73489
L-α-新戊基甘氨酸
≥98.0% (TLC)
别名:
γ-甲基-L-亮氨酸, (S)-2-氨基-4,4-二甲基戊酸, L-γ-甲基亮氨酸
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关于此项目
经验公式（希尔记法）:
C7H15NO2
化学文摘社编号:
分子量:
145.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Quality Level
assay
≥98.0% (TLC)
form
solid
reaction suitability
reaction type: solution phase peptide synthesis
application(s)
peptide synthesis
SMILES string
[H][C@](N)(CC(C)(C)C)C(O)=O
InChI
1S/C7H15NO2/c1-7(2,3)4-5(8)6(9)10/h5H,4,8H2,1-3H3,(H,9,10)/t5-/m0/s1
InChI key
LPBSHGLDBQBSPI-YFKPBYRVSA-N
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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)
J L Fauchère et al.
International journal of peptide and protein research, 18(3), 249-255 (1981-09-01)
The modified Strecker synthesis of Patel & Worsley was combined with an enzymatic deamidation in the final step, to produce the title compound. The amino acid is a member of the family of the "fat" amino-acids with high lipophilicity and
Xuejing Yu et al.
The FEBS journal, 281(1), 391-400 (2013-11-12)
Branched-chain amino acid aminotransferase (BCAT) plays a key role in the biosynthesis of hydrophobic amino acids (such as leucine, isoleucine and valine), and its substrate spectrum has not been fully explored or exploited owing to the inescapable restrictions of previous
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 73489-1G-F | 04061826104163 |