Marinoquinolines A-F, pyrroloquinolines from ohtaekwangia kribbensis (Bacteroidetes)

Journal of Natural Products

Volumn 74, Issue 4, 2011, Pages 603-608

  Okanya, Patrick W ^a,b   Mohr, Kathrin I ^a   Gerth, Klaus ^a   Jansen, Rolf ^a   Müller, Rolf ^a,b  

^a HELMHOLTZ CENTRE FOR INFECTION RESEARCH   (Germany)

^b SAARLAND UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIBIOTIC AGENT; ANTIFUNGAL AGENT; MARINOQUINOLINE A; MARINOQUINOLINE B; MARINOQUINOLINE C; MARINOQUINOLINE D; MARINOQUINOLINE E; MARINOQUINOLINE F; PYRROLOQUINOLINEQUINONE; UNCLASSIFIED DRUG;

ANIMAL CELL; ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ANTIPROTOZOAL ACTIVITY; ARTICLE; BACTEROIDETES; CONTROLLED STUDY; CYTOTOXICITY; DRUG STRUCTURE; FEMALE; HUMAN; HUMAN CELL; IC 50; MOUSE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OHTAEKWANGIA KRIBBENSIS; PLASMODIUM FALCIPARUM;

ANTI-BACTERIAL AGENTS; ANTIFUNGAL AGENTS; ANTIMALARIALS; ANTINEOPLASTIC AGENTS; BACTEROIDETES; DRUG SCREENING ASSAYS, ANTITUMOR; FEMALE; HUMANS; INDIA; INHIBITORY CONCENTRATION 50; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE, BIOMOLECULAR; PLASMODIUM FALCIPARUM; PYRROLES; QUINOLINES;

BACTERIA (MICROORGANISMS); BACTEROIDETES; MAMMALIA; PLASMODIUM FALCIPARUM;

EID: 79955449444     PISSN: 01633864     EISSN: 15206025     Source Type: Journal    
DOI: 10.1021/np100625a     Document Type: Article

References (13)

1. Srisukchayakul, P.; Suwanachart, C.; Sangnoi, Y; Kanjana-Opas, A.; Hosoya, S.; Yokota, A.; Arunpairojana, V. Int. J. Syst. Evol. Microbiol. 2007, 57, 2275-2279
2. Kanjana-opas, A.; Panphon, S.; Fun, H.; Chantrapromma, S. Acta Crystallogr. 2006, E62, 2728-2730
3. Sangnœ, Y.; Sakulkeo, O.; Yuenyongsawad, S.; Kanjana-opas, A.; Ingkaninan, K.; Plubrukarn, A.; Suwanborirux, K. Mar. Drugs 2008, 6, 578-586
4. Yoon, J. H.; Kang, S. J.; Lee, S. Y.; Lee, J. S.; Park, S. Int. J. Syst. Evol. Microbiol. 2010, (in press) doi: 10.1099/ijs.0.025874-0.
5. Dictionary of Natural Products on DVD, Ver. 19.1, CRC Press: London, UK, 2010.
6. In a pyridine-type ring a vicinal coupling of about 5.5 Hz would be expected. In a simple pyridine ring the direct H,C coupling of methine 5 would be expected near 163 Hz compared to 168 Hz for a corresponding pyrrole.
7. Abraham, R. J.; Mobli, M.; Smith, R. J. Magn. Reson. Chem. 2003, 41, 26-36
8. Mayser, P.; Schäfer, U.; Krämer, H. J.; Irlinger, B.; Steglich, W. Dermatol. Res. 2002, 294, 131-134
9. Mosmann, T. J. Immunol. Methods 1983, 65, 56-63
10. Becher, P. G.; Beuchat, J.; Gademann, K.; Jüttner, F. J. Nat. Prod. 2005, 68, 1793-1795
11. Bonazzi, S.; Barbaras, D.; Patiny, L.; Scopelliti, R.; Schneider, P.; Cole, S. T.; Kaiser, M.; Brun, R.; Gademann, K. Biorg. Med. Chem. 2010, 18, 1464-1476
12. Van Baelen, G.; Hostyn, S.; Dhooghe, L.; Tapolcsanyi, P.; Matyus, P.; Lemiere, G.; Dommisse, R.; Kaiser, M.; Brun, R.; Cos, P.; Maes, L.; Hajos, G.; Riedl, Z.; Nagy, I.; Maes, B. U. W.; Pieters, L. Biorg. Med. Chem. 2009, 17, 7209-7217
13. Shimkets, L. J.; Dworkin, M.; Reichenbach, H. The myxobacteria. In The Prokaryotes: A Handbook on the Biology of Bacteria; Dworkin, M.; Falkow, S.; Rosenberg, E.; Schleifer, K. H.; Stackebrandt, E., Eds.; Springer: New York, 2006; Vol. 7, pp 31 - 115.