nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Analogues of 1-(3,10-Dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]-cyclohepta[1,2-b]pyridin-11-yl)piperidine as inhibitors of farnesyl protein transferase
|
Afonso, Adriano |
|
1999 |
7 |
9 |
p. 1845-1855 11 p. |
artikel |
2 |
Anti-AIDS agents. Part 36: 1 17-carboxylated steroids as potential anti-HIV agents
|
Xia, Peng |
|
1999 |
7 |
9 |
p. 1907-1911 5 p. |
artikel |
3 |
Biomimetic degradation of lignin and lignin model compounds by synthetic anionic and cationic water soluble manganese and iron porphyrins
|
Crestini, Claudia |
|
1999 |
7 |
9 |
p. 1897-1905 9 p. |
artikel |
4 |
Chemical modification of apomorphine to discover σ ligands: 6H-dibenzo[b,d]pyran and carbazole analogues
|
Nakazato, Atsuro |
|
1999 |
7 |
9 |
p. 2027-2035 9 p. |
artikel |
5 |
Chemoenzymatic synthesis and antitumor promoting activity of 6′- and 3-esters of 2-O-β-d-glucosylglycerol
|
Colombo, Diego |
|
1999 |
7 |
9 |
p. 1867-1871 5 p. |
artikel |
6 |
CH/π interaction in the conformation of peptides. A database study † † This paper is dedicated to the memory of the late Professor Sir Derek H. R. Barton, the founder of the concept of conformation. The authors sincerely regret the immeasurable loss of an outstanding figure in the world of science.
|
Umezawa, Yoji |
|
1999 |
7 |
9 |
p. 2021-2026 6 p. |
artikel |
7 |
Combinatorial discovery process yields antimicrobial peptoids
|
Ng, Simon |
|
1999 |
7 |
9 |
p. 1781-1785 5 p. |
artikel |
8 |
Corrigendum to “dolichylpyrophosphate oligosaccharides: large-scale isolation and evaluation of oligosaccharyltransferase substrates” [Bioorg. Med. Chem. 7 (1999) 441–447]
|
Gibbs, Barbara S |
|
1999 |
7 |
9 |
p. 2121- 1 p. |
artikel |
9 |
design and synthesis of a novel series of HIV-1 protease inhibitors
|
Takashiro, Eiji |
|
1999 |
7 |
9 |
p. 2105-2114 10 p. |
artikel |
10 |
Direct solid-phase synthesis of octreotide conjugates
|
Hsieh, Hsing-Pang |
|
1999 |
7 |
9 |
p. 1797-1803 7 p. |
artikel |
11 |
Evaluation of [18F]VUF 5000 as a potential PET ligand for brain imaging of the histamine H3 receptor
|
Windhorst, Albert D. |
|
1999 |
7 |
9 |
p. 1761-1767 7 p. |
artikel |
12 |
Heterocyclic analogues of l-citrulline as inhibitors of the isoforms of nitric oxide synthase (NOS) and identification of N δ-(4,5-dihydrothiazol-2-yl)ornithine as a potent inhibitor
|
Ulhaq, Saraj |
|
1999 |
7 |
9 |
p. 1787-1796 10 p. |
artikel |
13 |
Imidazole-containing amino acids as selective inhibitors of nitric oxide synthases
|
Lee, Younghee |
|
1999 |
7 |
9 |
p. 1941-1951 11 p. |
artikel |
14 |
Imidazole substituted biphenyls: A new class of highly potent and in vivo active inhibitors of P450 17 as potential therapeutics for treatment of prostate cancer
|
Wachall, Bertil G. |
|
1999 |
7 |
9 |
p. 1913-1924 12 p. |
artikel |
15 |
In vitro cytotoxicity of 5-aminosubstituted 20(S)-camptothecins. part 1
|
Subrahmanyam, Duvvuri |
|
1999 |
7 |
9 |
p. 2013-2020 8 p. |
artikel |
16 |
Lipase-catalysed regio- and enantioselective deacetylation of 2,4-diacetoxyphenyl alkyl ketones
|
Prasad, Ashok K. |
|
1999 |
7 |
9 |
p. 1973-1977 5 p. |
artikel |
17 |
Lucidenic acid O and lactone, new terpene inhibitors of eukaryotic DNA polymerases from a basidiomycete, ganoderma lucidum
|
Mizushina, Yoshiyuki |
|
1999 |
7 |
9 |
p. 2047-2052 6 p. |
artikel |
18 |
Mechanism of biochemical action of substituted 4-Methylbenzopyran-2-ones. Part 5: Pulse radiolysis studies on the antioxidant action of 7,8-diacetoxy-4-methylcoumarin
|
Raj, Hanumantharao G |
|
1999 |
7 |
9 |
p. 2091-2094 4 p. |
artikel |
19 |
Mechanism of hemolysis and erythrocyte transformation caused by lipogrammistin-A, a lipophilic and acylated cyclic polyamine from the skin secretion of soapfishes (Grammistidae)
|
Kobayashi, Yoshimasa |
|
1999 |
7 |
9 |
p. 2073-2081 9 p. |
artikel |
20 |
Melanocyte-directed enzyme prodrug therapy (MDEPT): development of a targeted treatment for malignant melanoma
