nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A colorimetric nano-biosensor for simultaneous detection of prevalent cancers using unamplified cell-free ribonucleic acid biomarkers
|
Mollasalehi, Hamidreza |
|
|
107 |
C |
p. |
artikel |
2 |
Alginate hydrogels: Sustained release system to analyze the effect of traditional excipients on curcumin availability
|
Mor, Nitika |
|
|
107 |
C |
p. |
artikel |
3 |
Alkaloids from Tabernaemontana divaricata combined with fluconazole to overcome fluconazole resistance in Candida albicans
|
Zhang, Yu |
|
|
107 |
C |
p. |
artikel |
4 |
Alkaloids of Zephyranthes citrina (Amaryllidaceae) and their implication to Alzheimer's disease: Isolation, structural elucidation and biological activity
|
Kohelová, Eliška |
|
|
107 |
C |
p. |
artikel |
5 |
Analgesic bisbenzylisoquinoline alkaloids from the rhizoma of Menispermum dauricum DC
|
Wei, Hongli |
|
|
107 |
C |
p. |
artikel |
6 |
A newly identified small molecular compound acts as a protein kinase inhibitor to suppress metastasis of colorectal cancer
|
Qi, Lu |
|
|
107 |
C |
p. |
artikel |
7 |
A NMR study of binding the metabolite of SN38 derivatives to a model nicked DNA decamer mimicking target of Topo I inhibitors
|
Naumczuk, Beata |
|
|
107 |
C |
p. |
artikel |
8 |
A novel carbon-11 radiolabeled maternal embryonic leucine zipper kinase inhibitor for PET imaging of triple-negative breast cancer
|
Tang, Rongmei |
|
|
107 |
C |
p. |
artikel |
9 |
Antibacterial activity of xylose-derived LpxC inhibitors – Synthesis, biological evaluation and molecular docking studies
|
Dreger, Alexander |
|
|
107 |
C |
p. |
artikel |
10 |
Application of cyclohexane-1,3-diones for six-membered oxygen-containing heterocycles synthesis
|
Sharma, Dharminder |
|
|
107 |
C |
p. |
artikel |
11 |
Benzannulated 5,5-spiroketal sesquiterpenes from the roots of Angelica Pubescens
|
Tian, Danmei |
|
|
107 |
C |
p. |
artikel |
12 |
Bioactive sesquiterpene derivatives from mangrove endophytic fungus Phomopsis sp. SYSU-QYP-23: Structures and nitric oxide inhibitory activities
|
Chen, Yan |
|
|
107 |
C |
p. |
artikel |
13 |
Bioactive sesquiterpenoids from the flower buds of Tussilago farfara
|
Song, Xiu-Qing |
|
|
107 |
C |
p. |
artikel |
14 |
Biological evaluation and molecular docking of novel 1,3,4-thiadiazole-resorcinol conjugates as multifunctional cholinesterases inhibitors
|
Skrzypek, Alicja |
|
|
107 |
C |
p. |
artikel |
15 |
Biological evaluation, radiosensitizing activity and structural insights of novel halogenated quinazoline-sulfonamide conjugates as selective human carbonic anhydrases IX/XII inhibitors
|
Ghorab, Mostafa M. |
|
|
107 |
C |
p. |
artikel |
16 |
Biphenylurea/thiourea derivatives tagged with heteroarylsulfonamide motifs as novel VEGFR2 inhibitors; Design, synthesis and anti-angiogenic activity
|
Al-Ansary, Ghada H. |
|
|
107 |
C |
p. |
artikel |
17 |
Broad-spectrum antivirals of protoporphyrins inhibit the entry of highly pathogenic emerging viruses
|
Lu, Shengsheng |
|
|
107 |
C |
p. |
artikel |
18 |
Butyl methyl imidazolium silica sulfate (BMIm)SS: A novel hybrid nano‐catalyst for highly efficient synthesis of new 1,2-diol monoesters of ibuprofen as the novel prodrugs of ibuprofen having potent analgesic property
|
Soltani Rad, Mohammad Navid |
|
|
107 |
C |
p. |
artikel |
19 |
