nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Activity of 2,6,9-trisubstituted purines as potent PDGFRα kinase inhibitors with antileukaemic activity
|
Řezníčková, Eva |
|
2019 |
182 |
C |
p. |
artikel |
2 |
A fluorine scan on the Zn2+-binding thiolate side chain of HDAC inhibitor largazole: Synthesis, biological evaluation, and molecular modeling
|
Zhang, Bingbing |
|
2019 |
182 |
C |
p. |
artikel |
3 |
β-Amino acid derivatives as mitochondrial complex III inhibitors of L. donovani: A promising chemotype targeting visceral leishmaniasis
|
Chandrakar, Pragya |
|
2019 |
182 |
C |
p. |
artikel |
4 |
14- and 15-membered lactone macrolides and their analogues and hybrids: structure, molecular mechanism of action and biological activity
|
Janas, Anna |
|
2019 |
182 |
C |
p. |
artikel |
5 |
An epidermal growth factor receptor-targeted and endoplasmic reticulum-localized organic photosensitizer toward photodynamic anticancer therapy
|
Zhao, Xuan |
|
2019 |
182 |
C |
p. |
artikel |
6 |
An overview of recent progress in siderophore-antibiotic conjugates
|
Kong, Huimin |
|
2019 |
182 |
C |
p. |
artikel |
7 |
Application of glycosylation in targeted drug delivery
|
Chen, Fang |
|
2019 |
182 |
C |
p. |
artikel |
8 |
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells
|
Bozdag, Murat |
|
2019 |
182 |
C |
p. |
artikel |
9 |
Chromenone derivatives as a versatile scaffold with dual mode of inhibition of HIV-1 reverse transcriptase-associated Ribonuclease H function and integrase activity
|
Esposito, Francesca |
|
2019 |
182 |
C |
p. |
artikel |
10 |
Conformational restriction design of thiophene-biphenyl-DAPY HIV-1 non-nucleoside reverse transcriptase inhibitors
|
Sang, Yali |
|
2019 |
182 |
C |
p. |
artikel |
11 |
Curcumin analogues and their hybrid molecules as multifunctional drugs
|
Noureddin, Sawsan A. |
|
2019 |
182 |
C |
p. |
artikel |
12 |
Cyclic enaminone as new chemotype for selective cyclooxygenase-2 inhibitory, anti-inflammatory, and analgesic activities
|
Kumar, Raj |
|
2019 |
182 |
C |
p. |
artikel |
13 |
De novo design approaches targeting an envelope protein pocket to identify small molecules against dengue virus
|
Leal, Emilse S. |
|
2019 |
182 |
C |
p. |
artikel |
14 |
Design and synthesis of new N-terminal fatty acid modified-antimicrobial peptide analogues with potent in vitro biological activity
|
Zhong, Chao |
|
2019 |
182 |
C |
p. |
artikel |
15 |
Design and synthesis of novel artemisinin derivatives with potent activities against colorectal cancer in vitro and in vivo
|
Wang, Liang-Liang |
|
2019 |
182 |
C |
p. |
artikel |
16 |
Design and synthesis of pentacyclic triterpene conjugates and their use in medicinal research
|
Hodon, Jiri |
|
2019 |
182 |
C |
p. |
artikel |
17 |
Design of fluorinated cyclopropane derivatives of 2-phenylcyclopropylmethylamine leading to identification of a selective serotonin 2C (5-HT2C) receptor agonist without 5-HT2B agonism
|
Zhang, Guiping |
|
2019 |
182 |
C |
p. |
artikel |
18 |
Design, synthesis and biological evaluation of a new series of thiazolyl-pyrazolines as dual EGFR and HER2 inhibitors
|
Sever, Belgin |
|
2019 |
182 |
C |
p. |
artikel |
19 |
Design, synthesis and biological evaluation of 1-benzyl-5-oxopyrrolidine-2-carboximidamide derivatives as novel neuroprotective agents
|
Zhang, Linkui |
|
2019 |
182 |
C |
p. |
artikel |
20 |
Design, synthesis, and biological evaluation of novel benzodiazepine derivatives as anticancer agents through inhibition of tubulin polymerization in vitro and in vivo
