nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A FRET-based multifunctional fluorescence probe for the simultaneous detection of sulfite and viscosity in living cells
|
Zhang, Xin |
|
|
148 |
C |
p. |
artikel |
2 |
A novel selenium nanocomposite modified by AANL inhibits tumor growth by upregulating CLK2 in lung cancer
|
Zhang, Yueyang |
|
|
148 |
C |
p. |
artikel |
3 |
Antidote-controlled DNA aptamer modulates human factor IXa activity
|
Fang, Liang |
|
|
148 |
C |
p. |
artikel |
4 |
Antimicrobial activity and structure–activity relationships of molecules containing mono- or di- or oligosaccharides: An update
|
Zhou, Tiantian |
|
|
148 |
C |
p. |
artikel |
5 |
A review of chemical signaling mechanisms underlying quorum sensing and its inhibition in Staphylococcus aureus
|
Vadakkan, Kayeen |
|
|
148 |
C |
p. |
artikel |
6 |
Azaphilone pigments from the marine-derived Penicillium sclerotium UJNMF 0503 and their neuroprotective potential against H2O2-induced cell apoptosis through modulating PI3K/Akt pathway
|
Bao, Jie |
|
|
148 |
C |
p. |
artikel |
7 |
Biological impact and therapeutic potential of a novel camptothecin derivative (FLQY2) in pancreatic cancer through inactivation of the PDK1/AKT/mTOR pathway
|
Wang, Wenchao |
|
|
148 |
C |
p. |
artikel |
8 |
Blocking potential metabolic sites on NAT to improve its safety profile while retaining the pharmacological profile
|
Flammia, Rachael |
|
|
148 |
C |
p. |
artikel |
9 |
Brunonianines D-F, three new C19-diterpenoid alkaloids from the Delphinium brunonianum, with therapeutic effect on ovarian cancer in vitro and in vivo
|
Li, Qing |
|
|
148 |
C |
p. |
artikel |
10 |
Chemical sensors detect and resolve proteome aggregation in peripheral neuropathy cell model induced by chemotherapeutic agents
|
Wang, Zhiming |
|
|
148 |
C |
p. |
artikel |
11 |
Corrigendum to “DEFB114 protein enhances host resistance to fungal infection through the NOD1/2-ATG16L1-NF-κB signaling pathway” [Bioorg. Chem. 146 (2024) 107245]
|
Chen, Jingyun |
|
|
148 |
C |
p. |
artikel |
12 |
Dauresorcinols A and B, two pairs of merosesquiterpenoid enantiomers with new carbon skeletons from Rhododendron dauricum
|
Zhang, Hanqi |
|
|
148 |
C |
p. |
artikel |
13 |
Design and one-pot synthesis of new substituted pyrrolo[1,2-a]thieno[3,2-e]pyrimidine as potential antitumor agents: in vitro and in vivo studies
|
Gorbunova, Irina A. |
|
|
148 |
C |
p. |
artikel |
14 |
Design and synthesis of sulfonamide phenothiazine derivatives as novel ferroptosis inhibitors and their therapeutic effects in spinal cord injury
|
Bai, Xinyue |
|
|
148 |
C |
p. |
artikel |
15 |
Design, synthesis, and biological evaluation of 2,4-diaminopyrimidine derivatives as potent Hematopoietic Progenitor Kinase 1 (HPK1) inhibitors
|
Fu, Siyu |
|
|
148 |
C |
p. |
artikel |
16 |
Design, synthesis and biological evaluation of new RNF126-based p300/CBP degraders
|
Lei, Yan-Hua |
|
|
148 |
C |
p. |
artikel |
17 |
Design, synthesis, and biological evaluation of 2-(2-oxoindolin-3-ylidene)hydrazinecarbothioamides as a potential EGR-1 inhibitor for targeted therapy of atopic dermatitis
|
Ahn, Seunghyun |
|
|
148 |
C |
p. |
artikel |
18 |
