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SKF-86002

    
99%

6-(4-FLUOROPHENYL)-2,3-DIHYDRO-5-(4-PYRIDINYL)IMIDAZO[2,1-B]THIAZOLE DIHYDROCHLORIDE

源葉(MedMol)
S86339 一鍵復制產品信息
72873-74-6
C16H12FN3S
297.36
6-(4-氟苯基)-5-(4-吡啶基)-2,3-二氫咪唑并[2,1-B]-噻唑;6-(4-FLUOROPHENYL)-5-(4-PYRIDYL)-2,3-DIHYDROIMIDAZO[2,1-B]-THIAZOLE;6-(4-FLUOROPHENYL)-2,3-DIHYDRO-5-(4-PRIDYL)IMIDAZO-[2,1,B]-THAIZOLE;6-(4-FLUOROPHENYL)-2,3-D
貨號 規格 價格 上海 北京 武漢 南京 購買數量
S86339-1mg 99% ¥120.00 9 - - -
S86339-2mg 99% ¥190.00 7 - - -
S86339-5mg 99% ¥320.00 7 - - -
S86339-10mg 99% ¥590.00 6 - - -
S86339-25mg 99% ¥990.00 5 - - -
S86339-50mg 99% ¥1400.00 貨期:2-3天 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

SKF-86002 is an orally active p38 MAPK inhibitor, with anti-inflammatory, anti-arthritic and analgesic activities. SKF-86002 inhibits lipopolysaccharide (LPS)-stimulate human monocyte IL-1 and TNF-α production (IC50 = 1 μM). SKF-86002 inhibits lipoxygenase- and cyclooxygenase-mediated metabolism of arachidonic acid

產品描述: SKF-86002 is an orally active p38 MAPK inhibitor, with anti-inflammatory, anti-arthritic and analgesic activities. SKF-86002 inhibits lipopolysaccharide (LPS)-stimulate human monocyte IL-1 and TNF-α production (IC50 = 1 μM). SKF-86002 inhibits lipoxygenase- and cyclooxygenase-mediated metabolism of arachidonic acid
靶點: p38 MAPK;p38MAPK;TNF
體內研究: SKF-86002 (10-90 mg/kg; p.o.; daily; for 22 days) has antiarthritic activity
參考文獻: 1. Frasch SC, et al. p38 mitogen-activated protein kinase-dependent and -independent intracellular signal transduction pathways leading to apoptosis in human neutrophils. J Biol Chem. 1998 Apr 3;273(14):8389-97. 2. Griswold DE, et al. SK&F 86002: a structurally novel anti-inflammatory agent that inhibits lipoxygenase- and cyclooxygenase-mediated metabolism of arachidonic acid. Biochem Pharmacol. 1987 Oct 15;36(20):3463-70. 3. Lee JC, et al. A protein kinase involved in the regulation of inflammatory cytokine biosynthesis. Nature. 1994;372(6508):739-746. 4. L A Marshall, et al. Inhibitors of the p38 mitogen-activated kinase modulate IL-4 induction of low affinity IgE receptor (CD23) in human monocytes. J Immunol. 1998 Dec 1;161(11):6005-13. 5. M J DiMartino, et al. Pharmacologic characterization of the antiinflammatory properties of a new dual inhibitor of lipoxygenase and cyclooxygenase. Agents Actions. 1987 Feb;20(1-2):113-23.
溶解性: Soluble  in  DMSO
保存條件: 2-8℃,避光
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.363 ml 16.815 ml 33.629 ml
5 mM 0.673 ml 3.363 ml 6.726 ml
10 mM 0.336 ml 1.681 ml 3.363 ml
50 mM 0.067 ml 0.336 ml 0.673 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。

參考文獻

質檢證書(COA)

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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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