2-Deoxy-D-galactose
CAS No. 1949-89-9
2-Deoxy-D-galactose ( —— )
产品货号. M37322 CAS No. 1949-89-9
2-Deoxy-D-galactose 是葡萄糖的类似物。2-Deoxy-D-galactose 通过抑制糖酵解来抑制肿瘤生长。2-Deoxy-D-galactose 是一种干扰糖大分子聚焦化的物质,在各种学习任务中损害记忆巩固。2-Deoxy-D-galactose 阻碍体内糖蛋白集中化。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 50MG | ¥235 | 有现货 |
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| 100MG | ¥367 | 有现货 |
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| 200MG | ¥520 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称2-Deoxy-D-galactose
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述2-Deoxy-D-galactose 是葡萄糖的类似物。2-Deoxy-D-galactose 通过抑制糖酵解来抑制肿瘤生长。2-Deoxy-D-galactose 是一种干扰糖大分子聚焦化的物质,在各种学习任务中损害记忆巩固。2-Deoxy-D-galactose 阻碍体内糖蛋白集中化。
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产品描述2-Deoxy-D-galactose is a glucose analog. 2-Deoxy-D-galactose inhibits glycolysis to inhibits tumor growth. 2-Deoxy-D-galactose is a substance interfering with the fucosylation of glycomacromolecules and impairing memory consolidation in various learning tasks. 2-Deoxy-d-galactose hinders glycoprotein fucosylation in vivo.
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体外实验2-Deoxy-D-galactose (1 mM/L; 5 h) is rapid phosphorylation during the first 30 min and decreases to approximately 20% of this rate during the subsequent hours in ascites hepatoma cells.
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体内实验2-Deoxy-D-galactose (380 mg/kg; i.p.; for 6 times) strongly decreases contents of UMP, UDPG, and UDP galactose in rat livers.2-Deoxy-D-galactose (2-8 μM; intracerebroventricularly injection; once) shows PAR impairment 30 min before the acquisition trial a dose of 4 μM and 15 min delay after do-gal administration.Animal Model:Male adult Wistar rats with passive avoidance response (PAR) acquisition trial Dosage:2, 4 and 8 μM Administration:Intracerebroventricularly injection; 2-8 μM; once Result:Exhibited PAR disruption at a dose of 4 μM.
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同义词——
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通路Others
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靶点Other Targets
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受体Others
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研究领域——
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适应症——
化学信息
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CAS Number1949-89-9
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分子量164.16
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分子式C6H12O5
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纯度>98% (HPLC)
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溶解度In Vitro:?H2O 中的溶解度 : 250 mg/mL (1522.90 mM; 超声助溶) Methanol 中的溶解度 : 125 mg/mL (761.45 mM; 超声助溶)
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SMILESOC[C@@H](O)[C@H](O)[C@H](O)CC=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Keppler DO, et al. The trapping of uridine phosphates by D-galactosamine. D-glucosamine, and 2-deoxy-D-galactose. A study on the mechanism of galactosamine hepatitis. Eur J Biochem. 1970 Dec;17(2):246-53.?
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