Linamarin

SKU
L-1045
  • CAS:554-35-8
  • Formula:C10H17NO6
  • MW:247.2
  • Appearance:White Solid
  • Purity:97%

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Product Name Qty
Linamarin
25 mg
$284.76

Carbohydrate which acts as a cyanogenic glycoside.Genetic Screening Identifies Cyanogenesis-Deficient Mutants of Lotus japonicus and Reveals Enzymatic Specificity in Hydroxynitrile Glucoside Metabolism.TheGlucosidases Responsible for Bioactivation of Hydroxynitrile Glucosides in Lotus japonicus.

More Information
Alternate Name/Synonyms
hydroxyisobutyronitrile-D-glucopyranoside
SKU
L-1045
CAS #
554-35-8
Chemical Name
α-hydroxyisobutyronitrile-β-D-glucopyranoside
Chemical Formula
C10H17NO6
Molecular Weight
247.2
Appearance
White Solid
Purity
97%
Solubility
Soluble in Water, Methanol
Storage Temp
-20°C
THERAPEUTIC AREA
Not Available
USE
Linamarin is a cyanogenic glycoside
MDL NUMBER
MFCD00036209
CHEMACX
X1036566-7
INCHI
InChI=1S/C10H17NO6/c1-10(2,4-11)17-9-8(15)7(14)6(13)5(3-12)16-9/h5-9,12-15H,3H2,1-2H3/t5-,6-,7+,8-,9+/m1/s1
SMILES
CC(C)(C#N)O[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
Peptide sequence
Not Applicable
RTECS
TZ4850000
UN #'S
Not Applicable
PACKING GROUP
Not Applicable
HAZARD CLASS
Not Applicable
Handling
Store in Tightly Sealed Vial Packaged under inert atmosphere.
Citations
RESEARCH ARTICLES: Genetic Screening Identifies Cyanogenesis-Deficient Mutants of Lotus japonicus and Reveals Enzymatic Specificity in Hydroxynitrile Glucoside Metabolism Adam Takos, Daniela Lai, Lisbeth Mikkelsen, Maher Abou Hachem, Dale Shelton, Mohammed Saddik Motawia, Carl Erik Olsen, Trevor L. Wang, Cathie Martin, and Fred Rook PLANT CELL, May 2010; 22: 1605 - 1619.
Citations_Hyperlink
http://www.plantcell.org/cgi/reprint/22/5/1605
Certificate of Analysis 1
Certificate of Analysis 2
Certificate of Analysis 3
GHS PICTOGRAMS
Handling Store in Tightly Sealed Vial Packaged under inert atmosphere.
UN #'S Not Applicable
Packing Group Not Applicable
Citations Genetic screening identifies cyanogenesis-deficient mutants of Lotus japonicus and reveals enzymatic specificity in hydroxynitrile glucoside metabolism
The beta-glucosidases responsible for bioactivation of hydroxynitrile glucosides in Lotus japonicus
The evolutionary appearance of non-cyanogenic hydroxynitrile glucosides in the Lotus genus is accompanied by the substrate specialization of paralogous β-glucosidases resulting from a crucial amino acid substitution
Genomic clustering of cyanogenic glucoside biosynthetic genes aids their identification in Lotus japonicus and suggests the repeated evolution of this chemical defence pathway
Purification and detection of linamarin from cassava root cortex by high performance liquid chromatography
Diversified glucosinolate metabolism: biosynthesis of hydrogen cyanide and of the hydroxynitrile glucoside alliarinoside in relation to sinigrin metabolism in Alliaria petiolata
On the biomarkers and mechanisms of konzo, a distinct upper motor neuron disease associated with food (cassava) cyanogenic exposure
Cyanogenic glycosides content in two edible leaves of tree spinach (Cnidoscolus spp.)
Glucosinolate-related glucosides in Alliaria petiolata: sources of variation in the plant and different metabolism in an adapted specialist herbivore, Pieris rapae
Raman spectroscopic analysis of cyanogenic glucosides in plants: development of a flow injection surface-enhanced Raman scatter (FI-SERS) method for determination of cyanide
In vitro degradation of poly (D, L-lactide-co-glycolide) nanoparticles loaded with linamarin
An in vitro inhibition of human malignant cell growth of crude water extract of cassava (Manihot esculenta Crantz) and commercial linamarin
Dissipation of cyanogenic glucosides and cyanide in soil amended with white clover (Trifolium repens L.)
Molecular evolution of the Li/li chemical defence polymorphism in white clover (Trifolium repens L.)
Cyanide content of cassava and cassava products in some pacific island countries
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