Abstract
Bioassay-guided fractionation of the cell extract of the insect pathogenic fungus
Aschersonia tubulata BCC 1785 led to the isolation of dustanin (1), 3β,15α,22-trihydroxyhopane (3), 5α,8α-epidioxy-24(R)-methylcholesta-6,22-diene-3β-ol (6), together with the new 3β-acetoxy-15α,22-dihydroxyhopane (4). Chemical structures of these compounds were elucidated by spectral analyses as
well as chemical transformation. Compounds 1 and 4 exhibited antimycobacterial activity with the minimum inhibitory concentration (MIC)
of 12.5 μg/ml.
References
- 1
Tsuda Y, Isobe K.
A new pentacyclic triterpenoid as a fungal metabolite.
Tetrahedron Letters.
1965;
3337-43
- 2
Corbett R E, Young H.
Lichens and fungi. Part III. Structural elucidation of 15α,22-dihydroxyhopane from
Sticta billardierii Del.
J. Chem. Soc. (C).
1966;
1564-7
- 3
Van Eijk G W, Roeijmans H J, Seykens D.
Hopanoids from the entomogenous fungus Aschersonia aleyrodis
.
Tetrahedron Letters.
1986;
27
2533-4
- 4
Takahashi R, Tanaka O, Shibata S.
Occurrence of 15α-acetoxy-22-hydroxyhopane and phlebic acid A in the lichen, Peltigera aphthosa
.
Phytochemistry.
1969;
8
2345-9
- 5
Sheffer M, Fried A, Gottlieb H E, Tietz A, Avron M.
Lipid composition of the plasma membrane of the halotolerant alga, Dunaliella salina
.
Biochim. Biophys. Acta.
1986;
857
165-72
- 6
Collins L, Franzblau S G.
Microplate alamar blue assay versus BACTEC 460 system for high-throughput screening
of compounds against Mycobacterium tuberculosis and Mycobacterium avium
.
Antimicrobial Agents and Chemotherapy.
1997;
4
1004-9
- 7
Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren J T, Bokesch H,
Kenney S, Boyd M R.
New colorimetric cytotoxicity assay for anticancer-drug screening.
Journal of National Cancer Institute.
1990;
82
1107-12
- 8
Cantrell C L, Rajab M S, Franzblau S G, Fronczek F R, Fischer N H.
Antimycobacterial ergosterol-5,8-endoperoxide from Ajuga remota
.
Planta Medica.
1999;
65
732-4
- 9
Cantrell C L, Lu T, Fronczek F R, Fischer N H, Adams L B, Franzblau S G.
Antimycobacterial cycloartanes from Borrichia frutescens
.
J. Nat. Prod..
1996;
59 (12)
1131-6
- 10
Cantrell C L, Rajab M S, Franzblau S G, Fischer N H.
Antimycobacterial triterpenes from Melia volkensii
.
J. Nat. Prod..
1999;
62 (4)
546-8
- 11
Fischer N H, Lu T, Cantrell C L, Castañeda-Acosta J, Quijano L, Franzblau S G.
Antimycobacterial evaluation of germacranolides.
Phytochemistry.
1998;
49 (2)
559-64
- 12
Cantrell C L, Abate L, Fronczek F R, Franzblau S G, Quijano L, Fischer N H.
Antimycobacterial Eudesmanolides from Inula helenium and Rudbeckia subtomentosa
.
Planta Medica.
1999;
65 (4)
351-5
- 13
Rajab M S, Cantrell C L, Franzblau S G, Fischer N H.
Antimycobacterial activity of (E)-phytol and derivatives: a preliminary structure-activity study.
Planta Medica.
1998;
64 (1)
2-4
- 14
Lu T, Cantrell C L, Robbs S L, Franzblau S G, Fischer N H.
Antimycobacterial matricaria esters and lactones from Astereae species.
Planta Medica.
1998;
64 (7)
665-7
Dr. Prasat Kittakoop
National Center for Genetic Engineering and Biotechnology
National Science and Technology Development Agency
73/1, Rama VI Road
Bangkok 10400
Thailand
Email: prasat@biotec.or.th
Fax: +66-2-6448107