Baijayantimala Swain

National Institutes of Health — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index293citations27works1.42yr avg
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Research Topics

Enzyme function and inhibition(18), Synthesis and Catalytic Reactions(17), Cholinesterase and Neurodegenerative Diseases(7), Phenothiazines and Benzothiazines Synthesis and Activities(7), Synthesis and Biological Evaluation(5)

Publications27 total

Corrigendum to ‘Synthesis and investigation of substituted 1,5-diaryl-1H-1,2,4-triazoles for the discovery of 18F-labeled probes for imaging brain cyclooxygenase-1’ [Eur. J. Med. Chem. 2025, 118523]
European Journal of Medicinal Chemistry·2026
Discovery of Fluorinated Ultrapotent Chemogenetic Ligands for PET Imaging and Neural Modulation in Nonhuman Primates
Journal of Medicinal Chemistry·2026
Synthesis and antimicrobial evaluation of novel 8-hydroxyquinoline containing benzimidazole hybrids
Discover Chemistry.·2025· 2 citedOpen Access
Facile synthesis, antimicrobial activity, and molecular docking analysis of 8-hydroxyquinoline-4-thiazolidinone hybrids
Future Medicinal Chemistry·2025· 1 citedOpen Access
Synthesis of Chromene-linked Bis-indole Derivatives as Selective Tumor-associated Carbonic Anhydrase IX Inhibitors
Anti-Cancer Agents in Medicinal Chemistry·2024· 1 cited
Design, synthesis and in vitro evaluation of novel thiazole-coumarin hybrids as selective and potent human carbonic anhydrase IX and XII inhibitors
International Journal of Biological Macromolecules·2024· 4 cited
Design, synthesis, and biological evaluation of 3‐benzenesulfonamide‐linked 3‐hydrazinoisatin derivatives as carbonic anhydrase inhibitors
Archiv der Pharmazie·2024· 2 citedOpen Access
Development of Novel Indole-3-sulfonamide-heteroaryl Hybrids as CarbonicAnhydrase Inhibitors: Design, Synthesis and in-vitro Screening
Anti-Cancer Agents in Medicinal Chemistry·2023· 3 cited
Design, Synthesis and Biological Assessment of Rhodanine-Linked Benzenesulfonamide Derivatives as Selective and Potent Human Carbonic Anhydrase Inhibitors
Molecules·2022· 7 citedOpen Access
Synthesis of a new series of quinoline/pyridine indole-3-sulfonamide hybrids as selective carbonic anhydrase IX inhibitors
Bioorganic & Medicinal Chemistry Letters·2022· 15 citedOpen Access
Microwave‐Assisted Copper‐Catalyzed One‐Pot Synthesis of 2‐Aryl/Heteroaryl‐4‐Quinolones <i>via</i> Sequential Intramolecular Aza‐Michael Addition and Oxidation
Asian Journal of Organic Chemistry·2022· 5 cited
Exploration of 2-phenylquinoline-4-carboxamide linked benzene sulfonamide derivatives as isoform selective inhibitors of transmembrane human carbonic anhydrases
European Journal of Medicinal Chemistry·2022· 18 citedOpen Access
Efficient One-pot Synthesis of 3,3-di(indolyl)indolin-2-ones from Isatin and Indole Catalyzed by VOSO<sub>4</sub> as Non-Sulfonamide Carbonic Anhydrase Inhibitors
Anti-Cancer Agents in Medicinal Chemistry·2022· 3 cited
Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII Inhibitors
ChemMedChem·2021· 12 cited
Design and development of novel series of indole‐3‐sulfonamide ureido derivatives as selective carbonic anhydrase II inhibitors
Archiv der Pharmazie·2021· 11 cited
Synthesis and Biological Evaluation of Coumarin-Linked 4-Anilinomethyl-1,2,3-Triazoles as Potent Inhibitors of Carbonic Anhydrases IX and XIII Involved in Tumorigenesis
Metabolites·2021· 14 citedOpen Access
Design and synthesis of benzenesulfonamide‐linked imidazo[2,1‐<i>b</i>][1,3,4]thiadiazole derivatives as carbonic anhydrase I and II inhibitors
Archiv der Pharmazie·2021· 9 cited
3-Functionalised benzenesulphonamide based 1,3,4-oxadiazoles as selective carbonic anhydrase XIII inhibitors: Design, synthesis and biological evaluation
Bioorganic & Medicinal Chemistry Letters·2021· 10 citedOpen Access
Discovery of a novel series of indolylchalcone-benzenesulfonamide hybrids acting as selective carbonic anhydrase II inhibitors
Bioorganic Chemistry·2021· 14 cited
New coumarin/sulfocoumarin linked phenylacrylamides as selective transmembrane carbonic anhydrase inhibitors: Synthesis and in-vitro biological evaluation
Bioorganic & Medicinal Chemistry·2020· 21 citedOpen Access
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Frequent Co-authors

Mohammed Arifuddin(21), Andrea Angeli(18), Claudiu T. Supuran(18), Priti Singh(16), Venkata Madhavi Yaddanapudi(10), Sridhar Goud Nerella(7), Santosh K. Sahoo(6), Pavitra S. Thacker(4), Dilep Kumar Sigalapalli(4), Chander Singh Digwal(3), Abhishek Choli(3), Qasim Ullah(3), Pooja Yadav(2), Upasana Yadav(2), P. Ramya(2), Ähmed Kamal(2), Kamtam Aashritha(2), Abrar Ahmad Khan(2), Vaibhav S. Marde(2), Krishna Kartheek Chinchilli(2)