ChemicalBook--->CAS DataBase List--->132489-69-1

132489-69-1

132489-69-1 Structure

132489-69-1 Structure
IdentificationBack Directory
[Name]

O-[2-ACETAMIDO-2-DEOXY-D-GLUCOPYRANOSYLI
[CAS]

132489-69-1
[Synonyms]

(Z)-Pugnac
(Z)-PUGNAc min. 99%
O-[2-ACETAMIDO-2-DEOXY-D-GLUCOPYRANOSYLI
n-acetylglucosaminono-1,5-lactoneo-(phenylcarbamoyl)oxime
acetamidodeoxy-D-glucopyranosylideneamino phenylcarbamate
O-(2-Acetamido-2-deoxy-D-glucopyranosylidenamino) N-phenylcarbamate
O-(2-Acetamido-2-deoxy-D-glucopyranosylidene)amino-Z-N-phenylcarbamate
(Z)-O-(2-Acetamido-2-deoxy-D-glucopyranosylidene)amino N-phenylcarbamate
O-(2-Acetamido-2-deoxy-D-glucopyranosylidene)amino N-phenyl carbamate ,97%
2-(AcetylaMino)-2-deoxy-N-[[(phenylaMino)carbonyl]oxy]-D-gluconiMidic Acid δ-Lactone
(1Z)-2-(Acetylamino)-2-deoxy-N-[[(phenylamino)carbonyl]oxy]-D-gluconimidic acid delta-lactone
D-Gluconimidic acid, 2-(acetylamino)-2-deoxy-N-[[(phenylamino)carbonyl]oxy]-, δ-lactone, (1Z)-
(5R,6R,7S,8R,Z)-6,7-Dihydroxy-8-(hydroxymethyl)-2,3-dioxo-N-((phenylcarbamoyl)oxy)-1,4-oxazocane-5-carbimidic acid
[EINECS(EC#)]

1533716-785-6
[Molecular Formula]

C15H19N3O7
[MDL Number]

MFCD00145022
[MOL File]

132489-69-1.mol
[Molecular Weight]

353.33
Chemical PropertiesBack Directory
[Melting point ]

172-175°C
[density ]

1.53
[storage temp. ]

-20°C
[solubility ]

Soluble in DMSO (up to 35 mg/ml)
[form ]

solid
[pka]

11.85±0.70(Predicted)
[color ]

White
[BRN ]

4274031
[Stability:]

Moisture and Temperature Sensitive
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

29329990
Hazard InformationBack Directory
[Description]

Proteins can be modified post-translationally by the addition of O-linked N-acetylglucosamine (O-GlcNAc). Nuclear cytoplasmic O-GlcNAcase and acetyltransferase (NCOAT) is a β-N-acetylglucosaminidase that removes GlcNAc from O-glycosylated proteins. PUGNAc is a (phenylcarbamoyl)oxime analog of GlcNAc that reversibly inhibits NCOAT (Ki = 40-110 nM). It also less potently inhibits other hexosaminidases and exochitinases. (Z)-PUGNAc is a stereoisomer of PUGNAc that is a more potent inhibitor of NCOAT than the (E) isomer, both in vitro and in cells.
[Chemical Properties]

White to Off-White Solid
[Uses]

O-(2-acetamido-2deoxy-D-glucopyranosylidene)amino-N-phenylcarbamate (PUGNAc) has been used to evaluate the effects of silibinin on O-GlcNAc levels of glycoproteins in Adult Retinal Pigment Epithelial-19 (ARPE-19) cells. It has also been used as a component of the HEPES lysis buffer for rat brain samples.
[Uses]

An inhibitor of O-GlcNAcase, hexosaminidase A, and hexosaminidase B
[Biological Activity]

O -GlcNAc- β - N -acetylglucosaminidase ( O -GlcNAcase) and β -hexosaminidase inhibitor (K i values are 46 and 36 nM respectively) that increases O -GlcNAc levels ~ 2-fold in HT29 cells. Z -linked isomer is more potent than the E isomer.
[Biochem/physiol Actions]

O-(2-acetamido-2deoxy-D-glucopyranosylidene)amino-N-phenylcarbamate (PUGNAc) induces insulin resistance in 3T3-L1 adipocytes by reducing insulin-prompting phosphorylation of protein kinase B (Akt) and glycogen synthase kinase 3β (GSK3β).
[storage]

Desiccate at -20°C
[References]

1) Macauley et al. (2005), O-GlcNAcase uses substrate-assisted catalysis: kinetic analysis and development of highly selective mechanism-inspired inhibitors; J. Biol. Chem., 280 25313 2) Kneass and Marchase (2005), Protein O-GlcNAc modulates motility-associated signaling intermediates in neutrophils; J. Biol. Chem., 280 14579 3) Zou et al. (2007), The protective effects of PUGNAC on cardiac function after trauma-hemorrhage are mediated via increased protein O-GlcNAc levels; Shock, 27 402 4) Arias et al. (2004), Prolonged incubation in PUGNAc results in increased protein O-Linked glycosylation and insulin resistance in rat skeletal muscle; Diabetes, 53 921
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