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经验公式(希尔记法):
C19H19NO4
化学文摘社编号:
分子量:
325.36
UNSPSC Code:
12352209
NACRES:
NA.26
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5604328
产品名称
Fmoc-α-Me-Ala-OH, ≥97.0% (HPLC)
InChI
1S/C19H19NO4/c1-19(2,17(21)22)20-18(23)24-11-16-14-9-5-3-7-12(14)13-8-4-6-10-15(13)16/h3-10,16H,11H2,1-2H3,(H,20,23)(H,21,22)
SMILES string
CC(C)(NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O
InChI key
HOZZVEPRYYCBTO-UHFFFAOYSA-N
assay
≥97.0% (HPLC)
reaction suitability
reaction type: Fmoc solid-phase peptide synthesis
mp
182-188 °C
application(s)
peptide synthesis
functional group
Fmoc
storage temp.
2-8°C
Quality Level
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Aleksandra Balliu et al.
Chembiochem : a European journal of chemical biology, 18(14), 1396-1407 (2017-04-23)
A 42-residue polypeptide conjugated to a small-molecule organic ligand capable of targeting the phosphorylated side chain of Ser15 was shown to bind glycogen phosphorylase a (GPa) with a K
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