nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
8-Alkylmercaptocaffeine derivatives: antioxidant, molecular docking, and in-vitro cytotoxicity studies
|
Sargazi, Saman |
|
|
111 |
C |
p. |
artikel |
2 |
Antiproliferative and cytotoxic activities of C-Geranylated flavonoids from Paulownia tomentosa Steud. Fruit
|
Molčanová, Lenka |
|
|
111 |
C |
p. |
artikel |
3 |
Biomimetic synthesis and anti-inflammatory evaluation of violacin A analogues
|
Wu, Wenxi |
|
|
111 |
C |
p. |
artikel |
4 |
Blended polar/nonpolar peptide conjugate interferes with human insulin amyloid-mediated cytotoxicity
|
Sen, Shantanu |
|
|
111 |
C |
p. |
artikel |
5 |
Butyrolactone and sesquiterpene derivatives as inhibitors of iNOS from the roots of Lindera glauca
|
Ruan, Qing-Feng |
|
|
111 |
C |
p. |
artikel |
6 |
Chemical space exploration of novel naphthyl-carboxamide-diarylpyrimidine derivatives with potent anti-HIV-1 activity
|
Sang, Yali |
|
|
111 |
C |
p. |
artikel |
7 |
Controlling the selectivity of aminergic GPCR ligands from the extracellular vestibule
|
Egyed, Attila |
|
|
111 |
C |
p. |
artikel |
8 |
Design and linkage optimization of ursane-thalidomide-based PROTACs and identification of their targeted-degradation properties to MDM2 protein
|
Qi, Zhiwen |
|
|
111 |
C |
p. |
artikel |
9 |
Design and synthesis of β-carboline and combretastatin derivatives as anti-neutrophilic inflammatory agents
|
Kumar, Sunil |
|
|
111 |
C |
p. |
artikel |
10 |
Design of molecular hybrids of phthalimide-triazole agents with potent selective MCF-7/HepG2 cytotoxicity: Synthesis, EGFR inhibitory effect, and metabolic stability
|
Ihmaid, Saleh K. |
|
|
111 |
C |
p. |
artikel |
11 |
Design, synthesis and antitumor activity evaluation of Chrysamide B derivatives
|
Zhu, Longqing |
|
|
111 |
C |
p. |
artikel |
12 |
Design, synthesis, and biological activity evaluation of a series of novel sulfonamide derivatives as BRD4 inhibitors against acute myeloid leukemia
|
Feng, Ziying |
|
|
111 |
C |
p. |
artikel |
13 |
Design, synthesis and biological evaluation of anilide (dicarboxylic acid) shikonin esters as antitumor agents through targeting PI3K/Akt/mTOR signaling pathway
|
Ma, Yingying |
|
|
111 |
C |
p. |
artikel |
14 |
Design, synthesis, and biological evaluation of new pyrimidine-5-carbonitrile derivatives bearing 1,3-thiazole moiety as novel anti-inflammatory EGFR inhibitors with cardiac safety profile
|
Abdel-Aziz, Salah A. |
|
|
111 |
C |
p. |
artikel |
15 |
Design, synthesis and biological evaluation of novel bischalcone derivatives as potential anticancer agents
|
Burmaoglu, Serdar |
|
|
111 |
C |
p. |
artikel |
16 |
Design, synthesis and biological evaluation of selective histone deacetylase 6 (HDAC6) inhibitors bearing benzoindazole or pyrazoloindazole scaffold as surface recognition motif
|
Xu, Qihao |
|
|
111 |
C |
p. |
artikel |
17 |
Design, synthesis and evaluation of cholinesterase hybrid inhibitors using a natural steroidal alkaloid as precursor
|
Borioni, José L. |
|
|
111 |
C |
p. |
artikel |
18 |
Design, synthesis, and evaluation of N-benzylpyrrolidine and 1,3,4-oxadiazole as multitargeted hybrids for the treatment of Alzheimer’s disease
|
Choubey, Priyanka Kumari |
|
|
111 |
C |
p. |
artikel |
19 |
Design, synthesis, and in vitro evaluation of 4-aminoalkyl-1(2H)-phthalazinones as potential multifunctional anti-Alzheimer’s disease agents
|
Ye, Chanyuan |
|
|
111 |
C |
p. |
artikel |
20 |
Design, synthesis and in vivo anticancer activity of novel parthenolide and micheliolide derivatives as NF-κB and STAT3 inhibitors
|
Zeng, Binglin |
|
|
111 |
C |
p. |
artikel |
21 |
Design, synthesis and mechanistic study of new 1,2,4-triazole derivatives as antimicrobial agents
|
Amin, Noha H. |
|
|
111 |
C |
p. |
artikel |
22 |
