6493-06-7

(±)-Lisofylline Chemical Structure
6493-06-7

Chemical Structure

(±)-Lisofylline

Synonym(s): (±)-Lisophylline

  • CAS No.: 6493-06-7
  • Formula:C13H20N4O3
  • Molecular Weight:280.33

IUPAC Name: 1-(5-hydroxyhexyl)-3,7-dimethyl-3,7-dihydro-1H-purine-2,6-dione

InChIKey: NSMXQKNUPPXBRG-UHFFFAOYSA-N

SMILES: O=C(N1CCCCC(O)C)N(C)C2=C(N(C)C=N2)C1=O

Biological Activity: (±)-Lisofylline ((±)-Lisophylline) is the racemate of Lisofylline. Lisofylline inhibits the generation of phosphatidic acid and free fatty acids. Lisofylline also blocks the release of pro-inflammatory cytokines in oxidative tissue injury, in response to cancer chemotherapy and in experimental sepsis. Lisofylline can be used for Type 1 diabetes research[1].

Cat. No. Product Name Purity Description Pricing
HY-126042
(±)-Lisofylline 98.57% (±)-Lisofylline ((±)-Lisophylline) is the racemate of Lisofylline. Lisofylline inhibits the generation of phosphatidic acid and free fatty acids. Lisofylline also blocks the release of pro-inflammatory cytokines in oxidative tissue injury, in response to cancer chemotherapy and in experimental sepsis. Lisofylline can be used for Type 1 diabetes research.
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HY-126042R
(±)-Lisofylline (Standard) ≥98% (±)-Lisofylline (Standard) is the analytical standard of (±)-Lisofylline. This product is intended for research and analytical applications. (±)-Lisofylline ((±)-Lisophylline) is the racemate of Lisofylline. Lisofylline inhibits the generation of phosphatidic acid and free fatty acids. Lisofylline also blocks the release of pro-inflammatory cytokines in oxidative tissue injury, in response to cancer chemotherapy and in experimental sepsis. Lisofylline can be used for Type 1 diabetes research.
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HY-126042S
(±)-Lisofylline-d6 (±)-Lisofylline-d6 is the deuterium labeled (±)-Lisofylline.
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HY-126042S4
(±)-Lisofylline-d4 (±)-Lisofylline-d4 ((±)-Lisophylline-d4) is deuterium labeled (±)-Lisofylline. (±)-Lisofylline ((±)-Lisophylline) is the racemate of Lisofylline. Lisofylline inhibits the generation of phosphatidic acid and free fatty acids. Lisofylline also blocks the release of pro-inflammatory cytokines in oxidative tissue injury, in response to cancer chemotherapy and in experimental sepsis. Lisofylline can be used for Type 1 diabetes research.
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