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CEF3

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CEF3 (SIIPSGPLK) corresponds to aa 13-21 of the influenza A virus M1 protein, and was first described in the yeast Saccharomyces cerevisiae and has subsequently been identified in a wide range of fungal species including Candida albicans and Schizosaccharomyces pombe. The matrix (M1) protein of influenza A virus is a multifunctional protein that plays essential structural and functional roles in the virus life cycle.

Category
Peptide Inhibitors
Catalog number
BAT-010629
CAS number
199727-62-3
Molecular Formula
C42H74N10O12
Molecular Weight
911.09
CEF3
IUPAC Name
(2S)-6-amino-2-[[(2S)-2-[[[(2S)-1-[2-[[(2S)-2-[[[(2S)-1-[(2S,3S)-2-[[(2S,3S)-2-[[(2S)-2-amino-1,3-dihydroxy-propylidene]amino]-1-hydroxy-3-methyl-pentylidene]amino]-3-methyl-pentanoyl]pyrrolidin-2-yl]-hydroxy-methylene]amino]-1,3-dihydroxy-propylidene]amino]acetyl]pyrrolidin-2-yl]-hydroxy-methylene]amino]-1-hydroxy-4-methyl-pentylidene]amino]hexanoic acid
Synonyms
Influenza Virus M1 (13-21); Ser-Ile-Ile-Pro-Ser-Gly-Pro-Leu-Lys; L-seryl-L-isoleucyl-L-isoleucyl-L-prolyl-L-seryl-glycyl-L-prolyl-L-leucyl-L-lysine
Appearance
White or Off-white Lyophilized Powder
Purity
≥95%
Density
1.4±0.1 g/cm3
Boiling Point
1104.4±75.0°C at 760 mmHg
Sequence
SIIPSGPLK
Storage
Store at -20°C
Solubility
Soluble in DMSO
InChI
InChI=1S/C42H74N10O12/c1-7-24(5)33(49-35(56)26(44)21-53)40(61)50-34(25(6)8-2)41(62)52-18-12-15-31(52)39(60)48-29(22-54)36(57)45-20-32(55)51-17-11-14-30(51)38(59)47-28(19-23(3)4)37(58)46-27(42(63)64)13-9-10-16-43/h23-31,33-34,53-54H,7-22,43-44H2,1-6H3,(H,45,57)(H,46,58)(H,47,59)(H,48,60)(H,49,56)(H,50,61)(H,63,64)/t24-,25-,26-,27-,28-,29-,30-,31-,33-,34-/m0/s1
InChI Key
ZTJURUPAUNLCRP-BBCPKTBMSA-N
Canonical SMILES
CCC(C)C(C(=O)NC(C(C)CC)C(=O)N1CCCC1C(=O)NC(CO)C(=O)NCC(=O)N2CCCC2C(=O)NC(CC(C)C)C(=O)NC(CCCCN)C(=O)O)NC(=O)C(CO)N
1. Functionalized Mesoporous SBA-15 with CeF3: Eu3+ Nanoparticle by Three Different Methods: Synthesis, Characterization, and Photoluminescence
Ying Li,Bing Yan Nanoscale Res Lett . 2010 Jan 16;5(4):701-8. doi: 10.1007/s11671-010-9534-0.
Luminescence functionalization of the ordered mesoporous SBA-15 silica is realized by depositing a CeF3: Eu3+ phosphor layer on its surface (denoted as CeF3: Eu3+/SBA-15/IS, CeF3: Eu3+/SBA-15/SI and CeF3: Eu3+/SBA-15/SS) using three different methods, which are reaction in situ (I-S), solution impregnation (S-I) and solid phase grinding synthesis (S-S), respectively. The structure, morphology, porosity, and optical properties of the materials are well characterized by X-ray diffraction, Fourier transform infrared spectroscopy, transmission electron microscopy, N2 adsorption, and photoluminescence spectra. These materials all have high surface area, uniformity in the mesostructure and crystallinity. As expected, the pore volume, surface area, and pore size of SBA-15 decrease in sequence after deposition of the CeF3: Eu3+ nanophosphors. Furthermore, the efficient energy transfer in mesoporous material mainly occurs between the Ce3+ and the central Eu3+ ion. They show the characteristic emission of Ce3+ 5d → 4f (200-320 nm) and Eu3+5D0 → 7FJ(J = 1-4, with 5D0 → 7F1 orange emission at 588 nm as the strongest one) transitions, respectively. In addition, for comparison, the mesoporous material CeF3: Eu3+/SBA-15/SS exhibits the characteristic emission of Eu3+ ion under UV irradiation with higher luminescence intensity than the other materials.
