Fmoc-4,4-dimethyl-L-proline
Need Assistance?
  • US & Canada:
    +
  • UK: +

Fmoc-4,4-dimethyl-L-proline

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
Cyclic Amino Acids
Catalog number
BAT-008402
CAS number
1380336-01-5
Molecular Formula
C22H23NO4
Molecular Weight
365.4
IUPAC Name
1-(9H-fluoren-9-ylmethoxycarbonyl)-4,4-dimethylpyrrolidine-2-carboxylic acid
Synonyms
1-Fmoc-4,4-dimethyl-L-proline
InChI
InChI=1S/C22H23NO4/c1-22(2)11-19(20(24)25)23(13-22)21(26)27-12-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h3-10,18-19H,11-13H2,1-2H3,(H,24,25)/t19-/m0/s1
InChI Key
OUDJCOWHKHEGGK-IBGZPJMESA-N
Canonical SMILES
CC1(CC(N(C1)C(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C(=O)O)C
1. Strategy to Identify Improved N-Terminal Modifications for Supramolecular Phenylalanine-Derived Hydrogelators
Brittany L Abraham, Wathsala Liyanage, Bradley L Nilsson Langmuir. 2019 Nov 19;35(46):14939-14948. doi: 10.1021/acs.langmuir.9b02971. Epub 2019 Nov 8.
Supramolecular hydrogels formed by self-assembly of low molecular weight (LMW) compounds have been identified as promising materials for applications in tissue engineering and regenerative medicine. In many cases, the relationship between the chemical structure of the gelator and the emergent hydrogel properties is poorly understood. As a result, empirical screening strategies instead of rational design approaches are often relied upon to tune the emergent properties of the gels. Herein, we describe a novel strategy to identify improved phenylalanine (Phe) derived gelators using a focused empirical approach. Fluorenylmethoxycarbonyl (Fmoc) protected Phe derivatives are a privileged class of gelators that spontaneously self-assemble into fibrils that entangle to form a hydrogel network upon dissolution into water. However, the Fmoc group has been shown to have toxicity drawbacks for potential biological applications, requiring the identification of new N-terminal modifications that promote efficient self-assembly but lack the shortcomings of the Fmoc group. We previously discovered that fibrils in Fmoc-p-nitrophenylalanine (Fmoc-4-NO2-Phe) hydrogels transition to crystalline microtubes after several hours by a mechanism that involves the hierarchical assembly and fusion of the hydrogel fibrils. We hypothesized that this hierarchical crystallization behavior could form the basis of a screening approach to identify alternative N-terminal functional groups to replace Fmoc in Phe-derived LMW gelators. Specifically, screening N-terminal modifying groups for 4-NO2-Phe that stabilize the hydrogel state by preventing subsequent hierarchical crystallization would facilitate empirical identification of functional Fmoc replacements. To test this approach, we screened a small series of 4-NO2-Phe derivatives with various N-terminal modifying groups to determine if any provided stable LMW supramolecular hydrogels. All but one of the 4-NO2-Phe derivatives assembled into crystalline forms. Only the 1-naphthaleneacetic acid (1-Nap) 4-NO2-Phe derivative self-assembled into a stable hydrogel network. Additional Phe derivatives were modified by N-terminal 1-Nap groups to confirm the general potential of 1-Nap as a suitable replacement for Fmoc, and all derivatives formed stable hydrogels under similar conditions to their Fmoc-Phe counterparts. These results illustrate the potential of this approach to identify next-generation Phe-derived LMW gelators with improved emergent properties.
2. Multivalent peptide dendrimers inhibit the fusion of viral-cellular membranes and the cellular NF-κB signaling pathway
Xi Xie, Jian He Eur J Med Chem. 2022 Feb 15;230:114140. doi: 10.1016/j.ejmech.2022.114140. Epub 2022 Jan 19.
The binding of the influenza A virus (IAV) to host cells is multivalent interactions between the hemagglutinin (HA) trimer and sialic acid residues on the cell surface, which present a challenge for the development of efficient antiviral drugs interfering with the entry of IAV into host cells. In this study, a number of multivalent peptide dendrimers targeting the HA2 subunit of HA to block the fusion between viral-cellular membranes have been created, of which FMOC-4-KKWK showed the lowest cytotoxicity, while in the nanomolar concentration range of antiviral effects. In addition to being active against a panel of various subtypes of influenza viruses, these dendrimers reduced the levels of NF-κB in RAW 264.7 cells and inhibited the overexpression of proinflammatory cytokines of TNF-α, IL-1β, and IL-6 that are associated with the influenza infection. Further tests in mice infected with a lethal dose of PR8 virus showed that these dendrimers increased the survival rate of mice, and reduced the viral load in the lungs. Significantly, this is the first report describing peptide dendrimers that target the HA2 subunit of IAV, differing from those using carbohydrates as ligands to block the adsorption of viruses to host cells.
3. Hydrogels of halogenated Fmoc-short peptides for potential application in tissue engineering
Yuqin Wang, Zhaoliang Zhang, Lu Xu, Xingyi Li, Hao Chen Colloids Surf B Biointerfaces. 2013 Apr 1;104:163-8. doi: 10.1016/j.colsurfb.2012.11.038. Epub 2012 Dec 20.
Molecular hydrogels formed by Fmoc-short peptides have been demonstrated to be a class of promising scaffolds/carrier for in vitro cell cultures/drug delivery. In this paper, we firstly studied the gelation property of Fmoc-halogenated phenylalanine and found that the halogenated compounds had better gelation properties than the Fmoc-phenylalanine in aqueous solutions. The most efficient gelator is Fmoc-4-fluoro-phenylalanine, which can gel PBS buffer solution at the minimum gelation concentration of 0.15 wt%. All of the hydrogels formed by halogenated or non-halogenated Fmoc-phenylalanine were characterized by SEM and fluorescence spectrometer. But unfortunately, they were not suitable for NIH 3T3 cell culture. Based on these information and the fact that arginine-glycine-aspartic acid (RGD) peptide could promote cells adhesion and division, we then synthesized a Fmoc-peptide (Fmoc-fFfFGRGD) based on the best gelator of 4-fluoro-phenylalanine (fF) and the cell adhesion peptide of RGD. We observed the formation of molecular hydrogels from Fmoc-fFfFGRGD and the hydrogels could promote NIH 3T3 cell adhesion and proliferation efficiently. This study provides useful information about the gelation property of peptides containing halogenated phenylalanine and the hydrogels reported in this paper had potentials to be used as materials for tissue engineering and drug delivery.
Online Inquiry
Verification code
Inquiry Basket