83434-88-2
83434-88-2
Chemical Structure
D-Erythrose-2-13C
- CAS No.: 83434-88-2
- Formula:C313CH8O4
- Molecular Weight:121.10
IUPAC Name: (2R,3R)-2,3,4-trihydroxybutanal-2-13C
InChIKey: YTBSYETUWUMLBZ-XNJVPAERSA-N
SMILES: O=C[13C@H](O)[C@H](O)CO
Biological Activity: D-Erythrose-2-13C is the 13C labeled D-Erythrose[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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D-Erythrose-2-13C | D-Erythrose-2-13C is the 13C labeled D-Erythrose. | |||||||||||||||||||||
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D-Erythrose-3-13C | D-Erythrose-3-13C is the 13C labeled D-Erythrose. | |||||||||||||||||||||
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D-Erythrose-4-13C | 99.18% | D-Erythrose-4-13C is the 13C labeled D-Erythrose. | ||||||||||||||||||||
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D-Erythrose-1-13C | D-Erythrose-1-13C is the 13C labeled D-Erythrose. | |||||||||||||||||||||
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D-Erythrose (50%w/w in water) | 95.41% | D-Erythrose is a four-carbon sugar classified as an aldose. D-Erythrose has unique chemical properties that make it an important intermediate in various metabolic pathways, especially in the biosynthesis of amino acids and nucleotides. It also plays a role in the pentose phosphate pathway, which generates reducing equivalents for biosynthetic reactions and cellular defense against oxidative damage. | ||||||||||||||||||||
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References
