Papyracon D

Papyracon D

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Category Bioactive by-products
Catalog number BBF-02362
CAS
Molecular Weight 266.29
Molecular Formula C14H18O5

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Description

It is produced by the strain of Lachnum papyraceum. It has weak effect against nematodes and has inhibitory effect on L1210 and HL60 cells. It also has weak anti-gram-positive bacterial effect.

Specification

IUPAC Name (1aR,3aS,7S,7aS)-3a,7-dihydroxy-2,2-dimethyl-5-(2-oxopropyl)-1a,7-dihydro-1H-cyclopropa[c][1]benzofuran-4-one
Canonical SMILES CC(=O)CC1=CC(C23CC2C(OC3(C1=O)O)(C)C)O
InChI InChI=1S/C14H18O5/c1-7(15)4-8-5-10(16)13-6-9(13)12(2,3)19-14(13,18)11(8)17/h5,9-10,16,18H,4,6H2,1-3H3/t9-,10-,13-,14+/m0/s1
InChI Key ILUWWIMJTKGGNJ-TXFQPVFDSA-N

Properties

Appearance Yellow Oily Matter
Antibiotic Activity Spectrum Gram-positive bacteria; Neoplastics (Tumor); Parasites
Solubility Soluble in Chloroform

Reference Reading

1. New metabolites with nematicidal and antimicrobial activities from the ascomycete Lachnum papyraceum (Karst.) Karst. VIII. Isolation, structure determination and biological activities of minor metabolites structurally related to mycorrhizin A
R Shan, M Stadler, O Sterner, H Anke J Antibiot (Tokyo). 1996 May;49(5):447-52. doi: 10.7164/antibiotics.49.447.
Five new minor metabolites, papyracon D (6), 6-O-methylpapyracon B (9), 6-O-methylpapyracon C (10), lachnumfuran A (11) and lachnumlactone A (12a), together with the known chloromycorrhizinol A (4), have been isolated from extracts of the culture fluids of the ascomycete Lachnum papyraceum. The compounds, which structures were determined by spectroscopic methods, are structurally related to the nematicidal and antibiotic mycorrhizin A (1), which also is produced by the fungus. The nematicidal, antibiotic and cytotoxic activities of the new compounds are weaker compared to those of mycorrhizin A (1). Papyracon D (6) possesses the highest antibiotic activities while lachnumlactone A (12a) is the most nematicidal and cytotoxic.

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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