L7286
赖氨酸 乙酸盐
meets USP testing specifications
别名:
L-赖氨酸 乙酸盐, (S)-2,6-二氨基己酸
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关于此项目
经验公式（希尔记法）:
C6H14N2O2 · C2H4O2
CAS Number:
分子量:
206.24
EC 号:
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
Agency
meets USP testing specifications
应用
pharmaceutical (small molecule)
SMILES字符串
CC(O)=O.NCCCC[C@H](N)C(O)=O
InChI
1S/C6H14N2O2.C2H4O2/c7-4-2-1-3-5(8)6(9)10;1-2(3)4/h5H,1-4,7-8H2,(H,9,10);1H3,(H,3,4)/t5-;/m0./s1
InChI key
RRNJROHIFSLGRA-JEDNCBNOSA-N
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储存分类代码
13 - Non Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
Kenneth Matthew Scaglione et al.
The Journal of biological chemistry, 288(26), 18784-18788 (2013-05-23)
Attachment of ubiquitin to substrate is typically thought to occur via formation of an isopeptide bond between the C-terminal glycine residue of ubiquitin and a lysine residue in the substrate. In vitro, Ube2w is nonreactive with free lysine yet readily
Lubin Jiang et al.
Nature, 499(7457), 223-227 (2013-07-05)
The variant antigen Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1), which is expressed on the surface of P. falciparum-infected red blood cells, is a critical virulence factor for malaria. Each parasite has 60 antigenically distinct var genes that each code
Krystyna Midura-Nowaczek et al.
Acta poloniae pharmaceutica, 70(3), 431-434 (2013-06-14)
Effects of eight short peptides containing lysine and epsilon-aminocaproic acid (EACA) on prolongation of the clot lysis time, as well as hemolytic and antibacterial activities were investigated. Interaction with plasmids pBR322 and pUC19 with the use of ethidium bromide assay
Scott R Floyd et al.
Nature, 498(7453), 246-250 (2013-06-04)
DNA damage activates a signalling network that blocks cell-cycle progression, recruits DNA repair factors and/or triggers senescence or programmed cell death. Alterations in chromatin structure are implicated in the initiation and propagation of the DNA damage response. Here we further
Jeongsoon Park et al.
Molecular cell, 50(6), 919-930 (2013-06-29)
Protein function is regulated by diverse posttranslational modifications. The mitochondrial sirtuin SIRT5 removes malonyl and succinyl moieties from target lysines. The spectrum of protein substrates subject to these modifications is unknown. We report systematic profiling of the mammalian succinylome, identifying
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