Royal Society of Chemistry (RSC)
SCOPUS (2010-2019)
2040-2503
2040-2511
Cơ quản chủ quản: N/A
Các bài báo tiêu biểu
Are pyridazines privileged structures?
Tập 2 Số 10 - Trang 935-941
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
Strategies to prolong the plasma residence time of peptidedrugs
Tập 1 Số 5 - Trang 319-324
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
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
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
Indomethacin belongs to the acetic acid derivative class of non-steroidal
anti-inflammatory drugs with diverse pharmacological and biological activities.
Structure–activity relationships for the synthesis of selective cyclooxygenase 2 inhibitors: an overview (2009–2016)
Tập 8 Số 3 - Trang 492-500
An original point of view inside the SAR studies to develop new selective COX-2
inhibitors.
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
Some of the hybrid compounds exhibited promising trypanocidal and anticancer
activities.
Synthesis and evaluation of a series of benzothiophene acrylonitrile analogs as anticancer agents
Tập 4 Số 7 - Trang 1073 - 2013
Design, synthesis and evaluation of cinnamic acid ester derivatives as mushroom tyrosinase inhibitors
Tập 9 Số 5 - Trang 853-861
Tyrosinase is a key enzyme in melanin biosynthesis, and is also involved in the
enzymatic browning of plant-derived foods.