<p>Cyclo (<em>N<sup>α</sup></em>-dinicotinoyl)-bis-[(L-valinyl)-L-lysinyl acid hydrazide]: Assessment of its Role in Cancer and Kinase Activity Inhibition</p>
Online Publishing @ NISCAIR
View Archive InfoField | Value | |
Authentication Code |
dc |
|
Title Statement |
<p>Cyclo (<em>N<sup>α</sup></em>-dinicotinoyl)-bis-[(L-valinyl)-L-lysinyl acid hydrazide]: Assessment of its Role in Cancer and Kinase Activity Inhibition</p> |
|
Added Entry - Uncontrolled Name |
Amr, A E; Pharmaceutical Chemistry Department, College of Pharmacy, Drug Exploration & Development Chair (DEDC), King Saud University, Riyadh 11 451, Saudi Arabia.
Applied Organic Chemistry Department, National Research Center, Cairo, Dokki 12 622, Egypt. Elsayed, E A; Bioproducts Research Chair, Zoology Department, College of Science, King Saud University, Riyadh 11 451, Kingdom of Saudi Arabia Natural and Microbial Products Department, National Research Centre, Dokki, Cairo 12 311, Egypt Al-Omar, M A; Pharmaceutical Chemistry Department, College of Pharmacy, Drug Exploration & Development Chair (DEDC), King Saud University, Riyadh 11 451, Saudi Arabia. Almehizia, A A; Pharmaceutical Chemistry Department, College of Pharmacy, Drug Exploration & Development Chair (DEDC), King Saud University, Riyadh 11 451, Saudi Arabia. Abdel-Mageid, Randa E.; 5Photochemistry Department, National Research Center, Cairo, Dokki 12 622, Egypt. |
|
Uncontrolled Index Term |
Anticancer, Hydrazide, Mechanism of action, Peptides, Synthesis |
|
Summary, etc. |
<p class="Abstract">Current research aimed at evaluating the <em>in vitro</em> as well as i<em>n vivo</em> anticancer activities of a newly synthesized <br /> peptide hydrazide; i.e. 4,14-diisopropyl-2,5,13,16-tetraoxo-3,6,12,15-tetraaza-1(3,5)-pyridinacyclohexadecaphane-7-carbohydrazide. The hydrazide was synthesized from methyl 4,14-diisopropyl-2,5,13,16-tetraoxo-3,6,12,15-tetraaza-1(3,5)-pyridinacyclohexadecaphane-7-carboxylate <strong>2 </strong>by acting of hydrazine hydrate. It showed significant anticancer effects against different tested cell lines, where cervical, breast, liver, colon, prostate, brain, fibrosarcoma, leukemia and melanoma cell lines were the most affected cell types. The prepared derivative also inhibited VEGF-2 kinase enzyme significantly and exhibited an <em>in vivo</em> tumorigenic effects in mice model.<strong></strong></p> |
|
Publication, Distribution, Etc. |
Journal of Scientific & Industrial Research 2022-11-19 07:20:43 |
|
Electronic Location and Access |
application/pdf http://op.niscair.res.in/index.php/JSIR/article/view/68669 |
|
Data Source Entry |
Journal of Scientific & Industrial Research; ##issue.vol## 79, ##issue.no## 4 (2020): Journal of Scientific & Industrial Research |
|
Language Note |
en |
|