Fig. 2. 1H–1H COSY/HMBC (A-D) correlations of macrobrevin analogues (1–4). Key 1H–1H COSY correlations and HMBC pairings were characterized by bold-faced bonds and double-barbed arrows, respectively.Published as part of Chakraborty, Kajal, Kizhakkekalam, Vinaya Kizhakkepatt & Joy, Minju, 2022, Polyketide-derived macrobrevins from marine macroalga-associated Bacillus amyloliquefaciens as promising antibacterial agents against pathogens causing nosocomial infections, pp. 1-13 in Phytochemistry (112983) 193 on page 5, DOI: 10.1016/j.phytochem.2021.112983, http://zenodo.org/record/823515
Fig. 3. Selected HMBC correlations (A B: proton A to carbon B; A B: proton A to carbon B and proton ...
Not AvailablePreviously unreported aryl - enclosed 12 - membered macrocyclic polyketide characterise...
Previously unreported aryl-enclosed 12-membered macrocyclic polyketide characterised as 2′-[(8-ethyl...
Fig. 1. Structural representation of (A) trihydroxy-decahydro-37-methyl-macrobrevin (compound 1), (B...
Chakraborty, Kajal, Kizhakkekalam, Vinaya Kizhakkepatt, Joy, Minju (2022): Polyketide-derived macrob...
Fig. 5. (A) Molecular docking interfaces of 41-hydroxy-macrobrevin-31-acetate (compound 3) with S. a...
Fig. 4. Proposed biosynthesis of 21- membered macrocyclic lactones classified as macrobrevin analogu...
Fig. 3. (A) Biosynthetic gene cluster coding for biosynthesis of macrobrevin analogues in B. amyloli...
Fig. 2. Key HMBC and COSY correlations of 1–5.Published as part of Wang, Wenxue, Feng, Huimin, Sun, ...
Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.Published as part of X...
Fig. 2. (A1-C1) 1H–1H COSY (bold-face bonds), selected HMBCs (double-barbed arrows), (A2-C2) NOE (co...
Fig. 2. The key HMBC and COSY (bold line) correlations of compounds 1–6.Published as part of Wongsom...
Fig. 4. Key 1H–1H COSY (¡), HMBC (→), and NOESY (↔) correlations of compound 1.Published as part of ...
Fig. 8. Key HMBC correlations in 7.Published as part of Kumla, Decha, Sousa, Emilia, Marengo, Alessi...
Fig. 2. Selected HMBC correlations (A B: proton A to carbon B; A B: proton A to carbon B and proton ...
Fig. 3. Selected HMBC correlations (A B: proton A to carbon B; A B: proton A to carbon B and proton ...
Not AvailablePreviously unreported aryl - enclosed 12 - membered macrocyclic polyketide characterise...
Previously unreported aryl-enclosed 12-membered macrocyclic polyketide characterised as 2′-[(8-ethyl...
Fig. 1. Structural representation of (A) trihydroxy-decahydro-37-methyl-macrobrevin (compound 1), (B...
Chakraborty, Kajal, Kizhakkekalam, Vinaya Kizhakkepatt, Joy, Minju (2022): Polyketide-derived macrob...
Fig. 5. (A) Molecular docking interfaces of 41-hydroxy-macrobrevin-31-acetate (compound 3) with S. a...
Fig. 4. Proposed biosynthesis of 21- membered macrocyclic lactones classified as macrobrevin analogu...
Fig. 3. (A) Biosynthetic gene cluster coding for biosynthesis of macrobrevin analogues in B. amyloli...
Fig. 2. Key HMBC and COSY correlations of 1–5.Published as part of Wang, Wenxue, Feng, Huimin, Sun, ...
Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.Published as part of X...
Fig. 2. (A1-C1) 1H–1H COSY (bold-face bonds), selected HMBCs (double-barbed arrows), (A2-C2) NOE (co...
Fig. 2. The key HMBC and COSY (bold line) correlations of compounds 1–6.Published as part of Wongsom...
Fig. 4. Key 1H–1H COSY (¡), HMBC (→), and NOESY (↔) correlations of compound 1.Published as part of ...
Fig. 8. Key HMBC correlations in 7.Published as part of Kumla, Decha, Sousa, Emilia, Marengo, Alessi...
Fig. 2. Selected HMBC correlations (A B: proton A to carbon B; A B: proton A to carbon B and proton ...
Fig. 3. Selected HMBC correlations (A B: proton A to carbon B; A B: proton A to carbon B and proton ...
Not AvailablePreviously unreported aryl - enclosed 12 - membered macrocyclic polyketide characterise...
Previously unreported aryl-enclosed 12-membered macrocyclic polyketide characterised as 2′-[(8-ethyl...