Reaction Details |
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Target | Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase |
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Ligand | BDBM201314 |
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Substrate/Competitor | n/a |
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Meas. Tech. | MGAT LCMS Assay |
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pH | 7.4±n/a |
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IC50 | 4±n/a nM |
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Comments | extracted |
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Citation | Turdi, H; Hangeland, JJ; Lawrence, RM; Cheng, D; Ahmad, S; Meng, W; Brigance, RP; Devasthale, P; Zhao, G Aryl dihydropyridinones and piperidinone MGAT2 inhibitors US Patent US9187424 Publication Date 11/17/2015 |
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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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BDBM201314 |
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n/a |
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Name | BDBM201314 |
Synonyms: | US9187424, 144 | US9187424, 78 |
Type | Small organic molecule |
Emp. Form. | C24H18F8N2O3 |
Mol. Mass. | 534.3985 |
SMILES | FC(F)Oc1ccc(cc1)C1=C(C#N)C(=O)NC(C1)(c1ccc(OCCCC(F)(F)F)cc1)C(F)(F)F |c:11| |
Structure |
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