Chuanxiongdiolides R4 and R5, phthalide dimers with a complex polycyclic skeleton from the aerial parts of Ligusticum chuanxiong and their vasodilator activity
|
Tang, Fei |
|
|
107 |
C |
p. |
artikel |
20 |
Combining photo-redox and enzyme catalysis for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives in one pot
|
Yu, Yuan |
|
|
107 |
C |
p. |
artikel |
21 |
Computational and Synthetic approach with Biological Evaluation of Substituted Quinoline derivatives as small molecule L858R/T790M/C797S triple mutant EGFR inhibitors targeting resistance in Non-Small Cell Lung Cancer (NSCLC)
|
Karnik, Kshipra S. |
|
|
107 |
C |
p. |
artikel |
22 |
Cytotoxic polyprenylated phloroglucinol derivatives from Hypericum elodeoides Choisy modulating the transactivation of RXRα
|
Qiu, Da-Ren |
|
|
107 |
C |
p. |
artikel |
23 |
Design and synthesis of methoxyphenyl- and coumarin-based chalcone derivatives as anti-inflammatory agents by inhibition of NO production and down-regulation of NF-κB in LPS-induced RAW264.7 macrophage cells
|
Emam, Soha H. |
|
|
107 |
C |
p. |
artikel |
24 |
Design, molecular docking, in vitro, and in vivo studies of new quinazolin-4(3H)-ones as VEGFR-2 inhibitors with potential activity against hepatocellular carcinoma
|
Eissa, Ibrahim.H. |
|
|
107 |
C |
p. |
artikel |
25 |
Design, synthesis and antitumour evaluation of novel anthraquinone derivatives
|
Lin, Kai-Wei |
|
|
107 |
C |
p. |
artikel |
26 |
Design, synthesis, and biological evaluation of benzo[d]imidazole-2-carboxamides as new anti-TB agents
|
Dhameliya, Tejas M. |
|
|
107 |
C |
p. |
artikel |
27 |
Design, synthesis, and biological evaluation of new series of pyrrol-2(3H)-one and pyridazin-3(2H)-one derivatives as tubulin polymerization inhibitors
|
Abdelbaset, Mahmoud S. |
|
|
107 |
C |
p. |
artikel |
28 |
Design, synthesis and biological evaluation of water soluble and non-aggregated silicon phthalocyanines, naphthalocyanines against A549, SNU-398, SK-MEL128, DU-145, BT-20 and HFC cell lines as potential anticancer agents
|
Keleş, Turgut |
|
|
107 |
C |
p. |
artikel |
29 |
Design, synthesis and in silico insights of new 7,8-disubstituted-1,3-dimethyl-1H-purine-2,6(3H,7H)-dione derivatives with potent anticancer and multi-kinase inhibitory activities
|
Mohamed, Abdalla R. |
|
|
107 |
C |
p. |
artikel |
30 |
Design, synthesis, biological evaluation of 3,5-diaryl-4,5-dihydro-1H-pyrazole carbaldehydes as non-purine xanthine oxidase inhibitors: Tracing the anticancer mechanism via xanthine oxidase inhibition
|
Joshi, Gaurav |
|
|
107 |
C |
p. |
artikel |
31 |
Design, synthesis, spectral characterization and molecular docking studies of novel pyranoquinolinyl dihydropyridine carboxylates as potential antibacterial agents including Vibrio cholerae with minimal cytotoxity towards fibroblast cell line (L-929)
|
Lavanya, G. |
|
|
107 |
C |
p. |
artikel |
32 |
Development of genistein-O-alkylamines derivatives as multifunctional agents for the treatment of Alzheimer’s disease
|
Sang, Zhipei |
|
|
107 |
C |
p. |
artikel |
33 |
Diaryl-substituted thiosemicarbazone: A potent scaffold for the development of New Delhi metallo-β-lactamase-1 inhibitors
|
Li, Jia-Qi |
|
|
107 |
C |
p. |
artikel |
34 |
Discovery of anti-cell migration activity of an anti-HIV heterocyclic compound by identification of its binding protein hnRNP M
