메뉴 건너뛰기




Volumn 5, Issue 11, 2006, Pages 903-918

PI3Kγ inhibition: Towards an 'aspirin of the 21st century'?

Author keywords

[No Author keywords available]

Indexed keywords

2 AMINOTHIAZOLE DERIVATIVE; 2 MORPHOLINO 8 PHENYLCHROMONE; 2,4 THIAZOLIDINEDIONE DERIVATIVE; ACETYLSALICYLIC ACID; BENZOXAZINE DERIVATIVE; BENZOXAZINONE DERIVATIVE; IMIDAZO[1,2 C]QUINAZOLINE DERIVATIVE; MYRICETIN; NEUTRALIZING ANTIBODY; NORVIRIDIN; PHOSPHATIDYLINOSITOL 3 KINASE; PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR; PHOSPHATIDYLINOSITOL 3 KINASE P100 GAMMA; PHOSPHOTRANSFERASE INHIBITOR; PROSTAGLANDIN SYNTHASE INHIBITOR; QUERCETIN; STAUROSPORINE; TETRAZOLE DERIVATIVE; TG 100 115; UNCLASSIFIED DRUG; VIRIDIN; WORTMANNIN; CHEMOKINE; CHEMOKINE RECEPTOR; ENZYME INHIBITOR; NONSTEROID ANTIINFLAMMATORY AGENT;

EID: 33750525089     PISSN: 14741776     EISSN: 14741784     Source Type: Journal    
DOI: 10.1038/nrd2145     Document Type: Review
Times cited : (223)

References (160)
  • 1
    • 33750524111 scopus 로고    scopus 로고
    • PI3-kinase inhibition: A target for therapeutic intervention
    • Finan, P. M. & Ward, S. G. PI3-kinase inhibition: A target for therapeutic intervention. Protein Tyrosine Kinases 53-69 (2006).
    • (2006) Protein Tyrosine Kinases , pp. 53-69
    • Finan, P.M.1    Ward, S.G.2
  • 2
    • 15044338824 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase in disease: Timing, location, and scaffolding
    • Wymann, M. P. & Marone, R. Phosphoinositide 3-kinase in disease: Timing, location, and scaffolding. Curr. Opin. Cell Biol. 17, 141-149 (2005).
    • (2005) Curr. Opin. Cell Biol. , vol.17 , pp. 141-149
    • Wymann, M.P.1    Marone, R.2
  • 3
    • 25644454404 scopus 로고    scopus 로고
    • Pharmaceuticals: A new grammar for drug discovery
    • Fishman, M. C. & Porter, J. A. Pharmaceuticals: A new grammar for drug discovery. Nature 437, 491-493 (2005).
    • (2005) Nature , vol.437 , pp. 491-493
    • Fishman, M.C.1    Porter, J.A.2
  • 4
    • 0037205048 scopus 로고    scopus 로고
    • The phosphoinositide 3-kinase pathway
    • Cantley, L. C. The phosphoinositide 3-kinase pathway. Science 296, 1655-1657 (2002).
    • (2002) Science , vol.296 , pp. 1655-1657
    • Cantley, L.C.1
  • 5
    • 0033605718 scopus 로고    scopus 로고
    • The role of phosphoinositide 3-kinase lipid products in cell function
    • Rameh, L. E. & Cantley, L. C. The role of phosphoinositide 3-kinase lipid products in cell function. J. Biol. Chem. 274, 8347-8350 (1999).
    • (1999) J. Biol. Chem. , vol.274 , pp. 8347-8350
    • Rameh, L.E.1    Cantley, L.C.2
  • 6
    • 33750514221 scopus 로고    scopus 로고
    • Fishing for pharmaceutically relevant phosphoinositide-binding proteins using chemical proteomics
    • Pasquali, C. & Rommel, C. Fishing for pharmaceutically relevant phosphoinositide-binding proteins using chemical proteomics. Functional Lipidomics 211-241 (2006).
    • (2006) Functional Lipidomics , pp. 211-241
    • Pasquali, C.1    Rommel, C.2
  • 7
    • 5644222583 scopus 로고    scopus 로고
    • Involvement of phosphoinositide 3-kinase γ, Rac, and PAK signaling in chemokine-induced macrophage migration
    • Weiss-Haljiti, C. et al. Involvement of phosphoinositide 3-kinase γ, Rac, and PAK signaling in chemokine-induced macrophage migration. J. Biol. Chem. 41, 43273-84 (2004).
    • (2004) J. Biol. Chem. , vol.41 , pp. 43273-43284
    • Weiss-Haljiti, C.1
  • 9
    • 0034911881 scopus 로고    scopus 로고
    • Synthesis and function of 3-phosphorylated inositol lipids
    • Vanhaesebroeck, B. et al. Synthesis and function of 3-phosphorylated inositol lipids. Annu. Rev. Biochem. 70, 535-602 (2001).
    • (2001) Annu. Rev. Biochem. , vol.70 , pp. 535-602
    • Vanhaesebroeck, B.1
  • 10
    • 33746257209 scopus 로고    scopus 로고
    • The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism
    • Engelman J. A., Luo J., Cantley L. C. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nature Rev. Genet. 7, 606-619 (2006).
    • (2006) Nature Rev. Genet. , vol.7 , pp. 606-619
    • Engelman, J.A.1    Luo, J.2    Cantley, L.C.3
  • 11
    • 0033574429 scopus 로고    scopus 로고
    • Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110α subunit of phosphoinositide 3-kinase
    • Bi, L., Okabe, I., Bernard, D. J., Wynshaw-Boris, A. & Nussbaum, R. L. Proliferative defect and embryonic lethality in mice homozygous for a deletion in the p110α subunit of phosphoinositide 3-kinase. J. Biol. Chem. 274, 10963-10968 (1999).
    • (1999) J. Biol. Chem. , vol.274 , pp. 10963-10968
    • Bi, L.1    Okabe, I.2    Bernard, D.J.3    Wynshaw-Boris, A.4    Nussbaum, R.L.5
  • 12
    • 0036185944 scopus 로고    scopus 로고
    • Early embryonic lethality in mice deficient in the p110β catalytic subunit of PI 3-kinase
    • Bi, L., Okabe, I., Bernard, D. J. & Nussbaum, R. L. Early embryonic lethality in mice deficient in the p110β catalytic subunit of PI 3-kinase. Mammalian Genome 13, 169-172 (2002).
    • (2002) Mammalian Genome , vol.13 , pp. 169-172
    • Bi, L.1    Okabe, I.2    Bernard, D.J.3    Nussbaum, R.L.4
  • 13
    • 33744990592 scopus 로고    scopus 로고
    • Critical role for the p110α phosphoinositide-3-OH kinase in growth and metabolic regulation
    • Foukas, L. C., et al. Critical role for the p110α phosphoinositide-3-OH kinase in growth and metabolic regulation. Nature 441, 366-370 (2006).
    • (2006) Nature , vol.441 , pp. 366-370
    • Foukas, L.C.1
  • 14
    • 33646383684 scopus 로고    scopus 로고
    • A pharmacological map of the PI3-K family defines a role for p110α in insulin signaling
    • Knight, Z. A., et al. A pharmacological map of the PI3-K family defines a role for p110α in insulin signaling. Cell 125, 733-747 (2006).
    • (2006) Cell , vol.125 , pp. 733-747
    • Knight, Z.A.1
  • 15
    • 11144358645 scopus 로고    scopus 로고
    • Brevia: High frequency of mutations of the PIK3Ca gene in human cancers
    • Samuels, Y. et al. Brevia: High frequency of mutations of the PIK3Ca gene in human cancers. Science 304, 554 (2004).
    • (2004) Science , vol.304 , pp. 554
    • Samuels, Y.1
  • 16
    • 28844448182 scopus 로고    scopus 로고
    • Oncogenic PI3K deregulates transcription and translation
    • Bader, A. G., Kang, S., Zhao, L. Vogt, P. K. Oncogenic PI3K deregulates transcription and translation. Nature Rev. Cancer 5, 921-929 (2005).
    • (2005) Nature Rev. Cancer , vol.5 , pp. 921-929
    • Bader, A.G.1    Kang, S.2    Zhao, L.3    Vogt, P.K.4
  • 17
    • 21044454703 scopus 로고    scopus 로고
    • PI3-kinase p110β: A new target for antithrombotic therapy
    • Jackson, S. P. PI3-kinase p110β: A new target for antithrombotic therapy. Nature Med. 11, 507-514 (2005).
    • (2005) Nature Med. , vol.11 , pp. 507-514
    • Jackson, S.P.1
  • 18
    • 0038549067 scopus 로고    scopus 로고
    • PI3K in lymphocyte development, differentiation and activation
    • Okkenhaug, K., Vanhaesebroeck, B. PI3K in lymphocyte development, differentiation and activation. Nature Rev. Immunol. 3, 317-330 (2003).
    • (2003) Nature Rev. Immunol. , vol.3 , pp. 317-330
    • Okkenhaug, K.1    Vanhaesebroeck, B.2
  • 19
    • 0028334738 scopus 로고
    • A novel phosphoinositide 3 kinase activity in myeloid-derived cells is activated by G-protein βγ subunits
    • Stephens, L. et al. A novel phosphoinositide 3 kinase activity in myeloid-derived cells is activated by G-protein βγ subunits. Cell 77, 83-93 (1994).
