Literature DB >> 1880062

Herbicidal nucleosides from microbial sources.

B G Isaac1, S W Ayer, L J Letendre, R J Stonard.   

Abstract

The structures of five naturally-occurring herbicidal nucleosides have been determined by spectral analysis. Three (5'-deoxyguanosine, coaristeromycin and 5'-deoxytoyocamycin) are novel natural products while the remaining two (coformycin and adenine 9-beta-D-arabinofuranoside) are known natural products which have not previously been reported to be herbicidal.

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Year:  1991        PMID： 1880062     DOI： 10.7164/antibiotics.44.729

Source DB:  PubMed          Journal:  J Antibiot (Tokyo)        ISSN： 0021-8820            Impact factor:   2.649


  5 in total

1.  Phosphine-catalyzed β'-umpolung addition of nucleophiles to activated α-alkyl allenes.

Authors:  Tioga J Martin; Venus G Vakhshori; Yang S Tran; Ohyun Kwon
Journal:  Org Lett       Date:  2011-04-14       Impact factor: 6.005

2.  Deciphering deazapurine biosynthesis: pathway for pyrrolopyrimidine nucleosides toyocamycin and sangivamycin.

Authors:  Reid M McCarty; Vahe Bandarian
Journal:  Chem Biol       Date:  2008-08-25

Review 3.  Biosynthesis of pyrrolopyrimidines.

Authors:  Reid M McCarty; Vahe Bandarian
Journal:  Bioorg Chem       Date:  2012-01-31       Impact factor: 5.275

4.  Adenine nucleotide pool perturbation is a metabolic trigger for AMP deaminase inhibitor-based herbicide toxicity.

Authors:  Richard L Sabina; Anna-Lisa Paul; Robert J Ferl; Bernd Laber; Stephen D Lindell
Journal:  Plant Physiol       Date:  2007-02-16       Impact factor: 8.340

5.  Evolution of new function in the GTP cyclohydrolase II proteins of Streptomyces coelicolor.

Authors:  James E Spoonamore; Annie L Dahlgran; Neil E Jacobsen; Vahe Bandarian
Journal:  Biochemistry       Date:  2006-10-03       Impact factor: 3.162
  5 in total

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