UDP-GlcNAc Disodium Salt
CAS No. 91183-98-1
UDP-GlcNAc Disodium Salt( UDP-α-D-N-Acetylglucosamine Disodium Salt,Uridine 5′-diphospho-N-acetylglucosamine )
Catalog No. M22577 CAS No. 91183-98-1
UDP-GlcNAc Disodium Salt is a nucleotide sugar.?It is synthesized from glucose via the hexosamine biosynthetic pathway (HBP).OGT is a nucleocytoplasmic glycosyltransferase assigned to the GT41 family in the CAZY database.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 36 | In Stock |
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| 5MG | 58 | In Stock |
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| 10MG | 97 | In Stock |
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| 25MG | 177 | In Stock |
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| 50MG | 264 | In Stock |
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| 100MG | 393 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameUDP-GlcNAc Disodium Salt
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NoteResearch use only, not for human use.
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Brief DescriptionUDP-GlcNAc Disodium Salt is a nucleotide sugar.?It is synthesized from glucose via the hexosamine biosynthetic pathway (HBP).OGT is a nucleocytoplasmic glycosyltransferase assigned to the GT41 family in the CAZY database.
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DescriptionUDP-GlcNAc Disodium Salt is a nucleotide sugar.?It is synthesized from glucose via the hexosamine biosynthetic pathway (HBP).OGT is a nucleocytoplasmic glycosyltransferase assigned to the GT41 family in the CAZY database. Using UDP-GlcNAc Disodium Salt (UDP-GlcNAc) as the donor substrate, this enzyme modifies thousands of proteins by adding a unique N-acetylglucosamine residue onto acceptor substrates mainly confined within cytosol and nucleus.
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In Vitro——
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In Vivo——
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SynonymsUDP-α-D-N-Acetylglucosamine Disodium Salt,Uridine 5′-diphospho-N-acetylglucosamine
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number91183-98-1
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Formula Weight651.32
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Molecular FormulaC17H25N3Na2O17P2
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (383.84 mM)
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SMILES[Na+].[Na+].CC(=O)N[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1OP([O-])(=O)OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Aldosterone
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Thymidylate Kinase I...
YMU1 is a human thymidylate kinase (hTMPK) inhibitor. YMU1 stabilizes the conformation of ligand-induced degradation (LID) region of hTMPK and blocks the catalytic site or ATP-binding site.
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