    • (1994) Cell , vol.77 , pp. 83-93
    • Stephens, L.1
  • 20
    • 0029090212 scopus 로고
    • Cloning and characterization of a G-protein activated human phosphoinositide 3-kinase
    • Stoyanov, B. et al. Cloning and characterization of a G-protein activated human phosphoinositide 3-kinase. Science 269, 690-693 (1995).
    • (1995) Science , vol.269 , pp. 690-693
    • Stoyanov, B.1
  • 21
    • 0030887632 scopus 로고    scopus 로고
    • The Gβγ sensitivity of a PI3K is dependent upon a tightly associated adaptor, p101
    • Stephens, L. R. et al. The Gβγ sensitivity of a PI3K is dependent upon a tightly associated adaptor, p101. Cell 89, 105-114 (1997).
    • (1997) Cell , vol.89 , pp. 105-114
    • Stephens, L.R.1
  • 22
    • 0033546148 scopus 로고    scopus 로고
    • Characterizing the interactions between the two subunits of the p101/p110 phosphoinositide 3-kinase and their role in the activation of this enzyme by G subunits
    • Krugmann, S., Hawkins, P. T., Pryer, N. & Braselmann, S. Characterizing the interactions between the two subunits of the p101/p110 phosphoinositide 3-kinase and their role in the activation of this enzyme by G subunits. J. Biol. Chem. 274, 17152-17158 (1999).
    • (1999) J. Biol. Chem. , vol.274 , pp. 17152-17158
    • Krugmann, S.1    Hawkins, P.T.2    Pryer, N.3    Braselmann, S.4
  • 23
    • 0033635157 scopus 로고    scopus 로고
    • Crystal structure and functional analysis of Ras binding to its effector phosphoinositide 3-kinase γ
    • Pacold, M. E. et al. Crystal structure and functional analysis of Ras binding to its effector phosphoinositide 3-kinase γ. Cell 103, 931-943 (2000).
    • (2000) Cell , vol.103 , pp. 931-943
    • Pacold, M.E.1
  • 24
    • 0037046799 scopus 로고    scopus 로고
    • Activation of phosphoinositide 3-kinase γ by Ras
    • Suire, S., Hawkins, P. & Stephens, L. Activation of phosphoinositide 3-kinase γ by Ras. Curr. Biol. 12, 1068-1075 (2002).
    • (2002) Curr. Biol. , vol.12 , pp. 1068-1075
    • Suire, S.1    Hawkins, P.2    Stephens, L.3
  • 25
    • 0032500730 scopus 로고    scopus 로고
    • Bifurcation of lipid and protein kinase signals of PI3Kγ to the protein kinases PKB and MAPK
    • Bondeva, T. et al. Bifurcation of lipid and protein kinase signals of PI3Kγ to the protein kinases PKB and MAPK. Science. 282, 293-296 (1998).
    • (1998) Science , vol.282 , pp. 293-296
    • Bondeva, T.1
  • 26
    • 0032579244 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase γ is a mediator of Gβγ-dependent Jun kinase activation
    • Lopez-Ilasaca, M., Gutkind, J. S. & Wetzker, R. Phosphoinositide 3-kinase γ is a mediator of Gβγ-dependent Jun kinase activation. J. Biol. Chem. 273, 2505-2508 (1998).
    • (1998) J. Biol. Chem. , vol.273 , pp. 2505-2508
    • Lopez-Ilasaca, M.1    Gutkind, J.S.2    Wetzker, R.3
  • 27
    • 0032158834 scopus 로고    scopus 로고
    • Tissue distribution and subcellular localization of a G-protein coupled phosphoinositide 3-kinase. An immunohistochemical study
    • Bernstein, H.-G., Keilhoff, G., Reiser, M., Freese, S. & Wetzker, R. Tissue distribution and subcellular localization of a G-protein coupled phosphoinositide 3-kinase. An immunohistochemical study. Cell. Mol. Biol. 44, 973-983 (1998).
    • (1998) Cell. Mol. Biol. , vol.44 , pp. 973-983
    • Bernstein, H.-G.1    Keilhoff, G.2    Reiser, M.3    Freese, S.4    Wetzker, R.5
  • 28
    • 2442596885 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinases as targets for therapeutic intervention
    • Wetzker, R. & Rommel, C. Phosphoinositide 3-kinases as targets for therapeutic intervention. Curr. Pharm. Des. 10, 1915-1922 (2004).
    • (2004) Curr. Pharm. Des. , vol.10 , pp. 1915-1922
    • Wetzker, R.1    Rommel, C.2
  • 31
    • 0028133063 scopus 로고
    • Distinct patterns of bidirectional regulation of mammalian adenylyl cyclases
    • Taussig, R., Tang, W. J., Hepler, J. R. & Gilman, A. G. Distinct patterns of bidirectional regulation of mammalian adenylyl cyclases. J. Biol. Chem. 269, 6093-6100 (1994).
    • (1994) J. Biol. Chem. , vol.269 , pp. 6093-6100
    • Taussig, R.1    Tang, W.J.2    Hepler, J.R.3    Gilman, A.G.4
  • 32
    • 0027132929 scopus 로고
    • Activation of phospholipase C-β2 mutants by G protein αθ and βγ subunits
    • Lee, S. B., Shin, S. H., Hepler, J. R., Gilman, A. G. & Rhee, S. G. Activation of phospholipase C-β2 mutants by G protein αθ and βγ subunits. J. Biol. Chem. 268, 25952-25957 (1993).
    • (1993) J. Biol. Chem. , vol.268 , pp. 25952-25957
    • Lee, S.B.1    Shin, S.H.2    Hepler, J.R.3    Gilman, A.G.4    Rhee, S.G.5
  • 33
    • 0034635221 scopus 로고    scopus 로고
    • Roles of PLC-β2 and-β3 and PI3Kγ in chemoattractant-mediated signal transduction
    • Li, Z. et al. Roles of PLC-β2 and-β3 and PI3Kγ in chemoattractant-mediated signal transduction. Science 287, 1046-1049 (2000).
    • (2000) Science , vol.287 , pp. 1046-1049
    • Li, Z.1
  • 34
    • 0037309099 scopus 로고    scopus 로고
    • Chemoattractant receptor-stimulated F-actin polymerization in the human neutrophil is signaled by 2 distinct pathways
    • Chodniewicz, D. & Zhelev, D. V. Chemoattractant receptor-stimulated F-actin polymerization in the human neutrophil is signaled by 2 distinct pathways. Blood 101, 1181-1184 (2003).
    • (2003) Blood , vol.101 , pp. 1181-1184
    • Chodniewicz, D.1    Zhelev, D.V.2
  • 35
    • 0034625002 scopus 로고    scopus 로고
    • Role of Rac in controlling the actin cytoskeleton and chemotaxis in motile cells
    • Chung, C. Y., Lee, S., Briscoe, C., Ellsworth, C. & Firtel, R. A. Role of Rac in controlling the actin cytoskeleton and chemotaxis in motile cells. Proc. Natl Acad. Sci. USA 97, 5225-5230 (2000).
    • (2000) Proc. Natl Acad. Sci. USA , vol.97 , pp. 5225-5230
    • Chung, C.Y.1    Lee, S.2    Briscoe, C.3    Ellsworth, C.4    Firtel, R.A.5
  • 36
    • 0035511611 scopus 로고    scopus 로고
    • Ion-channel regulation by G proteins
    • Dascal, N. Ion-channel regulation by G proteins. Trends Endocrinol. Metab. 12, 391-398 (2001).
    • (2001) Trends Endocrinol. Metab. , vol.12 , pp. 391-398
    • Dascal, N.1
  • 37
    • 0034635452 scopus 로고    scopus 로고
    • Central role for G protein-coupled phosphoinositide 3-kinase γ in inflammation
    • Hirsch, E. et al. Central role for G protein-coupled phosphoinositide 3-kinase γ in inflammation. Science 287, 1049-1053 (2000).
    • (2000) Science , vol.287 , pp. 1049-1053
    • Hirsch, E.1
  • 38
    • 0034635264 scopus 로고    scopus 로고
    • Function of PI3Kγ in thymocyte development, T cell activation, and neutrophil migration
    • Sasaki, T. et al. Function of PI3Kγ in thymocyte development, T cell activation, and neutrophil migration. Science 287, 1040-1046 (2000).
    • (2000) Science , vol.287 , pp. 1040-1046
    • Sasaki, T.1
  • 39
    • 4344714889 scopus 로고    scopus 로고
    • PI3Kγ modulates the cardiac response to chronic pressure overload by distinct kinase-dependent and-independent effects
    • Patrucco, E. et al. PI3Kγ modulates the cardiac response to chronic pressure overload by distinct kinase-dependent and-independent effects. Cell 118, 375-387 (2004).
    • (2004) Cell , vol.118 , pp. 375-387
    • Patrucco, E.1
  • 40
    • 0035950131 scopus 로고    scopus 로고
    • Tumour biology. Weakening link to colorectal cancer?
    • Barbier, M. et al. Tumour biology. Weakening link to colorectal cancer? Nature 413, 796 (2001).
    • (2001) Nature , vol.413 , pp. 796
    • Barbier, M.1
  • 42
    • 2342486058 scopus 로고    scopus 로고
    • Chemokine inhibition - Why, when, where, which and how?
    • Johnson, Z. et al. Chemokine inhibition - why, when, where, which and how? Biochem. Soc. Trans. 32, 366-377 (2004).
