Reaction Details |
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Target | Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
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Ligand | BDBM529346 |
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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 |
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) |
Type: | n/a |
Mol. Mass.: | 51567.80 |
Organism: | Homo sapiens (Human) |
Description: | Q10469 |
Residue: | 447 |
Sequence: | MRFRIYKRKVLILTLVVAACGFVLWSSNGRQRKNEALAPPLLDAEPARGAGGRGGDHPSV
AVGIRRVSNVSAASLVPAVPQPEADNLTLRYRSLVYQLNFDQTLRNVDKAGTWAPRELVL
VVQVHNRPEYLRLLLDSLRKAQGIDNVLVIFSHDFWSTEINQLIAGVNFCPVLQVFFPFS
IQLYPNEFPGSDPRDCPRDLPKNAALKLGCINAEYPDSFGHYREAKFSQTKHHWWWKLHF
VWERVKILRDYAGLILFLEEDHYLAPDFYHVFKKMWKLKQQECPECDVLSLGTYSASRSF
YGMADKVDVKTWKSTEHNMGLALTRNAYQKLIECTDTFCTYDDYNWDWTLQYLTVSCLPK
FWKVLVPQIPRIFHAGDCGMHHKKTCRPSTQSAQIESLLNNNKQYMFPETLTISEKFTVV
AISPPRKNGGWGDIRDHELCKSYRRLQ
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BDBM529346 |
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n/a |
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Name | BDBM529346 |
Synonyms: | US11198695, Example II-283 |
Type | Small organic molecule |
Emp. Form. | C24H26F6N4O5S |
Mol. Mass. | 596.542 |
SMILES | CS(=O)(=O)CC(=O)Nc1c2c(C[C@]3(CCc4cc(CCC(F)(F)F)ccc34)NC2=O)nn1CCCOC(F)(F)F |r| |
Structure |
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