Title of article :
Resolution and comparative anti-HIV evaluation of the enantiomers of calanolides A and B
Author/Authors :
John H. Cardellina II، نويسنده , , Heidi R. Bokesch، نويسنده , , Tawnya C. McKee، نويسنده , , Michael R. Boyd، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1995
Pages :
4
From page :
1011
To page :
1014
Abstract :
Methods for the chiral resolution of (+)-calanolide A and (−)-calanolide A from synthetic (±)-calanolide A, and of (+)-calanolide B and (−)-calanolide B (costatolide) from a scalemic mixture isolated from C. lanigerium, have been developed. Calanolide A was originally isolated as the pure (+) enantiomer from C. lanigerum, but now is also shown to occur as a scalemic mixture in latex of C. teysmannii. Interestingly, (+)-calanolide A and (−)-calanolide B are potent HIV-1 inhibitors, while (−)-calanolide A and (+)-calanolide B are inactive against the virus.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
1995
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
787460
Link To Document :
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