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Number of references found for the '' category : 31

(1)Wei, et al. (2011). A simple reverse genetics approach to elucidating the biosynthetic pathway of nocathiacin. Biotechnol Lett. 33(3):585-91. [PudMed:21107653]
(2)Zhang, et al. (2011). Characterization of NocL Involved in Thiopeptide Nocathiacin I Biosynthesis: A [4Fe-4S] CLUSTER AND THE CATALYSIS OF A RADICAL S-ADENOSYLMETHIONINE ENZYME. J Biol Chem. 286(24):21287-94. [PudMed:21454624]
(3)Ding, et al. (2010). Moving posttranslational modifications forward to biosynthesize the glycosylated thiopeptide nocathiacin I in Nocardia sp. ATCC202099. Mol Biosyst. 6(7):1180-5. [PudMed:20473441]
(4)Wei, et al. (2010). Separation of structurally similar nocathiacin analogues by reversed phase chromatography. J Chromatogr A. 1217(18):3038-43. [PudMed:20303091]
(5)Wei, et al. (2010). Microbial generation of nocathiacin acid from nocathiacin I. Bioresour Technol. 101(10):3617-22. [PudMed:20106660]
(6)Xu, et al. (2009). Nocathiacin analogs: Synthesis and antibacterial activity of novel water-soluble amides. Bioorg Med Chem Lett. 19(13):3531-5. [PudMed:19447613]
(7)Junker, et al. (2009). Actinomycetes scale-up for the production of the antibacterial, nocathiacin. Biotechnol Prog. 25(1):176-88. [PudMed:19205044]
(8)Li, et al. (2008). N-Demethylation of nocathiacin I via photo-oxidation. Bioorg Med Chem Lett. 18(14):4051-3. [PudMed:18556203]
(9)Nicolaou, et al. (2007). New synthetic technology for the construction of N-hydroxyindoles and synthesis of nocathiacin I model systems.. Tetrahedron.. 63(27):6088-6114.. [PudMed:20606766]
(10)Xu, et al. (2007). Conversion of nocathiacin I to nocathiacin acid by a mild and selective cleavage of dehydroalanine. J Org Chem. 72(19):7447-50. [PudMed:17705543]
(11)Huang, et al. (2007). Observation of O-H...N scalar coupling across a hydrogen bond in nocathiacin I. Magn Reson Chem. 45(6):447-50. [PudMed:17431856]
(12)Naidu, et al. (2006). Synthesis and antibacterial activity of nocathiacin I analogues. Bioorg Med Chem Lett. 16(13):3545-9. [PudMed:16621551]
(13)Nicolaou, et al. (2005). Construction of substituted N-hydroxyindoles: synthesis of a nocathiacin I model system. Angew Chem Int Ed Engl. 44(24):3736-40. [PudMed:15892095]
(14)Naidu, et al. (2005). Synthesis, in vitro, and in vivo antibacterial activity of nocathiacin I thiol-Michael adducts. Bioorg Med Chem Lett. 15(8):2069-72. [PudMed:15808470]
(15)Connolly, et al. (2005). Chemical conversion of nocathiacin I to nocathiacin II and a lactone analogue of glycothiohexide alpha. J Nat Prod. 68(4):550-3. [PudMed:15844946]
(16)Naidu, et al. (2004). Synthesis and antibacterial activity of O-substituted nocathiacin I derivatives. Bioorg Med Chem Lett. 14(14):3743-6. [PudMed:15203154]
(17)Naidu, et al. (2004). Nocathiacin I analogues: synthesis, in vitro and in vivo biological activity of novel semi-synthetic thiazolyl peptide antibiotics. Bioorg Med Chem Lett. 14(22):5573-7. [PudMed:15482927]
(18)Regueiro-Ren, et al. (2004). Novel semi-synthetic nocathiacin antibiotics: synthesis and antibacterial activity of bis- and mono-O-alkylated derivatives. Bioorg Med Chem Lett. 14(1):171-5. [PudMed:14684322]
(19)Pucci, et al. (2004). Antimicrobial evaluation of nocathiacins, a thiazole peptide class of antibiotics. Antimicrob Agents Chemother. 48(10):3697-701. [PudMed:15388422]
(20)Leet, et al. (2003). Nocathiacins, new thiazolyl peptide antibiotics from Nocardia sp. II. Isolation, characterization, and structure determination. J Antibiot (Tokyo). 56(3):232-42. [PudMed:12760679]
(21)Regueiro-Ren, et al. (2002). Mild method for cleavage of dehydroalanine units: highly efficient conversion of nocathiacin I to nocathiacin IV. J Org Chem. 67(24):8699-702. [PudMed:12444665]
(22)Hrnciar, et al. (2002). Synthesis of novel nocathiacin-class antibiotics. Condensation of glycolaldehyde with primary amides and tandem reductive amination of amadori-rearranged 2-oxoethyl intermediates. J Org Chem. 67(25):8789-93. [PudMed:12467390]
(23) Singh, et al. (2008). Biosynthetic studies of Nocathiacin-I. Tetrahedron Lett. 49(43): 6265-6268. [on SciFinder(R)]
(24) Hudyma, et al. (2004). Preparation of nocathiacin O-derivatives. . 53 pp. [on SciFinder(R)]
(25) Naidu, et al. (2004). Organic reactions in frozen water: Michael addition of amines and thiols to the dehydroalanine side chain of nocathiacins. Tetrahedron Lett. 45(5): 1059-1063. [on SciFinder(R)]
(26) Li, et al. (2002). Nocathiacin antibiotics prepared by biotransformation or chemical methods. . 53 pp.. [on SciFinder(R)]
(27) Constantine, et al. (2002). Conformation and absolute configuration of nocathiacin I determined by NMR spectroscopy and chiral capillary electrophoresis. [Erratum to document cited in CA137:140768]. J. Am. Chem. Soc. 124(49): 14810. [on SciFinder(R)]
(28) Naidu, et al. (2002). Synthesis and Antibacterial Activity of Novel Nocathiacin I Analogs. . . [on SciFinder(R)]
(29) Leet, et al. (2000). Nocathiacin antibiotics. . 55 pp. [on SciFinder(R)]
(30) Li, et al. (2000). Nocathiacin antibiotic derivatives prepared by microbial biotransformation. . 50 pp. [on SciFinder(R)]
(31) Li, et al. (2000). Halo- or hydroxy-substituted nocathiacin antibiotics. . 43 pp. [on SciFinder(R)]