|
Kamo, Masahiro |
|
|
107 |
C |
p. |
artikel |
35 |
Discovery of CAPE derivatives as dual EGFR and CSK inhibitors with anticancer activity in a murine model of hepatocellular carcinoma
|
Liu, Xiaoyu |
|
|
107 |
C |
p. |
artikel |
36 |
Discovery of degradable niclosamide derivatives able to specially inhibit small cell lung cancer (SCLC)
|
He, XingGang |
|
|
107 |
C |
p. |
artikel |
37 |
Discovery of novel indole derivatives that inhibit NEDDylation and MAPK pathways against gastric cancer MGC803 cells
|
Fu, Dong-Jun |
|
|
107 |
C |
p. |
artikel |
38 |
Discovery of Thai mangrove tetranortriterpenoids as agonists of human pregnane–X–receptor and inhibitors against human carboxylesterase 2
|
Ren, Yan-Xia |
|
|
107 |
C |
p. |
artikel |
39 |
Diverse diterpenoids and sesquiterpenoids from Siegesbeckia pubescens and their activity against RANKL-induced osteoclastogenesis
|
Sun, Zhejun |
|
|
107 |
C |
p. |
artikel |
40 |
Editorial Board
|
|
|
|
107 |
C |
p. |
artikel |
41 |
Efficient synthesis of cyano-containing multi-substituted indoles catalyzed by lipase
|
Li, Fengxi |
|
|
107 |
C |
p. |
artikel |
42 |
Facile green bio-fabricated silver nanoparticles from Microchaete infer dose-dependent antioxidant and anti-proliferative activity to mediate cellular apoptosis
|
Husain, Shaheen |
|
|
107 |
C |
p. |
artikel |
43 |
Fast and high-efficiency synthesis of 2-substituted benzothiazoles via combining enzyme catalysis and photoredox catalysis in one-pot
|
Yang, Zeng-Jie |
|
|
107 |
C |
p. |
artikel |
44 |
Flavonoids from the peels of Citrus unshiu Markov. and their inhibitory effects on RANKL-induced osteoclastogenesis through the downregulation of c-Fos signaling in vitro
|
Vu, Thi Oanh |
|
|
107 |
C |
p. |
artikel |
45 |
Generation of potent Nrf2 activators via tuning the electrophilicity and steric hindrance of vinyl sulfones for neuroprotection
|
Song, Zi-Long |
|
|
107 |
C |
p. |
artikel |
46 |
Gramine-based structure optimization to enhance anti-gastric cancer activity
|
Zhang, Xin-Hui |
|
|
107 |
C |
p. |
artikel |
47 |
Identification of aplysinopsin as a blood-brain barrier permeable scaffold for anti-cholinesterase and anti-BACE-1 activity
|
Nuthakki, Vijay K. |
|
|
107 |
C |
p. |
artikel |
48 |
Isolation and characterization of neolignan derivatives with hepatoprotective and neuroprotective activities from the fruits of Citrus medica L. var. Sarcodactylis Swingle
|
Ma, Qin-Ge |
|
|
107 |
C |
p. |
artikel |
49 |
Issue TOC
|
|
|
|
107 |
C |
p. |
artikel |
50 |
Modulatory influences of antiviral bioactive compounds on cell viability, mRNA and protein expression of cytochrome P450 3A4 and P-glycoprotein in HepG2 and HEK293 cells
|
Kehinde, Idowu |
|
|
107 |
C |
p. |
artikel |
51 |
Monoterpenoid indole alkaloids from the fruits of Gelsemium elegans and their anti-inflammatory activities
|
Li, Ni-Ping |
|
|
107 |
C |
p. |
artikel |
52 |
Multipodal insulin mimetics built on adamantane or proline scaffolds
|
Hajduch, Jan |
|
|
107 |
C |
p. |
artikel |
53 |
Mycotoxins as inhibitors of protein tyrosine phosphatases from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021
|
Liang, Xiao |
|
|
107 |
C |
p. |
artikel |
54 |
Natural potential neuroinflammatory inhibitors from Stephania epigaea H.S. Lo
|
Xiao, Jiao |
|
|
107 |
C |
p. |
artikel |
55 |