    • (2004) Biochem. Soc. Trans. , vol.32 , pp. 366-377
    • Johnson, Z.1
  • 43
    • 0036803279 scopus 로고    scopus 로고
    • Chemokines, chemokine receptors and small-molecule antagonists: Recent developments
    • Onuffer, J. J. & Horuk, R. Chemokines, chemokine receptors and small-molecule antagonists: Recent developments. Trends Pharm. Sci. 23, 459-467 (2002).
    • (2002) Trends Pharm. Sci. , vol.23 , pp. 459-467
    • Onuffer, J.J.1    Horuk, R.2
  • 44
    • 20444375419 scopus 로고    scopus 로고
    • The clinical potential of chemokine receptor antagonists
    • Ribeiro, S. & Horuk, R. The clinical potential of chemokine receptor antagonists. Pharm. Ther. 107, 44-58 (2005).
    • (2005) Pharm. Ther. , vol.107 , pp. 44-58
    • Ribeiro, S.1    Horuk, R.2
  • 45
    • 23844499144 scopus 로고    scopus 로고
    • The toxicology of chemokine inhibition
    • Schroff, R. W. et al. The toxicology of chemokine inhibition. Mini-Rev. Med. Chem. 5, 849-855 (2005).
    • (2005) Mini-Rev. Med. Chem. , vol.5 , pp. 849-855
    • Schroff, R.W.1
  • 46
    • 0027432424 scopus 로고
    • Wortmannin is a potent phosphatidylinositol 3-kinase inhibitor: The role of phosphatidylinositol 3,4,5-triphosphate in neutrophil responses
    • Arcaro, A. & Wymann, M. P. Wortmannin is a potent phosphatidylinositol 3-kinase inhibitor: The role of phosphatidylinositol 3,4,5-triphosphate in neutrophil responses. Biochem. J. 296, 297-301 (1993).
    • (1993) Biochem. J. , vol.296 , pp. 297-301
    • Arcaro, A.1    Wymann, M.P.2
  • 47
    • 0028170210 scopus 로고
    • A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002)
    • Vlahos, C. J., Matter, W. F., Hui, K. Y. & Brown, R. F. A specific inhibitor of phosphatidylinositol 3-kinase, 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one (LY294002). J. Biol. Chem. 269, 5241-5248 (1994).
    • (1994) J. Biol. Chem. , vol.269 , pp. 5241-5248
    • Vlahos, C.J.1    Matter, W.F.2    Hui, K.Y.3    Brown, R.F.4
  • 48
    • 0033559497 scopus 로고    scopus 로고
    • Recruitment of pleckstrin and phosphoinositide 3-kinase γ into the cell membranes, and their association with Gβγ after activation of NK cells with chemokines
    • Al-Aoukaty, A., Rolstad, B. & Maghazachi, A. A. Recruitment of pleckstrin and phosphoinositide 3-kinase γ into the cell membranes, and their association with Gβγ after activation of NK cells with chemokines. J. Immunol. 162, 3249-3255 (1999).
    • (1999) J. Immunol. , vol.162 , pp. 3249-3255
    • Al-Aoukaty, A.1    Rolstad, B.2    Maghazachi, A.A.3
  • 50
    • 20244364825 scopus 로고    scopus 로고
    • Airway inflammation: Chemokine-induced neutrophilia and the class I phosphoinositide 3-kinases
    • Thomas, M. J. et al. Airway inflammation: Chemokine-induced neutrophilia and the class I phosphoinositide 3-kinases. Eur. J. Immunol. 35, 1283-1291 (2005).
    • (2005) Eur. J. Immunol. , vol.35 , pp. 1283-1291
    • Thomas, M.J.1
  • 51
    • 23744492188 scopus 로고    scopus 로고
    • Sequential activation of class IB and class IA PI3K is important for the primed respiratory burst of human but not murine neutrophils
    • Condliffe, A. M. et al. Sequential activation of class IB and class IA PI3K is important for the primed respiratory burst of human but not murine neutrophils. Blood 106, 1432-1440 (2005).
    • (2005) Blood , vol.106 , pp. 1432-1440
    • Condliffe, A.M.1
  • 52
    • 22044442679 scopus 로고    scopus 로고
    • The role of endothelial PI3Kγ activity in neutrophil trafficking
    • Puri, K. D. et al. The role of endothelial PI3Kγ activity in neutrophil trafficking. Blood 106, 150-157 (2005).
    • (2005) Blood , vol.106 , pp. 150-157
    • Puri, K.D.1
  • 53
    • 0141569194 scopus 로고    scopus 로고
    • Requirement for PI 3-kinase γ in macrophage migration to MCP-1 and CSF-1
    • Jones, G. E. et al. Requirement for PI 3-kinase γ in macrophage migration to MCP-1 and CSF-1. Exp. Cell Res. 290, 120-131 (2003).
    • (2003) Exp. Cell Res. , vol.290 , pp. 120-131
    • Jones, G.E.1
  • 54
    • 4644232654 scopus 로고    scopus 로고
    • Defective dendritic cell migration and activation of adaptive immunity in PI3Kγ-deficient mice
    • Del Prete, A. et al. Defective dendritic cell migration and activation of adaptive immunity in PI3Kγ-deficient mice. EMBO J. 23, 3505-3515 (2004).
    • (2004) EMBO J. , vol.23 , pp. 3505-3515
    • Del Prete, A.1
  • 55
    • 18244373430 scopus 로고    scopus 로고
    • Phosphoinositide-3 kinases critically regulate the recruitment and survival of eosinophils in vivo: Importance for the resolution of allergic inflammation
    • Pinho, V. et al. Phosphoinositide-3 kinases critically regulate the recruitment and survival of eosinophils in vivo: Importance for the resolution of allergic inflammation. J. Leukoc. Biol. 77, 800-810 (2005).
    • (2005) J. Leukoc. Biol. , vol.77 , pp. 800-810
    • Pinho, V.1
  • 56
    • 4043082729 scopus 로고    scopus 로고
    • Differential roles for phosphoinositide 3-kinases, p110γ and p110δ, in lymphocyte chemotaxis and homing
    • Reif, K. et al. Differential roles for phosphoinositide 3-kinases, p110γ and p110δ, in lymphocyte chemotaxis and homing. J. Immunol. 173, 2236-2240 (2004).
    • (2004) J. Immunol. , vol.173 , pp. 2236-2240
    • Reif, K.1
  • 57
    • 0842346270 scopus 로고    scopus 로고
    • Do phosphoinositide 3-kinases direct lymphocyte navigation?
    • Ward, S. G. Do phosphoinositide 3-kinases direct lymphocyte navigation? Trends Immunol. 25, 67-74 (2004).
    • (2004) Trends Immunol. , vol.25 , pp. 67-74
    • Ward, S.G.1
  • 58
    • 2942625693 scopus 로고    scopus 로고
    • Activation of phosphoinositide 3-kinases by the CCR4 ligand macrophage-derived chemokine is a dispensable signal for T lymphocyte chemotaxis
    • Cronshaw, D. G., Owen, C., Brown, Z. & Ward, S. G. Activation of phosphoinositide 3-kinases by the CCR4 ligand macrophage-derived chemokine is a dispensable signal for T lymphocyte chemotaxis. J. Immunol. 172, 7761-7770 (2004).
    • (2004) J. Immunol. , vol.172 , pp. 7761-7770
    • Cronshaw, D.G.1    Owen, C.2    Brown, Z.3    Ward, S.G.4
  • 59
    • 29644443728 scopus 로고    scopus 로고
    • Class IB-phosphatidylinositol 3-kinase (PI3K) deficiency ameliorates IA-PI3K-induced systemic lupus but not T cell invasion
    • Barber, D. F. et al. Class IB-phosphatidylinositol 3-kinase (PI3K) deficiency ameliorates IA-PI3K-induced systemic lupus but not T cell invasion. J. Immunol. 176, 589-593 (2006).
    • (2006) J. Immunol. , vol.176 , pp. 589-593
    • Barber, D.F.1
  • 60
    • 4444335344 scopus 로고    scopus 로고
    • Differential requirements for DOCK2 and phosphoinositide-3-kinase γ during T and B lymphocyte homing
    • Nombela-Arrieta, C. et al. Differential requirements for DOCK2 and phosphoinositide-3-kinase γ during T and B lymphocyte homing. Immunity 21, 429-441 (2004).
    • (2004) Immunity , vol.21 , pp. 429-441
    • Nombela-Arrieta, C.1
  • 61
    • 33344470236 scopus 로고    scopus 로고
    • Integrated signalling pathways for mast-cell activation
    • Gilfillan, A. M. & Tkaczyk, C. Integrated signalling pathways for mast-cell activation. Nature Rev. Immunol. 6, 218-230 (2006).
    • (2006) Nature Rev. Immunol. , vol.6 , pp. 218-230
    • Gilfillan, A.M.1    Tkaczyk, C.2
  • 62
    • 0036200415 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase γ is an essential amplifier of mast cell function
    • Laffargue, M. et al. Phosphoinositide 3-kinase γ is an essential amplifier of mast cell function. Immunity 16, 441-451 (2002).
    • (2002) Immunity , vol.16 , pp. 441-451
    • Laffargue, M.1
  • 63
    • 0035464192 scopus 로고    scopus 로고
    • Resistance to thromboembolism in PI3Kγ-deficient mice
    • Hirsch, E. et al. Resistance to thromboembolism in PI3Kγ-deficient mice. FASEB J. 15, 2019-2021 (2001).
