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Year Number of Results
1966 3
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1970 2
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1975 4
1980 2
1981 1
1983 2
1984 3
1985 5
1986 3
1987 4
1988 6
1989 3
1990 3
1991 2
1992 2
1993 3
1994 4
1995 4
1996 2
1997 1
1998 1
1999 4
2000 3
2001 7
2002 5
2003 2
2004 1
2005 2
2006 3
2007 1
2008 3
2009 7
2010 2
2011 1
2012 2
2013 4
2014 2
2015 1
2016 4
2017 2
2018 4
2019 3
2020 2
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2023 2
2024 0

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The following term was not found in PubMed: 20Mersyah
Page 1
Showing results for roridin%20Mersyah
Your search for Rohidin%20Mersyah retrieved no results
Isolation and characterization of roridin E.
Ridge CD, Mazzola EP, Coles MP, Hinkley SF. Ridge CD, et al. Magn Reson Chem. 2017 Apr;55(4):337-340. doi: 10.1002/mrc.4539. Epub 2016 Nov 10. Magn Reson Chem. 2017. PMID: 27737497
The commonly occurring, high-cytotoxicity macrolide roridin E has been re-isolated from Stachybotrys chartarum and characterized by 1-D and 2-D NMR spectroscopy. ...For the first time confirmation of structure was provided by a crystallographic solution for roridin
The commonly occurring, high-cytotoxicity macrolide roridin E has been re-isolated from Stachybotrys chartarum and characterized by 1 …
Recent Advances on Macrocyclic Trichothecenes, Their Bioactivities and Biosynthetic Pathway.
Zhu M, Cen Y, Ye W, Li S, Zhang W. Zhu M, et al. Toxins (Basel). 2020 Jun 23;12(6):417. doi: 10.3390/toxins12060417. Toxins (Basel). 2020. PMID: 32585939 Free PMC article. Review.
According to the search results in database and phylogenetic trees generated in the review, the species of the genera Podostroma and Monosporascus would probably be great sources for producing macrocyclic trichothecenes. Moreover, we propose that the macrocyclic trichothecene …
According to the search results in database and phylogenetic trees generated in the review, the species of the genera Podostroma and Monospo …
Enzyme immunoassay for the macrocyclic trichothecene roridin A: production, properties, and use of rabbit antibodies.
Märtlbauer E, Gareis M, Terplan G. Märtlbauer E, et al. Appl Environ Microbiol. 1988 Jan;54(1):225-30. doi: 10.1128/aem.54.1.225-230.1988. Appl Environ Microbiol. 1988. PMID: 3278686 Free PMC article.
Antisera against roridin A were prepared by using a roridin A-hemisuccinate derivative coupled to human serum albumin as the immunogen. ...The assay was most specific for the tested macrocyclic trichothecenes, and the relative cross-reactivities with roridin
Antisera against roridin A were prepared by using a roridin A-hemisuccinate derivative coupled to human serum albumin as the i …
Production and characterization of monoclonal antibodies to the macrocyclic trichothecene roridin A.
Hack R, Märtlbauer E, Terplan G. Hack R, et al. Appl Environ Microbiol. 1988 Sep;54(9):2328-30. doi: 10.1128/aem.54.9.2328-2330.1988. Appl Environ Microbiol. 1988. PMID: 3190229 Free PMC article.
The antibodies, designated 5G11 and 4H10, had affinity constants for roridin A of 9.25 X 10(7) and 1.7 X 10(7) liters/mol, respectively. ...Both antibodies were most specific for the tested macrocyclic trichothecenes. The relative cross-reactivities of antibody 5G11 with …
The antibodies, designated 5G11 and 4H10, had affinity constants for roridin A of 9.25 X 10(7) and 1.7 X 10(7) liters/mol, respective …
Verrucarin A and roridin E produced on spinach by Myrothecium verrucaria under different temperatures and CO(2) levels.
Siciliano I, Bosio P, Gilardi G, Gullino ML, Garibaldi A. Siciliano I, et al. Mycotoxin Res. 2017 May;33(2):139-146. doi: 10.1007/s12550-017-0273-2. Epub 2017 Mar 9. Mycotoxin Res. 2017. PMID: 28281009 Free article.
The isolate used for this study was growing well on spinach, and the mycotoxins verrucarin A and roridin E were produced under all tested temperature and CO(2) conditions. The maximum levels of verrucarin A (18.59 ng/g) and roridin E (49.62 ng/g) were found at a tem …
The isolate used for this study was growing well on spinach, and the mycotoxins verrucarin A and roridin E were produced under all te …
[Structure of antibiotic Roridin H].
Traxler P, Tamm C. Traxler P, et al. Helv Chim Acta. 1970;53(7):1846-69. doi: 10.1002/hlca.19700530733. Helv Chim Acta. 1970. PMID: 5530851 German. No abstract available.
Macrocyclic trichothecenes as antifungal and anticancer compounds.
de Carvalho MP, Weich H, Abraham WR. de Carvalho MP, et al. Curr Med Chem. 2016;23(1):23-35. doi: 10.2174/0929867323666151117121521. Curr Med Chem. 2016. PMID: 26572613 Review.
This review is focused on compounds belonging to the macrocyclic type, where a cyclic diester or triester ring binds to the trichothecane moiety at C-4 and C- 15 leading to natural products belonging to the groups of satratoxins, verrucarins, roridins, myrotoxins and bacch …
This review is focused on compounds belonging to the macrocyclic type, where a cyclic diester or triester ring binds to the trichothecane mo …
131 results