14687-15-1
Chemical Structure
Methyl α-L-fucopyranoside
Synonym(s): Methyl alpha-L-fucopyranoside
- CAS No.: 14687-15-1
- Formula:C7H14O5
- Molecular Weight:178.18
IUPAC Name: (2R,3S,4R,5S,6S)-2-methoxy-6-methyltetrahydro-2H-pyran-3,4,5-triol
InChIKey: OHWCAVRRXKJCRB-CXNFULCWSA-N
SMILES: CO[C@H]1[C@H]([C@@H]([C@@H]([C@@H](O1)C)O)O)O
Biological Activity: Methyl α-L-fucopyranoside (Methyl alpha-L-fucopyranoside) is a fucopyranoside derivative with weak phagostimulatory activity against Spodoptera litura larvae. Methyl α-L-fucopyranoside serves as a starting material for the synthesis of isomeric methyl α-L-fucopyranoside sulfates. Methyl α-L-fucopyranoside shows potential for use in pest control-related research[1][2].
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Methyl α-L-fucopyranoside | 99.88% | Methyl α-L-fucopyranoside (Methyl alpha-L-fucopyranoside) is a fucopyranoside derivative with weak phagostimulatory activity against Spodoptera litura larvae. Methyl α-L-fucopyranoside serves as a starting material for the synthesis of isomeric methyl α-L-fucopyranoside sulfates. Methyl α-L-fucopyranoside shows potential for use in pest control-related research. | ||||||||||||||||||||
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- [1]. Flowers H M, et al. The feeding response of the larva of the Egyptian cotton leafworm, Spodoptera littoralis Boisd., to sugars and related compounds—IV. Ingestion and excretion of some phagostimulatory weak or inactive carbohydrates. Comparative Biochemistry and Physiology Part A: Physiology. 1975;51A:145-149. [Content Brief]
- [2]. Leder I G. Synthesis of the Sodium Salts of Methyl α-L-Fucopyranoside 2-, 3-, and 4-Sulfates. Journal of Carbohydrate Chemistry. 1993;12(1):95-103.
Keywords
