| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Acetylcholinesterase inhibition by fused dihydroquinazoline compounds
|
Jaén, Juan C.
|
|
1996
|
6 |
6 |
p. 737-742
6 p.
|
artikel
|
| 2 |
A Hammett correlation for CC-1065 and duocarmycin analogs: Magnitude of substituent electronic effects on functional reactivity
|
Boger, Dale L.
|
|
1996
|
6 |
6 |
p. 659-664
6 p.
|
artikel
|
| 3 |
A Non-peptidic photoactivatable antagonist for mapping the antagonist binding site of the tachykinin NK2 receptor
|
Kersey, Ian D.
|
|
1996
|
6 |
6 |
p. 605-608
4 p.
|
artikel
|
| 4 |
Anti-HIV activity of quassinoids
|
Okano, Masayoshi
|
|
1996
|
6 |
6 |
p. 701-706
6 p.
|
artikel
|
| 5 |
Carboxylic acid bioisosteres of γ-linked dipeptide analogues of the folate-based thymidylate synthase (TS) inhibitor, 2-desamino-2-methyl-N 10-propargyl-5,8-dideazafolic acid (ICI 198583)
|
Bavetsias, Vassilios
|
|
1996
|
6 |
6 |
p. 631-636
6 p.
|
artikel
|
| 6 |
Chemical synthesis, DNA cleavage and antitumor activity of molecules with (Z)-7-sulfonyl-3-hexene-1,5-diyne functionalities
|
Wu, Ming-Jung
|
|
1996
|
6 |
6 |
p. 675-678
4 p.
|
artikel
|
| 7 |
Contributors to this issue
|
|
|
1996
|
6 |
6 |
p. iii-iv
nvt p.
|
artikel
|
| 8 |
Design and synthesis of bisubstrate analogues for 3-hydroxy-3-methyl-glutaryl coenzyme a reductase
|
Taillefumier, C
|
|
1996
|
6 |
6 |
p. 615-618
4 p.
|
artikel
|
| 9 |
Design, synthesis, and characterization of dipeptide isostere containing cis-epoxide for the irreversible inactivation of HIV protease
|
Sun Lee, Chang
|
|
1996
|
6 |
6 |
p. 589-594
6 p.
|
artikel
|
| 10 |
Evaluation of tea polyphenols as anti-HIV agents
|
Hashimoto, Fumio
|
|
1996
|
6 |
6 |
p. 695-700
6 p.
|
artikel
|
| 11 |
From indomethacin to a selective COX-2 inhibitor: Development of indolalkanoic acids as potent and selective cyclooxygenase-2 inhibitors
|
Black, W.C.
|
|
1996
|
6 |
6 |
p. 725-730
6 p.
|
artikel
|
| 12 |
Graphical abstracts
|
|
|
1996
|
6 |
6 |
p. v-xii
nvt p.
|
artikel
|
| 13 |
Imino 1,2,3,4-tetrahydrocyclopent[b]indole carbamates as dual inhibitors of acetylcholinesterase and monoamine oxidase
|
Fink, David M.
|
|
1996
|
6 |
6 |
p. 625-630
6 p.
|
artikel
|
| 14 |
Inhibitors of acyl-CoA: cholesterol O-acyl transferase (ACAT) as hypocholesterolemic agents. The synthesis and biological activity of a series of malonester amides
|
Sliskovic, D.R.
|
|
1996
|
6 |
6 |
p. 713-718
6 p.
|
artikel
|
| 15 |
Inhibitory potency of lithocholic acid analogs and other bile acids on glucuronosyltransferase activity in a colon cancer cell line
|
Schneider, H.
|
|
1996
|
6 |
6 |
p. 637-642
6 p.
|
artikel
|
| 16 |
β-Methanesulfonyl-L-valine as a novel, unnatural amino acid surrogate for P2 in the design of HIV protease inhibitors.
|
Park, Chihyo
|
|
1996
|
6 |
6 |
p. 585-588
4 p.
