2018年9月13日星期四

New convenient reagent for peptide syntheses

New convenient reagent for peptide syntheses

B Belleau, G Malek - Journal of the American Chemical Society, 1968 - ACS Publications
12,500). Catalytic hydrogenation of 16a,b gave me- thoxyibogamine (17a; 55%) and methoxyepiibogamine
(17b; 67%) (17a: mp 152-154°; 17b: mp 144-147°), which were reduced14 smoothly to dZ-ibogamine
(la) and dZ-epiibogamine (lb) (la: mp 127-128°; lb: mp 196.5-197.5°). The samples of la and …

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*Peptide Synthesis: From short peptides to long peptides, linear peptides to cyclic peptides.
*Peptide Modifications: Peptide-protein conjugation, D-amino acid peptides, isotope peptides, fluorescent peptides, multiple antigen peptides, multiple disulfide bridge peptides, phosphopeptides etc.
*Catalog Peptides: ACE Inhibitors, Amyloids & Related Peptides, Antimicrobial Peptides, Apelin Peptides, Myelin Oligodendrocyte Glycoprotein (MOG) Peptides, TAT Proteins etc.
*Peptide Salt: TFA, Desalt, Acetate, HCl.
*Peptide Purity: From crude to >99.5%.
*Production Capacity: From mg to kg, with a capacity of synthesizing 15,000 peptides/month.
*Peptide Library Synthesis: Alanine Scan, Overlapping, Positional Scan, T-cell Truncated, Scrambled ect.

Eva He
eva@pepmic.com
Pepmic Co., Ltd
www.pepmic.com


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