|
Pang, Yanqing |
|
2019 |
182 |
C |
p. |
artikel |
21 |
Design, synthesis and biological evaluation of novel diazaspiro[4.5]decan-1-one derivatives as potential chitin synthase inhibitors and antifungal agents
|
Li, Bing |
|
2019 |
182 |
C |
p. |
artikel |
22 |
Design, synthesis and biological evaluation of stereo- and regioisomers of amino aryl esters as multidrug resistance (MDR) reversers
|
Teodori, Elisabetta |
|
2019 |
182 |
C |
p. |
artikel |
23 |
Design, synthesis of oleanolic acid-saccharide conjugates using click chemistry methodology and study of their anti-influenza activity
|
Su, Yangqing |
|
2019 |
182 |
C |
p. |
artikel |
24 |
Developing a binuclear multi-target Bi(III) complex by optimizing 2-acetyl-3-ethylpyrazine thiosemicarbazides
|
Khan, Muhammad Hamid |
|
2019 |
182 |
C |
p. |
artikel |
25 |
Development of novel chromeno[4,3-c]pyrazol-4(2H)-one derivates bearing sulfonylpiperazine as antitumor inhibitors targeting PI3Kα
|
Yin, Yong |
|
2019 |
182 |
C |
p. |
artikel |
26 |
Discovery and biological evaluation of darolutamide derivatives as inhibitors and down-regulators of wild-type AR and the mutants
|
Yu, Jiang |
|
2019 |
182 |
C |
p. |
artikel |
27 |
Discovery and synthesis of 3- and 21-substituted fusidic acid derivatives as reversal agents of P-glycoprotein-mediated multidrug resistance
|
Guo, Mengqi |
|
2019 |
182 |
C |
p. |
artikel |
28 |
Discovery of aryl-substituted indole and indoline derivatives as RORγt agonists
|
Zhu, Yan |
|
2019 |
182 |
C |
p. |
artikel |
29 |
Discovery of dual-acting opioid ligand and TRPV1 antagonists as novel therapeutic agents for pain
|
Lee, Hobin |
|
2019 |
182 |
C |
p. |
artikel |
30 |
Discovery of fused heterocyclic carboxamide derivatives as novel α7-nAChR agonists: Synthesis, preliminary SAR and biological evaluation
|
Xue, Yu |
|
2019 |
182 |
C |
p. |
artikel |
31 |
Discovery of novel functionalized 1,2,4-triazoles as PARP-1 inhibitors in breast cancer: Design, synthesis and antitumor activity evaluation
|
Boraei, Ahmed T.A. |
|
2019 |
182 |
C |
p. |
artikel |
32 |
Discovery of novel indolylarylsulfones as potent HIV-1 NNRTIs via structure-guided scaffold morphing
|
Zhao, Tong |
|
2019 |
182 |
C |
p. |
artikel |
33 |
Discovery of novel series of 2-substituted benzo[d]oxazol-5-amine derivatives as multi-target directed ligands for the treatment of Alzheimer's disease
|
Gutti, Gopichand |
|
2019 |
182 |
C |
p. |
artikel |
34 |
Discovery of phosphonamidate IDO1 inhibitors for the treatment of non-small cell lung cancer
|
Du, Qianming |
|
2019 |
182 |
C |
p. |
artikel |
35 |
Discovery of potent 4-aminoquinoline hydrazone inhibitors of NRH:quinoneoxidoreductase-2 (NQO2)
|
Hussein, Buthaina |
|
2019 |
182 |
C |
p. |
artikel |
36 |
Discovery of potent p38α MAPK inhibitors through a funnel like workflow combining in silico screening and in vitro validation
|
Astolfi, Andrea |
|
2019 |
182 |
C |
p. |
artikel |
37 |
Discovery of tissue selective liver X receptor agonists for the treatment of atherosclerosis without causing hepatic lipogenesis
|
Li, Chanjuan |
|
2019 |
182 |
C |
p. |
artikel |
38 |
Discovery, structural insight, and bioactivities of BY27 as a selective inhibitor of the second bromodomains of BET proteins
|
Chen, Deheng |
|
2019 |
182 |
C |
p. |
artikel |
39 |
Editorial Board
|
|
|
2019 |
182 |
C |
p. |
artikel |
40 |
