Search Results - "Dutia, Minu" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Optimization of 4-Phenylamino-3-quinolinecarbonitriles as Potent Inhibitors of Src Kinase Activity

Optimization of 4-Phenylamino-3-quinolinecarbonitriles as Potent Inhibitors of Src Kinase Activity

by Boschelli, Diane H, Ye, Fei, Wang, Yanong D, Dutia, Minu, Johnson, Steve L, Wu, Biqi, Miller, Karen, Powell, Dennis W, Yaczko, Deanna, Young, Mairead, Tischler, Mark, Arndt, Kim, Discafani, Carolyn, Etienne, Carlo, Gibbons, Jay, Grod, Janet, Lucas, Judy, Weber, Jennifer M, Boschelli, Frank
Published in Journal of medicinal chemistry (08.11.2001)

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Journal Article

Synthesis and Src Kinase Inhibitory Activity of a Series of 4-Phenylamino-3-quinolinecarbonitriles

Synthesis and Src Kinase Inhibitory Activity of a Series of 4-Phenylamino-3-quinolinecarbonitriles

by Boschelli, Diane H, Wang, Yanong D, Ye, Fei, Wu, Biqi, Zhang, Nan, Dutia, Minu, Powell, Dennis W, Wissner, Allan, Arndt, Kim, Weber, Jennifer M, Boschelli, Frank
Published in Journal of medicinal chemistry (01.03.2001)

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Journal Article

Indazolylpyrazolopyrimidine as Highly Potent B-Raf Inhibitors with in Vivo Activity

Indazolylpyrazolopyrimidine as Highly Potent B-Raf Inhibitors with in Vivo Activity

by Wang, Xiaolun, Berger, Dan M, Salaski, Edward J, Torres, Nancy, Dutia, Minu, Hanna, Cilien, Hu, Yongbo, Levin, Jeremy I, Powell, Dennis, Wojciechowicz, Donald, Collins, Karen, Frommer, Eileen, Lucas, Judy
Published in Journal of medicinal chemistry (11.11.2010)

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Lead identification to generate 3-cyanoquinoline inhibitors of insulin-like growth factor receptor (IGF-1R) for potential use in cancer treatment

Lead identification to generate 3-cyanoquinoline inhibitors of insulin-like growth factor receptor (IGF-1R) for potential use in cancer treatment

by Miller, Lori M., Mayer, Scott C., Berger, Dan M., Boschelli, Diane H., Boschelli, Frank, Di, Li, Du, Xuemei, Dutia, Minu, Floyd, Middleton B., Johnson, Mark, Kenny, Cynthia Hess, Krishnamurthy, Girija, Moy, Franklin, Petusky, Susan, Tkach, Diane, Torres, Nancy, Wu, Biqi, Xu, Weixin
Published in Bioorganic & medicinal chemistry letters (2009)

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Disodium (R,R)-5-[2-[[2-(3-chlorophenyl)-2-hydroxyethyl]amino]propyl]-1,3-benzodioxole-2,2-dicarboxylate (CL 316,243). A potent .beta.-adrenergic agonist virtually specific for .beta.3 receptors. A promising antidiabetic and antiobesity agent

Disodium (R,R)-5-[2-[[2-(3-chlorophenyl)-2-hydroxyethyl]amino]propyl]-1,3-benzodioxole-2,2-dicarboxylate (CL 316,243). A potent .beta.-adrenergic agonist virtually specific for .beta.3 receptors. A promising antidiabetic and antiobesity agent

by Bloom, Jonathan D, Dutia, Minu D, Johnson, Bernard D, Wissner, Allan, Burns, Michael G, Largis, Elwood E, Dolan, Jo Alene, Claus, Thomas H
Published in Journal of medicinal chemistry (01.08.1992)

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Journal Article

Potential antiatherosclerotic agents. 6. Hypocholesterolemic trisubstituted urea analogs

Potential antiatherosclerotic agents. 6. Hypocholesterolemic trisubstituted urea analogs

by DeVries, Vern G, Bloom, Jonathan D, Dutia, Minu D, Katocs, Andrew S, Largis, Elwood E
Published in Journal of medicinal chemistry (01.10.1989)

