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publishDate:"[2000 TO 2009]"
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PubPharm (88)
1
New 2-aryloxy-3-phenyl-propanoic acids as peroxisome proliferator-activated receptors alpha/gamma dual agonists with improved potency and reduced adverse effects on skeletal muscle function
enthalten in:
Journal of medicinal chemistry
| 2009
von
Fracchiolla, G.
|
Laghezza, A.
|
Piemontese, L.
| +9
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2
Benzothiopyranoindole-based antiproliferative agents : synthesis, cytotoxicity, nucleic acids interaction, and topoisomerases inhibition properties
enthalten in:
Journal of medicinal chemistry
| 2009
von
Dalla Via, L.
|
Magno, S.
|
Gia, O.
| +11
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3
Synthesis, cannabinoid receptor affinity, molecular modeling studies and in vivo pharmacological evaluation of new substituted 1-aryl-5-(1H-pyrrol-1-yl)-1H-pyrazole-3-carboxamides. 2. Effect of the 3-carboxamide substituent on the affinity and selectivity profile
enthalten in:
Bioorganic & medicinal chemistry
| 2009
von
Silvestri, R.
|
Ligresti, A.
|
La Regina, G.
| +12
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4
N6-Cycloalkyl- and N6-bicycloalkyl-C5'(C2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice
enthalten in:
Journal of medicinal chemistry
| 2009
von
Franchetti, P.
|
Cappellacci, L.
|
Vita, P.
| +8
ErratumIn: J Med Chem. 2009 May 28;52(10):3430
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5
Indolylarylsulfones bearing natural and unnatural amino acids. Discovery of potent inhibitors of HIV-1 non-nucleoside wild type and resistant mutant strains reverse transcriptase and coxsackie B4 virus
enthalten in:
Journal of medicinal chemistry
| 2009
von
Piscitelli, F.
|
Coluccia, A.
|
Brancale, A.
| +12
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6
Exploiting the pyrazolo[3,4-d]pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors
enthalten in:
Journal of medicinal chemistry
| 2009
von
La Motta, C.
|
Sartini, S.
|
Mugnaini, L.
| +11
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7
CDC25A and B dual-specificity phosphatase inhibitors : potential agents for cancer therapy
enthalten in:
Current medicinal chemistry
| 2009
von
Lavecchia, A.
|
Di Giovanni, C.
|
Novellino, E.
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8
Exploiting the Pyrazolo[3,4-d]pyrimidin-4-one Ring System as a Useful Template To Obtain Potent Adenosine Deaminase Inhibitors
enthalten in:
Journal of medicinal chemistry
| 2009
von
La Motta, C.
|
Sartini, S.
|
Mugnaini, L.
| +11
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9
Indolylarylsulfones Bearing Natural and Unnatural Amino Acids. Discovery of Potent Inhibitors of HIV-1 Non-Nucleoside Wild Type and Resistant Mutant Strains Reverse Transcriptase and Coxsackie B4 Virus
enthalten in:
Journal of medicinal chemistry
| 2009
von
Piscitelli, F.
|
Coluccia, A.
|
Brancale, A.
| +12
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10
N6-Cycloalkyl- and N6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1 Adenosine Receptor with Antinociceptive Effects in Mice
enthalten in:
Journal of medicinal chemistry
| 2009
von
Franchetti, P.
|
Cappellacci, L.
|
Vita, P.
| +8
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Erscheinungsjahr: 2000-2009
Medienart
88
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71
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17
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17
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Zeitschriftentitel
46
Journal of medicinal chemistry
11
Bioorganic & medicinal chemistry
5
ChemMedChem
3
Notiziario chimico farmaceutico
2
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2
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2
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2
Journal of pharmaceutical and biomedical analysis
1
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1
Anti-cancer agents in medicinal chemistry
1
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1
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1
Current medicinal chemistry / Anti-cancer agents
1
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1
European journal of organic chemistry
1
Journal of molecular graphics & modelling
1
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1
Journal of the American Chemical Society
1
Organic & biomolecular chemistry
1
Tetrahedron
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Thema
55
Journal Article
41
Research Support, Non-U.S. Gov't
17
Ligands
11
Antineoplastic Agents
7
Enzyme Inhibitors
7
Indoles
6
PPAR gamma
6
Pyrroles
5
9007-49-2
5
DNA
5
PPAR alpha
4
Adenosine
4
Aldehyde Reductase
4
EC 1.1.1.21
4
EC 2.7.7.49
4
EC 3.5.1.11
4
HIV Reverse Transcriptase
4
K72T3FS567
4
Oxazines
4
Penicillin Amidase
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Erscheinungszeitraum
2000-2009
15
2009
20
2008
13
2007
12
2006
10
2005
3
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6
2003
4
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3
2001
2
2000
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Englisch
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