A6950
Acetyl-Lys-D-Ala-D-Ala
≥95% (HPLC), powder
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10 MG
$219.60
50 MG
$831.00
$219.60
Precio de catálogo$244.00Ahorre 10 %En stockDetalles
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10 MG
$219.60
50 MG
$831.00
About This Item
Fórmula empírica (notación de Hill):
C14H26N4O5
Número de CAS:
Peso molecular:
330.38
MDL number:
UNSPSC Code:
12352204
PubChem Substance ID:
NACRES:
NA.32
$219.60
Precio de catálogo$244.00Ahorre 10 %En stockDetalles
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Nombre del producto
Acetyl-Lys-D-Ala-D-Ala, ≥95% (HPLC)
Quality Level
assay
≥95% (HPLC)
form
powder
solubility
water: 10 mg/mL, clear, colorless
storage temp.
−20°C
SMILES string
CC(NC(=O)C(C)NC(=O)C(CCCCN)NC(C)=O)C(O)=O
InChI
1S/C14H26N4O5/c1-8(12(20)17-9(2)14(22)23)16-13(21)11(18-10(3)19)6-4-5-7-15/h8-9,11H,4-7,15H2,1-3H3,(H,16,21)(H,17,20)(H,18,19)(H,22,23)
InChI key
GMSXMADYKTYBCP-UHFFFAOYSA-N
Substrates
Substrate for carboxypeptidase G and DD from Streptomyces albus.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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The structure of an asymmetric dimer relevant to the mode of action of the glycopeptide antibiotics.
P Groves et al.
Structure (London, England : 1993), 2(8), 747-754 (1994-08-15)
Glycopeptide antibiotics of the vancomycin group are of crucial clinical importance in the treatment of methicillin resistant Staphylococcus aureus (MRSA)--the often lethal 'super-bug'--characterized by its resistance to a wide range of antibiotics in common use. The antibiotics exert their physiological
D H Williams et al.
Science (New York, N.Y.), 280(5364), 711-714 (1998-05-23)
The cooperativity between binding of cell wall precursor analogs (ligands) to and antibiotic dimerization of the clinically important vancomycin group antibiotics was investigated by nuclear magnetic resonance. When dimerization was weak in the absence of a ligand, the increase in
L Varetto et al.
European journal of biochemistry, 162(3), 525-531 (1987-02-02)
Titration of the active-site serine DD-peptidase of Streptomyces R61 shows that formation of acyl enzyme during hydrolysis of the substrate Ac2-L-Lys-D-Ala-D-Ala and enzyme inactivation by the beta-lactam compounds benzylpenicillin, N-acetylampicillin and ampicillin relies on the acidic form of an enzyme's
Eric C DiBiasio et al.
Journal of bacteriology, 202(20) (2020-08-12)
Uropathogenic Escherichia coli (UPEC) is the leading cause of human urinary tract infections (UTIs), and many patients experience recurrent infection after successful antibiotic treatment. The source of recurrent infections may be persistent bacterial reservoirs in vivo that are in a
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