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14699

Sigma-Aldrich

2-Deoxy-D-ribonic acid lithium salt

≥95.0% (TLC)

Sinonimo/i:

2-Deoxy-D-erythro-pentonic acid lithium salt

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About This Item

Formula empirica (notazione di Hill):
C5H10O5 · xLi+
Numero CAS:
7284-15-3
Peso molecolare:
150.13 (free acid basis)
Codice UNSPSC:
12352201
ID PubChem:
329750581
NACRES:
NA.25

Saggio

≥95.0% (TLC)

Attività ottica

[α]/D 12.0±2.0°, 24 hr, c = 1 in 1 M HCl

Temperatura di conservazione

2-8°C

Stringa SMILE

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

InChI

1S/C5H10O5/c6-2-4(8)3(7)1-5(9)10/h3-4,6-8H,1-2H2,(H,9,10)/t3-,4+/m0/s1
VBUWJOHKCBQXNU-IUYQGCFVSA-N

Azioni biochim/fisiol

2-Deoxyribonic acid is the acid form of deoxyribonate, intercovertible with 2-Deoxy-ribonolactone, produced as part of bistranded lesions by DNA damaging agents, by ionizing radiation, organometallic oxidants, and is a metastable intermediate in DNA damage mediated by copper phenanthroline nucleases, and is also formed under anaerobic conditions in the presence of the radiosensitizing agent tirapazamine. It has been found in normal human biofluids.

Altre note

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

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Cleavage of the intermediate hydroperoxides in the oxidation of D-glucose and D-fructose with oxygen.
Vuorinen, T.
Carbohydrate Research, 141, 319-322 (1985)
M Davies et al.
Acta endocrinologica, 104(2), 210-215 (1983-10-01)
Serum vitamin D metabolites, the renal tubular maximum reabsorptive rate for phosphate (TMP/GFR) nephrogenic cyclic AMP (NcAMPI, and CaE (urinary calcium excretion per litre of glomerular filtrate) were measured in 14 adults with familial hypocalciuric hypercalcaemia (FHH). The findings were
Kelly M Kroeger et al.
Biochemistry, 42(8), 2449-2455 (2003-02-26)
2-Deoxyribonolactone (3) is produced in DNA as a result of reaction with a variety of DNA damaging agents. The lesion undergoes beta-elimination to form a second metastable electrophilic product (4). In this study, DNA containing 2-deoxyribonolactone (3) and its beta-elimination
Formation of carboxylic acids during degradation of mono- saccharides.
Novotny, O., et al.
Czech Journal of Food Sciences, 26, 117-131 (2008)
Isolation of 2-deoxy-D-erythro-pentonic acid from an alkali-labile site in gamma-irradiated DNA.
M Dizdaroglu et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 32(5), 481-483 (1977-11-01)
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