nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
An Artificial CuII complex with intriguing oxygen radical-quenching profile. X-ray structure, cytochrome C assay, and ESR study
|
Otsuka, Masami |
|
1996 |
4 |
10 |
p. 1703-1708 6 p. |
artikel |
2 |
Cholecystokinin B antagonists. Synthesis and quantitative structure-activity relationships of a series of C-terminal analogues of CI-988
|
Augelli-Szafran, Corinne E. |
|
1996 |
4 |
10 |
p. 1733-1745 13 p. |
artikel |
3 |
Computational and molecular modeling evaluation of the structural basis for tubulin polymerization inhibition by colchicine site agents
|
ter Haar, Ernst |
|
1996 |
4 |
10 |
p. 1659-1671 13 p. |
artikel |
4 |
Conformational analysis of phthalein derivatives acting as thymidylate synthase inhibitors by means of 1H NMR and quantum chemical calculations
|
Ghelli, Stefano |
|
1996 |
4 |
10 |
p. 1783-1794 12 p. |
artikel |
5 |
Contributors to this issue
|
|
|
1996 |
4 |
10 |
p. iii-iv nvt p. |
artikel |
6 |
1,4-Dihydropyridines bearing a pharmacophoric fragment of lidoflazine
|
Chiarini, A. |
|
1996 |
4 |
10 |
p. 1629-1635 7 p. |
artikel |
7 |
Exploration of the effects of linker chain modifications on anti-HIV activities in a series of cosalane analogues
|
Marek Golebiewski, W. |
|
1996 |
4 |
10 |
p. 1637-1648 12 p. |
artikel |
8 |
Graphical abstracts
|
|
|
1996 |
4 |
10 |
p. v-x nvt p. |
artikel |
9 |
Hybrid oligonucleotides: Synthesis, biophysical properties, stability studies, and biological activity
|
Yu, Dong |
|
1996 |
4 |
10 |
p. 1685-1692 8 p. |
artikel |
10 |
Investigation on QSAR and binding mode of a new class of human rhinovirus-14 inhibitors by CoMFA and docking experiments
|
Artico, Marino |
|
1996 |
4 |
10 |
p. 1715-1724 10 p. |
artikel |
11 |
Key analogues of the tetrapeptide subunit of RA-VII and deoxybouvardin
|
Boger, Dale L. |
|
1996 |
4 |
10 |
p. 1597-1603 7 p. |
artikel |
12 |
New 19-acetoxyingol diterpenes from the latex of Euphorbia poisonii (Euphorbiaceae)
|
Fatope, Majekodunmi O. |
|
1996 |
4 |
10 |
p. 1679-1683 5 p. |
artikel |
13 |
New amino-nitroxide spin labels
|
Dragutan, Ileana |
|
1996 |
4 |
10 |
p. 1577-1583 7 p. |
artikel |
14 |
New carbamate supports for the preparation of 3′-amino-modified oligonucleotides
|
Aviñó, Anna |
|
1996 |
4 |
10 |
p. 1649-1658 10 p. |
artikel |
15 |
Nitric oxide-induced oxidation of α-tocopherol
|
d'Ischia, Marco |
|
1996 |
4 |
10 |
p. 1747-1753 7 p. |
artikel |
16 |
Phosphatase inhibitors—III. Benzylaminophosphonic acids as potent inhibitors of human prostatic acid phosphatase
|
Beers, Scott A. |
|
1996 |
4 |
10 |
p. 1693-1701 9 p. |
artikel |
17 |
Prediction of relative potency of ketone protease inhibitors using molecular orbital theory
|
Edith Chan, A.W. |
|
1996 |
4 |
10 |
p. 1673-1677 5 p. |
artikel |
18 |
Some aspect of the interactions of adriamycin with human serum albumin
|
Trynda-Lemiesz, Lilianna |
|
1996 |
4 |
10 |
p. 1709-1713 5 p. |
artikel |
19 |
Stereoselective syntheses of substituted pterocarpans with anti-HIV activity, and 5-aza-/5-thia-pterocarpan and 2-aryl-2,3-dihydrobenzofuran analogues
|
Engler, Thomas A. |
|
1996 |
4 |
10 |
p. 1755-1769 15 p. |
artikel |
20 |
Structure determination of metabolites isolated from urine and bile after administration of AY4166, a novel d-phenylalanine-derivative hypoglycemic agent
|
Takesada, Hiroko |
|
1996 |
4 |
10 |
p. 1771-1781 11 p. |
artikel |
21 |
Synthesis and biochemical activity of novel amidine derivatives as m1 muscarinic receptor agonists
|
Ojo, Babatunde |
|
1996 |
4 |
10 |
p. 1605-1615 11 p. |
artikel |
22 |
Synthesis and evaluation of estradiol derivatives with 16α-(bromoalkylamide), 16α-(bromoalkyl) or 16α-(bromoalkynyl) side chain as inhibitors of 17β-hydroxysteroid dehydrogenase type 1 without estrogenic activity
|
Pelletier, Joëlle D |
|
1996 |
4 |
10 |
p. 1617-1628 12 p. |
artikel |
23 |
Synthesis of chemoreversible prodrugs of ara-C with variable time-release profiles. Biological evaluation of their apoptotic activity
|
Wipf, Peter |
|
1996 |
4 |
10 |
p. 1585-1596 12 p. |
artikel |
24 |
The synthesis and biological evaluation of 4-p-nitrobenzylthio-v-triazolo [4,5-d]pyridazine and imidazo[4,5-d]pyridazine ribosides as potential nucleoside transport inhibitors
|
Bussolari, Jacqueline C. |
|
1996 |
4 |
10 |
p. 1725-1731 7 p. |
artikel |
25 |
Use of the chemical structure of peptides as the starting point to design nonpeptide agonists and antagonists at peptide receptors: Examples with cholecystokinin and tachykinins
|
Horwell, David C. |
|
1996 |
4 |
10 |
p. 1573-1576 4 p. |
artikel |