| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Activation of the 20S proteasome as a possible strategy to counteract amylin oligomerization in type 2 diabetes
|
Sowik, Daria
|
|
|
155 |
C |
p.
|
artikel
|
| 2 |
2-Acylpyrrole-based alkaloids from the leaves of Sauropus spatulifolius and their α-glucosidase inhibitory activities
|
Xia, Xiao
|
|
|
155 |
C |
p.
|
artikel
|
| 3 |
Application of a near-infrared viscosity-responsive fluorescent probe for lysosomal targeting in fatty liver mice
|
Hao, Junlei
|
|
|
155 |
C |
p.
|
artikel
|
| 4 |
Benzothiazole-triazole hybrids: Novel anticancer agents inducing cell cycle arrest and apoptosis through Bcl-2 inhibition in triple-negative breast cancer
|
Shama, Aamir R.
|
|
|
155 |
C |
p.
|
artikel
|
| 5 |
Citrus maxima extract-coated versatile gold nanoparticles display ROS-mediated inhibition of MDR-Pseudomonas aeruginosa and cancer cells
|
Jha, Diksha
|
|
|
155 |
C |
p.
|
artikel
|
| 6 |
Design, synthesis and activity evaluation of novel quinazolinone compounds as TRPC5 inhibitors
|
Bai, Longhui
|
|
|
155 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis and biological evaluation of Alisol B derivatives for potential treatment of non-alcoholic steatohepatitis
|
Yu, Nai-Rong
|
|
|
155 |
C |
p.
|
artikel
|
| 8 |
Design, synthesis, and biological evaluation of N 1-(2-(adamantan-1-yl)-1H-indol-5-yl)-N 2-(substituent)-1,2-dicarboxamides as anticancer agents targeting Nur77-mediated endoplasmic reticulum stress
|
Hu, Hongyu
|
|
|
155 |
C |
p.
|
artikel
|
| 9 |
Design, synthesis, and biological evaluation of novel FGFR1 PROTACs
|
Wang, Yu-Wei
|
|
|
155 |
C |
p.
|
artikel
|
| 10 |
Design, synthesis, and biological evaluation of novel thiourea derivatives as small molecule inhibitors for prostate specific membrane antigen
|
Sengupta, Sagnik
|
|
|
155 |
C |
p.
|
artikel
|
| 11 |
Design, synthesis, and structure–activity relationships of five-membered heterocyclic incorporated aryl(alkyl)azoles: From antiproliferative thiazoles to safer anticonvulsant oxadiazoles
|
Valipour, Mehdi
|
|
|
155 |
C |
p.
|
artikel
|
| 12 |
Discovery of novel tris-1,2,3-triazole-based hybrids as VEGFR2 inhibitors with potent anti-proliferative and cytotoxicity through apoptosis induction
|
Alsehli, Mosa
|
|
|
155 |
C |
p.
|
artikel
|
| 13 |
Discovery of potent antiosteoporotic cyclic depsipeptides with an unusual nitrile hydroxy acid from Microascus croci
|
Li, Shasha
|
|
|
155 |
C |
p.
|
artikel
|
| 14 |
Editorial Board
|
|
|
|
155 |
C |
p.
|
artikel
|
| 15 |
Exploration of triazole derivatives, SAR profiles, and clinical pipeline against Mycobacterium tuberculosis
|
Pakeeraiah, Kakarla
|
|
|
155 |
C |
p.
|
artikel
|
| 16 |
Exploring the therapeutic potential of acridines: Synthesis, structure, and biological applications
|
Marques, Diego Santa Clara
|
|
|
155 |
C |
p.
|
artikel
|
| 17 |
Exploring 1,2,3-triazole-Schiff’s base hybrids as innovative EGFR inhibitors for the treatment of breast cancer: In vitro and in silico study
|
Nawareg, Nareman A.
|
|
|
155 |
C |
p.
|
artikel
|
| 18 |
Hederagenin ameliorates ferroptosis-induced damage by regulating PPARα/Nrf2/GPX4 signaling pathway in HT22 cells: An in vitro and in silico study
|
Feng, Yuxin
|
|
|
155 |
C |
p.
|
artikel
|
| 19 |
Heterologous expression of calcium-independent mesophilic α-amylase from Priestia megaterium: Immobilization on genipin-modified multi-walled carbon nanotubes and silica supports to enhance thermostability and catalytic activity
|
Akbulut, Kübra
|
|
|
155 |
C |
p.
|
artikel
|
| 20 |
Homopregnane-type ferrocene-steroid conjugates exhibit immunomodulatory activity
|
Raičević, Vidak
|
|
|
155 |
C |
p.
|
artikel
|
| 21 |
Identification of mitoxantrone as a potent inhibitor of CDK7/Cyclin H via structure-based virtual screening and In-Vitro validation by ADP-Glo kinase assay
|
Somarowthu, Tejaswi
|
|
|
155 |
C |
p.
