CAS
|
188062-50-2
|
中文名称
|
硫酸阿巴卡韦
|
英文名称
|
Abacavir Sulfate
|
别名
|
阿巴卡韦硫酸盐;赛进
|
纯度
|
≥98%
|
分子式
|
C28H36N12O2·H2SO4
|
分子量
|
670.74
|
外观(性状)
|
White to off-white Solid
|
储存条件
|
Powder : -20℃, 2 years;In solvent(母液): -20℃, 1 month; -80℃, 6 months
|
溶解性
|
Soluble in DMSO
|
EC
|
EINECS 620-488-4
|
MDL
|
MFCD04112763
|
SMILES
|
NC1=NC(NC2CC2)=C3N=CN([C@H]4C=C[C@@H](CO)C4)C3=N1.O=S(O)(O)=O.NC5=NC(NC6CC6)=C7N=CN([C@H]8C=C[C@@H](CO)C8)C7=N5
|
描述
|
是核苷类似物逆转录酶抑制剂(NRTI),可用于HIV和AIDS的相关研究。(It is a nucleoside analog reverse transcriptase inhibitor (NRTI), which can be used for HIV and AIDS related research.)
|
靶点
|
Reverse Transcriptase
|
通路
|
Anti-infection
|
生物活性
|
Abacavir is a nucleoside reverse transcriptase inhibitor marketed the treatment of infection with the human immunodeficiency virus type 1 (HIV). [1] Abacavir is a carbocyclic 2'-deoxyguanosine nucleoside analogue. It is metabolised intracellularly to a 2'-deoxyguanosine nucleoside analogue which competitively inhibits HIV reverse transcriptase and terminates proviral DNA chain extension. [2]
|
数据来源文献
|
[1]. Charneira C, et al. Reactive aldehyde metabolites from the anti-HIV drug abacavir: amino acid adducts as possible factors in abacavir toxicity. Chem Res Toxicol. 2011 Dec 19;24(12):2129-41.
[2]. Hervey PS, et al. Abacavir: a review of its clinical potential in patients with HIV infection. Drugs. 2000 Aug;60(2):447-79.
|
规格
|
10mg
|
单位
|
瓶
|