standard fmoc solid-phase Search Results


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  • 99
    Millipore standard fmoc solid phase peptide synthesis
    Standard Fmoc Solid Phase Peptide Synthesis, supplied by Millipore, used in various techniques. Bioz Stars score: 99/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 15 article reviews
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    standard fmoc solid phase peptide synthesis - by Bioz Stars, 2020-04
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    86
    INTAVIS standard solid phase fmoc chemistry
    Standard Solid Phase Fmoc Chemistry, supplied by INTAVIS, used in various techniques. Bioz Stars score: 86/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    AnaSpec standard fmoc solid phase peptide synthesis
    Standard Fmoc Solid Phase Peptide Synthesis, supplied by AnaSpec, used in various techniques. Bioz Stars score: 86/100, based on 7 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    85
    New England Peptide standard fmoc solid phase
    Standard Fmoc Solid Phase, supplied by New England Peptide, used in various techniques. Bioz Stars score: 85/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    INTAVIS standard fmoc solid phase
    Standard Fmoc Solid Phase, supplied by INTAVIS, used in various techniques. Bioz Stars score: 88/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    SPSS Inc standard fmoc solid phase peptide synthesis
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 94/100, based on 108 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    GL Biochem standard solid phase fmoc
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Solid Phase Fmoc, supplied by GL Biochem, used in various techniques. Bioz Stars score: 94/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    GenScript standard fmoc solid phase synthesis methods
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Fmoc Solid Phase Synthesis Methods, supplied by GenScript, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    87
    CEM Corporation standard fmoc solid phase peptide synthesis
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Fmoc Solid Phase Peptide Synthesis, supplied by CEM Corporation, used in various techniques. Bioz Stars score: 87/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    SPSS Inc peptide synthesis standard fmoc based solid phase peptide synthesis fmoc spps
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Peptide Synthesis Standard Fmoc Based Solid Phase Peptide Synthesis Fmoc Spps, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    86
    INTAVIS standard solid phase fmoc chemistry peptide synthesizer
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Solid Phase Fmoc Chemistry Peptide Synthesizer, supplied by INTAVIS, used in various techniques. Bioz Stars score: 86/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    21st Century Biochemicals standard solid phase 9 fluoronylmethoxycarbonyl fmoc chemistry
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Solid Phase 9 Fluoronylmethoxycarbonyl Fmoc Chemistry, supplied by 21st Century Biochemicals, used in various techniques. Bioz Stars score: 92/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    SPSS Inc standard 9 fluorenyl methoxycarbonyl fmoc solid phase peptide synthesis
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard 9 Fluorenyl Methoxycarbonyl Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 92/100, based on 4 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    SPSS Inc standard fluorenylmethoxycarbonyl fmoc solid phase peptide synthesis
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Fluorenylmethoxycarbonyl Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 90/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    SPSS Inc standard fmoc tbu solid phase peptide synthesis
    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) <t>Fmoc</t> <t>SPPS</t> from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).
    Standard Fmoc Tbu Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 94/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    91
    SPSS Inc f labeled analogs standard fmoc based solid phase peptide synthesis
    Diarylethene (DAET) building blocks for <t>SPPS:</t> <t>Fmoc-protected</t> amino acid ( 1 ), and a dicarboxylic acid ( 2 ) used to prepare the model compounds studied in this work.
    F Labeled Analogs Standard Fmoc Based Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 91/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    88
    SPSS Inc microwave assisted standard fmoc solid phase peptide synthesis
    Diarylethene (DAET) building blocks for <t>SPPS:</t> <t>Fmoc-protected</t> amino acid ( 1 ), and a dicarboxylic acid ( 2 ) used to prepare the model compounds studied in this work.
    Microwave Assisted Standard Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 88/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    92
    SPSS Inc conventional stepwise standard 9 fluorenylmethoxycarbonyl based solid phase peptide synthesis fmoc spps
    Diarylethene (DAET) building blocks for <t>SPPS:</t> <t>Fmoc-protected</t> amino acid ( 1 ), and a dicarboxylic acid ( 2 ) used to prepare the model compounds studied in this work.
    Conventional Stepwise Standard 9 Fluorenylmethoxycarbonyl Based Solid Phase Peptide Synthesis Fmoc Spps, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 92/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    94
    Peptides International solid phase fmoc
    Diarylethene (DAET) building blocks for <t>SPPS:</t> <t>Fmoc-protected</t> amino acid ( 1 ), and a dicarboxylic acid ( 2 ) used to prepare the model compounds studied in this work.
    Solid Phase Fmoc, supplied by Peptides International, used in various techniques. Bioz Stars score: 94/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    97
    SPSS Inc fmoc solid phase peptide synthesis
    A synthetic scheme that shows the approach used to synthesize the linear precursor of wollamide B using <t>SPPS.</t> Reagents and conditions: a) <t>Fmoc-L-Leu-OH,</t> DIPEA, DCM, 2 h; b) 20% piperidine/DMF, 10 min (2X); c) Fmoc-L-Trp (Boc)-OH, HATU, DIPEA, NMP, 1 h; d) Fmoc-D-Orn (Boc)-OH, HATU, DIPEA, NMP, 1 h; e) Fmoc-L-Asn (Trt)-OH, HATU, DIPEA, NMP, 1 h; f) Fmoc-L-Val-OH, HATU, DIPEA, NMP, 1 h; g) Fmoc-D-Leu-OH, HATU, DIPEA, NMP, 1 h; h) 20% HFIP/DC, 1 h.
    Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 97/100, based on 342 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    90
    AnaSpec fmoc solid phase peptide synthesis
    A synthetic scheme that shows the approach used to synthesize the linear precursor of wollamide B using <t>SPPS.</t> Reagents and conditions: a) <t>Fmoc-L-Leu-OH,</t> DIPEA, DCM, 2 h; b) 20% piperidine/DMF, 10 min (2X); c) Fmoc-L-Trp (Boc)-OH, HATU, DIPEA, NMP, 1 h; d) Fmoc-D-Orn (Boc)-OH, HATU, DIPEA, NMP, 1 h; e) Fmoc-L-Asn (Trt)-OH, HATU, DIPEA, NMP, 1 h; f) Fmoc-L-Val-OH, HATU, DIPEA, NMP, 1 h; g) Fmoc-D-Leu-OH, HATU, DIPEA, NMP, 1 h; h) 20% HFIP/DC, 1 h.
    Fmoc Solid Phase Peptide Synthesis, supplied by AnaSpec, used in various techniques. Bioz Stars score: 90/100, based on 22 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    CEM Corporation fmoc solid phase techniques
    A synthetic scheme that shows the approach used to synthesize the linear precursor of wollamide B using <t>SPPS.</t> Reagents and conditions: a) <t>Fmoc-L-Leu-OH,</t> DIPEA, DCM, 2 h; b) 20% piperidine/DMF, 10 min (2X); c) Fmoc-L-Trp (Boc)-OH, HATU, DIPEA, NMP, 1 h; d) Fmoc-D-Orn (Boc)-OH, HATU, DIPEA, NMP, 1 h; e) Fmoc-L-Asn (Trt)-OH, HATU, DIPEA, NMP, 1 h; f) Fmoc-L-Val-OH, HATU, DIPEA, NMP, 1 h; g) Fmoc-D-Leu-OH, HATU, DIPEA, NMP, 1 h; h) 20% HFIP/DC, 1 h.
    Fmoc Solid Phase Techniques, supplied by CEM Corporation, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    95
    SPSS Inc automated fmoc solid phase peptide synthesis
    (a) Synthesis of building blocks with incorporated cleavable linkers. N -methylmorpholine (NMM) (b) synthesis of peptide segment 6 and incorporation of linker building block 5a by standard <t>Fmoc-SPPS.</t>
    Automated Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 95/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    93
    SPSS Inc fluorenylmethyloxycarbonyl fmoc solid phase peptide synthesis
    (a) Synthesis of building blocks with incorporated cleavable linkers. N -methylmorpholine (NMM) (b) synthesis of peptide segment 6 and incorporation of linker building block 5a by standard <t>Fmoc-SPPS.</t>
    Fluorenylmethyloxycarbonyl Fmoc Solid Phase Peptide Synthesis, supplied by SPSS Inc, used in various techniques. Bioz Stars score: 93/100, based on 16 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) Fmoc SPPS from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).

