| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Amino acids that specify structure through hydrophobic clustering and histidine-aromatic interactions lead to biologically active peptidomimetics
|
Graciani, Nilsa R.
|
|
1994
|
2 |
9 |
p. 999-1006
8 p.
|
artikel
|
| 2 |
Benzodiazepine peptidomimetic inhibitors of farnesyltransferase
|
Marsters Jr, James C.
|
|
1994
|
2 |
9 |
p. 949-957
9 p.
|
artikel
|
| 3 |
Conformationally constrained o-tolylpiperazine camphorsulfonamide oxytocin antagonists. Structural modifications that provide high receptor affinity and suggest a bioactive conformation.
|
Williams, Peter D.
|
|
1994
|
2 |
9 |
p. 971-985
15 p.
|
artikel
|
| 4 |
Design of a potent and orally active nonpeptide platelet fibrinogen receptor (GPIIb/IIIa) antagonist
|
Bondinell, William E.
|
|
1994
|
2 |
9 |
p. 897-908
12 p.
|
artikel
|
| 5 |
Design of orally active, non-peptide fibrinogen receptor antagonists. An evolutionary process from the RGD sequence to novel anti-platelet aggregation agents
|
Bovy, P.R.
|
|
1994
|
2 |
9 |
p. 881-895
15 p.
|
artikel
|
| 6 |
Design of orally bioavailable, symmetry-based inhibitors of HIV protease
|
Kempf, Dale J.
|
|
1994
|
2 |
9 |
p. 847-858
12 p.
|
artikel
|
| 7 |
Graphical Abstracts
|
|
|
1994
|
2 |
9 |
p. vii-x
nvt p.
|
artikel
|
| 8 |
Herpes simplex virus ribonucleotide reductase subunit association inhibitors: the effect and conformation of β-alkylated aspartic acid derivatives
|
Moss, Neil
|
|
1994
|
2 |
9 |
p. 959-970
12 p.
|
artikel
|
| 9 |
HIV-1 protease inhibitors: Ketomethylene isosteres with unusually high affinity compared with hydroxyethylene isostere analogs
|
Marinier, Aime
|
|
1994
|
2 |
9 |
p. 919-925
7 p.
|
artikel
|
| 10 |
Peptidomimetic antagonists designed to inhibit the binding of CD4 to HIV GP120
|
Ramurthy, Savithri
|
|
1994
|
2 |
9 |
p. 1007-1013
7 p.
|
artikel
|
| 11 |
Preface
|
Sikorski, James A.
|
|
1994
|
2 |
9 |
p. xi-xii
nvt p.
|
artikel
|
| 12 |
Renin inhibitor SC-51106 complexed with human renin: Discovery of a new binding site adjacent to P3
|
Hanson, Gunnar J.
|
|
1994
|
2 |
9 |
p. 909-918
10 p.
|
artikel
|
| 13 |
Renin inhibitors: C-terminal oxetanes as potent transition-state mimics
|
Rosenberg, Saul H.
|
|
1994
|
2 |
9 |
p. 927-937
11 p.
|
artikel
|
| 14 |
Selective non-peptide ligands for an accommodating peptide receptor. Imidazobenzodiazepines as potent cholecystokinin type b receptor antagonists
|
Bock, Mark G.
|
|
1994
|
2 |
9 |
p. 987-998
12 p.
|
artikel
|
| 15 |
Synthesis and biological activity of ras farnesyl protein transferase inhibitors. Tetrapeptide analogs with amino methyl and carbon linkages
|
Wai, John S.
|
|
1994
|
2 |
9 |
p. 939-947
9 p.
|
artikel
|
| 16 |
Synthesis, antiviral activity, and bioavailability studies of γ-lactam derived HIV protease inhibitors
|
Hungate, Randall W.
|
|
1994
|
2 |
9 |
p. 859-879
21 p.
|
artikel
|
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