跳转至内容
Merck
CN

14699

Sigma-Aldrich

2-Deoxy-D-ribonic acid lithium salt

≥95.0% (TLC)

别名:

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

登录查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C5H10O5 · xLi+
化学文摘社编号:
分子量:
150.13 (free acid basis)
UNSPSC代码:
12352201
PubChem化学物质编号:
NACRES:
NA.25
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

方案

≥95.0% (TLC)

旋光性

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

储存温度

2-8°C

SMILES字符串

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

生化/生理作用

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.

其他说明

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

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)
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
Cleavage of the intermediate hydroperoxides in the oxidation of D-glucose and D-fructose with oxygen.
Vuorinen, T.
Carbohydrate Research, 141, 319-322 (1985)
Kinetics and mechanism of the reduction of CrVI to CrIII by D-ribose and 2-deoxy-D-ribose.
Daier, V., et al.
Canadian Journal of Chemistry, 77, 57-64 (1999)
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

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持