Neuraminidase inhibitory diarylheptanoids from Alpinia officinarum: In vitro and molecular docking studies
|
Yoo, Guijae |
|
|
107 |
C |
p. |
artikel |
56 |
New alkaloids from the diversity-enhanced extracts of an endophytic fungus Aspergillus flavus GZWMJZ-288
|
He, Wenwen |
|
|
107 |
C |
p. |
artikel |
57 |
New 5-carba-pterocarpans: Synthesis and preliminary antiproliferative activity on a panel of human cancer cells
|
Gaspar, Francisco V. |
|
|
107 |
C |
p. |
artikel |
58 |
New lipophilic glycomimetic DC-SIGN ligands: Stereoselective synthesis and SPR-based binding inhibition assays
|
Di Pietro, Sebastiano |
|
|
107 |
C |
p. |
artikel |
59 |
New phenylpropanoid-conjugated pentacyclic triterpenoids from the whole plants of Leptopus lolonum with their antiproliferative activities on cancer cells
|
Qi, Shi-Zhou |
|
|
107 |
C |
p. |
artikel |
60 |
Nine prenylated acylphloroglucinols with potential anti-depressive and hepatoprotective activities from Hypericum scabrum
|
Ma, Jie |
|
|
107 |
C |
p. |
artikel |
61 |
Novel Mannich bases of ciprofloxacin with improved physicochemical properties, antibacterial, anticancer activities and caspase-3 mediated apoptosis
|
Abdel-Rahman, Islam M. |
|
|
107 |
C |
p. |
artikel |
62 |
Novel Schiff base-bridged multi-component sulfonamide imidazole hybrids as potentially highly selective DNA-targeting membrane active repressors against methicillin-resistant Staphylococcus aureus
|
Hu, Yuanyuan |
|
|
107 |
C |
p. |
artikel |
63 |
Oleanolic acid indole derivatives as novel α-glucosidase inhibitors: Synthesis, biological evaluation, and mechanistic analysis
|
Wu, Panpan |
|
|
107 |
C |
p. |
artikel |
64 |
Oxaliplatin derived monofunctional triazole-containing platinum(II) complex counteracts oxaliplatin-induced drug resistance in colorectal cancer
|
Li, Yaru |
|
|
107 |
C |
p. |
artikel |
65 |
Palladium-catalyzed cross-coupling reactions on a bromo-naphthalene scaffold in the search for novel human CC chemokine receptor 8 (CCR8) antagonists
|
Verhaegen, Yenthel |
|
|
107 |
C |
p. |
artikel |
66 |
Pharmacophore hybridization approach to discover novel pyrazoline-based hydantoin analogs with anti-tumor efficacy
|
Upadhyay, Neha |
|
|
107 |
C |
p. |
artikel |
67 |
pH-promoted O-α-glucosylation of flavonoids using an engineered α-glucosidase mutant
|
Li, Chao |
|
|
107 |
C |
p. |
artikel |
68 |
Polymethylated acylphloroglucinols from Rhodomyrtus tomentosa exert acetylcholinesterase inhibitory effects
|
Qin, Xu-Jie |
|
|
107 |
C |
p. |
artikel |
69 |
Prediction of biological activity of compounds containing a 1,3,5-triazinyl sulfonamide scaffold by artificial neural networks using simple molecular descriptors
|
Havránková, Eva |
|
|
107 |
C |
p. |
artikel |
70 |
Probing 4-(diethylamino)-salicylaldehyde-based thiosemicarbazones as multi-target directed ligands against cholinesterases, carbonic anhydrases and α-glycosidase enzymes
|
Hashmi, Sadaf |
|
|
107 |
C |
p. |
artikel |
71 |
Probing phenylcarbamoylazinane-1,2,4-triazole amides derivatives as lipoxygenase inhibitors along with cytotoxic, ADME and molecular docking studies
|
Muzaffar, Saima |
|
|
107 |
C |
p. |
artikel |
72 |
Structurally modified glycyrrhetinic acid derivatives as anti-inflammatory agents
|
Bian, Ming |
|
|
107 |
C |
p. |
artikel |
73 |
