162663
DL -2-氨基丁酸
99%, for peptide synthesis, ReagentPlus®
别名:
AABA, Homoalanine, alpha-amino-n-butyric acid
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关于此项目
线性分子式:
C2H5CH(NH2)CO2H
化学文摘社编号:
分子量:
103.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
220-616-5
MDL number:
Beilstein/REAXYS Number:
635889
产品名称
DL -2-氨基丁酸, ReagentPlus®, 99%
InChI key
QWCKQJZIFLGMSD-UHFFFAOYSA-N
InChI
1S/C4H9NO2/c1-2-3(5)4(6)7/h3H,2,5H2,1H3,(H,6,7)
SMILES string
CCC(N)C(O)=O
product line
ReagentPlus®
assay
99%
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
mp
291 °C (dec.) (lit.)
application(s)
peptide synthesis
Quality Level
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Application
DL-2-氨基丁酸可用于合成2-(2,5-二氧代吡咯烷-1-基)丁酸。
General description
DL-2-氨基丁酸，又称为α-氨基丁酸，常用于液相多肽合成法。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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)
Design, synthesis, and anticonvulsant activity of new hybrid compounds derived from 2-(2, 5-dioxopyrrolidin-1-yl) propanamides and 2-(2, 5-dioxopyrrolidin-1-yl) butanamides
Journal of Medicinal Chemistry, 58, 5274-5286 (2015)
Ryan J Martinie et al.
Journal of the American Chemical Society, 137(21), 6912-6919 (2015-05-13)
The iron(II)- and 2-(oxo)glutarate-dependent (Fe/2OG) oxygenases catalyze an array of challenging transformations, but how individual members of the enzyme family direct different outcomes is poorly understood. The Fe/2OG halogenase, SyrB2, chlorinates C4 of its native substrate, l-threonine appended to the
Izumi Kawabata et al.
Nature communications, 3, 722-722 (2012-03-08)
Synaptic remodelling coordinated with dendritic growth is essential for proper development of neural connections. After establishment of synaptic contacts, synaptic junctions are thought to become stationary and provide fixed anchoring points for further dendritic growth. However, the possibility of active
Danica P Galonić et al.
Nature chemical biology, 3(2), 113-116 (2007-01-16)
Enzymatic incorporation of a halogen atom is a common feature in the biosyntheses of more than 4,500 natural products. Halogenation of unactivated carbon centers in the biosyntheses of several compounds of nonribosomal peptide origin is carried out by a class
Christian Rausch et al.
Proteins, 81(5), 774-787 (2012-12-15)
Apart from their crucial role in metabolism, pyridoxal 5'-phosphate (PLP)-dependent aminotransferases (ATs) constitute a class of enzymes with increasing application in industrial biotechnology. To provide better insight into the structure-function relationships of ATs with biotechnological potential we performed a fundamental
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