nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A biaryl peptide crosslink in a MetJ peptide model confers cooperative, nonspecific binding to DNA that ablates both repressor binding and In vitro transcription
|
Yoburn, Joshua C |
|
2003 |
11 |
6 |
p. 811-816 6 p. |
artikel |
2 |
A frame shifted disulfide bridged analogue of angiotensin II
|
Schmidt, Boris |
|
2003 |
11 |
6 |
p. 985-990 6 p. |
artikel |
3 |
Antitumor agents 220. Antitumor-Promoting effects of cimigenol and related compounds on Epstein–Barr virus activation and two-stage mouse skin carcinogenesis
|
Sakurai, Nobuko |
|
2003 |
11 |
6 |
p. 1137-1140 4 p. |
artikel |
4 |
A substrate variant as a high-affinity, reversible inhibitor: insight from the X-ray structure of cilastatin bound to membrane dipeptidase
|
Smyth, Timothy P |
|
2003 |
11 |
6 |
p. 991-998 8 p. |
artikel |
5 |
Bis-4-aminoquinolines: novel triple-helix DNA intercalators and antagonists of immunostimulatory CpG-oligodeoxynucleotides
|
Strekowski, Lucjan |
|
2003 |
11 |
6 |
p. 1079-1085 7 p. |
artikel |
6 |
Chiral 3,3′-(1,2-Ethanediyl)-bis[2-(3,4-dimethoxyphenyl)-4-thiazolidinones] with anti-inflammatory activity. Part 11: Evaluation of COX-2 selectivity and modelling
|
Vigorita, M.G |
|
2003 |
11 |
6 |
p. 999-1006 8 p. |
artikel |
7 |
Curcumin differentially modulates mRNA profiles in Jurkat T and human peripheral blood mononuclear cells
|
Gertsch, Jürg |
|
2003 |
11 |
6 |
p. 1057-1063 7 p. |
artikel |
8 |
Design and synthesis of HIV-1 protease inhibitors. Novel tetrahydrofuran P2/P2′-groups interacting with Asp29/30 of the HIV-1 protease. Determination of binding from X-ray crystal structure of inhibitor protease complex
|
Oscarsson, Karin |
|
2003 |
11 |
6 |
p. 1107-1115 9 p. |
artikel |
9 |
6-Dimethylamino 1H-Pyrazolo[3,4-d]pyrimidine derivatives as new inhibitors of inflammatory mediators in intact cells
|
Quintela, José M |
|
2003 |
11 |
6 |
p. 863-868 6 p. |
artikel |
10 |
2,3-Disubstituted quinuclidines as a novel class of dopamine transporter inhibitors
|
Sakamuri, Sukumar |
|
2003 |
11 |
6 |
p. 1123-1136 14 p. |
artikel |
11 |
Editorial Board
|
|
|
2003 |
11 |
6 |
p. IFC- 1 p. |
artikel |
12 |
Graphical Abstracts
|
|
|
2003 |
11 |
6 |
p. 801-809 9 p. |
artikel |
13 |
Ibogaine analogues. Synthesis and preliminary pharmacological evaluation of 7-heteroaryl-2-azabicyclo[2.2.2]oct-7-enes
|
Passarella, Daniele |
|
2003 |
11 |
6 |
p. 1007-1014 8 p. |
artikel |
14 |
Inhibition of nucleoside transport By new analogues of nitrobenzylthioinosine
|
Deghati, Paymaneh Y.F |
|
2003 |
11 |
6 |
p. 899-908 10 p. |
artikel |
15 |
Mechanism of biochemical action of substituted 4-methylbenzopyran-2-ones. Part 10: identification of inhibitors for the liver microsomal acetoxycoumarin: protein transacetylase
|
Raj, Hanumantharao G |
|
2003 |
11 |
6 |
p. 1015-1019 5 p. |
artikel |
16 |
Modes of antifungal action of alkanols against Saccharomyces cerevisiae
|
Kubo, Isao |
|
2003 |
11 |
6 |
p. 1117-1122 6 p. |
artikel |
17 |
New fluorinated derivatives as esterase inhibitors. Synthesis, hydration and crossed specificity studies
|
Quero, Carmen |
|
2003 |
11 |
6 |
p. 1047-1055 9 p. |
artikel |
18 |
New insights into protein crosslinking via the Maillard reaction: structural requirements, the effect on enzyme function, and predicted efficacy of crosslinking inhibitors as anti-ageing therapeutics
|
Miller, Antonia G |
|
2003 |
11 |
6 |
p. 843-852 10 p. |
artikel |
19 |
N-Morpholino- and N-diethyl-analogues of palmitoylethanolamide increase the sensitivity of transfected human vanilloid receptors to activation by anandamide without affecting fatty acid amidohydrolase activity
|
Vandevoorde, Séverine |
|
2003 |
11 |
6 |
p. 817-825 9 p. |
artikel |
20 |
ortho-Halogen naphthaleins as specific inhibitors of Lactobacillus casei thymidylate synthase. Conformational properties and biological activity
|
Ghelli, Stefano |
|
2003 |
11 |
6 |
p. 951-963 13 p. |
artikel |
21 |
Prodrugs of biologically active phosphate esters
|
Schultz, Carsten |
|
2003 |
11 |
6 |
p. 885-898 14 p. |
artikel |
22 |
Purification and characterization of an alkaline lipase from a newly isolated Pseudomonas mendocina PK-12CS and chemoselective hydrolysis of fatty acid ester † † CDRI Communication No. 6212.
