| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A novel pregnene analogs: synthesis, cytotoxicity on prostate cancer of PC-3 and LNCPa-AI cells and in silico molecular docking study
|
Abdul-Rida, Nabeel A.
|
|
|
25 |
2 |
p. 661-671
|
artikel
|
| 2 |
A system-level approach to investigate alloxan-induced toxicity in microtubule-binding protein to lead type 2 diabetes mellitus
|
Sathish Kumar, Paramashivam
|
|
|
25 |
2 |
p. 911-924
|
artikel
|
| 3 |
Calix[4]API-s: fully functionalized calix[4]arene-based facial active pharmaceutical ingredients
|
Pur, Fazel Nasuhi
|
|
|
25 |
2 |
p. 1247-1258
|
artikel
|
| 4 |
Data science-driven analyses of drugs inducing hypertension as an adverse effect
|
Sharma, Reetu
|
|
|
25 |
2 |
p. 801-810
|
artikel
|
| 5 |
Design and synthesis of 4,5-diphenyl-imidazol-1,2,3-triazole hybrids as new anti-diabetic agents: in vitro α-glucosidase inhibition, kinetic and docking studies
|
Asgari, Mohammad Sadegh
|
|
|
25 |
2 |
p. 877-888
|
artikel
|
| 6 |
Design, synthesis, and anticancer activity of novel 4-thiazolidinone-phenylaminopyrimidine hybrids
|
Türe, Aslı
|
|
|
25 |
2 |
p. 1025-1050
|
artikel
|
| 7 |
Design, synthesis and evaluation of dihydrotriazine derivatives-bearing 5-aryloxypyrazole moieties as antibacterial agents
|
Zhang, Tian-Yi
|
|
|
25 |
2 |
p. 861-876
|
artikel
|
| 8 |
Design, synthesis and evaluation of 3-hydroxypyridin-4-ones as inhibitors of catechol-O-methyltransferase
|
de Beer, Johannie
|
|
|
25 |
2 |
p. 753-762
|
artikel
|
| 9 |
Design, synthesis and evaluation of new chromone-derived aminophosphonates as potential acetylcholinesterase inhibitor
|
Shaikh, Sarfaraz
|
|
|
25 |
2 |
p. 811-825
|
artikel
|
| 10 |
Design, synthesis, crystal structure and in vitro antimicrobial activity of novel 1,2,4-triazolo[1,5-a]pyrimidine-containing quinazolinone derivatives
|
Du, Huan
|
|
|
25 |
2 |
p. 711-722
|
artikel
|
| 11 |
Dipolar cycloaddition strategy for three-component synthesis of chromeno[3′,4′:3,4]pyrido[2,1-a]isoquinoline derivatives
|
Alizadeh, Abdolali
|
|
|
25 |
2 |
p. 701-710
|
artikel
|
| 12 |
Distinguishing drug/non-drug-like small molecules in drug discovery using deep belief network
|
Hooshmand, Seyed Aghil
|
|
|
25 |
2 |
p. 827-838
|
artikel
|
| 13 |
DNA interaction, in vivo and in vitro cytotoxicity, reactive oxygen species, lipid peroxidation of –N, S donor Re(I) metal complexes
|
Varma, Reena R.
|
|
|
25 |
2 |
p. 687-699
|
artikel
|
| 14 |
Drug design by machine-trained elastic networks: predicting Ser/Thr-protein kinase inhibitors’ activities
|
Toussi, Cyrus Ahmadi
|
|
|
25 |
2 |
p. 899-909
|
artikel
|
| 15 |
Hydrazine clubbed 1,3-thiazoles as potent urease inhibitors: design, synthesis and molecular docking studies
|
Channar, Pervaiz Ali
|
|
|
25 |
2 |
p. 1-13
|
artikel
|
| 16 |
Introducing a pyrazolopyrimidine as a multi-tyrosine kinase inhibitor, using multi-QSAR and docking methods
|
Bahmani, Asrin
|
|
|
25 |
2 |
p. 949-965
|
artikel
|
| 17 |
Metal-free visible-light-mediated organophotoredox catalysis: synthesis of 3-functionalized indole via C–C, C–N bond formation
|
Yadav, Neetu
|
|
|
25 |
2 |
p. 1103-1109
|
artikel
|
| 18 |
Modeling and insights into molecular basis of low molecular weight respiratory sensitizers
|
Cui, Xueyan
|
|
|
25 |
2 |
p. 847-859
|
artikel
|
| 19 |
Molecular modeling and LC–MS-based metabolomics of a glutamine-valproic acid (Gln-VPA) derivative on HeLa cells
|
Fragoso-Vázquez, M. J.
|
|
|
25 |
2 |
p. 1077-1089
|
artikel
|
| 20 |
N-Benzylation of 6-aminoflavone by reductive amination and efficient access to some novel anticancer agents via topoisomerase II inhibition
|
Thorat, Nitin M.