|
artikel
|
| 22 |
In situ labeling of pretargeted hyaluronan for PET/MR imaging of CD44+ tumors
|
Hai, Wangxi
|
|
|
155 |
C |
p.
|
artikel
|
| 23 |
In vitro and in vivo Investigations of 4-Substituted 2-Phenylquinazoline derivatives as multipotent ligands for the treatment of Alzheimer’s disease
|
Kumar, Vijay
|
|
|
155 |
C |
p.
|
artikel
|
| 24 |
Issue TOC
|
|
|
|
155 |
C |
p.
|
artikel
|
| 25 |
Modular cascade with engineered HpaB for efficient synthesis of hydroxytyrosol
|
Liu, Wen-Kai
|
|
|
155 |
C |
p.
|
artikel
|
| 26 |
N-glycosylation-modifications-driven conformational dynamics attenuate substrate inhibition of d-lactonohydrolase
|
Sun, Ruobin
|
|
|
155 |
C |
p.
|
artikel
|
| 27 |
Nidustrin A, cysteine-retained emestrin with a unique 18-membered macrocyclic lactone from the endophytic fungus Aspergillus nidulans
|
Fu, Aimin
|
|
|
155 |
C |
p.
|
artikel
|
| 28 |
Peptide nucleic acids: Recent advancements and future opportunities in biomedical applications
|
Sannigrahi, Achinta
|
|
|
155 |
C |
p.
|
artikel
|
| 29 |
pH-sensitive phthalocyanine-loaded polymeric nanoparticles as a novel treatment strategy for breast cancer
|
Malarz, Katarzyna
|
|
|
155 |
C |
p.
|
artikel
|
| 30 |
Preclinical pharmacokinetics, absolute bioavailability and dose proportionality evaluation of bioactive phytochemical Withanone in rats
|
Singh, Sandeep K.
|
|
|
155 |
C |
p.
|
artikel
|
| 31 |
Recent advancements in the quest of benzazoles as anti-Mycobacterium tuberculosis agents
|
Patel, Kshitij I.
|
|
|
155 |
C |
p.
|
artikel
|
| 32 |
Spermidine synthase promotes liver cancer progression in a paracrine manner by altering the macrophage immunometabolic state
|
Yu, Sihang
|
|
|
155 |
C |
p.
|
artikel
|
| 33 |
Surface display and characterization of recombinant α-l-Rhamnosidase from Emiliania huxleyi on Pichia pastoris
|
Xie, Xi
|
|
|
155 |
C |
p.
|
artikel
|
| 34 |
Synthesis and biological evaluation of 4-((3-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-4-yl)oxy)quinoline derivatives as novel potential transforming growth factor-β type 1 receptor inhibitors for hepatocellular carcinoma
|
Liu, Siyuan
|
|
|
155 |
C |
p.
|
artikel
|
| 35 |
Synthesis and exploration of anticancer potential of spirocyclic 1,2,3-triazoline and aziridine derivatives of natural eudesmanolide isoalantolactone
|
Patrushev, Sergey S.
|
|
|
155 |
C |
p.
|
artikel
|
| 36 |
Synthesis and potential anti-inflammatory response of indole and amide derivatives of ursolic acid in LPS-induced RAW 264.7 cells and systemic inflammation mice model: Insights into iNOS, COX2 and NF-κB
|
Choudhary, Rupali
|
|
|
155 |
C |
p.
|
artikel
|
| 37 |
Synthesis, biological evaluation, and in silico studies of phenyl naphthalene-2-sulfonate derived thiosemicarbazones as potential carbonic anhydrase inhibitors
|
Eshal, Javeria
|
|
|
155 |
C |
p.
|
artikel
|
| 38 |
Synthesis of bioisosteres of caffeic acid phenethyl ester: 1,3,4-oxadiazole derivatives containing a catechol fragment with anti-inflammatory activities in vitro and in vivo
|
Sun, Jing
|
|
|
155 |
C |
p.
|
artikel
|
| 39 |
Synthesis of BODIPYs using organoindium reagents and survey of their cytotoxicity and cell uptake on nervous system cells
|
Lama, Ana Da
|
|
|
155 |
C |
p.
|
artikel
|
| 40 |
Synthesis of tetra-substituted thiophene derivatives as potential Hits combating antibiotic resistant bacteria ESKAPE
|
Abd El-Mawgoud, Heba K.
|
|
|
155 |
C |
p.
|
artikel
|
| 41 |
Triphenylphosphine-modified cyclometalated iridiumIII complexes as mitochondria-targeting anticancer agents with enhanced selectivity
|
Fu, Hanxiu
|
|
|
155 |
C |
p.
|
artikel
|
| 42 |
Unveiling the chemistry of antibody conjugation for enhanced PET imaging: Current trends and future directions
|
Saccullo, Erika
|
|
|
155 |
C |
p.
|
artikel
|
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