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Merck
CN

D1542

1,4-二脱氧-1,4-亚氨基-D-阿拉伯糖醇 盐酸盐

≥98% (TLC), Glycogen phosphorylase inhibitor, solid

别名:

2-羟甲基-3,4-吡咯烷二醇 盐酸盐

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关于此项目

经验公式(希尔记法):
C5H11NO3 · HCl
化学文摘社编号:
分子量:
169.61
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.77
MDL number:
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产品名称

1,4-二脱氧-1,4-亚氨基-D-阿拉伯糖醇 盐酸盐, enzyme inhibitor

SMILES string

Cl.OC[C@H]1NC[C@@H](O)[C@@H]1O

InChI key

PZGVJCJRMKIVLJ-DEVUXVJFSA-N

InChI

1S/C5H11NO3.ClH/c7-2-3-5(9)4(8)1-6-3;/h3-9H,1-2H2;1H/t3-,4-,5-;/m1./s1

assay

≥98% (TLC)

form

solid

storage condition

under inert gas

solubility

water: 19.60-20.40 mg/mL, clear, colorless to faintly yellow

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

糖原磷酸化酶和α-葡萄糖苷酶的抑制剂。

Disclaimer

极易吸湿,在氩中储存和处理

General description

1,4-二脱氧-1,4-亚氨基-D-阿拉伯糖醇是一种天然存在的吡咯烷生物碱。它存在于Arachniodes standishii Angylocalyx boutiqueanus中。

Application

1,4-二脱氧-1,4-亚氨基-D-阿拉伯糖醇盐酸盐已用作α-葡萄糖苷酶(GAA)抑制剂。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A new resorufin-based $\alpha$-glucosidase assay for high-throughput screening
Motabar O, et al.
Analytical Biochemistry, 390(1), 79-84 (2009)
Tetrahedron Letters, 42, 5685-5685 (1986)
The synthesis from d-xylose of the potent and specific enantiomeric glucosidase inhibitors, 1, 4-dideoxy-1, 4-imino-d-arabinitol and 1, 4-dideoxy-1, 4-imin
Fleet GWJ and Smith PW
Tetrahedron, 42(20), 5685-5692 (1986)
Ze Fan et al.
Neuroscience bulletin, 36(12), 1513-1523 (2020-10-14)
General anesthesia severely affects the metabolites in the brain. Glycogen, principally stored in astrocytes and providing the short-term delivery of substrates to neurons, has been implicated as an affected molecule. However, whether glycogen plays a pivotal role in modulating anesthesia-arousal
Omid Motabar et al.
Analytical biochemistry, 390(1), 79-84 (2009-04-18)
Mutations in alpha-glucosidase cause accumulation of glycogen in lysosomes, resulting in Pompe disease, a lysosomal storage disorder. Small molecule chaperones that bind to enzyme proteins and correct the misfolding and mistrafficking of mutant proteins have emerged as a new therapeutic

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