIQLAHELGLLVILR
PGPYICAEWDMGGLPAWLLEKKSIVLRSSDPDYLAAVDKWLGVLLPKMRPLLYKNGGPII
TVQVENEYGSYLSCDYDYLRFLQKRFHDHLGEDVLLFTTDGVNERLLQCGALQGLYATVD
FSPGTNLTAAFMLQRKFEPTGPLVNSEFYTGWLDHWGQRHSTVSSKAVAFTLHDMLALGA
NVNMYMFIGGTNFAYWNGANIPYQPQPTSYDYDAPLSEAGDLTEKYFALRDIIQKFAKVP
EGPIPPSTPKFAYGKVALNKLKTVEDALNILCPSGPIKSVYPLTFIDVKQYFGFVLYRTM
LPEDCSDPTPLSSPLSGVHDRAYVSVNGVAQGILERESVITLNITGKAGATLDLLVENMG
RVNYGSSINDFKGLVSNLTLGSKILTNWEIFPLDMEDAVRSHLGTWGGRDRGYHNKARAH
SPPTYALPTFYVGNFTIPSGIADLPQDTFIQFPGWTKGQVWINGFNLGRYWPVRGPQMTL
FVPQHILVTSTPNTIVVLELEHAPCQDGGPELCTVEFVDKPVFRTVQTHRHAN
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50118923
n/a
NameBDBM50118923
Synonyms:(1S,2S,3R)-4-Methyl-6-octylamino-cyclohexane-1,2,3-triol | 4-Methyl-6-octylamino-cyclohexane-1,2,3-triol | CHEMBL314757
TypeSmall organic molecule
Emp. Form.C15H31NO3
Mol. Mass.273.4115
SMILESCCCCCCCCNC1CC(C)C(O)C(O)C1O
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: