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品質水準
アッセイ
≥95% (TLC)
フォーム
liquid
solid (semi solid, viscous liquid)
色
beige to very dark red-brown
保管温度
2-8°C
SMILES記法
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
生物化学的/生理学的作用
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
底の開いたガラス瓶内容物は内部に挿入され接着された円錐部に入っています。
その他情報
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
保管分類コード
10 - Combustible liquids
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
07532-50MG-BULK:
07532-50MG:
07532-VAR:
07532-10MG:
07532-BULK:
07532-10MG-BULK:
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
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
Determination of minor carbohydrates in carrot (Daucus carota L.) by GC?MS.
Food Chemistry, 114(2), 758-762 (2009)
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
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
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