所有图片(1)
About This Item
经验公式（希尔记法）:
C31H38N4O6S
CAS号:
分子量:
594.72
MDL编号:
UNSPSC代码:
12352209
eCl@ss:
34058011
PubChem化学物质编号:
NACRES:
NA.26
质量水平
检测方案
≥95.0% (HPLC)
形式
powder
反应适用性
reaction type: Fmoc solid-phase peptide synthesis
应用
peptide synthesis
官能团
Fmoc
SMILES字符串
[H][C@@]12CS[C@H](CCCCC(=O)NCCCC[C@H](NC(=O)OCC3c4ccccc4-c5ccccc35)C(O)=O)[C@]1([H])NC(=O)N2
InChI
1S/C31H38N4O6S/c36-27(15-6-5-14-26-28-25(18-42-26)33-30(39)35-28)32-16-8-7-13-24(29(37)38)34-31(40)41-17-23-21-11-3-1-9-19(21)20-10-2-4-12-22(20)23/h1-4,9-12,23-26,28H,5-8,13-18H2,(H,32,36)(H,34,40)(H,37,38)(H2,33,35,39)/t24-,25-,26-,28-/m0/s1
InChI key
OFIBQNGDYNGUEZ-OBXRUURASA-N
相关类别
其他说明
位点特异性生物素酰化探针的合成
WGK
WGK 3
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
M J Macielag et al.
International journal of peptide and protein research, 44(6), 582-588 (1994-12-01)
The solid-phase synthesis of two porcine motilin derivatives, specifically biotinylated on the side chain of Lys20, was accomplished by preactivation of the protected amino acids N alpha-(9-fluorenylmethoxycarbonyl)-N epsilon-biotinyl-L-lysine and N alpha-(9-fluorenylmethoxycarbonyl)-N epsilon-[N-(biotinyl)-6-aminohexanoyl]-L-lysine with BOP/HOBt/DIEA (1:1:2.5) followed by coupling to the
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