| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An alkali tolerant α-l-rhamnosidase from Fusarium moniliforme MTCC-2088 used in de-rhamnosylation of natural glycosides
|
Kumar, Dhirendra
|
|
2019
|
84 |
C |
p. 24-31
|
artikel
|
| 2 |
A new class of diamide scaffold: Design, synthesis and biological evaluation as potent antimitotic agents, tubulin polymerization inhibition and apoptosis inducing activity studies
|
Mohamed, Khaled O.
|
|
2019
|
84 |
C |
p. 399-409
|
artikel
|
| 3 |
Antibody recognition by a novel microgel photonic crystal
|
Sai, Na
|
|
2019
|
84 |
C |
p. 389-393
|
artikel
|
| 4 |
Anti-melanogenesis potential of a new series of Morita-Baylis-Hillman adducts in B16F10 melanoma cell line
|
Ketata, Emna
|
|
2019
|
84 |
C |
p. 17-23
|
artikel
|
| 5 |
Antiproliferative 3-deoxysphingomyelin analogs: Design, synthesis, biological evaluation and molecular docking of pyrrolidine-based 3-deoxysphingomyelin analogs as anticancer agents
|
Hassan, Ahmed H.E.
|
|
2019
|
84 |
C |
p. 444-455
|
artikel
|
| 6 |
Antitrypanosomal activity of epi-polygodial from Drimys brasiliensis and its effects in cellular membrane models at the air-water interface
|
Gonçalves, Giulia Elisa Guimarães
|
|
2019
|
84 |
C |
p. 186-191
|
artikel
|
| 7 |
Artemisianins A-D, new stereoisomers of seco-guaianolide involved heterodimeric [4+2] adducts from Artemisia argyi induce apoptosis via enhancement of endoplasmic reticulum stress
|
Xue, Gui-Min
|
|
2019
|
84 |
C |
p. 295-301
|
artikel
|
| 8 |
Bioactive butylphthalide derivatives from Ligusticum chuanxiong
|
Zhang, Xu
|
|
2019
|
84 |
C |
p. 505-510
|
artikel
|
| 9 |
Biological evaluation and structure activity relationship of 9-methyl-1-phenyl-9H-pyrido[3,4-b]indole derivatives as anti-leishmanial agents
|
Ashok, Penta
|
|
2019
|
84 |
C |
p. 98-105
|
artikel
|
| 10 |
Combined molecular modeling and cholinesterase inhibition studies on some natural and semisynthetic O-alkylcoumarin derivatives
|
Orhan, Ilkay Erdogan
|
|
2019
|
84 |
C |
p. 355-362
|
artikel
|
| 11 |
Design and analysis of EphA2-SAM peptide ligands: A multi-disciplinary screening approach
|
Mercurio, Flavia Anna
|
|
2019
|
84 |
C |
p. 434-443
|
artikel
|
| 12 |
Design, synthesis and biological evaluation of novel indole derivatives as potential HDAC/BRD4 dual inhibitors and anti-leukemia agents
|
Cheng, Gaoliang
|
|
2019
|
84 |
C |
p. 410-417
|
artikel
|
| 13 |
Design, synthesis and biological evaluation of novel β-pinene-based thiazole derivatives as potential anticancer agents via mitochondrial-mediated apoptosis pathway
|
Wang, Yunyun
|
|
2019
|
84 |
C |
p. 468-477
|
artikel
|
| 14 |
Design, synthesis and cytotoxicity of chimeric erlotinib-alkylphospholipid hybrids
|
Alam, Md. Maqusood
|
|
2019
|
84 |
C |
p. 51-62
|
artikel
|
| 15 |
Design, synthesis and structure-activity relationship optimization of phenanthridine derivatives as new Wnt/β-catenin signalling pathway agonists
|
Chen, Duo-zhi
|
|
2019
|
84 |
C |
p. 285-294
|
artikel
|
| 16 |
Design, synthesis, DNA assessment and molecular docking study of novel 2-(pyridin-2-ylimino)thiazolidin-4-one derivatives as potent antifungal agents
|
Metwally, Nadia Hanafy
|
|
2019
|
84 |
C |
p. 456-467
|
artikel
|
| 17 |
1,4-Dihydroquinazolin-3(2H)-yl benzamide derivatives as anti-inflammatory and analgesic agents with an improved gastric profile: Design, synthesis, COX-1/2 inhibitory activity and molecular docking study
|
Sakr, Asmaa
|
|
2019
|
84 |
C |
p. 76-86
|
artikel
|
| 18 |
Discovery of a novel cathepsin inhibitor with dual autophagy-inducing and metastasis-inhibiting effects on breast cancer cells
|
Yuan, Lei
|
|
2019
|
84 |
C |
p. 239-253
|
artikel
|
| 19 |
3D-QSAR assisted identification of FABP4 inhibitors: An effective scaffold hopping analysis/QSAR evaluation
|
Floresta, Giuseppe
|
|
2019
|
84 |
C |
p. 276-284
|
artikel
|
| 20 |
Ebsulfur as a potent scaffold for inhibition and labelling of New Delhi metallo-β-lactamase-1 in vitro and in vivo
|
Su, Jianpeng
|
|
2019
|
84 |
C |
p. 192-201
|
artikel
|
| 21 |
Editorial Board
|
|
|
2019
|
84 |
C |
p. i
|
artikel
|
| 22 |
Encapsulation of ciprofloxacin within modified xanthan gum- chitosan based hydrogel for drug delivery
|
Hanna, Demiana H.
