1. GPCR/G Protein Immunology/Inflammation
  2. CXCR
  3. 17:0 Lyso PI-d5

LN5972 是一种选择性的 ACKR3 激动剂,EC50 为 3.40 μM,对 ACKR3 的选择性高于 CXCR4。LN5972 可诱导 β-抑制蛋白募集至 ACKR3/CXCR7。LN5972 可降低 P-selectin 的表面表达。LN5972 可用于血小板介导的血栓形成相关研究。

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17:0 Lyso PI-d<sub>5</sub>

17:0 Lyso PI-d5 Chemical Structure

CAS No. : 3035425-93-2

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

LN5972 is a selective ACKR3 agonist with an EC50 of 3.40 μM, showing higher selectivity for ACKR3 over CXCR4. LN5972 induces β-arrestin recruitment to ACKR3/CXCR7. LN5972 reduces the surface expression of P-selectin. LN5972 is applicable to studies related to platelet-mediated thrombosis[1].

IC50 & Target[1]

ACKR3

3.40 μM (EC50)

体外研究
(In Vitro)

LN5972 (0.3 nM-100 μM) 可作为 HEK293T 细胞中 ACKR3 的超激动剂,诱导 β-arrestin 募集,其 EC50 为 3.40 μM,最大效能为 CXCL12 的 161%[1]
LN5972 (100 μM; 15 min) 可在富血小板血浆中使 CRP-XL 诱导的 P-选择素表达降低 76%[1]
LN5972 (0.3 nM-100 μM) 对 ACKR3 具有选择性,在 HEK293T 细胞中对 CXCR4 无活性[1]
LN5972 在肝微粒体 HLM 中表现出较高的代谢稳定性 (87% remaining at 120 min),而在小鼠肝微粒体中的稳定性较低[1]
LN5972 (up to 100 μM; 72 h) 对 THP1 和 HEK293 细胞无细胞毒性[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

422.54

Formula

C19H30N6O3S

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
17:0 Lyso PI-d5
目录号:
HY-182533
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