P4126
苯丙氨酸-苯丙氨酸
≥98% (TLC)
别名:
L -苯丙氨酰- L -苯丙氨酸, 二- L -苯丙氨酸
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关于此项目
线性分子式:
C6H5CH2CH(NH2)CONHCH(CH2C6H5)COOH · H2O
化学文摘社编号:
分子量:
312.36 (anhydrous basis)
NACRES:
NA.26
PubChem Substance ID:
UNSPSC Code:
12352202
EC Number:
219-930-5
MDL number:
产品名称
苯丙氨酸-苯丙氨酸,
InChI key
GKZIWHRNKRBEOH-HOTGVXAUSA-N
InChI
1S/C18H20N2O3/c19-15(11-13-7-3-1-4-8-13)17(21)20-16(18(22)23)12-14-9-5-2-6-10-14/h1-10,15-16H,11-12,19H2,(H,20,21)(H,22,23)/t15-,16-/m0/s1
SMILES string
N[C@@H](Cc1ccccc1)C(=O)N[C@@H](Cc2ccccc2)C(O)=O
assay
≥98% (TLC)
form
powder
color
white
storage temp.
−20°C
Quality Level
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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)
Dmitriy Berillo et al.
Journal of colloid and interface science, 368(1), 226-230 (2011-12-02)
In this study, it was found that macroporous hydrogels were formed when self-assembly of fluorenyl-9-methoxycarbonyl (Fmoc)-diphenylalanine (Phe-Phe) peptides was induced using glucono-δ-lactone (GdL) in apparently frozen samples. Formed cryogels exhibited a heterogeneous structure with pore walls of densely packed fibres
H Mozsolits et al.
Biophysical journal, 77(3), 1428-1444 (1999-08-31)
The interaction of three bioactive peptides, bombesin, beta-endorphin, and glucagon with a phosphatidylcholine monolayer that was immobilized to porous silica particles and packed into a stainless steel column cartridge, has been studied using dynamic elution techniques. This immobilized lipid monolayer
Supramolecular nanofibers and hydrogels of nucleopeptides.
Xinming Li et al.
Angewandte Chemie (International ed. in English), 50(40), 9365-9369 (2011-09-29)
Robert C Dunbar et al.
Journal of the American Chemical Society, 133(5), 1212-1215 (2011-01-05)
Chirality reversal of a residue in a peptide can change its mode of binding to a metal ion, as shown here experimentally by gas-phase IR spectroscopy of peptide-metal ion complexes. The binding conformations of Li(+), Na(+), and H(+) with the
G B Dreyer et al.
Biochemistry, 32(3), 937-947 (1993-01-26)
Potential advantages of C2-symmetric inhibitors designed for the symmetric HIV-1 protease include high selectivity, potency, stability, and bioavailability. Pseudo-C2-symmetric monools and C2-symmetric diols, containing central hydroxymethylene and (R,R)-dihydroxyethylene moieties flanked by a variety of hydrophobic P1/P1' side chains, were studied
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