| Weight | 247.247 g/mol |
|---|---|
| Formula | C10H17NO6 |
| Hydrogen Acceptors | 7 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
LINAMARIN (554-35-8)
Score:
#1306 in Biochemistry
,
#3199 in Biology
,
#4001 in Chemistry
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- Cytochromes P-450 from cassava (Manihot esculenta Crantz) catalyzing the first steps in the biosynthesis of the cyanogenic glucosides linamarin and lotaustralin: cloning, functional expression in Pichia pastoris, and substrate specificity of the isolated recombinant enzymes. (Journal of Biological Chemistry, 2000)
- Studies on cassava, Manihot utilissima PohlI. Cyanogenesis: The biosynthesis of linamarin and lotaustralin in etiolated seedlings (Phytochemistry, 1968)
- Biosynthesis of the Nitrile Glucosides Rhodiocyanoside A and D and the Cyanogenic Glucosides Lotaustralin and Linamarin in Lotus japonicus (Plant Physiology, 2004)
- The distribution of the cyanoglucosides linamarin and lotaustralin in higher plants (Phytochemistry, 1965)
- Geographical and seasonal association between linamarin and cyanide exposure from cassava and the upper motor neurone disease konzo in former Zaire (Tropical Medicine & International Health, 1997)
- OCCURRENCE, VARIATION AND BIOSYNTHESIS OF THE CYANOGENIC GLUCOSIDES LINAMARIN AND LOTAUSTRALIN IN SPECIES OF THE HELICONIINI (INSECTA: LEPIDOPTERA) (Comparative Biochemistry and Physiology B, 1983)
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SMILESCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O
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InChIKeyQLTCHMYAEJEXBT-UHFFFAOYSA-N
- Pubchem - LINAMARIN
- Wikipedia - linamarin
Linamarin is a cyanogenic glucoside found in the leaves and roots of plants such as cassava, lima beans, and flax. It is a glucoside of acetone cyanohydrin. Upon exposure to enzymes and gut flora in the human intestine, linamarin and its methylated relative lotaustralin can decompose to the toxic chemical hydrogen cyanide; hence food uses of plants that contain significant quantities of linamarin require extensive preparation and detoxification.
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