| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Abenzyl 10-formyl-trideazafolic acid (abenzyl 10-formyl-TDAF): An effective inhibitor of glycinamide ribonucleotide transformylase
|
Boger, Dale L.
|
|
1997
|
5 |
9 |
p. 1847-1852
6 p.
|
artikel
|
| 2 |
A molecular modeling analysis of the binding interactions between the okadaic acid class of natural product inhibitors and the ser-thr phosphatases, PP1 and PP2A
|
Gauss, Carla-Maria
|
|
1997
|
5 |
9 |
p. 1751-1773
23 p.
|
artikel
|
| 3 |
Contributors to this issue
|
|
|
1997
|
5 |
9 |
p. iii-iv
nvt p.
|
artikel
|
| 4 |
E-64 analogues as inhibitors of cathepsin B. On the role of the absolute configuration of the epoxysuccinyl group
|
Schaschke, Norbert
|
|
1997
|
5 |
9 |
p. 1789-1797
9 p.
|
artikel
|
| 5 |
Effect of stereochemistry on the transport of Aca-linked β-turn peptidomimetics across a human intestinal cell line
|
Tamura, Kiyoshi
|
|
1997
|
5 |
9 |
p. 1859-1866
8 p.
|
artikel
|
| 6 |
Embodying a stable α-helical protein structure through efficient chemical ligation via thioether formation
|
Futaki, Shiroh
|
|
1997
|
5 |
9 |
p. 1883-1891
9 p.
|
artikel
|
| 7 |
10-formyl-5,8,10-trideazafolic acid (10-formyl-TDAF): A potent inhibitor of glycinamide ribonucleotide transformylase
|
Boger, Dale L.
|
|
1997
|
5 |
9 |
p. 1817-1830
14 p.
|
artikel
|
| 8 |
Functionalized analogues of 5,8,10-trideazafolate as potential inhibitors of GAR Tfase or AICAR Tfase
|
Boger, Dale L.
|
|
1997
|
5 |
9 |
p. 1831-1838
8 p.
|
artikel
|
| 9 |
Functionalized analogues of 5,8,10-trideazafolate: Development of an enzyme-assembled tight binding inhibitor of GAR Tfase and a potential irreversible inhibitor of AICAR Tfase
|
Boger, Dale L.
|
|
1997
|
5 |
9 |
p. 1839-1846
8 p.
|
artikel
|
| 10 |
Graphical abstract
|
|
|
1997
|
5 |
9 |
p. v-viii
nvt p.
|
artikel
|
| 11 |
Inhibition of the ser-thr phosphatases PP1 and PP2A by naturally occurring toxins
|
Sheppeck II, James E.
|
|
1997
|
5 |
9 |
p. 1739-1750
12 p.
|
artikel
|
| 12 |
Libraries of opiate and anti-opiate peptidomimetics containing 2,3-methanoleucine
|
Burgess, Kevin
|
|
1997
|
5 |
9 |
p. 1867-1871
5 p.
|
artikel
|
| 13 |
Multisubstrate analogue based on 5,8,10-trideazafolate
|
Boger, Dale L.
|
|
1997
|
5 |
9 |
p. 1853-1857
5 p.
|
artikel
|
| 14 |
Myrosinase-generated isothiocyanate from glucosinolates: Isolation, characterization and in vitro antiproliferative studies
|
Leoni, O.
|
|
1997
|
5 |
9 |
p. 1799-1806
8 p.
|
artikel
|
| 15 |
Structure-activity relationship for DNA topoisomerase II-induced DNA cleavage by azatoxin analogues
|
Madalengoitia, Jose S.
|
|
1997
|
5 |
9 |
p. 1807-1815
9 p.
|
artikel
|
| 16 |
Structure-activity studies of the inhibition of serine β-lactamases by phosphonate monoesters
|
Li, Naixin
|
|
1997
|
5 |
9 |
p. 1783-1788
6 p.
|
artikel
|
| 17 |
Synthesis and α-adrenoceptor blocking activity of the enantiomers of benzyl-(2-chloroethyl)-[2-(2-methoxyphenoxy)-1-methylethl]amine hydrochloride
|
Giardinà, Dario
|
|
1997
|
5 |
9 |
p. 1775-1782
8 p.
|
artikel
|
| 18 |
Synthesis and protein kinase C inhibitory activities of balanol analogues with modification of 4-hydroxybenzamido moiety
|
Hu, Hong
|
|
1997
|
5 |
9 |
p. 1873-1882
10 p.
|
artikel
|
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