You Searched For: Boc-D-Tyr(ME)-OH


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Supplier: Ambeed
Description: (2S,4S)-1-(tert-Butoxycarbonyl)-4-methoxypyrrolidine-2-carboxylic acid 98%

New Product

Catalog Number: (100292-982)
Supplier: Indofine Chemical Company
Description: Boc-(S)-2-amino-3-methoxypropionicacid dicyclohexylammonium salt ≥99%, crystals

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Supplier: TCI America
Description: CAS Number: 70642-86-3
MDL Number: MFCD00063030
Molecular Formula: C14H19NO5
Molecular Weight: 281.31
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Specific rotation [a]20/D: -2 deg (C=2, AcOH)

SDS

Supplier: Ambeed
Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-((tert-butoxycarbonyl)amino)-2-methylhexanoic acid 97%

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Supplier: Ambeed
Description: (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-6-((tert-butoxycarbonyl)amino)hexanoic acid 95%

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Catalog Number: (77618-504)
Supplier: Ambeed
Description: (R)-3-(4-(tert-Butoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid 97%

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Catalog Number: (B-4320.0005BA)
Supplier: Bachem Americas
Description: 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.


Supplier: TCI America
Description: CAS Number: 2130-96-3
MDL Number: MFCD00065597
Molecular Formula: C21H25NO5
Molecular Weight: 371.43
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 113
Specific rotation [a]20/D: 29.5 deg (C=2, EtOH)

SDS

Catalog Number: (B-4315.0005BA)
Supplier: Bachem Americas
Description: 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.


Catalog Number: (B-3930.0005BA)
Supplier: Bachem Americas
Description: 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.


Catalog Number: (101855-764)
Supplier: Matrix Scientific
Description: N-(tert-Butoxycarbonyl)-N-methyl-D-alanine


Catalog Number: (B-4295.0005BA)
Supplier: Bachem Americas
Description: 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.


Supplier: TCI America
Description: CAS Number: 47375-34-8
MDL Number: MFCD00065598
Molecular Formula: C18H27NO5
Molecular Weight: 337.42
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 117
Specific rotation [a]20/D: -16 deg (C=1, DMF)
Storage Temperature: 0-10°C

SDS

Supplier: Ambeed
Description: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-((tert-butoxycarbonyl)(methyl)amino)propanoic acid 97%

New Product

Catalog Number: (M-2115.0001BA)
Supplier: Bachem Americas
Description: This internally quenched fluorogenic peptide substrate contains anthranilic acid as fluorescent donor and m-nitro-tyrosine as acceptor (quencher). The sequence Abz-RVKRGLAY(NO₂)E is based on the sequence of hemagglutinin. The FRET substrate is efficiently cleaved by furin, a subtilisin-like eukaryotic serine endoprotease with Km = 3.8 µM and kcat = 29.3 s⁻¹ (kcat/Km = 7'710'000 M⁻¹s⁻¹). Its kcat/Km value is over 2000-fold higher than that of the commonly used substrate Boc-Arg-Val-Arg-Arg-AMC (I-1645). FRET Substrate for the basic residue-specific yeast aspartyl protease yapsin 1.


Catalog Number: (76985-272)
Supplier: Ambeed
Description: Dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)-3-methoxypropanoate, Purity: 95%, CAS number: 69912-63-6, Appearance: White to off-white powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G


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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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