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Journal Article

Synthesis of 7-( E)-alkenyl-4-amino-3-quinolinecarbonitriles via Pd-mediated Heck, Stille, and Suzuki reactions

Synthesis of 7-( E)-alkenyl-4-amino-3-quinolinecarbonitriles via Pd-mediated Heck, Stille, and Suzuki reactions

by Wang, Yanong D., Dutia, Minu, Floyd, M. Brawner, Prashad, Amar S., Berger, Dan, Lin, Melissa
Published in Tetrahedron (03.01.2009)

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Non-hinge-binding pyrazolo[1,5- a]pyrimidines as potent B-Raf kinase inhibitors

Non-hinge-binding pyrazolo[1,5- a]pyrimidines as potent B-Raf kinase inhibitors

by Berger, Dan M., Torres, Nancy, Dutia, Minu, Powell, Dennis, Ciszewski, Greg, Gopalsamy, Ariamala, Levin, Jeremy I., Kim, Kyung-Hee, Xu, Weixin, Wilhelm, James, Hu, YongBo, Collins, Karen, Feldberg, Larry, Kim, Steven, Frommer, Eileen, Wojciechowicz, Donald, Mallon, Robert
Published in Bioorganic & medicinal chemistry letters (01.12.2009)

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Novel pyrazolopyrimidines as highly potent B-Raf inhibitors

Novel pyrazolopyrimidines as highly potent B-Raf inhibitors

by Di Grandi, Martin J., Berger, Dan M., Hopper, Darrin W., Zhang, Chunchun, Dutia, Minu, Dunnick, Alejandro L., Torres, Nancy, Levin, Jeremy I., Diamantidis, George, Zapf, Christoph W., Bloom, Jonathan D., Hu, YongBo, Powell, Dennis, Wojciechowicz, Donald, Collins, Karen, Frommer, Eileen
Published in Bioorganic & medicinal chemistry letters (15.12.2009)

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Observation of differential reactivity of cyclic amines in SN2 and SNAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors

Observation of differential reactivity of cyclic amines in SN2 and SNAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors

by Hopper, Darrin W., Dutia, Minu, Berger, Dan M., Powell, Dennis W.
Published in Tetrahedron letters (01.01.2008)

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Observation of differential reactivity of cyclic amines in S(N)2 and SNAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors

Observation of differential reactivity of cyclic amines in S(N)2 and SNAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors

by Hopper, Darrin W., Dutia, Minu, Berger, Dan M., Powell, Dennis W.
Published in Tetrahedron letters (01.01.2008)

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Journal Article

4-Anilino-7-alkenylquinoline-3-carbonitriles as potent MEK1 kinase inhibitors

4-Anilino-7-alkenylquinoline-3-carbonitriles as potent MEK1 kinase inhibitors

by Berger, Dan M., Dutia, Minu, Powell, Dennis, Floyd, Middleton B., Torres, Nancy, Mallon, Robert, Wojciechowicz, Donald, Kim, Steven, Feldberg, Larry, Collins, Karen, Chaudhary, Inder
Published in Bioorganic & medicinal chemistry (15.10.2008)

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Observation of differential reactivity of cyclic amines in S N2 and S NAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors

Observation of differential reactivity of cyclic amines in S N2 and S NAr displacement reactions in the course of synthesizing C-6, C-7 substituted quinolinecarbonitrile MEK1 kinase inhibitors

by Hopper, Darrin W., Dutia, Minu, Berger, Dan M., Powell, Dennis W.
Published in Tetrahedron letters (2008)

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Journal Article

Novel Multidrug Resistance Reversal Agents

Novel Multidrug Resistance Reversal Agents

by Berger, Dan, Citarella, Ron, Dutia, Minu, Greenberger, Lee, Hallett, William, Paul, Rolf, Powell, Dennis
Published in Journal of medicinal chemistry (17.06.1999)

