478529-67-8
478529-67-8
Chemical Structure
Glycolaldehyde-2-13C
- CAS No.: 478529-67-8
- Formula:C13CH4O2
- Molecular Weight:61.04
IUPAC Name: (2S,3R,4S,5R)-2,3,4,5,6-pentahydroxyhexanal-2-13C
InChIKey: WGCNASOHLSPBMP-VQEHIDDOSA-N
SMILES: O=C[13CH2]O
Biological Activity: Glycolaldehyde-2-13C is the 13C labeled Glycolaldehyde[1].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Glycolaldehyde-2-13C | 99.30% | Glycolaldehyde-2-13C is the 13C labeled Glycolaldehyde. | ||||||||||||||||||||
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2-Hydroxyacetaldehyde-13C2 | 2-Hydroxyacetaldehyde-13C2 is the 13C-labeled 2-Hydroxyacetaldehyde (HY-28911). | |||||||||||||||||||||
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Glycolaldehyde-1-13C | 99.0% | Glycolaldehyde-1-13C is the 13C labeled Glycolaldehyde. | ||||||||||||||||||||
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2-Hydroxyacetaldehyde | 2-Hydroxyacetaldehyde acts as a ribonucleotide synthesis precursor and a LDL modifier. 2-Hydroxyacetaldehyde specifically targets lysine residues of high-affinity LDL receptors and their apolipoproteins. By blocking the ε-amino groups of apolipoproteins, 2-Hydroxyacetaldehyde prevents receptor recognition, thereby reducing LDL degradation by macrophages. 2-Hydroxyacetaldehyde generates modified LDL, which serves as a probe for investigating non-receptor-dependent catabolic pathways. | |||||||||||||||||||||
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