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1.
Acta Pharmaceutica Sinica ; (12): 364-366, 2012.
Article in English | WPRIM | ID: wpr-323035

ABSTRACT

One new sesquiterpene was isolated from the fermentation broth of Streptomyces sp. and the structure was elucidated by spectral analysis as caryolane-1, 6beta-diol (1). An intermediate 1alpha, 6beta, 11-eudesmanetriol (2) in the biosynthesis of geosmin was also found in this strain which proved sequence for the reactions, especially bicyclization preceding dealkylation.


Subject(s)
Magnetic Resonance Spectroscopy , Molecular Structure , Naphthols , Chemistry , Sesquiterpenes , Chemistry , Streptomyces , Chemistry
2.
China Journal of Chinese Materia Medica ; (24): 337-339, 2003.
Article in Chinese | WPRIM | ID: wpr-272862

ABSTRACT

<p><b>OBJECTIVE</b>[corrected] To study the cyclic peptides from Psammosilene tunicoides.</p><p><b>METHOD</b>The constituents were separated and purified with chromatographic methods, identified by NMR, MS, UV and IR.</p><p><b>RESULT</b>Three cyclic dipeptides: cyclo(-Pro-Val-) (1), cyclo(-Pro-Ala-) (2) and cyclo(-Pro-Pro-) (3), were isolated and identified.</p><p><b>CONCLUSION</b>Compound 1 and 2 are new natural products, compound 3 was isolated for the first time from Psammosilene tunicoides.</p>


Subject(s)
Caryophyllaceae , Chemistry , Dipeptides , Chemistry , Molecular Structure , Peptides, Cyclic , Chemistry , Plant Roots , Chemistry , Plants, Medicinal , Chemistry
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