nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A chemoenzymatic process for preparation of highly purified dehydroepiandrosterone in high space-time yield
|
Su, Bing-Mei |
|
|
133 |
C |
p. |
artikel |
2 |
Advances in antitumor research of HIF-1α inhibitor YC-1 and its derivatives
|
Ouyang, Chenglin |
|
|
133 |
C |
p. |
artikel |
3 |
Affinity-based protein profiling-driven discovery of myricanol as a Nampt activator
|
Lyu, Peng |
|
|
133 |
C |
p. |
artikel |
4 |
A novel CDK8 inhibitor with poly-substituted pyridine core: Discovery and anti-inflammatory activity evaluation in vivo
|
Chen, Xing |
|
|
133 |
C |
p. |
artikel |
5 |
A novel co-culture assay to evaluate the effects of sympathetic innervation on vascular smooth muscle differentiation
|
Jafarkhani, Saeed |
|
|
133 |
C |
p. |
artikel |
6 |
Anti-gout activity and the interaction mechanisms between Sanghuangporus vaninii active components and xanthine oxidase
|
Song, Jiling |
|
|
133 |
C |
p. |
artikel |
7 |
Biogenic synthesis, molecular docking, biomedical and environmental applications of multifunctional CuO nanoparticles mediated Phragmites australis
|
Kocabas, Buket Bulut |
|
|
133 |
C |
p. |
artikel |
8 |
Biotinylated selenocyanates: Potent and selective cytostatic agents
|
Roldán-Peña, Jesús M. |
|
|
133 |
C |
p. |
artikel |
9 |
Cationic lipid-conjugated bis-arylidene oxindole derivatives as broad-spectrum breast cancer-selective therapeutics
|
Yousuf, Md |
|
|
133 |
C |
p. |
artikel |
10 |
6-C-Linked trehalose glycolipids signal through Mincle and exhibit potent adjuvant activity
|
Thathsaranie P. Manthrirathna, M.A. |
|
|
133 |
C |
p. |
artikel |
11 |
Design, synthesis, and evaluation of hydrazones as dual inhibitors of ryanodine receptors and acetylcholinesterases for Alzheimer’s disease
|
Yang, Fan |
|
|
133 |
C |
p. |
artikel |
12 |
Design, synthesis and structure-activity relationship of N-phenyl aromatic amide derivatives as novel xanthine oxidase inhibitors
|
Hu, Sen-sen |
|
|
133 |
C |
p. |
artikel |
13 |
Design, synthesis, anticonvulsant activity and structure-activity relationships of novel 7-Azaindole derivatives
|
Meng, Qingfei |
|
|
133 |
C |
p. |
artikel |
14 |
Design, Synthesis, Molecular docking, and biological evaluation of novel 2,3-diaryl-1,3-thiazolidine-4-one derivatives as potential anti-inflammatory and cytotoxic agents
|
Mekhlef, Yosra O. |
|
|
133 |
C |
p. |
artikel |
15 |
Development of Yin-Yang ligand for cannabinoid receptors
|
Qiu, Yanli |
|
|
133 |
C |
p. |
artikel |
16 |
Dimeric pyrrole-imidazole alkaloids: sources, structures, bioactivities and biosynthesis
|
Chu, Mei-Jun |
|
|
133 |
C |
p. |
artikel |
17 |
Discovery and optimization of olanzapine derivatives as new ferroptosis inhibitors
|
Jiang, Xiufen |
|
|
133 |
C |
p. |
artikel |
18 |
Discovery of pterostilbene analogs as novel NLRP3 inflammasome inhibitors for potential treatment of DSS-induced colitis in mice
|
Ruan, Banfeng |
|
|
133 |
C |
p. |
artikel |
19 |
Disulfiram reduces the severity of mouse acute pancreatitis by inhibiting RIPK1-dependent acinar cell necrosis
|
Huang, Qiu-Yang |
|
|
133 |
C |
p. |
artikel |
20 |
Diversity oriented synthesis and SAR studies of new quinazolinones and related compounds as insecticidal agents against Culex pipiens L. Larvae and associated predator
|
Hekal, Mohamed H. |
|
|
133 |
C |
p. |
artikel |
21 |
Dual–target platinum(IV) complexes reverse cisplatin resistance in triple negative breast via inhibiting poly(ADP–ribose) polymerase (PARP–1) and enhancing DNA damage
|
Li, Rui |
|
|
133 |
C |
p. |
artikel |
22 |
Editorial Board
|
|
|
|
133 |
C |
p. |
artikel |
23 |
Exploring the cytotoxic effect and CDK-9 inhibition potential of novel sulfaguanidine-based azopyrazolidine-3,5-diones and 3,5-diaminoazopyrazoles
|
Husseiny, Ebtehal M. |
|
|
133 |
C |