    • (2001) FASEB J. , vol.15 , pp. 2019-2021
    • Hirsch, E.1
  • 64
    • 22044443427 scopus 로고    scopus 로고
    • The relative role of PLCβ and PI3Kγ in platelet activation
    • Lian, L. et al. The relative role of PLCβ and PI3Kγ in platelet activation. Blood 106, 110-117 (2005).
    • (2005) Blood , vol.106 , pp. 110-117
    • Lian, L.1
  • 65
    • 1342292522 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase: Diverse roles in immune cell activation
    • Deane, J. A. & Fruman, D. A. Phosphoinositide 3-kinase: Diverse roles in immune cell activation. Annu. Rev. Immunol. 22, 563-598 (2004).
    • (2004) Annu. Rev. Immunol. , vol.22 , pp. 563-598
    • Deane, J.A.1    Fruman, D.A.2
  • 66
    • 0242416992 scopus 로고    scopus 로고
    • Phosphatidylinositol 3-kinase regulates the CD4/CD8 T cell differentiation ratio
    • Rodriguez-Borlado, L. et al. Phosphatidylinositol 3-kinase regulates the CD4/CD8 T cell differentiation ratio. J. Immunol. 170, 4475-4482 (2003).
    • (2003) J. Immunol. , vol.170 , pp. 4475-4482
    • Rodriguez-Borlado, L.1
  • 67
    • 0033113636 scopus 로고    scopus 로고
    • 2+ channels via phosphoinositide 3-kinase
    • 2+ channels via phosphoinositide 3-kinase. FASEB J. 13, 685-694 (1999).
    • (1999) FASEB J. , vol.13 , pp. 685-694
    • Viard, P.1
  • 69
    • 0035979994 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase γ mediates angiotensin II-induced stimulation of L-type calcium channels in vascular myocytes
    • Quignard, J-F. et al. Phosphoinositide 3-kinase γ mediates angiotensin II-induced stimulation of L-type calcium channels in vascular myocytes. J. Biol. Chem. 276, 32545-32551 (2001).
    • (2001) J. Biol. Chem. , vol.276 , pp. 32545-32551
    • Quignard, J.-F.1
  • 70
    • 0035851221 scopus 로고    scopus 로고
    • PI3King the L-type calcium channel activation mechanism
    • Steinberg, S. F. PI3King the L-type calcium channel activation mechanism. Circulation Res. 89, 641-644 (2001).
    • (2001) Circulation Res. , vol.89 , pp. 641-644
    • Steinberg, S.F.1
  • 71
    • 20944433770 scopus 로고    scopus 로고
    • Protection from angiotensin II-mediated vasculotoxic and hypertensive response in mice lacking PI3Kγ
    • Vecchione, C. et al. Protection from angiotensin II-mediated vasculotoxic and hypertensive response in mice lacking PI3Kγ. J. Exp. Med. 201, 1217-1228 (2005).
    • (2005) J. Exp. Med. , vol.201 , pp. 1217-1228
    • Vecchione, C.1
  • 74
    • 18644372367 scopus 로고    scopus 로고
    • Regulation of myocardial contractility and cell size by distinct PI3K-PTEN signaling pathways
    • Crackower, M. A. et al. Regulation of myocardial contractility and cell size by distinct PI3K-PTEN signaling pathways. Cell 110, 737-749 (2002).
    • (2002) Cell , vol.110 , pp. 737-749
    • Crackower, M.A.1
  • 75
    • 0242381308 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase γ-deficient mice are protected from isoproterenol-induced heart failure
    • Oudit, G. Y. et al. Phosphoinositide 3-kinase γ-deficient mice are protected from isoproterenol-induced heart failure. Circulation 108, 2147-2152 (2003).
    • (2003) Circulation , vol.108 , pp. 2147-2152
    • Oudit, G.Y.1
  • 76
    • 0033807680 scopus 로고    scopus 로고
    • CC chemokine receptor 2 is critical for induction of experimental autoimmune encephalomyelitis
    • Fife, B. T., Huffnagle, G. B., Kuziel, W. A. & Karpus, W. J. CC chemokine receptor 2 is critical for induction of experimental autoimmune encephalomyelitis. J. Exp. Med. 192, 899-905 (2000).
    • (2000) J. Exp. Med. , vol.192 , pp. 899-905
    • Fife, B.T.1    Huffnagle, G.B.2    Kuziel, W.A.3    Karpus, W.J.4
  • 77
    • 0037011022 scopus 로고    scopus 로고
    • Essential role for the C5a receptor in regulating the effector phase of synovial infiltration and joint destruction in experimental arthritis
    • Grant, E. P. et al. Essential role for the C5a receptor in regulating the effector phase of synovial infiltration and joint destruction in experimental arthritis. J. Exp. Med. 196, 1461-1471 (2002).
    • (2002) J. Exp. Med. , vol.196 , pp. 1461-1471
    • Grant, E.P.1
  • 78
    • 0037300296 scopus 로고    scopus 로고
    • Chemokines and chemokine receptors in reumatoid arthritis
    • Szekanecz, Z., Kim, J. & Koch, A. E. Chemokines and chemokine receptors in reumatoid arthritis. Semin. Immunol. 15, 15-21 (2003).
    • (2003) Semin. Immunol. , vol.15 , pp. 15-21
    • Szekanecz, Z.1    Kim, J.2    Koch, A.E.3
  • 79
    • 0037031680 scopus 로고    scopus 로고
    • Mast cells: A cellular link between autoantibodies and inflammatory arthritis
    • Lee, D. M. et al. Mast cells: A cellular link between autoantibodies and inflammatory arthritis. Science 297, 1689-1692 (2002).
    • (2002) Science , vol.297 , pp. 1689-1692
    • Lee, D.M.1
  • 80
    • 24744435115 scopus 로고    scopus 로고
    • A small molecule inhibitor of PI3Kγ suppresses joint inflammation and damage in a murine model of rheumatoid arthritis
    • Camps, M. et al. A small molecule inhibitor of PI3Kγ suppresses joint inflammation and damage in a murine model of rheumatoid arthritis. Nature Med. 11, 936-943 (2005).
    • (2005) Nature Med. , vol.11 , pp. 936-943
    • Camps, M.1
  • 81
    • 9644302717 scopus 로고    scopus 로고
    • Ablation of phosphoinositide 3-kinase-γ reduces the severity of acute pancreatitis
    • Lupia, E. et al. Ablation of phosphoinositide 3-kinase-γ reduces the severity of acute pancreatitis. Am. J. Pathol. 165, 2003-2011 (2004).
    • (2004) Am. J. Pathol. , vol.165 , pp. 2003-2011
    • Lupia, E.1
  • 82
    • 24744449495 scopus 로고    scopus 로고
    • PI3Kγ inhibition blocks glomerulonephritis and extends lifespan in murine models of systemic lupus
    • Barber, D. F. et al. PI3Kγ inhibition blocks glomerulonephritis and extends lifespan in murine models of systemic lupus. Nature Med. 11, 933-935 (2005).
    • (2005) Nature Med. , vol.11 , pp. 933-935
    • Barber, D.F.1
  • 83
    • 4043067193 scopus 로고    scopus 로고
    • Gene targeting: Attention to detail
    • Vanhaesebroeck, B., Rohn, J. L. & Waterfield, M. D. Gene targeting: attention to detail. Cell 118, 274-276 (2004).
    • (2004) Cell , vol.118 , pp. 274-276
    • Vanhaesebroeck, B.1    Rohn, J.L.2    Waterfield, M.D.3
  • 84
    • 0037119630 scopus 로고    scopus 로고
    • A crucial role for the p110δ subunit of phosphatidylinositol 3-kinase in B cell development and activation
    • Clayton, E. et al. A crucial role for the p110δ subunit of phosphatidylinositol 3-kinase in B cell development and activation. J. Exp. Med. 196, 753-763 (2002).
    • (2002) J. Exp. Med. , vol.196 , pp. 753-763
    • Clayton, E.1
  • 85
    • 0037695593 scopus 로고    scopus 로고
    • Essential, nonredundant role for the phosphoinositide 3-kinase p110δ in signaling by the B-cell receptor complex
    • Jou, S-T., Carpino, N., Takahashi, Y., Piekorz, R., Chao, J-R., Carpino, N., Wang, D. & Ihle, J. N. Essential, nonredundant role for the phosphoinositide 3-kinase p110δ in signaling by the B-cell receptor complex. Mol. Cell. Biol. 22, 8580-8591 (2002).
    • (2002) Mol. Cell. Biol. , vol.22 , pp. 8580-8591
    • Jou, S.-T.1    Carpino, N.2    Takahashi, Y.3    Piekorz, R.4    Chao, J.-R.5    Carpino, N.6    Wang, D.7    Ihle, J.N.8
  • 86
    • 0037047590 scopus 로고    scopus 로고
    • Impaired B and T cell antigen receptor signaling in p110δ PI 3-kinase mutant mice
    • Okkenhaug, K. et al. Impaired B and T cell antigen receptor signaling in p110δ PI 3-kinase mutant mice. Science 297, 1031-1034 (2002).
    • (2002) Science , vol.297 , pp. 1031-1034
    • Okkenhaug, K.1
  • 87
    • 0033581886 scopus 로고    scopus 로고
    • Structural insights into phosphoinositide 3-kinase signaling
    • Walker, E. H., Perisic, O., Ried, C., Stephens, L. & Williams, R. L. Structural insights into phosphoinositide 3-kinase signaling. Nature 402, 313-320 (1999).