Design, synthesis and biological evaluation of Thiazolo[3, 2-a]Pyrimidine derivatives as novel RNase H inhibitors
|
Zhao, Ke-Xin |
|
|
148 |
C |
p. |
artikel |
19 |
Design, synthesis and evaluation of thieno[3,2-d]pyrimidine derivatives as novel potent CDK7 inhibitors
|
Zhang, Hongjin |
|
|
148 |
C |
p. |
artikel |
20 |
Design, synthesis, biological evaluation of novel piperidine-based derivatives as potent poly(ADP-ribose) polymerase-1 (PARP-1) inhibitors
|
Lin, Chao |
|
|
148 |
C |
p. |
artikel |
21 |
Development of erythrina-based PARP-1/FTase dual-target inhibitors against lung cancer epithelial-mesenchymal transition (EMT) in vivo and in vitro
|
Yu, Ling |
|
|
148 |
C |
p. |
artikel |
22 |
Diaminocyclopentane – l-Lysine Adducts: Potent and selective inhibitors of human O-GlcNAcase
|
Weber, Patrick |
|
|
148 |
C |
p. |
artikel |
23 |
Discovery of a first-in-class degrader for the protein arginine methyltransferase 6 (PRMT6)
|
Yang, Hongling |
|
|
148 |
C |
p. |
artikel |
24 |
Discovery of highly potent PARP7 inhibitors for cancer immunotherapy
|
Yang, Jieping |
|
|
148 |
C |
p. |
artikel |
25 |
Discovery of novel biphenyl derivatives as androgen receptor degraders for the treatment of enzalutamide-resistant prostate cancer
|
Zhang, Wenqiang |
|
|
148 |
C |
p. |
artikel |
26 |
Discovery of novel coumarin-based KRAS-G12C inhibitors from virtual screening and Rational structural optimization
|
Shi, Jian-Tao |
|
|
148 |
C |
p. |
artikel |
27 |
Discovery of novel natural cardiomyocyte protectants from a toxigenic fungus Stachybotrys chartarum
|
Lin, Shuang |
|
|
148 |
C |
p. |
artikel |
28 |
Discovery of novel octahydroquinazoline scaffolds endowed with dual inhibition of tubulin polymerization/Eg5 against HCC: Apoptotic and radio-chemotherapeutic studies
|
Abdelhameid, Mohammed K. |
|
|
148 |
C |
p. |
artikel |
29 |
Discovery of selective TYK2 inhibitors: Design, synthesis, in vitro and in silico studies of promising hits with triazolopyrimidinone scaffold
|
Istanbullu, Huseyin |
|
|
148 |
C |
p. |
artikel |
30 |
Discovery, optimization and biological activity evaluation of genipin derivatives as potential KRAS G12D inhibitors
|
Sun, Ran |
|
|
148 |
C |
p. |
artikel |
31 |
Editorial Board
|
|
|
|
148 |
C |
p. |
artikel |
32 |
Evaluation of anticancer activity of novel platinum(II) bis(thiosemicarbazone) complex against breast cancer
|
Radomska, Dominika |
|
|
148 |
C |
p. |
artikel |
33 |
Exploring flavylium-based SWIR emitters: Design, synthesis and optical characterization of dyes derivatized with polar moieties
|
Blua, Federica |
|
|
148 |
C |
p. |
artikel |
34 |
Exploring the unexplored chemical space: Rational identification of new Tafenoquine analogs with antimalarial properties
|
Manen-Freixa, Leticia |
|
|
148 |
C |
p. |
artikel |
35 |
Golgi-targeted NIR fluorescent probe with large stokes shift for real-time monitoring of nitric oxide in depression model
|
Xi, Yanbei |
|
|
148 |
C |
p. |
artikel |
36 |
Identification and optimization of nitrophenolic analogues as dopamine metabolic enzyme inhibitors for the treatment of Parkinson’s disease
|
Zou, Manxing |
|
|
148 |
C |
p. |
artikel |
37 |
Issue TOC
|
|
|
|
148 |
C |
p. |
artikel |
38 |
