| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A novel molecular modelling study of inhibitors of the 17α-hydroxylase component of the enzyme system 17α-hydroxylase/17,20-lyase (P-45017α)
|
Ahmed, Sabbir
|
|
1999
|
7 |
8 |
p. 1487-1496
10 p.
|
article
|
| 2 |
A reversible monoamine oxidase a inhibitor, befloxatone: structural approach of its mechanism of action
|
Wouters, Johan
|
|
1999
|
7 |
8 |
p. 1683-1693
11 p.
|
article
|
| 3 |
A synthetic heparan sulfate pentasaccharide, exclusively containing l-iduronic acid, displays higher affinity for FGF-2 than its d-glucuronic acid-containing isomers
|
Kovensky, José
|
|
1999
|
7 |
8 |
p. 1567-1580
14 p.
|
article
|
| 4 |
Bacteria targeted by human natural antibodies using α-gal conjugated receptor-specific glycopolymers
|
Li, Jun
|
|
1999
|
7 |
8 |
p. 1549-1558
10 p.
|
article
|
| 5 |
2-Benzyl-2-methylsuccinic acid as inhibitor for carboxypeptidase A. synthesis and evaluation
|
Lee, Mijoon
|
|
1999
|
7 |
8 |
p. 1755-1760
6 p.
|
article
|
| 6 |
Bis-N-nitroso-caged nitric oxides: photochemistry and biological performance test by rat aorta vasorelaxation
|
Namiki, Shigeyuki
|
|
1999
|
7 |
8 |
p. 1695-1702
8 p.
|
article
|
| 7 |
7-Chloro-5-hydroxy-1-[2-methyl-4-(2-methylbenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-1-benzazepine (OPC-41061): A potent, orally active nonpeptide arginine vasopressin V2 receptor antagonist
|
Kondo, Kazumi
|
|
1999
|
7 |
8 |
p. 1743-1754
12 p.
|
article
|
| 8 |
α-Cyanocinnamide derivatives: a new family of non-peptide, non-sulfhydryl inhibitors of ras farnesylation
|
Poradosu, Enrique
|
|
1999
|
7 |
8 |
p. 1727-1736
10 p.
|
article
|
| 9 |
Cytotoxic and tubulin-interactive hemiasterlins from Auletta sp. and Siphonochalina spp. sponges
|
Gamble, William R.
|
|
1999
|
7 |
8 |
p. 1611-1615
5 p.
|
article
|
| 10 |
1,3-Disubstituted benzazepines as neuropeptide Y Y1 receptor antagonists
|
Murakami, Yasushi
|
|
1999
|
7 |
8 |
p. 1703-1714
12 p.
|
article
|
| 11 |
Effects of escins Ia, Ib, IIa, and IIb from horse chestnuts on gastrointestinal transit and ileus in mice
|
Matsuda, Hisashi
|
|
1999
|
7 |
8 |
p. 1737-1741
5 p.
|
article
|
| 12 |
Imidazothiadiazine dioxides: synthesis and antiviral activity
|
Martı́nez, Ana
|
|
1999
|
7 |
8 |
p. 1617-1623
7 p.
|
article
|
| 13 |
Indolo[3,2-c]cinnolines with antiproliferative, antifungal, and antibacterial activity
|
Barraja, Paola
|
|
1999
|
7 |
8 |
p. 1591-1596
6 p.
|
article
|
| 14 |
Isolation and characterization of the product of inactivation of γ-aminobutyric acid aminotransferase by gabaculine
|
Fu, Mengmeng
|
|
1999
|
7 |
8 |
p. 1581-1590
10 p.
|
article
|
| 15 |
New calcium antagonists: synthesis, X-ray analysis, and smooth muscle relaxing effect of 3-[O-(Benzyl-substituted)-oximino-ethers]-hexahydroazepin-2,3-diones
|
El From, Hayat
|
|
1999
|
7 |
8 |
p. 1655-1663
9 p.
|
article
|
| 16 |
Novel anthracycline-spacer-β-glucuronide, -β-glucoside, and -β-galactoside prodrugs for application in selective chemotherapy
|
Leenders, Ruben G.G.
|
|
1999
|
7 |
8 |
p. 1597-1610
14 p.
|
article
|
| 17 |
Preparation and pharmacological evaluation of the R- and S-enantiomers of 3-(2′-butylamino)-4H- and 3-(3′-methyl-2′-butylamino)-4H-pyrido[4,3-e]-1,2,4-thiadiazine 1,1-dioxide, two tissue selective ATP-sensitive potassium channel openers
|
Khelili, Smail
|
|
1999
|
7 |
8 |
p. 1513-1520
8 p.
|
article
|
| 18 |
Stereoselective synthesis of a conformationally defined cyclohexyl carnitine analogue that binds CPT-1 with high affinity
|
Hutchison, Tracy L.
|
|
1999
|
7 |
8 |
p. 1505-1511
7 p.
|
article
|
| 19 |
Stereospecificity of Pseudomonas fluorescens kynureninase for diastereomers of β-methylkynurenine
|
Cyr, Lakshmi V.
|
|
1999
|
7 |
8 |
p. 1497-1503
7 p.
|
article
|
| 20 |
Syntheses of benzoquinolizidine and benzoindolizidine derivatives as anti-amnesic agents
|
Zhao, Shikai
|
|
1999
|
7 |
8 |
p. 1637-1646
10 p.
|
article
|
| 21 |
Syntheses of 1,2-diamino and 1,2-aminoalcohol derivatives in the piperidine and pyrrolidine series as anti-amnesic agents
|
Zhao, Shikai
|
|
1999
|
7 |
8 |
p. 1647-1654
8 p.
|
article
|
| 22 |
Syntheses of (Z)- and (E)-4-amino-2-(trifluoromethyl)-2-butenoic acid and Their inactivation of γ-aminobutyric acid aminotransferase
|
Johnson, Theodore R.
|
|
1999
|
7 |
8 |
p. 1625-1636
12 p.
|
article
|
| 23 |
Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems. Part III:
|
Azami, Hidenori
|
|
1999
|
7 |
8 |
p. 1665-1682
18 p.
|
article
|
| 24 |
Synthesis and antiviral activity of monobactams inhibiting the human cytomegalovirus protease
|
Ogilvie, W.W.
|
|
1999
|
7 |
8 |
p. 1521-1531
11 p.
|
article
|
| 25 |
Synthesis and evaluation of 2-Amino-9-(3-acyloxymethyl-4-alkoxycarbonyloxybut-1-yl)purines and 2-Amino-9-(3-alkoxycarbonyloxymethyl-4-alkoxycarbonyloxybut-1-yl)purines as potential prodrugs of penciclovir
|
Kim, Dae-Kee
|
|
1999
|
7 |
8 |
p. 1715-1725
11 p.
|
article
|
| 26 |
Synthesis and functional characterization of novel derivatives related to oxotremorine and oxotremorine-M
|
Dallanoce, Clelia
|
|
1999
|
7 |
8 |
p. 1539-1547
9 p.
|
article
|
| 27 |
Synthesis and properties of some novel anti-calmodulin drugs
|
Sakai, Ted T.
|
|
1999
|
7 |
8 |
p. 1559-1565
7 p.
|
article
|
| 28 |
Synthesis and structure–affinity relationships at the central benzodiazepine receptor of pyridazino[4,3-b]indoles and Indeno[1,2-c]pyridazines
|
Campagna, F
|
|
1999
|
7 |
8 |
p. 1533-1538
6 p.
|
article
|
Journal description