nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Aggregation-Induced emission photosensitizer with lysosomal response for photodynamic therapy against cancer
|
Pan, Zhenxing |
|
|
132 |
C |
p. |
artikel |
2 |
An AIE luminogen targeting the endoplasmic reticulum inhibits cancer cell growth via multicellular organelle oxidative stress
|
Yang, Li |
|
|
132 |
C |
p. |
artikel |
3 |
A near infrared two-channel fluorescent probe for the detection of hydrogen sulfide and viscosity with a negligible crosstalk influence
|
Liu, Meng |
|
|
132 |
C |
p. |
artikel |
4 |
Antibiotic resistance and drug modification: Synthesis, characterization and bioactivity of newly modified potent pleuromutilin derivatives with a substituted piperazine moiety
|
Yi, Yunpeng |
|
|
132 |
C |
p. |
artikel |
5 |
Anti-inflammatory activity of fluorine-substituted benzo[h]quinazoline-2-amine derivatives as NF-κB inhibitors
|
Luan, Ming-Zhu |
|
|
132 |
C |
p. |
artikel |
6 |
Design, synthesis and biological evaluation of novel 9-methyl-9H-purine and thieno[3, 2-d]pyrimidine derivatives as potent mTOR inhibitors
|
Yang, Ying-Yue |
|
|
132 |
C |
p. |
artikel |
7 |
Design, synthesis and biological evaluation of purine-based derivatives as novel JAK2/BRD4(BD2) dual target inhibitors
|
Guo, Yong |
|
|
132 |
C |
p. |
artikel |
8 |
Design, synthesis, and biological evaluation of quinolinedione-linked sulfonylpiperazine derivatives as NQO1-directed antitumor agents
|
Guo, Kerong |
|
|
132 |
C |
p. |
artikel |
9 |
Design, synthesis, biological evaluation, and docking study of chromone-based phenylhydrazone and benzoylhydrazone derivatives as antidiabetic agents targeting α‐glucosidase
|
Fan, Meiyan |
|
|
132 |
C |
p. |
artikel |
10 |
Discovery of β-cyclocitral-derived mono-carbonyl curcumin analogs as anti-hepatocellular carcinoma agents via suppression of MAPK signaling pathway
|
Han, Haoyi |
|
|
132 |
C |
p. |
artikel |
11 |
Editorial Board
|
|
|
|
132 |
C |
p. |
artikel |
12 |
Enantiomeric pairs of macrocyclic acylphloroglucinols from Syzygium szemaoense
|
Huang, Jin-Chang |
|
|
132 |
C |
p. |
artikel |
13 |
Fluorescence sensing and glycosidase inhibition effect of multivalent glycosidase inhibitors based on Naphthalimide-deoxynojirimycin conjugates
|
Wang, Guang-Yuan |
|
|
132 |
C |
p. |
artikel |
14 |
Ganoapplins A and B with an unprecedented 6/6/6/5/6-fused pentacyclic skeleton from Ganoderma inhibit Tau pathology through activating autophagy
|
Peng, Xingrong |
|
|
132 |
C |
p. |
artikel |
15 |
Highly oxygenated grayanane diterpenoids with structural diversity from the flowers of Rhododendron dauricum and their analgesic activities
|
Feng, Yuanyuan |
|
|
132 |
C |
p. |
artikel |
16 |
8-Hydroxyquinoline derivatives suppress GLI1-mediated transcription through multiple mechanisms
|
Wen, Jiachen |
|
|
132 |
C |
p. |
artikel |
17 |
Issue TOC
|
|
|
|
132 |
C |
p. |
artikel |
18 |
Neuroprotective effect of a Keap1-Nrf2 Protein-Protein Inter-action inhibitor on cerebral Ischemia/Reperfusion injury
|
Qi, Zengxin |
|
|
132 |
C |
p. |
artikel |
19 |
Novel 2,6-disubstituted benzofuran-3-one analogues improve cerebral ischemia/reperfusion injury via neuroprotective and antioxidative effects
|
Yang, Zunhua |
|
|
132 |
C |
p. |
artikel |
20 |
