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A1878
L-Alanyl-L-leucin
≥99% (TLC)
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About This Item
Empirische Formel (Hill-System):
C9H18N2O3
CAS-Nummer:
Molekulargewicht:
202.25
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352202
PubChem Substanz-ID:
NACRES:
NA.26
Empfohlene Produkte
Produktbezeichnung
L-Alanyl-L-leucin,
Assay
≥99% (TLC)
Qualitätsniveau
Form
powder
Farbe
white
Lagertemp.
−20°C
SMILES String
CC(C)C[C@H](NC(=O)[C@H](C)N)C(O)=O
InChI
1S/C9H18N2O3/c1-5(2)4-7(9(13)14)11-8(12)6(3)10/h5-7H,4,10H2,1-3H3,(H,11,12)(H,13,14)/t6-,7-/m0/s1
InChIKey
RDIKFPRVLJLMER-BQBZGAKWSA-N
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Biochem./physiol. Wirkung
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.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Alice B Nongonierma et al.
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Víctor Cruz et al.
The journal of physical chemistry. B, 115(16), 4880-4886 (2011-04-08)
An exhaustive umbrella sampling simulation of the alanine dipeptide in solution is reported. The presence of stable Y conformations in solution is assessed by both quantum calculations and experimental data from X-ray and NMR protein-solved structures available in the protein
Voislav Blagojevic et al.
Analytical chemistry, 83(9), 3470-3476 (2011-04-21)
The ability to resolve isomeric protonated dipeptides was investigated with the new technique of differential ion mobility mass spectrometry that uses "modifier" molecules to enhance differential mobility. Two pairs of protonated peptides [glycine-alanine (GlyAla) and alanine-glycine (AlaGly), glycine-serine (GlySer) and
Marie-Pierre Gaigeot
Physical chemistry chemical physics : PCCP, 12(35), 10198-10209 (2010-06-12)
Following our previous work [J. Phys. Chem. B. Lett., 2009, 113, 10059], DFT-based molecular dynamics (DFTMD) simulations of 2-Ala peptide (i.e. Ac-Ala-NHMe dialanine peptide analog with methyl group caps at the extremities) immersed in liquid water at room temperature are
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