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DF3016A

Chemical Structure : DF3016A

CAS No.: 2351103-44-9

DF3016A (DF 3016A)

货号: PC-38338Not For Human Use, Lab Use Only.

DF3016A (DF 3016A) is a potent and selective C5aR inhibitor with IC50 of 50 nM (C5a-induced human PMN migration and IC50 of 45 and 37 nM against rat and mouse C5aR, respectively.

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

    生物&药学活性

    DF3016A (DF 3016A) is a potent and selective C5aR inhibitor with IC50 of 50 nM (C5a-induced human PMN migration and IC50 of 45 and 37 nM against rat and mouse C5aR, respectively.
    DF3016A exhibited a high degree of selectivity with no effect on PMN migration induced by other leukocyte activators such as CXCL8, CXCL1, CCL3, fMLP, CXCL12, and on LPS-induced PGE2 accumulation at 10 uM.
    DF3016A protects neuronal viability by restoring intracellular calcium levels, thus opposing the increase in pro-inflammatory cytokine levels and miR-181 expression in rat model of neuroinflammatory injury.
    DF3016A also inhibits osteoclast degradation activity through inhibition of C5aR signal transduction and transcription.

    物理化学性质&存储条件

    分子量 362.31
    分子式 C13H10F3N6NaS
    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 1 Month
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    sodium (R)-5-(1-(4-((4-(trifluoromethyl)thiazol-2-yl)amino)phenyl)ethyl)tetrazol-1-ide

    参考文献

    1. Rosa D'Angelo, et al. Biomed Pharmacother. 2020 Mar;123:109764.

    2. Laura Brandolini, et al. Neurotox Res. 2019 Jul;36(1):163-174.

    3. Grannonico M, et al. Brain Res. 2020 Dec 1;1748:147057.

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