Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies-Reference-Cited by-同舟云学术

Synthesis of novel derivatives of oxindole, their urease inhibition and molecular docking studies

Published:2015-08 Issue:16 Volume:25 Page:3285-3289
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Taha Muhammad,Ismail Nor Hadiani,Khan Ajmal,Shah Syed Adnan Ali,Anwar Ammarah,Halim Sobia Ahsan,Fatmi M. Qaiser,Imran Syahrul,Rahim Fazal,Khan Khalid Mohammed

Funder

The Ministry of Agriculture (MOA) Malaysia

Universiti Teknologi MARA

Atta-ur-Rahman Institute for Natural product Discovery (RiND)

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference46 articles.

1. Synthesis of Potent Oxindole CDK2 Inhibitors

2. Oxindole Derivatives as Orally Active Potent Growth Hormone Secretagogues

3. Paratunamides A−D, Oxindole Alkaloids from Cinnamodendron axillare

4. TMC-95A, B, C, and D, Novel Proteasome Inhibitors Produced by Apiospora montagnei Sacc. TC 1093. Taxonomy, Production, Isolation, and Biological Activities.

5. A Novel Series of Piperidin-4-yl-1,3-Dihydroindol-2-ones as Agonist and Antagonist Ligands at the Nociceptin Receptor

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