p. |
artikel |
24 |
Garcinol and its analogues: Synthesis, cytotoxic activity and mechanistic investigation
|
Wang, Xueying |
|
|
133 |
C |
p. |
artikel |
25 |
Gastroprotective 2-(2-phenylethyl)chromone-sesquiterpene hybrids from the resinous wood of Aquilaria sinensis (Lour.) Gilg
|
Zhang, Hang |
|
|
133 |
C |
p. |
artikel |
26 |
Gliotoxin, a natural product with ferroptosis inducing properties
|
Chen, Huabin |
|
|
133 |
C |
p. |
artikel |
27 |
1H-Indazoles derivatives targeting PI3K/AKT/mTOR pathway: Synthesis, anti-tumor effect and molecular mechanism
|
Wang, Shuai |
|
|
133 |
C |
p. |
artikel |
28 |
Imidazo[1,2-a]quinazolines as novel, potent EGFR-TK inhibitors: Design, synthesis, bioactivity evaluation, and in silico studies
|
Hasanvand, Zaman |
|
|
133 |
C |
p. |
artikel |
29 |
Inspired by bis-β-carboline alkaloids: Construction and antitumor evaluation of a novel bis-β-carboline scaffold as potent antitumor agents
|
Liu, Wei |
|
|
133 |
C |
p. |
artikel |
30 |
Issue TOC
|
|
|
|
133 |
C |
p. |
artikel |
31 |
New trends in synthetic drugs and natural products targeting 20S proteasomes in cancers
|
Atta, Hind |
|
|
133 |
C |
p. |
artikel |
32 |
Novel N1 or N9 modified α-carboline analogues as potential ligands in Alzheimer's disease therapy: Synthesis and neurobiological activity evaluation
|
Dan, Wenjia |
|
|
133 |
C |
p. |
artikel |
33 |
Novel tools to study West Nile virus NS3 protease activity
|
Pianka, Joanna |
|
|
133 |
C |
p. |
artikel |
34 |
PET radiotracers and fluorescent probes for imaging human carbonic anhydrase IX and XII in hypoxic tumors
|
Nerella, Sridhar Goud |
|
|
133 |
C |
p. |
artikel |
35 |
Pharmacological evaluation of a novel skeleton compound isobavachin (4′,7-dihydroxy-8-prenylflavanone) as a hypouricemic agent: Dual actions of URAT1/GLUT9 and xanthine oxidase inhibitory activity
|
Zhao, Zean |
|
|
133 |
C |
p. |
artikel |
36 |
Phthalazone tethered 1,2,3-triazole conjugates: In silico molecular docking studies, synthesis, in vitro antiproliferative, and kinase inhibitory activities
|
Abdelgawad, Mohamed A |
|
|
133 |
C |
p. |
artikel |
37 |
Piperazine-derived small molecules as potential Flaviviridae NS3 protease inhibitors. In vitro antiviral activity evaluation against Zika and Dengue viruses
|
del Rosario García-Lozano, María |
|
|
133 |
C |
p. |
artikel |
38 |
Protective effects of berberine against β-amyloid-induced neurotoxicity in HT22 cells via the Nrf2/HO‐1 pathway
|
Zhang, Ru-lan |
|
|
133 |
C |
p. |
artikel |
39 |
Recent development of multi-target VEGFR-2 inhibitors for the cancer therapy
|
Liu, Xiu-Juan |
|
|
133 |
C |
p. |
artikel |
40 |
Structure-directed linker optimization of novel HEPTs as non-nucleoside inhibitors of HIV-1 reverse transcriptase
|
Hao, Qing-Qing |
|
|
133 |
C |
p. |
artikel |
41 |
Switching of newly synthesized linker-based derivatives of non-steroidal anti-inflammatory drugs toward anti-inflammatory and anticancer activity
|
Kaur, Mandeep |
|
|
133 |
C |
p. |
artikel |
42 |
Synthesis, antimicrobial, antibiofilm and computational studies of isatin-semicarbazone tethered 1,2,3-triazoles
|
Kumar, Aman |
|
|
133 |
C |
p. |
artikel |
43 |
Synthesis of amide derivatives of 3-aryl-3H-benzopyrans as osteogenic agent concomitant with anticancer activity
|
Singh, Sarita |
|
|
133 |
C |
p. |
artikel |
44 |
The role of lysine-specific demethylase 6A (KDM6A) in tumorigenesis and its therapeutic potentials in cancer therapy
|
Chen, Li-Juan |
|
|
133 |
C |
p. |
artikel |
45 |
Thiazolidin-4-one-based derivatives – Efficient tools for designing antiprotozoal agents. A review of the last decade
|
Tuszewska, Helena |
|
|
133 |
C |
p. |
artikel |
46 |
(±)-Yanhusuomide A, a pair of ornithine-fused benzylisoquinoline enantiomers from Corydalis yanhusuo
|
Wang, Ling-Yan |
|
|
133 |
C |
p. |
artikel |