Home 
Last Update: June 1, 2012

Categories
Reviews Isolation and structure characterization Fermentation and production Biosynthesis
Bioactivity Chemical synthesis Anticancer Others
Relative Books                                           All
Search
    

Number of references found for the '' category : 50

(1)Yang, et al. (2010). Crystallization and preliminary crystallographic analysis of nosiheptide-resistance methyltransferase from Streptomyces actuosus in complex with SAM. Acta Crystallogr Sect F Struct Biol Cryst Commun. 66(Pt 5):579-82. [PudMed:20445264]
(2)Yu, et al. (2010). NosA catalyzing carboxyl-terminal amide formation in nosiheptide maturation via an enamine dealkylation on the serine-extended precursor peptide. J Am Chem Soc. 132(46):16324-6. [PudMed:21047073]
(3)Yang, et al. (2010). Crystal structure of the nosiheptide-resistance methyltransferase of Streptomyces actuosus. Biochemistry. 49(30):6440-50. [PudMed:20550164]
(4)Yu, et al. (2009). Nosiheptide biosynthesis featuring a unique indole side ring formation on the characteristic thiopeptide framework. ACS Chem Biol. 4(10):855-64. [PudMed:19678698]
(5)Lu, et al. (2009). Aza-Wittig-supported synthesis of the A ring of nosiheptide. Angew Chem Int Ed Engl. . 48(43):8137-40.. [PudMed:19784984]
(6)Feng, et al. (2008). Recombinant high-density lipoprotein complex as a targeting system of nosiheptide to liver cells. J Drug Target. 16(6):502-8. [PudMed:18604663]
(7)Zhang, et al. (2008). Overexpression of yeast S-adenosylmethionine synthetase metK in Streptomyces actuosus leads to increased production of nosiheptide. Appl Microbiol Biotechnol. 78(6):991-5. [PudMed:18330566]
(8)Kimber, et al. (2008). Construction of macrocyclic thiodepsipeptides: synthesis of a nosiheptide 'southern hemisphere' model system. Chem Commun (Camb). (5):591-3. [PudMed:18209799]
(9)Lu, et al. (2007). Hetero Diels-Alder synthesis of 3-hydroxypyridines: access to the nosiheptide core.. J Org Chem.. 72(11):4205-12.. [PudMed:17447818]
(10)Bentley, et al. (2004). Synthesis of the 2,3,4-trisubstituted indole fragments of nosiheptide and glycothiohexide. Org Biomol Chem. 2(5):701-8. [PudMed:14985810]
(11)Horii, et al. (2000 ). Rapid determination of nosiheptide in meat and egg by liquid chromatography with fluorescence detection.. J AOAC Int.. 83(1):17-9.. [PudMed:10692999]
(12)Li, et al. (1991). Transcriptional organization and regulation of the nosiheptide resistance gene in Streptomyces actuosus. J Ind Microbiol. 8(1):1-12. [PudMed:1367329]
(13)Li, et al. (1990). Nucleotide sequence and transcriptional analysis of the nosiheptide-resistance gene from Streptomyces actuosus. Gene. 91(1):9-17. [PudMed:2401410]
(14)Mocek, et al. (1989). 1H and 13C NMR assignments of the thiopeptide antibiotic nosiheptide. J Antibiot (Tokyo). 42(11):1643-8. [PudMed:2584148]
(15)Dary, et al. (1989). Cloning of a nosiheptide-resistant gene from Streptomyces actuosus. C R Acad Sci III.. 308(2):35-41. [PudMed:2493312]
(16)Dosch, et al. (1988). Molecular cloning of the nosiheptide resistance gene from Streptomyces actuosus ATCC 25421. Biochem Biophys Res Commun. 156(1):517-23. [PudMed:2845982]
