nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Design, synthesis, and biological evaluation of anti-HIV double-drugs
|
Matsumoto, Hikaru |
|
2001 |
9 |
6 |
p. 1589-1600 12 p. |
artikel |
2 |
Dicaffeoyl- or digalloyl pyrrolidine and furan derivatives as HIV integrase inhibitors
|
Hwang, Dong Jin |
|
2001 |
9 |
6 |
p. 1429-1437 9 p. |
artikel |
3 |
Dicationic dithiocarbamate carbapenems with anti-MRSA activity
|
Imamura, Hideaki |
|
2001 |
9 |
6 |
p. 1571-1578 8 p. |
artikel |
4 |
3D-QSAR Analysis of 2,4,5- and 2,3,4,5-substituted imidazoles as potent and nontoxic modulators of P-glycoprotein mediated MDR
|
Kim, Ki H |
|
2001 |
9 |
6 |
p. 1517-1523 7 p. |
artikel |
5 |
Effect of C-ring modifications in benzo[c]quinolizin-3-ones, new selective inhibitors of human 5α-reductase 1
|
Guarna, Antonio |
|
2001 |
9 |
6 |
p. 1385-1393 9 p. |
artikel |
6 |
Graphical Abstracts
|
|
|
2001 |
9 |
6 |
p. VII-XIII nvt p. |
artikel |
7 |
Identification of new triarylethylene oxyalkanoic acid analogues as bone selective estrogen mimetics
|
Rubin, Valeria N |
|
2001 |
9 |
6 |
p. 1579-1587 9 p. |
artikel |
8 |
Inhibition of serine proteases by functionalized sulfonamides coupled to the 1,2,5-thiadiazolidin-3-one 1,1 dioxide scaffold
|
Groutas, William C |
|
2001 |
9 |
6 |
p. 1543-1548 6 p. |
artikel |
9 |
Introduction of the new dipeptide isostere 7-endo-BtA as reverse turn inducer in a Bowman-Birk proteinase inhibitor
|
Scarpi, Dina |
|
2001 |
9 |
6 |
p. 1625-1632 8 p. |
artikel |
10 |
Investigation of the biological mode of action of clerocidin using whole cell assays
|
Jamora, Colin |
|
2001 |
9 |
6 |
p. 1365-1370 6 p. |
artikel |
11 |
Melanocyte-Directed enzyme prodrug therapy (MDEPT)
|
Jordan, Allan M. |
|
2001 |
9 |
6 |
p. 1549-1558 10 p. |
artikel |
12 |
Molecular cloning, expression and characterization of the first three genes in the mevalonate-independent isoprenoid pathway in Streptomyces coelicolor
|
Cane, David E |
|
2001 |
9 |
6 |
p. 1467-1477 11 p. |
artikel |
13 |
Novel mimics of sialyl Lewis X
|
Marinier, Anne |
|
2001 |
9 |
6 |
p. 1395-1427 33 p. |
artikel |
14 |
N-Terminal carboxyl and tetrazole-containing amides as adjuvants to Grb2 SH2 domain ligand binding
|
Burke Jr, Terrence R |
|
2001 |
9 |
6 |
p. 1439-1445 7 p. |
artikel |
15 |
Salen complexes with bulky substituents as useful tools for biomimetic phenol oxidation research
|
Haikarainen, Anssi |
|
2001 |
9 |
6 |
p. 1633-1638 6 p. |
artikel |
16 |
Selenotyrosine and related phenylalanine derivatives
|
Ganther, Howard E |
|
2001 |
9 |
6 |
p. 1459-1466 8 p. |
artikel |
17 |
Signaling pathways and effector mechanisms pre-programmed cell death
|
Blatt, Neal B. |
|
2001 |
9 |
6 |
p. 1371-1384 14 p. |
artikel |
18 |
Structures of withanosides I, II, III, IV, V, VI, and VII, new withanolide glycosides, from the roots of Indian Withania somnifera Dunal. and inhibitory activity for tachyphylaxis to clonidine in isolated guinea-pig ileum
|
Matsuda, Hisashi |
|
2001 |
9 |
6 |
p. 1499-1507 9 p. |
artikel |
19 |
Studies on selectin blocker. 9. SARs of non-sugar selectin blocker against E-, P-, L-selectin bindings
|
Moriyama, Hideki |
|
2001 |
9 |
6 |
p. 1479-1491 13 p. |
artikel |
20 |
Synthesis and antimicrobial activity of the symmetric dimeric form of temporin A based on 3-N,N-di(3-aminopropyl)amino propanoic acid as the branching unit
|
Hujakka, Helena |
|
2001 |
9 |
6 |
p. 1601-1607 7 p. |
artikel |
21 |
Synthesis and DNA nicking studies of a novel cyclic peptide: Cyclo[Lys-Trp-Lys-Ahx-]
|
Cheng, Chong-Teh |
|
2001 |
9 |
6 |
p. 1493-1498 6 p. |
artikel |
22 |
Synthesis and phosphodiesterase 5 inhibitory activity of novel phenyl ring modified sildenafil analogues
|
Kim, Dae-Kee |
|
2001 |
9 |
6 |
p. 1609-1616 8 p. |
artikel |
23 |
Synthesis and preliminary pharmacological evaluation of 5-Hydroxy- and 5,6-dihydroxy-1,2,3,7,12,12a-hexahydrobenzo[5,6]cyclohepta[1,2,3-ij]isoquinoline derivatives as dopamine receptor ligands
|
Cingolani, Gian Mario |
|
2001 |
9 |
6 |
p. 1447-1458 12 p. |
artikel |
24 |
Synthesis and Properties of Triple Helix-Forming Oligodeoxyribonucleotides containing 7-Chloro-7-deaza-2′-deoxyguanosine
|
Aubert, Yves |
|
2001 |
9 |
6 |
p. 1617-1624 8 p. |
artikel |
25 |
Synthesis and structure–mutagenicity relationship of benzo-annulated cyclopentaphenanthrenes
|
Marrocchi, Assunta |
|
2001 |
9 |
6 |
p. 1509-1515 7 p. |
artikel |
26 |
Synthesis and study of a cyclic angiotensin II antagonist analogue reveals the role of π*–π* interactions in the C-terminal aromatic residue for agonist activity and its structure resemblance with AT1 non-peptide antagonists
|
Polevaya, Ludmila |
|
2001 |
9 |
6 |
p. 1639-1647 9 p. |
artikel |
27 |
Synthesis, chemical and enzymatic reactivity, and toxicity of dithymidylyl-3′,5′-phosphorofluoridate and -phosphorothiofluoridate
|
Misiura, Konrad |
|
2001 |
9 |
6 |
p. 1525-1532 8 p. |
artikel |
28 |
Synthesis, cytotoxicity, DNA interaction and topoisomerase II inhibition properties of tetrahydropyrrolo[3,4-a]carbazole-1,3-dione and tetrahydropyrido-[3,2-b]pyrrolo[3,4-g]indole-1,3-dione derivatives
|
Joseph, Benoı̂t |
|
2001 |
9 |
6 |
p. 1533-1541 9 p. |
artikel |
29 |
Synthesis, molecular modeling and QSAR studies in chiral 2,3-disubstituted-1,2,3,4-tetrahydro-9H-pyrido(3,4-b)indoles as potential modulators of opioid antinociception
|
Saxena, Anil K |
|
2001 |
9 |
6 |
p. 1559-1570 12 p. |
artikel |