nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('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. |
artikel |
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. |
artikel |
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. |
artikel |
4 |
Bacteria targeted by human natural antibodies using α-gal conjugated receptor-specific glycopolymers
|
Li, Jun |
|
1999 |
7 |
8 |
p. 1549-1558 10 p. |
artikel |
5 |
2-Benzyl-2-methylsuccinic acid as inhibitor for carboxypeptidase A. synthesis and evaluation
|
Lee, Mijoon |
|
1999 |
7 |
8 |
p. 1755-1760 6 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
9 |
Cytotoxic and tubulin-interactive hemiasterlins from Auletta sp. and Siphonochalina spp. sponges
|
Gamble, William R. |
|
1999 |
7 |
8 |
p. 1611-1615 5 p. |
artikel |
10 |
1,3-Disubstituted benzazepines as neuropeptide Y Y1 receptor antagonists
|
Murakami, Yasushi |
|
1999 |
7 |
8 |
p. 1703-1714 12 p. |
artikel |
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. |
artikel |
12 |
Imidazothiadiazine dioxides: synthesis and antiviral activity
|
Martı́nez, Ana |
|
1999 |
7 |
8 |
p. 1617-1623 7 p. |
artikel |
13 |
Indolo[3,2-c]cinnolines with antiproliferative, antifungal, and antibacterial activity
|
Barraja, Paola |
|
1999 |
7 |
8 |
p. 1591-1596 6 p. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
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. |
artikel |
19 |
Stereospecificity of Pseudomonas fluorescens kynureninase for diastereomers of β-methylkynurenine
|
Cyr, Lakshmi V. |
|
1999 |
7 |
8 |
p. 1497-1503 7 p. |
artikel |
20 |
Syntheses of benzoquinolizidine and benzoindolizidine derivatives as anti-amnesic agents
|
Zhao, Shikai |
|
1999 |
7 |
8 |
p. 1637-1646 10 p. |
artikel |
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. |
artikel |
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. |
artikel |
23 |
Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems. Part III:
|
Azami, Hidenori |
|
1999 |
7 |
8 |
p. 1665-1682 18 p. |
artikel |
24 |
Synthesis and antiviral activity of monobactams inhibiting the human cytomegalovirus protease
|
Ogilvie, W.W. |
|
1999 |
7 |
8 |
p. 1521-1531 11 p. |
artikel |
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. |
artikel |
26 |
Synthesis and functional characterization of novel derivatives related to oxotremorine and oxotremorine-M
|
Dallanoce, Clelia |
|
1999 |
7 |
8 |
p. 1539-1547 9 p. |
artikel |
27 |
Synthesis and properties of some novel anti-calmodulin drugs
|
Sakai, Ted T. |
|
1999 |
7 |
8 |
p. 1559-1565 7 p. |
artikel |
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. |
artikel |