nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Acyloxymethyl as a drug protecting group. Part 7: Tertiary sulfonamidomethyl ester prodrugs of benzylpenicillin: chemical hydrolysis and anti-bacterial activity
|
Iley, Jim |
|
2000 |
8 |
7 |
p. 1629-1636 8 p. |
artikel |
2 |
Analyses of insulin-potentiating fragments of human growth hormone by computative simulation; essential unit for insulin-Involved biological responses
|
Ohkura, Kazuto |
|
2000 |
8 |
7 |
p. 1733-1740 8 p. |
artikel |
3 |
Analysis of stereoelectronic properties of camptothecin analogues in relation to biological activity
|
Werbovetz, Karl A. |
|
2000 |
8 |
7 |
p. 1741-1747 7 p. |
artikel |
4 |
Anti-tumor promoting effects of sesquiterpenes from Maytenus cuzcoina (celastraceae)
|
González, Antonio G. |
|
2000 |
8 |
7 |
p. 1773-1778 6 p. |
artikel |
5 |
Attempts to obtain more efficient GAC-cleaving hammerhead ribozymes by in vitro selection
|
Kore, Anilkumar R |
|
2000 |
8 |
7 |
p. 1767-1771 5 p. |
artikel |
6 |
Aurine tricarboxylic acid, a potent metal-chelating inhibitor of NFκB–DNA binding
|
Kumar Sharma, Rakesh |
|
2000 |
8 |
7 |
p. 1819-1823 5 p. |
artikel |
7 |
Comparative QSAR studies on substituted bis-(acridines) and bis-(phenazines)-carboxamides: a new class of anticancer agents
|
Garg, Rajni |
|
2000 |
8 |
7 |
p. 1835-1839 5 p. |
artikel |
8 |
Conformations in solution and bound to bacterial ribosomes of ketolides, HMR 3647 (telithromycin) and RU 72366: A new class of highly potent antibacterials
|
Evrard-Todeschi, Nathalie |
|
2000 |
8 |
7 |
p. 1579-1597 19 p. |
artikel |
9 |
Controlled site-selective protein glycosylation for precise glycan structure–catalytic activity relationships
|
Davis, Benjamin G |
|
2000 |
8 |
7 |
p. 1527-1535 9 p. |
artikel |
10 |
Design, synthesis and binding at cloned muscarinic receptors of N-[5-(1′-substituted-acetoxymethyl)-3-oxadiazolyl] and N-[4-(1′-substituted-acetoxymethyl)-2-dioxolanyl] dialkyl amines
|
Manfredini, Stefano |
|
2000 |
8 |
7 |
p. 1559-1566 8 p. |
artikel |
11 |
Design, synthesis and cytotoxicity evaluation of 1-chloromethyl-5-hydroxy-1,2-dihydro-3H-benz[e]indole (seco-CBI) dimers
|
Jia, Guofeng |
|
2000 |
8 |
7 |
p. 1607-1617 11 p. |
artikel |
12 |
Development of a 3D pharmacophore for nonspecific ligand recognition of α1, α2, α3, α5, and α6 containing gabaA/benzodiazepine receptors
|
Filizola, Marta |
|
2000 |
8 |
7 |
p. 1799-1807 9 p. |
artikel |
13 |
Flavonols from Heterotheca inuloides: Tyrosinase Inhibitory Activity and Structural Criteria
|
Kubo, Isao |
|
2000 |
8 |
7 |
p. 1749-1755 7 p. |
artikel |
14 |
Hydrogen bonding isosteres: bimolecular carboxylic acid and amine-N-oxide interactions mediated via CH···O hydrogen bonds
|
Baures, P.W |
|
2000 |
8 |
7 |
p. 1599-1605 7 p. |
artikel |
15 |
Mechanism of biochemical action of substituted 4-methylbenzopyran-2-ones. Part 7: assay and characterization of 7,8-diacetoxy-4-methylcoumarin:protein transacetylase from rat liver microsomes based on the irreversible inhibition of cytosolic glutathione S-Transferase
