nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An exhaustive compilation on chemistry of triazolopyrimidine: A journey through decades
|
Singh, Pankaj Kumar |
|
|
88 |
C |
p. |
artikel |
2 |
α-bisabolol β-D-fucopyranoside as a potential modulator of β-amyloid peptide induced neurotoxicity: An in vitro & in silico study
|
Jeyakumar, Mahalingam |
|
|
88 |
C |
p. |
artikel |
3 |
Chemical constituents from Vietnamese mangrove Calophyllum inophyllum and their anti-inflammatory effects
|
Van Thanh, Nguyen |
|
|
88 |
C |
p. |
artikel |
4 |
Chiral β-lactam-based integrin ligands through Lipase-catalysed kinetic resolution and their enantioselective receptor response
|
Martelli, Giulia |
|
|
88 |
C |
p. |
artikel |
5 |
Cisplatin: The first metal based anticancer drug
|
Ghosh, Sumit |
|
|
88 |
C |
p. |
artikel |
6 |
Click chemistry-assisted synthesis of novel aminonaphthoquinone-1,2,3-triazole hybrids and investigation of their cytotoxicity and cancer cell cycle alterations
|
Gholampour, Maryam |
|
|
88 |
C |
p. |
artikel |
7 |
Current development of 5-nitrofuran-2-yl derivatives as antitubercular agents
|
Elsaman, Tilal |
|
|
88 |
C |
p. |
artikel |
8 |
Design and synthesis of the novel oleanolic acid-cinnamic acid ester derivatives and glycyrrhetinic acid-cinnamic acid ester derivatives with cytotoxic properties
|
Wang, Rui |
|
|
88 |
C |
p. |
artikel |
9 |
Design, synthesis and anticancer evaluation of thieno[2,3-d]pyrimidine derivatives as dual EGFR/HER2 inhibitors and apoptosis inducers
|
Elmetwally, Souad A. |
|
|
88 |
C |
p. |
artikel |
10 |
Design, synthesis and molecular docking of 1,4-benzodioxane thiazolidinedione piperazine derivatives as FabH inhibitors
|
Sun, Juan |
|
|
88 |
C |
p. |
artikel |
11 |
Design, synthesis and molecular docking of new N-4-piperazinyl ciprofloxacin-triazole hybrids with potential antimicrobial activity
|
Mohammed, Hamada H.H. |
|
|
88 |
C |
p. |
artikel |
12 |
Design, synthesis and molecular modeling studies on novel moxifloxacin derivatives as potential antibacterial and antituberculosis agents
|
Türe, Aslı |
|
|
88 |
C |
p. |
artikel |
13 |
Design, synthesis and photoinduced DNA cleavage studies of [1,2,4]-triazolo[4,3-a]quinoxalin-4(5H)-ones
|
Sumran, Garima |
|
|
88 |
C |
p. |
artikel |
14 |
Design, synthesis, anticancer evaluation, molecular docking and cell cycle analysis of 3-methyl-4,7-dihydropyrazolo[1,5-a]pyrimidine derivatives as potent histone lysine demethylases (KDM) inhibitors and apoptosis inducers
|
Metwally, Nadia Hanafy |
|
|
88 |
C |
p. |
artikel |
15 |
Dipyridamole inhibits α-amylase/α-glucosidase at sub-micromolar concentrations; in-vitro, in-vivo and theoretical studies
|
Esmaeili, Sajjad |
|
|
88 |
C |
p. |
artikel |
16 |
Discovery and development of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid derivatives as Bcl-2/Mcl-1 inhibitors
|
Liu, Renshuai |
|
|
88 |
C |
p. |
artikel |
17 |
Discovery of Baicalin as NDM-1 inhibitor: Virtual screening, biological evaluation and molecular simulation
|
Shi, Cheng |
|
|
88 |
C |
p. |
artikel |
18 |
Discovery of cycloneolignan enantiomers from Isatis indigotica Fortune with neuroprotective effects against MPP+-induced SH-SY5Y cell injury
|
Xi, Yu-Fei |
|
|
88 |
C |
p. |
artikel |
19 |
Editorial Board
|
|
|
|
88 |
C |
p. |
artikel |
20 |
