A3253
Ala-Pro hydrate
≥98% (TLC), suitable for ligand binding assays
别名:
L-Alanyl-L-proline hydrate
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关于此项目
经验公式(希尔记法):
C8H14N2O3 · xH2O
CAS Number:
分子量:
186.21 (anhydrous basis)
Beilstein:
3546017
EC 号:
MDL编号:
UNSPSC代码:
12352202
PubChem化学物质编号:
NACRES:
NA.26
Product Name
Ala-Pro hydrate,
方案
≥98% (TLC)
质量水平
表单
powder
技术
ligand binding assay: suitable
颜色
white to off-white
储存温度
−20°C
SMILES字符串
O.C[C@H](N)C(=O)N1CCC[C@H]1C(O)=O
InChI
1S/C8H14N2O3.H2O/c1-5(9)7(11)10-4-2-3-6(10)8(12)13;/h5-6H,2-4,9H2,1H3,(H,12,13);1H2/t5-,6-;/m0./s1
InChI key
SSUWZOPYGFOQJA-GEMLJDPKSA-N
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相关类别
生化/生理作用
Alanyl dipeptides such as ala-leu, ala-lys, ala-gly, ala-pro, ala-tyr and ala-phe may be used in physicochemical studies or to evaluate dipeptide separation technologies. Alanyl dipeptides may also be used for studying cell uptake mechanisms, dipeptide metabolism or cell growth supplementation benefits.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
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I Naasani et al.
Biochimica et biophysica acta, 1231(2), 163-168 (1995-09-12)
The transport characteristics of ceftibuten, a dianionic cephem antibiotic, in rat renal and intestinal brush-border membranes were compared. Ceftibuten transport was mediated by two transport systems in the renal brush-border membrane and by one transport system in the intestinal brush-border
J Butterworth et al.
Journal of inherited metabolic disease, 8(4), 193-197 (1985-01-01)
Two forms of prolidase can be separated for all the human cells and tissues examined by DEAE-cellulose column chromatography or batch methods. Serum had a very low prolidase activity eluting as a single peak prior to tissue peak I prolidase.
Lijiang Yang et al.
The Journal of chemical physics, 130(12), 124111-124111 (2009-04-02)
Recently, we introduced an integrated tempering approach to enhance sampling in the energy and configuration space for large systems. In this paper, we show that this new method has a higher efficiency than bias potential and generalized ensemble methods, such
S Capasso et al.
Peptides, 19(2), 389-391 (1998-03-11)
Diketopiperazine formation from the N-terminal residues of a peptide chain is accelerated by aprotic dipolar protophobic solvents and catalyzed in organic solvents by alkylammonium carboxylate salts. The t1/2 for the first-order reaction of H-Ala-Pro-NH2 x TFA falls from 20 d
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