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Merck
CN

V7755

Sigma-Aldrich

疣孢漆斑菌原 来源于疣孢青霉菌

~95%

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关于此项目

经验公式(希尔记法):
C27H33N3O7
化学文摘社编号:
分子量:
511.57
MDL编号:
UNSPSC代码:
12352200
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方案

~95%

储存温度

2-8°C

SMILES字符串

COc1ccc2c3[C@H](O)[C@]4(O)N([C@H]5CC(C)(C)OO[C@H](\C=C(\C)C)n(c35)c2c1)C(=O)[C@@H]6CCCN6C4=O

生化/生理作用

A neurotoxin produced as a secondary metabolite of Aspergillus fumigatus. Inhibits Ca2+-activated K+ channels. Arrests the cell cycle in M phase.

象形图

Skull and crossbones

警示用语:

Danger

危险声明

预防措施声明

危险分类

Acute Tox. 3 Oral

储存分类代码

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

新产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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C B Cui et al.
The Journal of antibiotics, 49(6), 534-540 (1996-06-01)
Two novel diketopiperazines named tryprostatins A and B and a new natural product belonging to the diketopiperazine series, designated as demethoxyfumitremorgin C, together with four known diketopiperazines, fumitremorgin C, 12,13-dihydroxyfumitremorgin C, fumitremorgin B and verruculogen, are new M phase inhibitors
C B Cui et al.
The Journal of antibiotics, 49(6), 527-533 (1996-06-01)
Two novel diketopiperazines named tryprostatins A (1) and B (2) and a new natural product belonging to the diketopiperazine series, designated as demethoxyfumitremorgin C (3), together with four known diketopiperazines, fumitremorgin C (4), 12,13-dihydroxyfumitremorgin C (5), fumitremorgin B (6) and
H G Knaus et al.
Biochemistry, 33(19), 5819-5828 (1994-05-17)
Tremorgenic indole alkaloids produce neurological disorders (e.g., staggers syndromes) in ruminants. The mode of action of these fungal mycotoxins is not understood but may be related to their known effects on neurotransmitter release. To determine whether these effects could be

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