(S)-Lisofylline

 化学構造式
100324-80-9
CAS番号.
100324-80-9
化学名:
别名:
英語名:
(S)-Lisofylline
英語别名:
(S)-Lisofylline;(S)-Lisophylline;(S)-Lisofylline Exclusive;(S)Lisofylline,(S) Lisofylline;1-[(5S)-5-hydroxyhexyl]-3,7-dimethylpurine-2,6-dione;1H-Purine-2,6-dione, 3,7-dihydro-1-[(5S)-5-hydroxyhexyl]-3,7-dimethyl-
CBNumber:
CB02589835
化学式:
C13H20N4O3
分子量:
280.32
MOL File:
100324-80-9.mol

(S)-Lisofylline 物理性質

貯蔵温度 :
Store at -20°C
溶解性:
≤15mg/ml in ethanol;3mg/ml in DMSO;12mg/ml in dimethyl formamide
外見 :
crystalline solid
色:
Off-white to light yellow

安全性情報

(S)-Lisofylline 価格

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入

(S)-Lisofylline 化学特性,用途語,生産方法

説明

LSF, a chiral metabolite of pentoxifylline, acts as a potent anti-inflammatory agent. (S)-LSF is the pharmacologically inactive optical enantiomer of (R)-LSF, the biologically active isomer. When metabolized by isolated human liver cells, pentoxifylline is exclusively reduced to (S)-LSF in the cytosol, while reduction in liver microsomes is 85% stereoselective in favor of (S)-LSF formation. Thus, pentoxifylline is an inefficient prodrug for the delivery of therapeutically relevant lisofylline.

使用

LSF, a chiral metabolite of pentoxifylline, acts as a potent anti-inflammatory agent. (S)-LSF is the pharmacologically inactive optical enantiomer of (R)-LSF, the biologically active isomer. When metabolized by isolated human liver cells, pentoxifylline is exclusively reduced to (S)-LSF in the cytosol, while reduction in liver microsomes is 85% stereoselective in favor of (S)-LSF formation. Thus, pentoxifylline is an inefficient prodrug for the delivery of therapeutically relevant lisofylline.[Cayman Chemical]

(S)-Lisofylline 上流と下流の製品情報

原材料

準備製品


(S)-Lisofylline 生産企業

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  スペクトルデータ(1HNMR)



  • 100324-80-9
  • (S)-Lisofylline
  • 1H-Purine-2,6-dione, 3,7-dihydro-1-[(5S)-5-hydroxyhexyl]-3,7-dimethyl-
  • (S)-Lisofylline Exclusive
  • 1-[(5S)-5-hydroxyhexyl]-3,7-dimethylpurine-2,6-dione
  • (S)-Lisophylline
  • (S)Lisofylline,(S) Lisofylline
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