07532
D-Sedoheptulose
≥95% (TLC)
别名:
D-altro-2-Heptulose
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关于此项目
经验公式（希尔记法）:
C7H14O7
化学文摘社编号:
分子量:
210.18
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
221-166-2
MDL number:
Beilstein/REAXYS Number:
1726427
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
assay
≥95% (TLC)
form
liquid, solid (semi solid, viscous liquid)
color
beige to very dark red-brown
Biochem/physiol Actions
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.
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
flash_point_f
Not applicable
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_c
Not applicable
法规信息
涉药品监管产品
此项目有
P P Hipps et al.
Carbohydrate research, 96(1), 1-6 (1981-10-01)
Sedoheptulose was observed to be formed at the rate of 12-120 nmol/g tissue/h in dialyzed rat and bovine tissue homogenates. The compound was identified by its gas-chromatographic retention time and by its mass spectrum. A standard of [14C]-sedoheptulose was prepared
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)
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
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
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