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Merck

F0537

Sigma-Aldrich

壳梭孢菌素 来源于扁桃壳梭菌

≥85% (HPLC)

别名:

Fusicoccin A

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About This Item

经验公式(希尔记法):
C36H56O12
CAS号:
分子量:
680.82
MDL號碼:
分類程式碼代碼:
12352201
PubChem物質ID:
NACRES:
NA.25

生物源

plant (Fusicoccum amygdali)

品質等級

化驗

≥85% (HPLC)

形狀

solid

儲存溫度

−20°C

SMILES 字串

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

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-

InChI 密鑰

KXTYBXCEQOANSX-QFEZKATASA-N

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應用

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。

其他說明

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。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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
Jan Hlavinka et al.
Plant science : an international journal of experimental plant biology, 209, 75-80 (2013-06-14)
It was reported earlier that 7B-1 mutant in tomato (Solanum lycopersicum L.), an ABA overproducer, is defective in blue light (BL) signaling leading to BL-specific resistance to abiotic and biotic stresses. In this work, we examine responses of stomata to
Yusuke Ono et al.
Journal of the American Chemical Society, 133(8), 2548-2555 (2011-02-09)
Fusicoccin A and cotylenin A are structurally related diterpene glucosides and show a phytohormone-like activity. However, only cotylenin A induces the differentiation of human myeloid leukemia cells. Since the cotylenin A producer lost its ability to proliferate during preservation, a
Ingrid J de Vries-van Leeuwen et al.
Cancer letters, 293(2), 198-206 (2010-02-16)
Active small molecules have a high potential for the development into new anti-cancer drugs. Here we analysed the effect of the natural occurring fusicoccanes, Fusicoccin-A (FC), Ophiobolin-A (OPH-A) and Ophiobolin-I (OPH-I) on various tumor cell lines. Both FC and OPH-A

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