홈MCP워크벤치Skills
홈워크벤치알림마이페이지
Huagongshe 오픈 프로젝트:[email protected]AI 접속: llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.7.8
돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HCID 23519621생성일: 2026년 11월 4일

(S)-리소필린

(S)-리소필린 · (S)-Lisofylline · (S)-Lisophylline · (S)-Lisofylline Exclusive · (S)-Lisofylline, 10 mM in DMSO · (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-

https://huagongshe.com/ko/chemical/23519621

(S)-리소필린 분자 구조식

식별자 및 물리적 특성

CAS No.100324-80-9
분자식C13H20N4O3
평균 분자량280.32 g/mol
SMILESC[C@H](O)CCCCn1c(=O)c2c(ncn2C)n(C)c1=O
InChIKeyNSMXQKNUPPXBRG-VIFPVBQESA-N
PubChem CID23519621
ChEMBLCHEMBL4300766
ChEBICHEBI:143564
현지명(S)-리소필린

화학 및 물리적 성질

저장 조건Store at -20°C
용해도≤15mg/ml in ethanol3mg/ml in DMSO12mg/ml in dimethyl formamide
물리적 상태결정질 고체
색상Off-white to light yellow

용도

개요

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.

용도

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]