A3253
Ala-Pro hydrate
≥98% (TLC), suitable for ligand binding assays
Synonym(s):
L-Alanyl-L-proline hydrate
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About This Item
Empirical Formula (Hill Notation):
C8H14N2O3 · xH2O
CAS Number:
Molecular Weight:
186.21 (anhydrous basis)
Beilstein:
3546017
EC Number:
MDL number:
UNSPSC Code:
12352202
PubChem Substance ID:
NACRES:
NA.26
Pricing and availability is not currently available.
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Product Name
Ala-Pro hydrate,
Assay
≥98% (TLC)
form
powder
technique(s)
ligand binding assay: suitable
color
white to off-white
storage temp.
−20°C
SMILES string
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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Biochem/physiol Actions
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Justin F Shaffer et al.
Journal of muscle research and cell motility, 30(7-8), 303-306 (2010-03-11)
Cardiac myosin binding protein-C (cMyBP-C) is an accessory protein found in the A-bands of vertebrate sarcomeres and mutations in the cMyBP-C gene are a leading cause of familial hypertrophic cardiomyopathy. The regulatory functions of cMyBP-C have been attributed to the
M Sugawara et al.
The Journal of pharmacy and pharmacology, 46(8), 680-684 (1994-08-01)
The types of inhibitory effects caused by compound V (an analogue of ceftibuten) and alanylproline (dipeptide) on the uptake of ceftibuten by brush-border membrane vesicles (BBMV) prepared from human and rat small intestine were analysed. In the presence of an
R Hanai et al.
Journal of chromatography, 394(2), 273-278 (1987-05-22)
The "elution-band relaxation method" has been applied to the analysis of the cis-trans kinetics isomerization of the proline of L-Ala-L-Pro using reversed-phase liquid chromatography. A procedure suitable for cases where neither isomer can be injected separately is described.
Young-Ok Kim et al.
The Journal of general and applied microbiology, 55(5), 345-350 (2009-11-27)
Citrobacter braakii produced an intracellular acid glucose phosphatase (AgpC) which was purified 986 fold to homogeneity with the specific activity of 286 units/mg. AgpC hydrolyzed a wide variety of phosphorylated compounds with high activity for glucose-1-phosphate and glucose-6-phosphate. The optimum
G Sterner et al.
Nephron, 34(2), 104-109 (1983-01-01)
Small intestinal dipeptidases (substrate: glycyl-L-leucine, L-methionyl-L-methionine, and L-alanyl-L-proline) were determined in uraemic and sham-operated rats given normal protein diet (24%), low protein diet (6%), and total parenteral nutrition for 10-14 days. Disaccharidases (substrate: maltose, sucrose, trehalose, and lactose) were measured
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