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(S)-Lisofylline

CAS No.
100324-80-9
Chemical Name:
(S)-Lisofylline
Synonyms
(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
Molecular Formula:
C13H20N4O3
Molecular Weight:
280.32
MDL Number:
MOL File:
100324-80-9.mol
Last updated:2023-09-04 15:50:00

(S)-Lisofylline Properties

storage temp. Store at -20°C
solubility ≤15mg/ml in ethanol;3mg/ml in DMSO;12mg/ml in dimethyl formamide
form crystalline solid
FDA UNII N939YFB9KP

(S)-Lisofylline price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 13617 (S)-Lisofylline ≥98% 100324-80-9 1mg $71 2024-03-01 Buy
Cayman Chemical 13617 (S)-Lisofylline ≥98% 100324-80-9 5mg $313 2024-03-01 Buy
Cayman Chemical 13617 (S)-Lisofylline ≥98% 100324-80-9 10mg $554 2024-03-01 Buy
ApexBio Technology C4161 (S)-Lisofylline 100324-80-9 10mg $632 2021-12-16 Buy
ApexBio Technology C4161 (S)-Lisofylline 100324-80-9 5mg $356 2021-12-16 Buy
Product number Packaging Price Buy
13617 1mg $71 Buy
13617 5mg $313 Buy
13617 10mg $554 Buy
C4161 10mg $632 Buy
C4161 5mg $356 Buy

(S)-Lisofylline Chemical Properties,Uses,Production

Description

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.

Uses

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]

Definition

ChEBI: (S)-lisofylline is a 1-(5-hydroxyhexyl)-3,7-dimethyl-3,7-dihydro-1H-purine-2,6-dione that has (S)-configuration. It is the inactive optical enantiomer of (R)-lisofylline, an anti-inflammatory agent. It is an enantiomer of a (R)-lisofylline.

in vivo

in rats subjected to hemorrhagic shock and resuscitation, lsf increased the intestinal and hepatic blood flow. treatment with lsf (15 mg/kg) ameliorated the development of mucosal damage and hyperpermeability. rats treated with lsf showed lower plasma concentrations of the intracellular hepatic enzyme, aspartate aminotransferase. lsf treatment increased concentrations of adenosine triphosphate in intestinal and hepatic tissue [1]. in nod mice, lisofylline suppressed ifn-γ production, reduced the onset of insulitis and diabetes, and inhibited diabetes after transfer of splenocytes from lisofylline-treated donors to nod.scid recipients [3].

References

[1] wattanasirichaigoon s, menconi m j, fink m p. lisofylline ameliorates intestinal and hepatic injury induced by hemorrhage and resuscitation in rats[j]. critical care medicine, 2000, 28(5): 1540-1549.
[2] lillibridge, j. a.,kalhorn, t.f. and slattery, j.t. metabolism of lisofylline and pentoxifylline in human liver microsomes and cytosol. drug metabolism and disposition 24(11), 1174-1179 (1996).
[3] yang z d, chen m, wu r, et al. the anti-inflammatory compound lisofylline prevents type i diabetes in non-obese diabetic mice[j]. diabetologia, 2002, 45(9): 1307-1314.
[4] chen m, yang z, wu r, et al. lisofylline, a novel antiinflammatory agent, protects pancreatic β-cells from proinflammatory cytokine damage by promoting mitochondrial metabolism[j]. endocrinology, 2002, 143(6): 2341-2348.

6493-05-6
100324-81-0
100324-80-9
Synthesis of (S)-Lisofylline from Pentoxifylline

(S)-Lisofylline Preparation Products And Raw materials

Raw materials

Preparation Products

(S)-Lisofylline Suppliers

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Hangzhou MolCore BioPharmatech Co.,Ltd.
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Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
ApexBio Technology -- sales@apexbt.com United States 6254 58

(S)-Lisofylline Spectrum

(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 100324-80-9