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                             56 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 7-Amine-spiro[chromeno[4,3-b]quinoline-6,1′-cycloalkanes]: Synthesis and cholinesterase inhibitory activity of structurally modified tacrines Silva, Letícia B.
108 C p.
 artikel
2 A novel series of benzothiazepine derivatives as tubulin polymerization inhibitors with anti-tumor potency Wang, Bin
108 C p.
 artikel
3 Antiamoebic effects of sesquiterpene lactones isolated from the zoanthid Palythoa aff. clavata Rodríguez-Expósito, Rubén L.
108 C p.
 artikel
4 Antibiotic resistance and drug modification: Synthesis, characterization and bioactivity of newly modified potent ciprofloxacin derivatives Alsughayer, Abdulhakeem
108 C p.
 artikel
5 Anti-hyperlipidemic potential of natural product based labdane-pyrroles via inhibition of cholesterol and triglycerides synthesis Jalaja, Renjitha
108 C p.
 artikel
6 Antiinflammatory triterpenoids from the fruiting bodies of Fomitopsis pinicola Kuo, Ping-Chung
108 C p.
 artikel
7 Bioactive constituents from Thunbergia erecta as potential anticholinesterase and anti-ageing agents: Experimental and in silico studies Refaey, Mohamed S.
108 C p.
 artikel
8 Chalcone and its analogs: Therapeutic and diagnostic applications in Alzheimer’s disease Thapa, Pritam
108 C p.
 artikel
9 Chemical mining of heterotrophic Shewanella algae reveals anti-infective potential of macrocyclic polyketides against multidrug-resistant pathogens Chakraborty, Kajal
108 C p.
 artikel
10 Combined 3D-QSAR and docking analysis for the design and synthesis of chalcones as potent and selective monoamine oxidase B inhibitors Mellado, Marco
108 C p.
 artikel
11 Combined in silico and in vitro studies to identify novel antidiabetic flavonoids targeting glycogen phosphorylase Brás, Natércia F.
108 C p.
 artikel
12 Corrigendum to “Acylphloroglucinols with acetylcholinesterase inhibitory effects from the fruits of Eucalyptus robusta”. [Bioorg. Chem. 103 (2020) 104127] Liu, Hui
108 C p.
 artikel
13 Dehydroepiandrosterone derived imidazolium salts and their antimicrobial efficacy Hryniewicka, Agnieszka
108 C p.
 artikel
14 Design and synthesis of pyrimidine-5-carbonitrile hybrids as COX-2 inhibitors: Anti-inflammatory activity, ulcerogenic liability, histopathological and docking studies Alfayomy, Abdallah M.
108 C p.
 artikel
15 Design, synthesis and antitumor activity evaluation of novel HDAC inhibitors with tetrahydrobenzothiazole as the skeleton Sun, Simin
108 C p.
 artikel
16 Design, synthesis and biological evaluation of potential anti-AD hybrids with monoamine oxidase B inhibitory and iron-chelating effects Guo, Jianan
108 C p.
 artikel
17 Design, synthesis, biological evaluation and molecular docking of new 1,3,4-oxadiazole homonucleosides and their double-headed analogs as antitumor agents EL Mansouri, Az-eddine
108 C p.
 artikel
18 Design, synthesis, molecular docking, in silico ADMET profile and anticancer evaluations of sulfonamide endowed with hydrazone-coupled derivatives as VEGFR-2 inhibitors Sayed, Asmaa M
108 C p.
 artikel
19 Diarylheptanoid-chalcone hybrids with PTP1B and α-glucosidase dual inhibition from Alpinia katsumadai He, Xiao-Feng
108 C p.
 artikel
20 Dimeric guaianes from leaves of Xylopia vielana as snail inhibitors identified by high content screening Xu, Qi-Qi
108 C p.
 artikel
21 Discovery and SAR studies of 3-amino-4-(phenylsulfonyl)tetrahydrothiophene 1,1-dioxides as non-electrophilic antioxidant response element (ARE) activators Jo, Jeyun
108 C p.
 artikel
22 Discovery of andrastones from the deep-sea-derived Penicillium allii-sativi MCCC 3A00580 by OSMAC strategy Xie, Chun-Lan
108 C p.
 artikel
23 Discovery of a novel series of indolylchalcone-benzenesulfonamide hybrids acting as selective carbonic anhydrase II inhibitors Singh, Priti
108 C p.
 artikel
24 Discovery of 5-(3-bromo-2-(2,3-dibromo-4,5-dimethoxybenzyl)-4,5-dimethoxybenzylidene)thiazolidine-2,4-dione as a novel potent protein tyrosine phosphatase 1B inhibitor with antidiabetic properties Jiang, Bo
108 C p.
 artikel
25 Eco-friendly sequential one-pot synthesis, molecular docking, and anticancer evaluation of arylidene-hydrazinyl-thiazole derivatives as CDK2 inhibitors El-Naggar, Abeer M.
