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About This Item
经验公式（希尔记法）:
C11H21N3O5
CAS号:
分子量:
275.30
MDL號碼:
分類程式碼代碼:
12352209
PubChem物質ID:
NACRES:
NA.26
推荐产品
product name
γ-Glu-ε-Lys,
化驗
≥98.0% (TLC)
形狀
powder
顏色
white
儲存溫度
−20°C
SMILES 字串
NC(CCCCNC(=O)CCC(N)C(O)=O)C(O)=O
InChI
1S/C11H21N3O5/c12-7(10(16)17)3-1-2-6-14-9(15)5-4-8(13)11(18)19/h7-8H,1-6,12-13H2,(H,14,15)(H,16,17)(H,18,19)
InChI 密鑰
JPKNLFVGUZRHOB-UHFFFAOYSA-N
相关类别
應用
GammaGlu-epsilonLys（γ-Glu-ε-Lys）用于研究内-ε（-γ-Glu）-Lys异肽键在生物过程中的功能和加工。
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
Julian L Wong et al.
Development (Cambridge, England), 136(11), 1835-1847 (2009-05-01)
Fertilization is accompanied by the construction of an extracellular matrix that protects the new zygote. In sea urchins, this structure is built from glycoproteins residing at the egg surface and in secretory vesicles at the egg cortex. Four enzymatic activities
L Zavalova et al.
Molecular & general genetics : MGG, 253(1-2), 20-25 (1996-11-27)
We previously detected in salivary gland secretions of the medicinal leech (Hirudo medicinalis) a novel enzymatic activity, endo-epsilon(gamma-Glu)-Lys isopeptidase, which cleaves isopeptide bonds formed by transglutaminase (Factor XIIIa) between glutamine gamma-carboxamide and the epsilon-amino group of lysine. Such isopeptide bonds
Damien M O Halloran et al.
Tissue engineering, 12(6), 1467-1474 (2006-07-19)
This study investigated the effect on the mechanical and physicochemical properties of type II collagen scaffolds after cross-linking with microbial transglutaminase (mTGase). It is intended to develop a collagen-based scaffold to be used for the treatment of degenerated intervertebral discs.
I P Baskova et al.
Biochemistry. Biokhimiia, 66(12), 1368-1373 (2002-01-29)
Destabilase, endo-epsilon-(gamma-Glu)-Lys-isopeptidase, was prepared from the salivary gland secretion of the medicinal leech (Hirudo medicinalis). The secretion prepared by the known method of Rigbi et al. (1987) (secretion-K) lacks the destabilase-characteristic highly specific isopeptidase activity (the D-dimer-monomerizing activity) because of
Thomas M Jeitner et al.
Amino acids, 44(1), 129-142 (2012-03-13)
Transglutaminases catalyze the formation of γ-glutamylamines utilizing glutamyl residues and amine-bearing compounds such as lysyl residues and polyamines. These γ-glutamylamines can be released from proteins by proteases in an intact form. The free γ-glutamylamines can be catabolized to 5-oxo-L-proline and
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