07743
Dhurrin
≥95% (HPLC)
Synonym(s):
(S)-(β-D-Glucopyranosyloxy)(4-hydroxyphenyl)acetonitrile, (S)-4-Hydroxymandelonitrile β-D-glucoside
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About This Item
Empirical Formula (Hill Notation):
C14H17NO7
CAS Number:
Molecular Weight:
311.29
PubChem Substance ID:
UNSPSC Code:
12352201
NACRES:
NA.25
EC Number:
207-878-6
MDL number:
Quality Level
assay
≥95% (HPLC)
form
powder or crystals
color
white to light brown
storage temp.
room temp
InChI
1S/C14H17NO7/c15-5-9(7-1-3-8(17)4-2-7)21-14-13(20)12(19)11(18)10(6-16)22-14/h1-4,9-14,16-20H,6H2/t9-,10-,11-,12+,13-,14-/m1/s1
InChI key
NVLTYOJHPBMILU-YOVYLDAJSA-N
General description
Dhurrin is a cyanogenic glucoside found expressed in the leaves of Sorghum plants. Studies have shown that as the plant ages, dhurrin expression depends are nitrogen availability. Dhurrin production shifts from the leaves to the stems during development.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
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Toni M Kutchan
Trends in biotechnology, 23(8), 381-383 (2005-06-01)
In an important recent paper Kristensen et al. address a question of fundamental importance in plant biotechnology: how are metabolic pathways affected upon introduction of a transgene? Analysis of the transcriptome and metabolome of Arabidopsis thaliana engineered to produce the
Brenda S J Winkel
Annual review of plant biology, 55, 85-107 (2005-02-24)
The organization of cooperating enzymes into macromolecular complexes is a central feature of cellular metabolism. A major advantage of such spatial organization is the transfer of biosynthetic intermediates between catalytic sites without diffusion into the bulk phase of the cell.
Charlotte Kristensen et al.
Proceedings of the National Academy of Sciences of the United States of America, 102(5), 1779-1784 (2005-01-25)
Focused and nontargeted approaches were used to assess the impact associated with introduction of new high-flux pathways in Arabidopsis thaliana by genetic engineering. Transgenic A. thaliana plants expressing the entire biosynthetic pathway for the tyrosine-derived cyanogenic glucoside dhurrin as accomplished