N,O-Bis-Boc-L-tyrosine
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N,O-Bis-Boc-L-tyrosine

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
BOC-Amino Acids
Catalog number
BAT-002903
CAS number
20866-48-2
Molecular Formula
C19H27NO7
Molecular Weight
381.40
N,O-Bis-Boc-L-tyrosine
IUPAC Name
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[4-[(2-methylpropan-2-yl)oxycarbonyloxy]phenyl]propanoic acid
Synonyms
Boc-L-Tyr(Boc)-OH; (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-[4-[(2-methylpropan-2-yl)oxycarbonyloxy]phenyl]propanoic acid; N,O-Bis[(1,1-dimethylethoxy)carbonyl]-L-tyrosine; N,O-di-tert-butyloxycarbonyl-L-tyrosine; Boc-L-Tyr(Boc)-OH; N-Boc-L-Tyr(OBoc)-OH
Appearance
White to off-white powder
Purity
≥ 98% (HPLC)
Density
1.183±0.06 g/cm3
Melting Point
93-103 °C
Boiling Point
528.4±50.0 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C19H27NO7/c1-18(2,3)26-16(23)20-14(15(21)22)11-12-7-9-13(10-8-12)25-17(24)27-19(4,5)6/h7-10,14H,11H2,1-6H3,(H,20,23)(H,21,22)/t14-/m0/s1
InChI Key
MRYIHKCPPKHOPJ-AWEZNQCLSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CC=C(C=C1)OC(=O)OC(C)(C)C)C(=O)O
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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