108 C p.
 artikel
26 Editorial Board
108 C p.
 artikel
27 Evaluation of thionolactones as a new type of hydrogen sulfide (H2S) donors for a blood pressure regulation Zaorska, Ewelina
108 C p.
 artikel
28 Exploring the potential intracellular targets of vascular normalization based on active candidates Shan, Yuanyuan
108 C p.
 artikel
29 Furan-2-carboxamide derivative, a novel microtubule stabilizing agent induces mitotic arrest and potentiates apoptosis in cancer cells Shwetha, B
108 C p.
 artikel
30 Identification of fenoldopam as a novel LSD1 inhibitor to abrogate the proliferation of renal cell carcinoma using drug repurposing strategy Zheng, Yan
108 C p.
 artikel
31 Influence of core extension and side chain nature in targeting G-quadruplex structures with perylene monoimide derivatives Busto, Natalia
108 C p.
 artikel
32 Insights of 8-hydroxyquinolines: A novel target in medicinal chemistry Gupta, Rohini
108 C p.
 artikel
33 Investigation of pyrazolo[1,5-a]quinoxalin-4-ones as novel monoamine oxidase inhibitors Panova, Valeria A.
108 C p.
 artikel
34 Issue TOC
108 C p.
 artikel
35 Minor immunosuppressive spiroorthoester group-containing pregnane glycosides from the root barks of Periploca sepium Shao, Xing-Cheng
108 C p.
 artikel
36 Multivalent butyrylcholinesterase inhibitor discovered by exploiting dynamic combinatorial chemistry Zhao, Shuang
108 C p.
 artikel
37 Novel phenylpyrimidine derivatives containing a hydrazone moiety protect rice seedlings from injury by metolachlor Deng, Xile
108 C p.
 artikel
38 Pentacyclic triterpenes with nitric oxide inhibitory activity from Potentilla chinensis Han, Jae Sang
108 C p.
 artikel
39 Pesimquinolones I–S, eleven new quinolone alkaloids produced by Penicillium simplicissimum and their inhibitory activity on NO production Dai, Chong
108 C p.
 artikel
40 Pinocembrin and its linolenoyl ester derivative induce wound healing activity in HaCaT cell line potentially involving a GPR120/FFA4 mediated pathway Mazzotta, Sarah
108 C p.
 artikel
41 Pyrazoline analogs as potential anticancer agents and their apoptosis, molecular docking, MD simulation, DNA binding and antioxidant studies Rana, Manish
108 C p.
 artikel
42 QM/MM analysis, synthesis and biological evaluation of epalrestat based mutual-prodrugs for diabetic neuropathy and nephropathy Choudhary, Shalki
108 C p.
 artikel
43 Quinazolin-4(3H)-one based agents bearing thiadiazole-urea: Synthesis and evaluation of anti-proliferative and antiangiogenic activity Faraji, Aram
108 C p.
 artikel
44 Quinoline carboxamide core moiety-based compounds inhibit P. falciparum falcipain-2: Design, synthesis and antimalarial efficacy studies Singh, Anju
108 C p.
 artikel
45 Research progress in biological activities of succinimide derivatives Zhao, Zefeng
108 C p.
 artikel
46 Scope and limitations of biocatalytic carbonyl reduction with white-rot fungi Zhuk, Tatyana S.
108 C p.
 artikel
47 Structural insights into the desymmetrization of bulky 1,2-dicarbonyls through enzymatic monoreduction Rabuffetti, Marco
108 C p.
 artikel
48 Swertiamarin from Enicostemma littorale, counteracts PD associated neurotoxicity via enhancement α-synuclein suppressive genes and SKN-1/NRF-2 activation through MAPK pathway Pandey, Taruna
108 C p.
 artikel
49 Synthesis and biological evaluation of novel withangulatin A derivatives as potential anticancer agents Zhou, Wu-Xi
108 C p.
 artikel
50 Synthesis, biological evaluation and molecular docking studies of novel quinazolinones as antitubercular and antimicrobial agents Kumar Pandey, Sarvesh
108 C p.
 artikel
51 Synthesis, inhibition properties against xanthine oxidase and molecular docking studies of dimethyl N-benzyl-1H-1,2,3-triazole-4,5-dicarboxylate and (N-benzyl-1H-1,2,3-triazole-4,5-diyl)dimethanol derivatives Yagiz, Güler
108 C p.
 artikel
52 Synthesis of 6-epi-tuberiferin and the biological activities of tuberiferin, dehydrobrabrachylaenolide, 6-epi-tuberiferin, and their synthetic intermediates Li, Dan
108 C p.
 artikel
53 Synthesis of imidazole-pyrazole conjugates bearing aryl spacer and exploring their enzyme inhibition potentials Chaudhry, Faryal
108 C p.
 artikel
54 Synthesis of indole-based-thiadiazole derivatives as a potent inhibitor of α-glucosidase enzyme along with in silico study Alomari, Munther
108 C p.
 artikel
55 Synthesis of novel sulfonamide derivatives containing pyridin-3-ylmethyl 4-(benzoyl)piperazine-1-carbodithioate moiety as potent PKM2 activators Li, Ridong
108 C p.
 artikel
56 Target separation and antitumor metastasis activity of sesquiterpene-based lysine-specific demethylase 1 inhibitors from zedoary turmeric oil Ren, Chunling
108 C p.
 artikel
                             56 gevonden resultaten
 
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