D-Alanyl-D-alanine
D-Alanyl-D-alanine Basic information
- Product Name:
- D-Alanyl-D-alanine
- Synonyms:
-
- (R)-N-(D-Alanyl)-2-methylglycine
- D-Ala-D-Ala-OH
- N-(D-Alanyl)-D-alanine
- (R)-2-((R)-2-aminopropanamido)-3-(4-fluorophenyl)propanoic acid
- (R)-2-((R)-2-aMinopropanaMido)propanoic acid
- D-Ala-D-Ala-OH≥ 95% (HPLC)
- 2-[[(2R)-2-amino-1-oxopropyl]amino]propanoic acid
- H-D-ALA-D-ALA-OH
- CAS:
- 923-16-0
- MF:
- C6H12N2O3
- MW:
- 160.17
- Product Categories:
-
- Peptide
- Dipeptides
- Dipeptides and Tripeptides
- Peptides
- Mol File:
- 923-16-0.mol
D-Alanyl-D-alanine Chemical Properties
- Melting point:
- 120 °C
- Boiling point:
- 402.6±30.0 °C(Predicted)
- Density
- 1.208±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,2-8°C
- form
- Solid
- pka
- 3.16±0.10(Predicted)
- color
- White to off-white
- CAS DataBase Reference
- 923-16-0(CAS DataBase Reference)
MSDS
- Language:English Provider:SigmaAldrich
D-Alanyl-D-alanine Usage And Synthesis
Chemical Properties
White to off-white powder
Uses
D-Ala-D-Ala is a bacterial endogenous metabolite. D-Ala-D-Ala constitutes the terminus of the peptide part of the peptidoglycan monomer unit and is involved in the transpeptidation reaction as the substrate. D-Ala-D-Ala is catalyzed by D-Alanine-D-Alanine ligase[1][2][3].
Definition
ChEBI: D-alanyl-D-alanine is a dipeptide comprising D-alanine with a D-alanyl residue attached to the alpha-nitrogen. It is a component of bacterial peptidoglycan and forms an important target for development of antibacterial drugs. It has a role as an Escherichia coli metabolite. It is a tautomer of a D-alanyl-D-alanine zwitterion.
Biological Activity
D-Ala-D-Ala is found in the stem termini of peptidoglycan side-chain pentapeptide found in the cell walls of gram positive bacteria. The D-ala-d-ala stem termini is the site of interaction of glycopeptide antibiotics such as vancomycin and teicoplanin. D-ala-D-ala is a substrate used to study kinetics of UDPMurNAc-tripeptide D-alanyl-D-alanine-adding (ligase) enzyme.', 'D-Ala-D-Ala, a terminus moiety of bacterial peptidoglycans, is used for affinity chromatography and binding mechanism studies of antibiotics such as teicoplanin, ristocetin, vancomycin.
IC 50
Microbial Metabolite
References
[1] Kitamura Y, et al. Structure of D-alanine-D-alanine ligase from Thermus thermophilus HB8: cumulative conformational change and enzyme-ligand interactions. Acta Crystallogr D Biol Crystallogr. 2009 Oct;65(Pt 10):1098-106. DOI:10.1107/S0907444909029710
[2] Tytgat I, et al. DD-ligases as a potential target for antibiotics: past, present and future. Curr Med Chem. 2009;16(20):2566-80. DOI:10.2174/092986709788682029
[3] Trivedi RR, et al. Mechanical Genomic Studies Reveal the Role of d-Alanine Metabolism in Pseudomonas aeruginosa Cell Stiffness. mBio. 2018 Sep 11;9(5):e01340-18. DOI:10.1128/mBio.01340-18
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D-Alanyl-D-alanine(923-16-0)Related Product Information
- L-Alanyl-L-Glutamine
- L-Alanine
- D-Alanine
- D-Alanine Methyl Ester Hydrochloride
- D-Alanine tert-butyl ester hydrochloride
- D-Phenylalanine methyl ester hydrochloride
- D-Prolinamide
- D-Phenylalanine
- N-ACETYL-D-ALA-D-ALA
- Boc-Phe-Phe-OH
- N-L-alanyl-L-alanine
- L-Alanyl-L-alanine
- N-DL-Alanyl-DL-alanine
- SUCCINYL-L-ALANYL-L-ALANYL-L-ALANINE P-NITROANILIDE,SUCCINYL-L-ALANYL-L-ALANYL-L-ALANINE-4-NITROANILIDE
- 3-phenyl-N-(3-phenyl-L-alanyl)-L-alanine
- Ammonia
- H-D-ALA-D-ALA-OME HCL
- AC-LYS-D-ALA-D-ALA-OH