| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A drug–biomarker interaction model to predict the key targets of Scutellaria barbata D. Don in adverse-risk acute myeloid leukaemia
|
Wang, Teng
|
|
|
25 |
4 |
p. 2351-2365
|
artikel
|
| 2 |
A facile green synthesis of MgCoFe2O4 nanomaterials with robust catalytic performance in the synthesis of pyrano[2,3-d]pyrimidinedione and their bis-derivatives
|
Atarod, Monireh
|
|
|
25 |
4 |
p. 2183-2200
|
artikel
|
| 3 |
Anticancer activity and evaluation of apoptotic genes expression of 2-azetidinones containing anthraquinone moiety
|
Mohamadzadeh, Masoud
|
|
|
25 |
4 |
p. 2429-2439
|
artikel
|
| 4 |
Antiproliferative activity of cardenolides on cell line A549: structure–activity relationship analysis
|
Meneses-Sagrero, Salvador Enrique
|
|
|
25 |
4 |
p. 2289-2305
|
artikel
|
| 5 |
Antiproliferative and antiinflammatory coxib–combretastatin hybrids suppress cell cycle progression and induce apoptosis of MCF7 breast cancer cells
|
Ngo, Quoc Anh
|
|
|
25 |
4 |
p. 2307-2319
|
artikel
|
| 6 |
A three-component cyclocondensation reaction for the synthesis of new triazolo[1,5-a]pyrimidine scaffolds using 3-aminotriazole, aldehydes and ketene N,S-acetal
|
Karami, Solmaz
|
|
|
25 |
4 |
p. 2053-2062
|
artikel
|
| 7 |
Chemistry and anti-herpes simplex virus type 1 evaluation of 4-substituted-1H-1,2,3-triazole-nitroxyl-linked hybrids
|
Cunha, Anna C.
|
|
|
25 |
4 |
p. 2035-2043
|
artikel
|
| 8 |
Comparative biological study between quinazolinyl–triazinyl semicarbazide and thiosemicarbazide hybrid derivatives
|
Patel, Janki J.
|
|
|
25 |
4 |
p. 2271-2287
|
artikel
|
| 9 |
Construction of hybrid polycyclic quinolinobenzo[a]phenazinone architectures using solid-state melt reaction (SSMR)
|
Bakthadoss, Manickam
|
|
|
25 |
4 |
p. 2447-2458
|
artikel
|
| 10 |
Dehydroabietylamine-based thiazolidin-4-ones and 2-thioxoimidazolidin-4-ones as novel tyrosyl-DNA phosphodiesterase 1 inhibitors
|
Kovaleva, Kseniya
|
|
|
25 |
4 |
p. 2389-2397
|
artikel
|
| 11 |
Design and exploration of 5-nitro-3-trinitromethyl-1H-1,2,4-triazole and its derivatives as energetic materials
|
Zhang, Jian-ying
|
|
|
25 |
4 |
p. 2107-2121
|
artikel
|
| 12 |
Design and in vitro analysis of SIRT2 inhibitor targeting Parkinson’s disease
|
Singh, Amrendra Pratap
|
|
|
25 |
4 |
p. 2261-2270
|
artikel
|
| 13 |
Design and synthesis of novel (Z)-5-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)-3-((1-substituted phenyl-1H-1,2,3-triazol-4-yl)methyl)thiazolidine-2,4-diones: a potential cytotoxic scaffolds and their molecular modeling studies
|
Subhashini, N. J. P.
|
|
|
25 |
4 |
p. 2017-2033
|
artikel
|
| 14 |
Design, antihuman immunodeficiency activity and molecular docking studies of synthesized 2-aryl and 2-pyrimidinyl pyrrolidines
|
Gasparyan, Sahak P.
|
|
|
25 |
4 |
p. 2045-2052
|
artikel
|
| 15 |
Domino ring opening and selective O/S-alkylation of cyclic ethers and thioethers
|
Bakthadoss, Manickam
|
|
|
25 |
4 |
p. 2467-2478
|
artikel
|
| 16 |
Facile synthesis of pyrrolo[2,1-a]isoquinolines by domino reaction of 1-aroyl-3,4-dihydroisoquinolines with conjugated ketones, nitroalkenes and nitriles
|
Astakhov, Grigorii S.
|
|
|
25 |
4 |
p. 2441-2446
|
artikel
|
| 17 |
gem-Difunctionalization of α-diazoarylketones with diaryldiselenides and N-halosuccinimides: facile synthesis of α-halo-α-arylseleno ketones
|
Li, Jiuling
|
|
|
25 |
4 |
p. 2459-2466
|
artikel
|
| 18 |
4H-benzochromene derivatives as novel tyrosinase inhibitors and radical scavengers: synthesis, biological evaluation, and molecular docking analysis
|
Karimian, Somaye
|
|
|
25 |
4 |
p. 2339-2349
|
artikel
|
| 19 |
Head-to-head bisbenzazole derivatives as antiproliferative agents: design, synthesis, in vitro activity, and SAR analysis
|
Ersan, Ronak Haj
|
|
|
25 |
4 |
p. 2247-2259
|
artikel
|
| 20 |
Indole-fused spirochromenes as potential anti-tubercular agents: design, synthesis and in vitro evaluation
|
Dogamanti, Ashok
|
|
|
25 |
4 |
p. 2137-2148
|
artikel
|
| 21 |
Novel 1,2,4-triazole analogues as mushroom tyrosinase inhibitors: synthesis, kinetic mechanism, cytotoxicity and computational studies
|
Vanjare, Balasaheb D.
