| Identification | Back Directory | [Name]
CALANOLIDE A | [CAS]
142632-32-4 | [Synonyms]
NSC675451
NSC-675451
NSC 675451
CALANOLIDE A
(+)-Calanolide A
(+) Calanolide A
(10R,11S,12S)-12-hydroxy-6,6,10,11-tetramethyl-4-propyl-11,12-dihydro-2H,6H,10H-dipyrano[2,3-f:2',3'-h]chromen-2-one
(+)-(10R,11S,12S)-12-HYDROXY-6,6,10,11-TETRAMETHYL-4-PROPYL-11,12-DIHYDRO-2H,6H,10H-BENZO(1,2-B:3,4-B':5,6-B'']TRIPYRAN-2-ONE
2H,6H,10H-Dipyrano[2,3-f:2',3'-h][1]benzopyran-2-one, 11,12-dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-propyl-, (10R,11S,12S)-
CALANOLIDE A,(+)-(10R,11S，12S)-12-HYDROXY-6,6,10,11-TETRAMETHYL-4-PROPYL-11，12-DIHYDRO-2H，6H,10H-BENZO(1，2-B：3,4-B'：5,6-B ]TRIPYRAN-2-ONE | [Molecular Formula]
C22H26O5 | [MDL Number]
MFCD00867485 | [MOL File]
142632-32-4.mol | [Molecular Weight]
370.44 |
| Hazard Information | Back Directory | [Uses]
(+)-Calanolide A is an experimental non-nucleoside reverse transcriptase inhibitor. It has potent anti-HIV activity. | [Definition]
ChEBI:(+)-calanolide A is an organic heterotetracyclic compound that is 11,12-dihydro-2H,6H,10H-dipyrano[2,3-f:2',3'-h]chromen-2-one substituted by a hydroxy group at position 12, methyl groups at positions 6, 6, 10 and 11 and a propyl group at position 4 (the 10R,11S,12S stereoisomer). Isolated from Calophyllum lanigerum var austrocoriaceum and Calophyllum brasiliense, it exhibits potent activity against HIV-1 reverse transcriptase. It has a role as a HIV-1 reverse transcriptase inhibitor and a plant metabolite. It is an organic heterotetracyclic compound, a delta-lactone, a cyclic ether and a secondary alcohol. |
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