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03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Calophyllum brasiliense (6)
Calophyllum lanigerum var austrocoriaceum (3)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
fruit [PO:0009001] (81)
leaf [PO:0025034] (351)
08. Chemical Category
08. Chemical Category
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
(+)-calanolide A [CHEBI:65552] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65552]
ChEBI Compound Description :
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.
ChEBI Compound Identification Number :
65552
ChEBI InChI Value :
InChI=1S/C22H26O5/c1-6-7-13-10-15(23)26-21-16(13)20-14(8-9-22(4,5)27-20)19-17(21)18(24)11(2)12(3)25-19/h8-12,18,24H,6-7H2,1-5H3/t11-,12-,18+/m1/s1
ChEBI InChIKey Value :
NIDRYBLTWYFCFV-FMTVUPSXSA-N
ChEBI Compound Name :
(+)-calanolide A
ChEBI SMILES Value :
CCCc1cc(=O)oc2c3[C@@H](O)[C@H](C)[C@@H](C)Oc3c3C=CC(C)(C)Oc3c12
ChEBI Substance ID :
160655758
ChEBI URL :
ChEBI:65552
ChemSpider ID :
NS
Ontomatica Chemical Accession Key (OnChAKey) :
NIDRYBLTWYFCFV_FMTVUPSXSA_N_000_000000
PubChem Compound ID :
64972