Enceleamycins A-C, Furo-Naphthoquinones from Amycolatopsis sp. MCC0218: Isolation, Structure Elucidation, and Antimicrobial Activity.
Abujunaid KhanMadhukar S SaidBalasaheb R BoradeRajesh G GonnadeVitthal T BarvkarRavindar KonthamSyed Gulam DastagerPublished in: Journal of natural products (2022)
Three novel furo-naphthoquinones, enceleamycins A-C ( 1 - 3 ), and a new N -hydroxypyrazinone acid ( 4 ) were identified from the strain Amycolatopsis sp. MCC 0218, isolated from a soil sample collected from the Western Ghats of India. Their chemical structure and absolute and relative configurations were established by 1D and 2D NMR spectroscopy, single-crystal X-ray crystallography, and high-resolution mass spectrometry. Compounds 1 and 3 were active against methicillin-susceptible and -resistant Staphylococcus aureus with MIC values of 2-16 μg/mL.
Keyphrases
- staphylococcus aureus
- high resolution mass spectrometry
- liquid chromatography
- ultra high performance liquid chromatography
- biofilm formation
- methicillin resistant staphylococcus aureus
- high resolution
- gas chromatography
- mass spectrometry
- south africa
- tandem mass spectrometry
- magnetic resonance
- pseudomonas aeruginosa
- candida albicans