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Volumn 337, Issue 2, 2011, Pages 479-486

Proteasome regulator marizomib (NPI-0052) Exhibits prolonged inhibition, attenuated efflux, and greater cytotoxicity than its reversible analogs

Author keywords

[No Author keywords available]

Indexed keywords

1 [(CYCLOHEX 2 ENYL)(HYDROXY)METHYL] 4 ETHYL 5 METHYL 6 OXA 2 AZABICYCLO[3.2.0]HEPTANE 3,7 DIONE; 1 [(CYCLOHEX 2 ENYL)(HYDROXY)METHYL] 4,5 DIMETHYL 6 OXA 2 AZABICYCLO[3.2.0]HEPTANE 3,7 DIONE; 1 [(CYCLOHEX 2 ENYL)(HYDROXY)METHYL] 5 METHYL 4 PROPYL 6 OXA 2 AZABICYCLO[3.2.0]HEPTANE 3,7 DIONE; 2 1 [[(CYCLOHEX 2 ENYL)(HYDROXY)METHYL] 5 METHYL 3,7 DIOXO 6 OXA 2 AZABICYCLO[3.2.0]HEPTAN 4 YL]ETHYL BENZENESULFONATE; 2 1 [[(CYCLOHEX 2 ENYL)(HYDROXY)METHYL] 5 METHYL 3,7 DIOXO 6 OXA 2 AZABICYCLO[3.2.0]HEPTANE 4 YL] METHANESULFONATE; ABC TRANSPORTER; NPI 0047; NPI 2063; NPI 2080; NPI 2150; NPI 2151; PROTEASOME; SALINOSPORAMIDE A; UNCLASSIFIED DRUG;

EID: 79954990288     PISSN: 00223565     EISSN: 15210103     Source Type: Journal    
DOI: 10.1124/jpet.110.177824     Document Type: Article
Times cited : (25)