Design, synthesis and molecular docking of new pyrazole-thiazolidinones as potent anti-inflammatory and analgesic agents with TNF-α inhibitory activity
|
Abd El-Karim, Somaia S. |
|
|
111 |
C |
p. |
artikel |
23 |
Design, synthesis, biological evaluation, and computational studies of novel thiazolo-pyrazole hybrids as promising selective COX-2 inhibitors: Implementation of apoptotic genes expression for ulcerogenic liability assessment
|
Marzouk, Adel A. |
|
|
111 |
C |
p. |
artikel |
24 |
Design, synthesis, modelling studies and biological evaluation of 1,3,4-oxadiazole derivatives as potent anticancer agents targeting thymidine phosphorylase enzyme
|
Bajaj, Shalini |
|
|
111 |
C |
p. |
artikel |
25 |
Discovery of nor-bicyclic polyprenylated acylphloroglucinols possessing diverse architectures with anti-hepatoma activities from Hypericum patulum
|
Duan, Yulin |
|
|
111 |
C |
p. |
artikel |
26 |
Discovery of novel celastrol-triazole derivatives with Hsp90-Cdc37 disruption to induce tumor cell apoptosis
|
Li, Na |
|
|
111 |
C |
p. |
artikel |
27 |
Discovery of novel dihydroartemisinin-cinnamic hybrids inducing lung cancer cells apoptosis via inhibition of Akt/Bad signal pathway
|
Hu, Yanping |
|
|
111 |
C |
p. |
artikel |
28 |
Discovery of pyridine- sulfonamide hybrids as a new scaffold for the development of potential VEGFR-2 inhibitors and apoptosis inducers
|
Ahmed, Marwa F. |
|
|
111 |
C |
p. |
artikel |
29 |
Diversity-oriented synthesis of cembranoid derivatives as potential anti-inflammatory agents
|
Zhang, Cong |
|
|
111 |
C |
p. |
artikel |
30 |
Dysiscalarones A-E, scalarane sesterterpenoids with nitric oxide production inhibitory activity from marine sponge Dysidea granulosa
|
Sun, Jia-Bao |
|
|
111 |
C |
p. |
artikel |
31 |
Editorial Board
|
|
|
|
111 |
C |
p. |
artikel |
32 |
Exploring the quorum sensing inhibition of isolated chrysin from Penicillium chrysogenum DXY-1
|
Chang, Aiping |
|
|
111 |
C |
p. |
artikel |
33 |
Ginsenoside derivatives inhibit advanced glycation end-product formation and glucose–fructose mediated protein glycation in vitro via a specific structure–activity relationship
|
Yousof Ali, Md |
|
|
111 |
C |
p. |
artikel |
34 |
α-Glucosidase inhibitory and anti-inflammatory activities of dammarane triterpenoids from the leaves of Cyclocarya paliurus
|
Li, Chenguo |
|
|
111 |
C |
p. |
artikel |
35 |
α-Glucosidase inhibitory triterpenoids from Euonymus fortunei
|
Zhao, Ke |
|
|
111 |
C |
p. |
artikel |
36 |
Granatripodins A–B, limonoids featuring a Tricyclo[3.3.1.02,8]nonane motif: Absolute configuration and agonistic effects on human pregnane–X–receptor
|
Shen, Li |
|
|
111 |
C |
p. |
artikel |
37 |
High-level expression of a novel multifunctional GH3 family β-xylosidase/α-arabinosidase/β-glucosidase from Dictyoglomus turgidum in Escherichia coli
|
Tong, Xinyi |
|
|
111 |
C |
p. |
artikel |
38 |
Inverse Virtual Screening for the rapid re-evaluation of the presumed biological safe profile of natural products. The case of steviol from Stevia rebaudiana glycosides on farnesoid X receptor (FXR)
|
Potenza, Marianna |
|
|
111 |
C |
p. |
artikel |
39 |
In vitro and in vivo degradation of programmed cell death ligand 1 (PD-L1) by a proteolysis targeting chimera (PROTAC)
|
Wang, Yubo |
|
|
111 |
C |
p. |
artikel |
40 |
Issue TOC
|
|
|
|
111 |
C |
p. |
artikel |
41 |
Lithocholic acid-based design of noncalcemic vitamin D receptor agonists
|
Gaikwad, Sunil |
|
|
111 |
C |
p. |
artikel |
42 |
New benzimidazolequinones as trypanosomicidal agents
|
López-Lira, Claudia |
|
|
111 |
C |
p. |
artikel |
43 |
New dammarane-type glycosides from Gynostemma pentaphyllum and their lipid-lowering activity
|
Weng, Xin |
|
|
111 |
C |
p. |
artikel |
44 |
New quinolone derivatives as neuropeptide S receptor antagonists: Design, synthesis, homology modeling, dynamic simulations and modulation of Gq/Gs signaling pathways
