Molecular structure of Fmoc-Phe-OH, CAS Number: 35661-40-6
Fmoc-Phe-OH (CAS 35661-40-6)
Alternate Names:
N-9-Fmoc-L-phenylglycine; N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine; Fmoc-L-phenylalanine
CAS Number:
35661-40-6
Molecular Weight:
387.43
Molecular Formula:
C24H21NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Fmoc-Phe-OH is a derivative of L-Phenylalanine with inherent antimicrobial qualities. This natural substance plays a role in the preparation deltorphin derivatives. It is an inhibitor of the IGF-I and IGF-Binding Protein-5 complex. Fmoc-Phe-OH is particularly utilized in the solid-phase peptide synthesis method for preparing peptide sequences.
Fmoc-Phe-OH (CAS 35661-40-6) References
- Peptide recognition via hierarchical imprinting. | Titirici, MM. and Sellergren, B. 2004. Anal Bioanal Chem. 378: 1913-21. PMID: 14758460
- Solid-phase peptide synthesis using nanoparticulate amino acids in water. | Hojo, K., et al. 2007. J Pept Sci. 13: 493-7. PMID: 17554805
- Effect of C-terminal modification on the self-assembly and hydrogelation of fluorinated Fmoc-Phe derivatives. | Ryan, DM., et al. 2011. Langmuir. 27: 4029-39. PMID: 21401045
- Novel nanoparticles generated by polymeric amphiphiles with pi-pi conjugated small molecules for anti-tumor drug delivery. | Deng, X., et al. 2013. J Biomed Nanotechnol. 9: 1336-44. PMID: 23926799
- Synthesis of Macromolecules Containing Phenylalanine and Aliphatic Building Blocks. | Chan-Seng, D., et al. 2018. Macromol Rapid Commun. 39: e1700764. PMID: 29409141
- Technetium-99 m-PEGylated dendrimer-G2-(Dabcyle-Lys6,Phe7)-pHBSP: A novel Nano-Radiotracer for molecular and early detecting of cardiac ischemic region. | Mohtavinejad, N., et al. 2020. Bioorg Chem. 98: 103731. PMID: 32171100
- Single Amino-Acid Based Self-Assembled Biomaterials with Potent Antimicrobial Activity. | Misra, S., et al. 2021. Chemistry. 27: 16744-16753. PMID: 34468048
- Synthesis of gem-diamino derivatives on solid support | Sonia Cantel, Damien Boeglin, Marc Rolland, Jean Martinez, Jean-Alain Fehrentz. 2003. Tetrahedron Letters. 44: 4797-4799.
- Development of a Method for the Solid-Phase Peptide Synthesis in Water | Keiko Hojo, Hideki Ichikawa, Yoshinobu Fukumori & Koichi Kawasaki. 2008. International Journal of Peptide Research and Therapeutics. 14: 373–380.
- Amino acid based smart hydrogel: formation, characterization and fluorescence properties of silver nanoclusters within the hydrogel matrix | Subhasish Roya and Arindam Banerjee*a. 2011. Soft Matter,. 7: 5300-5308.
- Functionalized single walled carbon nanotube containing amino acid based hydrogel: a hybrid nanomaterial | Subhasish Roy and Arindam Banerjee *. 2012. RSC Adv. 2: 2105-2111.
- Nioplexes encapsulated in supramolecular hybrid biohydrogels as versatile delivery platforms for nucleic acids | Santiago Grijalvo abc, Gustavo Puras cd, Jon Zárate cd, Ramon Pons b, Jose Luis Pedraz cd, Ramon Eritja bc and David Díaz Díaz *ab. 2016. RSC Adv. 6: 39688-39699.
- Photoresponsive Supramolecular Hydrogel Co-assembled from Fmoc-Phe-OH and 4,4′-Azopyridine for Controllable Dye Release | Xiao-Qiu Dou, Chang-Li Zhao, Nabila Mehwish, Ping Li, Chuan-Liang Feng & Holger Schönherr. 2019. Chinese Journal of Polymer Science. 37: 437–443.
- Supramolecular nanofiber-reinforced Puerarin hydrogels as drug carriers with synergistic controlled release and antibacterial properties | Wan Li. 2020. Journal of Materials Science. 55: 6669–6677.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-Phe-OH, 5 g | sc-300739 | 5 g | $20.00 | |||
Fmoc-Phe-OH, 25 g | sc-300739A | 25 g | $64.00 |