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Merck
CN

F0537

壳梭孢菌素 来源于扁桃壳梭菌

≥85% (HPLC)

别名:

Fusicoccin A

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关于此项目

经验公式(希尔记法):
C36H56O12
化学文摘社编号:
分子量:
680.82
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
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InChI

1S/C36H56O12/c1-10-35(6,7)45-17-26-30(41)33(46-21(5)38)31(42)34(47-26)48-32-28-24(18(2)15-44-20(4)37)13-27(39)36(28,8)14-25-22(16-43-9)11-12-23(25)19(3)29(32)40/h10,14,18-19,22-23,26-27,29-34,39-42H,1,11-13,15-17H2,2-9H3/b25-14-

SMILES string

COCC1CCC2C(C)C(O)C(OC3OC(COC(C)(C)C=C)C(O)C(OC(C)=O)C3O)C4=C(CC(O)C4(C)C=C12)C(C)COC(C)=O

InChI key

KXTYBXCEQOANSX-QFEZKATASA-N

biological source

plant (Fusicoccum amygdali)

assay

≥85% (HPLC)

form

solid

storage temp.

−20°C

Quality Level

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Application

壳梭孢菌素(壳梭孢菌素A)是一种二萜葡萄糖苷植物毒素,用于研究14-3-3-依赖性过程,例如植物和其他具有模式III结合基序的客户蛋白中H+-ATPase的激活。壳梭孢菌素是过氧化氢酶抑制剂的诱导剂,可导致植物氧化损伤。

Other Notes

一种对植物具有多种生理效应的二萜糖苷。
为了全面了解我们针对客户研究提供的各种单糖产品,建议您访问我们的碳水化合物分类页面。

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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访问文档库

Identification and structure of small-molecule stabilizers of 14-3-3 protein-protein interactions.
Rolf Rose et al.
Angewandte Chemie (International ed. in English), 49(24), 4129-4132 (2010-05-04)
A H de Boer
Biochemical Society transactions, 30(4), 416-421 (2002-08-28)
Turgor pressure is a cellular parameter, important for a range of physiological processes in plants, like cell elongation, gas exchange and gravitropic/phototropic bending. Regulation of turgor pressure involves ion and water transport at the expense of metabolic energy (ATP). The
Xiao-Ping She et al.
Physiologia plantarum, 140(3), 258-268 (2010-07-17)
Fusicoccin (FC) treatment prevents dark-induced stomatal closure, the mechanism of which is still obscure. By using pharmacological approaches and laser-scanning confocal microscopy, the relationship between FC inhibition of dark-induced stomatal closure and the hydrogen peroxide (H₂O₂) levels in guard cells
Anja Richter et al.
The Journal of organic chemistry, 76(16), 6694-6702 (2011-07-16)
A synthesis of the fully protected C-ring fragment of the tricyclic diterpene fusicoccin A is reported. The desired cyclopentenyl halides 5a,b are obtained in a total of nine steps. Key transformations of the synthesis sequence are a nonconventional Cr-catalyzed allylic
Renata Kurtyka et al.
Archives of environmental contamination and toxicology, 61(4), 568-577 (2011-03-23)
The effects of cadmium (Cd; 0.1-1000 μM) and fusicoccin (FC) on growth, Cd(2+) content, and membrane potential (E(m)) in maize coleoptile segments were studied. In addition, the E(m) changes and accumulation of Cd and calcium (Ca) in coleoptile segments treated

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