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About This Item
经验公式（希尔记法）:
C9H13N3O3
CAS号:
分子量:
211.22
Beilstein:
654956
MDL號碼:
分類程式碼代碼:
41106305
PubChem物質ID:
NACRES:
NA.52
推荐产品
生物源
synthetic (organic)
化驗
≥98% (HPLC)
形狀
powder
顏色
colorless
mp
217-218 °C (lit.)
溶解度
water: 50 mg/mL, clear, colorless to faintly yellow
儲存溫度
−20°C
SMILES 字串
NC1=NC(=O)N(C=C1)[C@H]2CC[C@@H](CO)O2
InChI
1S/C9H13N3O3/c10-7-3-4-12(9(14)11-7)8-2-1-6(5-13)15-8/h3-4,6,8,13H,1-2,5H2,(H2,10,11,14)/t6-,8+/m0/s1
InChI 密鑰
WREGKURFCTUGRC-POYBYMJQSA-N
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應用
2′,3′-二脱氧胞苷用于:
- 作为基于 Sanger 链终止法的 DNA 测序方法的 DNA 链终止核苷酸
- 作为核苷逆转录酶抑制剂（NRTI）用于研究其对衰老小鼠机械性机械性触诱发痛发展的影响
- 作为线粒体 DNA（mtDNA） 复制抑制剂，用于抑制 cGAS-STING 通路的激活，并研究其对小鼠海马和小胶质细胞中信号蛋白-干扰素基因刺激因子 (STING)、环状 GMP-AMP 合酶 (cGAS) 和磷酸化干扰素调节因子 3 (p-IRF3)表达的影响
- 作为 NRTI 抑制剂用于研究其对秀丽隐杆线虫中药物诱导的线粒体毒性的影响
生化／生理作用
2′,3′-二脱氧胞苷（ddC） 是一种离子化合物和核苷类似物。它可作为核苷类逆转录酶抑制剂，并对人类免疫缺陷病毒（HIV）感染具有治疗作用。2′,3′-二脱氧胞苷具有抗腺病毒活性并抑制腺病毒聚合酶。
Maja M Janas et al.
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For oligonucleotide therapeutics, chemical modifications of the sugar-phosphate backbone are frequently used to confer drug-like properties. Because 2'-deoxy-2'-fluoro (2'-F) nucleotides are not known to occur naturally, their safety profile was assessed when used in revusiran and ALN-TTRSC02, two short interfering
Shuang-Xi Gu et al.
Bioorganic & medicinal chemistry, 19(17), 5117-5124 (2011-08-10)
A series of 26 diarylpyrimidines, characterized by the hydroxymethyl linker between the left wing benzene ring and the central pyrimidine, were synthesized and evaluated for in vitro anti-HIV activity. Most of the compounds exhibited moderate to excellent activities against wild-type
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Cellular & molecular immunology, 18(9), 2211-2223 (2020-05-14)
Exposure to ionizing radiation, a physical treatment that inactivates live tumor cells, has been extensively applied to enhance the antitumor responses induced by cancer cell vaccines in both animal research and human clinical trials. However, the mechanisms by which irradiated
Anindya Roy Chowdhury et al.
iScience, 23(8), 101370-101370 (2020-08-02)
This study shows that multiple modes of mitochondrial stress generated by partial mtDNA depletion or cytochrome c oxidase disruption cause ryanodine receptor channel (RyR) dysregulation, which instigates the release of Ca2+ in the cytoplasm of C2C12 myoblasts and HCT116 carcinoma
Didier Desmaële et al.
Journal of controlled release : official journal of the Controlled Release Society, 161(2), 609-618 (2011-08-16)
Squalene is a triterpene widely distributed in nature that is an intermediate in the cholesterol biosynthesis pathway. The remarkable dynamic folded conformation of squalene has been used to chemically conjugate this lipid with various therapeutic molecules to construct nanoassemblies of
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