92122-45-7
Chemical Structure
Fmoc-D-Lys(Boc)-OH
- CAS No.: 92122-45-7
- Formula:C26H32N2O6
- Molecular Weight:468.54
IUPAC Name: N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-D-lysine
InChIKey: UMRUUWFGLGNQLI-JOCHJYFZSA-N
SMILES: O=C(O)[C@@H](CCCCNC(OC(C)(C)C)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O
Biological Activity: Fmoc-D-Lys (Boc)-OH is an Fmoc- and Boc-protected D-lysine derivative. Fmoc-D-Lys (Boc)-OH ensures the precise incorporation of D-lysine into peptide chains, maintaining the specific conformation and biological activity of peptides. Fmoc-D-Lys (Boc)-OH can be used in research on the synthesis of peptides containing unnatural amino acids[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Fmoc-D-Lys(Boc)-OH | 99.87% | Fmoc-D-Lys (Boc)-OH is an Fmoc- and Boc-protected D-lysine derivative. Fmoc-D-Lys (Boc)-OH ensures the precise incorporation of D-lysine into peptide chains, maintaining the specific conformation and biological activity of peptides. Fmoc-D-Lys (Boc)-OH can be used in research on the synthesis of peptides containing unnatural amino acids. | ||||||||||||||||||||
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- [1]. Humphrey JM, et al. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides. Chem Rev. 1997 Oct 1;97(6):2243-2266. [Content Brief]
- [2]. Hooks JC, et al. Development of homomultimers and heteromultimers of lung cancer-specific peptoids. Biopolymers. 2011;96(5):567-577. [Content Brief]
Keywords
