L9250
亮氨酸-丙氨酸 水合物
Bulk package
别名:
L -亮氨酰- L -丙氨酸 水合物
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线性分子式:
(CH3)2CHCH2CH(NH2)CONHCH(CH3)COOH · xH2O
化学文摘社编号:
分子量:
202.25 (anhydrous basis)
UNSPSC Code:
12352209
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1726165
产品名称
亮氨酸-丙氨酸 水合物, Bulk package
InChI
1S/C9H18N2O3.H2O/c1-5(2)4-7(10)8(12)11-6(3)9(13)14;/h5-7H,4,10H2,1-3H3,(H,11,12)(H,13,14);1H2/t6-,7-;/m0./s1
SMILES string
O.CC(C)C[C@H](N)C(=O)N[C@@H](C)C(O)=O
InChI key
FTDFAGANYJVHDA-LEUCUCNGSA-N
assay
≥98% (TLC)
form
powder
technique(s)
ligand binding assay: suitable
color
white
storage temp.
2-8°C
Quality Level
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Application
亮氨酰丙氨酸 (Leu-Ala) 被用于制备非电解三有机锡 (IV) 衍生物（通式 R3Sn (HL)），以研究金属蛋白相互作用的模型。
以 Leu-Ala 水合物为底物，在三-盐酸（HCl）缓冲液中分析了幼虫中亮氨酸-丙氨酸肽酶（LAP）的活性。
General description
亮氨酰丙氨酸（Leu-Ala）被用于制备非电解三有机锡（IV）衍生物（通式 R3Sn（HL)），以研究金属蛋白相互作用的模型。
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)
David S Milner et al.
Proceedings of the National Academy of Sciences of the United States of America, 116(12), 5613-5622 (2019-03-08)
Many microbes acquire metabolites in a "feeding" process where complex polymers are broken down in the environment to their subunits. The subsequent uptake of soluble metabolites by a cell, sometimes called osmotrophy, is facilitated by transporter proteins. As such, the
New triorganotin (IV) derivatives of dipeptides as models for metal-protein interactions: synthesis, structural characterization and biological studies.
Nath M, Pokharia S, Eng G, Song X, Kumar A.
Spectrochimica Acta Part A: Molecular Spectroscopy, 63, 66-75 (2006)
Arun K Ghosh et al.
Journal of medicinal chemistry, 50(10), 2399-2407 (2007-04-17)
Structure-based design and synthesis of a number of potent and selective memapsin 2 inhibitors are described. These inhibitors were designed based upon the X-ray structure of memapsin 2-bound inhibitor 3 that incorporates methylsulfonyl alanine as the P2-ligand and a substituted
Marie Terpager et al.
Journal of receptor and signal transduction research, 29(5), 235-245 (2009-09-15)
7TM receptors are easily fused to proteins such as G proteins and arrestin but because of the fact that their terminals are found on each side of the membrane they cannot be joined directly in covalent dimers. Here, we use
L P Biały et al.
Folia histochemica et cytobiologica, 40(2), 135-136 (2002-06-12)
We have used the dipeptide Leu-Ala in an attempt to prevent the formation of ubiquitin-protein conjugates in U937 cells by inhibition of cellular E3 enzymes (ubiquitin ligases). Proteasome inhibitors induce the formation of perinuclear aggregates of ubiquitinated proteins and proteasomes
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