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Merck

75617

Sigma-Aldrich

2-Deoxy-L-ribose

≥97.0% (TLC)

Sinónimos:

2-Deoxy-L-erythro-pentose

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About This Item

Fórmula empírica (notación de Hill):
C5H10O4
Número de CAS:
Peso molecular:
134.13
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

Quality Level

assay

≥97.0% (TLC)

form

powder

optical activity

[α]/D 54.0±2.0°, 24 hr, c = 1 in H2O

storage temp.

2-8°C

SMILES string

O=CC[C@@H](O)[C@@H](O)CO

InChI

1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m1/s1

InChI key

ASJSAQIRZKANQN-UHNVWZDZSA-N

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Biochem/physiol Actions

Inhibitor of enzymes and valuable building block for synthesis

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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The reaction of 70 unprotected, diversely functionalized free reducing sugars with methoxyamine-appended colchicine led to the production of a 58-member glycorandomized library. High-throughput cytotoxicity assays revealed glycosylation to modulate specificity and potency. Library members were also identified which, unlike the
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Thymidine phosphorylase (TP) catalyzes the reversible conversion of thymidine to thymine, thereby generating 2-deoxy-D-ribose-1-phosphate, which upon dephosphorylation forms 2-deoxy-D-ribose (D-dRib), a degradation product of thymidine. We have previously shown that D-dRib promotes angiogenesis and chemotaxis of endothelial cells and also

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