Search Results - "al-Rashida, Mariya"

Piperidinium‐Based Deep Eutectic Solvents: Efficient and Sustainable Eco‐Friendly Medium for One‐Pot N‐Heterocycles Synthesis.

Authors: Ali, Shujaat Al‐Rashida, Mariya Younus, Hafiza Amna et al.

Source: ChemistrySelect. 11/6/2020, Vol. 5 Issue 41, p12697-12703. 7p.

Carbonic anhydrase inhibition by 1-aroyl-3-(4-aminosulfonylphenyl)thioureas.

Authors: Saeed, Aamer al-Rashida, Mariya Hamayoun, Mehwish et al.

Source: Journal of Enzyme Inhibition & Medicinal Chemistry. Dec2014, Vol. 29 Issue 6, p901-905. 5p.

Sulfa Drugs as Inhibitors of Carbonic Anhydrase: New Targets for the Old Drugs.

Authors: Al-Rashida, Mariya Hussain, Sajad Hamayoun, Mehwish et al.

Source: BioMed Research International. 2014, Vol. 2014, p1-10. 10p.

Chromone containing sulfonamides as potent carbonic anhydrase inhibitors.

Authors: Ekinci, Deniz al-Rashida, Mariya Abbas, Ghulam et al.

Source: Journal of Enzyme Inhibition & Medicinal Chemistry. Oct2012, Vol. 27 Issue 5, p744-747. 4p.

Synthesis of new 1,2,3-triazole analogues of metronidazole and their identification as α-glucosidase inhibitors.

Authors: Batool, Farhana Ullah, Saeed Khan, Maria Aqeel et al.

Source: Discover Chemistry. 6/23/2026, Vol. 3 Issue 1, p1-27. 27p.

Acridine-based (thio)semicarbazones and hydrazones: Synthesis, in vitro urease inhibition, molecular docking and in-silico ADME evaluation.

Authors: Isaac, Ibanga Okon al-Rashida, Mariya Rahman, Shafiq Ur et al.

Source: Bioorganic Chemistry. Feb2019, Vol. 82, p6-16. 11p.

Synthesis, in vitro, and in silico studies of 4-chlorophenyl-sulfonyl Indole based thiosemicarbazones as competitive α-glucosidase inhibitors.

Authors: Naseer, Iqra Ullah, Saeed Batool, Zahra et al.

Source: Scientific Reports. 11/6/2025, Vol. 15 Issue 1, p1-22. 22p.

2-Alkoxy-3-(sulfonylarylaminomethylene)-chroman-4-ones as potent and selective inhibitors of ectonucleotidases.

Authors: al-Rashida, Mariya Batool, Gazala Sattar, Almas et al.

Source: European Journal of Medicinal Chemistry. Jun2016, Vol. 115, p484-494. 11p.

Diarylsulfonamides and their bioisosteres as dual inhibitors of alkaline phosphatase and carbonic anhydrase: Structure activity relationship and molecular modelling studies.

Authors: al-Rashida, Mariya Ejaz, Syeda Abida Ali, Sharafat et al.

Source: Bioorganic & Medicinal Chemistry. May2015, Vol. 23 Issue 10, p2435-2444. 10p.

Recent Developments of Carbonic Anhydrase Inhibitors as Potential Drugs.

Authors: Iqbal, Jamshed Al-Rashida, Mariya Durdagi, Serdar et al.

Source: BioMed Research International. 3/2/2015, Vol. 2015, p1-2. 2p.

Identification of novel chromone based sulfonamides as highly potent and selective inhibitors of alkaline phosphatases.

Authors: al-Rashida, Mariya Raza, Rabia Abbas, Ghulam et al.

Source: European Journal of Medicinal Chemistry. Aug2013, Vol. 66, p438-449. 12p.

Discovery of new chromone containing sulfonamides as potent inhibitors of bovine cytosolic carbonic anhydrase

Authors: al-Rashida, Mariya Ashraf, Muhammad Hussain, Bushra et al.

Source: Bioorganic & Medicinal Chemistry. Jun2011, Vol. 19 Issue 11, p3367-3371. 5p.

Dihydropyrimidines Emerge as Promising Dual‐Acting Inhibitors Targeting Acetylcholinesterase and Monoamine Oxidases for Alzheimer's and Other Neurological Disorders.

Authors: Saleem Khan, Maria Islam, Talha Farooq, Muhammad Umer et al.

Source: ChemistrySelect. 2/12/2025, Vol. 10 Issue 6, p1-22. 22p.

Integrated Experimental and Computational Investigation of 7‐Bromoochromone Thiosemicarbazones as α‐Glucosidase Inhibitors.

Authors: Shahzadi, Eshah Ghaffar, Uzma Khan, Ajmal et al.

Source: Chemical Biology & Drug Design. Feb2026, Vol. 107 Issue 2, p1-10. 10p.

Optimization study and application of box-behnken model for probing eggshell supported transition metals based catalysts to synthesize hydrazone & dihydropyrimidinones.

Authors: Perveen, Rabia Latif, Fiza Abbas, Minahil et al.

Source: Scientific Reports. 10/10/2024, Vol. 14 Issue 1, p1-16. 16p.

Design, synthesis, in vitro and in silico studies of novel piperidine derived thiosemicarbazones as inhibitors of dihydrofolate reductase.

Authors: Aftab, Hina Ullah, Saeed Khan, Ajmal et al.

Source: Scientific Reports. 9/30/2024, Vol. 14 Issue 1, p1-18. 18p.

Synthesis, In-vitro evaluation and molecular docking studies of oxoindolin phenylhydrazine carboxamides as potent and selective inhibitors of ectonucleoside triphosphate diphosphohydrolase (NTPDase).

Authors: Afzal, Saira al-Rashida, Mariya Hameed, Abdul et al.

Source: Bioorganic Chemistry. Jul2021, Vol. 112, pN.PAG-N.PAG. 1p.

N-hexylsulfonyl indole based thiosemicarbazones as potent and selective ecto-5′-nucleotidase and NTPDase inhibitors.

Authors: Batool, Zahra Dutt, Shireen Mona al-Rashida, Mariya et al.

Source: Bioorganic Chemistry. Aug2025, Vol. 163, pN.PAG-N.PAG. 1p.

Probing Solid‐Supported Alkali and Alkaline Earth Metal Salts‐Based Catalysts in the Multicomponent Synthesis of Acridine‐1,8‐diones: Box–Behnken and Density Functional Theory (DFT) Study.

Authors: Ali, Nisar Sarfaraz, Sehrish Asif, Hina et al.

Source: ChemistrySelect. 10/6/2025, Vol. 10 Issue 37, p1-13. 13p.

Functionalized Diazabenzo[a]anthracenediones: Regioselective Multicomponent Synthesis and Biological and Computational Studies as Potential Cholinesterase Inhibitors.

Authors: Tariq Riaz, Muhammad Taslimi, Parham Yaqub, Muhammad et al.

Source: ChemistrySelect. 6/13/2023, Vol. 8 Issue 22, p1-12. 12p.