nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An exit beyond the pharmacophore model for 5-HT6R agents - a new strategy to gain dual 5-HT6/5-HT2A action for triazine derivatives with procognitive potential
|
Kucwaj-Brysz, Katarzyna |
|
|
121 |
C |
p. |
artikel |
2 |
Chemical synthesis, biological activities and action on nuclear receptors of 20S(OH)D3, 20S,25(OH)2D3, 20S,23S(OH)2D3 and 20S,23R(OH)2D3
|
Brzeminski, Pawel |
|
|
121 |
C |
p. |
artikel |
3 |
Combinatorial assembly, traceless generation and in situ evaluation of inhibitors for therapeutically relevant serine proteases
|
Vu, Lan Phuong |
|
|
121 |
C |
p. |
artikel |
4 |
Design and synthesis of new 2-oxoquinoxalinyl-1,2,4-triazoles as antitumor VEGFR-2 inhibitors
|
Zengin, Merve |
|
|
121 |
C |
p. |
artikel |
5 |
Design, molecular Docking, synthesis and evaluation of xanthoxylin hybrids as dual inhibitors of IL-6 and acetylcholinesterase for Alzheimer's disease
|
Kaur, Sukhvir |
|
|
121 |
C |
p. |
artikel |
6 |
Design, synthesis and anticancer evaluation of 6,7-disubstituted-4-phenoxyquinoline derivatives bearing 1,8-naphthyridine-3-carboxamide moiety as novel multi-target TKIs
|
Chen, Pengqin |
|
|
121 |
C |
p. |
artikel |
7 |
Design, synthesis and biological evaluation of 2-aminopyrimidine-based LSD1 inhibitors
|
Wang, Xinran |
|
|
121 |
C |
p. |
artikel |
8 |
Design, synthesis and biological evaluation of hydantoin derivatives as Mcl-1 selective inhibitors
|
Liang, Xiao |
|
|
121 |
C |
p. |
artikel |
9 |
Design, synthesis, and biological evaluation of quinazoline derivatives with covalent reversible warheads as potential FGFR4 inhibitors
|
Nie, Wenwen |
|
|
121 |
C |
p. |
artikel |
10 |
Design, synthesis, and biological evaluation of thiazole bioisosteres of goniofufurone through in vitro antiproliferative activity and in vivo toxicity
|
Svirčev, Miloš |
|
|
121 |
C |
p. |
artikel |
11 |
Design, synthesis and evaluation of novel thienopyridazine derivatives as Chk1/2 inhibitors
|
Shen, Dadong |
|
|
121 |
C |
p. |
artikel |
12 |
Design, synthesis, biological assessment, and in-Silico studies of 1,2,4-triazolo[1,5-a]pyrimidine derivatives as tubulin polymerization inhibitors
|
Mohamed, Heba S. |
|
|
121 |
C |
p. |
artikel |
13 |
Discovery and structural optimization of 9-O-phenylsulfonyl-berberines as new lipid-lowering agents
|
Kong, Yuan |
|
|
121 |
C |
p. |
artikel |
14 |
Discovery of a Nur77-mediated cytoplasmic vacuolation and paraptosis inducer (4-PQBH) for the treatment of hepatocellular carcinoma
|
Li, Baicun |
|
|
121 |
C |
p. |
artikel |
15 |
Discovery of ARS-1620 analogs as KRas G12C inhibitors with high in vivo antitumor activity
|
Zhao, Huiting |
|
|
121 |
C |
p. |
artikel |
16 |
Discovery of EGFR-Targeted Environment-Sensitive fluorescent probes for cell imaging and efficient tumor detection
|
Wang, Li-Xia |
|
|
121 |
C |
p. |
artikel |
17 |
Discovery of new pyrimido[5,4-c]quinolines as potential antiproliferative agents with multitarget actions: Rapid synthesis, docking, and ADME studies
|
Mekheimer, Ramadan A. |
|
|
121 |
C |
p. |
artikel |
18 |
Discovery of PHGDH inhibitors by virtual screening and preliminary structure–activity relationship study
|
Zhang, Fu-Mao |
|
|
121 |
C |
p. |
artikel |
19 |
Editorial Board
|
|
|
|
121 |
C |
p. |
artikel |
20 |
Evaluation of the effects of natural isoquinoline alkaloids on low density lipoprotein receptor (LDLR) and proprotein convertase subtilisin/kexin type 9 (PCSK9) in hepatocytes, as new potential hypocholesterolemic agents
|
Maharjan, Binita |
|
|
121 |
C |
p. |
artikel |
21 |
Facile synthesis of C1-substituted β-carbolines as CDK4 inhibitors for the treatment of cancer
|
Li, Deping |
|
|
121 |
C |
p. |
artikel |
22 |
Fe(III)-catalyzed regioselective and faster synthesis of isocoumarins with 3-oxoalkyl moiety at C-4: Identification of new inhibitors of PDE4
|
Thirupataiah, B. |
|
|
121 |
C |
p. |
artikel |
23 |
Identification of a dual FLT3 and MNK2 inhibitor for acute myeloid leukemia treatment using a structure-based virtual screening approach
|
Yen, Shih-Chung |
|
|
121 |
C |
p. |
artikel |
24 |
