<span style="font-size:11.0pt;mso-bidi-font-size: 10.0pt;font-family:"Times New Roman";mso-fareast-font-family:"Times New Roman"; mso-ansi-language:EN-US;mso-fareast-language:EN-US;mso-bidi-language:AR-SA" lang="EN-US">A phyto-pharmacological overview on <i>Physalis minima</i> Linn.</span>

477-482Physalis minima Linn. (Family <span style="font-family:Symbol;mso-ascii-font-family: " times="" new="" roman";mso-hansi-font-family:"times="" roman";mso-char-type:symbol;="" mso-symbol-font-family:symbol"="" lang="EN-GB">¾ Solanaceae) is commonly known as Ground Cherry or Sunberry. It is traditionally used as diuretic, purgative, analgesic, anthelmentic, febrifuge, vermifuge, abortificient, etc. Many steroidal lactones have been identified from the plant and it has been reported to possess antifertility, hypoglycemic, cytotoxic, antiulcer, antibacterial, anti-inflammatory, analgesic, antipyretic, antimalarial, amylase, lipase and alpha glucosidase inhibitor activity and anti-gonorrhoeal activity. Present review summarizes the traditional claims, phytochemistry and pharmacology of P. minima reported so far in scientific literature. </span

Anti-hyperlipidemic effect of carcia papaya L in sprague dawley rats

No Abstract.Nigerian Journal of Natural Products and Medicine Vol. 10 () 2006: pp.69-7

Oxidative cyanide-free cyanation on arylboronic acid derivatives using aryl/heteroaryl thiocyanate using novel IL-PdCl₄ catalyst under mild condition

<p>An efficient and simple method is reported for the cyanation on arylboronic acid using various simple/indole thiocyanates using a new IL-PdCl₄ catalyst. The cascade process involves a coupling reaction without any additive to give a wide range of cyanide derivatives. Cyanation on various arylboronic acids underwent smoothly affording the corresponding arylnitriles in good to high yields.</p

Novel Pyranopyrazoles: Synthesis and Theoretical Studies

A series of pyranopyrazoles, namely, 7-(2-aminoethyl)-3,4-dimethyl-1-phenyl-1&lt;em&gt;H&lt;/em&gt;-pyrazolo[3,4-b]pyridin-6(7&lt;em&gt;H&lt;/em&gt;)-one (&lt;strong&gt;2&lt;/strong&gt;), (&lt;em&gt;Z&lt;/em&gt;)-3,4-dimethyl-1-(4-((4-nitrobenzylidene)amino)phenyl)pyrano[2,3-c]pyrazol-6(1&lt;em&gt;H&lt;/em&gt;)-one (&lt;strong&gt;5&lt;/strong&gt;), 1-(4-(3,4-dimethyl-6-oxopyrano[2,3-c]pyrazol-1(6&lt;em&gt;H&lt;/em&gt;)-yl)phenyl)-3-(naphthalen-1-yl)urea (&lt;strong&gt;6&lt;/strong&gt;), (&lt;em&gt;Z&lt;/em&gt;)-ethyl 4-((3,4-dimethyl-6-oxo-1,6-dihydropyrano[2,3-c]pyrazol-5-yl)diazenyl)benzoate (&lt;strong&gt;8&lt;/strong&gt;) and 3,4-dimethyl-&lt;em&gt;N&lt;/em&gt;-(naphthalen-1-yl)-6-oxopyrano[2,3-c]pyrazole-1(6H)-carboxamide (&lt;strong&gt;9&lt;/strong&gt;) were synthesized and characterized by means of their UV-VIS, FT-IR, &lt;sup&gt;1&lt;/sup&gt;H-NMR and &lt;sup&gt;13&lt;/sup&gt;C-NMR spectral data. Density Functional Theory calculations of the synthesized pyranopyrazoles were performed using molecular structures with optimized geometries. Molecular orbital calculations have provided detail description of the orbitals, including spatial characteristics, nodal patterns, and the contributions of individual atoms