Structurally various sorbicillinoids from the deep-sea sediment derived fungus Penicillium sp. SCSIO06871
|
Pang, Xiaoyan |
|
|
107 |
C |
p. |
artikel |
74 |
Structure-activity relationship studies of dipeptide-based hepsin inhibitors with Arg bioisosteres
|
Kwon, Hongmok |
|
|
107 |
C |
p. |
artikel |
75 |
4-Substituted-1,2,3-triazolo nucleotide analogues as CD73 inhibitors, their synthesis, in vitro screening, kinetic and in silico studies
|
Ghoteimi, Rayane |
|
|
107 |
C |
p. |
artikel |
76 |
Synthesis and biological evaluation of modified laminin peptide (N2S2-KDP) with enhanced affinity for neuronal growth and targeted molecular imaging (SPECT)
|
Varshney, Raunak |
|
|
107 |
C |
p. |
artikel |
77 |
Synthesis and biological evaluation of new nicotinate derivatives as potential anti-inflammatory agents targeting COX-2 enzyme
|
El-Dash, Yara |
|
|
107 |
C |
p. |
artikel |
78 |
Synthesis and evaluation of novel fluorinated hematoporphyrin ether derivatives for photodynamic therapy
|
Li, Man-Yi |
|
|
107 |
C |
p. |
artikel |
79 |
Synthesis and in vitro study of nitro- and methoxy-2-phenylbenzofurans as human monoamine oxidase inhibitors
|
Delogu, Giovanna L. |
|
|
107 |
C |
p. |
artikel |
80 |
Synthesis and pharmacological characterization of mitochondrial KATP channel openers with enhanced mitochondriotropic effects
|
Testai, Lara |
|
|
107 |
C |
p. |
artikel |
81 |
Synthesis, anti-inflammatory and analgesic evaluation of thiazole/oxazole substituted benzothiazole derivatives
|
Kumar, Gajendra |
|
|
107 |
C |
p. |
artikel |
82 |
Synthesis, crystal structure and Hirshfeld Surface analysis of benzamide derivatives of thiourea as potent inhibitors of α-glucosidase in-vitro
|
Akhter, Sidra |
|
|
107 |
C |
p. |
artikel |
83 |
Synthesis, design, and assessment of novel morpholine-derived Mannich bases as multifunctional agents for the potential enzyme inhibitory properties including docking study
|
Boy, Songül |
|
|
107 |
C |
p. |
artikel |
84 |
Synthesis, inverse docking-assisted identification and in vitro biological characterization of Flavonol-based analogs of fisetin as c-Kit, CDK2 and mTOR inhibitors against melanoma and non-melanoma skin cancers
|
Roy, Tithi |
|
|
107 |
C |
p. |
artikel |
85 |
Synthesis of N-2(5H)-furanonyl sulfonyl hydrazone derivatives and their biological evaluation in vitro and in vivo activity against MCF-7 breast cancer cells
|
Yang, Kai |
|
|
107 |
C |
p. |
artikel |
86 |
Synthesis of novel 1,2,3 triazole derivatives and assessment of their potential cholinesterases, glutathione S-transferase enzymes inhibitory properties: An in vitro and in silico study
|
Çelik, Fatih |
|
|
107 |
C |
p. |
artikel |
87 |
Synthesis, structural characterization, molecular docking study, biological activity of carbon monoxide release molecules as potent antitumor agents
|
Liu, Hua-Peng |
|
|
107 |
C |
p. |
artikel |
88 |
Tacrine – Benzothiazoles: Novel class of potential multitarget anti-Alzheimeŕs drugs dealing with cholinergic, amyloid and mitochondrial systems
|
Nepovimova, Eugenie |
|
|
107 |
C |
p. |
artikel |
89 |
Targeted dendrimers for antagonizing the migration and viability of NALM-6 lymphoblastic leukemia cells
|
Chittasupho, Chuda |
|
|
107 |
C |
p. |
artikel |
90 |
Vincamine, a safe natural alkaloid, represents a novel anticancer agent
|
Al-Rashed, Sarah |
|
|
107 |
C |
p. |
artikel |