| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A combined network pharmacology and molecular biology approach to investigate the potential mechanisms of G-M6 on ovarian cancer
|
Ding, Meng
|
|
|
138 |
C |
p.
|
artikel
|
| 2 |
A mitochondria-targeted dual-response sensor for monitoring viscosity and peroxynitrite in living cells with distinct fluorescence signals
|
Li, Yaqian
|
|
|
138 |
C |
p.
|
artikel
|
| 3 |
A multidisciplinary functional proteomics-aided strategy as a tool for the profiling of a novel cytotoxic thiadiazolopyrimidone
|
Morretta, Elva
|
|
|
138 |
C |
p.
|
artikel
|
| 4 |
A novel fluorescent probe for rapid detection of sulfatase in vitro and in living cells
|
Chen, Junqing
|
|
|
138 |
C |
p.
|
artikel
|
| 5 |
Anti-inflammatory effects of naringenin 8-sulphonate from Parinari excelsa Sabine stem bark and its semi-synthetic derivatives
|
Macedo, Tiago
|
|
|
138 |
C |
p.
|
artikel
|
| 6 |
Apocarotenoids from Equisetum debile Roxb. ex Vaucher regulate the lipid metabolism via the activation of the AMPK/ACC/SREBP-1c signaling pathway
|
Xu, Qiannan
|
|
|
138 |
C |
p.
|
artikel
|
| 7 |
Chemoenzymatic approach towards the synthesis of the antitumor and antileishmanial marine metabolite (+)-Harzialactone A via the stereoselective, biocatalyzed reduction of a prochiral ketone
|
Artasensi, Angelica
|
|
|
138 |
C |
p.
|
artikel
|
| 8 |
Construction of HPQ-based activatable fluorescent probe for peroxynitrite and its application in ferroptosis and mice model of LPS-induced inflammation
|
Ji, Yuxiang
|
|
|
138 |
C |
p.
|
artikel
|
| 9 |
Corrigendum to “Synthesis, DFT study, theoretical and experimental spectroscopy of fatty amides based on extra-virgin olive oil and their antibacterial activity” [Bioorganic Chem., 135 (2023), 106511]
|
Farhan, Nesrain
|
|
|
138 |
C |
p.
|
artikel
|
| 10 |
Design and synthesis of pseudo-rutaecarpines as potent anti-inflammatory agents via regulating MAPK/NF-κB pathways to relieve inflammation-induced acute liver injury in mice
|
Qin, Li-Qing
|
|
|
138 |
C |
p.
|
artikel
|
| 11 |
Design and synthesis of salidroside analogs and their bioactivity against septic myocardial injury
|
Wang, Zongyuan
|
|
|
138 |
C |
p.
|
artikel
|
| 12 |
Design of novel water-soluble isoxazole-based antimicrobial agents and evaluation of their cytotoxicity and acute toxicity
|
Kondrashov, Evgeniy V.
|
|
|
138 |
C |
p.
|
artikel
|
| 13 |
Design of thiamine analogues for inhibition of thiamine diphosphate (ThDP)-dependent enzymes: Systematic investigation through Scaffold-Hopping and C2-Functionalisation
|
Chan, Alex H.Y.
|
|
|
138 |
C |
p.
|
artikel
|
| 14 |
Design, structure–activity relationships, and enzyme kinetic studies of tricyclic and tetracyclic coumarin–based sulfamates as steroid sulfatase inhibitors
|
Chiu, Pei-Fang
|
|
|
138 |
C |
p.
|
artikel
|
| 15 |
Design, synthesis, and anticancer activity of some novel 1H-benzo[d]imidazole-5-carboxamide derivatives as fatty acid synthase inhibitors
|
Singh, Shailendra
|
|
|
138 |
C |
p.
|
artikel
|
| 16 |
Design, synthesis and anticancer evaluation of novel oncolytic peptide-chlorambucil conjugates
|
Yin, Hao
|
|
|
138 |
C |
p.
|
artikel
|
| 17 |
Design, synthesis and biological evaluation of antiparasitic dinitroaniline-ether phospholipid hybrids
|
Roussaki, Marina
|
|
|
138 |
C |
p.
|
artikel
|
| 18 |
Design, synthesis, and biological evaluation of a series of indolone derivatives as novel FLT3 inhibitors for the treatment of acute myeloid leukemia
|
Jin, Jiaming
|
|
|
138 |
C |
p.
|
artikel
|
| 19 |
Design, synthesis and biological evaluation of new multi-target scutellarein hybrids for treatment of Alzheimer’s disease
|
Luo, Keke
|
|
|
138 |
C |
p.
|
artikel
|
| 20 |
Design, synthesis, and biological evaluation studies of novel carboxylesterase 2 inhibitors for the treatment of irinotecan-induced delayed diarrhea
|
Yang, Zhongcheng
|
|
|
138 |
C |
p.
|
artikel
|
| 21 |
Design, synthesis and evaluation of 2-aryl quinoline derivatives against 12R-lipoxygenase (12R-LOX): Discovery of first inhibitor of 12R-LOX
|
Bhuktar, Harshavardhan
|
|
|
138 |
C |
p.
