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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
RT
- 保质期:
见标签
- 库存:
999
- 供应商:
联硕生物
- CAS号:
3056-17-5
- 规格:
10MG
Application
2′,3′-Didehydro-3′-deoxythymidine has been used in cell treatment.[1] It has also been used as a drug in Caenorhabditis elegans to study drug induced mitochondrial toxicity.[2] It has also been used in the preclinical evaluation of GS-9160.[3]
Biochem/physiol Actions
2′,3′-Didehydro-3′-deoxythymidine is a nucleoside analog, which inhibits HIV replication in vitro. Stavudine has the ability to enter the cells by non-facilitated diffusion. It possesses inhibitory activity against moloney murine leukemia virus, friend murine leukemia virus and simian immunodeficiency virus.[4]
General description
2′,3′-Didehydro-3′-deoxythymidine (d4T), a pyrimidine analogue is the inhibitor of reverse transcriptase.
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文献和实验缩写为 cGMp。分 2′, 3′- cGMP和 3′, 5′ -cGMP二种。前者为 RNA的酶催化分解的产物,后者在生理上具有重要作用。 3′, 5′ -cGMP是 D. F. Ashman等( 1963)在鼠尿中发现的。在动物的各种组织中广泛存在,在大肠杆菌中也有发现,在小脑和肺中含量最高。与 3′, 5′- cAMP一样,能将从细胞外来的刺激向细胞内传递,起所谓的第二信使作用。在鸟苷酸环化酶( guanylate cyclase)的作用下,由 GTA生成。可由特异的磷酸
ribonucleoside 2′‐conjugates S.11 a‐d and of the 5′‐pyrenylated 2′‐deoxythymidine conjugate S.12 . Abbreviations: B, a uracil‐1‐yl, b cytosin‐1‐yl, c adenin‐9‐yl, d guanin‐9‐yl; Thy, thymin‐1‐yl. Adapted from Cieślak et al. () by permission of Oxford University
Analysis of Bases, Nucleosides, and (Oligo)nucleotides by Capillary Electrophoresis
(Chapter 13 ) and in recent reviews (1 –3 ). A number of nucleosides and nucleotides have been used in chemotherapy as antiviral agents, e.g., 3′-azido-3′-deoxythymidine (azT), and 2′,3′-dideoxyinosine (ddI), and 2′,3′-dideoxycytidine (ddC
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