103478-62-2
Chemical Structure
Fmoc-N-Me-Leu-OH
- CAS No.: 103478-62-2
- Formula:C22H25NO4
- Molecular Weight:367.44
IUPAC Name: N-(((9H-fluoren-9-yl)methoxy)carbonyl)-N-methyl-L-leucine
InChIKey: BUJQSIPFDWLNDC-FQEVSTJZSA-N
SMILES: CC(C[C@H](N(C(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O)C)C(O)=O)C
Biological Activity: Fmoc-N-Me-Leu-OH is an N-Fmoc-N-methyl amino acid that can be used in peptide coupling reactions. Fmoc-N-Me-Leu-OH is primarily used as a standard building block in solid-phase peptide synthesis (SPPS) to introduce N-methylleucine residues into peptide chains, thereby enhancing the enzymatic stability, altering conformational flexibility, and modifying the biological activity of the target peptide[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Fmoc-N-Me-Leu-OH | 99.72% | Fmoc-N-Me-Leu-OH is an N-Fmoc-N-methyl amino acid that can be used in peptide coupling reactions. Fmoc-N-Me-Leu-OH is primarily used as a standard building block in solid-phase peptide synthesis (SPPS) to introduce N-methylleucine residues into peptide chains, thereby enhancing the enzymatic stability, altering conformational flexibility, and modifying the biological activity of the target peptide. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
Keywords