메뉴 건너뛰기




Volumn 53, Issue 4, 2010, Pages 1048-1052

Determination of SNX-2112, a selective Hsp90 inhibitor, in plasma samples by high-performance liquid chromatography and its application to pharmacokinetics in rats

Author keywords

HPLC; Pharmacokinetics; Rat plasma; SNX 2112; UV detector

Indexed keywords

4 (6,6 DIMETHYL 4 O 3 TRIFLUOROMETHYL 4,5,6,7 TETRAHYDRO 1 INDOLEYL) 2 [1 (4 HYDROXYCYCLOHEXANE)AMINO]BENZAMIDE; HEAT SHOCK PROTEIN 90 INHIBITOR; SNX 2112; UNCLASSIFIED DRUG;

EID: 77955588946     PISSN: 07317085     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpba.2010.06.031     Document Type: Article
Times cited : (9)

References (14)
  • 2
    • 0035718899 scopus 로고    scopus 로고
    • Structure, function, and mechanism of the Hsp90 molecular chaperone
    • Pearl L.H., Prodromou C. Structure, function, and mechanism of the Hsp90 molecular chaperone. Adv. Protein Chem. 2001, 59:157-186.
    • (2001) Adv. Protein Chem. , vol.59 , pp. 157-186
    • Pearl, L.H.1    Prodromou, C.2
  • 3
    • 0031895351 scopus 로고    scopus 로고
    • The Hsp902 based chaperone system: involvement in signal transduction from a variety of hormone and growth factor receptors
    • Pratt W.B. The Hsp902 based chaperone system: involvement in signal transduction from a variety of hormone and growth factor receptors. Proc. Soc. Exp. Biol. Med. 1998, 217:420-434.
    • (1998) Proc. Soc. Exp. Biol. Med. , vol.217 , pp. 420-434
    • Pratt, W.B.1
  • 4
    • 0027081145 scopus 로고
    • Potent and specific inhibition of p60v-src protein kinase both in vivo and in vitro by radicicol
    • Kwon H.J., Yoshida M., Fukui Y., Horinouchi S., Beppu T. Potent and specific inhibition of p60v-src protein kinase both in vivo and in vitro by radicicol. Cancer Res. 1992, 52:6926-6930.
    • (1992) Cancer Res. , vol.52 , pp. 6926-6930
    • Kwon, H.J.1    Yoshida, M.2    Fukui, Y.3    Horinouchi, S.4    Beppu, T.5
  • 6
    • 0033863883 scopus 로고    scopus 로고
    • The heat shock protein 90 antagonist geldanamycin alters chaperone association with p210bcr-abl and v-src proteins before their degradation by the proteasome
    • An W.G., Schulte T.W., Neckers L.M. The heat shock protein 90 antagonist geldanamycin alters chaperone association with p210bcr-abl and v-src proteins before their degradation by the proteasome. Cell Growth Differ. 2000, 11:355-360.
    • (2000) Cell Growth Differ. , vol.11 , pp. 355-360
    • An, W.G.1    Schulte, T.W.2    Neckers, L.M.3
  • 8
    • 0032101569 scopus 로고    scopus 로고
    • Metabolism of 17-(allylamino)-17-demethoxygeldanamycin (NSC330507) bymurine and human hepatic preparations
    • Egorin M.J., Rosen D.M., Wolff J.H., Callery P.S., Musser S.M., Eiseman J.L. Metabolism of 17-(allylamino)-17-demethoxygeldanamycin (NSC330507) bymurine and human hepatic preparations. Cancer Res. 1998, 58:2385-2396.
    • (1998) Cancer Res. , vol.58 , pp. 2385-2396
    • Egorin, M.J.1    Rosen, D.M.2    Wolff, J.H.3    Callery, P.S.4    Musser, S.M.5    Eiseman, J.L.6
  • 9
    • 0031875042 scopus 로고    scopus 로고
    • The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin
    • Schulte T.W., Neckers L.M. The benzoquinone ansamycin 17-allylamino-17-demethoxygeldanamycin binds to HSP90 and shares important biologic activities with geldanamycin. Cancer Chemother. Pharmacol. 1998, 42:273-279.
    • (1998) Cancer Chemother. Pharmacol. , vol.42 , pp. 273-279
    • Schulte, T.W.1    Neckers, L.M.2
  • 12
    • 59649086503 scopus 로고    scopus 로고
    • SNX-2112, a selective Hsp90 inhibitor, potently inhibits tumor cell growth, angiogenesis, and osteoclastogenesis in multiple myeloma and other hematological tumors by abrogating signaling via Akt and ERK
    • Okawa Y., Hideshima T., Steed P., Vallet S., Hall S., Huang K., Rice J., Barabasz A., Foley B., Ikeda H., Raje N., Kiziltepe T., Yasui H., Enatsu S., Anderson K.C. SNX-2112, a selective Hsp90 inhibitor, potently inhibits tumor cell growth, angiogenesis, and osteoclastogenesis in multiple myeloma and other hematological tumors by abrogating signaling via Akt and ERK. Blood 2009, 113:846-855.
    • (2009) Blood , vol.113 , pp. 846-855
    • Okawa, Y.1    Hideshima, T.2    Steed, P.3    Vallet, S.4    Hall, S.5    Huang, K.6    Rice, J.7    Barabasz, A.8    Foley, B.9    Ikeda, H.10    Raje, N.11    Kiziltepe, T.12    Yasui, H.13    Enatsu, S.14    Anderson, K.C.15
  • 13
    • 67349255247 scopus 로고    scopus 로고
    • Transcriptomic and proteomic approach to studying SNX-2112-induced K562 cells apoptosis and anti-leukemia activity in K562-NOD/SCID mice
    • Jin L., Xiao C.L., Lu C.H., Xia M., Xing G.W., Xiong S., Liu Q.Y., Liu H., Li Y.C., Ge F., Wang Q.D., He Q.Y., Wang Y.F. Transcriptomic and proteomic approach to studying SNX-2112-induced K562 cells apoptosis and anti-leukemia activity in K562-NOD/SCID mice. FEBS Lett. 2009, 583:1859-1866.
    • (2009) FEBS Lett. , vol.583 , pp. 1859-1866
    • Jin, L.1    Xiao, C.L.2    Lu, C.H.3    Xia, M.4    Xing, G.W.5    Xiong, S.6    Liu, Q.Y.7    Liu, H.8    Li, Y.C.9    Ge, F.10    Wang, Q.D.11    He, Q.Y.12    Wang, Y.F.13
  • 14
    • 51449115938 scopus 로고    scopus 로고
    • A phase 1 dose-escalation study of the safety and pharmacokinetics (PK) of the oral Hsp90 inhibitor SNX-5422
    • Bryson J.C., Infante J.R., Ramanathan R.K., Jones S.F., Von Hoff D.D., Burris H.A. A phase 1 dose-escalation study of the safety and pharmacokinetics (PK) of the oral Hsp90 inhibitor SNX-5422. J. Clin. Oncol. 2008, 26:14613.
    • (2008) J. Clin. Oncol. , vol.26 , pp. 14613
    • Bryson, J.C.1    Infante, J.R.2    Ramanathan, R.K.3    Jones, S.F.4    Von Hoff, D.D.5    Burris, H.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.