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Volumn 2, Issue 11, 2011, Pages 809-813

Erratum: Correction to highly selective and potent thiophenes as PI3K inhibitors with oral antitumor activity (ACS Medicinal Chemistry Letters (2011) 2:11 (809-813) DOI: 10.1021/ml200126j);Highly selective and potent thiophenes as PI3K inhibitors with oral antitumor activity

Author keywords

antitumor activity; Kinase inhibitor; mTOR; PI3K; thiophene; triazole

Indexed keywords

MAMMALIAN TARGET OF RAPAMYCIN; PHOSPHATIDYLINOSITOL 3 KINASE INHIBITOR; THIOPHENE DERIVATIVE;

EID: 80955128586     PISSN: None     EISSN: 19485875     Source Type: Journal    
DOI: 10.1021/ml300020u     Document Type: Erratum
Times cited : (33)

References (11)
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    • DOI 10.1038/nrg1879, PII NRG1879
    • Engelman, J. A.; Luo, J.; Cantley, L. C. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism Nat. Rev. Genet. 2006, 7, 606-619 (Pubitemid 44100518)
    • (2006) Nature Reviews Genetics , vol.7 , Issue.8 , pp. 606-619
    • Engelman, J.A.1    Luo, J.2    Cantley, L.C.3
  • 2
    • 67749122122 scopus 로고    scopus 로고
    • Targeting PI3K signalling in cancer: Opportunities, challenges and limitations
    • Engelman, J. A. Targeting PI3K signalling in cancer: Opportunities, challenges and limitations Nat. Rev. Genet. 2009, 9, 550-62
    • (2009) Nat. Rev. Genet. , vol.9 , pp. 550-562
    • Engelman, J.A.1
  • 3
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    • Emerging Therapies based on inhibitors of phosphatidyl-inositol-3-kinases
    • Nuss, J. M; Tsuhako, A. L; Anand, N. K. Emerging Therapies based on inhibitors of phosphatidyl-inositol-3-kinases Annu. Rep. Med. Chem. 2009, 44, 339-356
    • (2009) Annu. Rep. Med. Chem. , vol.44 , pp. 339-356
    • Nuss, J.M.1    Tsuhako, A.L.2    Anand, N.K.3
  • 9
    • 84866762779 scopus 로고    scopus 로고
    • 1(Metabolism, Pharmacokinetics and Toxicity of Functional Groups), Carboxylic acids and their bioisosteres
    • Kalgutkar, A. S.; Daniels, J. S. 1(Metabolism, Pharmacokinetics and Toxicity of Functional Groups), Carboxylic acids and their bioisosteres RSC Drug Discovery Ser. 2010, 99-167
    • (2010) RSC Drug Discovery Ser. , pp. 99-167
    • Kalgutkar, A.S.1    Daniels, J.S.2
  • 11
    • 79957451449 scopus 로고    scopus 로고
    • Development of Scalable Syntheses of Selective PI3K inhibitors
    • For a detailed discussion of the synthetic chemistry, see; ()
    • For a detailed discussion of the synthetic chemistry, see Huang, Q; Richardson, P. F.; Sach, N. W.; Zhu, J; Liu, K. K.-C.; Smith, G. L.; Bowles, D. M. Development of Scalable Syntheses of Selective PI3K inhibitors Org. Process Res. Dev. 2011, 15 (3) 556-564
    • (2011) Org. Process Res. Dev. , vol.15 , Issue.3 , pp. 556-564
    • Huang, Q.1    Richardson, P.F.2    Sach, N.W.3    Zhu, J.4    Liu, K.K.-C.5    Smith, G.L.6    Bowles, D.M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.