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A3253

Sigma-Aldrich

Ala-Pro hydrate

≥98% (TLC), suitable for ligand binding assays

Sinónimos:

L-Alanyl-L-proline hydrate

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About This Item

Fórmula empírica (notación de Hill):
C8H14N2O3 · xH2O
Número de CAS:
13485-59-1
Peso molecular:
186.21 (anhydrous basis)
Beilstein/REAXYS Number:
3546017
EC Number:
236-795-8
MDL number:
MFCD00150505
UNSPSC Code:
12352202
PubChem Substance ID:
24890751
NACRES:
NA.26

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

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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
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
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
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
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.
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