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Target
Beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase
Ligand
BDBM50090510
Substrate
n/a
Meas. Tech.
ChEMBL_1498284 (CHEMBL3583805)
IC50
>30000±n/a nM
Citation
 Sato, K; Takahagi, H; Yoshikawa, T; Morimoto, S; Takai, T; Hidaka, K; Kamaura, M; Kubo, O; Adachi, R; Ishii, T; Maki, T; Mochida, T; Takekawa, S; Nakakariya, M; Amano, N; Kitazaki, T Discovery of a Novel Series of N-Phenylindoline-5-sulfonamide Derivatives as Potent, Selective, and Orally Bioavailable Acyl CoA:Monoacylglycerol Acyltransferase-2 Inhibitors. J Med Chem 58:3892-909 (2015) [PubMed]  Article 
Target
Name:
Beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase
Synonyms:
GGNT3 | GNT-III | GlcNAc-T III | MGAT3 | MGAT3_HUMAN | N-acetylglucosaminyltransferase III | N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase III
Type:
PROTEIN
Mol. Mass.:
61324.81
Organism:
Homo sapiens (Human)
Description:
ChEMBL_107586
Residue:
533
Sequence:
MKMRRYKLFLMFCMAGLCLISFLHFFKTLSYVTFPRELASLSPNLVSSFFWNNAPVTPQASPEPGGPDLLRTPLYSHSPLLQPLPPSKAAEELHRVDLVLPEDTTEYFVRTKAGGVCFKPGTKMLERPPPGRPEEKPEGANGSSARRPPRYLLSARERTGGRGARRKWVECVCLPGWHGPSCGVPTVVQYSNLPTKERLVPREVPRRVINAINVNHEFDLLDVRFHELGDVVDAFVVCESNFTAYGEPRPLKFREMLTNGTFEYIRHKVLYVFLDHFPPGGRQDGWIADDYLRTFLTQDGVSRLRNLRPDDVFIIDDADEIPARDGVLFLKLYDGWTEPFAFHMRKSLYGFFWKQPGTLEVVSGCTVDMLQAVYGLDGIRLRRRQYYTMPNFRQYENRTGHILVQWSLGSPLHFAGWHCSWCFTPEGIYFKLVSAQNGDFPRWGDYEDKRDLNYIRGLIRTGGWFDGTQQEYPPADPSEHMYAPKYLLKNYDRFHYLLDNPYQEPRSTAAGGWRHRGPEGRPPARGKLDEAEV
  
Inhibitor
Name:
BDBM50090510
Synonyms:
CHEMBL3581716
Type:
Small organic molecule
Emp. Form.:
C24H23F2N3O3S
Mol. Mass.:
471.52
SMILES:
CC(=O)Nc1cc(cc2CCN(CCc3ccccc3)c12)S(=O)(=O)Nc1ccc(F)cc1F
Structure:
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