|
artikel
|
| 17 |
2-[4-(o-methoxyphenyl)piperazin-1-ylmethyl]-1,3-dioxoperhydroimidazo[1,5-a]pyridine as a new selective 5-HT1A receptor ligand
|
López-Rodríguez, María L.
|
|
1996
|
6 |
6 |
p. 689-694
6 p.
|
artikel
|
| 18 |
Optimization of retro-thiorphan for inhibition of endothelin converting enzyme
|
Kukkola, Paivi J.
|
|
1996
|
6 |
6 |
p. 619-624
6 p.
|
artikel
|
| 19 |
6-Phenyl-6-alkylamido-5,6-dihydro-2H-pyran-2-ones: novel HIV protease inhibitors
|
Hamilton, Harriet W.
|
|
1996
|
6 |
6 |
p. 719-724
6 p.
|
artikel
|
| 20 |
Solid phase synthesis and purification of 5′-mercaptoalkylated oligonucleotides
|
Kumar, P.
|
|
1996
|
6 |
6 |
p. 683-688
6 p.
|
artikel
|
| 21 |
Synthesis and antitumor activity of a new class of water soluble camptothecin derivatives
|
Bedeschi, Angelo
|
|
1996
|
6 |
6 |
p. 671-674
4 p.
|
artikel
|
| 22 |
Synthesis and antitumor activity of (2R,3R)-2,3-dihydroxy- and -2,3-dialkoxy-1,4-diaminobutane platinum(II) complexes
|
Kim, Dae-Kee
|
|
1996
|
6 |
6 |
p. 647-652
6 p.
|
artikel
|
| 23 |
Synthesis and biological evaluation of both enantiomers of L-761,000 as inhibitors of cyclooxygenase 1 and 2
|
Leblanc, Y.
|
|
1996
|
6 |
6 |
p. 731-736
6 p.
|
artikel
|
| 24 |
Synthesis and evaluation of 2-aryl-4H-3,1-benzoxazin-4-ones as C1r serine protease inhibitors
|
Gilmore, John L.
|
|
1996
|
6 |
6 |
p. 679-682
4 p.
|
artikel
|
| 25 |
Synthesis and in vitro cytotoxicity of cis-dichloro[(2S,3R,4S)-2-aminomethyl-3,4-(O-isopropylidene)dihydroxy- or -3,4-dihydroxypyrrolidine]platinum(II)
|
Kim, Dae-Kee
|
|
1996
|
6 |
6 |
p. 643-646
4 p.
|
artikel
|
| 26 |
Synthesis and preliminary pharmacological evaluation of analogues of caracasanamide, a hypotensive natural product
|
Corelli, Federico
|
|
1996
|
6 |
6 |
p. 653-658
6 p.
|
artikel
|
| 27 |
Synthesis of monooleoyl glycerophospho heptapeptide as a candidate of pathogen of essential hypertension
|
Inami, Kaoru
|
|
1996
|
6 |
6 |
p. 601-604
4 p.
|
artikel
|
| 28 |
Synthesis of polyamide nucleic acids (PNAs) using a novel Fmoc/Mmt protecting-group combination
|
Breipohl, G.
|
|
1996
|
6 |
6 |
p. 665-670
6 p.
|
artikel
|
| 29 |
The identification of cyclooxygenase-1 inhibitors from 4-thiazolidinone combinatorial libraries
|
Look, Gary C.
|
|
1996
|
6 |
6 |
p. 707-712
6 p.
|
artikel
|
| 30 |
Thiophenoxy peptides: A new class of HIV replication inhibitors
|
Niddam, Valérie
|
|
1996
|
6 |
6 |
p. 609-614
6 p.
|
artikel
|
| 31 |
Trishomocubanes, a new class of selective and high affinity ligands for the sigma binding site
|
Kassiou, Michael
|
|
1996
|
6 |
6 |
p. 595-600
6 p.
|
artikel
|
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