531480
N-芴甲氧羰基-L-丙氨酸
95%, for peptide synthesis
别名:
N-芴甲氧羰基-L-丙氨酸, Fmoc-L-丙氨酸
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关于此项目
经验公式（希尔记法）:
C18H17NO4
化学文摘社编号:
分子量:
311.33
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
252-660-6
MDL number:
Beilstein/REAXYS Number:
2225975
产品名称
N-芴甲氧羰基-L-丙氨酸, 95%
Quality Level
assay
95%
optical activity
[α]20/D −18°, c = 1 in DMF
reaction suitability
reaction type: C-H Activation, reaction type: Fmoc solid-phase peptide synthesis, reagent type: ligand
reaction type: Peptide Synthesis
mp
147-153 °C (lit.)
application(s)
peptide synthesis
functional group
Fmoc, amine, carboxylic acid
storage temp.
2-8°C
SMILES string
C[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI
1S/C18H17NO4/c1-11(17(20)21)19-18(22)23-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,19,22)(H,20,21)/t11-/m0/s1
InChI key
QWXZOFZKSQXPDC-NSHDSACASA-N
General description
Fmoc-Ala-OH又称为Fmoc-L-丙氨酸, 在Fmoc固相肽合成中起多种作用。
Application
Fmoc-Ala-OH的一般用途：
- 作为制备三唑肽和氮杂肽的构件
- 通过标准Fmoc固相肽合成法合成双阳离子卟啉肽
- 不经过氮杂环丙烷化作用，将曼尼希加合物转化为α-卤化酰胺
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存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Fabian Schnitter et al.
Nature protocols, 16(8), 3901-3932 (2021-07-02)
Many supramolecular materials in biological systems are driven to a nonequilibrium state by the irreversible consumption of high-energy molecules such as ATP or GTP. As a result, they exhibit unique dynamic properties such as a tunable lifetime, adaptivity or the
Xue Zhi Zhao et al.
Molecules (Basel, Switzerland), 23(8) (2018-07-28)
HIV-1 integrase (IN) inhibitors represent a new class of highly effective anti-AIDS therapeutics. Current FDA-approved IN strand transfer inhibitors (INSTIs) share a common mechanism of action that involves chelation of catalytic divalent metal ions. However, the emergence of IN mutants
Leixia Mei et al.
Organic & biomolecular chemistry, 17(4), 939-944 (2019-01-11)
We report the synthesis and self-assembly of fluorescent peptide amphiphiles (NBD-PA) composed of a fluorescent NBD probe and a peptide derivative VVAADD with a C12-alkyl-chain as the linker (NBD-C12-VVAADD). The self-assembly of NBD-PA formed beta-sheet structures at neutral pH in
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 531480-100G | 04061832558714 |
| 531480-1KG | 04061832642710 |
| 531480-25G | 04061832558721 |
| 531480-5G | 04061832558738 |