- Title
- Ferrocenyl and organic novobiocin derivatives: synthesis and their in vitro biological activity
- Creator
- Mbaba, Mziyanda, Mabhula, Amanda N, Boel, Natasha, Edkins, Adrienne L, Isaacs, Michelle, Hoppe, Heinrich C, Khanye, Setshaba D
- Date
- 2017
- Type
- text
- Type
- article
- Identifier
- http://hdl.handle.net/10962/66189
- Identifier
- vital:28914
- Identifier
- https://doi.org/10.1016/j.jinorgbio.2017.04.014
- Description
- publisher version
- Description
- A focused series of novobiocin derivatives containing a ferrocene unit together with their corresponding organic novobiocin analogues have been synthesized in modest to good yields. These compounds were screened for biological activity against a chloroquine-sensitive strain of Plasmodium falciparum (3D7) and human breast cancer cell line (HCC38). With the exception of compounds 5c and 5d, the general trend observed is that incorporation of the ferrocene moiety into novobiocin scaffold resulted in compounds 6a–d/6f showing enhanced activity compared to organic analogues 5a–b and 5e–f.
- Format
- 6 pages, pdf
- Language
- English
- Relation
- Journal of Inorganic Biochemistry, Mbaba, Mziyanda, Mabhula, Amanda N., Boel, Natasha, Edkins, Adrienne L., Isaacs, Michelle, Hoppe, Heinrich C., Khanye, Setshaba D. (2017) Ferrocenyl and organic novobiocin derivatives: Synthesis and their in vitro biological activity. Journal of Inorganic Biochemistry, 172, p. 88 – 93. SN - 0162-0134. https://doi.org/10.1016/j.jinorgbio.2017.04.014, Journal of Inorganic Biochemistry volume 172 number 88 93 July 2017 0162-0134
- Rights
- Elsevier B.V.
- Rights
- Use of this resource is governed by the terms and conditions of the Journal of Inorganic Biochemistry Guide for Authors Open Access Statement (https://www.elsevier.com/journals/journal-of-inorganic-biochemistry/0162-0134/guide-for-authors)
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