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<title>06. Shree Manibhai Virani and Smt. Navalben Virani Science College (Autonomous)</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/239" rel="alternate"/>
<subtitle>Sister Institute on the campus Affiliated to Saurashtra University, Rajkot</subtitle>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/239</id>
<updated>2026-05-10T15:05:43Z</updated>
<dc:date>2026-05-10T15:05:43Z</dc:date>
<entry>
<title>Synthesis, Characterization and Biological Evaluation of Ethyl-4'-(cyclopropane carboxamido-N-yl)-5-ary-3-oxo-3,4,5,6- tetrahydro-biphenyl-4-carboxylate</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/2205" rel="alternate"/>
<author>
<name>Akbari, P.M</name>
</author>
<author>
<name>Shah, V.R.</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/2205</id>
<updated>2025-01-01T11:26:08Z</updated>
<published>2019-01-01T00:00:00Z</published>
<summary type="text">Synthesis, Characterization and Biological Evaluation of Ethyl-4'-(cyclopropane carboxamido-N-yl)-5-ary-3-oxo-3,4,5,6- tetrahydro-biphenyl-4-carboxylate
Akbari, P.M; Shah, V.R.
A series of new substituted cyclohexenone derivatives have been&#13;
synthesized by the reaction of various substituted chalcones with&#13;
ethylacetoacetate. Some new N-(4-(3-aryl-acryloyl)phenyl)cyclopropane&#13;
carboxamide were prepared by Claisen-Schmidt condensation&#13;
method in presence of sodium hydroxide in ethanol solvent under&#13;
stirring. The synthesized compounds were characterized by their&#13;
spectral (IR, NMR, Mass) data and screened for their antimicrobial&#13;
activities against Gram-positive and Gram-negative bacteria by using&#13;
standard antimicrobial drugs.
</summary>
<dc:date>2019-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Synthesis, Characterization and in vitro Antimicrobial Evaluation of Pyrazole Based Oxothiazolidine Hybrids</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/2194" rel="alternate"/>
<author>
<name>Sanghani, Yogesh J.</name>
</author>
<author>
<name>Koradiya, Suresh B.</name>
</author>
<author>
<name>Jilariya, Krushnakumar J.</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/2194</id>
<updated>2025-01-01T10:58:27Z</updated>
<published>2020-01-01T00:00:00Z</published>
<summary type="text">Synthesis, Characterization and in vitro Antimicrobial Evaluation of Pyrazole Based Oxothiazolidine Hybrids
Sanghani, Yogesh J.; Koradiya, Suresh B.; Jilariya, Krushnakumar J.
In this work, pyrazole based oxothiazolidine hybrids, 4-{4-[2-(1-&#13;
phenyl-3-(substituted)phenyl-1H-pyrazol-4-yl)-4-oxo-thiazolidin-3-&#13;
yl]-phenyl}-morpholin-3-one (11a-l) were synthesized using molecular&#13;
hybridization approach through Vilsmeier-Haack reaction. The titled&#13;
compounds 11a-l were characterized by using elemental analysis, IR,&#13;
1H NMR and mass spectral studies. The antibacterial activity of 11a-l&#13;
was evaluated in vitro by agar cup plate method against B. cocous, B.&#13;
subtillis, E. coli and P. vulgaris. The antifungal activity of compounds&#13;
11a-l was evaluated in vitro by agar based disk diffusion method&#13;
against A. niger. The results of antibacterial and antifungal evaluation&#13;
were reported in terms of zone of inhibition measured in mm. The&#13;
synthesized compounds 11a-l exhibited moderate to good antibacterial&#13;
and antifungal potential. Compound 4-{4-[2-(1-phenyl-3-(2-methoxyphenyl)&#13;
phenyl-1H-pyrazol-4-yl)-4-oxo-thiazolidin-3-yl]-phenyl}-&#13;
morpholin-3-one (11h) emerged as a most potent antimicrobial agent&#13;
displaying zone of inhibition 21, 20, 21, 24 and 20 mm against B.&#13;
cocous, B. subtillis, E. coli, P. vulgaris and A. niger, respectively.
