nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Accurate detection depression cell model with a dual-locked fluorescence probe in response to noradrenaline and HClO
|
Xiong, Xinyi |
|
|
146 |
C |
p. |
artikel |
2 |
A comprehensive review of synthetic strategies and SAR studies for the discovery of PfDHODH inhibitors as antimalarial agents. Part 1: triazolopyrimidine, isoxazolopyrimidine and pyrrole-based (DSM) compounds
|
Sharma, Manmohan |
|
|
146 |
C |
p. |
artikel |
3 |
A novel natural Syk inhibitor suppresses IgE-mediated mast cell activation and passive cutaneous anaphylaxis
|
Wang, Lele |
|
|
146 |
C |
p. |
artikel |
4 |
Antimicrobial properties of triazolato terpyridine Pd(II) and Pt(II) complexes formed by [3+2] cycloaddition coupling reaction
|
Mansour, Ahmed M. |
|
|
146 |
C |
p. |
artikel |
5 |
Arylacryl amides: Design, synthesis and the protection against cisplatin-induced acute kidney injury via TLR4/STING/NF-κB pathway
|
Wu, Xiaoming |
|
|
146 |
C |
p. |
artikel |
6 |
A turn-on fluorescence probe for imaging tyrosinase at the wound site in broken tail of zebrafish
|
Chen, Dingguo |
|
|
146 |
C |
p. |
artikel |
7 |
Benzimidazole-oxindole hybrids as multi-kinase inhibitors targeting melanoma
|
Allam, Rasha M. |
|
|
146 |
C |
p. |
artikel |
8 |
Bis-arylidene oxindoles for colorectal cancer nanotherapy
|
Bhattacharyya, Tithi |
|
|
146 |
C |
p. |
artikel |
9 |
Corrigendum to “A novel Cereblon E3 ligase modulator with antitumor activity in gastrointestinal cancer” [Bioorgan. Chem. 119 (2022) 105505]
|
Lier, Svenja |
|
|
146 |
C |
p. |
artikel |
10 |
D-A-D type based NIR fluorescence probe for monitoring the cysteine levels in pancreatic cancer cell during ferroptosis
|
Qin, Jingcan |
|
|
146 |
C |
p. |
artikel |
11 |
DEFB114 protein enhances host resistance to fungal infection through the NOD1/2-ATG16L1-NF-κB signaling pathway
|
Chen, Jingyun |
|
|
146 |
C |
p. |
artikel |
12 |
Design and application of a novel “turn-on” fluorescent probe for imaging sulfite in living cells and inflammation models
|
Yao, Kun |
|
|
146 |
C |
p. |
artikel |
13 |
Design, synthesis and Anti-Plasmodial activity of Mortiamide-Lugdunin conjugates
|
Trirattanaporn, Nattamon |
|
|
146 |
C |
p. |
artikel |
14 |
Design, synthesis and biological evaluation of new 2,6-difluorinated phenyl 4-(2-oxoimidazolidin-1-yl)benzenesulfonates as new antimicrotubule agents
|
Bouzriba, Chahrazed |
|
|
146 |
C |
p. |
artikel |
15 |
2,3-Dichloronaphthoquinone derivatives: Synthesis, antimicrobial activity, molecular modelling and ADMET studies
|
Kolancılar, Hakan |
|
|
146 |
C |
p. |
artikel |
16 |
Discovery of a novel class of rosmarinic acid derivatives as antibacterial agents: Synthesis, structure-activity relationship and mechanism of action
|
Wang, Yong |
|
|
146 |
C |
p. |
artikel |
17 |
Discovery of a novel small-molecule activator of SIRT3 that inhibits cell proliferation and migration by apoptosis and autophagy-dependent cell death pathways in colorectal cancer
|
Mou, Yi |
|
|
146 |
C |
p. |
artikel |
18 |
Discovery of cinnamylaldehyde-derived mono-carbonyl curcumin analogs as anti-gastric cancer agents via suppression of STAT3 and AKT pathway
|
Chen, Xi |
|
|
146 |
C |
p. |
artikel |
19 |
Discovery of indoleninyl-pyrazolo[3,4-b]pyridines as potent chemotherapeutic agents against colorectal cancer cells
|
Basir, Nur Husnaini |
|
|
146 |
C |
p. |
artikel |
20 |
Discovery of macrocyclic CDK2/4/6 inhibitors with improved potency and DMPK properties through a highly efficient macrocyclic drug design platform