Exploring the new horizons of drug repurposing: A vital tool for turning hard work into smart work
|
Kumar, Rajesh |
|
2019 |
182 |
C |
p. |
artikel |
41 |
From random to rational: A discovery approach to selective subnanomolar inhibitors of human carbonic anhydrase IV based on the Castagnoli-Cushman multicomponent reaction
|
Kalinin, Stanislav |
|
2019 |
182 |
C |
p. |
artikel |
42 |
Galloyl esters of trans-stilbenes are inhibitors of FASN with anticancer activity on non-small cell lung cancer cells
|
Tan, Yu-Jia |
|
2019 |
182 |
C |
p. |
artikel |
43 |
Graphene quantum dots (GQDs)-based nanomaterials for improving photodynamic therapy in cancer treatment
|
Fan, Hua-yang |
|
2019 |
182 |
C |
p. |
artikel |
44 |
Graphical abstract TOC
|
|
|
2019 |
182 |
C |
p. |
artikel |
45 |
Graphical abstract TOC
|
|
|
2019 |
182 |
C |
p. |
artikel |
46 |
Graphical abstract TOC continued
|
|
|
2019 |
182 |
C |
p. |
artikel |
47 |
Highly potent non-steroidal FXR agonists protostane-type triterpenoids: Structure-activity relationship and mechanism
|
Luan, Zhi-Lin |
|
2019 |
182 |
C |
p. |
artikel |
48 |
Hitting on the move: Targeting intrinsically disordered protein states of the MDM2-p53 interaction
|
Neochoritis, Constantinos G. |
|
2019 |
182 |
C |
p. |
artikel |
49 |
Identification and characterization of benzo[d]oxazol-2(3H)-one derivatives as the first potent and selective small-molecule inhibitors of chromodomain protein CDYL
|
Yang, Lixin |
|
2019 |
182 |
C |
p. |
artikel |
50 |
Imidazo[2,1-a]isoindole scaffold as an uncharted structure active on Leishmania donovani
|
Arsène, Sobinson |
|
2019 |
182 |
C |
p. |
artikel |
51 |
Immunoproteasome-selective inhibitors: An overview of recent developments as potential drugs for hematologic malignancies and autoimmune diseases
|
Xi, Jianjun |
|
2019 |
182 |
C |
p. |
artikel |
52 |
Natural dimers of coumarin, chalcones, and resveratrol and the link between structure and pharmacology
|
Menezes, José C.J.M.D.S. |
|
2019 |
182 |
C |
p. |
artikel |
53 |
Natural products as important tyrosine kinase inhibitors
|
Yin, Bo |
|
2019 |
182 |
C |
p. |
artikel |
54 |
Neurobehavioral investigation and acetylcholinesterase inhibitory activity study for some new coumarin derivatives
|
Mahmoud, Walaa R. |
|
2019 |
182 |
C |
p. |
artikel |
55 |
Novel antiacanthamoebic compounds belonging to quinazolinones
|
Anwar, Ayaz |
|
2019 |
182 |
C |
p. |
artikel |
56 |
Novel class of 7-Oxabicyclo[2.2.1]heptene sulfonamides with long alkyl chains displaying improved estrogen receptor α degradation activity
|
Hu, Zhiye |
|
2019 |
182 |
C |
p. |
artikel |
57 |
Novel derivatives of anaplastic lymphoma kinase inhibitors: Synthesis, radiolabeling, and preliminary biological studies of fluoroethyl analogues of crizotinib, alectinib, and ceritinib
|
Radaram, Bhasker |
|
2019 |
182 |
C |
p. |
artikel |
58 |
Novel multi target-directed ligands targeting 5-HT4 receptors with in cellulo antioxidant properties as promising leads in Alzheimer's disease
|
Lanthier, Caroline |
|
2019 |
182 |
C |
p. |
artikel |
59 |
Novel N-Substituted oseltamivir derivatives as potent influenza neuraminidase inhibitors: Design, synthesis, biological evaluation, ADME prediction and molecular docking studies
|
Ye, Jiqing |
|
2019 |
182 |
C |
p. |
artikel |
60 |
Novel 4-quinoline-thiosemicarbazone derivatives: Synthesis, antiproliferative activity, in vitro and in silico biomacromolecule interaction studies and topoisomerase inhibition
|
Ribeiro, Amélia Galdino |
