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2-NBDG

2-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-D-glucose

CAS: 186689-07-6

Molecular Formula: C12H14N4O8

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2-NBDG - Names and Identifiers

Name 2-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-D-glucose
Synonyms 2-NBDG
2-NBD-Glucose
2-Deoxy-2-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]-D-glucose
2-(N-(7-NITROBENZ-2-OXA-1,3-DIAZOL-4-YL)AMINO)-2-DEOXYGLUCOSE
2-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-D-glucose
2-NBDG,2-(N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino)-2-deoxyglucose
2-NBDG [2-(N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)Amino)-2-Deoxyglucose]
CAS 186689-07-6

2-NBDG - Physico-chemical Properties

Molecular FormulaC12H14N4O8
Molar Mass342.26
Density1.750±0.06 g/cm3(Predicted)
Melting Point137 - 140°C
Boling Point740.0±70.0 °C(Predicted)
Solubility Soluble in DMSO (up to 10 mg/ml).
Appearancesolid
ColorDark yellow to orange/red
BRN7603370
pKa12.96±0.20(Predicted)
Storage ConditionInert atmosphere,Store in freezer, under -20°C
StabilityStable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 1 month.
Physical and Chemical PropertiesBioactive 2-NBDG, a fluorescent deoxyglucose derivative, is a marker for detecting glucose uptake and is also used to detect cell viability.
In vitro study It has since been demonstrated in living mammalian cells that the uptake of 2-NBDG takes place through glucose transporters (GLUTs) in a concentration-, time- and temperature-dependent manner. A short-period application of 2-NBDG produced a remarkable increase in the fluorescence intensity in COS-1 cells over-expressing GLUT2, whereas the increase was barely detectable in mock-transfected cells. In mouse insulin-secreting clonal MIN6 cells, uptake was inhibited by cytochalasin B, a specific blocker for GLUTs, and by D-glucose in a dose-dependent manner.

2-NBDG - Risk and Safety

WGK Germany3

2-NBDG - Reference

Reference
Show more
1. [IF=4.192] Jing Xu et al."Dietary Ginsenoside T19 Supplementation Regulates Glucose and Lipid Metabolism via AMPK and PI3K Pathways and Its Effect on Intestinal Microbiota."J Agr Food Chem. 2020;68(49):14452–14462

2-NBDG - Uses and synthesis methods

in vitro studies

It has since been demonstrated in living mammalian cells that the uptake of 2-NBDG takes place through glucose transporters (GLUTs) in a concentration-, time- and temperature-dependent manner. A short-period application of 2-NBDG produced a remarkable increase in the fluorescence intensity in COS-1 cells over-expressing GLUT2, whereas the increase was barely detectable in mock-transfected cells. In mouse insulin-secreting clonal MIN6 cells, uptake was inhibited by cytochalasin B, a specific blocker for GLUTs, and by D-glucose in a dose-dependent manner.

Last Update:2024-04-09 21:01:54
2-NBDG
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Product Name: (2R,3R,4S,5R)-3,4,5,6-Tetrahydroxy-2-((7-nitrobenzo[c][1,2,5]oxadiazol-4-yl)amino)hexanal Visit Supplier Webpage Request for quotation
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Product Name: 2-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-D-glucose Visit Supplier Webpage Request for quotation
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View History
2-NBDG
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Europium iodide
ART-CHEM-BB B024892
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