| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
[12]aneN3-based lipid with naphthalimide moiety for enhanced gene transfection efficiency
|
Gao, Yong-Guang
|
|
2018
|
79 |
C |
p. 334-340
|
artikel
|
| 2 |
A novel derivatives of thiazol-4(5H)-one and their activity in the inhibition of 11β-hydroxysteroid dehydrogenase type 1
|
Studzińska, Renata
|
|
2018
|
79 |
C |
p. 115-121
|
artikel
|
| 3 |
Catalytic asymmetric synthesis of indole derivatives as novel α-glucosidase inhibitors in vitro
|
Islam, Mohammad Shahidul
|
|
2018
|
79 |
C |
p. 350-354
|
artikel
|
| 4 |
Chalcones and bis-chalcones: As potential α-amylase inhibitors; synthesis, in vitro screening, and molecular modelling studies
|
Tajudeen Bale, Adebayo
|
|
2018
|
79 |
C |
p. 179-189
|
artikel
|
| 5 |
1-[(4′-Chlorophenyl) carbonyl-4-(aryl) thiosemicarbazide derivatives as potent urease inhibitors: Synthesis, in vitro and in silico studies
|
Ali, Basharat
|
|
2018
|
79 |
C |
p. 363-371
|
artikel
|
| 6 |
Design and synthesis of aminocoumarin derivatives as DPP-IV inhibitors and anticancer agents
|
Soni, Rina
|
|
2018
|
79 |
C |
p. 277-284
|
artikel
|
| 7 |
Design and synthesis of some new carboxamide and propanamide derivatives bearing phenylpyridazine as a core ring and the investigation of their inhibitory potential on in-vitro acetylcholinesterase and butyrylcholinesterase
|
Kilic, Burcu
|
|
2018
|
79 |
C |
p. 235-249
|
artikel
|
| 8 |
Design, synthesis, biological evaluation, structure-activity relationship study, and mode of action of 2-phenol-4,6-dichlorophenyl-pyridines
|
Shrestha, Aarajana
|
|
2018
|
79 |
C |
p. 1-18
|
artikel
|
| 9 |
Discovery of antitumor ursolic acid long-chain diamine derivatives as potent inhibitors of NF-κB
|
Jiang, Wei
|
|
2018
|
79 |
C |
p. 265-276
|
artikel
|
| 10 |
Discovery of potent α-glucosidase inhibitor flavonols: Insights into mechanism of action through inhibition kinetics and docking simulations
|
Şöhretoğlu, Didem
|
|
2018
|
79 |
C |
p. 257-264
|
artikel
|
| 11 |
Drechmerin H, a novel 1(2), 2(18)-diseco indole diterpenoid from the fungus Drechmeria sp. as a natural agonist of human pregnane X receptor
|
Zhao, Jian-Chao
|
|
2018
|
79 |
C |
p. 250-256
|
artikel
|
| 12 |
Editorial Board
|
|
|
2018
|
79 |
C |
p. i
|
artikel
|
| 13 |
Fructose furoic acid ester: An effective quorum sensing inhibitor against uropathogenic Escherichia coli
|
Vinothkannan, Ravichandran
|
|
2018
|
79 |
C |
p. 310-318
|
artikel
|
| 14 |
Functional group and stereochemical requirements for substrate binding by ghrelin O-acyltransferase revealed by unnatural amino acid incorporation
|
Cleverdon, Elizabeth R.
|
|
2018
|
79 |
C |
p. 98-106
|
artikel
|
| 15 |
Hit optimization studies of 3-hydroxy-indolin-2-one analogs as potential anti-HIV-1 agents
|
Chander, Subhash
|
|
2018
|
79 |
C |
p. 212-222
|
artikel
|
| 16 |
Identification of novel indole based heterocycles as selective estrogen receptor modulator
|
Singla, Ramit
|
|
2018
|
79 |
C |
p. 72-88
|
artikel
|
| 17 |
Issue TOC
|
|
|
2018
|
79 |
C |
p. ii-xiii
|
artikel
|
| 18 |
Leveraging the cruzain S3 subsite to increase affinity for reversible covalent inhibitors
|
Cianni, Lorenzo
|
|
2018
|
79 |
C |
p. 285-292
|
artikel
|
| 19 |
Molecular dynamics guided development of indole based dual inhibitors of EGFR (T790M) and c-MET
|
Singh, Pankaj Kumar
|
|
2018
|
79 |
C |
p. 163-170
|
artikel
|
| 20 |
Molecular modelling and synthesis of spiroimidazolidine-2,4-diones with dual activities as hypoglycemic agents and selective inhibitors of aldose reductase
|
Salem, Manar G.