    • (1999) Nature , vol.402 , pp. 313-320
    • Walker, E.H.1    Perisic, O.2    Ried, C.3    Stephens, L.4    Williams, R.L.5
  • 88
    • 0033634827 scopus 로고    scopus 로고
    • Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myrecetin, and staurosporin
    • Walker, E. H. et al. Structural determinants of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myrecetin, and staurosporin. Mol. Cell 6, 909-919 (2000).
    • (2000) Mol. Cell , vol.6 , pp. 909-919
    • Walker, E.H.1
  • 89
    • 20844458056 scopus 로고    scopus 로고
    • Chemistry and biology of wortmannin
    • Wipf, P. & Halter, R. J. Chemistry and biology of wortmannin. Org. Biomol. Chem. 3, 2053-2061 (2005).
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 2053-2061
    • Wipf, P.1    Halter, R.J.2
  • 90
    • 0037350266 scopus 로고    scopus 로고
    • Therapeutic potential of phosphoinositide 3-kinase inhibitors
    • Ward, S., Sotsios, Y., Dowden, J., Bruce, I. & Finan, P. Therapeutic potential of phosphoinositide 3-kinase inhibitors. Chem. Biol. 10, 207-213 (2003).
    • (2003) Chem. Biol. , vol.10 , pp. 207-213
    • Ward, S.1    Sotsios, Y.2    Dowden, J.3    Bruce, I.4    Finan, P.5
  • 91
    • 33750501647 scopus 로고
    • Inhibition of phosphatidylinositol 3-kinase with viridin, demethoxyviridin, viridiol, demethoxyviridiol, virone, wortmannolone, and analogs thereof
    • US Patent 05,726,167
    • Dodge, J. A., Sato, M. & Vlahos, C. J. Inhibition of phosphatidylinositol 3-kinase with viridin, demethoxyviridin, viridiol, demethoxyviridiol, virone, wortmannolone, and analogs thereof. US Patent 05,726,167 (1995).
    • (1995)
    • Dodge, J.A.1    Sato, M.2    Vlahos, C.J.3
  • 92
    • 4444223702 scopus 로고    scopus 로고
    • Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling
    • Ihle, N. T. et al. Molecular pharmacology and antitumor activity of PX-866, a novel inhibitor of phosphoinositide-3-kinase signaling. Mol. Cancer Ther. 3, 763-772 (2004).
    • (2004) Mol. Cancer Ther. , vol.3 , pp. 763-772
    • Ihle, N.T.1
  • 93
    • 0029965452 scopus 로고    scopus 로고
    • Wortmannin inactivates phosphoinositide 3-kinase by covalent modification of Lys-802, a residue involved in the phosphate
    • Wymann, M. P. et al. Wortmannin inactivates phosphoinositide 3-kinase by covalent modification of Lys-802, a residue involved in the phosphate. Mol. Cell. Biol. 16, 1722-1733 (1996).
    • (1996) Mol. Cell. Biol. , vol.16 , pp. 1722-1733
    • Wymann, M.P.1
  • 94
    • 0037369696 scopus 로고    scopus 로고
    • Essential role of phosphoinositide 3-kinase in neutrophil directional movement
    • Sadhu C., Masinosky B., Dick K., Sowell C. G. & Staunton D. E. Essential role of phosphoinositide 3-kinase in neutrophil directional movement. J. Immunol. 170, 2647-2654 (2003).
    • (2003) J. Immunol. , vol.170 , pp. 2647-2654
    • Sadhu, C.1    Masinosky, B.2    Dick, K.3    Sowell, C.G.4    Staunton, D.E.5
  • 95
    • 33745662579 scopus 로고    scopus 로고
    • Furan-2-ylmethylene thiazolidinediones as novel, potent, and selective inhibitors of phosphoinositide 3-kinase γ
    • Pomel, V. et al. Furan-2-ylmethylene thiazolidinediones as novel, potent, and selective inhibitors of phosphoinositide 3-kinase γ. J. Med. Chem. 49, 3857-3871 (2006).
    • (2006) J. Med. Chem. , vol.49 , pp. 3857-3871
    • Pomel, V.1
  • 96
    • 3843135141 scopus 로고    scopus 로고
    • Isoform-specific phosphoinositide 3-kinase inhibitors from an arylmorpholine scaffold
    • Knight, Z. A. et al. Isoform-specific phosphoinositide 3-kinase inhibitors from an arylmorpholine scaffold. Bioorg. Med. Chem. 12, 4749-4759 (2004).
    • (2004) Bioorg. Med. Chem. , vol.12 , pp. 4749-4759
    • Knight, Z.A.1
  • 97
    • 3042636702 scopus 로고    scopus 로고
    • ATP-competitive inhibitors of cyclindependent kinases
    • Dermatakis, A. ATP-competitive inhibitors of cyclindependent kinases. Front. Biotech. Pharm. 3, 125-156 (2002).
    • (2002) Front. Biotech. Pharm. , vol.3 , pp. 125-156
    • Dermatakis, A.1
  • 98
    • 12144285797 scopus 로고    scopus 로고
    • N-(Cycloalkylamino)acyl-2-aminothiazole inhibitors of cyclin-dependent kinase 2. N-[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4- piperidinecarboxamide (BMS-387032), a highly efficacious and selective antitumor agent
    • Misra, R. N. et al. N-(Cycloalkylamino)acyl-2-aminothiazole inhibitors of cyclin-dependent kinase 2. N-[5-(1,1-dimethylethyl)-2-oxazolyl]methyl]thio]-2-thiazolyl]-4- piperidinecarboxamide (BMS-387032), a highly efficacious and selective antitumor agent. J. Med. Chem. 47, 1719-1728 (2004).
    • (2004) J. Med. Chem. , vol.47 , pp. 1719-1728
    • Misra, R.N.1
  • 99
    • 5144230218 scopus 로고    scopus 로고
    • Discovery and SAR of 2-aminothiazole inhibitors of cyclin-dependent kinase 5/p25 as a potential treatment for Alzheimer's disease
    • Helal, C. J. et al. Discovery and SAR of 2-aminothiazole inhibitors of cyclin-dependent kinase 5/p25 as a potential treatment for Alzheimer's disease. Bioorg. Med. Chem. Lett. 14, 5521-5525 (2004).
    • (2004) Bioorg. Med. Chem. Lett. , vol.14 , pp. 5521-5525
    • Helal, C.J.1
  • 100
    • 0037194619 scopus 로고    scopus 로고
    • Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: Synthesis, X-ray crystallographic analysis, and biological activities
    • Kim, K. S. et al. Discovery of aminothiazole inhibitors of cyclin-dependent kinase 2: Synthesis, X-ray crystallographic analysis, and biological activities. J. Med. Chem. 45, 3905-3927 (2002).
    • (2002) J. Med. Chem. , vol.45 , pp. 3905-3927
    • Kim, K.S.1
  • 101
    • 10744220619 scopus 로고    scopus 로고
    • Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56Lck
    • Wityak, J. et al. Discovery and initial SAR of 2-amino-5-carboxamidothiazoles as inhibitors of the Src-family kinase p56Lck. Bioorg. Med. Chem. Lett. 13, 4007-4010 (2003).
    • (2003) Bioorg. Med. Chem. Lett. , vol.13 , pp. 4007-4010
    • Wityak, J.1
  • 102
    • 33750525383 scopus 로고    scopus 로고
    • 5-Phenylthiazole derivatives and their use as phosphatidylinositol 3-kinase (PI3K) inhibitors for the treatment of allergic and inflammatory diseases
    • PCT Int. Appl., WO-03072557
    • Bruce, I. et al. 5-Phenylthiazole derivatives and their use as phosphatidylinositol 3-kinase (PI3K) inhibitors for the treatment of allergic and inflammatory diseases. PCT Int. Appl., WO-03072557 (2003).
    • (2003)
    • Bruce, I.1
  • 103
    • 33750528814 scopus 로고    scopus 로고
    • Preparation of 5-phenylthiazoles as phosphatidylinositol 3-kinase (PI3 kinase) inhibitors
    • PCT Int. Appl., WO-04078754
    • Bloomfield, G. C., Bruce, I., Leblanc, C., Oza, M. S. & Whitehead, L. Preparation of 5-phenylthiazoles as phosphatidylinositol 3-kinase (PI3 kinase) inhibitors. PCT Int. Appl., WO-04078754 (2004).
    • (2004)
    • Bloomfield, G.C.1    Bruce, I.2    Leblanc, C.3    Oza, M.S.4    Whitehead, L.5
  • 104
    • 33750529406 scopus 로고    scopus 로고
    • Preparation of pyrazinyl/pyridinyl thiazolylamines as inhibitors of phosphatidylinositol 3-kinase
    • PCT Int. Appl., WO-04096797
    • Bruce, I. et al. Preparation of pyrazinyl/pyridinyl thiazolylamines as inhibitors of phosphatidylinositol 3-kinase. PCT Int. Appl., WO-04096797 (2004).
    • (2004)
    • Bruce, I.1
  • 105
    • 33750529819 scopus 로고    scopus 로고
    • Preparation of phenylthiazolylureas as inhibitors of phosphatidylinositol 3-kinase
    • PCT Int. Appl., WO-05021519
    • Bloomfield, G. C. et al. Preparation of phenylthiazolylureas as inhibitors of phosphatidylinositol 3-kinase. PCT Int. Appl., WO-05021519 (2005).
