메뉴 건너뛰기




Volumn 4, Issue 5, 2001, Pages 586-589

MCC-555 Mitsubishi-Tokyo pharmaceuticals

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33646779132     PISSN: 13697056     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (34)
  • 2
    • 33746963095 scopus 로고    scopus 로고
    • Widdowson PS, Kadowaki S, Williams G BR J PHARMACOL 1997 122 Suppl 149P Reports the action of MCC-555 in Zucker and ZDF rats.
    • Improved insulin sensitivity in Zucker and ZDF rats following chronic treatment with novel thiazolidinedione MCC-555. Upton R, Widdowson PS, Kadowaki S, Williams G BR J PHARMACOL 1997 122 Suppl 149P Reports the action of MCC-555 in Zucker and ZDF rats.
    • Upton, R.1
  • 6
    • 0032484224 scopus 로고    scopus 로고
    • Bailey ST, KrakowSL, Minami C, LazarMAetalJBIOL CHEM1998 273 49 32679 32684
    • A potent antidiabetic thiazolidinedione with unique peroxisome proliferator-activated receptor -activating properties. Reginato MJ, Bailey ST, KrakowSL, Minami C, LazarMAetalJBIOL CHEM1998 273 49 32679 32684
  • 9
    • 33747007118 scopus 로고    scopus 로고
    • UK. Bums T IDDB MEETING REPORT 1999 April 21 Defines the potency of MCC-555.
    • Novel Drug Developments for NIDDM and Insulin Resistance IBC Conference London, UK. Bums T IDDB MEETING REPORT 1999 April 21 Defines the potency of MCC-555.
  • 16
    • 18544403720 scopus 로고    scopus 로고
    • BIOORG MED CHEM LETT 1998 8 19 2725 - 2730 Clarifies the characteristics of these novel thiazolidinediones.
    • Synthesis and biological activity of novel thiazolidinediones. Prabhakar C et al BIOORG MED CHEM LETT 1998 8 19 2725 - 2730 Clarifies the characteristics of these novel thiazolidinediones.
    • Synthesis and Biological Activity of Novel Thiazolidinediones.
    • Prabhakar, C.1
  • 17
    • 33746987494 scopus 로고    scopus 로고
    • and their use in therapeutic approaches to insulin resistance.
    • Therapeutic approaches to insulin resistance. Laight DW EXP OP/NTHERR4T20001011 1703-1709 Explains the nature and function of PPARy agonists, and their use in therapeutic approaches to insulin resistance.
  • 19
    • 33746981246 scopus 로고    scopus 로고
    • Nakamura J, Hamada Y, Nakayama M, Chaya S, Komori H, Kiriyama T, Kasuya Y, Yasuda Y, Hotta N DIABETOLOGIA 2000 43 Suppl 1 A190 Explains the action of MCC-555 on hepatocytes.
    • Acute effect of MCC-555 in isolated hepatocytes of Otsuka LongEvans Tokushima Fatty rats. Mizubayashi R, Nakamura J, Hamada Y, Nakayama M, Chaya S, Komori H, Kiriyama T, Kasuya Y, Yasuda Y, Hotta N DIABETOLOGIA 2000 43 Suppl 1 A190 Explains the action of MCC-555 on hepatocytes.
    • Acute Effect of MCC-555 in Isolated Hepatocytes of Otsuka LongEvans Tokushima Fatty Rats.
    • Mizubayashi, R.1
  • 29
    • 0034082510 scopus 로고    scopus 로고
    • Goldstein BJINTJ CLIN PRACT2000 54 5 333-337
    • Rosiglitazone. Goldstein BJINTJ CLIN PRACT2000 54 5 333-337
    • Rosiglitazone.
  • 30
    • 33746949285 scopus 로고    scopus 로고
    • disposition, and metabolism of rostglitazone, a potent thiazolidinedione insulin sensitizer, in humans. Cox PJ, Ryan DA, Mollis FJ, Harris AM, Miller AK, Vousden M, Cowley H DRUG METAB DISPOS 2000 174287-294
    • Absorption, disposition, and metabolism of rostglitazone, a potent thiazolidinedione insulin sensitizer, in humans. Cox PJ, Ryan DA, Mollis FJ, Harris AM, Miller AK, Vousden M, Cowley H DRUG METAB DISPOS 2000 174287-294
  • 33
    • 33746979707 scopus 로고    scopus 로고
    • Oe T, Suehiro I, Nakamura F MITSUBISHI-TOKYO PHARMACEUTICALS EP-00604983 1996
    • Naphthalene derivatives. Ueno H, Oe T, Suehiro I, Nakamura F MITSUBISHI-TOKYO PHARMACEUTICALS EP-00604983 1996
    • Naphthalene Derivatives.
    • Ueno, H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.