推荐产品
产品名称
Fmoc-Tyr(tBu)-OH, ≥98.0% (HPLC)
质量水平
方案
≥98.0% (HPLC)
表单
powder
旋光性
[α]20/D −29±2°, c = 1% in DMF
反应适用性
reaction type: Fmoc solid-phase peptide synthesis
mp
153-156 °C (lit.)
应用
peptide synthesis
官能团
Fmoc
储存温度
2-8°C
SMILES字符串
CC(C)(C)Oc1ccc(C[C@H](NC(=O)OCC2c3ccccc3-c4ccccc24)C(O)=O)cc1
InChI
1S/C28H29NO5/c1-28(2,3)34-19-14-12-18(13-15-19)16-25(26(30)31)29-27(32)33-17-24-22-10-6-4-8-20(22)21-9-5-7-11-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,29,32)(H,30,31)/t25-/m0/s1
InChI key
JAUKCFULLJFBFN-VWLOTQADSA-N
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一般描述
Fmoc-Tyr(tBu)-OH也称为Fmoc-O-叔丁基-L-酪氨酸，通常用于Fmoc固相法肽合成。
应用
Fmoc-Tyr(tBu)-OH可用于通过水中固相反应合成亮氨酸-脑啡肽酰胺(Leu-Enkephalin Amide)。也用于合成氨基酸衍生物，例如Fmoc-Tyr-OAllyl。
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 Total Synthesis of the Proposed Structure of Coibamide A and Its Derivative: Highly Methylated Cyclic Depsipeptides
GA Sable
European Journal of Organic Chemistry, 2015, 7043-7052 (2015)
Solid-phase peptide synthesis using nanoparticulate amino acids in water
K Hojo
Journal of Peptide Science, 13, 493-497 (2007)
Rini Roy et al.
Journal of the American Society for Mass Spectrometry, 29(6), 1086-1098 (2018-05-26)
Immunoglobulins, such as immunoglobulin G (IgG), are of prime importance in the immune system. Polyclonal human IgG comprises four subclasses, of which IgG1 and IgG2 are the most abundant in healthy individuals. In an effort to develop an absolute MALDI-ToF-MS
Chloé Guilbaud-Chéreau et al.
ACS applied materials & interfaces, 11(14), 13147-13157 (2019-03-14)
Molecular gels formed by the self-assembly of low-molecular-weight gelators have received increasing interest because of their potential applications in drug delivery. In particular, the ability of peptides and amino acids to spontaneously self-assemble into three-dimensional fibrous network has been exploited
Loay Awad et al.
Chembiochem : a European journal of chemical biology, 17(24), 2353-2360 (2016-10-28)
We present the design, synthesis, and characterization of a novel photocaged glutamine derivative (modified on the side chain of glutamine), and describe its use in enhancing peptide stability and solubility. Our results demonstrate that this approach can be used to
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