References (22)
  • 1
    • 2342613652 scopus 로고    scopus 로고
    • The proteasome: A suitable antineoplastic target
    • Adams J (2004) The proteasome: A suitable antineoplastic target. Nat Rev Cancer 4:349-360. (Pubitemid 38579481)
    • (2004) Nature Reviews Cancer , vol.4 , Issue.5 , pp. 349-360
    • Adams, J.1
  • 2
    • 4944261541 scopus 로고    scopus 로고
    • Bortezomib therapy for myeloma
    • Anderson KC (2004) Bortezomib therapy for myeloma. Curr Hematol Rep 3:65-66.
    • (2004) Curr Hematol Rep , vol.3 , pp. 65-66
    • Anderson, K.C.1
  • 5
    • 13844320703 scopus 로고    scopus 로고
    • Proteasome inhibition in multiple myeloma: Therapeutic implication
    • Chauhan D, Hideshima T, and Anderson KC (2005b) Proteasome inhibition in multiple myeloma: Therapeutic implication. Annu Rev Pharmacol Toxicol 45:465-476.
    • (2005) Annu Rev Pharmacol Toxicol , vol.45 , pp. 465-476
    • Chauhan, D.1    Hideshima, T.2    Anderson, K.C.3
  • 6
    • 34548013292 scopus 로고    scopus 로고
    • A mechanistic and kinetic study of the β-lactone hydrolysis of salinosporamide A (NPI-0052), a novel proteasome inhibitor
    • DOI 10.1002/jps.20835
    • Denora N, Potts BC, and Stella VJ (2007) A mechanistic and kinetic study of the β-lactone hydrolysis of Salinosporamide A (NPI-0052), a novel proteasome inhibitor. J Pharm Sci 96:2037-2047. (Pubitemid 47280100)
    • (2007) Journal of Pharmaceutical Sciences , vol.96 , Issue.8 , pp. 2037-2047
    • Denora, N.1    Potts, B.C.M.2    Stella, V.J.3
  • 7
    • 0037455147 scopus 로고    scopus 로고
    • Salinosporamide A: A highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus Salinospora
    • DOI 10.1002/anie.200390115
    • Feling RH, Buchanan GO, Mincer TJ, Kauffman CA, Jensen PR, and Fenical W (2003) Salinosporamide A: A highly cytotoxic proteasome inhibitor from a novel microbial source, a marine bacterium of the new genus salinospora. Angew Chem Int Ed Engl 42:355-357. (Pubitemid 36176323)
    • (2003) Angewandte Chemie - International Edition , vol.42 , Issue.3 , pp. 355-357
    • Feling, R.H.1    Buchanan, G.O.2    Mincer, T.J.3    Kauffman, C.A.4    Jensen, P.R.5    Fenical, W.6
  • 8
    • 33646137808 scopus 로고    scopus 로고
    • Crystal structures of Salinosporamide A (NPI-0052) and B (NPI-0047) in complex with the 20S proteasome reveal important consequences of β-lactone ring opening and a mechanism for irreversible binding
    • Groll M, Huber R, and Potts BC (2006) Crystal structures of Salinosporamide A (NPI-0052) and B (NPI-0047) in complex with the 20S proteasome reveal important consequences of β-lactone ring opening and a mechanism for irreversible binding. J Am Chem Soc 128:5136-5141.
    • (2006) J Am Chem Soc , vol.128 , pp. 5136-5141
    • Groll, M.1    Huber, R.2    Potts, B.C.3
  • 9
    • 69949108710 scopus 로고    scopus 로고
    • Snapshots of the fluorosalinosporamide/20S complex offer mechanistic insights for fine tuning proteasome inhibition
    • Groll M, McArthur KA, Macherla VR, Manam RR, and Potts BC (2009) Snapshots of the fluorosalinosporamide/20S complex offer mechanistic insights for fine tuning proteasome inhibition. J Med Chem 52:5420-5428.
    • (2009) J Med Chem , vol.52 , pp. 5420-5428
    • Groll, M.1    McArthur, K.A.2    Macherla, V.R.3    Manam, R.R.4    Potts, B.C.5
  • 11
    • 0036884062 scopus 로고    scopus 로고
    • Molecular mechanisms of novel therapeutic approaches for multiple myeloma
    • DOI 10.1038/nrc952
    • Hideshima T and Anderson KC (2002) Molecular mechanisms of novel therapeutic approaches for multiple myeloma. Nat Rev Cancer 2:927-937. (Pubitemid 37328894)
    • (2002) Nature Reviews Cancer , vol.2 , Issue.12 , pp. 927-937
    • Hideshima, T.1    Anderson, K.C.2
  • 15
    • 33847686427 scopus 로고    scopus 로고
    • Stereoselective enzymatic reduction of keto-salinosporamide to (-)-salinosporamide A (NPI-0052)
    • DOI 10.1016/j.tetlet.2007.02.017, PII S0040403907002857
    • Manam RR, Macherla VR, and Potts BCM (2007) Stereoselective enzymatic reduction of keto-salinosporamide to (β)-salinosporamide A (NPI-0052). Tetrahed Lett 48:2537-2540. (Pubitemid 46356466)
    • (2007) Tetrahedron Letters , vol.48 , Issue.14 , pp. 2537-2540
    • Manam, R.R.1    Macherla, V.R.2    Potts, B.C.M.3
  • 17
    • 4344701681 scopus 로고    scopus 로고
    • Aureoverticillactam, a novel 22-atom macrocyclic lactam from the marine actinomycete Streptomyces aureoverticillatus
    • DOI 10.1021/np049970g
    • Mitchell SS, Nicholson B, Teisan S, Lam KS, and Potts BC (2004) Aureoverticillactam, a novel 22-atom macrocyclic lactam from the marine actinomycete Streptomyces aureoverticillatus. J Nat Prod 67:1400-1402. (Pubitemid 39145651)
    • (2004) Journal of Natural Products , vol.67 , Issue.8 , pp. 1400-1402
    • Mitchell, S.S.1    Nicholson, B.2    Teisan, S.3    Lam, K.S.4    Potts, B.C.M.5
  • 20
    • 34249740069 scopus 로고    scopus 로고
    • The establishment of two paclitaxel-resistant prostate cancer cell lines and the mechanisms of paclitaxel resistance with two cell lines
    • DOI 10.1002/pros.20581
    • Takeda M, Mizokami A, Mamiya K, Li YQ, Zhang J, Keller ET, and Namiki M (2007) The establishment of two paclitaxel-resistant prostate cancer cell lines and the mechanisms of paclitaxel resistance with two cell lines. Prostate 67:955-967. (Pubitemid 46828929)
    • (2007) Prostate , vol.67 , Issue.9 , pp. 955-967
    • Takeda, M.1    Mizokami, A.2    Mamiya, K.3    You, Q.L.4    Zhang, J.5    Keller, E.T.6    Namiki, M.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.