CHEBI:65553 - (−)-calanolide B

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ChEBI Name (−)-calanolide B
ChEBI ID CHEBI:65553
ChEBI ASCII Name (-)-calanolide B
Definition 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.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C22H26O5
Net Charge 0
Average Mass 370.43880
Monoisotopic Mass 370.17802
InChI 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
InChIKey NIDRYBLTWYFCFV-PZROIBLQSA-N
SMILES CCCc1cc(=O)oc2c3[C@@H](O)[C@@H](C)[C@H](C)Oc3c3C=CC(C)(C)Oc3c12
Metabolite of Species Details
Calophyllum brasiliense (IPNI:427115-1) Found in leaf (BTO:0000713). See: PubMed
Calophyllum teysmannii var. inophylloide (IPNI:876299-1) Found in latex (BTO:0000710). See: PubMed
Roles Classification
Biological Role(s): HIV-1 reverse transcriptase inhibitor
An entity which inhibits the activity of HIV-1 reverse transcriptase.
plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (−)-calanolide B (CHEBI:65553) has role HIV-1 reverse transcriptase inhibitor (CHEBI:53756)
(−)-calanolide B (CHEBI:65553) has role plant metabolite (CHEBI:76924)
(−)-calanolide B (CHEBI:65553) is a δ-lactone (CHEBI:18946)
(−)-calanolide B (CHEBI:65553) is a cyclic ether (CHEBI:37407)
(−)-calanolide B (CHEBI:65553) is a organic heterotetracyclic compound (CHEBI:38163)
(−)-calanolide B (CHEBI:65553) is a secondary alcohol (CHEBI:35681)
IUPAC Name
(10S,11R,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
Synonyms Sources
(+)-(10S,11R,12S)-10,11-trans-dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-propyl-2H,6H-benzo[1,2-b:3,4-b':5,6-b'']tripyran-2-one ChEBI
(10S,11R,12S)-11,12-dihydro-12-hydroxy-6,6,10,11-tetramethyl-4-propyl-2H,6H,10H-benzo(1,2-b:3,4-b':5,6-b'')tripyran-2-one ChEBI
costatolide ChEBI
Manual Xref Database
WO9932492 Patent
View more database links
Registry Numbers Types Sources
7257193 Reaxys Registry Number Reaxys
909-14-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10428899 PubMed citation Europe PMC
11142630 PubMed citation Europe PMC
15340243 PubMed citation Europe PMC
9784162 PubMed citation Europe PMC
9934455 PubMed citation Europe PMC
Last Modified
25 March 2015