Molecular design, construction and analgesic mechanism insights into the novel transdermal fusion peptide ANTP-BgNPB
|
Peng, Xinmeng |
|
|
148 |
C |
p. |
artikel |
39 |
Novel BODIPY-based nano-biomaterials with enhanced D-A-D structure for NIR-triggered photodynamic and photothermal therapy
|
Chen, Gang |
|
|
148 |
C |
p. |
artikel |
40 |
Novel quinazolin-2-yl 1,2,3-triazole hybrids as promising multi-target anticancer agents: Design, synthesis, and molecular docking study
|
El Hamaky, Noura F.M. |
|
|
148 |
C |
p. |
artikel |
41 |
Novel trifluoromethyl ketone derivatives as oral cPLA2/COX-2 dual inhibitors for resolution of inflammation in rheumatoid arthritis
|
Cai, Nan |
|
|
148 |
C |
p. |
artikel |
42 |
Spectroscopic, biochemical and computational studies of bioactive DNA minor groove binders targeting 5′-WGWWCW-3′ motif
|
Alniss, Hasan Y. |
|
|
148 |
C |
p. |
artikel |
43 |
Synthesis and antitumor activities of novel 3-(6-aminopyridin-3-yl)benzamide derivatives: Inducing cell cycle arrest and apoptosis via AURKB transcription inhibition
|
zhao, Xinran |
|
|
148 |
C |
p. |
artikel |
44 |
Synthesis and evaluation of antisense oligonucleotides prodrug with G-quadruplex assembly and lysosome escape capabilities for oncotherapy
|
Chen, Zuyi |
|
|
148 |
C |
p. |
artikel |
45 |
Synthesis and in vitro antitumor evaluation of new thieno[2,3-d]pyrimidine derivatives as EGFR and DHFR inhibitors
|
Fouad, Mahasen M. |
|
|
148 |
C |
p. |
artikel |
46 |
Synthesis, design, and antiproliferative evaluation of 6-(N-Substituted-methyl)pyrazolo[3,4-d]pyrimidines as the potent anti-leukemia agents
|
Chung, Cheng-Yen |
|
|
148 |
C |
p. |
artikel |
47 |
Synthesis, evaluation of biological activity and SAR of new thioalkyl derivatives of pyridine
|
Sh. Dashyan, Shushanik |
|
|
148 |
C |
p. |
artikel |
48 |
Synthesis, kinetic studies, and QSAR of dinucleoside polyphosphate derivatives as human AK1 inhibitors
|
Kozakiewicz-Piekarz, Anna |
|
|
148 |
C |
p. |
artikel |
49 |
Synthesis of novel indol-3-acetamido analogues as potent anticancer agents, biological evaluation and molecular modeling studies
|
Doganc, Fatima |
|
|
148 |
C |
p. |
artikel |
50 |
Synthesis of triazole AD-1 derivatives and its mechanism of mediating DNA damage of ROS in lung cancer cells
|
Han, Linlin |
|
|
148 |
C |
p. |
artikel |
51 |
Taking advantage of the interaction between the sulfoxide and heme cofactor to develop indoleamine 2, 3-dioxygenase 1 inhibitors
|
Wang, Yuchen |
|
|
148 |
C |
p. |
artikel |
52 |
The cryptic metabolites and anti-phytopathogenic activities from Nigrospora lacticolonia and Penicillium rubens uncovered by the synergism with host Paris polyphylla, monoculture, and co-culture
|
Shi, Wenzhi |
|
|
148 |
C |
p. |
artikel |
53 |
Total Synthesis, structure revision and antifungal activity of palmarumycin B8 and B7
|
Xu, Leichuan |
|
|
148 |
C |
p. |
artikel |
54 |
Unique aminothiazolyl coumarins as potential DNA and membrane disruptors towards Enterococcus faecalis
|
Zang, Zhong-Lin |
|
|
148 |
C |
p. |
artikel |
55 |
Utility of sulfachloropyridazine in the synthesis of novel anticancer agents as antiangiogenic and apoptotic inducers
|
Zahran, Sally S. |
|
|
148 |
C |
p. |
artikel |