SPECTROSCOPIC DETERMINATION OF TOTAL PHENOL AND FLAVONOID CONTENTS OF CITRUS LIMON PEEL FROM NORTH EASTERN REGION OF INDIA

Citrus fruit plants are valuable sources of phenolic and other biologically active compounds.  Phenolic compounds have been reported to have multiple biological effects. In this paper quantitative determination of phenols and flavonoids of citrus limon peel extracts was carried out using spectrophotometric method. The plant material was collected from Assam, north-eastern region of India. Total phenolic content was determined by Folin-Ciocalteau method and aluminium chloride method was used for flavonoid determination. Methanol and ethanol extracts of ripe and unripe peel of the plant contain high amount of phenol contents compared to acetone and ethyl acetate extracts. Methanol extract contains maximum and the ethyl acetate shows minimum amount of flavonoid contents. However, all the extracts show significant results. Key Words: Citrus limon, Phenol, Flavonoid, Catechol and Quercetin.Â

Identification of Metals Found in the Leaves of Tabernaemontana alternifolia

Abstract: Tabernaemontana alternifolia, an Ayurvedic medicinal plant is found in the western ghats of Maharashtra. The leaves, roots, bark-stem are used in Ayurvedic system of medicines. Leaves are used in the form of churna/extract or in combination with the other plant materials in their formulations. It is administered orally. Metal analysis of the leaves of Tabernaemontana alternifolia shows a high percentage of metals like magnesium, calcium, iron, copper and manganese. The present results will prove to be useful in understanding the role of metal ions in the biogenesis of the secondary metabolites of the medicinally important plant

Role of Metal Ions in Reactions of ɑ-Bornane-2, 3-dione with Diamines

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Efficacy of 4-methyl-7-hydroxy coumarin derivatives against vectors <i style="">Aedes aegypti </i>and <i>Culex quinquefasciatus</i>

788-7924-Methyl-7-hydroxy coumarin is considered as a lead molecule as a biopesticide. Its mono bromo and tribromo derivatives were synthesized. Two more derivatives were synthesized by acylation. Compound 1 (3,6,8-tribromo-7-hydroxy-4-methyl-chromen-2-one) was found to be the most potent against IVth instar larvae of C. quinquefasciatus and A. aegypti the LC50 being 1.49 and 2.23 ppm respectively. It showed 100% larval mortality at 25 ppm against A. aegypti and at 10 ppm against C. quinquefasciatus. Compounds 1 and 2 (3,6,8-tribromo-7-hydroxy-4-methyl-chromen-2’-oxo-2H-chromen-7-yl acetate) showed remarkable ovicidal activity. Significant reduction of 80-85% hatching of eggs of both mosquito species was observed at the highest dose of 100 ppm. The hatched larvae showed 100% mortality in the successive instars. Compounds 3 and 4 (3-bromo-7-hydroxy-4-methyl-chromen-2-one and 3-bromo-4-methyl-2’-oxo-2H-chromen-7-yl acetate) showed moderate activity against both mosquito species