Abstract

Eight new <i>neo</i>-clerodane\nditerpenoids (<b>1</b>–<b>8</b>) were acquired\nfrom the aerial parts of <i>Ajuga pantantha</i>. Spectroscopic\ndata analysis permitted the\ndefinition of their structures, and experimental and calculated electronic\ncircular dichroism data were used to define their absolute configurations.\nCompounds <b>2</b> and <b>4</b>–<b>8</b> were\nfound to have NO inhibitory effects with IC<sub>50</sub> values of\n20.2, 45.5, 34.0, 27.0, 45.0, and 25.8 μM, respectively. The\nmore potent compounds <b>2</b>, <b>6</b>, and <b>8</b> were analyzed to establish their anti-inflammatory mechanism, including\nregulation of the expression of inducible nitric oxide synthase (iNOS)\nand cyclooxygenase-2 (COX-2) proteins as well as their binding interactions\nwith the two proteins.

Keywords:
Nitric oxide synthase Circular dichroism Nitric oxide Enzyme Inhibitory postsynaptic potential

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Topics

Wheat and Barley Genetics and Pathology
Life Sciences →  Agricultural and Biological Sciences →  Plant Science
Genetic diversity and population structure
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Genetics
Chromosomal and Genetic Variations
Life Sciences →  Agricultural and Biological Sciences →  Plant Science

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JOURNAL ARTICLE

<i>neo-</i>Clerodane Diterpenoids from <i>Ajuga bracteosa</i>

Amaya Castro (1452040)Josep Coll (5054)Mohammad Arfan (683671)

Journal:   OPAL (Open@LaTrobe) (La Trobe University) Year: 2016
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