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/vufind/Search/Results?lookfor=%22Skalitzky%2C+Donald+J.%22&type=Person&sort=year
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PubPharm (22)
1
Discovery of LYC-55716 : A Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor-γ (RORγ) Agonist for Use in Treating Cancer
enthalten in:
Journal of medicinal chemistry
| 2021
von
Aicher, T.
|
Van Huis, C.
|
Hurd, A.
| +23
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2
ISOXAZOLINE DERIVATIVES AS ANTIPARASITIC AGENTS
enthalten in:
Europäisches Patentamt
| 2018
von
VAILLANCOURT VALERIE A
|
CHUBB NATHAN ANTHONY LOGAN
|
CURTIS MICHAEL
| +6
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3
Discovery of potent, selective, bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model, part I : transformation of selective pyrazolodiazepinone phosphodiesterase 4 (PDE4) inhibitors into selective PDE2 inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2013
von
Plummer, M.
|
Cornicelli, J.
|
Roark, H.
| +23
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4
Discovery of potent selective bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model. Part II : optimization studies and demonstration of in vivo efficacy
enthalten in:
Bioorganic & medicinal chemistry letters
| 2013
von
Plummer, M.
|
Cornicelli, J.
|
Roark, H.
| +23
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5
Discovery of potent, selective, bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model, Part I: Transformation of selective pyrazolodiazepinone phosphodiesterase 4 (PDE4) inhibitors into selective PDE2 inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2013
von
Plummer, M.
|
Cornicelli, J.
|
Roark, H.
| +23
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6
Discovery of potent selective bioavailable phosphodiesterase 2 (PDE2) inhibitors active in an osteoarthritis pain model. Part II: Optimization studies and demonstration of in vivo efficacy
enthalten in:
Bioorganic & medicinal chemistry letters
| 2013
von
Plummer, M.
|
Cornicelli, J.
|
Roark, H.
| +23
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7
Design, synthesis, and biological evaluation of novel human 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP) substrates
enthalten in:
Bioorganic & medicinal chemistry letters
| 2005
von
Kung, P.
|
Zehnder, L.
|
Meng, J.
| +8
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8
Design, synthesis, and biological evaluation of novel human 5#8242-deoxy-5#8242-methylthioadenosine phosphorylase (MTAP) substrates
enthalten in:
Bioorganic & medicinal chemistry letters
| 2005
von
Kung, P.
|
Zehnder, L.
|
Meng, J.
| +6
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9
Potentiation of cytotoxic drug activity in human tumour cell lines, by amine-substituted 2-arylbenzimidazole-4-carboxamide PARP-1 inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2004
von
White, A.
|
Curtin, N.
|
Eastman, B.
| +9
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10
Potentiation of cytotoxic drug activity in human tumour cell lines, by amine-substituted 2-arylbenzimidazole-4-carboxamide PARP-1 inhibitors
enthalten in:
Bioorganic & medicinal chemistry letters
| 2004
von
White, A.
|
Curtin, N.
|
Eastman, B.
| +6
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Antineoplastic Agents
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135330-18-6
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7GR28W0FJI
2
Azirines
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Benzimidazoles
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Cyclic Nucleotide Phosphodiesterases, Type 2
2
Dacarbazine
2
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EC 3.1.4.17
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2
Phosphodiesterase Inhibitors
2
Poly(ADP-ribose) Polymerase Inhibitors
2
Temozolomide
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YF1K15M17Y
2
diazipine
1
3C Viral Proteases
1
5'-methylthioadenosine phosphorylase
1
615
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