Evaluation of cytotoxic activity and genotoxicity of structurally well characterized potent cobalt(II) phen–based antitumor drug entities: An in vitro and in vivo approach
|
Khan, Huzaifa Yasir |
|
|
88 |
C |
p. |
artikel |
21 |
Evaluation of thioamides, thiolactams and thioureas as hydrogen sulfide (H2S) donors for lowering blood pressure
|
Zaorska, Ewelina |
|
|
88 |
C |
p. |
artikel |
22 |
Excavating precursors from the traditional Chinese herb Polygala tenuifolia and Gastrodia elata: Synthesis, anticonvulsant activity evaluation of 3,4,5-trimethoxycinnamic acid (TMCA) ester derivatives
|
Zhao, Zefeng |
|
|
88 |
C |
p. |
artikel |
23 |
Exploration of N-alkyl-2-[(4-oxo-3-(4-sulfamoylphenyl)-3,4-dihydroquinazolin-2-yl)thio]acetamide derivatives as anticancer and radiosensitizing agents
|
Soliman, Aiten M. |
|
|
88 |
C |
p. |
artikel |
24 |
Facile one-pot synthesis, antiproliferative evaluation and structure-activity relationships of 3-amino-1H-indoles and 3-amino-1H-7-azaindoles
|
Diao, Peng-Cheng |
|
|
88 |
C |
p. |
artikel |
25 |
Fluoro-benzimidazole derivatives to cure Alzheimer’s disease: In-silico studies, synthesis, structure-activity relationship and in vivo evaluation for β secretase enzyme inhibition
|
Ali, Sayyad |
|
|
88 |
C |
p. |
artikel |
26 |
Glucosamine-6-phosphate synthase inhibiting C3-β-cholesterol tethered spiro heterocyclic conjugates: Synthesis and their insight of DFT and docking study
|
Periyasami, Govindasami |
|
|
88 |
C |
p. |
artikel |
27 |
Highly selective carbamate-based butyrylcholinesterase inhibitors derived from a naturally occurring pyranoisoflavone
|
Wu, Chuanhai |
|
|
88 |
C |
p. |
artikel |
28 |
Hydrazones as novel epigenetic modulators: Correlation between TET 1 protein inhibition activity and their iron(II) binding ability
|
Jakubek, Milan |
|
|
88 |
C |
p. |
artikel |
29 |
Hypoglycemic activity and mechanism of the sulfated rhamnose polysaccharides chromium(III) complex in type 2 diabetic mice
|
Ye, Han |
|
|
88 |
C |
p. |
artikel |
30 |
Identification of anti-inflammatory polyketides from the coral-derived fungus Penicillium sclerotiorin: In vitro approaches and molecular-modeling
|
Liu, Zhaoming |
|
|
88 |
C |
p. |
artikel |
31 |
Identification of 10-dehydrooxyglycyuralin E as a selective human estrogen receptor alpha partial agonist
|
Saito, Nao |
|
|
88 |
C |
p. |
artikel |
32 |
Identification of novel imidazole flavonoids as potent and selective inhibitors of protein tyrosine phosphatase
|
Zhang, Ling |
|
|
88 |
C |
p. |
artikel |
33 |
In-silico design and synthesis of N9-substituted β-Carbolines as PLK-1 inhibitors and their in-vitro/in-vivo tumor suppressing evaluation
|
Jeyapal, Gomathi Priya |
|
|
88 |
C |
p. |
artikel |
34 |
Introducing article numbering to Journal of Bioorganic Chemistry
|
|
|
|
88 |
C |
p. |
artikel |
35 |
Investigation of the interaction between salvianolic acid C and xanthine oxidase: Insights from experimental studies merging with molecular docking methods
|
Tang, Hongjin |
|
|
88 |
C |
p. |
artikel |
36 |
Isolation, identification, and quantification of Pentylcurcumene from Geophila repens: A new class of cholinesterase inhibitor for Alzheimer’s disease
|
Dash, Umesh Chandra |
|
|
88 |
C |
p. |
artikel |
37 |
Issue TOC
|
|
|
|
88 |
C |
p. |
artikel |
38 |
