720127
D-Glucose-1,2,3-13C3
99 atom % 13C, 99% (CP)
Synonym(s):
Labeled Glucose
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About This Item
Empirical Formula (Hill Notation):
13C3C3H12O6
Molecular Weight:
183.13
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
Note: This product can be packaged on demand. For information on pricing, availability and packaging of custom sizes, please contact Stable Isotopes Customer Service
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isotopic purity
99 atom % 13C
Assay
99% (CP)
form
powder
mp
150-152 °C (lit.)
mass shift
M+3
SMILES string
OC[C@H]1O[13CH](O)[13C@H](O)[13C@@H](O)[C@@H]1O
InChI
1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1/i4+1,5+1,6+1
InChI key
WQZGKKKJIJFFOK-VJPMIEPHSA-N
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Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Dongqing Yan et al.
Blood cancer discovery, 2(3), 266-287 (2021-05-25)
We discovered that the survival and growth of many primary acute myeloid leukemia (AML) samples and cell lines, but not normal CD34+ cells, are dependent on SIRT5, a lysine deacylase implicated in regulating multiple metabolic pathways. Dependence on SIRT5 is
Travis Nemkov et al.
JCI insight, 6(3) (2020-12-23)
Computational models based on recent maps of the RBC proteome suggest that mature erythrocytes may harbor targets for common drugs. This prediction is relevant to RBC storage in the blood bank, in which the impact of small molecule drugs or
Kaiqi Sun et al.
Scientific reports, 7(1), 15281-15281 (2017-11-12)
Elevated sphingosine 1-phosphate (S1P) is detrimental in Sickle Cell Disease (SCD), but the mechanistic basis remains obscure. Here, we report that increased erythrocyte S1P binds to deoxygenated sickle Hb (deoxyHbS), facilitates deoxyHbS anchoring to the membrane, induces release of membrane-bound
Daniel Hernandez-Saavedra et al.
Scientific reports, 10(1), 413-413 (2020-01-17)
Altered metabolism in pulmonary artery smooth muscle cells (PASMCs) and endothelial cells (PAECs) contributes to the pathology of pulmonary hypertension (PH), but changes in substrate uptake and how substrates are utilized have not been fully characterized. We hypothesized stable isotope
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