Synthesis and biological evaluation of phenyl-amino-pyrimidine and indole/oxindole conjugates as potential BCR-ABL inhibitors-Reference-Cited by-同舟云学术

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Synthesis and biological evaluation of phenyl-amino-pyrimidine and indole/oxindole conjugates as potential BCR-ABL inhibitors

Published:2019-03-16 Issue:5 Volume:28 Page:633-645
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

Rahim Abdul,Syed Riyaz,Poornachandra Y.,Malik M. Shaheer,Reddy Ch. Venkata Ramana,Alvala Mallika,Boppana Kiran,Sridhar B.,Amanchy Ramars,Kamal Ahmed

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-019-02318-4.pdf

Reference75 articles.

1. Amala K, Bhujanga Rao AK, Gorantla B, Gondi CS, Rao JS (2013) Design, synthesis and preclinical evaluation of NRC-AN-019. Int J Oncol 42:168–178

2. An X, Tiwari AK, Sun Y, Ding PR, Ashby Jr. CR, Chen ZH (2010) BCR-ABL tyrosine kinase inhibitors in the treatment of Philadelphia chromosome positive chronic myeloid leukemia: a review. Leuk Res 34:1255–1268

3. Ateyya H, Hassan ZA, El-Sherbeeny NA (2017) The selective tyrosine kinase-inhibitor nilotinib alleviates experimentally induced cisplatin nephrotoxicity and hepatotoxicity. Environ Toxicol Pharmacol 55:60–67

4. Azevedo AP, Reichert A, Afonso C, Alberca MD, Tavares P, Lima F (2017) BCR-ABL V280G mutation, potential role in Imatinib resistance: first case report. Clin Med Insights Oncol 11:1–5

5. Banavath HM, Sharma OP, Kumar MS, Baskaran R (2014) Identification of novel tyrosine kinase inhibitors for drug resistant T315I mutant BCR-ABL: a virtual screening and molecular dynamics simulations study. Sci Rep 4:6948

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