| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Carbonic anhydrases activation with 3-amino-1H-1,2,4-triazole-1-carboxamides: Discovery of subnanomolar isoform II activators
|
Le Duc, Yann
|
|
2017
|
25 |
5 |
p. 1681-1686
6 p.
|
artikel
|
| 2 |
Carbonic anhydrases from Trypanosoma and Leishmania as anti-protozoan drug targets
|
Vermelho, Alane B.
|
|
2017
|
25 |
5 |
p. 1543-1555
13 p.
|
artikel
|
| 3 |
Conjugates of phosphorylated zalcitabine and lamivudine with SiO2 nanoparticles: Synthesis by CuAAC click chemistry and preliminary assessment of anti-HIV and antiproliferative activity
|
Vasilyeva, Svetlana V.
|
|
2017
|
25 |
5 |
p. 1696-1702
7 p.
|
artikel
|
| 4 |
Cytotoxic and apoptotic effects of the combination of palladium (II) 5,5-diethylbarbiturate complex with bis(2-pyridylmethyl)amine and curcumin on non small lung cancer cell lines
|
Tunc, Duygu
|
|
2017
|
25 |
5 |
p. 1717-1723
7 p.
|
artikel
|
| 5 |
Discovery and structure activity relationship of the first potent cryptosporidium FIKK kinase inhibitor
|
Osman, Khan T.
|
|
2017
|
25 |
5 |
p. 1672-1680
9 p.
|
artikel
|
| 6 |
Discovery of 4-chloro-2-(2,4-dichloro-6-methylphenoxy)-1-methyl-7-(pentan-3-yl)-1H-benzimidazole, a novel CRF1 receptor antagonist
|
Mochizuki, Michiyo
|
|
2017
|
25 |
5 |
p. 1556-1570
15 p.
|
artikel
|
| 7 |
Discovery of N-(2-aminoethyl)-N-benzyloxyphenyl benzamides: New potent Trypanosoma brucei inhibitors
|
Buchynskyy, Andriy
|
|
2017
|
25 |
5 |
p. 1571-1584
14 p.
|
artikel
|
| 8 |
Editorial board
|
|
|
2017
|
25 |
5 |
p. IFC-
1 p.
|
artikel
|
| 9 |
Identification of novel inverse agonists of estrogen-related receptors ERRγ and ERRβ
|
Yu, Donna D.
|
|
2017
|
25 |
5 |
p. 1585-1599
15 p.
|
artikel
|
| 10 |
Influence of substituent heteroatoms on the cytoprotective properties of pyrimidinol antioxidants
|
Chevalier, Arnaud
|
|
2017
|
25 |
5 |
p. 1703-1716
14 p.
|
artikel
|
| 11 |
Lynamicin D an antimicrobial natural product affects splicing by inducing the expression of SR protein kinase 1
|
Sigala, Ioanna
|
|
2017
|
25 |
5 |
p. 1622-1629
8 p.
|
artikel
|
| 12 |
New insights into highly potent tyrosinase inhibitors based on 3-heteroarylcoumarins: Anti-melanogenesis and antioxidant activities, and computational molecular modeling studies
|
Pintus, Francesca
|
|
2017
|
25 |
5 |
p. 1687-1695
9 p.
|
artikel
|
| 13 |
Positively charged phthalocyanine-arginine conjugates as efficient photosensitizer for photodynamic therapy
|
Wang, Ao
|
|
2017
|
25 |
5 |
p. 1643-1651
9 p.
|
artikel
|
| 14 |
Synthesis and biological evaluation of 4 arylcoumarin analogues as tubulin-targeting antitumor agents
|
Mutai, Peggoty
|
|
2017
|
25 |
5 |
p. 1652-1665
14 p.
|
artikel
|
| 15 |
Synthesis and biological evaluation of cyclic imides incorporating benzenesulfonamide moieties as carbonic anhydrase I, II, IV and IX inhibitors
|
Abdel-Aziz, Alaa A.-M.
|
|
2017
|
25 |
5 |
p. 1666-1671
6 p.
|
artikel
|
| 16 |
Synthesis of new derivatives of 21-imidazolyl-16-dehydropregnenolone as inhibitors of 5α-reductase 2 and with cytotoxic activity in cancer cells
|
Silva-Ortiz, Aylin Viviana
|
|
2017
|
25 |
5 |
p. 1600-1607
8 p.
|
artikel
|
| 17 |
Total synthesis and cytotoxicity of Leucetta alkaloids
|
Koswatta, Panduka B.
|
|
2017
|
25 |
5 |
p. 1608-1621
14 p.
|
artikel
|
| 18 |
Tubulin-binding dibenz[c,e]oxepines: Part 2. 1 Structural variation and biological evaluation as tumour vasculature disrupting agents
|
Rossington, Steven B.
|
|
2017
|
25 |
5 |
p. 1630-1642
13 p.
|
artikel
|
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