|
Jordan, Allan M. |
|
1999 |
7 |
9 |
p. 1775-1780 6 p. |
artikel |
21 |
Modulating pyridoxamine-mediated transamination through a ββα motif peptide scaffold
|
Shogren-Knaak, Michael A |
|
1999 |
7 |
9 |
p. 1993-2002 10 p. |
artikel |
22 |
Molecular modeling of the dopamine D2 and serotonin 5-HT1A receptor binding modes of the enantiomers of 5-OMe-BPAT
|
Homan, Evert J. |
|
1999 |
7 |
9 |
p. 1805-1820 16 p. |
artikel |
23 |
Novel Cobalt Complex Inhibitors of Mitochondrial Calcium Uptake
|
Unitt, John F |
|
1999 |
7 |
9 |
p. 1891-1896 6 p. |
artikel |
24 |
Oligosaccharides corresponding to the regular sequence of heparin: chemical synthesis and interaction with FGF-2
|
Tabeur, Christine |
|
1999 |
7 |
9 |
p. 2003-2012 10 p. |
artikel |
25 |
Resolution, molecular structure and biological activities of the d- and l-enantiomers of potent anti-implantation agent, dl-2-[4-(2-Piperidinoethoxy)phenyl]-3-phenyl-2H-1-benzopyran
|
Hajela, K. |
|
1999 |
7 |
9 |
p. 2083-2090 8 p. |
artikel |
26 |
Semisynthesis and cytotoxicity of amino acetogenins and derivatives
|
Duret, Philippe |
|
1999 |
7 |
9 |
p. 1821-1826 6 p. |
artikel |
27 |
Stereoelectronic features of the cinchona alkaloids determine their differential antimalarial activity
|
Karle, Jean M. |
|
1999 |
7 |
9 |
p. 1769-1774 6 p. |
artikel |
28 |
Structure–activity relationship of HIV-1 protease inhibitors containing α-hydroxy-β-amino acids. Detailed study of P1 site
|
Takashiro, Eiji |
|
1999 |
7 |
9 |
p. 2063-2072 10 p. |
artikel |
29 |
Synthesis and antagonistic activity at muscarinic receptor subtypes of some 2-carbonyl derivatives of diphenidol
|
Varoli, Lucilla |
|
1999 |
7 |
9 |
p. 1837-1844 8 p. |
artikel |
30 |
Synthesis and antifungal activity of coumarins and angular furanocoumarins
|
Sardari, Soroush |
|
1999 |
7 |
9 |
p. 1933-1940 8 p. |
artikel |
31 |
Synthesis and antitumor activity of goniofufurone analogues
|
Mereyala, Hari Babu |
|
1999 |
7 |
9 |
p. 2095-2103 9 p. |
artikel |
32 |
Synthesis and binding properties of photoactivable biotin-conjugated verapamil derivatives for the study of P-170 glycoprotein
|
Teodori, Elisabetta |
|
1999 |
7 |
9 |
p. 1873-1880 8 p. |
artikel |
33 |
Synthesis and biological evaluation of 2-methoxy- and 2-Methylthio-6-[(2′-alkylamino)ethyl]-4(3H)-pyrimidinones with anti-rubella virus activity
|
Botta, Maurizio |
|
1999 |
7 |
9 |
p. 1925-1931 7 p. |
artikel |
34 |
Synthesis and biology of 3′-N-acyl-N-debenzoylpaclitaxel analogues
|
Roh, Eun Joo |
|
1999 |
7 |
9 |
p. 2115-2119 5 p. |
artikel |
35 |
Synthesis and deconvolution of the first combinatorial library of glycosidase inhibitors
|
Lohse, Anders |
|
1999 |
7 |
9 |
p. 1965-1971 7 p. |
artikel |
36 |
Synthesis and evaluation of homofarnesoyl-substituted CAAX-peptidomimetics as farnesyltransferase inhibitors and antiproliferative agents
|
Schlitzer, Martin |
|
1999 |
7 |
9 |
p. 2037-2045 9 p. |
artikel |
37 |
Synthesis and investigation of glycosylated mono- and diarylporphyrins for photodynamic therapy
|
Schell, Christian |
|
1999 |
7 |
9 |
p. 1857-1865 9 p. |
artikel |
38 |
Synthesis of an artificial glycoconjugate polymer carrying Pk-antigenic trisaccharide and its potent neutralization activity against Shiga-like toxin
|
Dohi, Hirofumi |
|
1999 |
7 |
9 |
p. 2053-2062 10 p. |
artikel |
39 |
Synthesis of heparin-like antithrombotics having perphosphorylated thrombin binding domains
|
Buijsman, Rogier C. |
|
1999 |
7 |
9 |
p. 1881-1890 10 p. |
artikel |
40 |
Synthesis of novel progestin–rhenium conjugates as potential ligands for the progesterone receptor
|
Wüst, F. |
|
1999 |
7 |
9 |
p. 1827-1835 9 p. |
artikel |
41 |
The synthesis and antibacterial activity of totarol derivatives. part 1: modifications of ring-C and pro-drugs
|
Evans, Gary B |
|
1999 |
7 |
9 |
p. 1953-1964 12 p. |
artikel |
42 |
tRNAPhe binds aminoglycoside antibiotics
|
Kirk, Sarah R. |
|
1999 |
7 |
9 |
p. 1979-1991 13 p. |
artikel |