H7270
HC毒素 来源于碳色长蠕孢菌
lyophilized powder
方案
90-95% (TLC)
表单
lyophilized powder
储存温度
2-8°C
SMILES字符串
CC1NC(=O)C(C)NC(=O)C2CCCN2C(=O)C(CCCCCC(=O)C3CO3)NC1=O
InChI
1S/C21H32N4O6/c1-12-18(27)22-13(2)19(28)24-14(7-4-3-5-9-16(26)17-11-31-17)21(30)25-10-6-8-15(25)20(29)23-12/h12-15,17H,3-11H2,1-2H3,(H,22,27)(H,23,29)(H,24,28)
InChI key
GNYCTMYOHGBSBI-UHFFFAOYSA-N
生化/生理作用
Cyclic tetrapeptide fungal toxin selectively toxic to plants with susceptible host genotype.
警示用语:
Danger
危险声明
预防措施声明
危险分类
Acute Tox. 2 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, Gloves, type N95 (US)
法规信息
新产品
此项目有
Jennifer Byers et al.
International journal for parasitology, 38(1), 57-64 (2007-08-21)
Treatment of higher eukaryotic cells with short-chain fatty acids (SCFA) such as butyrate causes decreased levels of histone deacetylase (HDAC) activity and hyperacetylation of histones, and thereby affects gene expression, cell growth and differentiation. Entamoeba parasites encounter high levels of
Jonathan D Walton
Phytochemistry, 67(14), 1406-1413 (2006-07-15)
HC-toxin is a cyclic tetrapeptide of structure cyclo(D-Pro-L-Ala-D-Ala-L-Aeo), where Aeo stands for 2-amino-9,10-epoxi-8-oxodecanoic acid. It is a determinant of specificity and virulence in the interaction between the producing fungus, Cochliobolus carbonum, and its host, maize. HC-toxin qualifies as one of
S J Darkin-Rattray et al.
Proceedings of the National Academy of Sciences of the United States of America, 93(23), 13143-13147 (1996-11-12)
A novel fungal metabolite, apicidin [cyclo(N-O-methyl-L-tryptophanyl-L -isoleucinyl-D-pipecolinyl-L-2-amino-8-oxodecanoyl)], that exhibits potent, broad spectrum antiprotozoal activity in vitro against Apicomplexan parasites has been identified. It is also orally and parenterally active in vivo against Plasmodium berghei malaria in mice. Many Apicomplexan parasites
Hedwig E Deubzer et al.
Cancer letters, 264(1), 21-28 (2008-02-12)
Treatment of high-risk neuroblastoma (NB) is difficult. Novel therapeutics improving survival rates are urgently required. We have previously shown that the histone deacetylase inhibitor (HDACI) Helminthosporium carbonum (HC)-toxin induces differentiation of neuroblastoma (NB) cells. Here, we show that HC-toxin inhibits
Host-selective toxins: agents of compatibility.
J D Walton
The Plant cell, 8(10), 1723-1733 (1996-10-01)
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