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FD028

Chemical Structure : FD028

CAS No.: 2563903-40-0

FD028 (FD-028, FD 028)

货号: PC-73248Not For Human Use, Lab Use Only.

FD028 is a small-molecule HIV-1 inactivator by conjugating FD016 (gp120-CD4 binding inhibitor) with FD017 (HIV-1 fusion inhibitor), inactivates cell-free virions (IC50=0.7 uM) of by targeting both HIV-1 gp120 and gp41.

规格 价格 库存 数量
25 mg Get quote
50 mg Get quote
100 mg Get quote

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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

    生物&药学活性

    FD028 is a small-molecule HIV-1 inactivator by conjugating FD016 (gp120-CD4 binding inhibitor) with FD017 (HIV-1 fusion inhibitor), inactivates cell-free virions (IC50=0.7 uM) of by targeting both HIV-1 gp120 and gp41.
    FD028 is not significantly toxic and has broad-spectrum HIV-1 inhibitory and inactivation activity, including T20-resistant viruses and T2635-resistant viruses.

    物理化学性质&存储条件

    分子量 881.812
    分子式 C42H39Cl2FN4O8S2
    外观性状 Solid
    CAS No.
    储存条件
    固体粉末
    -20°C 12 个月; 4°C 6 个月
    配置液
    -80°C 6 个月; -20°C 6 个月
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    (Z)-2-chloro-5-(5-((3-(4-(2-(4-(2-((4-chloro-3-fluorophenyl)amino)-2-oxoacetamido)-2,2,6,6-tetramethylpiperidin-1-yl)-2-oxoethoxy)phenethyl)-4-oxo-2-thioxothiazolidin-5-ylidene)methyl)furan-2-yl)benzoic acid

    参考文献

    1. Jing Pu, et al. Front Pharmacol. 2021 Jan 25;11:613361. doi: 10.3389/fphar.2020.613361.

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