07532
D-Sedoheptulose
≥95% (TLC)
别名:
D-altro-2-Heptulose
方案
≥95% (TLC)
表单
liquid
solid (semi solid, viscous liquid)
颜色
beige to very dark red-brown
储存温度
2-8°C
SMILES字符串
OC[C@@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO
OC[C@@H](O)[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO
InChI
1S/C7H14O7/c8-1-3(10)5(12)7(14)6(13)4(11)2-9/h3,5-10,12-14H,1-2H2/t3-,5-,6-,7-/m1/s1
InChI key
HSNZZMHEPUFJNZ-SHUUEZRQSA-N
生化/生理作用
D-Sedoheptulose, also known as D-altro-2-heptulose, facilitates the cyclic regeneration of D-ribulose for carbon dioxide fixation in plant photosynthesis.
Substrate for sedoheptulose kinase CARKL directing macro-phage polarization through control of glucose metabolism. Accumulation under carbondioxide enrichment in leaves. Patients with the autosomal recessive lysosomal storage disease cystinosis have elevated urinary concentrations of sedoheptulose.
包装
Bottomless glass bottle. Contents are inside inserted fused cone.
其他说明
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
涉药品监管产品
此项目有
Gonzalo R Lara-Issasi et al.
Journal of ethnopharmacology, 225, 159-168 (2018-07-11)
The medicinal plant Sedum oxypetalum Kunth (Crassulaceae), locally known as Jiote or in general Siempreviva (always alive) has been traditionally used by people of the Mexican community of Tenango del Valle as a home remedy to treat periodontal diseases, inducing
M M C Wamelink et al.
Molecular genetics and metabolism, 102(3), 339-342 (2011-01-05)
Cystinosis is an autosomal recessive lysosomal storage disease caused by mutations in CTNS. The most prevalent CTNS mutation is a homozygous 57-kb deletion that also includes an adjacent gene named SHPK (CARKL), encoding sedoheptulokinase. Patients with this deletion have elevated
Yupeng Xie et al.
Carbohydrate research, 342(11), 1510-1513 (2007-05-23)
A facile synthetic approach to 7-O-galloyl-D-sedoheptulose (1), a natural product with notable immunosuppressant activity, was developed. The starting material, 2,7-anhydro-d-sedoheptulose (2), was converted in three steps into 1,3,4,5-tetra-O-benzyl-d-sedoheptulose (5), a key intermediate that allows specific functionalization at C-7 of the
Johan Ceusters et al.
Journal of experimental botany, 64(6), 1497-1507 (2013-02-05)
In contrast to the well-documented roles of its mono- and bisphosphate esters, the occurrence of free sedoheptulose in plant tissues remains a matter of conjecture. The present work sought to determine the origin of sedoheptulose formation in planta, as well
Determination of minor carbohydrates in carrot (Daucus carota L.) by GC?MS.
Soria AC, et al.
Food Chemistry, 114(2), 758-762 (2009)
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