We have designed, synthesized, and evaluated the physical properties of some high birefringence (Án) isothiocyanato biphenyl-bistolane liquid crystals. These compounds exhibit Án $ 0:7{0:8 at room temperature and wavelength ¼ 633 nm. Laterally substituted short alkyl chains and fluorine atom eliminate smectic phase and lower the melting temperature. The moderate melting temperature and very high clearing temperature make those compounds attractive for eutectic mixture formulation. A eutectic mixture based on those compounds was formulated and its physical properties evaluated. The simulated absorption spectra agree reasonably well with the measured results.
: 1,3-disubstituted aliphatic and aromatic symmetrical and unsymmetrical thioureas were synthesised by novel routes and the antifungal activities of these compounds against two plant pathogens, Pyricularia oryzae and Drechslera oryzae were studied in Czapek-Dox medium at four di †erent concentrations using acetone as the control and the structure-activity relationship among the substituted thioureas is reported.
Prodrugs of (-)-beta-D-(2R,4R)-1,3-dioxolane-2,6-diamino purine (DAPD), organic salts of DAPD, 5'-L-valyl DAPD and N-1 substituted (-)-beta-D-(2R,4R)-1,3-dioxolane guanosine (DXG) have been synthesized with the objective of finding molecules which might be superior to DAPD and DXG in solubility as well as pharmacologic profiles. Synthesized prodrugs were evaluated for anti-HIV activity against HIV-1(LAI) in primary human lymphocytes (PBM cells) as well as their cytotoxicity in PBM, CEM and Vero cells. DAPD prodrugs, modified at the C6 position of the purine ring, demonstrated several folds of enhanced anti-HIV activity in comparison to the parent compound DAPD without increasing the toxicity. The presence of alkyl amino groups at the C6 position of the purine ring increased the antiviral potency several folds, and the most potent compound (-)-beta-D-(2R,4R)-1,3-dioxolane-2-amino-6-aminoethyl purine (8) was 17 times more potent than that of DAPD. 5'-L-Valyl DAPD 20 and organic acid salts 21-24 also exhibited enhanced anti-HIV activity in comparison to DAPD, while DXG prodrugs 16 and 17 exhibited lower potency than that of DXG or DAPD.
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