Last Update: June 1, 2012

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Number of references found for the '' category : 22

(1)LaMarche, et al. (2011). 4-Aminothiazolyl analogues of GE2270 A: antibacterial lead finding. J Med Chem. 54(7):2517-21. [PudMed:21405087]
(2)Lamarche, et al. (2011). 4-Aminothiazolyl analogs of GE2270 A: Design, synthesis and evaluation of imidazole analogs. Bioorg Med Chem Lett. 21(11):3210-5. [PudMed:21550238]
(3)Morris, et al. (2009). Ribosomally synthesized thiopeptide antibiotics targeting elongation factor Tu.. J Am Chem Soc.. 131(16):5946-55. [PudMed:19338336]
(4)Delgado, et al. (2008). Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A.. Chemistry.. 14(8):2322-39.. [PudMed:18270986]
(5)Müller, et al. (2007). Total synthesis of the thiazolyl peptide GE2270 A.. Angew Chem Int Ed Engl.. 46(25):4771-4. [PudMed:17503407]
(6)Delgado, et al. (2006). Synthesis and configurational assignment of the amino alcohol in the eastern fragment of the GE2270 antibiotics by regio- and stereoselective addition of 2-metalated 4-bromothiazoles to alpha-chiral electrophiles.. J Org Chem.. 71(12):4599-608. [PudMed:16749794]
(7)Parmeggiani, et al. (2006). Structural basis of the action of pulvomycin and GE2270 A on elongation factor Tu. Biochemistry. 45(22):6846-57. [PudMed:16734421]
(8)Clough, et al. (2003). Combinatorial modification of natural products: synthesis and in vitro analysis of derivatives of thiazole peptide antibiotic GE2270 A: A-ring modifications.. Bioorg Med Chem Lett.. 13(20):3409-14. [PudMed:14505638]
(9)Gastaldo, et al. (2003). Changes in GE2270 antibiotic production in Planobispora rosea through modulation of methylation metabolism. Microbiology. 149(Pt 6):1523-32. [PudMed:12777492]
(10)De, et al. (2001). Biosynthesis of the thiazolylpeptide antibiotic GE2270. J Antibiot (Tokyo). 54(12):1066-71. [PudMed:11858662]
(11)Kenny, et al. (1997). In vitro antimicrobial activity of the thiazolyl peptide antibiotic MDL 62,879 (GE2270 A). Chemotherapy. 43(4):254-63. [PudMed:9209782]
(12)Colombo, et al. (1995). Contribution of mass spectrometry to the structural confirmation of components of the antibiotic GE2270 complex. Rapid Commun Mass Spectrom. 9(8):717-22. [PudMed:7647369]
(13)Selva, et al. (1995). Components of the GE2270 complex produced by Planobispora rosea ATCC 53773. J Antibiot (Tokyo). 48(9):1039-42. [PudMed:7592050]
(14)King, et al. (1993). In vitro activity of MDL 62,879 (GE2270 A) against aerobic gram-positive and anaerobic bacteria. Antimicrob Agents Chemother. 37(4):746-9. [PudMed:8494370]
(15)Goldstein, et al. (1993). In vitro antimicrobial activity of a new antibiotic, MDL 62,879 (GE2270 A). Antimicrob Agents Chemother. 37(4):741-5. [PudMed:8494369]
(16)Anborgh, et al. (1993). Probing the reactivity of the GTP- and GDP-bound conformations of elongation factor Tu in complex with the antibiotic GE2270 A. J Biol Chem. 268(33):24622-8. [PudMed:8227020]
(17)Selva, et al. (1991). Antibiotic GE2270 a: a novel inhibitor of bacterial protein synthesis. I. Isolation and characterization. J Antibiot (Tokyo). 44(7):693-701. [PudMed:1908853]
(18) Beltrametti, et al. (2007). Protoplast fusion and gene recombination in the uncommon Actinomycete Planobispora rosea producing GE2270. J Antibiot (Tokyo). 60(7): 447-454.. [on SciFinder(R)]
(19) Heckmann, et al. (2005). Synthesis of the heterocyclic core of the GE2270 antibiotics and structure elucidation of a major degradation product. Angew. Chem., Int. Ed. 44(8): 1199-1201. [on SciFinder(R)]
(20) Colombo, et al. (1996). Characterization of the antibiotic GE2270 complex by combined liquid chromatography and mass spectrometry. Rapid Commun. Mass Spectrom. 0(4): 409-412. [on SciFinder(R)]
(21) Lociuro, et al. (1996). Preparation of basic prolineamide derivatives of GE2270 and GE2270-like antibiotics. . 83 pp. [on SciFinder(R)]
(22) Sosio, et al. (1996). An elongation factor Tu (EF-Tu) resistant to the EF-Tu inhibitor GE2270 in the producing organism Planobispora rosea. Mol Microbiol. 22(1): 43-51. [on SciFinder(R)]