(2'S,3'R,6'R)-2',3'-ジヒドロ-3',6'-ジヒドロキシ-2'-ヒドロキシメチル-2',4',6'-トリメチルスピロ[シクロプロパン-1,5'-[5H]インデン]-7'(6'H)-オン

(2'S,3'R,6'R)-2',3'-ジヒドロ-3',6'-ジヒドロキシ-2'-ヒドロキシメチル-2',4',6'-トリメチルスピロ[シクロプロパン-1,5'-[5H]インデン]-7'(6'H)-オン 価格

(2'S,3'R,6'R)-2',3'-ジヒドロ-3',6'-ジヒドロキシ-2'-ヒドロキシメチル-2',4',6'-トリメチルスピロ[シクロプロパン-1,5'-[5H]インデン]-7'(6'H)-オン 化学特性,用途語,生産方法

• 説明

  Illudins are fungal sesquiterpenes that, through their unique DNA alkylating actions, have anticancer potential. Illudin S is a cytotoxic illudin that is converted, intracellularly, to metabolites that cause a complete block of cell cycling at the G₁-S phase interface, particularly in myeloid and T-lymphocyte leukemia cells (IC₅₀ = 6-11 nM). T-lymphocyte leukemia CEM cells that are resistant to doxorubicin , epipodophyllotoxins, and 1-β-D-arabinofuranosylcytosine display only 2-fold increased resistance to illudin S. Illudin S metabolites induce DNA damage that is not repaired by the processes that counter conventional DNA alkylating agents.

• 使用

  Illudin S is potent antitumor sesquiterpene, first isolated from the fungus, Clitocybe illudens, in 1963. Illudin S is metabolically activated to reactive intermediates that bind DNA. The DNA damage appears to differ from that of other reactive metabolites. Importantly, illudin S exhibits in vitro and in vivo potency against multi-drug resistant tumours.

(2'S,3'R,6'R)-2',3'-ジヒドロ-3',6'-ジヒドロキシ-2'-ヒドロキシメチル-2',4',6'-トリメチルスピロ[シクロプロパン-1,5'-[5H]インデン]-7'(6'H)-オン 生産企業

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(2'S,3'R,6'R)-2',3'-ジヒドロ-3',6'-ジヒドロキシ-2'-ヒドロキシメチル-2',4',6'-トリメチルスピロ[シクロプロパン-1,5'-[5H]インデン]-7'(6'H)-オン スペクトルデータ(¹HNMR)

1149-99-1, (2'S,3'R,6'R)-2',3'-ジヒドロ-3',6'-ジヒドロキシ-2'-ヒドロキシメチル-2',4',6'-トリメチルスピロ[シクロプロパン-1,5'-[5H]インデン]-7'(6'H)-オン キーワード