|
Meng, Fanye |
|
|
146 |
C |
p. |
artikel |
21 |
Discovery of novel benzimidazole derivatives as potent HDACs inhibitors against leukemia with (Thio)Hydantoin as zinc-binding moiety: Design, synthesis, enzyme inhibition, and cellular mechanistic study
|
Abdulwahab, Hanan Gaber |
|
|
146 |
C |
p. |
artikel |
22 |
Discovery of novel biphenyl-sulfonamide analogues as NLRP3 inflammasome inhibitors
|
Huang, Chao |
|
|
146 |
C |
p. |
artikel |
23 |
Discovery of novel quinolin-2-one derivatives as potential GSK-3β inhibitors for treatment of Alzheimer’s disease: Pharmacophore-based design, preliminary SAR, in vitro and in vivo biological evaluation
|
Abdo Moustafa, Esraa |
|
|
146 |
C |
p. |
artikel |
24 |
Discovery of potential components characteristic by conjugated enone from the branches and leaves of Croton lauioides with anti-neuroinflammatory activity via regulating the NF-κB pathway
|
Jin, Yue |
|
|
146 |
C |
p. |
artikel |
25 |
Discovery of sesquiterpenoids from an actinomycete Crossiella cryophila through genome mining and heterologous expression
|
Yang, Qian |
|
|
146 |
C |
p. |
artikel |
26 |
Editorial Board
|
|
|
|
146 |
C |
p. |
artikel |
27 |
Efficient assembly and anti-tumor evaluation of novel polycyclic [1,2-a]-fused indoles
|
Guo, Hui |
|
|
146 |
C |
p. |
artikel |
28 |
Engineering an (R)-selective transaminase for asymmetric synthesis of (R)-3-aminobutanol
|
Liu, He |
|
|
146 |
C |
p. |
artikel |
29 |
Evaluation of antioxidant, antidiabetic and antiobesity potential of phenylpropanoids (PPs): Structure-activity relationship and insight into action mechanisms against dual digestive enzymes by comprehensive technologies
|
Li, Jiao |
|
|
146 |
C |
p. |
artikel |
30 |
Ferroptosis inducers: A new frontier in cancer therapy
|
Ma, Wenjing |
|
|
146 |
C |
p. |
artikel |
31 |
Four component Ugi reaction based small-molecule probes for integrated phenotypic screening
|
Thangaraj, Manikandan |
|
|
146 |
C |
p. |
artikel |
32 |
Identification of benzo[b]thiophene-1,1-dioxide derivatives as novel PHGDH covalent inhibitors
|
Cao, Xin-Yu |
|
|
146 |
C |
p. |
artikel |
33 |
Identifying eleven new ferroptosis inhibitors as neuroprotective agents from FDA-approved drugs
|
Tan, Qingyun |
|
|
146 |
C |
p. |
artikel |
34 |
Indole-based NNN donor Schiff base ligand and its complexes: Sonication-assisted synthesis, characterization, DNA binding, anti-cancer evaluation and in-vitro biological assay
|
Sanjurani, Thangjam |
|
|
146 |
C |
p. |
artikel |
35 |
Induction of breast cancer cell apoptosis by novel thiouracil-fused heterocyclic compounds through boosting of Bax/Bcl-2 ratio and DFT study
|
Mansour, Eman |
|
|
146 |
C |
p. |
artikel |
36 |
Insights into nucleoside hydrolase from Leishmania donovani inhibition: A new bioaffinity chromatography-based screening assay and docking studies
|
Anchau Wegermann, Camila |
|
|
146 |
C |
p. |
artikel |
37 |
Investigation on production and reaction conditions of sucrose synthase based glucosylation cascade towards flavonoid modification
|
Matera, Agata |
|
|
146 |
C |
p. |
artikel |
38 |
Issue TOC
|
|
|
|
146 |
C |
p. |
artikel |
39 |
Magnolol derivatives as specific and noncytotoxic inhibitors of breast cancer resistance protein (BCRP/ABCG2)
|
da Silva Zanzarini, Isadora |
|
|
146 |
C |
p. |
artikel |
40 |
Modular preparation of biphenyl triazoles via click chemistry as non-competitive hyaluronidase inhibitors
|
Qin, Yiman |
|
|
146 |
C |
p. |
artikel |
41 |
