2021
DOI: 10.1016/j.bioorg.2021.104668
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Antibacterial activity of a new monocarbonyl analog of curcumin MAC 4 is associated with divisome disruption

Abstract: Antibacterial activity of a new monocarbonyl analog of curcumin MAC 4 is associated with divisome disruption. Bioorganic Chemistry, 109, [104668].

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Cited by 12 publications
(9 citation statements)
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References 70 publications
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“…In an attempt to overcome increased antibacterial resistance, research into structural modifications of natural products to enhance their biological activities has been conducted (▶ Table 1). Due to its already well-established pharmacological activities, cur-cuminʼs structure has been studied and synthetically modified to form curcumin analogues to further enhance these antibacterial activities [28][29][30][31][32][33][34][35].…”
Section: Antibacterial Activity Of Curcumin Analoguesmentioning
confidence: 99%
“…In an attempt to overcome increased antibacterial resistance, research into structural modifications of natural products to enhance their biological activities has been conducted (▶ Table 1). Due to its already well-established pharmacological activities, cur-cuminʼs structure has been studied and synthetically modified to form curcumin analogues to further enhance these antibacterial activities [28][29][30][31][32][33][34][35].…”
Section: Antibacterial Activity Of Curcumin Analoguesmentioning
confidence: 99%
“…It was found that these derivatives at (MIC 90 = 7.8-27.9 μg/ml) were able to inhibit MTB growth. 117 To overcome the limited stability and pharmacokinetics associated with curcumin, Polaquini et al 118 synthesized a MACs having enhanced and broad-spectrum antibacterial activity against MTB, MRSA, and A. baumannii having MIC values lying between 0.9 and 15.6 μg/ml. 118 Future studies of this reported potential isomeric forms of curcumin and their principle of interaction with MTB may be carried out and compared with that of native crude curcumin, which may be helpful in future design and synthesis of highly efficient anti-MTB synthetic drug derived from curcumin.…”
Section: Curcumin and Its Important Nanoformulations Against Mtb Infe...mentioning
confidence: 99%
“…It was found that these derivatives at (MIC 90 = 7.8–27.9 μg/ml) were able to inhibit MTB growth 117 . To overcome the limited stability and pharmacokinetics associated with curcumin, Polaquini et al 118 . synthesized a MACs having enhanced and broad‐spectrum antibacterial activity against MTB , MRSA, and A. baumannii having MIC values lying between 0.9 and 15.6 μg/ml 118 .…”
Section: Curcumin and Its Important Nanoformulations Against Mtb Infe...mentioning
confidence: 99%
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