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. Macrae, C.F., Bruno, I.J., Chisholm, J.A., Edgington, P.R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. and Wood, P.A. (2008) Mercury CSD 2.0—New Features for the Visualization and Investigation of Crystal Structures. Journal Applied Crystallography, 41, 466-470.
http://dx.doi.org/10.1107/S0021889807067908
has been cited by the following article:
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TITLE:
Synthesis, Molecular Structure and Anti-Onchocercal Studies of 1-(Phthalazin-1(2H)-one)[(Pyridin-2-yl)ethylidene]hydrazone
AUTHORS:
Joseph N. Yong, Felicite Majoumo-Mbe, Moses Samje, Emmanuel N. Nfor
KEYWORDS:
Hydralazine Hydrochloride, Schiff Bases, Anti-Onchocercal Activity
JOURNAL NAME:
International Journal of Organic Chemistry,
Vol.6 No.1,
March
30,
2016
ABSTRACT: The novel ligand, 1-(phthalazin-1(2H)-one)[(pyridin-2-yl)ethylidene]hydrazone,(APN), derived from the antihypertensive drug, hydralazine hydrochloride, was synthesized and characterized by spectroscopic methods (IR, 1H NMR). The X-ray crystallographic data indicates that APN has an exocyclic C=N bond on the hydralazine moiety. APN revealed significant anti-onchocercal activity with IC50 values of 0.3125 μg/mL on microfilaria and 10 μg/mL on adult worms compared to the standard drug, ivermectin.