| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A diastereoselective three-component reaction for the assembly of succinimide and isatin hybrid molecules with potent anticancer activities
|
Yuan, Haoxuan
|
|
|
27 |
2 |
p. 837-843
|
artikel
|
| 2 |
Amentoflavone derivatives significantly act towards the main protease (3CLPRO/MPRO) of SARS-CoV-2: in silico admet profiling, molecular docking, molecular dynamics simulation, network pharmacology
|
Dey, Dipta
|
|
|
27 |
2 |
p. 857-871
|
artikel
|
| 3 |
Antibacterial and antioxidant assay of novel heteroaryl-substituted methane derivatives synthesized via ceric ammonium nitrate (CAN) catalyzed one-pot green approach
|
Verma, Monika
|
|
|
27 |
2 |
p. 889-900
|
artikel
|
| 4 |
Artificial intelligence and machine-learning approaches in structure and ligand-based discovery of drugs affecting central nervous system
|
Gautam, Vertika
|
|
|
27 |
2 |
p. 959-985
|
artikel
|
| 5 |
Aryl-n-hexanamide linked enaminones of usnic acid as promising antimicrobial agents
|
Bangalore, Pavan Kumar
|
|
|
27 |
2 |
p. 811-836
|
artikel
|
| 6 |
Correction to: Outliers in SAR and QSAR: 4. effects of allosteric protein–ligand interactions on the classical quantitative structure–activity relationships
|
Kim, Ki Hwan
|
|
|
27 |
2 |
p. 987
|
artikel
|
| 7 |
Creation of targeted compound libraries based on 3D shape recognition
|
Kyrylchuk, Andrii
|
|
|
27 |
2 |
p. 939-949
|
artikel
|
| 8 |
Design and synthesis of novel 2,2-dimethylchromene derivatives as potential antifungal agents
|
Li, Yong
|
|
|
27 |
2 |
p. 589-601
|
artikel
|
| 9 |
Design, synthesis and fungicidal evaluation of novel psoralen derivatives containing sulfonohydrazide or acylthiourea moiety
|
Dong, Jingyue
|
|
|
27 |
2 |
p. 571-588
|
artikel
|
| 10 |
Efficient regioselective five-component synthesis of novel thiazolo[3,2-a]pyridine carbohydrazides and oxazolo[3,2-a]pyridine carbohydrazides
|
Rouzban, Hadiseh
|
|
|
27 |
2 |
p. 667-678
|
artikel
|
| 11 |
Evaluation of xanthene-appended quinoline hybrids as potential leads against antimalarial drug targets
|
Jesu Jaya Sudan, R.
|
|
|
27 |
2 |
p. 709-727
|
artikel
|
| 12 |
Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents
|
Jesumoroti, Omobolanle Janet
|
|
|
27 |
2 |
p. 753-765
|
artikel
|
| 13 |
External oxidant-free and transition metal-free synthesis of 5-amino-1,2,4-thiadiazoles as promising antibacterials against ESKAPE pathogen strains
|
Shetnev, Anton
|
|
|
27 |
2 |
p. 651-666
|
artikel
|
| 14 |
High-throughput virtual screening of small-molecule inhibitors targeting immune cell checkpoints to discover new immunotherapeutics for human diseases
|
Singh, Satyendra
|
|
|
27 |
2 |
p. 729-751
|
artikel
|
| 15 |
Interactions between HIV protease inhibitor ritonavir and human DNA repair enzyme ALKBH2: a molecular dynamics simulation study
|
Shaji, Unnikrishnan Paruthiyezhath
|
|
|
27 |
2 |
p. 931-938
|
artikel
|
| 16 |
Microwave-assisted synthesis, spectroscopic characterization, and biological evaluation of fused thieno[2,3-d]pyrimidines as potential anti-cancer agents targeting EGFRWT and EGFRT790M
|
Aboelez, Moustafa O.
|
|
|
27 |
2 |
p. 901-917
|
artikel
|
| 17 |
Mining therapeutic targets from the antibiotic-resistant Campylobacter coli and virtual screening of natural product inhibitors against its riboflavin synthase
|
Jalal, Khurshid
|
|
|
27 |
2 |
p. 793-810
|
artikel
|
| 18 |
Molecular dynamic simulations reveal anti-SARS-CoV-2 activity of mitocurcumin by potentially blocking innate immune evasion proteins NSP3 and NSP16
|
Pal, Debojyoti
|
|
|
27 |
2 |
p. 635-649
|
artikel
|
| 19 |
Monoclonal antibody designed for SARS-nCoV-2 spike protein of receptor binding domain on antigenic targeted epitopes for inhibition to prevent viral entry
|
Abduljaleel, Zainularifeen
|
|
|
27 |
2 |
p. 695-708
|
artikel
|
| 20 |
Natural halloysite nanotubes as an efficient catalyst in strecker reaction: the synthesis of α-amino nitriles under solvent-free conditions
|
Mousavi-Mashhadi, Seyed Ali
|
|
|
27 |
2 |
p. 919-929
|
artikel
|
| 21 |
PTSA-catalyzed selective synthesis and antibacterial evaluation of 1,2-disubstituted benzimidazoles
|
Fu, Jiaxu
|
|
|
27 |
2 |
p. 873-887
|
artikel
|
| 22 |
Repositioning of experimentally validated anti-breast cancer peptides to target FAK-PAX complex to halt the breast cancer progression: a biomolecular simulation approach
|
Khan, Abbas
|
|
|
27 |
2 |
p. 603-618
|
artikel
|
| 23 |
Setomimycin as a potential molecule for COVID‑19 target: in silico approach and in vitro validation
|
Manhas, Ravi S.
|
|
|
27 |
2 |
p. 619-633
|
artikel
|
| 24 |
Syntheses, in vitro, and in silico studies of rhodanine-based schiff bases as potential α-amylase inhibitors and radicals (DPPH and ABTS) scavengers
|
Egu, Samuel Attah
|
|
|
27 |
2 |
p. 767-791
|
artikel
|
| 25 |
Synthesis of dihydrofuran-3-one and 9,10-phenanthrenequinone hybrid molecules and biological evaluation against colon cancer cells as selective Akt kinase inhibitors
|
Huang, Jingjing
|
|
|
27 |
2 |
p. 845-855
|
artikel
|
| 26 |
Synthesis of fused polycyclic β-carboline derivatives using Ugi-4CR followed by cascade cyclization
|
Kumar, Vipin
|
|
|
27 |
2 |
p. 951-957
|
artikel
|
| 27 |
Synthesis, spectral analysis, DFT calculations, biological potential and molecular docking studies of indole appended pyrazolo-triazine
|
Basavarajaiah, S. M.
|
|
|
27 |
2 |
p. 679-693
|
artikel
|
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