|
Raj, Hanumantharao G |
|
2000 |
8 |
7 |
p. 1707-1712 6 p. |
artikel |
16 |
Monoamine oxidase-catalyzed oxidation of endo,endo-2-amino-6-[(Z)-2′-phenyl]ethenylbicyclo[2.2.1]heptane, a potential probe for a radical cation intermediate
|
Wang, Xueqing |
|
2000 |
8 |
7 |
p. 1645-1651 7 p. |
artikel |
17 |
New aromatic iminoimidazolidine derivatives as α1-adrenoceptor antagonists: a novel synthetic approach and pharmacological activity
|
Dardonville, Christophe |
|
2000 |
8 |
7 |
p. 1567-1577 11 p. |
artikel |
18 |
Nicorandil analogues containing NO-donor furoxans and related furazans
|
Boschi, Donatella |
|
2000 |
8 |
7 |
p. 1727-1732 6 p. |
artikel |
19 |
Potent inhibition of serine proteases by heterocyclic sulfide derivatives of 1,2,5-thiadiazolidin-3-one 1,1 dioxide
|
He, Shu |
|
2000 |
8 |
7 |
p. 1713-1717 5 p. |
artikel |
20 |
Site-selective glycosylation of subtilisin Bacillus lentus causes dramatic increases in esterase activity
|
Lloyd, Richard C |
|
2000 |
8 |
7 |
p. 1537-1544 8 p. |
artikel |
21 |
Syntheses and biological activity of C-3′-difluoromethyl-taxoids
|
Ojima, Iwao |
|
2000 |
8 |
7 |
p. 1619-1628 10 p. |
artikel |
22 |
Synthesis and antitumor activity of duocarmycin derivatives
|
Amishiro, Nobuyoshi |
|
2000 |
8 |
7 |
p. 1637-1643 7 p. |
artikel |
23 |
Synthesis and biological activities of 2′-deoxy-2′-fluoro-4′-thioarabinofuranosylpyrimidine and -purine nucleosides
|
Yoshimura, Yuichi |
|
2000 |
8 |
7 |
p. 1545-1558 14 p. |
artikel |
24 |
Synthesis and biological activities of the marine bryozoan alkaloids convolutamines A, C and F, and lutamides A and C
|
Hashima, Hirofumi |
|
2000 |
8 |
7 |
p. 1757-1766 10 p. |
artikel |
25 |
Synthesis and biological evaluations of C-23-modified 26,26,26,27,27,27-F6-vitamin D3 analogues
|
Ikeda, Masahiko |
|
2000 |
8 |
7 |
p. 1809-1817 9 p. |
artikel |
26 |
Synthesis and characterisation of polyamine–poly(ethylene glycol) constructs for DNA binding and gene delivery
|
Garrett, Shane W |
|
2000 |
8 |
7 |
p. 1779-1797 19 p. |
artikel |
27 |
Synthesis and evaluation of fructose analogues as inhibitors of the d-fructose transporter GLUT5
|
Tatibouët, Arnaud |
|
2000 |
8 |
7 |
p. 1825-1833 9 p. |
artikel |
28 |
The design and synthesis of a new tumor-selective fluoropyrimidine carbamate, Capecitabine
|
Shimma, Nobuo |
|
2000 |
8 |
7 |
p. 1697-1706 10 p. |
artikel |
29 |
The synthesis and antibacterial activity of totarol derivatives. part 3: modification of ring-B
|
Evans, Gary B |
|
2000 |
8 |
7 |
p. 1663-1675 13 p. |
artikel |
30 |
The synthesis and antibacterial activity of totarol derivatives. part 2: modifications at C-12 and O-13
|
Evans, Gary B |
|
2000 |
8 |
7 |
p. 1653-1662 10 p. |
artikel |
31 |
Total synthesis and antifungal evaluation of cyclic aminohexapeptides
|
Klein, Larry L. |
|
2000 |
8 |
7 |
p. 1677-1696 20 p. |
artikel |
32 |
Triazene drug metabolites. Part 17: synthesis and plasma hydrolysis of acyloxymethyl carbamate derivatives of antitumour triazenes
|
Carvalho *, Emı́lia |
|
2000 |
8 |
7 |
p. 1719-1725 7 p. |
artikel |