| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Tumor-Targeting Dual-Modal imaging probe for nitroreductase in vivo
|
Li, Ting
|
|
|
149 |
C |
p.
|
artikel
|
| 2 |
Autophagy mediated targeting degradation, a promising strategy in drug development
|
Zhang, Jiantao
|
|
|
149 |
C |
p.
|
artikel
|
| 3 |
Bromo-substituted indirubins for inhibition of protein kinase-mediated signalling involved in inflammatory mediator release in human monocytes
|
Bachmann, Vivien
|
|
|
149 |
C |
p.
|
artikel
|
| 4 |
Characteristic terpenylated coumarins from Ferula ferulaeoides as potential inhibitors on overactivation of microglia
|
Jia, Yewen
|
|
|
149 |
C |
p.
|
artikel
|
| 5 |
Click-chemistry mediated synthesis of OTBN-1,2,3-Triazole derivatives exhibiting STK33 inhibition with diverse anti-cancer activities
|
Vala, Disha P.
|
|
|
149 |
C |
p.
|
artikel
|
| 6 |
Design, synthesis, and ex vivo anti-drug resistant cervical cancer activity of novel molecularly targeted chalcone derivatives
|
Yang, Zheng
|
|
|
149 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis and mechanistic studies of novel arylformylhydrazone butylphenyltin complexes as potential anticancer agents
|
Jiang, Wujiu
|
|
|
149 |
C |
p.
|
artikel
|
| 8 |
Design, Synthesis, DFT, docking Studies, and antimicrobial evaluation of novel benzimidazole containing sulphonamide derivatives
|
Singh, Kajal
|
|
|
149 |
C |
p.
|
artikel
|
| 9 |
Discovery of a potent Gilteritinib-based FLT3-PROTAC degrader for the treatment of Acute myeloid leukemia
|
Ye, Lei
|
|
|
149 |
C |
p.
|
artikel
|
| 10 |
Discovery of a prominent dual-target DDR1/EGFR inhibitor aimed DDR1/EGFR-positive NSCLC
|
Wang, Xuebao
|
|
|
149 |
C |
p.
|
artikel
|
| 11 |
Discovery of novel FUT8 inhibitors with promising affinity and in vivo efficacy for colorectal cancer therapy
|
Lv, Yixin
|
|
|
149 |
C |
p.
|
artikel
|
| 12 |
Dual-targeted NAMPT inhibitors as a progressive strategy for cancer therapy
|
Ozgencil, Fikriye
|
|
|
149 |
C |
p.
|
artikel
|
| 13 |
Editorial Board
|
|
|
|
149 |
C |
p.
|
artikel
|
| 14 |
Efficient conversion of hemoglobin to a non-vasoactive oxygen carrier by site-specific cross-linking with azido acyl methyl phosphates followed by bio-orthogonal CuAAC with a bis-alkyne
|
Kim, Yuju
|
|
|
149 |
C |
p.
|
artikel
|
| 15 |
Exploring antimalarial potential: Conjugating organometallic moieties with organic fragments for enhanced efficacy
|
Aqilah Zahirah Norazmi, Nur
|
|
|
149 |
C |
p.
|
artikel
|
| 16 |
Exploring the therapeutic potential of rutin through investigating its inhibitory mechanism on lactate dehydrogenase: Multi-spectral methods and computer simulation
|
Ding, Pei
|
|
|
149 |
C |
p.
|
artikel
|
| 17 |
Functionalized magnetic particles coupled with LC-MS strategy facilitated discovery of trace thioalkaloids with potent immunosuppressive activity
|
Lin, Chunyu
|
|
|
149 |
C |
p.
|
artikel
|
| 18 |
Important structural features of antimicrobial peptides towards specific activity: Trends in the development of efficient therapeutics
|
Fathi, Fariba
|
|
|
149 |
C |
p.
|
artikel
|
| 19 |
Incarvine C and its analogues inhibit the formation of cell cytoskeleton by targeting Rac1
|
Zhao, Pengxiang
|
|
|
149 |
C |
p.
|
artikel
|
| 20 |
Issue TOC
|
|
|
|
149 |
C |
p.
|
artikel
|
| 21 |
Novel imidazolone derivatives as potential dual inhibitors of checkpoint kinases 1 and 2: Design, synthesis, cytotoxicity evaluation, and mechanistic insights
|
Sheta, Yasmin S.
|
|
|
149 |
C |
p.
|
artikel
|
| 22 |
Old drug, new use: The thalidomide-based fluorescent probe for cysteine detection and imaging in living cells
|
Fu, Dingqiang
|
|
|
149 |
C |
p.
|
artikel
|
| 23 |
Rationale design of novel substituted 1,3,5-triazine candidates as dual IDH1(R132H)/ IDH2(R140Q) inhibitors with high selectivity against acute myeloid leukemia: In vitro and in vivo preclinical investigations
|
Tawfik, Haytham O.
|
|
|
149 |
C |
p.
|
artikel
|
| 24 |
Revisiting Structure-activity Relationships: Unleashing the potential of selective Janus kinase 1 inhibitors
|
Shan, Mengyi
|
|
|
149 |
C |
p.
|
artikel
|
| 25 |
Strategies for developing μ opioid receptor agonists with reduced adverse effects
|
Yuan, Yan
|
|
|
149 |
C |
p.
|
artikel
|
| 26 |
Structural characterization of polysaccharide from the peel of Trichosanthes kirilowii Maxim and its anti-hyperlipidemia activity by regulating gut microbiota and inhibiting cholesterol absorption
|
Jing, Yi
|
|
|
149 |
C |
p.
|
artikel
|
| 27 |
Structural optimization of Moracin M as novel selective phosphodiesterase 4 inhibitors for the treatment of idiopathic pulmonary fibrosis
|
Wang, Sen
|
|
|
149 |
C |
p.
|
artikel
|
| 28 |
Structural optimizations on the 7H-pyrrolo[2,3-d]pyrimidine scaffold to develop highly selective, safe and potent JAK3 inhibitors for the treatment of Rheumatoid arthritis
|
He, Linhong
|
|
|
149 |
C |
p.
|
artikel
|
| 29 |
Synthesis and evaluation of antibody-drug conjugates with high drug-to-antibody ratio using dimaleimide-DM1 as a linker- payload
|
Jeon, Joo-Hyun
|
|
|
149 |
C |
p.
|
artikel
|
| 30 |
Unveiling the promise of pyrimidine-modified CDK inhibitors in cancer treatment
|
Dubey, Rahul
|
|
|
149 |
C |
p.
|
artikel
|
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