|
|
2019
|
84 |
C |
p. 115-124
|
artikel
|
| 23 |
Evaluation of blood-brain barrier penetration and examination of binding to human serum albumin of 7-O-arylpiperazinylcoumarins as potential antipsychotic agents
|
Żołek, Teresa
|
|
2019
|
84 |
C |
p. 211-225
|
artikel
|
| 24 |
Heterocyclic cellular lipid peroxidation inhibitors inspired by the marine antioxidant barettin
|
Labrière, Christophe
|
|
2019
|
84 |
C |
p. 106-114
|
artikel
|
| 25 |
Hydrolases-mediated transformation of oleuropein into demethyloleuropein
|
Cariati, Luca
|
|
2019
|
84 |
C |
p. 384-388
|
artikel
|
| 26 |
1-(2-Hydroxy-5-((trimethylsilyl)ethynyl)phenyl)ethanone based α,β-unsaturated derivatives an alternate to non-sulfonamide carbonic anhydrase II inhibitors, synthesis via Sonogashira coupling, binding analysis, Lipinsk’s rule validation
|
Mahar, Jamaluddin
|
|
2019
|
84 |
C |
p. 170-176
|
artikel
|
| 27 |
Identification of osimertinib (AZD9291) as a lysine specific demethylase 1 inhibitor
|
Li, Zhong-Rui
|
|
2019
|
84 |
C |
p. 164-169
|
artikel
|
| 28 |
Immobilized Baliospermum montanum hydroxynitrile lyase catalyzed synthesis of chiral cyanohydrins
|
Jangir, Nisha
|
|
2019
|
84 |
C |
p. 32-40
|
artikel
|
| 29 |
Issue TOC
|
|
|
2019
|
84 |
C |
p. ii-xvi
|
artikel
|
| 30 |
Multi-target inhibitors against Alzheimer disease derived from 3-hydrazinyl 1,2,4-triazine scaffold containing pendant phenoxy methyl-1,2,3-triazole: Design, synthesis and biological evaluation
|
Yazdani, Mahnaz
|
|
2019
|
84 |
C |
p. 363-371
|
artikel
|
| 31 |
N-Alkyl-1,5-dideoxy-1,5-imino-l-fucitols as fucosidase inhibitors: Synthesis, molecular modelling and activity against cancer cell lines
|
Zhou, Jian
|
|
2019
|
84 |
C |
p. 418-433
|
artikel
|
| 32 |
New tirucallane triterpenoids from Picrasma quassioides with their potential antiproliferative activities on hepatoma cells
|
Zhao, Wen-Yu
|
|
2019
|
84 |
C |
p. 309-318
|
artikel
|
| 33 |
Nitric oxide inhibitory limonoids as potential anti-neuroinflammatory agents from Swietenia mahagoni
|
Shi, Zhaoyu
|
|
2019
|
84 |
C |
p. 177-185
|
artikel
|
| 34 |
Novel salicylamide derivatives as potent multifunctional agents for the treatment of Alzheimer's disease: Design, synthesis and biological evaluation
|
Song, Qing
|
|
2019
|
84 |
C |
p. 137-149
|
artikel
|
| 35 |
One-pot four-component synthesis of thiazolidin-2-imines using CuI/ZnII dual catalysis: A new class of acetylcholinesterase inhibitors
|
Shehzadi, Syeda Aaliya
|
|
2019
|
84 |
C |
p. 518-528
|
artikel
|
| 36 |
1,3,4-oxadiazole/chalcone hybrids: Design, synthesis, and inhibition of leukemia cell growth and EGFR, Src, IL-6 and STAT3 activities
|
Fathi, Marwa Ali A.
|
|
2019
|
84 |
C |
p. 150-163
|
artikel
|
| 37 |
Phenylpropanoids and lignans from Prunus tomentosa seeds as efficient β-amyloid (Aβ) aggregation inhibitors
|
Liu, Qingbo
|
|
2019
|
84 |
C |
p. 269-275
|
artikel
|
| 38 |
Repurposing approach identifies new treatment options for invasive fungal disease
|
Capoci, Isis Regina Grenier
|
|
2019
|
84 |
C |
p. 87-97
|
artikel
|
| 39 |
Structure-activity relationship of pyrazolo pyrimidine derivatives as inhibitors of mitotic kinesin Eg5 and anticancer agents
|
Muthuraja, P.
