Synthesis, molecular docking, and biological evaluation of 5‐alkyl(aryl)‐2‐isobutylthiazole derivatives: As α‐amylase, α‐glucosidase, and protein kinase inhibitors-Reference-Cited by-同舟云学术

Synthesis, molecular docking, and biological evaluation of 5‐alkyl(aryl)‐2‐isobutylthiazole derivatives: As α‐amylase, α‐glucosidase, and protein kinase inhibitors

Published:2022-03-07 Issue:5 Volume:36 Page:
ISSN:0268-2605
Container-title:Applied Organometallic Chemistry
language:en
Short-container-title:Applied Organom Chemis

Author:

Khan Siraj¹^ORCID,Buğday Nesrin²^ORCID,Rehman Asim Ur¹^ORCID,Haq Ihsan Ul¹^ORCID,Yaşar Sedat²³⁴^ORCID,Özdemir İsmail²³⁴^ORCID

Affiliation:

1. Department of Pharmacy, Faculty of Biological Sciences Quaid‐i‐Azam University Islamabad Pakistan

2. Department of Chemistry, Faculty of Science and Art İnönü University Malatya Turkey

3. Catalysis Research and Application Center Inönü University Malatya Turkey

4. Drug Application and Research Center İnönü University Malatya Turkey

Funder

Higher Education Commision, Pakistan

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/aoc.6641

Reference92 articles.

1. Recent Patents on Thiazole Derivatives Endowed with Antitumor Activity

2. Thiazole-containing compounds as therapeutic targets for cancer therapy

3. Pd-N-heterocyclic carbene complex catalysed C–H bond activation of 2-isobutylthiazole at the C5 position with aryl bromides

4. Identification and development of thiazole leads as COX-2/5-LOX inhibitors through in-vitro and in-vivo biological evaluation for anti-inflammatory activity

5. Synthesis of Novel Thiazole Derivatives Bearing β-Amino Acid and Aromatic Moieties as Promising Scaffolds for the Development of New Antibacterial and Antifungal Candidates Targeting Multidrug-Resistant Pathogens

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