|
Batran, Rasha Z. |
|
|
111 |
C |
p. |
artikel |
45 |
Novel antibody-drug conjugate with UV-controlled cleavage mechanism for cytotoxin release
|
Li, Jiaguo |
|
|
111 |
C |
p. |
artikel |
46 |
Novel 4,5-dihydrospiro[benzo[c]azepine-1,1′-cyclohexan]-3(2H)-one derivatives as PARP-1 inhibitors: Design, synthesis and biological evaluation
|
Li, Shuai |
|
|
111 |
C |
p. |
artikel |
47 |
Novel inhibitors of the main protease enzyme of SARS-CoV-2 identified via molecular dynamics simulation-guided in vitro assay
|
Loschwitz, Jennifer |
|
|
111 |
C |
p. |
artikel |
48 |
Novel 1,2,4-oxadiazole-chalcone/oxime hybrids as potential antibacterial DNA gyrase inhibitors: Design, synthesis, ADMET prediction and molecular docking study
|
Ibrahim, Tarek S. |
|
|
111 |
C |
p. |
artikel |
49 |
Novel 1,2,3-triazole-tethered Pam3CAG conjugates as potential TLR-2 agonistic vaccine adjuvants
|
Mhamane, Tukaram B. |
|
|
111 |
C |
p. |
artikel |
50 |
Oxygenated pentacyclic triterpenoids from the stems and branches of Enkianthus chinensis
|
Wang, Hai-Qiang |
|
|
111 |
C |
p. |
artikel |
51 |
Phenylpropanoid-conjugated pentacyclic triterpenoids from the whole plants of Leptopus lolonum induced cell apoptosis via MAPK and Akt pathways in human hepatocellular carcinoma cells
|
Qi, Shi-Zhou |
|
|
111 |
C |
p. |
artikel |
52 |
Small organic molecules accelerate the expansion of regulatory T cells
|
Afridi, Saifullah |
|
|
111 |
C |
p. |
artikel |
53 |
Structurally diverse diterpenoids with eight carbon skeletons from Rhododendron micranthum and their antinociceptive effects
|
Jin, Pengfei |
|
|
111 |
C |
p. |
artikel |
54 |
Structure and cytotoxicity of trichothecenes produced by the potato-associated fungus Trichothecium crotocinigenum
|
Yang, Hui-Xiang |
|
|
111 |
C |
p. |
artikel |
55 |
Synthesis and evaluation of technetium-99m labelled 1-(2-methoxyphenyl)piperazine derivative for single photon emission computed tomography imaging for targeting 5-HT1A
|
Kumari, Neelam |
|
|
111 |
C |
p. |
artikel |
56 |
Synthesis and structure-activity relationships of hydroxylated and halogenated 2,4-diaryl benzofuro[3,2-b]pyridin-7-ols as selective topoisomerase IIα inhibitors
|
Thapa Magar, Til Bahadur |
|
|
111 |
C |
p. |
artikel |
57 |
Synthesis, antioxidant activity and bioinformatics studies of L-3-hydroxytyrosine templated N-alkyl/aryl substituted urea/thioureas
|
Kollu, Umapriya |
|
|
111 |
C |
p. |
artikel |
58 |
Synthesis, in vitro evaluation, and molecular docking studies of novel hydrazineylideneindolinone linked to phenoxymethyl-1,2,3-triazole derivatives as potential α-glucosidase inhibitors
|
Shareghi-Boroujeni, Diba |
|
|
111 |
C |
p. |
artikel |
59 |
Synthesis, molecular modeling, selective aldose reductase inhibition and hypoglycemic activity of novel meglitinides
|
Salem, Manar G. |
|
|
111 |
C |
p. |
artikel |
60 |
Synthesis of new substituted pyridine derivatives as potent anti-liver cancer agents through apoptosis induction: In vitro, in vivo, and in silico integrated approaches
|
Boraei, Ahmed T.A. |
|
|
111 |
C |
p. |
artikel |
61 |
The discovery of novel sanjuanolide derivatives as chemotherapeutic agents targeting castration-resistant prostate cancer
|
Wang, Guangbao |
|
|
111 |
C |
p. |
artikel |
62 |
Therapeutic effect of cold atmospheric plasma and its combination with radiation as a novel approach on inhibiting cervical cancer cell growth (HeLa cells)
|
Kenari, Ali Jamaati |
|
|
111 |
C |
p. |
artikel |
63 |
The synthesis of furoquinolinedione and isoxazoloquinolinedione derivatives as selective Tyrosyl-DNA phosphodiesterase 2 (TDP2) inhibitors
|
Yang, Hao |
|
|
111 |
C |
p. |
artikel |
64 |
Tuning NO release of organelle-targeted furoxan derivatives and their cytotoxicity against lung cancer cells
|
Sodano, Federica |
|
|
111 |
C |
p. |
artikel |