N,N-Diacetyl-Lys-D-Ala-D-Ala
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N,N-Diacetyl-Lys-D-Ala-D-Ala

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N,N-Diacetyl-Lys-D-Ala-D-Ala is a substrate for penicillin-sensitive D-alanine carboxypeptidases (DD-carboxypeptidases).

Category
Others
Catalog number
BAT-015216
CAS number
24570-39-6
Molecular Formula
C16H28N4O6
Molecular Weight
372.42
N,N-Diacetyl-Lys-D-Ala-D-Ala
IUPAC Name
(2R)-2-[[(2R)-2-[[(2S)-2,6-diacetamidohexanoyl]amino]propanoyl]amino]propanoic acid
Synonyms
Diacetyl-Lys-D-Ala-D-Ala-OH; (Ac)2-L-Lys-D-Ala-D-Ala; N-acetyl-N6-acetyl-L-lysyl-D-alanyl-D-alanine; N2,N6-Diacetyl-L-lysyl-D-alanyl-D-alanine; Nα,Nepsilon-Diacetyl-Lys-D-Ala-D-Ala; D-Alanine, N-(N-(N2,N6-diacetyl-L-lysyl)-D-alanyl)-; (R)-2-((R)-2-((S)-2,6-Diacetamidohexanamido)propanamido)propanoic acid
Appearance
White Powder
Purity
95%
Density
1.193±0.06 g/cm3 (Predicted)
Boiling Point
840.0±65.0°C (Predicted)
Sequence
Ac-Lys(Ac)-D-Ala-D-Ala-OH
Storage
Store at -20°C
Solubility
Soluble in Methanol
InChI
InChI=1S/C16H28N4O6/c1-9(14(23)19-10(2)16(25)26)18-15(24)13(20-12(4)22)7-5-6-8-17-11(3)21/h9-10,13H,5-8H2,1-4H3,(H,17,21)(H,18,24)(H,19,23)(H,20,22)(H,25,26)/t9-,10-,13+/m1/s1
InChI Key
VIHGYLJIMMKSBR-BREBYQMCSA-N
Canonical SMILES
CC(C(=O)NC(C)C(=O)O)NC(=O)C(CCCCNC(=O)C)NC(=O)C
1. Advancing Pan-cancer Gene Expression Survial Analysis by Inclusion of Non-coding RNA
Bo Ye, et al. RNA Biol. 2020 Nov;17(11):1666-1673. doi: 10.1080/15476286.2019.1679585. Epub 2019 Oct 18.
Non-coding RNAs occupy a significant fraction of the human genome. Their biological significance is backed up by a plethora of emerging evidence. One of the most robust approaches to demonstrate non-coding RNA's biological relevance is through their prognostic value. Using the rich gene expression data from The Cancer Genome Altas (TCGA), we designed Advanced Expression Survival Analysis (AESA), a web tool which provides several novel survival analysis approaches not offered by previous tools. In addition to the common single-gene approach, AESA computes the gene expression composite score of a set of genes for survival analysis and utilizes permutation test or cross-validation to assess the significance of log-rank statistic and the degree of over-fitting. AESA offers survival feature selection with post-selection inference and utilizes expanded TCGA clinical data including overall, disease-specific, disease-free, and progression-free survival information. Users can analyse either protein-coding or non-coding regions of the transcriptome. We demonstrated the effectiveness of AESA using several empirical examples. Our analyses showed that non-coding RNAs perform as well as messenger RNAs in predicting survival of cancer patients. These results reinforce the potential prognostic value of non-coding RNAs. AESA is developed as a module in the freely accessible analysis suite MutEx.
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