所有图片(4)
About This Item
经验公式（希尔记法）:
C24H27NO6
CAS号:
分子量:
425.47
Beilstein:
3636375
EC 号:
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.26
推荐产品
产品名称
芴甲氧羰酰-色氨酸, ≥98.0% (HPLC)
方案
≥98.0% (HPLC)
表单
powder
旋光性
[α]20/D −5.0±2.0°, c = 1% in acetic acid: water (4:1)
反应适用性
reaction type: Fmoc solid-phase peptide synthesis
杂质
~4% water
应用
peptide synthesis
官能团
Fmoc
储存温度
2-8°C
SMILES字符串
CC(C)(C)OC(=O)CC[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
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此商品 | 71734 | 71745 | 93206 |
|---|---|---|---|
| Quality Level 200 | Quality Level 200 | Quality Level 100, 200 | Quality Level 200 |
| form crystals | form crystals | form powder | form solid |
| grade for ion-selective electrodes | grade for ion-selective electrodes | grade for ion-selective electrodes | grade for ion-selective electrodes |
| product line Selectophore™ | product line Selectophore™ | product line Selectophore™ | product line Selectophore™ |
| quality function tested | quality function tested | quality function tested | quality function tested |
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)
Solid phase synthesis of peptide C-terminal thioesters by Fmoc/t-Bu chemistry
Ingenito R, et al.
Journal of the American Chemical Society, 121(49), 11369-11374 (1999)
Multi-small molecule conjugations as new targeted delivery carriers for tumor therapy
Shan L, et al.
International journal of nanomedicine, 10(49), 5571-5571 (2015)
Stapled α-helical peptide drug development: A potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy
Chang YS, et al.
Proceedings of the National Academy of Sciences of the USA, 110(36), E3445-E3454 (2013)
Synthesis of peptides from alpha-and beta-tubulin containing glutamic acid side-chain linked oligo-glu with defined length
Tegge W, et al.
International Journal of Peptides, 2010 (2010)
Spectral characterization, solvation effects on topological aspects, and biological attributes of Fmoc-L-glutamic acid 5-tert-butyl ester: An effective reagent in anticancer evaluations
Thirunavukkarasu M, et al.
Journal of Molecular Structure, 1269, 133793-133793 (2022)
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