17428 Results for: "Boc-Ser-Otbu&"
(R)-tert-Butyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate 98%
Supplier: Ambeed
(R)-tert-Butyl 2-((tert-butoxycarbonyl)amino)-3-hydroxypropanoate 98%
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Fmoc-Ser(Ac3GalN3α)-OtBu 95
Supplier: AFG Bioscience
Fmoc-Ser(Ac3GalN3α)-OtBu 95
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(S)-tert-Butyl 2-(((benzyloxy)carbonyl)amino)-3-hydroxypropanoate 95%
Supplier: Ambeed
(S)-tert-Butyl 2-(((benzyloxy)carbonyl)amino)-3-hydroxypropanoate 95%
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N-Carbobenzoxy-O-tert-butyl-L-serine 97%
Supplier: Ambeed
N-Carbobenzoxy-O-tert-butyl-L-serine 97%
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N-Carbobenzoxy-O-tert-butyl-L-serine
Supplier: Bachem Americas
Sequence: Z-Ser(tBu)-OH
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O-tert-Butyl-N-carbobenzoxy-L-serine methyl ester 95%
Supplier: Ambeed
O-tert-Butyl-N-carbobenzoxy-L-serine methyl ester 95%
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Fmoc-Glu(Otbu)-Ser(Psi(Me,Me)Pro)-Oh
Supplier: Bachem Americas
These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
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Fmoc-Asp(Otbu)-Ser(Psi(Me,Me)Pro)-Oh
Supplier: Bachem Americas
These dipeptide building blocks containing Ser- or Thr-derived oxazolidines (pseudoprolines) proved to be versatile tools for overcoming some intrinsic problems in the field of peptide chemistry. The presence of pseudoprolines within a peptide sequence results in the disruption of β-sheet structures considered as a source of intermolecular aggregation during chain elongation, thus increasing solvation and coupling kinetics in peptide assembly. Therefore, use of pseudoprolines offer new possibilities for accessing large peptides by convergent strategies and chemoselective ligation techniques. Moreover, incorporation of a pseudoproline unit facilitates cyclization of peptides.
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(S)-tert-Butyl 2-amino-3-methoxypropanoate hydrochloride 97%
Supplier: Ambeed
(S)-tert-Butyl 2-amino-3-methoxypropanoate hydrochloride 97%
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N-Carbobenzoxy-O-tert-butyl-L-serine 98,0
Supplier: TCI America
CAS Number: 1676-75-1
MDL Number: MFCD00038275
Molecular Formula: C15H21NO5
Molecular Weight: 295.34
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 86
Specific rotation [a]20/D: 21 deg (C=2, EtOH)
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Boc-Asp-OtBu 95%
Supplier: Thermo Scientific Chemicals
N-Boc-L-aspartic acid 1-tert-butyl ester, 95%
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O-tert-Butyl-L-serine tert-butyl ester hydrochloride 97%
Supplier: Ambeed
O-tert-Butyl-L-serine tert-butyl ester hydrochloride 97%
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H-Trp(Boc)-OtBu·HCl
Supplier: Bachem Americas
Sequence: H-Trp(Boc)-OtBu · HCl
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Nɑ-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-serine-tert-butyl ester 98%
Supplier: Ambeed
Nɑ-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-serine-tert-butyl ester 98%
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H-D-Lys(boc)-OtBu·HCl
Supplier: Bachem Americas
Sequence: H-D-Lys(Boc)-OtBu · HCl
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Boc-Glu(OtBu)-OH 99%
Supplier: Thermo Scientific Chemicals
Boc-Glu(OtBu)-OH 99%
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Boc-Glu(OtBu)-OH ≥99%
Supplier: Indofine Chemical Company
Boc-Glu(OtBu)-OH ≥99%