nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Carboxymethyl tethered poly(disubstituted)triazoles built on nucleoside skeletons: A unique class of ribonuclease A inhibitors designed using chemical logic
|
Mondal, Pampa |
|
|
76 |
C |
p. |
artikel |
2 |
Computational design, synthesis and biological evaluation of PDE5 inhibitors based on N 2,N 4-diaminoquinazoline and N 2,N 6-diaminopurine scaffolds
|
Somnarin, Thanachon |
|
|
76 |
C |
p. |
artikel |
3 |
Design, synthesis, and bioevaluation of imidazo [1,2–a] pyrazine derivatives as tubulin polymerization inhibitors with potent anticancer activities
|
Deng, Bulian |
|
|
76 |
C |
p. |
artikel |
4 |
Editorial Board
|
|
|
|
76 |
C |
p. |
artikel |
5 |
Graphical Abstract Contents Continued
|
|
|
|
76 |
C |
p. |
artikel |
6 |
Graphical abstract TOC
|
|
|
|
76 |
C |
p. |
artikel |
7 |
Graphical abstract TOC
|
|
|
|
76 |
C |
p. |
artikel |
8 |
Hybrids of small CD4 mimics and gp41-related peptides as dual-target HIV entry inhibitors
|
Wang, Rongyi |
|
|
76 |
C |
p. |
artikel |
9 |
Radiolabelling Pt-based quadruplex DNA binders via click chemistry
|
Lo, Rainbow |
|
|
76 |
C |
p. |
artikel |
10 |
Revisiting recent unusual drug-DNA complex structures: Implications for cancer and neurological disease diagnostics and therapeutics
|
Satange, Roshan |
|
|
76 |
C |
p. |
artikel |
11 |
Symmetric lipophilic polyamines exhibiting antitumor activity
|
Perevoshchikova, Ksenia A. |
|
|
76 |
C |
p. |
artikel |
12 |
Synthesis and antibiofilm evaluation of N-acyl-2-aminopyrimidine derivatives against Acinetobacter baumannii
|
Jia, Xue-Min |
|
|
76 |
C |
p. |
artikel |
13 |
Synthesis and biological evaluation of novel photo-clickable adenosine and cyclic ADP-ribose analogs: 8-N3-2′-O-propargyladenosine and 8-N3-2′-O-propargyl-cADPR
|
Andy, Divya |
|
|
76 |
C |
p. |
artikel |
14 |
Synthesis and properties of fully-modified 4′-selenoRNA, an endonuclease-resistant RNA analog
|
Ota, Masashi |
|
|
76 |
C |
p. |
artikel |
15 |
Synthesis of estrone selenocyanate Compounds, anti-tumor activity evaluation and Structure-activity relationship analysis
|
Huang, Yanmin |
|
|
76 |
C |
p. |
artikel |
16 |
The discovery of (1R, 3R)-1-(3-chloro-5-fluorophenyl)-3-(hydroxymethyl)-1,2,3,4-tetrahydroisoquinoline-6-carbonitrile, a potent and selective agonist of human transient receptor potential cation channel subfamily m member 5 (TRPM5) and evaluation of as a potential gastrointestinal prokinetic agent
|
Sabat, M. |
|
|
76 |
C |
p. |
artikel |