| Reaction Details |
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 | Report a problem with these data |
| Target | Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
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| Ligand | BDBM529357 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | Inhibitory Activity |
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| IC50 | <1.000±n/a nM |
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| Citation |  Nodu, K; Tateno, Y; Masuda, K; Nishiura, Y; Sasaki, Y Fused ring derivative having MGAT-2 inhibitory activity US Patent US11198695 Publication Date 12/14/2021 |
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| More Info.: | Get all data from this article, Assay Method |
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| Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
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| Name: | Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
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| Synonyms: | 2.4.1.143 | Beta-1,2-N-acetylglucosaminyltransferase II | GNT-II | GlcNAc-T II | MGAT2 | MGAT2_HUMAN | Mannoside acetylglucosaminyltransferase 2 | Monoacylglycerol acyltransferase 2 (MGAT2) | Monoacylglycerol acyltransferase type 2 (h-MGAT2) | N-glycosyl-oligosaccharide-glycoprotein N-acetylglucosaminyltransferase II | h-MGAT2 (human monoacylglycerol acyltransferase type 2) |
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| Type: | n/a |
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| Mol. Mass.: | 51567.80 |
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| Organism: | Homo sapiens (Human) |
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| Description: | Q10469 |
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| Residue: | 447 |
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| Sequence: | MRFRIYKRKVLILTLVVAACGFVLWSSNGRQRKNEALAPPLLDAEPARGAGGRGGDHPSV
AVGIRRVSNVSAASLVPAVPQPEADNLTLRYRSLVYQLNFDQTLRNVDKAGTWAPRELVL
VVQVHNRPEYLRLLLDSLRKAQGIDNVLVIFSHDFWSTEINQLIAGVNFCPVLQVFFPFS
IQLYPNEFPGSDPRDCPRDLPKNAALKLGCINAEYPDSFGHYREAKFSQTKHHWWWKLHF
VWERVKILRDYAGLILFLEEDHYLAPDFYHVFKKMWKLKQQECPECDVLSLGTYSASRSF
YGMADKVDVKTWKSTEHNMGLALTRNAYQKLIECTDTFCTYDDYNWDWTLQYLTVSCLPK
FWKVLVPQIPRIFHAGDCGMHHKKTCRPSTQSAQIESLLNNNKQYMFPETLTISEKFTVV
AISPPRKNGGWGDIRDHELCKSYRRLQ
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| BDBM529357 |
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| n/a |
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| Name | BDBM529357 |
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| Synonyms: | US11198695, Example II-295 |
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| Type | Small organic molecule |
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| Emp. Form. | C24H21F4N5O6S |
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| Mol. Mass. | 583.512 |
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| SMILES | CS(=O)(=O)CC(=O)Nc1c2c(C[C@]3(CCOc4cc(OCC(F)(F)F)ccc34)NC2=O)nn1-c1ccc(F)cn1 |r| |
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| Structure | 
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