(17)Cromwell, et al. (1984). Efficacy of nosiheptide as a growth promotant for growing-finishing swine--a cooperative study. J Anim Sci. 59(5):1125-8. [PudMed:6511687]
(18)Cundliffe, et al. (1981). The mode of action of nosiheptide (multhiomycin) and the mechanism of resistance in the producing organism. J Gen Microbiol. 126(1):185-92. [PudMed:7038038]
(19)Cundliffe, et al. (1981). The mode of action of nosiheptide (multhiomycin) and the mechanism of resistance in the producing organism. J Gen Microbiol. 126(1):185-92. [PudMed:7038038]
(20)Benazet, et al. (1980). Effect of nosiheptide as a feed additive in chicks on the quantity, duration, prevalence of excretion, and resistance to antibacterial agents of Salmonella typhimurium; on the proportion of Escherichia coli and other coliforms resistant to antibacterial agents; and on their degree and spectrum of resistance. Poult Sci. 59(7):1405-15. [PudMed:6994088]
(21) Jiang, et al. (). LC Determination of Nosiheptide in Swine Kidney and Liver. Chromatographia. 71(1-2): 131-134. [on SciFinder(R)]
(22) Lu, et al. (2009). Aza-Wittig-supported synthesis of the A ring of nosiheptide. [Erratum to document cited in CA152:037890]. Angew. Chem., Int. Ed.. 48(49): 9211. [on SciFinder(R)]
(23) Gorugantula, et al. (2009). Syntheses of fused pyrroloheterocycles, isatins, approach towards the indole fragment of nosiheptide and a base-mediated formation of 3-hydroxycarbazoles. . 262 pp. [on SciFinder(R)]
(24) Lu, et al. (2008). Development of a Hetero-Diels-Alder reaction to synthesize 3-hydroxypyridines and its application toward the total synthesis of nosiheptide. . . [on SciFinder(R)]
(25) Taddei, et al. (2007). An expedient approach to the 2,3,5,6-tetrasubstituted pyridine core of nosiheptide using oxidative cleavage of 2,3,5,8-tetrasubstituted quinolines. ARKIVOC (Gainesville, FL, U. S.). (11): 56-63. [on SciFinder(R)]
(26) Belhadj, et al. (2006). Synthesis of the 'northern-hemisphere' fragments of the thiopeptide antibiotic nosiheptide. Synlett. (18): 3033-3036. [on SciFinder(R)]
(27) Umemura, et al. (1998). Synthesis of a fragment A derivative of an antibiotic, nosiheptide. Bull. Chem. Soc. Jpn.. 71(6): 1391-1396. [on SciFinder(R)]
(28) Umemura, et al. (1997). The synthesis of fragment A of an antibiotic, Nosiheptide. Tetrahedron Lett.. 38(20): 3539-3542. [on SciFinder(R)]
(29) Gasmi, et al. (1996). Improvements of HSQC and HMBC experiments by J-modulation, t1-noise reduction and spectral domain selection. Application to the study of nosiheptide. Magn. Reson. Chem. 34(3): 185-190. [on SciFinder(R)]
(30) Shin, et al. (1996). Convenient synthesis of fragment E of antibiotic, nosiheptide. Heterocycles. 43(4): 891-898. [on SciFinder(R)]
(31) Shin, et al. (1995). Syntheses of 2-[(1S,3S)-1-amino-3-carboxy-3-hydroxypropyl]thiazole-4-carboxylic acid and the tripeptide skeleton of nosiheptide containing the acid. Bull. Chem. Soc. Jpn. 68(11): 3151-3160 . [on SciFinder(R)]
(32) Koerber-Ple, et al. (1995). Total synthesis of nosiheptide. Synthesis of thiazole fragments. J. Heterocycl. Chem. . 32(4): 1309-1315. [on SciFinder(R)]
