| Reaction Details |
|---|
 | Report a problem with these data |
| Target | Beta-galactosidase |
|---|
| Ligand | BDBM50499768 |
|---|
| Substrate/Competitor | n/a |
|---|
| Meas. Tech. | ChEMBL_1540775 (CHEMBL3742526) |
|---|
| IC50 | 258000±n/a nM |
|---|
| Citation |  Cardullo, N; Spatafora, C; Musso, N; Barresi, V; Condorelli, D; Tringali, C Resveratrol-Related Polymethoxystilbene Glycosides: Synthesis, Antiproliferative Activity, and Glycosidase Inhibition. J Nat Prod78:2675-83 (2015) [PubMed] Article |
|---|
| More Info.: | Get all data from this article, Assay Method |
|---|
| |
| Beta-galactosidase |
|---|
| Name: | Beta-galactosidase |
|---|
| Synonyms: | 3.2.1.23 | Beta-galactosidase |
|---|
| Type: | PROTEIN |
|---|
| Mol. Mass.: | 100763.98 |
|---|
| Organism: | Aspergillus oryzae |
|---|
| Description: | ChEMBL_109122 |
|---|
| Residue: | 909 |
|---|
| Sequence: | MASLMKVYKLWVDIIAQNPANRHELTSQQRHVFSAEDPEKPLQDIVTWDEYSILVRGERI
LFFSGEFHPFRLPSPGLWLDVFQKIRALGYSGVSFYLMWGLLEGEPGHVRTEGVFALDGF
FNAASQAGIYLLARPGPYINAEVSGGGFPSWVQRIEGSVRTTDPTFLNATKNYISTIGEI
ISKVQITNGGPVILFQLENEYSICEGAPSHEELNFCLEKDYMAAIEQQFRDAEIVVPFVN
NDAVALGDWAPGTGQGAIDIYGFDNYPFGWGNGYASPENWTQITDPLTQYNFSQHQSMSP
GTPFSIIEFQGGAPDPWGGTGADVCAEMVSNIFARVFYKINYDFRITIFNLYMMLGGTNW
GNLGYSSGYTSYDVGAAIIEDRQITREKYSEIKLEAQFLQVSPAYITSKPHSPCSGCYTN
ASALMTTRLQGESTNFYIIRHSNYIVTQSTSYEWRANTSQGSITVPQPGGSSTLHGRDSK
FHVTDCDLGGINLIYPTAETFTWRRHGSKSVLVLYGGEDEIHEFAVDSNLGNATTIEGSN
VRLGKRGATFVVQWDHLDVYLLWRNEAYQYWVMDLPAPEPLDLHASPSRTNSSVIVKAGY
LLRNASISENTLHLTGDVNATSTVELISAPPGCCSDVLYDGNRLQNISNTNGRVSGVVPY
IDPKLAIPEMESLEWRYLDSLPEGEEKSLYLSTQGGYAYGHSVWLDSTYLGSWQGNPAIQ
NYNQTLQFPQSLQGDEHYVLTILIDNLGLDLNFELNTNTMKSPRGLLDYDLSGHNSWKIT
GNLGGEQYREHSRGPLNKGSTFVERQGYHLSGALNSTKAEWQTRTPQEGLSAAGVGLFAT
TFSLDYPQGYDIPTSVYVTIPTTHQSIVNNTGPQTEYPIPEGILNHHGGNHLAHHLLGSG
RKWGKAGRD
|
|
|
|---|
| BDBM50499768 |
|---|
| n/a |
|---|
| Name | BDBM50499768 |
|---|
| Synonyms: | CHEMBL3740658 |
|---|
| Type | Small organic molecule |
|---|
| Emp. Form. | C24H30O10 |
|---|
| Mol. Mass. | 478.489 |
|---|
| SMILES | COc1cc(OC)c(O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)c(\C=C\c2ccc(OC)c(OC)c2)c1 |r| |
|---|
| Structure | 
|
|---|
Search and Browse