|
artikel
|
| 22 |
Design, synthesis and molecular docking study of new pyrimidine-based hydrazones with selective anti-proliferative activity against MCF-7 and MDA-MB-231 human breast cancer cell lines
|
Badawi, Waleed A.
|
|
|
138 |
C |
p.
|
artikel
|
| 23 |
Determination of structural features that underpin the pannexin1 channel inhibitory activity of the peptide 10Panx1
|
Caufriez, Anne
|
|
|
138 |
C |
p.
|
artikel
|
| 24 |
Development of PROTAC degrader probe of CDK4/6 based on DCAF16
|
Pu, Chunlan
|
|
|
138 |
C |
p.
|
artikel
|
| 25 |
Discovery of berberine analogs as potent and highly selective p300/CBP HAT inhibitors
|
Zhong, Xue
|
|
|
138 |
C |
p.
|
artikel
|
| 26 |
Discovery of diaminotriazine carboxamides as potent inhibitors of hematopoetic progenitor kinase 1
|
Zhou, Lixin
|
|
|
138 |
C |
p.
|
artikel
|
| 27 |
Discovery of myrsinane-type Euphorbia diterpene derivatives through a skeleton conversion strategy from lathyrane diterpene for the treatment of Alzheimer's disease
|
Xiao, Yao
|
|
|
138 |
C |
p.
|
artikel
|
| 28 |
Discovery of potent and effective inhibitors containing sulfoxide structures targeting EML4-ALK rearrangement and EGFR mutant non-small cell lung cancer
|
An, Baijiao
|
|
|
138 |
C |
p.
|
artikel
|
| 29 |
Discovery of potent and selective PI3Kδ inhibitors bearing amino acid fragments
|
Lei, Hao
|
|
|
138 |
C |
p.
|
artikel
|
| 30 |
Discovery of potent natural product higenamine derivatives as novel Anti-Fusobacterium nucleatum agents
|
Su, Sijia
|
|
|
138 |
C |
p.
|
artikel
|
| 31 |
Diterpenoids with an unusual tricyclo[10.3.0.02,9]pentadecane skeleton from Pedilanthus tithymaloides as multidrug resistance modulators
|
Zhang, Lan-Jun
|
|
|
138 |
C |
p.
|
artikel
|
| 32 |
Editorial Board
|
|
|
|
138 |
C |
p.
|
artikel
|
| 33 |
Electro-organic synthesis of C-5 sulfenylated amino uracils: Optimization and exploring topoisomerase-I based anti-cancer profile
|
Rani, Payal
|
|
|
138 |
C |
p.
|
artikel
|
| 34 |
Enantiocomplementary synthesis of β-adrenergic blocker precursors via biocatalytic nitration of phenyl glycidyl ethers
|
Wang, Hui-Hui
|
|
|
138 |
C |
p.
|
artikel
|
| 35 |
Exploration of novel four-membered-heterocycle constructed peptidyl proteasome inhibitors with improved metabolic stability for cancer treatment
|
Wang, Hanlin
|
|
|
138 |
C |
p.
|
artikel
|
| 36 |
Fangchinoline derivatives inhibits PI3K signaling in vitro and in vivo in non-small cell lung cancer
|
Chen, Jia-shu
|
|
|
138 |
C |
p.
|
artikel
|
| 37 |
Fluorogenic substrates and pre‐column derivatization for monitoring the activity of bile salt hydrolase from Clostridium perfringens
|
Keuler, Tim
|
|
|
138 |
C |
p.
|
artikel
|
| 38 |
Genome-directed discovery of antiproliferative bafilomycins from a deepsea-derived Streptomyces samsunensis
|
Wang, Runyi
|
|
|
138 |
C |
p.
|
artikel
|
| 39 |
In-silico method for elucidation of prodigiosin as PARP-1 inhibitor a prime target of Triple-negative breast cancer
|
Sundararajan, Priya
|
|
|
138 |
C |
p.
|
artikel
|
| 40 |
Isatin-pyrimidine hybrid derivatives as enoyl acyl carrier protein reductase (InhA) inhibitors against Mycobacterium tuberculosis
|
Khalifa, Abdalrahman
|
|
|
138 |
C |
p.
|
artikel
|
| 41 |
Isolation and antihyperglycemic effects of garcibractinols A–H, intricate polycyclic polyprenylated acylphloroglucinols from the fruits of Garcinia bracteata
|
Li, Xueni
|
|
|
138 |
C |
p.
|
artikel
|
| 42 |
Issue TOC
|
|
|
|
138 |
C |
p.
|
artikel
|
| 43 |
Multivalent calix[4]arene-based mannosylated dendrons as new FimH ligands and inhibitors
|
Palmioli, Alessandro
|
|
|
138 |
C |
p.
|
artikel
|
| 44 |
New therapeutic approaches against pulmonary fibrosis
|
Yu, Dongke
|
|
|
138 |
C |
p.
|
artikel
|
| 45 |
Next generation of selenocyanate and diselenides with upgraded leishmanicidal activity
|
Henriquez-Figuereo, Andreina
|
|
|
138 |
C |
p.