Magmenthanes A-H: Eight new meroterpenoids from the bark of Magnolia officinalis var. Biloba
|
Li, Chuan |
|
|
88 |
C |
p. |
artikel |
39 |
6-Methoxyflavonols from the aerial parts of Tetragonia tetragonoides (Pall.) Kuntze and their anti-inflammatory activity
|
Lee, Yeong-Geun |
|
|
88 |
C |
p. |
artikel |
40 |
Multifunctional nanoparticles from albumin for stimuli-responsive efficient dual drug delivery
|
Nosrati, Hamed |
|
|
88 |
C |
p. |
artikel |
41 |
Naphthalimides in fluorescent imaging of tumor hypoxia – An up-to-date review
|
Kumari, Rashmi |
|
|
88 |
C |
p. |
artikel |
42 |
Natural urease inhibitors from Aloe vera resin and Lycium shawii and their structural-activity relationship and molecular docking study
|
Rehman, Najeeb Ur |
|
|
88 |
C |
p. |
artikel |
43 |
New perspective on the metabolism of AD-1 in vivo: Characterization of a series of dammarane-type derivatives with novel metabolic sites and anticancer mechanisms of active oleanane-type metabolites
|
Ding, Meng |
|
|
88 |
C |
p. |
artikel |
44 |
Nimesulide analogues: From anti-inflammatory to antitumor agents
|
Catarro, Mafalda |
|
|
88 |
C |
p. |
artikel |
45 |
Novel 9-(2-(1-arylethylidene)hydrazinyl)acridine derivatives: Target Topoisomerase 1 and growth inhibition of HeLa cancer cells
|
Haider, Md Rafi |
|
|
88 |
C |
p. |
artikel |
46 |
Novel eugenol bearing oxypropanolamines: Synthesis, characterization, antibacterial, antidiabetic, and anticholinergic potentials
|
Genç Bilgiçli, Hayriye |
|
|
88 |
C |
p. |
artikel |
47 |
Phenanthroimidazole derivatives act as potentinducer of autophagy by activating DNA damage pathway
|
Zhang, Hao |
|
|
88 |
C |
p. |
artikel |
48 |
Phytosynthesis of silver nanoparticles using Mangifera indica flower extract as bioreductant and their broad-spectrum antibacterial activity
|
Ameen, Fuad |
|
|
88 |
C |
p. |
artikel |
49 |
Potent and selective EGFR inhibitors based on 5-aryl-7H-pyrrolopyrimidin-4-amines
|
Reiersølmoen, Ann Christin |
|
|
88 |
C |
p. |
artikel |
50 |
Probing the high potency of pyrazolyl pyrimidinetriones and thioxopyrimidinediones as selective and efficient non-nucleotide inhibitors of recombinant human ectonucleotidases
|
Andleeb, Hina |
|
|
88 |
C |
p. |
artikel |
51 |
Selective cyclooxygenase inhibition and ulcerogenic liability of some newly prepared anti-inflammatory agents having thiazolo[4,5-d]pyrimidine scaffold
|
Bakr, Rania B. |
|
|
88 |
C |
p. |
artikel |
52 |
Structural modifications of 2,3-indolobetulinic acid: Design and synthesis of highly potent α-glucosidase inhibitors
|
Khusnutdinova, Elmira F. |
|
|
88 |
C |
p. |
artikel |
53 |
Substituted 1,3-dioxoisoindoline-4-aminoquinolines coupled via amide linkers: Synthesis, antiplasmodial and cytotoxic evaluation
|
Rani, Anu |
|
|
88 |
C |
p. |
artikel |
54 |
Synthesis and anti-tumor activity of [1,4] dioxino [2,3-f] quinazoline derivatives as dual inhibitors of c-Met and VEGFR-2
|
Wei, Dengshuai |
|
|
88 |
C |
p. |
artikel |
55 |
Synthesis and biological evaluation of flavone-8-acrylamide derivatives as potential multi-target-directed anti Alzheimer agents and investigation of binding mechanism with acetylcholinesterase
|
Shaik, Jeelan Basha |
|
|
88 |
C |
p. |
artikel |
56 |
Synthesis and biological evaluation of 3-functionalized 2-phenyl- and 2-alkylbenzo[b]furans as antiproliferative agents against human melanoma cell line