Novel terpestacin derivatives with l-amino acid residue as anticancer agents against U87MG-derived glioblastoma stem cells
|
Liao, Shengrong |
|
|
132 |
C |
p. |
artikel |
21 |
Onychiol B attenuates lipopolysaccharide-induced inflammation via MAPK/NF-κB pathways and acute lung injury in vivo
|
Pei, Xiaoxiao |
|
|
132 |
C |
p. |
artikel |
22 |
PD0325901, an ERK inhibitor, attenuates RANKL‐induced osteoclast formation and mitigates cartilage inflammation by inhibiting the NF-κB and MAPK pathways
|
Jiang, Ting |
|
|
132 |
C |
p. |
artikel |
23 |
Phenolic and quinone methide nor-triterpenes as selective NLRP3 inflammasome inhibitors
|
González-Cofrade, Laura |
|
|
132 |
C |
p. |
artikel |
24 |
Phosphine chalcogenides and their derivatives from red phosphorus and functionalized pyridines, imidazoles, pyrazoles and their antimicrobial and cytostatic activity
|
Malysheva, Svetlana |
|
|
132 |
C |
p. |
artikel |
25 |
Proximity-enhanced protein crosslinking through an alkene-tetrazine reaction
|
Ma, Bin |
|
|
132 |
C |
p. |
artikel |
26 |
Rational design, synthesis, antifungal evaluation and docking studies of antifungal peptide CGA-N12 analogues based on the target CtKRE9
|
Li, Ruifang |
|
|
132 |
C |
p. |
artikel |
27 |
Research progress on the structure and biological diversities of 2-phenylindole derivatives in recent 20 years
|
Wu, Pan |
|
|
132 |
C |
p. |
artikel |
28 |
Root-Extracted lignanamides from Limonium gmelinii (Willd.) Kuntze with a potential PTP1B inhibitory activity by regulating PI3K/AKT signaling pathway
|
Tuohongerbieke, Amanguli |
|
|
132 |
C |
p. |
artikel |
29 |
Screening and characterization of a β-xylosidase from Bifidobacterium breve K-110 and its application in the biotransformation of the total flavonoids of epimedium to icariin with α-l-rhamnosidase
|
Su, Jingwen |
|
|
132 |
C |
p. |
artikel |
30 |
Site-directed double monoubiquitination of the repeat domain of the amyloid-forming protein tau impairs self-assembly and coacervation
|
Trivellato, Daniele |
|
|
132 |
C |
p. |
artikel |
31 |
Structurally various p-terphenyls with neuraminidase inhibitory from a sponge derived fungus Aspergillus sp. SCSIO41315
|
Qi, Xin |
|
|
132 |
C |
p. |
artikel |
32 |
Structure optimization, synthesis, and biological evaluation of 6-(2-amino-1H-benzo[d]imidazole-6-yl)-quinazolin-4(3H)-one derivatives as potential multi-targeted anticancer agents via Aurora A/ PI3K/BRD4 inhibition
|
Fan, Yanhua |
|
|
132 |
C |
p. |
artikel |
33 |
Synthesis, biological evaluation and molecular docking study of some new 4-aminosalicylic acid derivatives as anti-inflammatory and antimycobacterial agents
|
Qahtan, Maha Q.M. |
|
|
132 |
C |
p. |
artikel |
34 |
The antimicrobial peptide LK2(6)A(L) exhibits anti-inflammatory activity by binding to the myeloid differentiation 2 domain and protects against LPS-induced acute lung injury in mice
|
Zhang, Juan |
|
|
132 |
C |
p. |
artikel |
35 |
The first peptide derivatives of dioxybiphenyl-bridged spiro cyclotriphosphazenes: In vitro cytotoxicity activities and DNA damage studies
|
Koran, Kenan |
|
|
132 |
C |
p. |
artikel |
36 |
Thioether-based novel transition metal complexes: Synthesis, DNA interaction, in vitro biological assay, DFT calculations, and molecular docking studies
|
Singh, Anmol |
|
|
132 |
C |
p. |
artikel |