| 000 -LEADER |
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a |
| 003 - CONTROL NUMBER IDENTIFIER |
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OSt |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
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| control field |
20211222131151.0 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
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211222b xxu||||| |||| 00| 0 eng d |
| 040 ## - CATALOGING SOURCE |
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| Original cataloging agency |
AIKTC-KRRC |
| Transcribing agency |
AIKTC-KRRC |
| 100 ## - MAIN ENTRY--PERSONAL NAME |
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| 9 (RLIN) |
14972 |
| Author |
Karumanchi, Srikanth Kumar |
| 245 ## - TITLE STATEMENT |
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| Title |
Design, Synthesis, Hypoglycemic Activity and Molecular Docking Studies of 3-substituted-5- [(furan-2-yl)-methylene]-thiazolidine-2,4-dione Derivatives |
| 250 ## - EDITION STATEMENT |
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| Volume, Issue number |
Vol.55(1), Jan-Mar |
| 260 ## - PUBLICATION, DISTRIBUTION, ETC. |
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| Place of publication, distribution, etc. |
Karnataka |
| Name of publisher, distributor, etc. |
Association of Pharmaceutical Teachers of India (APTI) |
| Year |
2021 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Pagination |
266-275p. |
| 520 ## - SUMMARY, ETC. |
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| Summary, etc. |
Background: From the wide range of previous literature studies indicated that thiazolidinedione’s reacts with substituted benzaldehydes undergoes knoevenagel condensation gives respective arylidene derivatives. In our attempt all the titled compounds were designed and developed by replacement of substituted benzaldehydes with furan- 2-aldehyde, so that furan moiety was introduced in the molecule. Materials and Methods: 5-[(furan-2-yl)-methylene]-thiazolidine-2,4-dione was prepared via knoevenagel condensation by the reaction of thiazolidine-2,4-dione and furfural. Further it was coupled with various alkyl/ aryl halides in alcoholic potassium hydroxide to produce various derivatives 2a-2j. The titled compounds furthermore prepared by microwave assisted synthesis technique. Synthesized compounds were analysed by physical and spectral characterization methods. Developed furan bearing thiazolidine-2,4-diones were evaluated for in-vivo hypoglycemic property. Molecular docking analysis was carried out to observe the binding interaction of designed ligands at PPARγ target receptor protein. Results and Conclusion: Microwave irradiation technique produced high yield at less reaction time in comparison with traditional conventional method. In-vivo hypoglycemic activity evaluation revealed that, electron releasing groups (-OH and –OCH3) containing compounds 2d and 2g found to possess significant activity in acute study as well as in chronic study. Even the molecular docking studies at PPARγ receptor protein (PDB ID- 2PRG), electron releasing groups containing compounds 2d and 2g exhibit significant binding affinity having high binding energy of -9.02 kcal/mol and -8.61 kcal/mol when compared with standard ligand rosiglitazone. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| 9 (RLIN) |
4639 |
| Topical term or geographic name entry element |
PHARMACEUTICS |
| 700 ## - ADDED ENTRY--PERSONAL NAME |
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| 9 (RLIN) |
14973 |
| Co-Author |
Rao, Atmakuri Lakshmana |
| 773 0# - HOST ITEM ENTRY |
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| Place, publisher, and date of publication |
Bengluru Association of Pharmaceutical Teachers of India (APTI) |
| International Standard Serial Number |
0019-5464 |
| Title |
Indian journal of pharmaceutical education and research |
| 856 ## - ELECTRONIC LOCATION AND ACCESS |
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| URL |
https://www.ijper.org/sites/default/files/IndJPhaEdRes_55_1_266.pdf |
| Link text |
Click here |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
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| Source of classification or shelving scheme |
|
| Koha item type |
Articles Abstract Database |
