Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues
A series of sixteen novel heterocyclic thiazolidine derivatives (3a-p) was synthesized upon reaction of L-cysteine with different substituted benzaldehyde. The synthesized compounds were extensively characterized by IR, 1H and 13C NMR spectral analysis. All compounds were evaluated for their anti-fu...
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my.utm.897482021-02-22T01:45:04Z http://eprints.utm.my/id/eprint/89748/ Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues Abid, F. M. A. Jamalis, J. Chander, S. Wahab, R. A. Bhagwat, D. P. Sankaranarayanan, M. Q Science (General) A series of sixteen novel heterocyclic thiazolidine derivatives (3a-p) was synthesized upon reaction of L-cysteine with different substituted benzaldehyde. The synthesized compounds were extensively characterized by IR, 1H and 13C NMR spectral analysis. All compounds were evaluated for their anti-fungal activity against Candida albicans and Aspergillus niger using fluconazole as reference drug. The assay revealed that, compound 3k showed significant activity (14 mm ZOI, 64 µg/mL IC50 and 15 mm ZOI, >32 µg/mL IC50) against C. albicans and A. niger, respectively. Elsevier B. V. 2019-06 Article PeerReviewed Abid, F. M. A. and Jamalis, J. and Chander, S. and Wahab, R. A. and Bhagwat, D. P. and Sankaranarayanan, M. (2019) Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues. Chemical Data Collections, 21 . ISSN 2405-8300 https://dx.doi.org/10.1016/j.cdc.2019.100219 DOI: 10.1016/j.cdc.2019.100219 |
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Q Science (General) Abid, F. M. A. Jamalis, J. Chander, S. Wahab, R. A. Bhagwat, D. P. Sankaranarayanan, M. Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
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A series of sixteen novel heterocyclic thiazolidine derivatives (3a-p) was synthesized upon reaction of L-cysteine with different substituted benzaldehyde. The synthesized compounds were extensively characterized by IR, 1H and 13C NMR spectral analysis. All compounds were evaluated for their anti-fungal activity against Candida albicans and Aspergillus niger using fluconazole as reference drug. The assay revealed that, compound 3k showed significant activity (14 mm ZOI, 64 µg/mL IC50 and 15 mm ZOI, >32 µg/mL IC50) against C. albicans and A. niger, respectively. |
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Article |
author |
Abid, F. M. A. Jamalis, J. Chander, S. Wahab, R. A. Bhagwat, D. P. Sankaranarayanan, M. |
author_facet |
Abid, F. M. A. Jamalis, J. Chander, S. Wahab, R. A. Bhagwat, D. P. Sankaranarayanan, M. |
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Abid, F. M. A. |
title |
Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
title_short |
Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
title_full |
Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
title_fullStr |
Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
title_full_unstemmed |
Synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
title_sort |
synthesis, characterization, in silico and antifungal studies of thiazolidine analogues |
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Elsevier B. V. |
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2019 |
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http://eprints.utm.my/id/eprint/89748/ https://dx.doi.org/10.1016/j.cdc.2019.100219 |
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