|
|
|
25 |
4 |
p. 2089-2106
|
artikel
|
| 22 |
Planning new Trypanosoma cruzi CYP51 inhibitors using QSAR studies
|
de Oliveira, Pedro Igor Camara
|
|
|
25 |
4 |
p. 2219-2235
|
artikel
|
| 23 |
Production of benzazepine derivatives via four-component reaction of isatins: study of antioxidant activity
|
Orimi, Fathali Gholami
|
|
|
25 |
4 |
p. 2171-2182
|
artikel
|
| 24 |
Recent strategies in the synthesis of thiophene derivatives: highlights from the 2012–2020 literature
|
Abedinifar, Fahimeh
|
|
|
25 |
4 |
p. 2571-2604
|
artikel
|
| 25 |
Recent synthetic strategies toward the synthesis of spirocyclic compounds comprising six-membered carbocyclic/heterocyclic ring systems
|
Babar, Kashaf
|
|
|
25 |
4 |
p. 2487-2532
|
artikel
|
| 26 |
Revisit to the synthesis of 1,2,3,4-tetrasubstituted pyrrole derivatives in lactic acid media as a green solvent and catalyst
|
Akbaslar, Dilek
|
|
|
25 |
4 |
p. 2321-2338
|
artikel
|
| 27 |
Selection of antileishmanial sesquiterpene lactones from SistematX database using a combined ligand-/structure-based virtual screening approach
|
Herrera-Acevedo, Chonny
|
|
|
25 |
4 |
p. 2411-2427
|
artikel
|
| 28 |
Synthesis and antimicrobial activities of some novel diastereoselective monocyclic cis-β-lactams using 2-ethoxy carbonyl DCPN as a carboxylic acid activator
|
Mishra, Mahesh Kumar
|
|
|
25 |
4 |
p. 2073-2087
|
artikel
|
| 29 |
Synthesis, antimicrobial evaluation, and in silico studies of quinoline—1H-1,2,3-triazole molecular hybrids
|
Awolade, Paul
|
|
|
25 |
4 |
p. 2201-2218
|
artikel
|
| 30 |
Synthesis of 4-alkylaminoimidazo[1,2-a]pyridines linked to carbamate moiety as potent α-glucosidase inhibitors
|
Saeedi, Mina
|
|
|
25 |
4 |
p. 2399-2409
|
artikel
|
| 31 |
Synthesis of mono- and bis-spirooxindole derivatives “on water” using double salt of aluminum sulfate–sulfuric acid as a reusable catalyst
|
Bashkar, Mohammad
|
|
|
25 |
4 |
p. 2001-2015
|
artikel
|
| 32 |
Synthesis of new curcumin-based aminocarbonitrile derivatives incorporating 4H-pyran and 1,4-dihydropyridine heterocycles
|
Khajeh Dangolani, Soheila
|
|
|
25 |
4 |
p. 2123-2135
|
artikel
|
| 33 |
Synthesis of polycyclic N-heterocyclic compounds via one-pot three-component cyclization strategy
|
Alizadeh, Abdolali
|
|
|
25 |
4 |
p. 2063-2072
|
artikel
|
| 34 |
Synthesis of pyrazole-4-carboxamides as potential fungicide candidates
|
Dong, Cuntao
|
|
|
25 |
4 |
p. 2379-2388
|
artikel
|
| 35 |
Synthesis of styryl-linked fused dihydropyridines by catalyst-free multicomponent reactions
|
Yadav, Rahul
|
|
|
25 |
4 |
p. 2161-2169
|
artikel
|
| 36 |
Synthesis of tetracyclic pyrido-fused dibenzodiazepines via a catalyst-free cascade reaction
|
Alizadeh, Abdolali
|
|
|
25 |
4 |
p. 2237-2246
|
artikel
|
| 37 |
Ultrasound-assisted, low-solvent and acid/base-free synthesis of 5-substituted 1,3,4-oxadiazole-2-thiols as potent antimicrobial and antioxidant agents
|
Yarmohammadi, Elahe
|
|
|
25 |
4 |
p. 2367-2378
|
artikel
|
| 38 |
Urease: a highly efficient biocatalyst for synthesis of polyhydroquinolines and polyhydroacridines from the ammonia formed in situ
|
Zhu, Gan
|
|
|
25 |
4 |
p. 2149-2159
|
artikel
|
| 39 |
Vinylazides: versatile synthons and magical precursors for the construction of N-heterocycles
|
Tashrifi, Zahra
|
|
|
25 |
4 |
p. 2533-2570
|
artikel
|
| 40 |
Visible-light-mediated one-pot efficient synthesis of 1-aryl-1H,3H-thiazolo[3,4-a]benzimidazoles: a metal-free photochemical approach in aqueous ethanol
|
Nazeef, Mohd
|
|
|
25 |
4 |
p. 2479-2486
|
artikel
|
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