Design, Synthesis, and Screening of Triazolopyrimidine–Pyrazole Hybrids as Potent Apoptotic Inducers. Issue 11 (16th October 2017)
- Record Type:
- Journal Article
- Title:
- Design, Synthesis, and Screening of Triazolopyrimidine–Pyrazole Hybrids as Potent Apoptotic Inducers. Issue 11 (16th October 2017)
- Main Title:
- Design, Synthesis, and Screening of Triazolopyrimidine–Pyrazole Hybrids as Potent Apoptotic Inducers
- Authors:
- Kamal, Raj
Kumar, Vipan
Kumar, Ravinder
Bhardwaj, Jitender K.
Saraf, Priyanka
Kumari, Priya
Bhardwaj, Vikas - Abstract:
- Abstract : An efficient synthesis of novel 3‐(3‐aryl‐1‐phenyl‐1 H ‐pyrazol‐4‐yl)‐5, 7‐dimethyl‐[1, 2, 4]triazolo[4, 3‐a]‐pyrimidines was accomplished by the oxidation of pyrimidinylhydrazones by using organoiodine(III) reagent. All new triazolopyrimidine derivatives bearing the pyrazole scaffold were screened to evaluate them as a reproductive toxicant in the testicular germ cells of goat ( Capra hircus ). This study aimed at assessing the cytological and biochemical changes in testicular germ cells after the exposure to triazolopyrimidines in a dose‐ and time‐dependent manner. Histomorphological analysis, fluorescence assays, apoptosis quantification, and terminal deoxynucleotidyl transferase dUTP‐mediated nick‐end labeling (TUNEL) assays were performed to determine cytological changes, whereas thiobarbituric acid‐reactive substance (TBARS) and ferric reducing antioxidant power (FRAP) assays were carried out to measure the oxidative stress in triazolopyrimidines treated germ cells. The parallel use of these methods enabled us to determine the role of triazolopyrimidines in inducing apoptosis as a consequence of cytogenetic damage and oxidative stress generated in testicular germ cells of goat. Abstract : Organoiodine(III)‐mediated oxidative methodology was used to design and synthesize triazolopyrimidine–pyrazole hybrid derivatives. The newly synthesized compounds were screened for their cytotoxicity and genotoxicity in goat ( Capra hircus ) testicular germ cells. TheAbstract : An efficient synthesis of novel 3‐(3‐aryl‐1‐phenyl‐1 H ‐pyrazol‐4‐yl)‐5, 7‐dimethyl‐[1, 2, 4]triazolo[4, 3‐a]‐pyrimidines was accomplished by the oxidation of pyrimidinylhydrazones by using organoiodine(III) reagent. All new triazolopyrimidine derivatives bearing the pyrazole scaffold were screened to evaluate them as a reproductive toxicant in the testicular germ cells of goat ( Capra hircus ). This study aimed at assessing the cytological and biochemical changes in testicular germ cells after the exposure to triazolopyrimidines in a dose‐ and time‐dependent manner. Histomorphological analysis, fluorescence assays, apoptosis quantification, and terminal deoxynucleotidyl transferase dUTP‐mediated nick‐end labeling (TUNEL) assays were performed to determine cytological changes, whereas thiobarbituric acid‐reactive substance (TBARS) and ferric reducing antioxidant power (FRAP) assays were carried out to measure the oxidative stress in triazolopyrimidines treated germ cells. The parallel use of these methods enabled us to determine the role of triazolopyrimidines in inducing apoptosis as a consequence of cytogenetic damage and oxidative stress generated in testicular germ cells of goat. Abstract : Organoiodine(III)‐mediated oxidative methodology was used to design and synthesize triazolopyrimidine–pyrazole hybrid derivatives. The newly synthesized compounds were screened for their cytotoxicity and genotoxicity in goat ( Capra hircus ) testicular germ cells. The cytological changes and oxidative stress levels in treated germ cells were determined to assess the role of triazolopyrimidines in inducing apoptosis by cytogenetic damage and oxidative stress. … (more)
- Is Part Of:
- Archiv der Pharmazie. Volume 350:Issue 11(2017)
- Journal:
- Archiv der Pharmazie
- Issue:
- Volume 350:Issue 11(2017)
- Issue Display:
- Volume 350, Issue 11 (2017)
- Year:
- 2017
- Volume:
- 350
- Issue:
- 11
- Issue Sort Value:
- 2017-0350-0011-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2017-10-16
- Subjects:
- Cytotoxic activity -- Pyrazole -- Synthesis -- Triazole
Pharmaceutical chemistry -- Periodicals
Pharmacology -- Periodicals
615.19 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-4184 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ardp.201700137 ↗
- Languages:
- English
- ISSNs:
- 0365-6233
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1622.800000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 8991.xml