推荐产品
product name
FFmoc-N-三苯甲基-L-谷氨酰胺, ≥98.0% (HPLC)
品質等級
化驗
≥98.0% (HPLC)
形狀
powder
光學活性
[α]/D -14.0±1.5°, c = 1% in DMF
反應適用性
reaction type: Fmoc solid-phase peptide synthesis
應用
peptide synthesis
官能基
Fmoc
儲存溫度
2-8°C
SMILES 字串
OC(=O)[C@H](CCC(=O)NC(c1ccccc1)(c2ccccc2)c3ccccc3)NC(=O)OCC4c5ccccc5-c6ccccc46
InChI
1S/C39H34N2O5/c42-36(41-39(27-14-4-1-5-15-27,28-16-6-2-7-17-28)29-18-8-3-9-19-29)25-24-35(37(43)44)40-38(45)46-26-34-32-22-12-10-20-30(32)31-21-11-13-23-33(31)34/h1-23,34-35H,24-26H2,(H,40,45)(H,41,42)(H,43,44)/t35-/m0/s1
InChI 密鑰
WDGICUODAOGOMO-DHUJRADRSA-N
正在寻找类似产品? 访问 产品对比指南
一般說明
Fmoc-Gln(Trt)-OH 也称 Nα-Fmoc-Nδ-三苯甲基-L-谷氨酰胺,它是 Fmoc 保护的氨基酸衍生物,可用作合成肽的试剂。 由于谷氨酰胺受到三苯甲基保护,因此可以防止在反应中出现不需要的取代产物。
應用
Fmoc-Gln(Trt)-OH可用作Fmoc 固相肽合成的原料,用于合成fellutamide B 和 fellutamide B的N-辛酰基类似物。
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 1
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Protection of carboxamide functions by the trityl residue. Application to peptide synthesis
Tetrahedron Letters, 32, 739-742 (1991)
Neurotrophic peptide aldehydes: Solid phase synthesis of fellutamide B and a simplified analog
Bioorganic & Medicinal Chemistry Letters, 16, 3855-3858 (2006)
Chembiochem : a European journal of chemical biology, 17(8), 719-726 (2015-11-18)
Serpin proteins irreversibly inhibit serine proteases, but only a small part of the serpin reactive-center loop (RCL) is responsible for the initial protein-protein interaction (PPI). To develop peptidic protease inhibitors, kallikrein-related peptidases 7 (KLK7) and 5 (KLK5) were chosen. Firstly
Journal of controlled release : official journal of the Controlled Release Society, 242, 35-41 (2016-07-30)
Nanogels offer many unique features rendering them as very attractive candidates for drug delivery. However, for their applications the loading capacity and specific encapsulation, in particular for hydrophobic drugs, in a complex media are two critical factors. In this work
Macromolecular bioscience, 19(4), e1800410-e1800410 (2018-12-24)
In this paper, a self-delivery chimeric peptide PpIX-PEG8 -KVPRNQDWL is designed for photodynamic therapy (PDT) amplified immunotherapy against malignant melanoma. After self-assembly into nanoparticles (designated as PPMA), this self-delivery system shows high drug loading rate, good dispersion, and stability as
相关内容
With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.
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