2. Enhanced visible and near infrared emissions via Ce(3+) to Ln(3+) energy transfer in Ln(3+)-doped CeF3 nanocrystals (Ln = Nd and Sm)
Shyam Sarkar,Tuhin Samanta,Athma E Praveen,Venkataramanan Mahalingam,Venkata N K B Adusumalli Dalton Trans . 2016 Jan 7;45(1):78-84. doi: 10.1039/c5dt02974k.
We report the enhancement of both visible and near infrared (NIR) emissions from Nd(3+) ions via Ce(3+) sensitization in colloidal nanocrystals for the first time. This is achieved in citrate capped Nd(3+)-doped CeF3 nanocrystals under ultraviolet (UV) irradiation (λex = 282 nm). The lasing transition ((4)F3/2 → (4)I11/2) at 1064 nm from Nd(3+)-doped CeF3 nanocrystals has much higher emission intensity via Ce(3+) ion sensitization compared to the direct excitation of Nd(3+) ions. The nanocrystals were prepared using a simple microwave irradiation route. Moreover, the study has been extended to Sm(3+)-doped CeF3 nanocrystals which show strong characteristic emissions of Sm(3+) ions via energy transfer from Ce(3+) ions. The energy transfer mechanism from Ce(3+) to Nd(3+) and Sm(3+) ions is proposed.
3. Transparent infrared-emitting CeF3:Yb-Er polymer nanocomposites for optical applications
Richard E Riman,Mei Chee Tan,Swanand D Patil ACS Appl Mater Interfaces . 2010 Jul;2(7):1884-91. doi: 10.1021/am100228j.
Bright infrared-emitting nanocomposites of unmodified CeF(3):Yb-Er with polymethyl-methacrylate (PMMA) and polystyrene (PS), which offer a vast range of potential applications, which include optical amplifiers, waveguides, laser materials, and implantable medical devices, were developed. For the optical application of these nanocomposites, it is critical to obtain highly transparent composites to minimize absorption and scattering losses. Preparation of transparent composites typically requires powder processing approaches that include sophisticated particle size control, deagglomeration, and dispersion stabilization methods leading to an increase in process complexity and processing steps. This work seeks to prepare transparent composites with high solids loading (>5 vol%) by matching the refractive index of the inorganic particle with low cost polymers like PMMA and PS, so as to circumvent the use of any complex processing techniques or particle surface modification. PS nanocomposites were found to exhibit better transparency than the PMMA nanocomposites, especially at high solids loading (>/=10 vol%). It was found that the optical transparency of PMMA nanocomposites was more significantly affected by the increase in solids loading and inorganic particle size because of the larger refractive index mismatch of the PMMA nanocomposites compared to that of PS nanocomposites. Rayleigh scattering theory was used to provide a theoretical estimate of the scattering losses in these ceramic-polymer nanocomposites.
4. A molecular precursor approach to monodisperse scintillating CeF3 nanocrystals
Andrei Belsky,Shashank Mishra,Bernadette Jouguet,Anne-Laure Bulin,Gilles Ledoux,David Amans,Stéphane Daniele,Christophe Dujardin,Erwann Jeanneau Dalton Trans . 2013 Sep 21;42(35):12633-43. doi: 10.1039/c3dt50605c.
A series of anhydrous cerium(III) trifluoroacetate complexes with neutral O-donor ligands, namely Ce2(OAc)(TFA)5(DMF)3 (1), Ce(TFA)3(L)x [x = 2, L = THF (2), DMF (3), DMSO (4); x = 1, L = diglyme (5)] and Ce2(TFA)6(DMSO)x(DMF)y [x = 6, y = 0 (6); x = 4, y = 2 (7)] (where OAc = acetate, TFA = trifluoroacetate, THF = tetrahydrofuran, DMF = dimethylformamide, DMSO = dimethylsulphoxide, and diglyme = MeO(C2H4O)2Me] were synthesized and completely characterized by elemental analysis, FT-IR spectroscopy and TG-DTA-MS studies. A partially hydrated complex [Ce(TFA)3(diglyme)(H2O)] (8) was obtained by slow evaporation of the THF solution of anhydrous 5 in the air. The single crystal X-ray diffraction analysis of 1, 3, 4, and 6-8 showed the versatile bonding mode of the TFA ligand (terminal, chelating and bridging). These complexes, on decomposition in 1-octadecene in inert atmosphere, gave CeF3 nanoparticles of 8-11 nm size. The complex 5 proved to be the best precursor in the series because of the ability of the diglyme ligand to act as capping reagent during decomposition to render the CeF3 particles monodisperse in organic solvents. The obtained CeF3 nanoparticles were characterized by FT-IR, EDX analysis and TEM studies and their luminescence and scintillation responses under UV and X-ray excitation were studied and compared with that of CeF3 single crystal.
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