|
Kwiecień, Halina |
|
|
88 |
C |
p. |
artikel |
57 |
Synthesis and evaluation of Quinoline-3-carbonitrile derivatives as potential antibacterial agents
|
Khan, Salman A. |
|
|
88 |
C |
p. |
artikel |
58 |
Synthesis and evaluation of redox-sensitive gonadotropin-releasing hormone receptor-targeting peptide conjugates
|
Dai, Yuxuan |
|
|
88 |
C |
p. |
artikel |
59 |
Synthesis and identification of quinoline derivatives as topoisomerase I inhibitors with potent antipsoriasis activity in an animal model
|
Zhang, Wen-Jin |
|
|
88 |
C |
p. |
artikel |
60 |
Synthesis and in vitro antitumor activity of novel acylspermidine derivative N-(4-aminobutyl)-N-(3-aminopropyl)-8-hydroxy-dodecanamide (AAHD) against HepG2 cells
|
Al-Malki, Abdulrahman L. |
|
|
88 |
C |
p. |
artikel |
61 |
Synthesis and molecular docking study of some 3,4-dihydrothieno[2,3-d]pyrimidine derivatives as potential antimicrobial agents
|
Shaaban, Omaima G. |
|
|
88 |
C |
p. |
artikel |
62 |
Synthesis and systemic toxicity assessment of quinine-triazole scaffold with antiprotozoal potency
|
Sahu, Adarsh |
|
|
88 |
C |
p. |
artikel |
63 |
Synthesis, antimicrobial, antioxidant, cytotoxic, antiurease and molecular docking studies of N-(3-trifluoromethyl)benzoyl-N′-aryl thiourea derivatives
|
Maalik, Aneela |
|
|
88 |
C |
p. |
artikel |
64 |
Synthesis, antitumor testing and molecular modeling study of some new 6-substituted amido, azo or thioureido-quinazolin-4(3H)-ones
|
Sabry, Mohamed A. |
|
|
88 |
C |
p. |
artikel |
65 |
Synthesis, characterization, anticancer evaluation and mechanisms of cytotoxic activity of novel 3-hydroxy-3-pyrrolin-2-ones bearing thenoyl fragment: DNA, BSA interactions and molecular docking study
|
Joksimović, Nenad |
|
|
88 |
C |
p. |
artikel |
66 |
Synthesis, computational molecular docking analysis and effectiveness on tyrosinase inhibition of kojic acid derivatives
|
Karakaya, Gülşah |
|
|
88 |
C |
p. |
artikel |
67 |
Synthesis of novel Schiff bases and azol-β-lactam derivatives starting from morpholine and thiomorpholine and investigation of their antitubercular, antiurease activity, acethylcolinesterase inhibition effect and antioxidant capacity
|
Cebeci, Yıldız Uygun |
|
|
88 |
C |
p. |
artikel |
68 |
Synthesis of oxazolidinone from enantiomerically enriched allylic alcohols and determination of their molecular docking and biologic activities
|
Atmaca, Ufuk |
|
|
88 |
C |
p. |
artikel |
69 |
Synthesis of some new C2 substituted dihydropyrimidines and their electrophysiological evaluation as L-/T-type calcium channel blockers
|
Teleb, Mohamed |
|
|
88 |
C |
p. |
artikel |
70 |
Synthesis of thymol-based pyrazolines: An effort to perceive novel potent-antimalarials
|
Raghuvanshi, Dushyant Singh |
|
|
88 |
C |
p. |
artikel |
71 |
Targeting hepatocellular carcinoma: Synthesis of new pyrazole-based derivatives, biological evaluation, DNA binding, and molecular modeling studies
|
Omran, Dina M. |
|
|
88 |
C |
p. |
artikel |
72 |
Vieloplains A-G, seven new guaiane-type sesquiterpenoid dimers from Xylopia vielana
|
Xie, Yangguo |
|
|
88 |
C |
p. |
artikel |
73 |
Virtual screening of active compounds from Artemisia argyi and potential targets against gastric ulcer based on Network pharmacology
|
Wang, Yue |
|
|
88 |
C |
p. |
artikel |