F6312
Fmoc-( S )-2-（4-戊烯基）Ala-OH
≥97%, for peptide synthesis
别名:
(S)-2-氨基-2-甲基-6-庚烯酸, (S)- N -Fmoc-α--4- n -戊烯丙氨酸, Fmoc-( S )-2-（4-戊烯基）丙氨酸
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关于此项目
经验公式（希尔记法）:
C23H25NO4
化学文摘社编号:
分子量:
379.45
MDL number:
UNSPSC Code:
12352209
NACRES:
NA.26
产品名称
Fmoc-( S )-2-（4-戊烯基）Ala-OH, ≥97%
SMILES string
N([C@](CCCC=C)(C)C(=O)O)C(=O)OCC1c2c(cccc2)c3c1cccc3
InChI
1S/C23H25NO4/c1-3-4-9-14-23(2,21(25)26)24-22(27)28-15-20-18-12-7-5-10-16(18)17-11-6-8-13-19(17)20/h3,5-8,10-13,20H,1,4,9,14-15H2,2H3,(H,24,27)(H,25,26)/t23-/m0/s1
InChI key
MRJFPZWLOJOINV-QHCPKHFHSA-N
assay
≥97%
form
solid
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
<30 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
−20°C
Application
Fmoc-( S )-2-（4-戊烯基）Ala-OH 是一种 Fmoc 保护的氨基酸，可用于创建肽库。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Z-selective olefin metathesis on peptides: Investigation of side chain influence, preorganization, and guidelines in substrate selection.
O?Leary D J and Grubbs R H
Amino Acids, 5, S13-S13 null
Young-Woo Kim et al.
Nature protocols, 6(6), 761-771 (2011-06-04)
This protocol provides a detailed procedure for the preparation of stapled α-helical peptides, which have proven their potential as useful molecular probes and as next-generation therapeutics. Two crucial features of this protocol are (i) the construction of peptide substrates containing
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