Works matching AU Al-Rifai, Nafisah
Results: 8
Synthesis, biological evaluation, and computational studies of N-benzyl pyridinium–curcumin derivatives as potent AChE inhibitors with antioxidant activity.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2023, v. 38, n. 1, p. 1, doi. 10.1080/14756366.2023.2281264
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α‐Substituted Chalcones: A Key Review.
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- ChemistrySelect, 2021, v. 6, n. 46, p. 13224, doi. 10.1002/slct.202103325
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High Throughput Screening and Characterization Methods of Jordanian Oil Shale as a Case Study.
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- Energies (19961073), 2019, v. 12, n. 16, p. 3148, doi. 10.3390/en12163148
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The Cytoprotective Effects of E-α-(4-Methoxyphenyl)-2’,3,4,4'-Tetramethoxychalcone (E-α-p-OMe-C<sub>6</sub>H<sub>4</sub>-TMC)—A Novel and Non-Cytotoxic HO-1 Inducer.
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- PLoS ONE, 2015, v. 10, n. 10, p. 1, doi. 10.1371/journal.pone.0142932
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Angiotensin Converting Enzyme (ACE) Gene Polymorphism in Jordanian Type-1 and Type-2 Diabetic Patients.
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- Jordan Journal of Biological Sciences, 2020, v. 13, n. 2, p. 207
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Synthesis, Isolation, Identification and Characterization of a Drug-Excipient Interaction Degradation Impurity in Pramipexole by HPLC, LC/MS and NMR.
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- Separations (2297-8739), 2023, v. 10, n. 1, p. 7, doi. 10.3390/separations10010007
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Opening or Closing the Lock? When Reactivity Is the Key to Biological Activity.
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- Chemistry - A European Journal, 2013, v. 19, n. 45, p. 15384, doi. 10.1002/chem.201302117
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- Article
The Synthetic α-Bromo-2′,3,4,4′-Tetramethoxychalcone (α-Br-TMC) Inhibits the JAK/STAT Signaling Pathway.
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- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0090275
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- Article