@article { ISI:000287374800008,
	title = {Phytochemical investigation of artemisia pallens},
	journal = {Helvetica Chimica Acta},
	volume = {94},
	number = {1},
	year = {2011},
	month = {JAN},
	pages = {73-77},
	publisher = {WILEY-BLACKWELL},
	address = {COMMERCE PLACE, 350 MAIN ST, MALDEN 02148, MA USA},
	abstract = {<p>Two new eudesmanolides, pallensin (1) and 4-epipallensin (2), along with a known eudesmanolide, santonin, and a known flavone, 4-epivalgarin, have been isolated from the aerial part of A. pallens. Their structures were established by detailed spectral studies (1D and 2D) and by comparison of their spectroscopic data with those of known compounds.</p>},
	issn = {0018-019X},
	doi = {10.1002/hlca.201000125},
	author = {Ruikar, Anjali D. and Jadhav, Ravindra B. and Phalgune, Usha D. and Rojatkar, Supada R. and Puranik, Vedavati G. and Deshpande, Nirmala R.}
}
@article { ISI:000295422000005,
	title = {Sesquiterpene lactone, a potent drug molecule from artemisia pallens wall with anti-inflammatory activity},
	journal = {Arzneimittel-Forschung-Drug Research},
	volume = {61},
	number = {9},
	year = {2011},
	month = {DEC},
	pages = {510-514},
	publisher = {ECV-EDITIO CANTOR VERLAG MEDIZIN NATURWISSENSCHAFTEN},
	address = {BANDELSTOCKWEG 20, POSTFACH 1255, D-88322 AULENDORF, GERMANY},
	abstract = {<p>The present study was carried out to investigate the anti-inflammatory activities of bioactive secondary metabolites of Artemisia pallens Wall, an aromatic herb from family Asteraceae. The results provide evidence for the topical anti-inflammatory properties of Artemisia pallens Wall. The compounds were isolated from the acetone extract of the plant material. The isolates were tested on Swiss albino mice using 12-O-tetradecanoyl phorbol-13-acetate (TPA) induced ear edema. One of the molecules from the extract indicated potent anti-inflammatory activity equivalent to indometacin (CAS 53-86-1). Elucidation of the molecular structures by single crystal x-ray diffraction studies revealed the conformational differences that the six membered rings in both the molecules are at an angle of 28.79 degrees. Presence of hydroxy function for compound 2 may be responsible for higher potency.</p>},
	keywords = {Anti-inflammatory activity, Artemisia pollens, Asteraceae, Mice, Single crystal x-ray structure},
	issn = {0004-4172},
	author = {Ruikar, Anjali D. and Misar, Ashwini V. and Jadhav, Ravindra B. and Rojatkar, Supada R. and Mujumdar, Arvind M. and Puranik, Vedavati G. and Deshpande, Nirmala R.}
}
@article { ISI:000308519200010,
	title = {Larvicidal potential of mimusops elengi against aedes aegypti (L) and Culex quinquefasciatus (Say)},
	journal = {Journal of Vector Borne Diseases},
	volume = {49},
	number = {2},
	year = {2012},
	month = {JUN},
	pages = {111-113},
	publisher = {MALARIA RESEARCH CENTRE, INDIAN COUNCIL MEDICAL RESEARCH-ICMR},
	address = {22 SHAM NATH MARG, DELHI, 00000, INDIA},
	keywords = {Aedes aegypti, Culex quinquefasciatus, larvicidal activity, Mimusops elengi},
	issn = {0972-9062},
	author = {Ruikar, Anjali D. and Pawar, Pushpa V. and Sen, Avalokiteswar and Phalgune, Usha D. and Puranik, Vedavati G. and Deshpande, Nirmala R.}
}