Identification of novel antiplatelet agents by targeting Glycoprotein VI: A combined virtual screening study
|
Olğaç, Simla |
|
|
121 |
C |
p. |
artikel |
25 |
Indirubin-3′-alkoxime derivatives for upregulation of Wnt signaling through dual inhibition of GSK-3β and the CXXC5-Dvl interaction
|
Song, Doona |
|
|
121 |
C |
p. |
artikel |
26 |
Inflammation: Biochemistry, cellular targets, anti-inflammatory agents and challenges with special emphasis on cyclooxygenase-2
|
Kaur, Baljit |
|
|
121 |
C |
p. |
artikel |
27 |
Interaction between CD44 and highly condensed hyaluronic acid through crosslinking with proteins
|
Tsuji, Reika |
|
|
121 |
C |
p. |
artikel |
28 |
Iridoids and sesquiterpenoids from Valeriana jatamansi and their anti-influenza virus activities
|
Quan, Li-Qiu |
|
|
121 |
C |
p. |
artikel |
29 |
Issue TOC
|
|
|
|
121 |
C |
p. |
artikel |
30 |
Mandelic acid-based spirothiazolidinones targeting M. tuberculosis: Synthesis, in vitro and in silico investigations
|
Trawally, Muhammed |
|
|
121 |
C |
p. |
artikel |
31 |
[99mTc-BBPA]: A possible SPECT agent to understand the role of 18-kDa translocator protein (PBR/TSPO) during neuro-glial interaction
|
Kumari, Neelam |
|
|
121 |
C |
p. |
artikel |
32 |
Novel sulfonyl thiazolyl-hydrazone derivatives as EGFR inhibitors: Design, synthesis, biological evaluation and molecular docking studies
|
Farghaly, Thoraya A. |
|
|
121 |
C |
p. |
artikel |
33 |
One-step purification and immobilization of thermostable β-glucosidase on Na-Y zeolite based on the linker and its application in the efficient production of baohuoside I from icariin
|
Lu, Shan |
|
|
121 |
C |
p. |
artikel |
34 |
Recent developments on 1,8-Naphthalimide moiety as potential target for anticancer agents
|
Tandon, Runjhun |
|
|
121 |
C |
p. |
artikel |
35 |
Recent updates on development of protein-tyrosine phosphatase 1B inhibitors for treatment of diabetes, obesity and related disorders
|
Singh, Sukhbir |
|
|
121 |
C |
p. |
artikel |
36 |
Revealing 2-dimethylhydrazino-2-alkyl alkynyl sphingosine derivatives as sphingosine kinase 2 inhibitors: Some hints on the structural basis for selective inhibition
|
Corro-Morón, Macarena |
|
|
121 |
C |
p. |
artikel |
37 |
Steroidal saponins from Trillium tschonoskii rhizome repress cancer stemness and proliferation of intrahepatic cholangiocarcinoma
|
Pang, Xu |
|
|
121 |
C |
p. |
artikel |
38 |
Structure-based discovery of a specific SHP2 inhibitor with enhanced blood–brain barrier penetration from PubChem database
|
Ma, Ying |
|
|
121 |
C |
p. |
artikel |
39 |
Structure-dependent of 3-fluorooxindole derivatives interacting with ctDNA: Binding effects and molecular docking approaches
|
Huang, Ze-Yue |
|
|
121 |
C |
p. |
artikel |
40 |
Synthesis and biological evaluation of 6-(pyrimidin-4-yl)-1H-pyrazolo[4,3-b]pyridine derivatives as novel dual FLT3/CDK4 inhibitors
|
Li, Xiandeng |
|
|
121 |
C |
p. |
artikel |
41 |
Synthesis and evaluation of biarylquinoline derivatives as novel HIF-1α inhibitors
|
Wu, Yu-Chieh |
|
|
121 |
C |
p. |
artikel |
42 |
Synthesis, biological evaluation, Structure − Activity relationship studies of quinoline-imidazole derivatives as potent antimalarial agents
|
Roy, Deblina |
|
|
121 |
C |
p. |
artikel |
43 |
Synthesis, photochemistry and computational study of novel 1,2,3-triazole heterostilbenes: Expressed biological activity of their electrocyclization photoproducts
|
Mlakić, Milena |
|
|
121 |
C |
p. |
artikel |
44 |
Synthesis, structural elucidation, in vitro antibacterial activity, DFT calculations, and molecular docking aspects of mixed-ligand complexes of a novel oxime and phenylalanine
|
Korkmaz, Ünal |
|
|
121 |
C |
p. |
artikel |
45 |
Synthesis, structure and acetylcholinesterase inhibition activity of new diarylpyrazoles
|
Zia, Mehwash |
|
|
121 |
C |
p. |
artikel |
46 |
Target identification of anti-diabetic and anti-obesity flavonoid derivative (Fla-CN)
|
Qin, Nan |
|
|
121 |
C |
p. |
artikel |
47 |
Triterpenoids and meroterpenoids from the edible Ganoderma resinaceum and their potential anti-inflammatory, antioxidant and anti-apoptosis activities
|
Kou, Rong-Wei |
|
|
121 |
C |
p. |
artikel |