About This Item
Fórmula empírica (Notação de Hill):
C9H18N2O3
Número CAS:
Peso molecular:
202.25
Número CE:
Número MDL:
Código UNSPSC:
12352202
ID de substância PubChem:
NACRES:
NA.26
Produtos recomendados
Nome do produto
Ala-Leu,
Ensaio
≥99% (TLC)
Nível de qualidade
Formulário
powder
cor
white
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
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
chave InChI
RDIKFPRVLJLMER-BQBZGAKWSA-N
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Ações bioquímicas/fisiológicas
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.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Matthew Rosati et al.
Molecular and biochemical parasitology, 217, 7-12 (2017-08-16)
The aminopeptidase PfA-M1 is a key contributor to peptide catabolism in the human malaria parasite Plasmodium falciparum. PfA-M1 substrate specificity is shaped by the cylindrical S1 subsite, which accommodates the sidechain of the substrate P1 residue. At the top of
Alice B Nongonierma et al.
Food research international (Ottawa, Ont.), 94, 79-89 (2017-03-16)
The release of dipeptidyl peptidase IV (DPP-IV) inhibitory peptides from bovine milk protein isolate (MPI) during trypsin hydrolysis was studied using a design of experiments (DOE) approach. A 3 factor×3 level DOE including temperature (40, 50 and 60°C), enzyme to
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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