more general categories
information about this item
03. Biological Effects of Specific Chemicals
03. Biological Effects of Specific Chemicals
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
06. Name of Biological Source of Chemical
06. Name of Biological Source of Chemical
Calophyllum brasiliense (6)
Calophyllum teysmannii var inophylloide (3)
07. Part of Biological Source of Chemical
07. Part of Biological Source of Chemical
leaf [PO:0025034] (351)
08. Chemical Category
08. Chemical Category
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
(-)-calanolide B [CHEBI:65553] (1)
ChEBI Compound Accession Identifier :
[CHEBI:65553]
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 10S,11R,12S stereoisomer). Isolated from Calophyllum lanigerum var austrocoriaceum and Calophyllum brasiliense, it exhibits potent activity against HIV-1 reverse transcriptase.
ChEBI Compound Identification Number :
65553
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-/m0/s1
ChEBI InChIKey Value :
NIDRYBLTWYFCFV-PZROIBLQSA-N
ChEBI Compound Name :
(-)-calanolide B
ChEBI SMILES Value :
CCCc1cc(=O)oc2c3[C@@H](O)[C@@H](C)[C@H](C)Oc3c3C=CC(C)(C)Oc3c12
ChEBI Substance ID :
160655739
ChEBI URL :
ChEBI:65553
ChemSpider ID :
405728
Ontomatica Chemical Accession Key (OnChAKey) :
NIDRYBLTWYFCFV_PZROIBLQSA_N_000_000000
PubChem Compound ID :
461128