Author:
Singh Shalini,Kanungo B. K.,Baral Minati
Publisher
Springer Science and Business Media LLC
Reference52 articles.
1. He, M., Fan, M., Peng, Z., Wang, G.: An overview of hydroxypyranone and hydroxypyridinone as privileged scaffolds for novel drug discovery. Eur. J. Med. Chem. 221, 113546 (2021). https://doi.org/10.1016/j.ejmech.2021.113546
2. Jiang, X., Zhou, T., Bai, R., Xie, Y.: Hydroxypyridinone-based iron chelators with broad-ranging biological activities. J. Med. Chem. 63, 14470–14501 (2020). https://doi.org/10.1021/acs.jmedchem.0c01480
3. Burgess, J., Rangel, M.: Hydroxypyranones, hydroxypyridinones, and their complexes. In: Advances in Inorganic Chemistry, pp. 167–243. Elsevier, Amsterdam (2008)
4. Saeedi, M., Eslamifar, M., Khezri, K.: Kojic acid applications in cosmetic and pharmaceutical preparations. Biomed. Pharmacother. 110, 582–593 (2019). https://doi.org/10.1016/j.biopha.2018.12.006
5. Baláž, Š, Uher, M., Brtko, J., Veverka, M., Bransová, J., Dobias, J., Pódová, M., Buchvald, J.: Relationship between antifungal activity and hydrophobicity of kojic acid derivatives. Folia Microbiol. 38, 387–391 (1993). https://doi.org/10.1007/BF02898762