772038
Fmoc- D -Gln (Trt)-OH
97%
别名:
Fmoc-N-trityl-D-glutamine
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关于此项目
经验公式（希尔记法）:
C39H34N2O5
化学文摘社编号:
分子量:
610.70
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
产品名称
Fmoc- D -Gln (Trt)-OH, 97%
InChI key
WDGICUODAOGOMO-PGUFJCEWSA-N
SMILES string
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-/m1/s1
assay
97%
form
powder or crystals
optical activity
[α]22/D +13.4°, c = 1% in DMF
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
232-237 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Kristina Najjar et al.
The Journal of biological chemistry, 292(3), 847-861 (2016-12-08)
Cell-penetrating peptides (CPPs) are well established as delivery agents for otherwise cell-impermeable cargos. CPPs can also theoretically be used to modulate intracellular processes. However, their susceptibility to proteolytic degradation often limits their utility in these applications. Previous studies have explored
Andreas Pech et al.
Nucleic acids research, 45(7), 3997-4005 (2017-02-06)
Biological evolution resulted in a homochiral world in which nucleic acids consist exclusively of d-nucleotides and proteins made by ribosomal translation of l-amino acids. From the perspective of synthetic biology, however, particularly anabolic enzymes that could build the mirror-image counterparts
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