|
|
|
25 |
2 |
p. 937-948
|
artikel
|
| 21 |
New nicotinic acid-based 3,5-diphenylpyrazoles: design, synthesis and antihyperlipidemic activity with potential NPC1L1 inhibitory activity
|
Shoman, Mai E.
|
|
|
25 |
2 |
p. 673-686
|
artikel
|
| 22 |
Novel quinolinone–pyrazoline hybrids: synthesis and evaluation of antioxidant and lipoxygenase inhibitory activity
|
Kostopoulou, Ioanna
|
|
|
25 |
2 |
p. 723-740
|
artikel
|
| 23 |
One-pot sequential coupling reactions as a new practical protocol for the synthesis of unsymmetrical 2,3-diethynyl quinoxalines and 4-ethynyl-substituted pyrrolo[1,2-a]quinoxalines
|
Keivanloo, Ali
|
|
|
25 |
2 |
p. 981-993
|
artikel
|
| 24 |
One-pot synthesis of dihydro-8H acenaphtho[1′,2′:4,5]pyrrolo[1,2-a]imidazole-diol derivatives
|
Vala, Masoud Mohammadi
|
|
|
25 |
2 |
p. 925-935
|
artikel
|
| 25 |
Pesticides, cosmetics, drugs: identical and opposite influences of various molecular features as measures of endpoints similarity and dissimilarity
|
Toropov, Andrey A.
|
|
|
25 |
2 |
p. 1137-1144
|
artikel
|
| 26 |
Pharmacophore-based designing of putative ROS-1 targeting agents for NSCLC
|
Pathak, Disha
|
|
|
25 |
2 |
p. 1091-1102
|
artikel
|
| 27 |
Prediction model of human ABCC2/MRP2 efflux pump inhibitors: a QSAR study
|
Le, Minh-Tri
|
|
|
25 |
2 |
p. 741-751
|
artikel
|
| 28 |
Recent development in the synthesis of heterocycles by 2-naphthol-based multicomponent reactions
|
Chaudhary, Ankita
|
|
|
25 |
2 |
p. 1211-1245
|
artikel
|
| 29 |
Solvent-free synthesis of isoindolo[2,1-c]pyrazolo[1,5-a]quinazoline and pyrazolo[5′,1′:2,3]pyrimido[6,1-a]isoindol derivatives through a one-pot three-component reaction
|
Alizadeh-Kouzehrash, Meysam
|
|
|
25 |
2 |
p. 1123-1130
|
artikel
|
| 30 |
Structure–activity relationship study of DEL-22379: ERK dimerization inhibitors with increased safety
|
Yang, Yang
|
|
|
25 |
2 |
p. 1051-1075
|
artikel
|
| 31 |
Synthesis and antitumor evaluation of (aryl)methyl-amine derivatives of dehydroabietic acid-based B ring-fused-thiazole as potential PI3K/AKT/mTOR signaling pathway inhibitors
|
Chen, Nai-Yuan
|
|
|
25 |
2 |
p. 967-979
|
artikel
|
| 32 |
Synthesis and evaluation of antitumor activity of dibenzodiazepine derivatives
|
Cao, Ke
|
|
|
25 |
2 |
p. 1111-1122
|
artikel
|
| 33 |
Synthesis, characterization, antimicrobial, antioxidant and computational evaluation of N-acyl-morpholine-4-carbothioamides
|
Aziz, Hamid
|
|
|
25 |
2 |
p. 763-776
|
artikel
|
| 34 |
Synthesis, computational study and cytotoxicity of 4-hydroxycoumarin-derived imines/enamines
|
Vaseghi, Samaneh
|
|
|
25 |
2 |
p. 1011-1024
|
artikel
|
| 35 |
Synthesis, β-glucuronidase inhibition and molecular docking studies of cyano-substituted bisindole hydrazone hybrids
|
Abid, Obaidurahman
|
|
|
25 |
2 |
p. 995-1009
|
artikel
|
| 36 |
Synthesis of the quinazolinone derivatives using an acid-functionalized magnetic silica heterogeneous catalyst in terms of green chemistry
|
Ahmadizadeh Shendy, Saeid
|
|
|
25 |
2 |
p. 889-897
|
artikel
|
| 37 |
Synthesis of thia- and thioxo-tetraazaspiro[4.4]nonenones from nitrile imines and arylidenethiohydantoins
|
Yavari, Issa
|
|
|
25 |
2 |
p. 777-785
|
artikel
|
| 38 |
Synthesis of triazolotriazine derivatives as c-Met inhibitors
|
Guo, Yuting
|
|
|
25 |
2 |
p. 839-846
|
artikel
|
| 39 |
The status of isocyanide-based multi-component reactions in Iran (2010–2018)
|
Shaabani, Ahmad
|
|
|
25 |
2 |
p. 1145-1210
|
artikel
|
| 40 |
Transition metal-free NaOH-catalyzed hydration of nitriles to primary amides in NH3·H2O–DMSO mixture
|
Wang, Nan
|
|
|
25 |
2 |
p. 1131-1136
|
artikel
|
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