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Boc-L-Lys-OH

CAS No.:
13734-28-6
Catalog Number:
AG0038XW
Molecular Formula:
C11H22N2O4
Molecular Weight:
246.3034
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$22
- +
25g
98%
In Stock USA
United States
$74
- +
100g
98%
In Stock USA
United States
$224
- +
500g
98%
In Stock USA
United States
$950
- +
Product Description
Catalog Number:
AG0038XW
Chemical Name:
Boc-L-Lys-OH
CAS Number:
13734-28-6
Molecular Formula:
C11H22N2O4
Molecular Weight:
246.3034
MDL Number:
MFCD00038203
IUPAC Name:
(2S)-6-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
InChI:
InChI=1S/C11H22N2O4/c1-11(2,3)17-10(16)13-8(9(14)15)6-4-5-7-12/h8H,4-7,12H2,1-3H3,(H,13,16)(H,14,15)/t8-/m0/s1
InChI Key:
DQUHYEDEGRNAFO-QMMMGPOBSA-N
SMILES:
NCCCC[C@@H](C(=O)O)NC(=O)OC(C)(C)C
EC Number:
237-303-4
Properties
Complexity:
261  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
246.158g/mol
Formal Charge:
0
Heavy Atom Count:
17  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
246.307g/mol
Monoisotopic Mass:
246.158g/mol
Rotatable Bond Count:
8  
Topological Polar Surface Area:
102A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.6  
Literature
Title Journal
Identification of modification sites on human serum albumin and human hemoglobin adducts with houttuynin using liquid chromatography coupled with mass spectrometry. Biomedical chromatography : BMC 20121101
Synthesis of a new amphiphilic glycodendrimer with antiviral functionality. Carbohydrate polymers 20121001
Well-defined homopolypeptides, copolypeptides, and hybrids of poly(l-proline). Biomacromolecules 20110613
Facile synthesis of multiamino vinyl poly(amino acid)s for promising bioapplications. Biomacromolecules 20101213
Synthesis of a l-lysine-based alternate alpha,epsilon-peptide: a novel linear polycation with nucleic acids-binding ability. International journal of pharmaceutics 20100915
Recognition of non-alpha-amino substrates by pyrrolysyl-tRNA synthetase. Journal of molecular biology 20090206
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor. Nature chemical biology 20090101
Asymmetrically simultaneous synthesis of L-homophenylalanine and N6-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferase. Biotechnology progress 20090101
Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases. Biochemical and biophysical research communications 20080711
Characterization of covalent addition products of chlorogenic acid quinone with amino acid derivatives in model systems and apple juice by high-performance liquid chromatography/electrospray ionization tandem mass spectrometry. Rapid communications in mass spectrometry : RCM 20080101
Magnesium-dependent phosphatase-1 is a protein-fructosamine-6-phosphatase potentially involved in glycation repair. The Journal of biological chemistry 20060707
Development of a mechanism-based assay for tissue transglutaminase--results of a high-throughput screen and discovery of inhibitors. Analytical biochemistry 20050315
2-ammonio-6-(3-oxidopyridinium-1-yl)hexanoate (OP-lysine) is a newly identified advanced glycation end product in cataractous and aged human lenses. The Journal of biological chemistry 20040220
Isolation and characterization of a new advanced glycation endproduct of dehydroascorbic acid and lysine. Biochimica et biophysica acta 20030317
Amides are novel protein modifications formed by physiological sugars. The Journal of biological chemistry 20011109
Evidence that malondialdehyde-derived aminoenimine is not a fluorescent age pigment. Chemical research in toxicology 20010501
Properties