Á Roxin, G Zheng - Future medicinal chemistry, 2012 - Taylor & Francis
Peptides can serve as versatile cancer-targeting ligands and have been used for clinically relevant applications such as cancer imaging and therapy. A current and long-standing …
Blockade of the interaction between programmed cell death ligand-1 (PD-L1) and its receptor PD-1 has shown great success in cancer immunotherapy. Peptides possess unique …
R Jagasia, JM Holub, M Bollinger… - The Journal of …, 2009 - ACS Publications
Head-to-tail cyclodimerization of resin-bound oligopeptides bearing azide and alkyne groups occurs readily by 1, 3-dipolar cycloaddition upon treatment with CuI. The process …
A series of two classes of 3-phenylpyrazolopyrimidine-1, 2, 3-triazole conjugates were synthesized using click chemistry approach. All compounds were evaluated for inhibition of …
D Sabatino, C Proulx, S Klocek, CB Bourguet… - Organic …, 2009 - ACS Publications
Submonomer synthesis of aza-peptides featuring regioselective alkylation of peptide-bound aza-Gly residues provided ten aza-analogues of the Growth Hormone Releasing Peptide-6 …
An efficient and economical method was developed for the synthesis of 3-substituted indoles by one-pot three-component coupling reaction of a substituted or unsubstituted …
KX2-391 (KX-01/Kinex Pharmaceuticals), N-benzyl-2-(5-(4-(2-morpholinoethoxy) phenyl) pyridin-2-yl) acetamide, is a highly selective Src substrate binding site inhibitor. To …
A Rafinejad, A Fallah-Tafti, R Tiwari, AN Shirazi… - DARU Journal of …, 2012 - Springer
Background A series of 2-amino-4-aryl-4 H-benzo [h or f] chromene-3-carbonitrile derivatives were synthesized and evaluated for inhibition of Src kinase and cell proliferation …
Peptides are unique class of biomolecules for pharmaceutics and industries, given their structural features that can be applied to many approaches. Although their advantages are …