|
|
2019
|
84 |
C |
p. 493-504
|
artikel
|
| 40 |
Switching of Trp-214 intrinsic rotamer population in human serum albumin: An insight into the aftermath of embracing therapeutic bioorganic luminophore azapodophyllotoxin into sudlow site I
|
Mukherjee, Soham
|
|
2019
|
84 |
C |
p. 63-75
|
artikel
|
| 41 |
Synthesis, ADME, docking studies and in vivo anti-hyperglycaemic potential estimation of novel Schiff base derivatives from octadec-9-enoic acid
|
Kapoor, Garima
|
|
2019
|
84 |
C |
p. 478-492
|
artikel
|
| 42 |
Synthesis and anti-inflammatory activity of sulfonamides and carboxylates incorporating trimellitimides: Dual cyclooxygenase/carbonic anhydrase inhibitory actions
|
Abdel-Aziz, Alaa A.-M.
|
|
2019
|
84 |
C |
p. 260-268
|
artikel
|
| 43 |
Synthesis and antioxidant activity of new lipophilic dihydropyridines
|
da Costa Cabrera, Diego
|
|
2019
|
84 |
C |
p. 1-16
|
artikel
|
| 44 |
Synthesis and bioactivities of pyrazoline benzensulfonamides as carbonic anhydrase and acetylcholinesterase inhibitors with low cytotoxicity
|
Ozmen Ozgun, Dilan
|
|
2019
|
84 |
C |
p. 511-517
|
artikel
|
| 45 |
Synthesis and biological evaluation of 7-(aminoalkyl)pyrazolo[1,5-a]pyrimidine derivatives as cathepsin K inhibitors
|
Petek, Nejc
|
|
2019
|
84 |
C |
p. 226-238
|
artikel
|
| 46 |
Synthesis and biological evaluation of new pyrazolone Schiff bases as monoamine oxidase and cholinesterase inhibitors
|
Tok, Fatih
|
|
2019
|
84 |
C |
p. 41-50
|
artikel
|
| 47 |
Synthesis and computer-aided analysis of the role of linker for novel ligands of the 5-HT6 serotonin receptor among substituted 1,3,5-triazinylpiperazines
|
Łażewska, Dorota
|
|
2019
|
84 |
C |
p. 319-325
|
artikel
|
| 48 |
Synthesis and identification of novel pyridazinylpyrazolone based diazo compounds as inhibitors of human islet amyloid polypeptide aggregation
|
Farrukh, Syed Usama Bin
|
|
2019
|
84 |
C |
p. 339-346
|
artikel
|
| 49 |
Synthesis, molecular docking and cholinesterase inhibitory activity of hydroxylated 2-phenylbenzofuran derivatives
|
Fais, Antonella
|
|
2019
|
84 |
C |
p. 302-308
|
artikel
|
| 50 |
Synthesis, molecular modeling and BACE-1 inhibitory study of tetrahydrobenzo[b] pyran derivatives
|
Bhaskar, Vijaya
|
|
2019
|
84 |
C |
p. 202-210
|
artikel
|
| 51 |
Synthesis of a new disulfide Fmoc monomer for creating biologically susceptible linkages in peptide nucleic acid oligomers
|
Campbell, Brandon
|
|
2019
|
84 |
C |
p. 394-398
|
artikel
|
| 52 |
Synthesis of 8-hydroxyquinoline glycoconjugates and preliminary assay of their β1,4-GalT inhibitory and anti-cancer properties
|
Krawczyk, Monika
|
|
2019
|
84 |
C |
p. 326-338
|
artikel
|
| 53 |
TDP-43 specific reduction induced by Di-hydrophobic tags conjugated peptides
|
Gao, Na
|
|
2019
|
84 |
C |
p. 254-259
|
artikel
|
| 54 |
The first target specific, highly diastereoselective synthesis, design and characterization of pyranoquinolinyl acrylic acid diastereomers as potential α-glucosidase inhibitors
|
Lavanya, G.
|
|
2019
|
84 |
C |
p. 125-136
|
artikel
|
| 55 |
The synthesis and anticancer activities of chiral epoxy-substituted chromone analogs
|
Jo, Hyunji
|
|
2019
|
84 |
C |
p. 347-354
|
artikel
|
| 56 |
Xanthenone-based hydrazones as potent α-glucosidase inhibitors: Synthesis, solid state self-assembly and in silico studies
|
Tariq, Qamar-un-Nisa
|
|
2019
|
84 |
C |
p. 372-383
|
artikel
|
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