|
artikel
|
| 46 |
Novel antimicrobial peptide DvAMP serves as a promising antifungal agent against Cryptococcus neoformans
|
Yang, Longbing
|
|
|
138 |
C |
p.
|
artikel
|
| 47 |
Novel flavonoid 1,3,4-oxadiazole derivatives ameliorate MPTP-induced Parkinson's disease via Nrf2/NF-κB signaling pathway
|
Meng, Hua-Wen
|
|
|
138 |
C |
p.
|
artikel
|
| 48 |
Novel hybrids of sclareol and 1,2,4-triazolo[1,5-a]pyrimidine show collateral sensitivity in multidrug-resistant glioblastoma cells
|
Stojković, Pavle
|
|
|
138 |
C |
p.
|
artikel
|
| 49 |
Novel organoboron complexes with robust core: Synthesis, functionalization, and subcellular targeting
|
Liu, Yanfei
|
|
|
138 |
C |
p.
|
artikel
|
| 50 |
Novel scaffolds targeting Mycobacterium tuberculosis plasma membrane Ca2+ transporter CtpF by structure-based strategy
|
A.Varon, Henry
|
|
|
138 |
C |
p.
|
artikel
|
| 51 |
Potential antioxidative components from Syringa oblata Lindl stems revealed by affinity ultrafiltration with multiple drug targets
|
Li, Zhiqiang
|
|
|
138 |
C |
p.
|
artikel
|
| 52 |
Recent advances in nitrogen-containing heterocyclic compounds as receptor tyrosine kinase inhibitors for the treatment of cancer: Biological activity and structural activity relationship
|
Taruneshwar Jha, Keshav
|
|
|
138 |
C |
p.
|
artikel
|
| 53 |
Recent development of selective inhibitors targeting the HDAC6 as anti-cancer drugs: Structure, function and design
|
Peng, Jie
|
|
|
138 |
C |
p.
|
artikel
|
| 54 |
Recent research of BTK inhibitors: Methods of structural design, pharmacological activities, manmade derivatives and structure–activity relationship
|
Wang, Lin
|
|
|
138 |
C |
p.
|
artikel
|
| 55 |
Structural and pharmacological diversity of 1,4-naphthoquinone glycosides in recent 20 years
|
Shen, Xuelian
|
|
|
138 |
C |
p.
|
artikel
|
| 56 |
Structure-regulated mitochondrial-targeted fluorescent probe for sensing and imaging SO2 in vivo
|
Tian, Qinqin
|
|
|
138 |
C |
p.
|
artikel
|
| 57 |
Substituted furan sulfonamides as carbonic anhydrase inhibitors: Synthesis, biological and in silico studies
|
Angeli, Andrea
|
|
|
138 |
C |
p.
|
artikel
|
| 58 |
Synthesis and antitubercular activity of novel 4-arylalkyl substituted thio-, oxy- and sulfoxy-quinoline analogues targeting the cytochrome bc1 complex
|
Murnane, Robert
|
|
|
138 |
C |
p.
|
artikel
|
| 59 |
Synthesis and biological evaluation of thieno[3,2-c]pyrazol-3-amine derivatives as potent glycogen synthase kinase 3β inhibitors for Alzheimer’s disease
|
Yan, Ning
|
|
|
138 |
C |
p.
|
artikel
|
| 60 |
Synthesis and evaluation of Piperine analogs as thioredoxin reductase inhibitors to cause oxidative stress-induced cancer cell apoptosis
|
Zhong, Miao
|
|
|
138 |
C |
p.
|
artikel
|
| 61 |
Synthesis of water-soluble novel bioactive pyridine-based azo coumarin derivative and competitive cytotoxicity, DNA binding, BSA binding study, and in silico analysis with coumarin
|
Karan, Putul
|
|
|
138 |
C |
p.
|
artikel
|
| 62 |
Synthetic and natural guanidine derivatives as antitumor and antimicrobial agents: A review
|
Gomes, Ana R.
|
|
|
138 |
C |
p.
|
artikel
|
| 63 |
Targeting histone deacetylases for heart diseases
|
Jin, Gang
|
|
|
138 |
C |
p.
|
artikel
|
| 64 |
Targeting the Grb2 cSH3 domain: Design, synthesis and biological evaluation of the first series of modulators
|
Bufano, Marianna
|
|
|
138 |
C |
p.
|
artikel
|
| 65 |
Targeting the Hedgehog pathway with novel Gli1 hydrophobic tagging degraders
|
Li, Xiangyang
|
|
|
138 |
C |
p.
|
artikel
|
| 66 |
Thalidomide derivatives as nanomolar human neutrophil elastase inhibitors: Rational design, synthesis, antiproliferative activity and mechanism of action
|
Donarska, Beata
|
|
|
138 |
C |
p.
|
artikel
|
| 67 |
β-Turn editing in Gramicidin S: Activity impact on replacing proline α-carbon with stereodynamic nitrogen
|
Lal, Jhajan
|
|
|
138 |
C |
p.
|
artikel
|
Tijdschrift beschrijving