    • (2005)
    • Bloomfield, G.C.1
  • 106
    • 33750523498 scopus 로고    scopus 로고
    • Preparation of thiazole derivatives as modulators of the phosphoinositide 3-kinases (PI3Ks)
    • PCT Int. Appl., WO-05068444
    • Quattropani, A. et al. Preparation of thiazole derivatives as modulators of the phosphoinositide 3-kinases (PI3Ks). PCT Int. Appl., WO-05068444 (2005).
    • (2005)
    • Quattropani, A.1
  • 107
    • 33750500779 scopus 로고    scopus 로고
    • PI3 kinases
    • PCT Int. Appl., WO-06040279
    • Breitfelder, S. et al. PI3 kinases. PCT Int. Appl., WO-06040279 (2006).
    • (2006)
    • Breitfelder, S.1
  • 108
    • 33750506795 scopus 로고    scopus 로고
    • Preparation of benzoxazin-3-ones and derivatives as inhibitors of PI3K kinase for treating inflammations, cardiovascular diseases and cancers
    • PCT Int. Appl., WO-04052373
    • Barvian, N. C., Kolz, C. N., Para, K. S., Patt, W. C. & Visnick, M. Preparation of benzoxazin-3-ones and derivatives as inhibitors of PI3K kinase for treating inflammations, cardiovascular diseases and cancers. PCT Int. Appl., WO-04052373 (2004).
    • (2004)
    • Barvian, N.C.1    Kolz, C.N.2    Para, K.S.3    Patt, W.C.4    Visnick, M.5
  • 109
    • 33750495035 scopus 로고    scopus 로고
    • Preparation of benzoxazines and related compounds as inhibitors of PI3Ks
    • PCT Int. Appl., WO-04056820
    • Gogliotti, R. D., Muccioli, K. L., Para, K. S. & Visnick, M. Preparation of benzoxazines and related compounds as inhibitors of PI3Ks. PCT Int. Appl., WO-04056820 (2004).
    • (2004)
    • Gogliotti, R.D.1    Muccioli, K.L.2    Para, K.S.3    Visnick, M.4
  • 110
    • 33750494600 scopus 로고    scopus 로고
    • Design and synthesis of 3-methyl-5-substituted benzyl and phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3kinase γ
    • MBCF meeting, Clearwater Beach, Feb. 26-March 1
    • Lanni, T. B. Jr et al. Design and synthesis of 3-methyl-5-substituted benzyl and phenethyl benzo[1,4]oxazine-3-ones as potent inhibitors of PI3kinase γ. MBCF meeting, Clearwater Beach, Feb. 26-March 1, 2006.
    • (2006)
    • Lanni Jr., T.B.1
  • 111
    • 33750508827 scopus 로고    scopus 로고
    • Preparation of azolidinone-vinyl fusedbenzene derivatives for therapeutic uses as PI3 kinase inhibitors
    • PCT Int. Appl., WO-04007491
    • Rueckle, T., Jiang, X., Gaillard, P., Church, D. D. & Vallotton, T. Preparation of azolidinone-vinyl fusedbenzene derivatives for therapeutic uses as PI3 kinase inhibitors. PCT Int. Appl., WO-04007491 (2004).
    • (2004)
    • Rueckle, T.1    Jiang, X.2    Gaillard, P.3    Church, D.D.4    Vallotton, T.5
  • 112
    • 33750498139 scopus 로고    scopus 로고
    • Identification and development of azolidinone vinyl-fused benzene derivatives, as potent and selective PI3Kγ inhibitors, orally active in models of rheumatoid arthritis
    • Abstracts of Papers, 230th National Meeting of the American Chemical Society, Washington, DC, August. 28 through September 1
    • Rueckle, T. et al. Identification and development of azolidinone vinyl-fused benzene derivatives, as potent and selective PI3Kγ inhibitors, orally active in models of rheumatoid arthritis. Abstracts of Papers, 230th National Meeting of the American Chemical Society, Washington, DC, August. 28 through September 1 2005.
    • (2005)
    • Rueckle, T.1
  • 113
    • 33750497916 scopus 로고    scopus 로고
    • Preparation of 3-substituted indoles as inhibitors of phosphoinositide-3 kinases (PI3Ks)
    • PCT Int. Appl., WO-04108708
    • Para, K. S., Stankovic, C. J. & Visnick, M. Preparation of 3-substituted indoles as inhibitors of phosphoinositide-3 kinases (PI3Ks PCT Int. Appl., WO-04108708 (2004).
    • (2004)
    • Para, K.S.1    Stankovic, C.J.2    Visnick, M.3
  • 114
    • 33750515729 scopus 로고    scopus 로고
    • Preparation of tetrazolyl benzofurancarboxamides as phosphoinositide-3-kinase (PI3K) inhibitors for the treatment of cancer, inflammatory and cardiovascular diseases
    • PCT Int. Appl., WO-04108709
    • Gogliotti, R. D., Lee, H. T., Sexton, K. E. & Visnick, M. Preparation of tetrazolyl benzofurancarboxamides as phosphoinositide-3-kinase (PI3K) inhibitors for the treatment of cancer, inflammatory and cardiovascular diseases. PCT Int. Appl., WO-04108709 (2004).
    • (2004)
    • Gogliotti, R.D.1    Lee, H.T.2    Sexton, K.E.3    Visnick, M.4
  • 115
    • 33750531939 scopus 로고    scopus 로고
    • Preparation of N-tetrazolyl benzo ]thiophenecarboxamides as phosphoinositide-3-kinase (PI3K) inhibitors for the treatment of cancer, inflammatory and cardiovascular diseases
    • PCT Int. Appl., WO-04108713
    • Connolly, M. et al. Preparation of N-tetrazolyl benzo [b#]thiophenecarboxamides as phosphoinositide-3-kinase (PI3K) inhibitors for the treatment of cancer, inflammatory and cardiovascular diseases. PCT Int. Appl., WO-04108713 (2004).
    • (2004)
    • Connolly, M.1
  • 116
    • 33750516383 scopus 로고    scopus 로고
    • Preparation of N-tetrazolyl benz o[b]thiophenecarboxamides as phosphoinositide-3-kinase (PI3K) inhibitors for the treatment of cancer, inflammatory and cardiovascular diseases
    • PCT Int. Appl., WO-04108715
    • Bruendl, M. M. et al. Preparation of N-tetrazolyl benz o[b]thiophenecarboxamides as phosphoinositide-3-kinase (PI3K) inhibitors for the treatment of cancer, inflammatory and cardiovascular diseases. PCT Int. Appl., WO-04108715 (2004).
    • (2004)
    • Bruendl, M.M.1
  • 117
    • 33750496665 scopus 로고    scopus 로고
    • Preparation of halo-substituted N-tetrazolylbenzo[b]thiophenecarboxamid es with PI3K inhibitory activity as therapeutic agents
    • PCT Int. Appl., WO-05023800
    • Connolly, M. K., Gogliotti, R. D., Hurt, C. R., Reichard, G. A. & Visnick, M. Preparation of halo-substituted N-tetrazolylbenzo[b]thiophenecarboxamid es with PI3K inhibitory activity as therapeutic agents. PCT Int. Appl., WO-05023800 (2005).
    • (2005)
    • Connolly, M.K.1    Gogliotti, R.D.2    Hurt, C.R.3    Reichard, G.A.4    Visnick, M.5
  • 118
    • 33750509918 scopus 로고    scopus 로고
    • Preparation of morpholinyl-pyrimidine derivatives as inhibitors of phosphoinositide-3-kinases
    • PCT Int. Appl., WO-05042519
    • Connolly, M. K., Gogliotti, R. D., Plummer, M. S. & Visnick, M. Preparation of morpholinyl-pyrimidine derivatives as inhibitors of phosphoinositide-3-kinases. PCT Int. Appl., WO-05042519 (2005).
    • (2005)
    • Connolly, M.K.1    Gogliotti, R.D.2    Plummer, M.S.3    Visnick, M.4
  • 119
    • 33750495676 scopus 로고    scopus 로고
    • Preparation of vasculostatic agents and methods of use
    • PCT Int. Appl., WO-04030635
    • Wrasidlo, W. et al. Preparation of vasculostatic agents and methods of use. PCT Int. Appl., WO-04030635 (2004).
    • (2004)
    • Wrasidlo, W.1
  • 120
    • 33750519333 scopus 로고    scopus 로고
    • Discovery of 3,3′-(2,4-diaminopteridine-6,7-diyl)diphenol, a PI3K inhibitor with potent activity against vascular leakage
    • Berlin, April, 13-14
    • Wrasidlo, W. Discovery of 3,3′-(2,4-diaminopteridine-6,7-diyl)diphenol, a PI3K inhibitor with potent activity against vascular leakage. Proceedings of MedChem Europe (Molecules that matter: Case studies in medicinal chemistry); Berlin, April, 13-14, 2005.
    • (2005) Proceedings of MedChem Europe (Molecules That Matter: Case Studies in Medicinal Chemistry)
    • Wrasidlo, W.1
  • 121
    • 33750521640 scopus 로고    scopus 로고
    • Preparation of fused azolepyrimidine derivatives as PI3K inhibitors with therapeutic uses
    • PCT Int. Appl., WO-04029055
    • Shimada, M. et al. Preparation of fused azolepyrimidine derivatives as PI3K inhibitors with therapeutic uses. PCT Int. Appl., WO-04029055 (2004).
