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You Searched For: Fmoc-Oic-OH


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Image Unavailable-B-4090.0005BA

Fmoc-Asn(Trt)-Ser(Psi(Me,Me)pro)-OH

Catalog Number: (B-4090.0005BA)
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.
Image Unavailable-D-1965.0025BA

2-Chlorotrityl chloride, polymer supported 200-400 mesh

Supplier: Bachem Americas
Description: A very acid sensitive resin suitable for the synthesis of protected peptide fragments by the Fmoc-strategy. ClTrt resin is in particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides (please see 2-Chlorotrityl Chloride Resin-Linked Amino Acids). Release from this resin is achieved by using 1-50 % TFA in CH₂Cl₂ containing 8 % triisopropylsilane, AcOH/CF₃CH₂OH/CH₂Cl₂, 0.5 % TFA or hexafluoroisopropanol/CH₂Cl₂. ClTrt resin has been used in cyclization reactions under Heck reaction conditions, the solid phase synthesis of β-peptides via the Arndt-Eistert homologation of Fmoc-protected amino acid diazoketones and in Mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt affording the corresponding aminomethylalkynyl adducts. 2-Chlorotrityl resin is highly suitable for the synthesis of peptide alcohols, e.g., peptaibols, and peptide ω-aminoalkylamides.

Image Unavailable-B-4330.0005BA

Fmoc-Val-Ser(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4330.0005BA)
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.
Image Unavailable-B-4320.0005BA

Fmoc-Trp(Boc)-Thr(Psi(Me,Me)Pro)-Oh

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.
Image Unavailable-B-4310.0005BA

Fmoc-Thr(Tbu)-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4310.0005BA)
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.
Image Unavailable-B-4295.0005BA

Fmoc-Lys(Boc)-Ser(Psi(Me,Me)Pro)-Oh

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.
Image Unavailable-B-4305.0005BA

Fmoc-Ser(Tbu)-Thr(Psi(Me,Me)Pro)-Oh

Catalog Number: (B-4305.0005BA)
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.
Product Image-97062-024

Sodium deoxycholate, high purity

Supplier: VWR
Description: Anionic - negatively-charged (carboxylates, sulfates or sulfonates in alkali metal form). Utilized for applications ranging from solubilizing membrane proteins in non-denaturing conditions to creating denaturing conditions during gel electrophoresis. Used for complete disruption of membranes.

SDS Certificates

Image Unavailable-TCA2526-100MG

1-Amino-3,6,9,12,15,18-hexaoxahenicosan-21-oic acid ≥95.0% (by HPLC)

Supplier: TCI America
Description: CAS Number: 905954-28-1
Molecular Formula: C15H31NO8
Molecular Weight: 353.41
Purity/Analysis Method: >95.0% (HPLC)
Form: Crystal

Certificates

Image Unavailable-TCH1645-200MG

Hederagenin ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America
Description: Hederagenin, Purity: >98.0%(HPLC)(T), CAS number: 465-99-6, Molecular Formula: C30H48O4, Molecular Weight: 472.71, Synonym: 3B,4A-3,23-Dihydroxyolean-12-en-28-oic Acid, Size: 50MG

Image Unavailable-TCM2666-25MG

Mal-amido-PEG4-acid ≥95.0% (by HPLC)

Supplier: TCI America
Description: 19-Maleimido-17-oxo-4,7,10,13-tetraoxa-16-azanonadecanoic Acid, Purity: >95.0%(HPLC), CAS Number: 1263045-16-4, MF: C18H28N2O9, MW: 416.43, Synonyms: 1-Maleimido-3-oxo-7,10,13,16-tetraoxa-4-azanonadecan-19-oic Acid, Size: 100MG

SDS

Product Image-89157-258

Ursolic acid ≥90%

Catalog Number: (89157-258)
Supplier: Enzo Life Sciences
Description: Inhibits angiogenesis
Product Image-89161-478

U-46619 ≥98%

Supplier: Enzo Life Sciences
Description: Prostaglandin H₂/thromboxane A₂ receptor agonist; stable analog of thromboxane A₂. Induces platelet aggregation at 32 nM and activates p38 MAPK.

Image Unavailable-CAAAAL05129-06

Methyl cholate 98+%

Supplier: Thermo Scientific Chemicals
Description: Methyl cholate 98+%

Certificates

Product Image-89149-396

Betulinic acid ≥99%, high purity

Supplier: Enzo Life Sciences
Description: Antitumor and anti-HIV agent

Product Image-89161-454

Prostaglandin F2α ≥99% (by TLC)

Catalog Number: (89161-454)
Supplier: Enzo Life Sciences
Description: A major uterine luteolytic prostaglandin. Endogenous agonist of the prostanoid FP receptor (KD=1.0nM). Inhibits differentiation of 3T3-L1 preadipocytes.
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