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Amara Mumtaz

Showing results (21-30 of 36) with videos related to

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International Journal of Biological Macromolecules|April 24, 2025
Development of novel cyclopropyl tethered iminothiazolidinone-isatin hybrids as effective multi target intestinal alkaline phosphatase, urease and α-glucosidase inhibitorsHina Zaman, Aamer Saeed, Tamknat Ul Muntaha, et al.
RSC Medicinal Chemistry|November 20, 2025
Design, synthesis, and biological evaluation of sulfonamide-functionalized pyridine carbothioamides as potent tubulin-targeting anticancer agentsFatima Younas, Jahan Zaib Arshad, Waqas Ali Shah, et al.
RSC Advances|January 6, 2025
Exploration of novel triazolo-thiadiazine hybrids of deferasirox as multi-target-directed anti-neuroinflammatory agents with structure-activity relationship (SAR): a new treatment opportunity for Alzheimer's diseaseSyed Ahmed Shakir, Umer Rashid, Marryum, et al.
Bioorganic Chemistry|September 18, 2020
Synthesis, in-vitro, in-vivo anti-inflammatory activities and molecular docking studies of acyl and salicylic acid hydrazide derivativesAbida Munir, Adil Khushal, Kiran Saeed, et al.
Bioorganic Chemistry|February 1, 2025
Corrigendum to "Synthesis of novel 1,2,3-triazole-tethered N-acyl hydrazones as a new class of carbonic anhydrase II inhibitors: In vitro and in silico potentials" [Bioorg. Chem. 153 (2024) 107822]Noor Fatima, Aamer Saeed, Saeed Ullah, et al.
Current Pharmaceutical Design|January 8, 2025
Bioactive Secondary Metabolites from <i>Bauhinia variegata</i> Linn. Roots: Isolation, Characterization, and Cytotoxic EvaluationYousaf Kamal, Nighat Fatima, Amara Mumtaz, et al.
Bioorganic Chemistry|July 19, 2019
Flavonols and 4-thioflavonols as potential acetylcholinesterase and butyrylcholinesterase inhibitors: Synthesis, structure-activity relationship and molecular docking studiesEhsan Ullah Mughal, Amina Sadiq, Jamshaid Ashraf, et al.
Bioorganic Chemistry|September 21, 2024
Synthesis of novel 1,2,3-triazole-tethered N-acyl hydrazones as a new class of carbonic anhydrase II inhibitors: In vitro and in silico potentialsNoor Fatima, Aamer Saeed, Saeed Ullah, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 29, 2019
Synthesis, computational studies, tyrosinase inhibitory kinetics and antimelanogenic activity of hydroxy substituted 2-[(4-acetylphenyl)amino]-2-oxoethyl derivativesMuhammad Rafiq, Yasir Nazir, Zaman Ashraf, et al.
Bioorganic Chemistry|May 5, 2019
Synthesis, antimicrobial, antioxidant, cytotoxic, antiurease and molecular docking studies of N-(3-trifluoromethyl)benzoyl-N'-aryl thiourea derivativesAneela Maalik, Hina Rahim, Muhammad Saleem, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
International Journal of Biological Macromolecules|April 24, 2025
Development of novel cyclopropyl tethered iminothiazolidinone-isatin hybrids as effective multi target intestinal alkaline phosphatase, urease and α-glucosidase inhibitorsHina Zaman, Aamer Saeed, Tamknat Ul Muntaha, et al.
RSC Medicinal Chemistry|November 20, 2025
Design, synthesis, and biological evaluation of sulfonamide-functionalized pyridine carbothioamides as potent tubulin-targeting anticancer agentsFatima Younas, Jahan Zaib Arshad, Waqas Ali Shah, et al.
RSC Advances|January 6, 2025
Exploration of novel triazolo-thiadiazine hybrids of deferasirox as multi-target-directed anti-neuroinflammatory agents with structure-activity relationship (SAR): a new treatment opportunity for Alzheimer's diseaseSyed Ahmed Shakir, Umer Rashid, Marryum, et al.
Bioorganic Chemistry|September 18, 2020
Synthesis, in-vitro, in-vivo anti-inflammatory activities and molecular docking studies of acyl and salicylic acid hydrazide derivativesAbida Munir, Adil Khushal, Kiran Saeed, et al.
Bioorganic Chemistry|February 1, 2025
Corrigendum to "Synthesis of novel 1,2,3-triazole-tethered N-acyl hydrazones as a new class of carbonic anhydrase II inhibitors: In vitro and in silico potentials" [Bioorg. Chem. 153 (2024) 107822]Noor Fatima, Aamer Saeed, Saeed Ullah, et al.
Current Pharmaceutical Design|January 8, 2025
Bioactive Secondary Metabolites from <i>Bauhinia variegata</i> Linn. Roots: Isolation, Characterization, and Cytotoxic EvaluationYousaf Kamal, Nighat Fatima, Amara Mumtaz, et al.
Bioorganic Chemistry|July 19, 2019
Flavonols and 4-thioflavonols as potential acetylcholinesterase and butyrylcholinesterase inhibitors: Synthesis, structure-activity relationship and molecular docking studiesEhsan Ullah Mughal, Amina Sadiq, Jamshaid Ashraf, et al.
Bioorganic Chemistry|September 21, 2024
Synthesis of novel 1,2,3-triazole-tethered N-acyl hydrazones as a new class of carbonic anhydrase II inhibitors: In vitro and in silico potentialsNoor Fatima, Aamer Saeed, Saeed Ullah, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|August 29, 2019
Synthesis, computational studies, tyrosinase inhibitory kinetics and antimelanogenic activity of hydroxy substituted 2-[(4-acetylphenyl)amino]-2-oxoethyl derivativesMuhammad Rafiq, Yasir Nazir, Zaman Ashraf, et al.
Bioorganic Chemistry|May 5, 2019
Synthesis, antimicrobial, antioxidant, cytotoxic, antiurease and molecular docking studies of N-(3-trifluoromethyl)benzoyl-N'-aryl thiourea derivativesAneela Maalik, Hina Rahim, Muhammad Saleem, et al.
Pageof 4