    • (2004)
    • Shimada, M.1
  • 122
    • 33644787284 scopus 로고    scopus 로고
    • Study on improving the selectivity of compounds that inhibit two PI3Ks (γ and δ)
    • Kuang, R-R., Qian, F., Li, Z. & Wei, D-Z. Study on improving the selectivity of compounds that inhibit two PI3Ks (γ and δ). J. Mol. Model. 12, 445-452 (2006).
    • (2006) J. Mol. Model. , vol.12 , pp. 445-452
    • Kuang, R.-R.1    Qian, F.2    Li, Z.3    Wei, D.-Z.4
  • 123
    • 33646147812 scopus 로고    scopus 로고
    • Action mechanisms and structure-activity relationships of PI3Kγ inhibitors on the enzyme: A molecular modeling study
    • Kuang, R.-R., Qian, F., Li, Z., Wei, D.-Z. & Tang, Y. Action mechanisms and structure-activity relationships of PI3Kγ inhibitors on the enzyme: a molecular modeling study. Eur. J. Med. Chem. 41, 558-565 (2006).
    • (2006) Eur. J. Med. Chem. , vol.41 , pp. 558-565
    • Kuang, R.-R.1    Qian, F.2    Li, Z.3    Wei, D.-Z.4    Tang, Y.5
  • 124
    • 24944497371 scopus 로고    scopus 로고
    • Features of selective kinase inhibitors
    • Knight, Z. A. & Shokat, K. M. Features of selective kinase inhibitors. Chem. Biol. 12, 621-637 (2005).
    • (2005) Chem. Biol. , vol.12 , pp. 621-637
    • Knight, Z.A.1    Shokat, K.M.2
  • 125
    • 0036636094 scopus 로고    scopus 로고
    • Apoptosis as a therapeutic tool in rheumatoid arthritis
    • Pope, R. M. Apoptosis as a therapeutic tool in rheumatoid arthritis. Nature Rev. Immunol. 2, 527-535 (2002).
    • (2002) Nature. Rev. Immunol. , vol.2 , pp. 527-535
    • Pope, R.M.1
  • 126
    • 7244232917 scopus 로고    scopus 로고
    • Essential role for the p110δ phosphoinositide 3-kinase in the allergic response
    • Ali, K. et al. Essential role for the p110δ phosphoinositide 3-kinase in the allergic response. Nature 431, 1007-1011 (2004).
    • (2004) Nature , vol.431 , pp. 1007-1011
    • Ali, K.1
  • 127
    • 0035575706 scopus 로고    scopus 로고
    • Involvement of phosphoinositide 3-kinases in neutrophil activation and the development of acute lung injury
    • Yum, H. K. et al. Involvement of phosphoinositide 3-kinases in neutrophil activation and the development of acute lung injury. J. Immunol. 167, 6601-6608 (2001).
    • (2001) J. Immunol. , vol.167 , pp. 6601-6608
    • Yum, H.K.1
  • 128
    • 10744230726 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase γ-deficient hearts are protected from the PAF-dependent depression of cardiac contractility
    • Alloatti, G. et al. Phosphoinositide 3-kinase γ-deficient hearts are protected from the PAF-dependent depression of cardiac contractility. Cardiovasc. Res. 60, 242-249 (2003).
    • (2003) Cardiovasc. Res. , vol.60 , pp. 242-249
    • Alloatti, G.1
  • 129
    • 19944381163 scopus 로고    scopus 로고
    • Phosphoinositide 3-kinase γ controls autonomic regulation of the mouse heart through Gi-independent downregulation of cAMP level
    • Alloatti, G. et al. Phosphoinositide 3-kinase γ controls autonomic regulation of the mouse heart through Gi-independent downregulation of cAMP level. FEBS Lett. 579, 133-140 (2005).
    • (2005) FEBS Lett. , vol.579 , pp. 133-140
    • Alloatti, G.1
  • 130
    • 33747134769 scopus 로고    scopus 로고
    • Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-γ and PTEN
    • Zhao, M. et al. Electrical signals control wound healing through phosphatidylinositol-3-OH kinase-γ and PTEN. Nature 442, 457-460 (2006).
    • (2006) Nature , vol.442 , pp. 457-460
    • Zhao, M.1
  • 131
    • 33750505743 scopus 로고
    • Preparation of antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones
    • PCT Int. Appl., WO-9119707
    • Gammill, R. B., Judge, T. M. & Morris, J. Preparation of antiatherosclerotic and antithrombotic 1-benzopyran-4-ones and 2-amino-1,3-benzoxazine-4-ones. PCT Int. Appl., WO-9119707 (1991).
    • (1991)
    • Gammill, R.B.1    Judge, T.M.2    Morris, J.3
  • 132
    • 0041493126 scopus 로고    scopus 로고
    • Preparation of condensed heteroaryl derivatives as phosphatidylinositol 3-kinase inhibitors and anticancer agents
    • PCT Int. Appl., WO-01083456
    • Hayakawa, M. et al. Preparation of condensed heteroaryl derivatives as phosphatidylinositol 3-kinase inhibitors and anticancer agents. PCT Int. Appl., WO-01083456 (2001).
    • (2001)
    • Hayakawa, M.1
  • 133
    • 0041493126 scopus 로고    scopus 로고
    • Preparation of imidazopyridine derivatives as phosphatidylinositol 3-kinase inhibitors and anticancer agents
    • PCT Int. Appl., WO-01083481
    • Hayakawa, M. et al. Preparation of imidazopyridine derivatives as phosphatidylinositol 3-kinase inhibitors and anticancer agents. PCT Int. Appl., WO-01083481 (2001).
    • (2001)
    • Hayakawa, M.1
  • 134
    • 33750530448 scopus 로고    scopus 로고
    • Quinolin-2-ones and isoxazolo[3,4-c]quinolin-2-ones as modulators of phosphoinositide 3-kinase
    • PCT Int. Appl., WO-03035618
    • Melese, T., Perkins, E. L., Nguyen, A. T. Q. & Sun, D. Quinolin-2-ones and isoxazolo[3,4-c]quinolin-2-ones as modulators of phosphoinositide 3-kinase. PCT Int. Appl., WO-03035618 (2003).
    • (2003)
    • Melese, T.1    Perkins, E.L.2    Nguyen, A.T.Q.3    Sun, D.4
  • 135
    • 33750496088 scopus 로고    scopus 로고
    • Cyclohexothienopyrimidotriazoles and tetrahydropyran othienopyrimidotriazoles as modulators of phosphoinositide 3-kinase
    • PCT Int. Appl., WO-03034997
    • Melese, T., Perkins, E. L., Nguyen, A. T. Q. & Sun, D. C yclohexothienopyrimidotriazoles and tetrahydropyran othienopyrimidotriazoles as modulators of phosphoinositide 3-kinase. PCT Int. Appl., WO-03034997 (2003).
    • (2003)
    • Melese, T.1    Perkins, E.L.2    Nguyen, A.T.Q.3    Sun, D.4
  • 136
    • 84882774063 scopus 로고    scopus 로고
    • Preparation of naphthoquinone derivatives as PI3 kinase inhibitors for treatment of cancer
    • Faming Zhuanli Shenqing Gongkai Shuomingshu, CN 1587255
    • Chang, J., Xie, W. & Wang, L. Preparation of naphthoquinone derivatives as PI3 kinase inhibitors for treatment of cancer. Faming Zhuanli Shenqing Gongkai Shuomingshu, CN 1587255 (2004).
    • (2004)
    • Chang, J.1    Xie, W.2    Wang, L.3
  • 137
    • 33750506153 scopus 로고    scopus 로고
    • Preparation of quaternized derivatives of (morpholinyl) phenylbenzopyranone as PI-3 kinase inhibitor prodrugs
    • PCT Int. Appl., WO-04089925
    • Garlich, J. R., Durden, D. L., Patterson, M., Su, J. & Suhr, R. G. Preparation of quaternized derivatives of (morpholinyl)phenylbenzopyranone as PI-3 kinase inhibitor prodrugs. PCT Int. Appl., WO-04089925 (2004).
    • (2004)
    • Garlich, J.R.1    Durden, D.L.2    Patterson, M.3    Su, J.4    Suhr, R.G.5
  • 138
    • 33750498138 scopus 로고    scopus 로고
    • Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer
    • PCT Int. Appl., WO-04048365
    • Nuss, J. M., Pecchi, S. & Renhowe, P. A. Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol (pi) 3-kinase inhibitors and their use in the treatment of cancer. PCT Int. Appl., WO-04048365 (2004).
    • (2004)
    • Nuss, J.M.1    Pecchi, S.2    Renhowe, P.A.3
  • 139
    • 33750507010 scopus 로고    scopus 로고
    • 2-Thioxo-oxazolidine inhibitors of phosphatidylinositol 3-kinase and their use in treatment of cancer, inflammation, and immune diseases
    • PCT Int. Appl., WO-05002514
    • Drees, B. E. et al. 2-Thioxo-oxazolidine inhibitors of phosphatidylinositol 3-kinase and their use in treatment of cancer, inflammation, and immune diseases. PCT Int. Appl., WO-05002514 (2005).
    • (2005)
    • Drees, B.E.1
  • 140
    • 33750532150 scopus 로고    scopus 로고
    • Preparation of pyrazoloquinolines and related derivatives as inhibitors of phosphatidylinositol 3-kinase
    • PCT Int. Appl., WO-05016245
    • Drees, B. E. et al. Preparation of pyrazoloquinolines and related derivatives as inhibitors of phosphatidylinositol 3-kinase. PCT Int. Appl., WO-05016245 (2005).