|
|
2018
|
79 |
C |
p. 131-144
|
artikel
|
| 21 |
New AChE inhibitors from microbial transformation of trachyloban-19-oic acid by Syncephalastrum racemosum
|
dos Santos, Gabriel Franco
|
|
2018
|
79 |
C |
p. 60-63
|
artikel
|
| 22 |
New fluorescent rosamine chelator showing promising antibacterial activity against Gram-positive bacteria
|
Novais, Ângela
|
|
2018
|
79 |
C |
p. 341-349
|
artikel
|
| 23 |
New α-Glucosidase inhibitors from the resins of Boswellia species with structure–glucosidase activity and molecular docking studies
|
Ur. Rehman, Najeeb
|
|
2018
|
79 |
C |
p. 27-33
|
artikel
|
| 24 |
Novel γ-lactone derivatives from Trigonostemon heterophyllus with their potential antiproliferative activities
|
Liu, Yan-Ping
|
|
2018
|
79 |
C |
p. 107-110
|
artikel
|
| 25 |
Novel 3-phenylcoumarin–lipoic acid conjugates as multi-functional agents for potential treatment of Alzheimer's disease
|
Jalili-Baleh, Leili
|
|
2018
|
79 |
C |
p. 223-234
|
artikel
|
| 26 |
Novel tetrahydrofuran derivatives from Trigonostemon howii with their potential anti-HIV-1 activities
|
Liu, Yan-Ping
|
|
2018
|
79 |
C |
p. 111-114
|
artikel
|
| 27 |
Oxidation at C-16 enhances butyrylcholinesterase inhibition in lupane triterpenoids
|
Castro, María Julia
|
|
2018
|
79 |
C |
p. 301-309
|
artikel
|
| 28 |
Pyran-2-one derivatives from Croton crassifolius as potent apoptosis inducers in HepG2 cells via p53-mediated Ras/Raf/ERK pathway
|
Tian, Jin-Long
|
|
2018
|
79 |
C |
p. 355-362
|
artikel
|
| 29 |
Selenides bearing benzenesulfonamide show potent inhibition activity against carbonic anhydrases from pathogenic bacteria Vibrio cholerae and Burkholderia pseudomallei
|
Angeli, Andrea
|
|
2018
|
79 |
C |
p. 319-322
|
artikel
|
| 30 |
Semicarbazone derivatives as urease inhibitors: Synthesis, biological evaluation, molecular docking studies and in-silico ADME evaluation
|
Qazi, Syeda Uroos
|
|
2018
|
79 |
C |
p. 19-26
|
artikel
|
| 31 |
Sophoflavanones A and B, two novel prenylated flavanones from the roots of Sophora flavescens
|
Zhu, Hui
|
|
2018
|
79 |
C |
p. 122-125
|
artikel
|
| 32 |
Spiropyrrolidine/spiroindolizino[6,7-b]indole heterocyclic hybrids: Stereoselective synthesis, cholinesterase inhibitory activity and their molecular docking study
|
Arumugam, Natarajan
|
|
2018
|
79 |
C |
p. 64-71
|
artikel
|
| 33 |
Steroids from Ganoderma sinense as new natural inhibitors of cancer-associated mutant IDH1
|
Zheng, Mengzhu
|
|
2018
|
79 |
C |
p. 89-97
|
artikel
|
| 34 |
Structure-activity relationships of rationally designed AMACR 1A inhibitors
|
Yevglevskis, Maksims
|
|
2018
|
79 |
C |
p. 145-154
|
artikel
|
| 35 |
Supramolecular nanofiber of pyrene-lactose conjugates and its two-photon fluorescence imaging
|
Sun, Qian
|
|
2018
|
79 |
C |
p. 126-130
|
artikel
|
| 36 |
Synthesis and molecular docking of N,N′-disubstituted thiourea derivatives as novel aromatase inhibitors
|
Pingaew, Ratchanok
|
|
2018
|
79 |
C |
p. 171-178
|
artikel
|
| 37 |
Synthesis, anticancer evaluation, and molecular docking studies of some novel 4,6-disubstituted pyrazolo[3,4-d]pyrimidines as cyclin-dependent kinase 2 (CDK2) inhibitors
|
Cherukupalli, Srinivasulu
|
|
2018
|
79 |
C |
p. 46-59
|
artikel
|
| 38 |
Synthesis, biological evaluation and molecular modeling of 2-amino-2-phenylethanol derivatives as novel β2-adrenoceptor agonists
|
Ge, Xinyue
|
|
2018
|
79 |
C |
p. 155-162
|
artikel
|
| 39 |
Synthesis, molecular docking and xanthine oxidase inhibitory activity of 5-aryl-1H-tetrazoles
|
Fatima, Itrat
|
|
2018
|
79 |
C |
p. 201-211
|
artikel
|
| 40 |
Synthesis of aryl pyrazole via Suzuki coupling reaction, in vitro mushroom tyrosinase enzyme inhibition assay and in silico comparative molecular docking analysis with Kojic acid
|
Channar, Pervaiz Ali
|
|
2018
|
79 |
C |
p. 293-300
|
artikel
|
| 41 |
Synthesis of steroidal imidazolidinthiones as potential apoptotic agents: Investigation by theoretical and experimental studies
|
Dar, Ayaz Mahmood
|
|
2018
|
79 |
C |
p. 190-200
|
artikel
|
| 42 |
Synthesis, SAR elucidations and molecular docking study of newly designed isatin based oxadiazole analogs as potent inhibitors of thymidine phosphorylase
|
Javid, Muhammad Tariq
|
|
2018
|
79 |
C |
p. 323-333
|
artikel
|
| 43 |
Synthetic nicotinic/isonicotinic thiosemicarbazides: In vitro urease inhibitory activities and molecular docking studies
|
Ali, Basharat
|
|
2018
|
79 |
C |
p. 34-45
|
artikel
|
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