Biomedical subjects

Consolacion Y Ragasa

Publications and source records attributed to Consolacion Y Ragasa.

8 recordsLinked to original sources

PubMed2005

Monoterpene lactones from the seeds of Nephelium lappaceum.

Dichloromethane extracts of the seeds of Nephelium lappaceum afforded two new diastereomeric monoterpene lactones, 1 and 2, and the known butenolide siphonodin (3), as well as kaempferol 3-O-beta-D-glucopyranoside-7-O-alpha-L-rhamnopyranoside. Compounds 1 and 2 represent a new monoterpene skeleton, and their structures were elucidated by extensive 1D and 2D NMR spectral data interpretation. Antimicrobial testing was carried out on 1 and 2 against a panel of bacteria and fungi.

Anti-Bacterial Agents↗

PubMed2005

Terpenoids and sterols from Lagerstroemia speciosa.

The leaves of Lagerstroemia speciosa afforded a new natural product, 31-norlargerenol acetate (4), along with known compounds 24-methylenecycloartanol acetate (1), its 31-nor analog (2), largerenol acetate (3), tinotufolins C (5) and D (6), lutein, phytol, sitosterol and sitosterol acetate. The structure of 4 was elucidated by 1D and 2D NMR and mass spectroscopy.

Lagerstroemia↗

PubMed2005

Antimicrobial terpenoids from Pterocarpus indicus.

A mixture of loliolide 1 (> 85%) and paniculatadiol 2 (< 15%) was obtained from the ethyl acetate leaf extract of Pterocarpus indicus by silica gel chromatography, while the air-dried flowers afforded lupeol 3 and phytol esters 4. The structures of 1-4 were determined by NMR spectroscopy. Antimicrobial tests on a mixture of 1 and 2 indicated that it has moderate activity against Candida albicans and low activity against Pseudomonas aeruginosa, Escherichia coli, and Aspergillus niger. It was found inactive against Staphylococcus aureus, Bacillus subtilis, and Trichophyton mentagrophytes.

Anti-Infective Agents↗

PubMed2005

Antifungal metabolites from Blumea balsamifera.

The leaves of Blumea balsamifera afforded icthyothereol acetate, cryptomeridiol, lutein, and beta-carotene. The structures of icthyothereol acetate (1) and cryptomeridiol (2) were elucidated by extensive 1D and 2D NMR spectroscopy, while those of lutein and beta-carotene were identified by comparison with literature data. Antimicrobial tests indicated that 1 has moderate activity against the fungi Aspergillus niger, Trichophyton mentagrophytes, and Candida albicans, while 2 has low activity against A. niger, T. mentagrophytes, and C. albicans. Both compounds have no antimicrobial activity against Psuedomonas aeruginosa, Staphylococcus aureus, Bacillus subtilis, and Escherichia coli.

Alkynes↗

PubMed2004

New cycloartenol esters from Ixora coccinea.

The air-dried flowers of Ixora coccinea L. afforded two new cycloartenol esters (1a and 1b), lupeol fatty ester, lupeol, ursolic acid, oleanolic acid, and sitosterol. The structures of 1a and 1b were elucidated by extensive 1D and 2D NMR spectroscopy and MS.

Esters↗

PubMed2003

A new furanoid diterpene from Caesalpinia pulcherrima.

A new cassane-type diterpene isovouacapenol E (1) was isolated from the leaves of Caesalpinia pulcherrima, together with the known compounds caesaldekarin A (3), spathulenol (4), caryophyllene oxide (5), phytol, and sitosterol. The structure of 1 was elucidated by spectral data interpretation.

Caesalpinia↗

PubMed2002

New furanoid diterpenes from Caesalpinia pulcherrima.

Four new cassane-type furanoditerpenoids (1-4) were isolated from the air-dried leaves of Caesalpinia pulcherrima. Their structures were elucidated by spectral data interpretation. The exocyclic methylene compound 1 readily isomerized and oxidized to the benzofuran 4. Benzyl 2,6-dimethoxybenzoate (5) was also identified in this study. Antimicrobial tests on 1-5 indicated that they were active against several bacteria (S. aureus, E. coli, P. aeruginosa, and B. subtilis) and fungi (C. albicans and T. mentagrophytes).

Anti-Bacterial Agents↗

PubMed2002

Ionone derivatives from Alternanthera sessilis.

The chloroform extract of the air-dried leaves of Alternanthera sessilis afforded a mixture of diastereomers of a new ionone derivative 1 whose structures were elucidated by extensive 1D and 2D NMR spectroscopy and mass spectrometry. Oxidative cleavage of 1 to aldehyde 3 with manganese dioxide confirmed diastereoisomerism arose from a racemic side chain chiral centre. Antimicrobial tests on the mixture of diastereomers and the derivative indicated that they have low activities against Pseudomonas aeruginosa and Trichophyton mentagrophytes.

Amaranthaceae↗