14699
2-Deoxy-D-ribonic acid lithium salt
≥95.0% (TLC)
Synonym(s):
2-Deoxy-D-erythro-pentonic acid lithium salt
SMILES string
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
InChI key
VBUWJOHKCBQXNU-IUYQGCFVSA-N
assay
≥95.0% (TLC)
optical activity
[α]/D 12.0±2.0°, 24 hr, c = 1 in 1 M HCl
storage temp.
2-8°C
Biochem/physiol Actions
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.
Other Notes
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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)
L S Kappen et al.
Biochemistry, 28(3), 1027-1032 (1989-02-07)
Neocarzinostatin- (NCS) induced release of cytosine from the deoxycytidylate residues of d(AGC) sequences of duplex oligonucleotides leaves a damaged sugar residue with intact phosphodiester linkages [Kappen, L.S., Chen, C., & Goldberg, I.H. (1988) Biochemistry 27, 4331-4340]. In order to isolate
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
Formation of carboxylic acids during degradation of mono- saccharides.
Novotny, O., et al.
Czech Journal of Food Sciences, 26, 117-131 (2008)
Cleavage of the intermediate hydroperoxides in the oxidation of D-glucose and D-fructose with oxygen.
Vuorinen, T.
Carbohydrate Research, 141, 319-322 (1985)
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