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Journal Article

4-Anilino-7-alkenylquinoIine-3-carbonitriles as potent MEI1 kinase inhibitors

4-Anilino-7-alkenylquinoIine-3-carbonitriles as potent MEI1 kinase inhibitors

by BERGER, Dan M, DUTIA, Minu, CHAUDHARY, Inder, POWELL, Dennis, FLOYD, Middleton B, TORRES, Nancy, MALLON, Robert, WOJCIECHOWICZ, Donald, KIM, Steven, FELDBERG, Larry, COLLINS, Karen
Published in Bioorganic & medicinal chemistry (2008)

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4-Anilino-7,8-dialkoxybenzo[g]quinoline-3-carbonitriles as Potent Src Kinase Inhibitors

4-Anilino-7,8-dialkoxybenzo[g]quinoline-3-carbonitriles as Potent Src Kinase Inhibitors

by Berger, Dan M, Dutia, Minu, Birnberg, Gary, Powell, Dennis, Boschelli, Diane H, Wang, Yanong D, Ravi, Malini, Yaczko, Deanna, Golas, Jennifer, Lucas, Judy, Boschelli, Frank
Published in Journal of medicinal chemistry (22.09.2005)

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Potential antiatherosclerotic agents. 5. An acyl-coenzyme A:cholesterol O-acyltransferase inhibitor with hypocholesterolemic activity

Potential antiatherosclerotic agents. 5. An acyl-coenzyme A:cholesterol O-acyltransferase inhibitor with hypocholesterolemic activity

by DeVries, Vern G, Schaffer, Sheldon A, Largis, Elwood E, Dutia, Minu D, Wang, Ching Hua, Bloom, Jonathan D, Katocs, Andrew S
Published in Journal of medicinal chemistry (01.07.1986)

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Journal Article

Substituted 4-anilino-7-phenyl-3-quinolinecarbonitriles as Src kinase inhibitors

Substituted 4-anilino-7-phenyl-3-quinolinecarbonitriles as Src kinase inhibitors

by BERGER, Dan, DUTIA, Minu, POWELL, Dennis, WISSNER, Allan, DEMORIN, Frenel, RAIFELD, Yuri, WEBER, Jennifer, BOSCHELLI, Frank
Published in Bioorganic & medicinal chemistry letters (21.10.2002)

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Disodium (R,R)-5[2-[[2-γ(3-chlorophenyl)-2-hydroxyethyl]-amino]propyl]-1,3-benzodioxole-2,2-dicarboxylate (CL 316,243). A potent β-adrenergic agonist virtually specific for β3 receptors. A promising antidiabetic and antiobesity agent

Disodium (R,R)-5[2-[[2-γ(3-chlorophenyl)-2-hydroxyethyl]-amino]propyl]-1,3-benzodioxole-2,2-dicarboxylate (CL 316,243). A potent β-adrenergic agonist virtually specific for β3 receptors. A promising antidiabetic and antiobesity agent

by BLOOM, J. D, DUTIA, M. D, JOHNSON, B. D, WISSNER, A, BURNS, M. G, LARGIS, E. E, DOLAN, J. A, CLAUS, T. H
Published in Journal of medicinal chemistry (01.08.1992)

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Journal Article

BRIDGED, BICYCLIC HETEROCYCLIC OR SPIRO BICYCLIC HETEROCYCLIC DERIVATIVES OF PYRAZOLO[1,5-A]PYRIMIDINES, METHODS FOR PREPARATION AND USES THEREOF

BRIDGED, BICYCLIC HETEROCYCLIC OR SPIRO BICYCLIC HETEROCYCLIC DERIVATIVES OF PYRAZOLO[1,5-A]PYRIMIDINES, METHODS FOR PREPARATION AND USES THEREOF

by TORRES NANCY, LEVIN JEREMY IAN, HOPPER DARRIN WILLIAM, WANG XIAOLUN, ZHANG CHUNCHUN, BERGER DAN MAARTEN, DUTIA MINU DHANJISH, DI GRANDI MARTIN JOSEPH, DUNNICK ALEJANDRO LEE
Year of Publication 24.11.2010

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