Synthesis of novel 2-alkyl-4-substituted-amino-pyrazolo[3,4-d]pyrimidines as new leads for anti-bacterial and anti-cancer activity-Reference-Cited by-同舟云学术

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Synthesis of novel 2-alkyl-4-substituted-amino-pyrazolo[3,4-d]pyrimidines as new leads for anti-bacterial and anti-cancer activity

Published:2012-06-04 Issue:3 Volume:22 Page:1090-1101
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Devarakonda Murty,Doonaboina Raghava,Vanga Sreedher,Vemu Jahnavi,Boni Sathoshini,Mailavaram Raghu Prasad

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-012-0084-0.pdf

Reference17 articles.

1. Abd El Razik HA, Abdel Wahab AE (2011) Synthesis and biological evaluation of some novel fused pyrazolopyrimidines as potential anticancer and antimicrobial agents. Arch Pharm 344:184–196

2. Ahmed OM, Mohamed MA, Ahmed RR, Ahmed SA (2009) Synthesis and anti-tumor activities of some new pyridines and pyrazolo[1,5-a]pyrimidines. Eur J Med Chem 44:3519–3523

3. Bakavoli M, Bagherzadeh G, Vaseghifar M, Shiri A, Pordel M, Mashreghi M, Pordeli P, Araghi M (2010) Molecular iodine promoted synthesis of new pyrazolo[3,4-d]pyrimidine derivatives as potential antibacterial agents. Eur J Med Chem 45:647–650

4. Bazgir A, Khanaposhtani MM, Soorki AA (2008) One-pot synthesis and antibacterial activities of pyrazolo[4′,3′:5,6]pyrido[2,3-d]pyrimidine-dione derivatives. Bioorg Med Chem Lett 18:5800–5803

5. Chern J, Shia K, Hsu T, Tai C, Lee C, Lee Y, Chang C, Tseng S, Shih S (2004) Design, synthesis, and structure–activity relationships of pyrazolo[3,4-d]pyrimidines: a novel class of potent enterovirus inhibitors. Bioorg Med Chem Lett 14:2519–2525

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1. N- and s-substituted Pyrazolopyrimidines: A promising new class of potent c-Src kinase inhibitors with prominent antitumor activity;Bioorganic Chemistry;2024-04

2. New pyrazolo[3,4-d]pyrimidine derivatives as EGFR-TK inhibitors: design, green synthesis, potential anti-proliferative activity and P-glycoprotein inhibition;RSC Advances;2024

3. Design, synthesis and chemoinformatic studies of new thiazolopyrimidine derivatives as potent anticancer agents via phosphodiesterase-5 inhibition and apoptotic inducing activity;Journal of Molecular Structure;2023-01

4. A New Insight into the Synthesis and Biological Activities of Pyrazole based Derivatives;Mini-Reviews in Organic Chemistry;2022-09

5. Synthesis Characterization and Molinspiration Analysis, Anti-bacterial activity of Novel 2,4,6-tri Substituted Pyrimidines;Journal of Young Pharmacists;2022-06-13

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