| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
ACAT inhibitors derived from hetero-Diels-Alder cycloadducts of thioaldehydes
|
Wilde, Richard G.
|
|
1996
|
4 |
9 |
p. 1493-1513
21 p.
|
artikel
|
| 2 |
20-Amino and 20,21-aziridinyl pregnene steroids: Development of potent inhibitors of 17α-hydroxylase/C17,20-lyase (P450 17)
|
Njar, Vincent C.O.
|
|
1996
|
4 |
9 |
p. 1447-1453
7 p.
|
artikel
|
| 3 |
A new class of HIV-1 protease inhibitor: The crystallographic structure, inhibition and chemical synthesis of an aminimide peptide isostere
|
Rutenber, Earl E.
|
|
1996
|
4 |
9 |
p. 1545-1558
14 p.
|
artikel
|
| 4 |
3-Carboxy-20-keto steroids are dual uncompetitive inhibitors of human steroid 5α-reductase types 1 and 2
|
Yamashita, Dennis S.
|
|
1996
|
4 |
9 |
p. 1481-1485
5 p.
|
artikel
|
| 5 |
Design, synthesis, and in vitro inhibitory activity toward human leukocyte elastase, cathepsin G, and proteinase 3 of saccharin-derived sulfones and congeners
|
Groutas, William C.
|
|
1996
|
4 |
9 |
p. 1393-1400
8 p.
|
artikel
|
| 6 |
Discovery and optimization of nonpeptide HIV-1 protease inhibitors
|
Tummino, Peter J.
|
|
1996
|
4 |
9 |
p. 1401-1410
10 p.
|
artikel
|
| 7 |
Graphical abstracts
|
|
|
1996
|
4 |
9 |
p. vii-xi
nvt p.
|
artikel
|
| 8 |
Inhibition of steroid C17(20) lyase with C-17-heteroaryl steroids
|
Burkhart, Joseph P.
|
|
1996
|
4 |
9 |
p. 1411-1420
10 p.
|
artikel
|
| 9 |
Inhibitors of farnesyl:protein transferase—A possible cancer chemotherapeutic
|
Scholten, Jeffrey D.
|
|
1996
|
4 |
9 |
p. 1537-1543
7 p.
|
artikel
|
| 10 |
Inhibitors of human nitric oxide synthase isoforms with the carbamidine moiety as a common structural element
|
Moore, William M.
|
|
1996
|
4 |
9 |
p. 1559-1564
6 p.
|
artikel
|
| 11 |
Mechanism-based inactivation of γ-aminobutyric acid aminotransferase by 3-amino-4-fluorobutanoic acid
|
Silverman, Richard B.
|
|
1996
|
4 |
9 |
p. 1521-1535
15 p.
|
artikel
|
| 12 |
Preface
|
Silverman, Richard B.
|
|
1996
|
4 |
9 |
p. xiii-
1 p.
|
artikel
|
| 13 |
Properties of analogues of an intermediate in the process of mechanism-based inactivation of carboxypeptidase A
|
Ghosh, Soumitra S.
|
|
1996
|
4 |
9 |
p. 1487-1492
6 p.
|
artikel
|
| 14 |
Quiescent affinity inactivators of protein tyrosine phosphatases
|
Taylor, William P.
|
|
1996
|
4 |
9 |
p. 1515-1520
6 p.
|
artikel
|
| 15 |
Solution conformations of KNI-272, a tripeptide HIV protease inhibitor designed on the basis of substrate transition state: Determined by NMR spectroscopy and simulated annealing calculations
|
Ohno, Yasushi
|
|
1996
|
4 |
9 |
p. 1565-1572
8 p.
|
artikel
|
| 16 |
Structure-based design of achiral, nonpeptidic hydroxybenzamide as a novel P2/P2′ replacement for the symmetry-based HIV protease inhibitors
|
Randad, Ramnarayan S.
|
|
1996
|
4 |
9 |
p. 1471-1480
10 p.
|
artikel
|
| 17 |
Structure-based design of parasitic protease inhibitors
|
Li, Rongshi
|
|
1996
|
4 |
9 |
p. 1421-1427
7 p.
|
artikel
|
| 18 |
Synthesis of complex δ-acetylenic amino acids as potential multisubstrate adduct inhibitors of methyltransferases
|
Burns, Mark R.
|
|
1996
|
4 |
9 |
p. 1455-1470
16 p.
|
artikel
|
| 19 |
The rationale for E2020 as a potent acetylcholinesterase inhibitor
|
Kawakami, Yoshiyuki
|
|
1996
|
4 |
9 |
p. 1429-1446
18 p.
|
artikel
|
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