所有图片(2)
About This Item
经验公式（希尔记法）:
C22H31N3O6 · C12H23N
CAS号:
分子量:
614.82
MDL编号:
UNSPSC代码:
12352209
PubChem化学物质编号:
NACRES:
NA.26
推荐产品
表单
solid
应用
peptide synthesis
储存温度
−20°C
SMILES字符串
C1CCC(CC1)NC2CCCCC2.CC(C)C[C@H](NC(=O)[C@@H]3CCCN3C(=O)[C@H](C)NC(=O)OCc4ccccc4)C(O)=O
InChI
1S/C22H31N3O6.C12H23N/c1-14(2)12-17(21(28)29)24-19(26)18-10-7-11-25(18)20(27)15(3)23-22(30)31-13-16-8-5-4-6-9-16;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,8-9,14-15,17-18H,7,10-13H2,1-3H3,(H,23,30)(H,24,26)(H,28,29);11-13H,1-10H2/t15-,17-,18-;/m0./s1
InChI key
BPZRECFZFZDXFS-OOAIBONUSA-N
应用
Cbz-Ala-Pro-Leu (Cbz-APL), an N-terminal carboxybenzyl blocked tripeptide, may be use in solid phase peptide synthesis (SPPS).
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Byunghee Yoo et al.
Bioconjugate chemistry, 18(3), 903-911 (2007-03-03)
A versatile method is disclosed for solid-phase peptide synthesis (SPPS) of molecular imaging contrast agents. A DO3A moiety was derivatized to introduce a CBZ-protected amino group and then coupled to a polymeric support. CBZ cleavage with Et2AlCl/thioanisole was optimized for
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