    Journal: ACS Chemical Biology

    Article Title: Chemical Control over T-Cell Activation in Vivo Using Deprotection of trans-Cyclooctene-Modified Epitopes

    doi: 10.1021/acschembio.8b00155

    Figure Lengend Snippet: Design and synthesis of caged peptides. (a) Inverse electron-demand Diels–Alder (IEDDA) pyridazine elimination between a silent trans -cyclooctene-modified epitope and a tetrazine liberates antigenicity of the peptide. After initial cycloaddition, tautomerization and elimination results in the free lysine ε-amine upon which a T-cell can recognize the epitope again and become activated. (b) Synthesis of SIINFEK[CCO]L ( 4 ), SIINFEK[TCO]L ( 5 ), and SIINFEK[mbTCO]L ( 7 ). Reagents/conditions: (a) Fmoc SPPS from Fmoc-Leu-Wang; (b) methylsulfonylethyl succinimido-carbonate, DIPEA, NMP, rt; (c) TFA/H2O/TIPS (95:2.5:2.5), rt, 23%; (d) NHS-CCO ( 2 ), NHS-TCO ( 3 ), or NHS-mbTCO ( 6 ), DIPEA, DMF, rt; (e) ethanolamine, DMF, rt; (f) dioxane/MeOH/4 M NaOH (7.5:2.25:0.25), rt, 16% ( 4 ), 20% ( 5 ), 14% ( 7 ).

