Molecular structure of Fmoc-Gly-Gly-Gly-OH, CAS Number: 170941-79-4
Fmoc-Gly-Gly-Gly-OH (CAS 170941-79-4)
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Alternate Names:
Fmoc-glycyl-glycyl-glycine
Application:
Fmoc-Gly-Gly-Gly-OH is an Fmoc protected glycine derivative
CAS Number:
170941-79-4
Purity:
≥98%
Molecular Weight:
411.41
Molecular Formula:
C21H21N3O6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Fmoc-Gly-Gly-Gly-OH is an Fmoc protected glycine derivative useful for proteomics studies and solid phase peptide synthesis techniques. Glycine is the simplest, and least sterically hindered of the amino acids, which confers a high level of flexibility when incorporated into polypeptides. This compound could be useful as an unusual amino acid analog to aid in the deconvolution of protein structure and function.
Fmoc-Gly-Gly-Gly-OH (CAS 170941-79-4) References
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- Synthesis of glycocluster peptides. | Shaikh, HA., et al. 2008. Carbohydr Res. 343: 1665-74. PMID: 18448085
- Kinetics of enzyme attack on substrates covalently attached to solid surfaces: influence of spacer chain length, immobilized substrate surface concentration and surface charge. | Deere, J., et al. 2008. Langmuir. 24: 11762-9. PMID: 18817422
- A phospholipid-PEG2000 conjugate of a vascular endothelial growth factor receptor 2 (VEGFR2)-targeting heterodimer peptide for contrast-enhanced ultrasound imaging of angiogenesis. | Pillai, R., et al. 2010. Bioconjug Chem. 21: 556-62. PMID: 20170116
- New method for effectively and quantitatively labeling cysteine residues on chicken eggshell membrane. | Wang, X., et al. 2012. Org Biomol Chem. 10: 8082-6. PMID: 22961406
- Scalable synthesis and post-modification of a mesoporous metal-organic framework called NU-1000. | Wang, TC., et al. 2016. Nat Protoc. 11: 149-62. PMID: 26678084
- Macrocyclization by asparaginyl endopeptidases. | James, AM., et al. 2018. New Phytol. 218: 923-928. PMID: 28322452
- One-Pot Dual Labeling of IgG 1 and Preparation of C-to-C Fusion Proteins Through a Combination of Sortase A and Butelase 1. | Harmand, TJ., et al. 2018. Bioconjug Chem. 29: 3245-3249. PMID: 30231608
- New Fmoc-Amino Acids/Peptides-Based Supramolecular Gels Obtained through Co-Assembly Process: Preparation and Characterization. | Croitoriu, A., et al. 2022. Polymers (Basel). 14: PMID: 36015611
- Injectable Networks Based on a Hybrid Synthetic/Natural Polymer Gel and Self-Assembling Peptides Functioning as Reinforcing Fillers. | Ghilan, A., et al. 2023. Polymers (Basel). 15: PMID: 36771937
- Amino-acids condensations in the preparation of N alpha-9-fluorenylmethyloxycarbonylamino-acids with 9-fluorenylmethylchloroformate. | Tessier, M., et al. 1983. Int J Pept Protein Res. 22: 125-8. PMID: 6885246
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fmoc-Gly-Gly-Gly-OH, 1 g | sc-285742 | 1 g | $238.00 | |||
Fmoc-Gly-Gly-Gly-OH, 5 g | sc-285742A | 5 g | $814.00 |