13171-93-2
13171-93-2
Chemical Structure
Z-Gly-Gly-Phe-OH
- CAS No.: 13171-93-2
- Formula:C21H23N3O6
- Molecular Weight:413.42
IUPAC Name: ((benzyloxy)carbonyl)glycylglycyl-L-phenylalanine
InChIKey: PARPWSYTROKYNG-KRWDZBQOSA-N
SMILES: O=C(O)[C@H](CC1=CC=CC=C1)NC(CNC(CNC(OCC2=CC=CC=C2)=O)=O)=O
Biological Activity: Z-Gly-Gly-Phe-OH is a substrate for pepsin and thermolysin. Z-Gly-Gly-Phe-OH has an IC50 of 15.8 μM for open sodium channels under pepsin catalysis. Z-Gly-Gly-Phe-OH forms peptide bonds with amine components (such as H-Leu-NHPh) through enzyme-catalyzed condensation reactions, and is active as an intermediate in peptide synthesis[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Z-Gly-Gly-Phe-OH | 99.46% | Z-Gly-Gly-Phe-OH is a substrate for pepsin and thermolysin. Z-Gly-Gly-Phe-OH has an IC50 of 15.8 μM for open sodium channels under pepsin catalysis. Z-Gly-Gly-Phe-OH forms peptide bonds with amine components (such as H-Leu-NHPh) through enzyme-catalyzed condensation reactions, and is active as an intermediate in peptide synthesis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
