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Royal Society of Chemistry (RSC)

  2040-2503

  2040-2511

 

Cơ quản chủ quản:  N/A

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Các bài báo tiêu biểu

Are pyridazines privileged structures?
Tập 2 Số 10 - Trang 935-941
Camille G. Wermuth

Compared to carbocyclic drug molecules, pyridazine-containing drugs present additional interaction possibilities, as illustrated here for the antirhinoviral agent R 61837.

The developability of heteroaromatic and heteroaliphatic rings – do some have a better pedigree as potential drug molecules than others?
Tập 3 Số 9 - Trang 1062 - 2012
Timothy J. Ritchie, Simon J. F. Macdonald, Simon Peace, Stephen D. Pickett, Christopher N. Luscombe
Strategies to prolong the plasma residence time of peptidedrugs
Tập 1 Số 5 - Trang 319-324
Lisa Pollaro, Christian Heinis

Well established as well as recently developed strategies to prevent the fast clearance of peptide drugs from the circulation are reviewed.

Synthesis and biological evaluation of coumarin–1,2,3-triazole–dithiocarbamate hybrids as potent LSD1 inhibitors
Tập 5 Số 5 - Trang 650-654
Xian-Wei Ye, Yi‐Chao Zheng, Ying‐Chao Duan, Mengmeng Wang, Bin Yu, Jingli Ren, Jinlian Ma, En Zhang, Hong‐Min Liu

Design of novel coumarin–1,2,3-triazole–dithiocarbamate hybrids as potent LSD1 inhibitors by introducing a coumarin scaffold.

Membranolytic anticancer peptides
Tập 7 Số 12 - Trang 2232-2245
Gisela Gabernet, Alex T. Müller, Jan A. Hiss, Gisbert Schneider

Understanding the structure–activity relationships and mechanisms of action of membranolytic anticancer peptides could help them advance to therapeutic success.

Interaction of indomethacin with calf thymus DNA: a multi-spectroscopic, thermodynamic and molecular modelling approach
Tập 8 Số 6 - Trang 1283-1296
Mohammed Amir Husain, Hassan Mubarak Ishqi, Tarique Sarwar, Sayeed Ur Rehman, Mohammad Tabish

Indomethacin belongs to the acetic acid derivative class of non-steroidal anti-inflammatory drugs with diverse pharmacological and biological activities.

Molecular hybridization as a powerful tool towards multitarget quinoidal systems: synthesis, trypanocidal and antitumor activities of naphthoquinone-based 5-iodo-1,4-disubstituted-, 1,4- and 1,5-disubstituted-1,2,3-triazoles
Tập 7 Số 8 - Trang 1555-1563
Samara Ben B. B. Bahia, Wallace J. Reis, Guilherme A. M. Jardim, Francielly T. Souto, Carlos A. de Simone, Claudia C. Gatto, Rubem F. S. Menna‐Barreto, Solange L. de Castro, Bruno C. Cavalcanti, Cláudia Pessoa, Maria H. Araújo, Eufrânio N. da Silva Júnior

Some of the hybrid compounds exhibited promising trypanocidal and anticancer activities.

Structure–activity relationships for the synthesis of selective cyclooxygenase 2 inhibitors: an overview (2009–2016)
Tập 8 Số 3 - Trang 492-500
Gabriele Carullo, F. Galligano, Francesca Aiello

An original point of view inside the SAR studies to develop new selective COX-2 inhibitors.

Synthesis and evaluation of a series of benzothiophene acrylonitrile analogs as anticancer agents
Tập 4 Số 7 - Trang 1073 - 2013
Narsimha Reddy Penthala, Vijayakumar N. Sonar, Jamie Horn, Markos Leggas, Jai Shankar K. Yadlapalli, Peter A. Crooks
Design, synthesis and evaluation of cinnamic acid ester derivatives as mushroom tyrosinase inhibitors
Tập 9 Số 5 - Trang 853-861
Zhaojun Sheng, Si-Yuan Ge, Ximing Xu, Yan Zhang, Panpan Wu, Kun Zhang, Xue-Tao Xu, Chen Li, Deng‐Gao Zhao, Xiaowen Tang

Tyrosinase is a key enzyme in melanin biosynthesis, and is also involved in the enzymatic browning of plant-derived foods.