3615-44-9
Chemical Structure
D-Mannoheptulose
- CAS No.: 3615-44-9
- Formula:C7H14O7
- Molecular Weight:210.18
IUPAC Name: (3S,4S,5R,6R)-1,3,4,5,6,7-hexahydroxyheptan-2-one
InChIKey: HSNZZMHEPUFJNZ-QMTIVRBISA-N
SMILES: OCC([C@H]([C@H]([C@@H]([C@@H](CO)O)O)O)O)=O
Biological Activity: D-Mannoheptulose is a 7-carbon keto sugar found in avocado. D-mannoheptulose is a specific inhibitor of D-glucose phosphorylation by hexokinase isoenzymes. D-Mannoheptulose can block insulin release and utilization of carbohydrate in rat. D-Mannoheptulose has various functions as anti-oxidants, anticancer effects and energy sources[1][2][3][4].
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D-Mannoheptulose | 99.9% | D-Mannoheptulose is a 7-carbon keto sugar found in avocado. D-mannoheptulose is a specific inhibitor of D-glucose phosphorylation by hexokinase isoenzymes. D-Mannoheptulose can block insulin release and utilization of carbohydrate in rat. D-Mannoheptulose has various functions as anti-oxidants, anticancer effects and energy sources. | ||||||||||||||||||||
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D-Mannoheptulose-13C | D-Mannoheptulose-13C is the 13C labeled D-Mannoheptulose (HY-U00462). D-Mannoheptulose is a 7-carbon keto sugar found in avocado. D-mannoheptulose is a specific inhibitor of D-glucose phosphorylation by hexokinase isoenzymes. D-Mannoheptulose can block insulin release and utilization of carbohydrate in rat. D-Mannoheptulose has various functions as anti-oxidants, anticancer effects and energy sources. | |||||||||||||||||||||
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- [1]. D-mannoheptulose and perseitol in ‘Hass’ avocado: Metabolism in seed and mesocarp tissue. South African Journal of Botany. 2012 Mar; 79:159-165.
- [2]. Courtois P, et al. D-mannoheptulose phosphorylation by hexokinase isoenzymes. Int J Mol Med. 2001 Apr;7(4):359-63. [Content Brief]
- [3]. Frenkel G, et al. Metabolic effects of insulin blockade by D-mannoheptulose in the sand rat (Psammomys obesus) and the rat. Gen Comp Endocrinol. 1972 Oct;19(2):341-4. [Content Brief]
- [4]. Al-Ziaydi, A.G. Evaluation of D-Mannoheptulose and Doxorubicin as Potential Therapeutic Agents for Breast Cancer by Targeting Glycolysis and Inducing Apoptosis. Ind J Clin Biochem (2024).
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