Synthesis of new isoquinoline-base-oxadiazole derivatives as potent inhibitors of thymidine phosphorylase and molecular docking study.

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第一作者： Khalid,Zaman

第一单位： Department of Chemistry, Hazara University, Mansehra, 21300, Khyber Pakhtunkhwa, Pakistan.

作者： Khalid,Zaman ^[1] ; Fazal,Rahim ^[1] ; Muhammad,Taha ^[2] ; Abdul,Wadood ^[3] ; Syed Adnan Ali,Shah ^[4] ; Qamar Uddin,Ahmed ^[5] ; Zainul Amiruddin,Zakaria ^[6]

作者单位： Department of Chemistry, Hazara University, Mansehra, 21300, Khyber Pakhtunkhwa, Pakistan. ^[1] Department of Clinical Pharmacy, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, P. O. Box 1982, Dammam, 31441, Saudi Arabia. mtaha@iau.edu.sa. ^[2] Department of Biochemistry, Abdul Wali Khan University Mardan, Mardan, 23200, Pakistan. ^[3] Faculty of Pharmacy, Universiti Teknologi MARA Cawangan Selangor Kampus Puncak Alam, 42300 Bandar Puncak Alam, Selangor, D.E., Malaysia. ^[4] Atta-ur-Rahman Institute for Natural Products Discovery (AuRIns), Universiti Teknologi MARA Cawangan Selangor Kampus Puncak Alam, 42300 Bandar Puncak Alam, Selangor, D.E., Malaysia. ^[5] Department of Pharmaceutical Chemistry, Kulliyyah of Pharmacy, International Islamic University Malaysia, Pahang DM, Kuantan, 25200, Malaysia. ^[6] Department of Biomedical Science, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia. zaz@upm.edu.my. ^[7] Halal Institute Research Institute, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia. zaz@upm.edu.my. ^[8]