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Alprostadil

    
≥98%

7-((1R,2R,3R)-3-hydroxy-2-((S,E)-3-hydroxyoct-1-en-1-yl)-5-oxocyclopentyl)heptanoic acid

源葉(MedMol)
S80930 一鍵復制產品信息
745-65-3
C20H34O5
354.48
前列地爾;Prostaglandin E1;7-((1R,2R,3R)-3-hydroxy-2-((S,E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl)heptanoic acid;l-PGE1; l-Prostaglandin E1; Lipoprost; Liprostin; Minprog; NSC 165559; ONO 1608; PGE-1; Prom
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S80930-5mg
≥98% ¥270.00 >10 - - -
S80930-10mg
99.5% ¥480.00 >10 - - -
S80930-50mg
99.5% ¥1400.00 >10 - - -
產品介紹 參考文獻(1篇) 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

Prostaglandin E1 (Alprostadil) is a prostanoid receptor ligand, with Kis of 1.1 nM, 2.1 nM, 10 nM, 33 nM and 36 nM for mouse EP3, EP4, EP2, IP and EP1, respectively. Prostaglandin E1 induces vasodilation and inhibits platelet aggregation. Prostaglandin E1 can be used as a vasodilator for the research of peripheral vascular diseases

產品描述:

Prostaglandin E1 (Alprostadil) is a prostanoid receptor ligand, with Kis of 1.1 nM, 2.1 nM, 10 nM, 33 nM and 36 nM for mouse EP3, EP4, EP2, IP and EP1, respectively. Prostaglandin E1 induces vasodilation and inhibits platelet aggregation. Prostaglandin E1 can be used as a vasodilator for the research of peripheral vascular diseases

靶點: Human Endogenous Metabolite;EndogenousMetabolite;ProstaglandinReceptor
體外研究: Prostaglandin E1 (1 nM-10 μM; 48 h) concentration-dependently reduces HUVECs proliferation (up to 100% inhibition) in the presence of VEGF (20 ng/mL), with an IC50 of 400 nM.
Prostaglandin E1 (0.01-10 μM; 6 h) inhibits VEGF-induced HUVECs migration in a concentration dependent manner, with an IC50 of 500 nM.
Prostaglandin E1 (1-5 μM; 12-18 h) inhibits in vitro angiogenesis.
Prostaglandin E1 (0.01-10 μM; 20 min) increases intracellular cAMP levels in HUVECs.
體內研究: Prostaglandin E1 (20 ng/animal/day; s.c. for 4 days) significantly inhibits the FGF-induced angiogenesis in mice. Animal Model: C57/bl6 female mice (6-8 weeks) were injected with Matrigel supplemented with aFGF and heparin Dosage: 20 ng/day/animal Administration: Minipump placed subcutaneously for 4 days Result: Visibly reduced the neovascularization process.
參考文獻: 1. Kiriyama M, et, al. Ligand binding specificities of the eight types and subtypes of the mouse prostanoid receptors expressed in Chinese hamster ovary cells. Br J Pharmacol. 1997 Sep;122(2):217-24. 2. Cattaneo MG, et, al. Alprostadil suppresses angiogenesis in vitro and in vivo in the murine Matrigel plug assay. Br J Pharmacol. 2003 Jan;138(2):377-85. 3. Hauck EW, et, al. Prostaglandin E1 long-term self-injection programme for treatment of erectile dysfunction--a follow-up of at least 5 years. Andrologia. 1999;31 Suppl 1:99-103.
溶解性: EtOH:40mg/ml,DMSO:40mg/ml
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.821 ml 14.105 ml 28.21 ml
5 mM 0.564 ml 2.821 ml 5.642 ml
10 mM 0.282 ml 1.411 ml 2.821 ml
50 mM 0.056 ml 0.282 ml 0.564 ml
注意: 部分產品我司僅能提供部分信息,我司不保證所提供信息的權威性,僅供客戶參考交流研究之用。

質檢證書(COA)

如何獲取質檢證書(COA)?
請輸入貨號和一個與之匹配的批號。
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批號:JS298415 貨號:S20001-25g
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摩爾濃度計算器

質量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

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