Molecular structure of Fmoc-GABA-OH, CAS Number: 116821-47-7
Fmoc-GABA-OH (CAS 116821-47-7)
Alternate Names:
4-(Fmoc-amino)butyric acid; Fmoc-GABA
CAS Number:
116821-47-7
Molecular Weight:
325.36
Molecular Formula:
C19H19NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
QUICK LINKS
Ordering Information
Description
Technical Information
Safety Information
SDS & Certificate of Analysis
Fmoc-GABA-OH, an amino acid derivative of gamma-aminobutyric acid (GABA), plays a role as a neurotransmitter in the brain. Scientists and researchers widely employ Fmoc-GABA-OH to investigate the effects of GABA on the brain and the body using in vitro studies. When it comes to its mechanism of action, Fmoc-GABA-OH acts as an agonist for the Fmoc-GABA-OH receptor. By binding to the receptor, Fmoc-GABA-OH triggers its activation.
Fmoc-GABA-OH (CAS 116821-47-7) References
- Design, synthesis, and NMR structure of linear and cyclic oligomers containing novel furanoid sugar amino acids. | Gruner, SA., et al. 2002. Chemistry. 8: 4365-76. PMID: 12355524
- Structure-activity and protraction relationship of long-acting glucagon-like peptide-1 derivatives: importance of fatty acid length, polarity, and bulkiness. | Madsen, K., et al. 2007. J Med Chem. 50: 6126-32. PMID: 17975905
- Synthetic Peptide libraries for T-cell epitope identification. | Hiemstra, HS., et al. 2000. Methods Mol Med. 41: 89-96. PMID: 21374434
- Synthesis of cyclic Py-Im polyamide libraries. | Li, BC., et al. 2013. J Org Chem. 78: 124-33. PMID: 23106218
- Dendrimer brain uptake and targeted therapy for brain injury in a large animal model of hypothermic circulatory arrest. | Mishra, MK., et al. 2014. ACS Nano. 8: 2134-47. PMID: 24499315
- Hydroxyl PAMAM dendrimer-based gene vectors for transgene delivery to human retinal pigment epithelial cells. | Mastorakos, P., et al. 2015. Nanoscale. 7: 3845-56. PMID: 25213606
- Design, synthesis, and characterization of fatty acid derivatives of a dimeric peptide-based postsynaptic density-95 (PSD-95) inhibitor. | Nissen, KB., et al. 2015. J Med Chem. 58: 1575-80. PMID: 25590984
- Synthesis of Nature-Inspired Medium-Sized Fused Heterocycles from Amino Acids. | Ventosa-Andrés, P., et al. 2015. Chemistry. 21: 13112-9. PMID: 26216626
- Dicyclohexylurea derivatives of amino acids as dye absorbent organogels and anion sensors. | Roy, K., et al. 2019. Org Biomol Chem. 17: 3026-3039. PMID: 30816399
- Total Synthesis and Antitrypanosomal Activity of Janadolide and Simplified Analogues. | Chung, JH., et al. 2020. Org Lett. 22: 3089-3093. PMID: 32251602
- Synthesis of a Peptide Derivative of MicrocinJ25 and Evaluation of Antibacterial and Biological Activities. | Mazaheri Tehrani, M., et al. 2019. Iran J Pharm Res. 18: 1264-1276. PMID: 32641937
- A Novel Small Molecule Neurotrophin-3 Analogue Promotes Inner Ear Neurite Outgrowth and Synaptogenesis In vitro. | Kempfle, JS., et al. 2021. Front Cell Neurosci. 15: 666706. PMID: 34335184
- Grafting Hydrophobic Amino Acids Critical for Inhibition of Protein-Protein Interactions on a Cell-Penetrating Peptide Scaffold. | Nagano, Y., et al. 2022. Mol Pharm. 19: 558-567. PMID: 34958576
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-GABA-OH, 5 g | sc-294841 | 5 g | $138.00 | |||
Fmoc-GABA-OH, 25 g | sc-294841A | 25 g | $535.00 |