英文名 | PF06447475 | CAS號 | 1527473-33-1 |
產品編號 | FSY0332 | 分子式 | C17H15N5O |
產品分類 | 化合物與抑制劑 | 分子量 | 305.3339 |
純度 | ≥98% | 儲存條件 | -20℃ |
產品簡介
PF-06447475是高效,選擇性,能透過血腦屏障的 LRRK2 抑制劑,IC50值為3 nM。Signaling Pathways(信號通路)→Autophagy(自噬)→LRRK2
體外研究 |
PF-06447475 inhibits LRRK2 enzyme and LRRK2 in the whole cell assay with IC50s of 3 and 25 nM, respectively. Cells incubated with PF-06447475 alone (0.5, 1, 3 μM) or in the presence of ROT significantly reduces (S935)-LRRK2 kinase phosphorylation to control. PF-06447475 significantly preserves the nucleus morphology and ΔΨm of NLCs exposed to ROT compared to untreated and control. PF-475 significantly diminishes ROT-induced ROS generation to a similar extent to cells exposed to PF-475 alone.
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體內研究 |
In G2019S+ rats treated with PF-06447475, a significant reduction in microgliosis to levels found in wild-type rats could be observed. The proinflammatory marker MHC-II expressed on myeloid cells but not neurons also appears to be less abundant in confocal sections in G2019S+ rats treated with PF-06447475. PF-06447475 treatment in G2019S+ rats significantly lowers the number of CD68 cells recruited to the SNpc. PF-06447475 successfully blocks the enhanced neuroinflammation associated with G2019S-LRRK2 expression. Treatment of G2019S+ rats with PF-06447475 preserves TH expression in the dorsal striatum, consistent with drug attenuating neurodegeneration in the SNpc. PF-06447475 is well tolerated in rats.
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分子式 |
C17H15N5O
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分子量 |
305.33
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CAS號 |
1527473-33-1
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儲存及運輸條件 |
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溶解性數據 |
In Vitro:
DMSO : 60 mg/mL (196.51 mM; Need ultrasonic) 配制儲備液
*
請根據產品在不同溶劑中的溶解度選擇合適的溶劑配制儲備液;一旦配成溶液,請分裝保存,避免反復凍融造成的產品失效。 In Vivo:
請根據您的實驗動物和給藥方式選擇適當的溶解方案。以下溶解方案都請先按照 In Vitro 方式配制澄清的儲備液,再依次添加助溶劑: ——為保證實驗結果的可靠性,澄清的儲備液可以根據儲存條件,適當保存;體內實驗的工作液,建議您現用現配,當天使用; 以下溶劑前顯示的百
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注意事項
1)本產品僅限于專業人員的科學研究用,不得用于臨床診斷或治療,不得用于食品或藥品,不得存放于普通住宅內。
2)為了您的安全和健康,請穿實驗服并戴一次性手套操作。
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