peptide synthesizer multipep rsi (INTAVIS Inc)
90
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INTAVIS Inc
peptide synthesizer multipep rsi
Peptide Synthesizer Multipep Rsi, supplied by INTAVIS Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/peptide+synthesizer+multipep+rsi/multipep+automated+peptide+synthesizer/us12312379-1282-85-91
Average 90 stars, based on 1 article reviews
Peptide Synthesizer Multipep Rsi, supplied by INTAVIS Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/peptide+synthesizer+multipep+rsi/multipep+automated+peptide+synthesizer/us12312379-1282-85-91
Average 90 stars, based on 1 article reviews
peptide synthesizer multipep rsi - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Rational Designed Hybrid Peptides Show up to a 6-Fold Increase in Antimicrobial Activity and Demonstrate Different Ultrastructural Changes as the Parental Peptides Measured by BioSAXS Article Snippet: Automated solid-phase peptide synthesis (SPPS) on a Article Title: Can BioSAXS detect ultrastructural changes of antifungal compounds in Candida albicans?–an exploratory study Article Snippet: Antimicrobial peptides were produced by automated solidphase peptide synthesis (SPPS) on a Article Title: The Actin-Binding Prolyl-Isomerase Par17 Sustains Its Substrate Selectivity by Interdomain Allostery. Article Snippet: β- Actin peptide libraries were produced by automatic SPOT synthesis by Fmoc (9- fluorenylmethyloxycarbonyl) chemistry on Residue:Article Title: Methods for producing cyclic compounds comprising N-substituted amino acid residues Article Snippet: .. The resulting residue was purified by reverse-phase column chromatography (acetonitrile containing 0.1% formic acid/distilled water containing 0.1% formic acid) to afford Compound aa113 ((2S)-2-[ethyl(9H-fluoren-9-ylmethoxycarbonyl)amino]-3-(4-methylphenyl)propanoic acid (Fmoc-EtPhe(4-Me)-OH)) (4.4 g, 73% in two steps) LCMS (ESI) m/z=430 (M+H)+ Retention time: 0.95 minutes, (analysis condition: SQDFA05) The following elongation of Fmoc-Pro-OH (CAS No. 71989-31-6), Fmoc-Hph (4-CF3-35-F2)-OH (Compound aa134), Fmoc-MeGly-OH (CAS No. 77128-70-2), Fmoc-EtPhe(4-Me)-OH (Compound aa113), Fmoc-Aze(2)-OH (CAS No. 136552-06-2), Fmoc-MeAla-OH (CAS No. 84000-07-7), and Fmoc-Ile-OH (CAS No. 71989-23-6) was performed by an Fmoc solid-phase synthesis method using a Purification:Article Title: Methods for producing cyclic compounds comprising N-substituted amino acid residues Article Snippet: .. The resulting residue was purified by reverse-phase column chromatography (acetonitrile containing 0.1% formic acid/distilled water containing 0.1% formic acid) to afford Compound aa113 ((2S)-2-[ethyl(9H-fluoren-9-ylmethoxycarbonyl)amino]-3-(4-methylphenyl)propanoic acid (Fmoc-EtPhe(4-Me)-OH)) (4.4 g, 73% in two steps) LCMS (ESI) m/z=430 (M+H)+ Retention time: 0.95 minutes, (analysis condition: SQDFA05) The following elongation of Fmoc-Pro-OH (CAS No. 71989-31-6), Fmoc-Hph (4-CF3-35-F2)-OH (Compound aa134), Fmoc-MeGly-OH (CAS No. 77128-70-2), Fmoc-EtPhe(4-Me)-OH (Compound aa113), Fmoc-Aze(2)-OH (CAS No. 136552-06-2), Fmoc-MeAla-OH (CAS No. 84000-07-7), and Fmoc-Ile-OH (CAS No. 71989-23-6) was performed by an Fmoc solid-phase synthesis method using a Column Chromatography:Article Title: Methods for producing cyclic compounds comprising N-substituted amino acid residues Article Snippet: .. The resulting residue was purified by reverse-phase column chromatography (acetonitrile containing 0.1% formic acid/distilled water containing 0.1% formic acid) to afford Compound aa113 ((2S)-2-[ethyl(9H-fluoren-9-ylmethoxycarbonyl)amino]-3-(4-methylphenyl)propanoic acid (Fmoc-EtPhe(4-Me)-OH)) (4.4 g, 73% in two steps) LCMS (ESI) m/z=430 (M+H)+ Retention time: 0.95 minutes, (analysis condition: SQDFA05) The following elongation of Fmoc-Pro-OH (CAS No. 71989-31-6), Fmoc-Hph (4-CF3-35-F2)-OH (Compound aa134), Fmoc-MeGly-OH (CAS No. 77128-70-2), Fmoc-EtPhe(4-Me)-OH (Compound aa113), Fmoc-Aze(2)-OH (CAS No. 136552-06-2), Fmoc-MeAla-OH (CAS No. 84000-07-7), and Fmoc-Ile-OH (CAS No. 71989-23-6) was performed by an Fmoc solid-phase synthesis method using a Liquid Chromatography with Mass Spectroscopy:Article Title: Methods for producing cyclic compounds comprising N-substituted amino acid residues Article Snippet: .. The resulting residue was purified by reverse-phase column chromatography (acetonitrile containing 0.1% formic acid/distilled water containing 0.1% formic acid) to afford Compound aa113 ((2S)-2-[ethyl(9H-fluoren-9-ylmethoxycarbonyl)amino]-3-(4-methylphenyl)propanoic acid (Fmoc-EtPhe(4-Me)-OH)) (4.4 g, 73% in two steps) LCMS (ESI) m/z=430 (M+H)+ Retention time: 0.95 minutes, (analysis condition: SQDFA05) The following elongation of Fmoc-Pro-OH (CAS No. 71989-31-6), Fmoc-Hph (4-CF3-35-F2)-OH (Compound aa134), Fmoc-MeGly-OH (CAS No. 77128-70-2), Fmoc-EtPhe(4-Me)-OH (Compound aa113), Fmoc-Aze(2)-OH (CAS No. 136552-06-2), Fmoc-MeAla-OH (CAS No. 84000-07-7), and Fmoc-Ile-OH (CAS No. 71989-23-6) was performed by an Fmoc solid-phase synthesis method using a |