nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An efficient one-pot synthesis of thiochromeno[3,4-d]pyrimidines derivatives: Inducing ROS dependent antibacterial and anti-biofilm activities
|
Suresh, Lingala |
|
2016 |
68 |
C |
p. 159-165 7 p. |
artikel |
2 |
Anticancer and structure-activity relationship evaluation of 3-(naphthalen-2-yl)-N,5-diphenyl-pyrazoline-1-carbothioamide analogs of chalcone
|
Lee, Youngshim |
|
2016 |
68 |
C |
p. 166-176 11 p. |
artikel |
3 |
A simple and efficient synthesis of novel inhibitors of alpha-glucosidase based on benzimidazole skeleton and molecular docking studies
|
Özil, Musa |
|
2016 |
68 |
C |
p. 226-235 10 p. |
artikel |
4 |
Candida parapsilosis: A versatile biocatalyst for organic oxidation-reduction reactions
|
Chadha, Anju |
|
2016 |
68 |
C |
p. 187-213 27 p. |
artikel |
5 |
Coumarin-thiazole and -oxadiazole derivatives: Synthesis, bioactivity and docking studies for aldose/aldehyde reductase inhibitors
|
Ibrar, Aliya |
|
2016 |
68 |
C |
p. 177-186 10 p. |
artikel |
6 |
Design, synthesis and biological evaluation of coumarin derivatives as novel acetylcholinesterase inhibitors that attenuate H2O2-induced apoptosis in SH-SY5Y cells
|
Yao, Dahong |
|
2016 |
68 |
C |
p. 112-123 12 p. |
artikel |
7 |
Design, synthesis and biological evaluation of dihydroquinoxalinone derivatives as BRD4 inhibitors
|
Yang, Yifei |
|
2016 |
68 |
C |
p. 236-244 9 p. |
artikel |
8 |
Editorial Board
|
|
|
2016 |
68 |
C |
p. i- 1 p. |
artikel |
9 |
Efficient synthesis and antioxidant activities of N-heterocyclyl substituted Coenzyme Q analogues
|
Wang, Jin |
|
2016 |
68 |
C |
p. 214-218 5 p. |
artikel |
10 |
Experimental, computational and chemometrics studies of BSA-vitamin B6 interaction by UV–Vis, FT-IR, fluorescence spectroscopy, molecular dynamics simulation and hard-soft modeling methods
|
Manouchehri, Firouzeh |
|
2016 |
68 |
C |
p. 124-136 13 p. |
artikel |
11 |
In silico binding analysis and SAR elucidations of newly designed benzopyrazine analogs as potent inhibitors of thymidine phosphorylase
|
Taha, Muhammad |
|
2016 |
68 |
C |
p. 80-89 10 p. |
artikel |
12 |
Issue TOC
|
|
|
2016 |
68 |
C |
p. ii-viii nvt p. |
artikel |
13 |
Rational derivation of CETP self-binding helical peptides by π-π stacking and halogen bonding: Therapeutic implication for atherosclerosis
|
Zhu, Jian |
|
2016 |
68 |
C |
p. 259-264 6 p. |
artikel |
14 |
Separation of enzymatic functions and variation of spin state of rice allene oxide synthase-1 by mutation of Phe-92 and Pro-430
|
Yoeun, Sereyvath |
|
2016 |
68 |
C |
p. 9-14 6 p. |
artikel |
15 |
Sulfotyrosine dipeptide: Synthesis and evaluation as HIV-entry inhibitor
|
Ju, Tong |
|
2016 |
68 |
C |
p. 105-111 7 p. |
artikel |
16 |
Synthesis and in vitro acetylcholinesterase and butyrylcholinesterase inhibitory potential of hydrazide based Schiff bases
|
Rahim, Fazal |
|
2016 |
68 |
C |
p. 30-40 11 p. |
artikel |
17 |
Synthesis and in vitro evaluation of novel rhodanine derivatives as potential cholinesterase inhibitors
|
Krátký, Martin |
|
2016 |
68 |
C |
p. 23-29 7 p. |
artikel |
18 |
Synthesis and proapoptotic activity of oleanolic acid derived amides
|
Heller, Lucie |
|
2016 |
68 |
C |
p. 137-151 15 p. |
artikel |
19 |
Synthesis and SAR studies of potent H+/K+-ATPase inhibitors of quinazolinone-Schiff’s base analogues
|
Rakesh, K.P. |
|
2016 |
68 |
C |
p. 1-8 8 p. |
artikel |
20 |
Synthesis, characterization and in silico designing of diethyl-3-methyl-5-(6-methyl-2-thioxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carboxamido) thiophene-2,4-dicarboxylate derivative as anti-proliferative and anti-microbial agents
|
Malani, Kalpesh |
|
2016 |
68 |
C |
p. 265-274 10 p. |
artikel |
21 |
Synthesis, β-glucuronidase inhibition and molecular docking studies of hybrid bisindole-thiosemicarbazides analogs
|
Taha, Muhammad |
|
2016 |
68 |
C |
p. 56-63 8 p. |
artikel |
22 |
Synthesis, in vitro α-glucosidase inhibitory activity and molecular docking studies of new thiazole derivatives
|
Khan, Khalid Mohammed |
|
2016 |
68 |
C |
p. 245-258 14 p. |
artikel |
23 |
Synthesis of novel bisindolylmethanes: New carbonic anhydrase II inhibitors, docking, and 3D pharmacophore studies
|
Imran, Syahrul |
|
2016 |
68 |
C |
p. 90-104 15 p. |
artikel |
24 |
Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor
|
Taha, Muhammad |
|
2016 |
68 |
C |
p. 15-22 8 p. |
artikel |
25 |
Synthesis of pyrimidine-2,4,6-trione derivatives: Anti-oxidant, anti-cancer, α-glucosidase, β-glucuronidase inhibition and their molecular docking studies
|
Barakat, Assem |
|
2016 |
68 |
C |
p. 72-79 8 p. |
artikel |
26 |
Synthesis of pyrimidin-4-one-1,2,3-triazole conjugates as glycogen synthase kinase-3β inhibitors with anti-depressant activity
|
Khan, Imran |
|
2016 |
68 |
C |
p. 41-55 15 p. |
artikel |
27 |
Synthesis of ring-C modified oleanolic acid derivatives and their cytotoxic evaluation
|
Pattnaik, Banita |
|
2016 |
68 |
C |
p. 152-158 7 p. |
artikel |
28 |
Synthetic assembly of novel avidin-biotin-GlcNAc (ABG) complex as an attractive bio-probe and its interaction with wheat germ agglutinin (WGA)
|
Kumari, Amrita |
|
2016 |
68 |
C |
p. 219-225 7 p. |
artikel |
29 |
The synthesis of novel pyrazole-3,4-dicarboxamides bearing 5-amino-1,3,4-thiadiazole-2-sulfonamide moiety with effective inhibitory activity against the isoforms of human cytosolic carbonic anhydrase I and II
|
Mert, Samet |
|
2016 |
68 |
C |
p. 64-71 8 p. |
artikel |