    Article Snippet: The peptide sequence was synthesized using standard Fmoc solid phase peptide synthesis (SPPS) conditions followed by N -terminal protection with the methylsulfonylethyloxycarbonyl (MSc) group to improve the solubility of the liberated peptide after acidic cleavage from the resin and to enable selective modification of the lysine ε-amine in the subsequent step ( b).

    Techniques: Modification

    Diarylethene (DAET) building blocks for SPPS: Fmoc-protected amino acid ( 1 ), and a dicarboxylic acid ( 2 ) used to prepare the model compounds studied in this work.

    Journal: Biochimica et Biophysica Acta

    Article Title: Flexibility vs rigidity of amphipathic peptide conjugates when interacting with lipid bilayers

    doi: 10.1016/j.bbamem.2017.09.021

    Figure Lengend Snippet: Diarylethene (DAET) building blocks for SPPS: Fmoc-protected amino acid ( 1 ), and a dicarboxylic acid ( 2 ) used to prepare the model compounds studied in this work.

    Article Snippet: 2.2 Synthesis of β/α-model peptides and their 19 F-labeled analogs Standard Fmoc-based solid-phase peptide synthesis (SPPS) and commercially available reagents were used for the peptide synthesis.

    Techniques:

    A synthetic scheme that shows the approach used to synthesize the linear precursor of wollamide B using SPPS. Reagents and conditions: a) Fmoc-L-Leu-OH, DIPEA, DCM, 2 h; b) 20% piperidine/DMF, 10 min (2X); c) Fmoc-L-Trp (Boc)-OH, HATU, DIPEA, NMP, 1 h; d) Fmoc-D-Orn (Boc)-OH, HATU, DIPEA, NMP, 1 h; e) Fmoc-L-Asn (Trt)-OH, HATU, DIPEA, NMP, 1 h; f) Fmoc-L-Val-OH, HATU, DIPEA, NMP, 1 h; g) Fmoc-D-Leu-OH, HATU, DIPEA, NMP, 1 h; h) 20% HFIP/DC, 1 h.

    Journal: PLoS ONE

    Article Title: Design, synthesis and structure-activity relationship study of wollamide B; a new potential anti TB agent

    doi: 10.1371/journal.pone.0176088

    Figure Lengend Snippet: A synthetic scheme that shows the approach used to synthesize the linear precursor of wollamide B using SPPS. Reagents and conditions: a) Fmoc-L-Leu-OH, DIPEA, DCM, 2 h; b) 20% piperidine/DMF, 10 min (2X); c) Fmoc-L-Trp (Boc)-OH, HATU, DIPEA, NMP, 1 h; d) Fmoc-D-Orn (Boc)-OH, HATU, DIPEA, NMP, 1 h; e) Fmoc-L-Asn (Trt)-OH, HATU, DIPEA, NMP, 1 h; f) Fmoc-L-Val-OH, HATU, DIPEA, NMP, 1 h; g) Fmoc-D-Leu-OH, HATU, DIPEA, NMP, 1 h; h) 20% HFIP/DC, 1 h.

    Article Snippet: Synthesis of the linear hexapeptide precursors The linear hexapeptides ( 1a - 25a ) (Table A in ) were synthesized following a standard Fmoc based solid phase peptide synthesis (SPPS) approach using 2-chlorotrityl chloride resin as a solid support as described by Chatterjee J et al. [ ].

    Techniques:

    (a) Synthesis of building blocks with incorporated cleavable linkers. N -methylmorpholine (NMM) (b) synthesis of peptide segment 6 and incorporation of linker building block 5a by standard Fmoc-SPPS.

    Journal: Chemical Science

    Article Title: Facile folding of insulin variants bearing a prosthetic C-peptide prepared by α-ketoacid-hydroxylamine (KAHA) ligation folding of insulin variants bearing a prosthetic C-peptide prepared by α-ketoacid-hydroxylamine (KAHA) ligation †Electronic supplementary information (ESI) available: Experimental procedures and analytical data of all new compounds. See DOI: 10.1039/c8sc03738h

    doi: 10.1039/c8sc03738h

    Figure Lengend Snippet: (a) Synthesis of building blocks with incorporated cleavable linkers. N -methylmorpholine (NMM) (b) synthesis of peptide segment 6 and incorporation of linker building block 5a by standard Fmoc-SPPS.

    Article Snippet: – We prepared both peptide segments 6 and 7 by standard automated Fmoc solid phase peptide synthesis (SPPS).

    Techniques: Blocking Assay