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Merck
CN

C1376

Sigma-Aldrich

Z-β-Ala-OH

别名:

N-Cbz-β-alanine, Z-β-alanine

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About This Item

经验公式(希尔记法):
C11H13NO4
CAS号:
分子量:
223.23
Beilstein:
1882542
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.26

方案

≥98% (TLC)

表单

powder

颜色

white

应用

peptide synthesis

储存温度

2-8°C

SMILES字符串

OC(=O)CCNC(=O)OCc1ccccc1

InChI

1S/C11H13NO4/c13-10(14)6-7-12-11(15)16-8-9-4-2-1-3-5-9/h1-5H,6-8H2,(H,12,15)(H,13,14)

InChI key

GEVGRLPYQJTKKS-UHFFFAOYSA-N

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应用

N-Cbz-β-alanine is N-terminal Cbz protected β-alanine, homologous N-(benzyloxycarbonyl)-omega-amino acid, used in design studies for anticonvulsant drugs.

储存分类代码

11 - Combustible Solids

WGK

WGK 2

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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Chu-Biao Xue et al.
The Journal of organic chemistry, 67(3), 865-870 (2002-02-22)
Asymmetric syntheses of (2S,3S)-3-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid (1b), (3R,4S)-4-(tert-butoxycarbonyl)-3-piperidinecarboxylic acid (2b), and their corresponding N-Boc and N-Cbz protected analogues 8a,b and 17a,b are described. Enantiomerically pure 1b has been synthesized in five steps starting from L-aspartic acid beta-tert-butyl ester. Tribenzylation of the
G K Scriba et al.
The Journal of pharmacy and pharmacology, 51(5), 549-553 (1999-07-20)
Glycine, which has weak anticonvulsant properties, has been shown to potentiate the activity of several antiepileptic drugs but not phenytoin. Recently, studies have shown that N-(benzyloxycarbonyl)glycine (Z-glycine) antagonized seizures more than glycine in addition to possessing activity in the maximal
Jiansheng Liu et al.
Biomaterials, 74, 64-76 (2015-10-09)
Despite optimal therapeutic regimen with currently available antiepileptic drugs (AEDs), approximately a third of epilepsy patients remain drug refractory. Region-specific overexpression of multidrug efflux transporters at the blood-brain barrier, such as P-glycoprotein (P-gp), might contribute to multidrug resistance (MDR) by

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