An efficient and scalable method for the isolation of costatolide, a naturally-occurring anti-HIV agent, from the latex of Calophyllum teysmannii var. inophylloide

被引:6
作者
Lin, YM
Anderson, HM
Jenta, TR
Williams, MJ
Flavin, MT
Xu, ZQ
机构
[1] MediChem Res Inc, Lemont, IL 60439 USA
[2] Sarawak MediChem Pharmaceut Inc, Lemont, IL 60439 USA
关键词
anti-HIV; NNRTI; costatolide; (-)-calanolide B; soulattrolide; production; isolation;
D O I
10.1076/phbi.37.1.71.6326
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
An efficient and scalable method is reported for the isolation of costatolide (2), a naturally-occurring and HIV-1-specific non-nucleoside reverse transcriptase inhibitor from the latex of Calophyllum teysmannii Mig. var inophylloide (King.) P. F. Stevens (Clusiaceae). An overall yield of 10.6% of costatolide (2), with a purity of 96%, was obtained by repetitive recrystallization of the latex from a single organic solvent, subsequent to the pre-treatment of latex with hexane and dichloromethane to remove undesirable oily material. A second major component of the latex, soulattrolide (3), another HIV-1 non-nuclecoside reverse transcriptase inhibitor was also isolated. Both compounds were characterized by spectroscopic and chromatographic analyses and their in vitro anti-HIV activities were also confirmed The results suggest that sufficient quantities of costatolide for preclinical and clinical development can be obtained in, a relatively low-cost manner from the natural source.
引用
收藏
页码:71 / 76
页数:6
相关论文
共 18 条
[1]   ANALYSIS OF NONNUCLEOSIDE DRUG-RESISTANT VARIANTS OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 REVERSE-TRANSCRIPTASE [J].
BOYER, PL ;
CURRENS, MJ ;
MCMAHON, JB ;
BOYD, MR ;
HUGHES, SH .
JOURNAL OF VIROLOGY, 1993, 67 (04) :2412-2420
[2]   STRUCTURE-ACTIVITY AND CROSS-RESISTANCE EVALUATIONS OF A SERIES OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE 1-SPECIFIC COMPOUNDS RELATED TO OXATHIIN CARBOXANILIDE [J].
BUCKHEIT, RW ;
KINJERSKI, TL ;
FLIAKASBOLTZ, V ;
RUSSELL, JD ;
STUP, TL ;
PALLANSCH, LA ;
BROUWER, WG ;
DAO, DC ;
HARRISON, WA ;
SCHULTZ, RJ ;
BADER, JP ;
YANG, SS .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (12) :2718-2727
[3]   RESISTANCE TO 1-[(2-HYDROXYETHOXY)METHYL]-6-(PHENYLTHIO)THYMINE DERIVATIVES IS GENERATED BY MUTATIONS AT MULTIPLE SITES IN THE HIV-1 REVERSE-TRANSCRIPTASE [J].
BUCKHEIT, RW ;
FLIAKASBOLTZ, V ;
YEAGYBARGO, S ;
WEISLOW, O ;
MAYERS, DL ;
BOYER, PL ;
HUGHES, SH ;
PAN, BC ;
CHU, SH ;
BADER, JP .
VIROLOGY, 1995, 210 (01) :186-193
[4]   COMPARITIVE ANTI-HIV EVALUATION OF DIVERSE HIV-1-SPECIFIC REVERSE-TRANSCRIPTASE INHIBITOR-RESISTANT VIRUS ISOLATES DEMONSTRATES THE EXISTENCE OF DISTINCT PHENOTYPIC SUBGROUPS [J].
BUCKHEIT, RW ;
FLIAKASBOLTZ, V ;
DECKER, WD ;
ROBERSON, JL ;
STUP, TL ;
PYLE, CA ;
WHITE, EL ;
MCMAHON, JB ;
CURRENS, MJ ;
BOYD, MR ;
BADER, JP .
ANTIVIRAL RESEARCH, 1995, 26 (02) :117-132
[5]   BIOLOGICAL AND BIOCHEMICAL ANTI-HIV ACTIVITY OF THE BENZOTHIADIAZINE CLASS OF NONNUCLEOSIDE REVERSE-TRANSCRIPTASE INHIBITORS [J].
BUCKHEIT, RW ;
FLIAKASBOLTZ, V ;
DECKER, WD ;
ROBERSON, JL ;
PYLE, CA ;
WHITE, EL ;
BOWDEN, BJ ;
MCMAHON, JB ;
BOYD, MR ;
BADER, JP ;
NICKELL, DG ;
BARTH, H ;
ANTONUCCI, TK .
ANTIVIRAL RESEARCH, 1994, 25 (01) :43-56
[6]   RESOLUTION AND COMPARATIVE ANTI-HIV EVALUATION OF THE ENANTIOMERS OF CALANOLIDE-A AND CALANOLIDE-B [J].
CARDELLINA, JH ;
BOKESCH, HR ;
MCKEE, TC ;
BOYD, MR .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1995, 5 (09) :1011-1014
[7]  
CREAGH T, 1998, 5 C RETR OPP INF CHI
[8]  
Currens MJ, 1996, J PHARMACOL EXP THER, V279, P652
[9]  
Currens MJ, 1996, J PHARMACOL EXP THER, V279, P645
[10]   SYNTHESIS OF OPTICALLY-ACTIVE CALANOLIDE-A AND CALANOLIDE-B [J].
DESHPANDE, PP ;
TAGLIAFERRI, F ;
VICTORY, SF ;
YAN, SJ ;
BAKER, DC .
JOURNAL OF ORGANIC CHEMISTRY, 1995, 60 (10) :2964-2965