Dihydropyrenophorin

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Dihydropyrenophorin
Category Others
Catalog number BBF-04890
CAS 1073287-13-4
Molecular Weight 310.34
Molecular Formula C16H22O6
Purity >95% by HPLC

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Description

Dihydropyrenophorin is a macrolide produced by Drechslera avenae. It is the pathogen of oat leaf spot. Dihydropyrenophorin has antifungal activity.

Specification

Synonyms 13S-hydroxy-8R,16R-dimethyl-1,9-dioxacyclohexadeca-3E,11E-diene-2,5,10-trione
Storage Store at -20°C
IUPAC Name (3E,8R,11E,13S,16R)-13-hydroxy-8,16-dimethyl-1,9-dioxacyclohexadeca-3,11-diene-2,5,10-trione
Canonical SMILES CC1CCC(C=CC(=O)OC(CCC(=O)C=CC(=O)O1)C)O
InChI InChI=1S/C16H22O6/c1-11-3-5-13(17)8-10-16(20)22-12(2)4-6-14(18)7-9-15(19)21-11/h7-13,17H,3-6H2,1-2H3/b9-7+,10-8+/t11-,12-,13+/m1/s1
InChI Key BKJDRLKIIICLOD-CEBWGLJESA-N

Properties

Boiling Point 565.5±50.0°C at 760 mmHg
Density 1.112±0.06 g/cm3 (Predicted)
Solubility Soluble in methanol, DMSO

Reference Reading

1. Antifungal metabolites from fungal endophytes of Pinus strobus
Mark W Sumarah, Julie R Kesting, J David Miller, Dan Sørensen Phytochemistry . 2011 Oct;72(14-15):1833-7. doi: 10.1016/j.phytochem.2011.05.003.
The extracts of five foliar fungal endophytes isolated from Pinus strobus (eastern white pine) that showed antifungal activity in disc diffusion assays were selected for further study. From these strains, the aliphatic polyketide compound 1 and three related sesquiterpenes 2-4 were isolated and characterized. Compound 2 is reported for the first time as a natural product and the E/Z conformational isomers 3 and 4 were hitherto unknown. Additionally, the three known macrolides; pyrenophorol (5), dihydropyrenophorin (6), and pyrenophorin (7) were isolated and identified. Their structures were elucidated by spectroscopic analyses including 2D NMR, HRMS and by comparison to literature data where available. The isolated compounds 1, 2, and 5 were antifungal against both the rust Microbotryum violaceum and Saccharomyces cerevisae.

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