|
2019 |
182 |
C |
p. |
artikel |
61 |
1,2,4-Oxadiazole derivatives targeting EGFR and c-Met degradation in TKI resistant NSCLC
|
Dokla, Eman M.E. |
|
2019 |
182 |
C |
p. |
artikel |
62 |
Phenylthiazoles with nitrogenous side chain: An approach to overcome molecular obesity
|
Elsebaei, Mohamed M. |
|
2019 |
182 |
C |
p. |
artikel |
63 |
Practical approaches to evaluating and optimizing brain exposure in early drug discovery
|
Freeman III, Burgess B. |
|
2019 |
182 |
C |
p. |
artikel |
64 |
Primaquine derivatives: Modifications of the terminal amino group
|
Zorc, Branka |
|
2019 |
182 |
C |
p. |
artikel |
65 |
Pyrazolo-benzothiazole hybrids: Synthesis, anticancer properties and evaluation of antiangiogenic activity using in vitro VEGFR-2 kinase and in vivo transgenic zebrafish model
|
Reddy, Velma Ganga |
|
2019 |
182 |
C |
p. |
artikel |
66 |
Recent advancements in mechanistic studies and structure activity relationship of FoF1 ATP synthase inhibitor as antimicrobial agent
|
Narang, Rakesh |
|
2019 |
182 |
C |
p. |
artikel |
67 |
Recent advances in the targeting of human DNA ligase I as a potential new strategy for cancer treatment
|
Saquib, Mohammad |
|
2019 |
182 |
C |
p. |
artikel |
68 |
ROS-responsive fluorinated polycations as non-viral gene vectors
|
Zhang, Ju-Hui |
|
2019 |
182 |
C |
p. |
artikel |
69 |
Scalable and cost-effective tosylation-mediated synthesis of antifungal and fungal diagnostic 6″-Modified amphiphilic kanamycins
|
Subedi, Yagya Prasad |
|
2019 |
182 |
C |
p. |
artikel |
70 |
STING modulators: Predictive significance in drug discovery
|
Cui, Xiangling |
|
2019 |
182 |
C |
p. |
artikel |
71 |
Structure-activity relationship with pyrazoline-based aromatic sulfamates as carbonic anhydrase isoforms I, II, IX and XII inhibitors: Synthesis and biological evaluation
|
Moi, Davide |
|
2019 |
182 |
C |
p. |
artikel |
72 |
Synthesis and in vitro biological evaluation of novel derivatives of Flexicaulin A condensation with amino acid trifluoroacetate
|
Ke, Yu |
|
2019 |
182 |
C |
p. |
artikel |
73 |
Synthesis and in vitro evaluation of piperazinyl-ureido sulfamates as steroid sulfatase inhibitors
|
Moi, Davide |
|
2019 |
182 |
C |
p. |
artikel |
74 |
Synthesis, biological evaluation and mechanism studies of C-23 modified 23-hydroxybetulinic acid derivatives as anticancer agents
|
Lu, Lixue |
|
2019 |
182 |
C |
p. |
artikel |
75 |
Synthesis, evaluation and structural investigations of potent purple acid phosphatase inhibitors as drug leads for osteoporosis
|
Feder, Daniel |
|
2019 |
182 |
C |
p. |
artikel |
76 |
Synthesis of polyfluoroalkyl sp2-iminosugar glycolipids and evaluation of their immunomodulatory properties towards anti-tumor, anti-leishmanial and anti-inflammatory therapies
|
Sánchez-Fernández, Elena M. |
|
2019 |
182 |
C |
p. |
artikel |
77 |
Synthesis, structure-activity relationship and trypanocidal activity of pyrazole-imidazoline and new pyrazole-tetrahydropyrimidine hybrids as promising chemotherapeutic agents for Chagas disease
|
Monteiro, M.E. |
|
2019 |
182 |
C |
p. |
artikel |
78 |
Targeting multiple G-quadruplex–forming DNA sequences: Design, biophysical and biological evaluations of indolo-naphthyridine scaffold derivatives
|
Catalano, Raffaella |
|
2019 |
182 |
C |
p. |
artikel |
79 |
The design of a cell-selective fowlicidin-1-derived peptide with both antimicrobial and anti-inflammatory activities
|
Rajasekaran, Ganesan |
|
2019 |
182 |
C |
p. |
artikel |