|
Jinwal, Umesh K |
|
2003 |
11 |
6 |
p. 1041-1046 6 p. |
artikel |
23 |
Role of solution conformation and flexibility of short peptide ligands that bind to the p56lck SH2 domain
|
Dekker, Frank J |
|
2003 |
11 |
6 |
p. 941-949 9 p. |
artikel |
24 |
Solid-phase library synthesis of reversed-statine type inhibitors of the malarial aspartyl proteases plasmepsin I and II
|
Dahlgren, Anders |
|
2003 |
11 |
6 |
p. 827-841 15 p. |
artikel |
25 |
Structure–activity relationships of xanthene carboxamides, novel CCR1 receptor antagonists
|
Naya, Akira |
|
2003 |
11 |
6 |
p. 875-884 10 p. |
artikel |
26 |
Substituted heterocyclic thiourea compounds as a new class of anti-allergic agents inhibiting IgE/FcεRI receptor mediated mast cell leukotriene release
|
Venkatachalam, T.K |
|
2003 |
11 |
6 |
p. 1095-1105 11 p. |
artikel |
27 |
Synthesis and antioxidant properties of a new lipophilic ascorbic acid analogue
|
Cotelle, Philippe |
|
2003 |
11 |
6 |
p. 1087-1093 7 p. |
artikel |
28 |
Synthesis and anti-tumor-promoting activity of glycoglycerolipid analogues lacking the glycerol backbone
|
Colombo, Diego |
|
2003 |
11 |
6 |
p. 909-912 4 p. |
artikel |
29 |
Synthesis and bioactivity of 4,10-dimethyl-pyridino[2,3-h]quinolin-2(1H)-one-9-carboxylic acid and its esters
|
Zhang, Qian |
|
2003 |
11 |
6 |
p. 1031-1034 4 p. |
artikel |
30 |
Synthesis and biological activity of 3,3-Diamino-sulfonylacrylonitriles as novel inhibitors of glucose induced insulin secretion from beta cells
|
Tagmose, Tina M |
|
2003 |
11 |
6 |
p. 931-940 10 p. |
artikel |
31 |
Synthesis and cytotoxicity of dihydroartemisinin ethers containing cyanoarylmethyl group
|
Li, Ying |
|
2003 |
11 |
6 |
p. 977-984 8 p. |
artikel |
32 |
Synthesis and DNA binding studies of a new asymmetric cyanine dye binding in the minor groove of [poly(dA-dT)]2
|
Karlsson, H.Jonas |
|
2003 |
11 |
6 |
p. 1035-1040 6 p. |
artikel |
33 |
Synthesis and evaluation of trans 3,4-cyclopropyl l-arginine analogues as isoform selective inhibitors of nitric oxide synthase
|
Fishlock, Dan |
|
2003 |
11 |
6 |
p. 869-873 5 p. |
artikel |
34 |
Synthesis and growth inhibition activity of α-Bromoacrylic heterocyclic and benzoheterocyclic derivatives of distamycin A modified on the amidino moiety
|
Baraldi, Pier Giovanni |
|
2003 |
11 |
6 |
p. 965-975 11 p. |
artikel |
35 |
Synthesis and structure–affinity relationship investigations of 5-aminomethyl and 5-carbamoyl analogues of the antipsychotic sertindole. A new class of selective α1 adrenoceptor antagonists
|
Balle, Thomas |
|
2003 |
11 |
6 |
p. 1065-1078 14 p. |
artikel |
36 |
Synthesis, characterization and in vitro anti-invasive activity screening of polyphenolic and heterocyclic compounds
|
Parmar, Virinder S |
|
2003 |
11 |
6 |
p. 913-929 17 p. |
artikel |
37 |
The role of dicarbonyl compounds in non-enzymatic crosslinking: a structure–activity study
|
Meade, Susie J |
|
2003 |
11 |
6 |
p. 853-862 10 p. |
artikel |
38 |
Water soluble prodrugs of the antitumor agent 3-[(3-amino-4-methoxy)phenyl]-2-(3,4,5-trimethoxyphenyl)cyclopent-2-ene-1-one
|
Nam, Nguyen-Hai |
|
2003 |
11 |
6 |
p. 1021-1029 9 p. |
artikel |