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The ester derivatives obtained by C-ring modification of podophyllotoxin  induce apoptosis and inhibited proliferation in PC-3M cells via  down-regulation of PI3K/Akt signaling pathway - ScienceDirect
The ester derivatives obtained by C-ring modification of podophyllotoxin induce apoptosis and inhibited proliferation in PC-3M cells via down-regulation of PI3K/Akt signaling pathway - ScienceDirect

Efficient and Practical Procedure for the Esterification of the Free α-Car-  boxylic Acid of Amino Acid Residues with β-(Trimet
Efficient and Practical Procedure for the Esterification of the Free α-Car- boxylic Acid of Amino Acid Residues with β-(Trimet

Ester coupling reactions – an enduring challenge in the chemical synthesis  of bioactive natural products
Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products

Design, Synthesis, and Biological Evaluation of the First Podophyllotoxin  Analogues as Potential Vascular‐Disrupting Agents - Labruère - 2010 -  ChemMedChem - Wiley Online Library
Design, Synthesis, and Biological Evaluation of the First Podophyllotoxin Analogues as Potential Vascular‐Disrupting Agents - Labruère - 2010 - ChemMedChem - Wiley Online Library

Ester coupling reactions – an enduring challenge in the chemical synthesis  of bioactive natural products - Natural Product Reports (RSC Publishing)  DOI:10.1039/C4NP00106K
Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products - Natural Product Reports (RSC Publishing) DOI:10.1039/C4NP00106K

Chem Soc Rev
Chem Soc Rev

A fundamental developmental transition in Physcomitrium patens is regulated  by evolutionarily conserved mechanisms - Jaeger - 2021 - Evolution &  Development - Wiley Online Library
A fundamental developmental transition in Physcomitrium patens is regulated by evolutionarily conserved mechanisms - Jaeger - 2021 - Evolution & Development - Wiley Online Library

Ester coupling reactions – an enduring challenge in the chemical synthesis  of bioactive natural products - Natural Product Reports (RSC Publishing)  DOI:10.1039/C4NP00106K
Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products - Natural Product Reports (RSC Publishing) DOI:10.1039/C4NP00106K

Designer Flared Pants - FARFETCH
Designer Flared Pants - FARFETCH

Ester coupling reactions – an enduring challenge in the chemical synthesis  of bioactive natural products - Natural Product Reports (RSC Publishing)  DOI:10.1039/C4NP00106K
Ester coupling reactions – an enduring challenge in the chemical synthesis of bioactive natural products - Natural Product Reports (RSC Publishing) DOI:10.1039/C4NP00106K

DU SIMON Ballerina con fiocco- blu - Boscaini Scarpe
DU SIMON Ballerina con fiocco- blu - Boscaini Scarpe

PDF) Versatile selective α-carboxylic acid esterification of N-protected  amino acids and peptides by alcalase
PDF) Versatile selective α-carboxylic acid esterification of N-protected amino acids and peptides by alcalase

Frontiers | Recent Approaches to the Identification of Novel  Microtubule-Targeting Agents
Frontiers | Recent Approaches to the Identification of Novel Microtubule-Targeting Agents

Vivi Pant
Vivi Pant

The ester derivatives obtained by C-ring modification of podophyllotoxin  induce apoptosis and inhibited proliferation in PC-3M cells via  down-regulation of PI3K/Akt signaling pathway - ScienceDirect
The ester derivatives obtained by C-ring modification of podophyllotoxin induce apoptosis and inhibited proliferation in PC-3M cells via down-regulation of PI3K/Akt signaling pathway - ScienceDirect

Characterization of novel heterocyclic compounds based on  4-aryl-4H-chromene scaffold as anticancer agents: Design, synthesis,  antiprofilerative activity against resistant cancer cells, dual  β-tubulin/c-Src inhibition, cell cycle arrest and apoptosis ...
Characterization of novel heterocyclic compounds based on 4-aryl-4H-chromene scaffold as anticancer agents: Design, synthesis, antiprofilerative activity against resistant cancer cells, dual β-tubulin/c-Src inhibition, cell cycle arrest and apoptosis ...

Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone  Derivatives Exerting Effective Antitumor Activity Through Microtubule  Destabilization in Vitro and in Vivo | Journal of Medicinal Chemistry
Synthesis, Evaluation, and Mechanism Study of Novel Indole-Chalcone Derivatives Exerting Effective Antitumor Activity Through Microtubule Destabilization in Vitro and in Vivo | Journal of Medicinal Chemistry