| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An investigation of antibody acyl hydrolysis catalysis using a large set of related haptens
|
Odenbaugh, Amy L.
|
|
2000
|
8 |
2 |
p. 413-426
14 p.
|
artikel
|
| 2 |
Benzamides derived from 1,2-diaminocyclopropane as novel ligands for human D2 and D3 dopamine receptors
|
Yang, Donglai
|
|
2000
|
8 |
2 |
p. 321-327
7 p.
|
artikel
|
| 3 |
Density functional and ab initio studies on N-acetyl-duocarmycin SA: insight into its DNA interaction properties
|
Kirschner, Karl N.
|
|
2000
|
8 |
2 |
p. 329-335
7 p.
|
artikel
|
| 4 |
DNA-binding peptides searched from the solid-phase combinatorial library with the use of the magnetic beads attaching the target duplex DNA
|
Rowshon Alam, Md
|
|
2000
|
8 |
2 |
p. 465-473
9 p.
|
artikel
|
| 5 |
Elucidation of strict structural requirements of Brefeldin A as an inducer of differentiation and apoptosis
|
Zhu, Ji-Wen
|
|
2000
|
8 |
2 |
p. 455-463
9 p.
|
artikel
|
| 6 |
gem-Diamine 1-N-iminosugars of l-fucose-type, the extremely potent l-fucosidase inhibitors
|
Shitara, Eiki
|
|
2000
|
8 |
2 |
p. 343-352
10 p.
|
artikel
|
| 7 |
Large scale, liquid phase oligonucleotide synthesis by alkyl H-phosphonate approach
|
Padiya, Kamlesh J.
|
|
2000
|
8 |
2 |
p. 337-342
6 p.
|
artikel
|
| 8 |
Novel potassium channel openers. Part 4: transformation of the 1,4-benzoxazine skeleton into 1,4-benzothiazine, 1,2,3,4-tetrahydroquinoline, 1,2,3,4-tetrahydroquinoxaline, indoline, and 1,5-benzoxazepine
|
Matsumoto, Yuzo
|
|
2000
|
8 |
2 |
p. 393-404
12 p.
|
artikel
|
| 9 |
Paclitaxel esters of malic acid as prodrugs with improved water solubility
|
Damen, Eric W.P
|
|
2000
|
8 |
2 |
p. 427-432
6 p.
|
artikel
|
| 10 |
para-substituted N-Nitroso-N-oxybenzenamine ammonium salts: a new class of redox-sensitive nitric oxide releasing compounds
|
McGill, Andrea D
|
|
2000
|
8 |
2 |
p. 405-412
8 p.
|
artikel
|
| 11 |
Steroidal derived acids as inhibitors of human Cdc25A protein phosphatase
|
Peng, Hairuo
|
|
2000
|
8 |
2 |
p. 299-306
8 p.
|
artikel
|
| 12 |
Syntheses and cytotoxicity evaluation of bis(indolyl)thiazole, bis(indolyl)pyrazinone and bis(indolyl)pyrazine: analogues of cytotoxic marine bis(indole) alkaloid
|
Jiang, Biao
|
|
2000
|
8 |
2 |
p. 363-371
9 p.
|
artikel
|
| 13 |
Synthesis and antitumor activity of duocarmycin derivatives: modification at C-8 position of A-ring pyrrole compounds bearing the simplified DNA-binding groups
|
Amishiro, Nobuyoshi
|
|
2000
|
8 |
2 |
p. 381-391
11 p.
|
artikel
|
| 14 |
Synthesis and biological activities of novel antiallergic agents with 5-lipoxygenase inhibiting action
|
Nakano, Hiroyuki
|
|
2000
|
8 |
2 |
p. 373-380
8 p.
|
artikel
|
| 15 |
Synthesis and Hybridization Properties of DNA–PNA Chimeras Carrying 5-Bromouracil and 5-Methylcytosine
|
Ferrer, Elisenda
|
|
2000
|
8 |
2 |
p. 291-297
7 p.
|
artikel
|
| 16 |
Synthesis and in vitro muscarinic activities of a series of 3-(pyrazol-3-yl)-1-azabicyclo[2.2.2]octanes
|
Plate, Ralf
|
|
2000
|
8 |
2 |
p. 449-454
6 p.
|
artikel
|
| 17 |
Synthesis and pharmacology of a hybrid cannabinoid
|
Huffman, John W.
|
|
2000
|
8 |
2 |
p. 439-447
9 p.
|
artikel
|
| 18 |
Synthesis and structure–activity relationships of a new class of selective EP3 receptor agonist, 13,14-didehydro-16-phenoxy analogues of prostaglandin E1
|
Shimazaki, Youichi
|
|
2000
|
8 |
2 |
p. 353-362
10 p.
|
artikel
|
| 19 |
Synthesis of C2-symmetric guanidino-sugars as potent inhibitors of glycosidases
|
Le Merrer, Yves
|
|
2000
|
8 |
2 |
p. 307-320
14 p.
|
artikel
|
| 20 |
The reactivity of phenolic and non-phenolic residual kraft lignin model compounds with Mn(II)-peroxidase from Lentinula edodes
|
Crestini, Claudia
|
|
2000
|
8 |
2 |
p. 433-438
6 p.
|
artikel
|
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