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Uzma Salar
Uzma Salar
International Center for Chemical & Biological Sciences, University of Karachi, Pakistan
Verified email at iccs.edu
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Cited by
Year
Multicomponent reactions (MCR) in medicinal chemistry: a patent review (2010-2020)
HA Younus, M Al-Rashida, A Hameed, M Uroos, U Salar, S Rana, ...
Expert Opinion on Therapeutic Patents 31 (3), 267-289, 2021
1412021
Syntheses of new 3-thiazolyl coumarin derivatives, in vitro α-glucosidase inhibitory activity, and molecular modeling studies
U Salar, M Taha, KM Khan, NH Ismail, S Imran, S Perveen, S Gul, ...
European journal of medicinal chemistry 122, 196-204, 2016
922016
Synthesis of benzotriazoles derivatives and their dual potential as α-amylase and α-glucosidase inhibitors in vitro: Structure-activity relationship, molecular docking, and …
S Hameed, F Seraj, R Rafique, S Chigurupati, A Wadood, AU Rehman, ...
European journal of medicinal chemistry 183, 111677, 2019
882019
5-Bromo-2-Aryl benzimidazole Derivatives as Non-Cytotoxic Potential Dual Inhibitors of α-Glucosidase and Urease Enzymes
T Arshad, KM Khan, N Rasool, U Salar, S Hussain, H Asghar, M Ashraf, ...
Bioorganic Chemistry 72, 21-31, 2017
852017
Synthesis, α-glucosidase inhibitory activity and in silico study of tris-indole hybrid scaffold with oxadiazole ring: As potential leads for the management of type-II diabetes …
M Taha, F Rahim, S Imran, NH Ismail, H Ullah, M Selvaraj, MT Javid, ...
Bioorganic chemistry 74, 30-40, 2017
832017
New Hybrid Hydrazinyl Thiazole Substituted Chromones: As Potential α-Amylase Inhibitors and Radical (DPPH & ABTS) Scavengers
U Salar, KM Khan, S Chigurupati, M Taha, A Wadood, S Vijayabalan, ...
Scientific Reports 7, 16980, 2017
812017
Biology-oriented drug synthesis (BIODS) of 2-(2-methyl-5-nitro-1H-imidazol-1-yl) ethyl aryl ether derivatives, in vitro α-amylase inhibitory activity and in silico studies
M Taha, S Imran, NH Ismail, M Selvaraj, F Rahim, S Chigurupati, H Ullah, ...
Bioorganic chemistry 74, 1-9, 2017
812017
Hydrazinyl arylthiazole based pyridine scaffolds: Synthesis, structural characterization, in vitro α-glucosidase inhibitory activity, and in silico studies
F Ali, KM Khan, U Salar, M Taha, NH Ismail, A Wadood, M Riaz, ...
European Journal of Medicinal Chemistry 138, 255-272, 2017
712017
Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs
M Taha, NH Ismail, S Imran, F Rahim, A Wadood, H Khan, H Ullah, ...
Bioorganic chemistry 68, 56-63, 2016
672016
2ʹ-Aryl and 4ʹ-arylidene substituted pyrazolones: As potential α-amylase inhibitors
S Yousuf, KM Khan, U Salar, S Chigurupati, MT Muhammad, A Wadood, ...
European journal of medicinal chemistry 159, 47-58, 2018
612018
New indole based hybrid oxadiazole scaffolds with N-substituted acetamides: As potent anti-diabetic agents
M Nazir, MA Abbasi, SZ Siddiqui, KM Khan, U Salar, M Shahid, M Ashraf, ...
Bioorganic chemistry 81, 253-263, 2018
592018
2-Aryl benzimidazoles: Synthesis, In vitro α-amylase inhibitory activity, and molecular docking study
AA Adegboye, KM Khan, U Salar, SA Aboaba, S Chigurupati, I Fatima, ...
European Journal of Medicinal Chemistry 150, 248-260, 2018
582018
Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives
KM Khan, S Qurban, U Salar, M Taha, S Hussain, S Perveen, A Hameed, ...
Bioorganic chemistry 68, 245-258, 2016
582016
2-Arylquinazolin-4 (3H)-ones: A new class of α-glucosidase inhibitors
K Javaid, SM Saad, S Rasheed, ST Moin, N Syed, I Fatima, U Salar, ...
Bioorganic & Medicinal Chemistry 23 (23), 7417-7421, 2015
572015
Synthesis of 6-chloro-2-Aryl-1H-imidazo [4, 5-b] pyridine derivatives: antidiabetic, antioxidant, β-glucuronidase inhibiton and their molecular docking studies
M Taha, NH Ismail, S Imran, H Rashwan, W Jamil, S Ali, SM Kashif, ...
Bioorganic chemistry 65, 48-56, 2016
542016
Dihydropyrimidones: as novel class of β-glucuronidase inhibitors
F Ali, KM Khan, U Salar, S Iqbal, M Taha, NH Ismail, S Perveen, ...
Bioorganic & Medicinal Chemistry 24 (16), 3624-3635, 2016
532016
Chalcones and Bis-Chalcones: As Potential α-Amylase Inhibitors; Synthesis, In Vitro Screening, and Molecular Modelling Studies
AT Bale, KM Khan, U Salar, S Chigurupati, T Fasina, F Ali, A Wadood, ...
Bioorganic chemistry 79, 179-189, 2018
522018
Flurbiprofen derivatives as novel α-amylase inhibitors: Biology-oriented drug synthesis (BIODS), in vitro, and in silico evaluation
M Khan, A Alam, KM Khan, U Salar, S Chigurupati, A Wadood, F Ali, ...
Bioorganic chemistry 81, 157-167, 2018
492018
Synthesis and evaluation of unsymmetrical heterocyclic thioureas as potent β-glucuronidase inhibitors
M Taha, NH Ismail, W Jamil, KM Khan, U Salar, SM Kashif, F Rahim, ...
Medicinal Chemistry Research, 1-8, 2015
492015
Synthesis, in vitro α-amylase inhibitory, and radicals (DPPH & ABTS) scavenging potentials of new N-sulfonohydrazide substituted indazoles
R Rafique, KM Khan, S Chigurupati, A Wadood, AU Rehman, U Salar, ...
Bioorganic chemistry 94, 103410, 2020
472020
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