| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A decade of tail-approach based design of selective as well as potent tumor associated carbonic anhydrase inhibitors
|
Kumar, Amit
|
|
|
126 |
C |
p.
|
artikel
|
| 2 |
Aromatic Schiff bases confer inhibitory efficacy against New Delhi metallo-β-lactamase-1 (NDM-1)
|
Zhai, Le
|
|
|
126 |
C |
p.
|
artikel
|
| 3 |
Bioactivity Study of Tricyclic and Tetracyclic Genipin Derivatives as Anti-inflammatory Agents
|
Li, Sin-Min
|
|
|
126 |
C |
p.
|
artikel
|
| 4 |
Design, semi-synthesis and bioactivity evaluation of novel podophyllotoxin derivatives as potent anti-tumor agents
|
Sun, Wenxue
|
|
|
126 |
C |
p.
|
artikel
|
| 5 |
Design, synthesis and anticancer activity of novel 2-arylbenzimidazole/2-thiopyrimidines and 2-thioquinazolin-4(3H)-ones conjugates as targeted RAF and VEGFR-2 kinases inhibitors
|
Ali, Islam H.
|
|
|
126 |
C |
p.
|
artikel
|
| 6 |
Design, synthesis and biological evaluation of novel pleuromutilin derivatives possessing 4-aminothiophenol linker as promising antibacterial agents
|
Chai, Fei
|
|
|
126 |
C |
p.
|
artikel
|
| 7 |
Design, synthesis, and biological evaluation of pseudo-bicyclic pyrimidine-based compounds as potential EGFR inhibitors
|
Farag, Ahmed Karam
|
|
|
126 |
C |
p.
|
artikel
|
| 8 |
Design, synthesis and evaluation of RGD peptidomimetic – Gold nanostar conjugates as M21 cell adhesion inhibitors
|
Innocenti, Riccardo
|
|
|
126 |
C |
p.
|
artikel
|
| 9 |
Discovery of novel benzofuro[3,2-b]quinoline derivatives as dual CDK2/Topo I inhibitors
|
Huang, Yaoguang
|
|
|
126 |
C |
p.
|
artikel
|
| 10 |
Discovery of novel tacrine derivatives as potent antiproliferative agents with CDKs inhibitory property
|
Liu, Wenwu
|
|
|
126 |
C |
p.
|
artikel
|
| 11 |
Discovery of pyrrolo[1,2-a]quinoxalin-4(5H)-one derivatives as novel non-covalent Bruton’s tyrosine kinase (BTK) inhibitors
|
Su, Rongrong
|
|
|
126 |
C |
p.
|
artikel
|
| 12 |
Diversity-oriented synthesis of marine polybrominated diphenyl ethers as potential KCNQ potassium channel activators
|
Liu, Lai-Xin
|
|
|
126 |
C |
p.
|
artikel
|
| 13 |
Editorial Board
|
|
|
|
126 |
C |
p.
|
artikel
|
| 14 |
Efficient synthesis of artificial pharmaceutical solid-phase modules for constructing aptamer-drug conjugates
|
Gao, Fei
|
|
|
126 |
C |
p.
|
artikel
|
| 15 |
Evaluating the effects of disubstituted 3-hydroxy-1H-pyrrol-2(5H)-one analog as novel tyrosinase inhibitors
|
Alizadeh, Naiemeh
|
|
|
126 |
C |
p.
|
artikel
|
| 16 |
Gallic acid derivatives as inhibitors of mussel (Mytilus galloprovincialis) larval settlement: Lead optimization, biological evaluation and use in antifouling coatings
|
Rita Neves, Ana
|
|
|
126 |
C |
p.
|
artikel
|
| 17 |
Generation of a poly-functionalized indolizine scaffold and its anticancer activity in pancreatic cancer cells
|
Lee, Yechan
|
|
|
126 |
C |
p.
|
artikel
|
| 18 |
Generation of wild-type rat Glucocerebrosidase homology modeling: Identification of putative interactions site and mechanism for chaperone using combined in-silico and in-vitro studies
|
Tripathi, Pratigya
|
|
|
126 |
C |
p.
|
artikel
|
| 19 |
Gypensapogenin H suppresses tumor growth and cell migration in triple-negative breast cancer by regulating PI3K/AKT/NF-κB/MMP-9 signaling pathway
|
Tan, Hongyan
|
|
|
126 |
C |
p.
|
artikel
|
| 20 |
Highly selective fluorescent probe based on AIE for identifying cysteine/homocysteine
|
Wang, Wei
|
|
|
126 |
C |
p.
|
artikel
|
| 21 |
Identification of selective homeodomain interacting protein kinase 2 inhibitors, a potential treatment for renal fibrosis
|
Hu, Liqing
|
|
|
126 |
C |
p.