</summary>
<dc:date>2020-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Isolation and screening of moderate halophiles for industrially important hydrolytic enzymes</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/998" rel="alternate"/>
<author>
<name>Lungariya, Amisha</name>
</author>
<author>
<name>Mehta, Hemangi</name>
</author>
<author>
<name>Patadia, Apexa</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/998</id>
<updated>2023-05-18T02:33:41Z</updated>
<published>2015-08-01T00:00:00Z</published>
<summary type="text">Isolation and screening of moderate halophiles for industrially important hydrolytic enzymes
Lungariya, Amisha; Mehta, Hemangi; Patadia, Apexa
Halophiles are the salt loving organisms, which are found to survive in wide range of salt concentration. Based on their salt &#13;
requirement, halophiles are categorized into different categories; 1. Slight, 2. Moderate, 3. Extreme. Moderate halophiles &#13;
were isolated from Jamnagar Vadinar Bandar area. Total 16 isolates were obtained on N-agar plates containing various &#13;
salt concentrations. These organisms were exploited for various hydrolytic enzyme activity i.e.; amylase, lipase, caseinase &#13;
etc. Among 16 isolates, 9 were amylase positive, 12 were lipase positive, 13 were caseinase positive. Identification of these &#13;
isolates was on the basis of morphology, physiology, biochemical activity. Further research on purification of one of these &#13;
enzymes is in progress.
</summary>
<dc:date>2015-08-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Steroid and fatty acid contents from  the leaves of Carica Papaya</title>
<link href="http://10.9.150.37:8080/dspace//handle/atmiyauni/990" rel="alternate"/>
<author>
<name>Devmurari, Vishvraj V.</name>
</author>
<author>
<name>Patel, Poojaben P.</name>
</author>
<author>
<name>Jadeja, Rajeshreeba A.</name>
</author>
<author>
<name>Bhadaniya, Cameykumari P.</name>
</author>
<author>
<name>Aghara, Priti P.</name>
</author>
<author>
<name>Patel, Anilkumar S.</name>
</author>
<author>
<name>Tala, Satishkumar D.</name>
</author>
<author>
<name>Savant, Mahesh M.</name>
</author>
<author>
<name>Ladva, Kartik D.</name>
</author>
<author>
<name>Nariya, Pankajkumar B.</name>
</author>
<id>http://10.9.150.37:8080/dspace//handle/atmiyauni/990</id>
<updated>2023-05-17T05:07:47Z</updated>
<published>2021-06-30T00:00:00Z</published>
<summary type="text">Steroid and fatty acid contents from  the leaves of Carica Papaya
Devmurari, Vishvraj V.; Patel, Poojaben P.; Jadeja, Rajeshreeba A.; Bhadaniya, Cameykumari P.; Aghara, Priti P.; Patel, Anilkumar S.; Tala, Satishkumar D.; Savant, Mahesh M.; Ladva, Kartik D.; Nariya, Pankajkumar B.
Aim: To extract and identify the non-polar entities from the leaves of Carica papaya, a plant used for medicinal purpose as folk medicine.&#13;
Materials and methods: Petroleum ether extract of the Carica papaya leaves was used for this study. Saponification process and &#13;
methylation process was performed to separate fatty acids and unsaponifiable matters. Phytochemical constituents were separated using &#13;
chemical process and separated fractions were analyzed by thin layer chromatography (TLC) and gas chromatography coupled with &#13;
mass spectroscopy (GC-MS).&#13;
Results: The chemical composition of the steroids, triterpenoids and fatty acid methyl esters (FAMEs) in leaves of Carica papaya, &#13;
which were analyzed by gas chromatography coupled with mass spectroscopy (GC-MS). A total of 15 fatty acid components were &#13;
identified in saponifiable matter, from unsaponifiable portion 2 steroids (campesterol, β- or γ-sitosterol), 1 triterpene (squalene), and 1 &#13;
diterpene (phytol) were identified.&#13;
Conclusions: The results indicate that the extract is rich in non-polar compounds. In this study, GC-MS method is at the central focus &#13;
for identification of these phytoconstituents. The current method can be used for direct analysis of non-polar entities of plant material.
We are grateful to the Department of Chemistry, Atmiya &#13;
University and Shri M. &amp; N. Virani Science College, Rajkot &#13;
for providing laboratory and other required facilities.
</summary>
<dc:date>2021-06-30T00:00:00Z</dc:date>
</entry>
</feed>