Multivalent pyrrolidines acting as pharmacological chaperones against Gaucher disease
|
Borie-Guichot, Marc |
|
|
146 |
C |
p. |
artikel |
42 |
New diarylcyclopentenone enantiomers and biphenyl derivatives from the fungus Talaromyces adpressus
|
Zheng, Meijia |
|
|
146 |
C |
p. |
artikel |
43 |
Novel chiral matrine derivatives as potential antitumor agents: Design, synthesis and biological evaluation
|
Qiu, Gan |
|
|
146 |
C |
p. |
artikel |
44 |
Potent, selective and reversible hMAO-B inhibition by benzalphthalides: Synthesis, enzymatic and cellular evaluations and virtual docking and predictive studies
|
Olmo, Esther del |
|
|
146 |
C |
p. |
artikel |
45 |
Qingkailing granule alleviates pulmonary fibrosis by inhibiting PI3K/AKT and SRC/STAT3 signaling pathways
|
Li, Hong |
|
|
146 |
C |
p. |
artikel |
46 |
Recent advances and structure-activity relationship studies of DPP-4 inhibitors as anti-diabetic agents
|
Singhal, Shipra |
|
|
146 |
C |
p. |
artikel |
47 |
Recent development of VEGFR small molecule inhibitors as anticancer agents: A patent review (2021–2023)
|
Zeng, Jing |
|
|
146 |
C |
p. |
artikel |
48 |
Riboflavin protects against pancreatic cancer metastasis by targeting TGF-β receptor 1
|
Zhao, Juanping |
|
|
146 |
C |
p. |
artikel |
49 |
Structure–activity relationship and biofilm formation-related gene targets of oleanolic acid-type saponins from Pulsatilla chinensis against Candida albicans
|
Tan, Junfeng |
|
|
146 |
C |
p. |
artikel |
50 |
Synergizing structure and function: Cinnamoyl hydroxamic acids as potent urease inhibitors
|
Viana, Luciana P.S. |
|
|
146 |
C |
p. |
artikel |
51 |
Synthesis and biological evaluation of lycoctonine derivatives with cardiotonic and calcium channels inhibitory activities
|
Wang, Jian–Zhu |
|
|
146 |
C |
p. |
artikel |
52 |
Synthesis and pharmacodynamic evaluation of Dihydropteridone derivatives against PDCoV in vivo and in vitro
|
Sun, Kai |
|
|
146 |
C |
p. |
artikel |
53 |
Synthesis and preclinical evaluation of a novel PET/fluorescence dual-modality probe targeting fibroblast activation protein
|
Zhang, Xiaojun |
|
|
146 |
C |
p. |
artikel |
54 |
Synthesis and preclinical evaluation of 11C-labeled 7-Oxo-2,4,5,7-tetrahydro-6H-pyrazolo[3,4-c]pyridine radioligands for RIPK1 positron emission tomography imaging
|
Luo, Tianwen |
|
|
146 |
C |
p. |
artikel |
55 |
Synthesis of narrow-spectrum anti-mycobacterial molecules without effect on the diversity of gut microbiota in mice based on the structure of rifampicin
|
Chen, Jun-Xian |
|
|
146 |
C |
p. |
artikel |
56 |
Synthesis of new trypanocidal agents from the hybridisation of metronidazole and eugenol analogues
|
Pelozo, Mônica Fraccarolli |
|
|
146 |
C |
p. |
artikel |
57 |
Synthesis, structure–activity relationship and biological evaluation of indole derivatives as anti-Candida albicans agents
|
Wu, Yandan |
|
|
146 |
C |
p. |
artikel |
58 |
The design, synthesis and bioactivity evaluation of novel androgen receptor degraders based on hydrophobic tagging
|
Sun, Ying |
|
|
146 |
C |
p. |
artikel |
59 |
The new N 2, N 4-diphenylpyridine-2,4-diamine deuterated derivatives as EGFR inhibitors to overcome C797S-mediated resistance
|
Liu, Jiadai |
|
|
146 |
C |
p. |
artikel |
60 |
Trisarcglaboids A and B, two cytotoxic lindenane sesquiterpenoid trimers with a unique polymerization mode isolated from Sarcandra glabra
|
Zhang, Danyang |
|
|
146 |
C |
p. |
artikel |
61 |
Unlocking InhA: Novel approaches to inhibit Mycobacterium tuberculosis
|
Wahan, Simranpreet K. |
|
|
146 |
C |
p. |
artikel |