|
artikel
|
| 22 |
Incensole derivatives from frankincense: Isolation, enhancement, synthetic modification, and a plausible mechanism of their anti-depression activity
|
Ur Rehman, Najeeb
|
|
|
126 |
C |
p.
|
artikel
|
| 23 |
Insights into the effect of elaborating coumarin-based aryl enaminones with sulfonamide or carboxylic acid functionality on carbonic anhydrase inhibitory potency and selectivity
|
Ibrahim, Hany S.
|
|
|
126 |
C |
p.
|
artikel
|
| 24 |
Insights into the mechanism for the high-alkaline activity of a novel GH43 β-xylosidase from Bacillus clausii with a promising application to produce xylose
|
Wang, Fenghua
|
|
|
126 |
C |
p.
|
artikel
|
| 25 |
Issue TOC
|
|
|
|
126 |
C |
p.
|
artikel
|
| 26 |
N-Acetyl-l-tryptophan inhibits CCl4-induced hepatic fibrogenesis via regulating TGF-β1/SMAD and Hippo/YAP1 signal
|
Ma, Tingting
|
|
|
126 |
C |
p.
|
artikel
|
| 27 |
New glycoconjugation strategies for Ruthenium(II) arene complexes via phosphane ligands and assessment of their antiproliferative activity
|
Iacopini, Dalila
|
|
|
126 |
C |
p.
|
artikel
|
| 28 |
Novel Azine Linked Hybrids of 2-Indolinone and Thiazolodinone Scaffolds as CDK2 Inhibitors with Potential Anticancer Activity: In Silico Design, Synthesis, Biological, Molecular Dynamics and Binding Free Energy Studies
|
Qayed, Wesam S.
|
|
|
126 |
C |
p.
|
artikel
|
| 29 |
Novel indazole derivatives as potent apoptotic antiproliferative agents by multi-targeted mechanism: Synthesis and biological evaluation
|
Obaid Arhema Frejat, Firas
|
|
|
126 |
C |
p.
|
artikel
|
| 30 |
Novel linezolid-based oxazolidinones as potent anticandidiasis and antitubercular agents
|
Faazil, Shaik
|
|
|
126 |
C |
p.
|
artikel
|
| 31 |
Novel N-benzoylimidazolium ionic liquids derived from benzoic and hydroxybenzoic acids as therapeutic alternative against Biofilm-forming bacteria in skin and soft-tissue infections
|
Forero-Doria, Oscar
|
|
|
126 |
C |
p.
|
artikel
|
| 32 |
Photostability investigation of a near-infrared-II heptamethine cyanine dye
|
Chen, Tingyan
|
|
|
126 |
C |
p.
|
artikel
|
| 33 |
Structure-Based design of [(2-Hydroxyethoxy)methyl]-6-(phenylthio)-thymine derivatives as nonnucleoside HIV-1 reverse transcriptase Inhibitors: From HEPTs to Sulfinyl-substituted HEPTs
|
Hao, Qingqing
|
|
|
126 |
C |
p.
|
artikel
|
| 34 |
Synthesis and bioactivity evaluation of novel nuciferine derivatives with antihyperuricemia and nephroprotective effects
|
Zhang, Yu-kai
|
|
|
126 |
C |
p.
|
artikel
|
| 35 |
Synthesis and in vitro/in vivo anticancer evaluation of pentacyclic triterpenoid derivatives linked with l -phenylalanine or l -proline
|
Yin, Yudong
|
|
|
126 |
C |
p.
|
artikel
|
| 36 |
Synthesis, biological evaluation and docking studies of methylene bearing cyanopyrimidine derivatives possessing a hydrazone moiety as potent Lysine specific demethylase-1 (LSD1) inhibitors: A promising anticancer agents
|
Tasneem, Sharba
|
|
|
126 |
C |
p.
|
artikel
|
| 37 |
Synthesis, characterization and antitubercular activities of heterocyclic selenosemicarbazones
|
Malhi, Rinku
|
|
|
126 |
C |
p.
|
artikel
|
| 38 |
Synthesis of 2-chloropurine ribosides with chiral amino acid amides at C6 and their evaluation as A1 adenosine receptor agonists
|
Berzina, Maria Ya.
|
|
|
126 |
C |
p.
|
artikel
|
| 39 |
Targeted modifications of neomycin and paromomycin: Towards resistance-free antibiotics?
|
Obszynski, J.
|
|
|
126 |
C |
p.
|
artikel
|
| 40 |
Triphenylphosphonium conjugation to a TRAP1 inhibitor, 2-amino-6-chloro-7,9-dihydro-8H-purin-8-one increases antiproliferative activity
|
Yang, Sujae
|
|
|
126 |
C |
p.
|
artikel
|
| 41 |
Triphenylphosphonium-linked derivative of allobetulin: preparation, anticancer properties and their mechanism of inhibiting SGC-7901 cells proliferation
|
Wang, Rui
|
|
|
126 |
C |
p.
|
artikel
|
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