Global Cancer Statistics 2022: the trends projection analysis

BS Chhikara, K Parang - Chemical Biology Letters, 2023 - pubs.thesciencein.org
Cancer is one of the most fatal diseases of recent times that causes several deaths every
year. The disease variations in different parts of the world, the impact of available medical …

Flexible or fixed: a comparative review of linear and cyclic cancer-targeting peptides

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 …

Discovery of cyclic peptide inhibitors targeting PD-L1 for cancer immunotherapy

J Fetse, Z Zhao, H Liu, UF Mamani… - Journal of medicinal …, 2022 - ACS Publications
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 …

Peptide Cyclization and Cyclodimerization by CuI-Mediated Azide−Alkyne Cycloaddition

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 …

Synthesis of 3-phenylpyrazolopyrimidine-1, 2, 3-triazole conjugates and evaluation of their Src kinase inhibitory and anticancer activities

A Kumar, I Ahmad, BS Chhikara, R Tiwari… - Bioorganic & medicinal …, 2011 - Elsevier
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 …

Exploring side-chain diversity by submonomer solid-phase aza-peptide synthesis

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 …

3-Substitued indoles: one-pot synthesis and evaluation of anticancer and Src kinase inhibitory activities

VK Rao, BS Chhikara, AN Shirazi, R Tiwari… - Bioorganic & medicinal …, 2011 - Elsevier
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 …

Thiazolyl N-benzyl-substituted acetamide derivatives: synthesis, Src kinase inhibitory and anticancer activities

A Fallah-Tafti, A Foroumadi, R Tiwari, AN Shirazi… - European journal of …, 2011 - Elsevier
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 …

4-Aryl-4H-naphthopyrans derivatives: one-pot synthesis, evaluation of Src kinase inhibitory and anti-proliferative activities

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 …

On the Cyclization of Non‐cyclic Peptides for Biological Applications: Inspiration from Naturally Cyclic Peptides

H Moulahoum, F Ghorbanizamani, K Tok… - …, 2023 - Wiley Online Library
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 …