(33) Umemura, et al. (1995). A facile synthesis of fragment D of antibiotic, nosiheptide. Synthesis. (11): 1423-1426. [on SciFinder(R)]
(34) Koerber-Ple, et al. (1994). Synthesis of an unusual 2,3,4-trisubstituted indole derivative found in the antibiotic nosiheptide. J. Chem. Soc., Chem. Commun. (9): 759-760. . [on SciFinder(R)]
(35) Mocek, et al. (1993). Biosynthesis of the modified peptide antibiotic nosiheptide in Streptomyces actuosus. J. Am. Chem. Soc. 115(17): 7557-7568. [on SciFinder(R)]
(36) Smith, et al. (1993). 3,4-Dimethylindole-2-carboxylate and 4-(1-hydroxyethyl)quinoline-2-carboxylate activating enzymes from the nosiheptide and thiostrepton producers, Streptomyces actuosus and Streptomyces laurentii. J. Chem. Soc., Chem. Commun.. (21): 1612-1614. [on SciFinder(R)]
(37) Smith, et al. (1993). 3,4-Dimethylindole-2-carboxylate and 4-(1-hydroxyethyl)quinoline-2-carboxylate activating enzymes from the nosiheptide and thiostrepton producers, Streptomyces actuosus and Streptomyces laurentii. J. Chem. Soc., Chem. Commun.. (21): 1612-1614. [on SciFinder(R)]
(38) Houck, et al. (1988). Biosynthesis of the modified peptide antibiotic nosiheptide in Streptomyces actuosus. J. Am. Chem. Soc.. 110(17): 5800-5806. [on SciFinder(R)]
(39) Houck, et al. (1987). Biosynthesis of the modified peptide antibiotic nosiheptide in Streptomyces actuosus. J. Am. Chem. Soc.. 109(4): 1250-1252. . [on SciFinder(R)]
(40) Houck, et al. (1986). Studies on the biosynthesis of the modified-peptide antibiotic, nosiheptide. . 114 pp. [on SciFinder(R)]
(41) Labeda, et al. (1983). Antibiotic nosiheptide. . 21 pp. [on SciFinder(R)]
(42) Iwakawa, et al. (1982). A facile synthetic approach to the fragment D of antibiotic nosiheptide, 2-[1-amino-3-carboxy-3-hydroxy-(1S,3S)-propyl]thiazole-4-carboxylic acid. Chem. Lett.. (12): 1975-1978. [on SciFinder(R)]
(43) Benazet, et al. (1980). Nosiheptide, a sulfur-containing peptide antibiotic isolated from Streptomyces actuosus 40037. Experientia. 36(4): 414-416. [on SciFinder(R)]
(44) Endo, et al. (1978). Identity of multhiomycin with nosiheptide. J. Antibiot.. 31(6): 623-625. [on SciFinder(R)]
(45) Depaire, et al. (1977). Acid and alkaline hydrolysis of the antibiotic nosiheptide. The structure elucidation of five fragments. Tetrahedron Lett.. (16): 1395-1396. [on SciFinder(R)]
(46) Prange, et al. (1977). Structure of nosiheptide, a polythiazole-containing antibiotic. Nature (London). 265(5590): 189-190. [on SciFinder(R)]
(47) Pascard, et al. (1977). Highly modified cysteine-containing antibiotics. Chemical structure and configuration of nosiheptide. J. Am. Chem. Soc.. 99(19): 6418-6423. [on SciFinder(R)]
(48) Depaire, et al. (1977). Carbon-13 NMR spectroscopy of nosiheptide. Tetrahedron Lett.. (16): 1397-1400. [on SciFinder(R)]
(49) Depaire, et al. (1977). The structure relation between the antibiotics nosiheptide and thiostrepton. Tetrahedron Lett.. (16): 1403-1406. [on SciFinder(R)]
(50) Depaire, et al. (1977). Nitrogen-15 NMR spectroscopy of nosiheptide. Determination of the elemental formula and the molecular weight of the antibiotic. Tetrahedron Lett. (16): 1401-1402. [on SciFinder(R)]