    • (2005)
    • Drees, B.E.1
  • 141
    • 33750513259 scopus 로고    scopus 로고
    • Preparation of 2-benzimidazolyl-4,6-dimorpholinylpyrimidine and 2-benzimidazolyl-4,6-dimorpholinyltriazine derivatives as antitumor agents
    • PCT Int. Appl., WO-05095389
    • Kawashima, S. et al. Preparation of 2-benzimidazolyl-4,6-dimorpholinylpyrimidine and 2-benzimidazolyl-4,6-dimorpholinyltriazine derivatives as antitumor agents. PCT Int. Appl., WO-05095389 (2005).
    • (2005)
    • Kawashima, S.1
  • 142
    • 79955807672 scopus 로고    scopus 로고
    • Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol 3 kinase inhibitors for treatment of cancer
    • PCT Int. Appl., WO-06005914
    • Bailey, J. P., Giles, M. B. & Pass, M. Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol 3 kinase inhibitors for treatment of cancer. PCT Int. Appl., WO-06005914 (2006).
    • (2006)
    • Bailey, J.P.1    Giles, M.B.2    Pass, M.3
  • 143
    • 33750503667 scopus 로고    scopus 로고
    • Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol 3-kinase inhibitors and their use in the treatment of cancer
    • PCT Int. Appl., WO-06005915
    • Pass, M. Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol 3-kinase inhibitors and their use in the treatment of cancer. PCT Int. Appl., WO-06005915 (2006).
    • (2006)
    • Pass, M.1
  • 144
    • 33750503667 scopus 로고    scopus 로고
    • Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol 3-kinase (PI3 kinase) inhibitors and their use in the treatment of cancer
    • PCT Int. Appl., WO-06005918
    • Pass, M. Preparation of 2,4,6-trisubstituted pyrimidines as phosphatidylinositol 3-kinase (PI3 kinase) inhibitors and their use in the treatment of cancer. PCT Int. Appl., WO-06005918 (2006).
    • (2006)
    • Pass, M.1
  • 145
    • 33750525869 scopus 로고    scopus 로고
    • Preparation of thiazoloindazoles for treatment and prevention of cancer
    • PCT Int. Appl., WO-06040281
    • Betzemeier, B. et al. Preparation of thiazoloindazoles for treatment and prevention of cancer. PCT Int. Appl., WO-06040281 (2006).
    • (2006)
    • Betzemeier, B.1
  • 146
    • 33750524702 scopus 로고    scopus 로고
    • Analogs of 17-hydroxywortmannin as PI3K inhibitors
    • PCT Int. Appl., WO-06044453
    • Zask, A. et al. Analogs of 17-hydroxywortmannin as PI3K inhibitors. PCT Int. Appl., WO-06044453 (2006).
    • (2006)
    • Zask, A.1
  • 147
    • 33750494601 scopus 로고    scopus 로고
    • Pharmaceutical compounds as PI3K inhibitors
    • PCT Int. Appl., WO-06046040
    • Shuttleworth, S. J. et al. Pharmaceutical compounds as PI3K inhibitors. PCT Int. Appl., WO-06046040 (2006).
    • (2006)
    • Shuttleworth, S.J.1
  • 148
    • 33750494601 scopus 로고    scopus 로고
    • Pharmaceutical compound as PI3K inhibitors
    • PCT Int. Appl., WO-06046031
    • Shuttleworth, S. J. et al. Pharmaceutical compound as PI3K inhibitors. PCT Int. Appl., WO-06046031 (2006).
    • (2006)
    • Shuttleworth, S.J.1
  • 149
    • 33750528616 scopus 로고    scopus 로고
    • 5-heteroaryl thiazoles and their use as PI3K inhibitors
    • PCT Int. Appl., WO-06051270
    • Bengtsson, M. et al. 5-heteroaryl thiazoles and their use as PI3K inhibitors. PCT Int. Appl., WO-06051270 (2006).
    • (2006)
    • Bengtsson, M.1
  • 150
    • 33750531507 scopus 로고    scopus 로고
    • Meroterpenoid inhibitors of phosphoinositide 3 kinase (PI3K)
    • PCT Int. Appl., WO-06081659
    • Andersen, R. et al. Meroterpenoid inhibitors of phosphoinositide 3 kinase (PI3K). PCT Int. Appl., WO-06081659 (2006).
    • (2006)
    • Andersen, R.1
  • 151
    • 31444457132 scopus 로고    scopus 로고
    • Liphagal, a selective inhibitor of PI3 kinase α isolated from the sponge Aka coralliphaga: Structure elucidation and biomimetic synthesis
    • Marion, F. et al. Liphagal, a selective inhibitor of PI3 kinase α isolated from the sponge Aka coralliphaga: Structure elucidation and biomimetic synthesis. Org. Lett. 8, 321-324 (2006).
    • (2006) Org. Lett. , vol.8 , pp. 321-324
    • Marion, F.1
  • 152
    • 33750513035 scopus 로고    scopus 로고
    • Preparation and formulation of morpholino-substituted heterocycles as phosphoinositide 3-kinase inhibitors for therapeutic use
    • PCT Int. Appl., WO-01053266
    • Robertson, A. D. et al. Preparation and formulation of morpholino-substituted heterocycles as phosphoinositide 3-kinase inhibitors for therapeutic use. PCT Int. Appl., WO-01053266 (2001).
    • (2001)
    • Robertson, A.D.1
  • 153
    • 33750506796 scopus 로고    scopus 로고
    • Preparation of morpholinyl- and pyridinyl-substituted heterobicyclic ketones as selective inhibitors of phosphoinositide 3-kinase β for use against thrombosis
    • PCT Int. Appl., WO-04016607
    • Jackson, S. P. et al. Preparation of morpholinyl- and pyridinyl-substituted heterobicyclic ketones as selective inhibitors of phosphoinositide 3-kinase β for use against thrombosis. PCT Int. Appl., WO-04016607 (2004).
    • (2004)
    • Jackson, S.P.1
  • 154
    • 33750496664 scopus 로고    scopus 로고
    • Quinazolinone derivatives as inhibitors of human phosphatidylinositol 3-kinase δ
    • PCT Int. Appl., WO-01081346
    • Sadhu, C. et al. Quinazolinone derivatives as inhibitors of human phosphatidylinositol 3-kinase δ. PCT Int. Appl., WO-01081346 (2001).
    • (2001)
    • Sadhu, C.1
  • 155
    • 33750533655 scopus 로고    scopus 로고
    • Preparation of purinylquinazolinones as inhibitors of human phosphatidylinositol 3-kinase δ
    • PCT Int. Appl., WO-03035075
    • Sadhu, C. et al. Preparation of purinylquinazolinones as inhibitors of human phosphatidylinositol 3-kinase δ. PCT Int. Appl., WO-03035075 (2003).
    • (2003)
    • Sadhu, C.1
  • 156
    • 33750494601 scopus 로고    scopus 로고
    • Pharmaceutical compounds as PI3K inhibitors
    • PCT Int. Appl., WO-06046035
    • Shuttleworth, S. J. et al. Pharmaceutical compounds as PI3K inhibitors. PCT Int. Appl., WO-06046035 (2006).
    • (2006)
    • Shuttleworth, S.J.1
  • 157
    • 33750533656 scopus 로고    scopus 로고
    • 3-arylsulfanyl and 3-heteroarylsulfanyl substituted benzo[b]thiophenes as therapeutic agents
    • PCT Int. Appl., WO-04108716
    • Gogliotti, R. D., Lee, H. T., Sexton, K. E. & Visnick, M. 3-arylsulfanyl and 3-heteroarylsulfanyl substituted benzo[b]thiophenes as therapeutic agents. PCT Int. Appl., WO-04108716 (2004).
    • (2004)
    • Gogliotti, R.D.1    Lee, H.T.2    Sexton, K.E.3    Visnick, M.4
  • 158
    • 33750520801 scopus 로고    scopus 로고
    • A preparation of (cycloalkylsulfanyl)benzo[b]thiophene derivatives, useful as selective PI3Kγ inhibitors
    • PCT Int. Appl., WO-04108714
    • Gogliotti, R. D., Lee, H. T., Sexton, K. E. & Visnick, M. A preparation of (cycloalkylsulfanyl)benzo[b]thiophene derivatives, useful as selective PI3Kγ inhibitors. PCT Int. Appl., WO-04108714 (2004).
    • (2004)
    • Gogliotti, R.D.1    Lee, H.T.2    Sexton, K.E.3    Visnick, M.4
  • 159
    • 33750497696 scopus 로고    scopus 로고
    • Preparation of 2-imino-4-(thio)oxo-5-polycyclovinylazolines as PI3 kinase inhibitors
    • WO-05011686
    • Rueckle, T., Shaw, J., Church, D. D. & Covini, D. Preparation of 2-imino-4-(thio)oxo-5-polycyclovinylazolines as PI3 kinase inhibitors. WO-05011686 (2005).
    • (2005)
    • Rueckle, T.1    Shaw, J.2    Church, D.D.3    Covini, D.4
  • 160
    • 33750506568 scopus 로고    scopus 로고
    • Pyridine methylene azolidinones and use thereof phosphoinositide inhibitors
    • PCT Int. Appl., WO-06024666
    • Rueckle, T. et al. Pyridine methylene azolidinones and use thereof phosphoinositide inhibitors. PCT Int. Appl., WO-06024666 (2006).
    • (2006)
    • Rueckle, T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.