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1.
J Ethnopharmacol ; 103(2): 297-301, 2006 Jan 16.
Article in English | MEDLINE | ID: mdl-16310995

ABSTRACT

The antibacterial activity of Haplopappus uncinatus is attributed to a new clerodane diterpenoid, 18-acetoxy-cis-cleroda-3-en-15-oic acid (10 betaH, 16 xi 19 beta, 17beta, 20 alpha form) (1), isolated as a major component from the resinous exudates of its twigs and leaves, together with the inactive 3,5-dihydroxy-6,7,3',4'-tetramethoxyflavone, n-alkanes and a few sesquiterpenoids.


Subject(s)
Anti-Infective Agents/chemistry , Diterpenes/chemistry , Haplopappus , Plant Extracts/chemistry , Anti-Infective Agents/isolation & purification , Diterpenes/isolation & purification , Microbial Sensitivity Tests , Plant Extracts/isolation & purification , Structure-Activity Relationship
2.
Carbohydr Res ; 338(12): 1309-12, 2003 Jun 16.
Article in English | MEDLINE | ID: mdl-12791284

ABSTRACT

The content of kappa, iota and lambda carrageenan in mixtures was determined by application of FT-IR spectroscopy combined with partial least-squares multivariate regression (PLS). This method allows the determination of the relative amounts of the different carrageenans in a rapid and accurate manner.


Subject(s)
Carrageenan/analysis , Spectroscopy, Fourier Transform Infrared/methods , Calibration , Carrageenan/chemistry , Disaccharides/analysis , Least-Squares Analysis , Magnetic Resonance Spectroscopy , Molecular Structure , Multivariate Analysis
3.
J Nat Prod ; 62(2): 381-2, 1999 Feb.
Article in English | MEDLINE | ID: mdl-10075795

ABSTRACT

Two new acylated flavonoids have been isolated from the resinous exudates of Pseudognaphalium robustum and Pseudognaphalium cheirantifolium. Their structures were elucidated by high-resolution spectroscopic methods as 5,7,8-trihydroxy-3-methoxyflavone 8-O-[(E)-2-methyl-2-butenoate] (1) and 5,7,8-trihydroxy-3, 6-dimethoxyflavone 8-O-[(E)-2-methyl-2-butenoate] (2).

4.
J Ethnopharmacol ; 62(3): 251-4, 1998 Oct.
Article in English | MEDLINE | ID: mdl-9849637

ABSTRACT

The antimicrobial properties of the resinous exudate from twigs and leaves of Eupatorium salvia were tested against five gram-negative and five gram-positive bacteria. Comparison of the antimicrobial activities of 7-hydroxy-8(17)-labden-15-oic acid (salvic acid) and of its acetate, both compounds isolated from the plant, with that of the crude extract suggested that the latter ester derivative was the major active component in the exudate. These results validate the vernacular medicinal use of Eupatorium salvia as an antiseptic agent.


Subject(s)
Anti-Bacterial Agents/pharmacology , Asteraceae/chemistry , Diterpenes/pharmacology , Plant Extracts/pharmacology , Ampicillin/pharmacology , Chloramphenicol/pharmacology , Colony Count, Microbial , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , In Vitro Techniques , Tetracycline/pharmacology
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