推荐产品
产品名称
D-allo-Isoleucine,
方案
≥98% (HPLC)
质量水平
表单
powder
旋光性
[α]20/D −38° in 6 M HCl
颜色
white to off-white
mp
291 °C (dec.) (lit.)
应用
peptide synthesis
SMILES字符串
CC[C@H](C)[C@@H](N)C(O)=O
InChI
1S/C6H13NO2/c1-3-4(2)5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)/t4-,5+/m0/s1
InChI key
AGPKZVBTJJNPAG-CRCLSJGQSA-N
正在寻找类似产品? 访问 产品对比指南
应用
D-allo-Isoleucine is used in the synthesis of a conjugate of epi-jasmonic acid and various antimicrobial peptides.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Koichi Narita et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(42), 11174-11186 (2009-09-18)
The bicyclic depsipeptide histone deacetylase (HDAC) inhibitors spiruchostatins A and B, 5''-epi-spiruchostatin B and FK228 were efficiently synthesized in a convergent and unified manner. The synthetic method involved the following crucial steps: i) a Julia-Kocienski olefination of a 1,3-propanediol-derived sulfone
G Kreil
Ciba Foundation symposium, 186, 77-85 (1994-01-01)
Over the past three decades, numerous peptides have been isolated from amphibian skin secretions. Many of these peptides were shown to be homologous to hormones and neurotransmitters of mammals. In recent years it has been shown that these secretions also
N Ogawa et al.
Amino acids, 42(5), 1955-1966 (2011-05-13)
The TES ether of the C6-hydroxy derivative of naturally occurring epi-jasmonic acid (epi-JA) was designed as epimerization-free equivalent of epi-JA. The TES ether was synthesized from (1R,4S)-4-hydroxycyclopent-2-enyl acetate in 13 steps. The acid part of the ether was activated with
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门