Pelopuradazole, a new imidazole derivative alkaloid from the marine bacteria Pelomonas puraquae sp. nov.

Natural Product Research

Volumn 28, Issue 9, 2014, Pages 680-682

  He, Xi Xin ^a   Chen, Xiao Jie ^a   Peng, Guang Tian ^a   Guan, Shan Yue ^b   Lei, Ling Fang ^a   Yao, Jun Hua ^b   Liu, Bing Xin ^a   Zhang, Cui Xian ^a  

^a GUANGZHOU UNIVERSITY OF CHINESE MEDICINE   (China)

^b SUN YAT SEN UNIVERSITY   (China)

Author keywords

alkaloid; cyclic dipeptide; Marine bacteria; Pelomonas puraquae sp. nov.; Pelopuradazole

Indexed keywords

1H PYRROLE 2 CARBOXYLIC ACID; 2 METHYL 3H IMIDAZOLE 4 CARBOXYLIC ACID; 3H IMIDAZOLE 4 CARBOXYLIC ACID; ALKALOID; ANTIFUNGAL AGENT; IMIDAZOLE DERIVATIVE; PELOPURADAZOLE; PELOPURIN A; PELOPURIN B; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ISOLATION; DRUG STRUCTURE; ELECTROSPRAY MASS SPECTROMETRY; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR SINGLE QUANTUM COHERENCE; MARINE BACTERIUM; NONHUMAN; PELOMONAS PURAQUAE; PROTON NUCLEAR MAGNETIC RESONANCE;

BACTERIA (MICROORGANISMS); PELOMONAS;

ALKALOID; CYCLIC DIPEPTIDE; MARINE BACTERIA; PELOMONAS PURAQUAE SP. NOV.; PELOPURADAZOLE;

ALKALOIDS; COMAMONADACEAE; IMIDAZOLES; MARINE BIOLOGY; PEPTIDES, CYCLIC; PROLINE;

EID: 84899471574     PISSN: 14786419     EISSN: 14786427     Source Type: Journal    
DOI: 10.1080/14786419.2014.891591     Document Type: Article

References (13)

1. Aguilar-Perez F, Gomez-Tagle P, Collado-Fregoso E, Yatsimirsky AK. 2006. Phosphate ester hydrolysis by hydroxo complexes of tri valent lanthanides stabilized by 4-imidazolecarboxylate. Inorg Chem. 45:9502-9517.
2. Anke D, Andreas H, Hans-Peter F, Goodfellow M, Muller WE, Brun R, Bringmann G. 2003. Biosynthetic capacitie s of Actinomycetes Pyrocoll, an antibiotic, antiparasitic and antitumor compound produced by a novel alkaliphilic Streptomyces strain. J Antibiot. 56:639-646.
3. Blunt JW, Copp BR, Keyzers RA, Munro MHG, Prinsep MR. 2013. Marine natural products. Nat Prod Rep. 30:237-323.
4. Franks A, Haywood P, Holmstro ̈m C, Egan S, Kjelleberg S, Kumar N. 2005. Isolation and structure elucidation of a novel yellow pigme nt from the marine bacterium Pseudoalteromonas tunicata. Molecules. 10:1286-1291.
5. Gao HF, Zhang DJ, Wei HG, Shen GM, Chen B, Li YG. 2008. Studies on the chemical constituents of the fermentation broth from Antarctic Marinomonas sp. BSw10005 strain. Chin J Marine Drug. 27:14-17.
6. Haeusler J Jahn R Schmidt U. 1978 Amino acids and peptides, XXIV. Radically and photochemically initiated oxidation of amino acid derivatives. Chem Ber. 111 361-366.
7. Korchak S, Ivanov K, Yurkovskaya A, Vieth HM. 2010. High resolution NMR study of T1 magnetic relaxation dispersion. II. Influence of spin-spin couplings on the longitudinal spin relaxation dispersion in multispin systems. J Chem Phys. 133:194502 /1-194502/11.
8. Kusebauch B, Brendel N, Kirchner H, Dahse HM, Hertweck C. 2011. Assessing oxazole bioisosteres as mutasynthons on the rhizoxin assembly line. ChemBioChem. 12:2284-2288.
9. Lu X, Xu QZ, Shen YH, Liu XY, Jiao BH, Zhang WD, Ni KY. 2008. Macrolactin S, a novel macrolactin antibiotic from marine Bacillus sp. Nat Prod Res. 22:342-347.
10. Mizuno CM, Kimes NE, Lopez-Perez M, AusóE, Rodriguez-Valera F, Ghai R. 2013. A hybrid NRPS-PKS gene cluster related to the bleomycin family of antitumor antibiotics in Alteromonas macleodii strains. PLOS One. 8:e76021.
11. Oehler E, Tataruch F, Schmidt U. 1973a . Amino acids and peptides. VI. Synthesis of the antibiotics gliotoxin, sporidesmin, aranotin, chaetocin, and verticillin. VI. Nucleophilic introduction of sulfur functions via sulfones and hydroxy derivatives of cyclic dip eptides (dioxopiperazines). Chem Ber. 106:165-176.
12. Oehler E, Tataruch F, Schmidt U. 1973b . Amino acids and peptides. VII. Synthesis of the antibiotics gliotoxin, sporidesmin, aranotin, chaetocin, and verticillin . VII. Introduction of oxygen functions in prolylproline anhydride with lead tetraacetate. A new way to epidithioprolylproline anhydride. Chem Ber. 106:396-398.
13. Zeng RY, Lin Y. 2006. Method for preparing compound with anti-HIV-I activity from deep sea bacteria strain[P]. Faming Zhuanli Shenqing, CN 1884479 A.