메뉴 건너뛰기




Volumn 62, Issue 9, 2009, Pages 501-505

Bingchamides a and b, two novel cyclic pentapeptides from the Streptomyces bingchenggensis: Fermentation, isolation, structure elucidation and biological properties

Author keywords

Antitumor activity; Bingchamides a and b; Cyclic pentapeptides; Streptomyces bingchenggensis

Indexed keywords

ANTINEOPLASTIC AGENT; BINGCHAMIDE A; BINGCHAMIDE B; PENTAPEPTIDE; SANSALVAMIDE A; UNCLASSIFIED DRUG;

EID: 70349594562     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.1038/ja.2009.60     Document Type: Article
Times cited : (24)

References (21)
  • 1
    • 34948876455 scopus 로고    scopus 로고
    • Two new-class milbemycins from Streptomyces bingchenggensis Fermentation, isolation, structure elucidation and biological properties
    • Xiang, W. S., Wang, J. D., Wang, X. J. & Zhang, J. Two new-class milbemycins from Streptomyces bingchenggensis Fermentation, isolation, structure elucidation and biological properties. J. Antibiot. 60, 351-356 (2007).
    • (2007) J. Antibiot. , vol.60 , pp. 351-356
    • Xiang, W.S.1    Wang, J.D.2    Wang, X.J.3    Zhang, J.4
  • 2
    • 38749153988 scopus 로고    scopus 로고
    • Further new milbemycin antibiotics from Streptomyces bingchenggensis
    • Xiang, W. S., Wang, J. D., Wang, X. J., Zhang, J. & Wang, Z. Further new milbemycin antibiotics from Streptomyces bingchenggensis. J. Antibiot. 60, 608-613 (2007).
    • (2007) J. Antibiot. , vol.60 , pp. 608-613
    • Xiang, W.S.1    Wang, J.D.2    Wang, X.J.3    Zhang, J.4    Wang, Z.5
  • 3
    • 44649176384 scopus 로고    scopus 로고
    • New Seco-milbemycins from Streptomyces bingchenggensis: Fermentation, isolation and structure elucidation
    • Xiang, W. S., Wang, J. D., Fan, H. M., Wang, X. J. & Zhang, J. New Seco-milbemycins from Streptomyces bingchenggensis: fermentation, isolation and structure elucidation. J. Antibiot. 60, 27-32 (2008).
    • (2008) J. Antibiot. , vol.60 , pp. 27-32
    • Xiang, W.S.1    Wang, J.D.2    Fan, H.M.3    Wang, X.J.4    Zhang, J.5
  • 4
    • 67249114338 scopus 로고    scopus 로고
    • A novel macrolide compound from Streptomyces bingchenggensis fermentation, isolation, structure elucidation and biological properties
    • Xiang, W. S., Wang, J. D., Wang, X. J. & Zhang, J. A novel macrolide compound from Streptomyces bingchenggensis fermentation, isolation, structure elucidation and biological properties. J. Antibiot. 62, 229-231 (2009).
    • (2009) J. Antibiot. , vol.62 , pp. 229-231
    • Xiang, W.S.1    Wang, J.D.2    Wang, X.J.3    Zhang, J.4
  • 5
    • 0032977819 scopus 로고    scopus 로고
    • Mechanism of inhibition of a poxvirus topoisomerase by the marine natural product sansalvamide
    • Hwang, Y. et al. Mechanism of inhibition of a poxvirus topoisomerase by the marine natural product sansalvamide. A. Mol. Pharmacol. 6, 1049-1053 (1999).
    • (1999) A. Mol. Pharmacol. , vol.6 , pp. 1049-1053
    • Hwang, Y.1
  • 6
    • 0034676534 scopus 로고    scopus 로고
    • Rapid high-yield, solid-phase synthesis of the antitumor antibiotic sansalvamide A using a side-chain-tethered phenylalanine building block
    • Lee, Y. & Silverman, R. B. Rapid, high-yield, solid-phase synthesis of the antitumor antibiotic sansalvamide A using a side-chain-tethered phenylalanine building block. Org. Lett. 2, 3743-3746 (2000).
    • (2000) Org. Lett. , vol.2 , pp. 3743-3746
    • Lee, Y.1    Silverman, R.B.2
  • 7
    • 0037078829 scopus 로고    scopus 로고
    • Solid-phase Pd-catalyzed siliconaryl carbon bond formation. Synthesis of sansalvamide A peptide
    • Gu, W., Liu, S. & Silverman, R. B. Solid-phase, Pd-catalyzed siliconaryl carbon bond formation. Synthesis of sansalvamide A peptide. Org. Lett. 4, 4171-4174 (2002).
    • (2002) Org. Lett. , vol.4 , pp. 4171-4174
    • Gu, W.1    Liu, S.2    Silverman, R.B.3
  • 8
    • 23944442706 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of novel sansalvamide A derivatives
    • Carroll, C. L. et al. Synthesis and cytotoxicity of novel sansalvamide A derivatives. Org. Lett. 7, 3481-3484 (2005).
    • (2005) Org. Lett. , vol.7 , pp. 3481-3484
    • Carroll, C.L.1
  • 9
    • 33244483270 scopus 로고    scopus 로고
    • Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives
    • Otrubova, K. et al. Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives. Chem. Commun. 9, 1033-1034 (2006).
    • (2006) Chem. Commun. , vol.9 , pp. 1033-1034
    • Otrubova, K.1
  • 10
    • 34247580055 scopus 로고    scopus 로고
    • Scaffold targeting drug-resistant colon cancers
    • Otrubova, K., McGuire, K. L. & McAlpine, S. R. Scaffold targeting drug-resistant colon cancers. J. Med. Chem. 9, 1999-2002 (2007).
    • (2007) J. Med. Chem. , vol.9 , pp. 1999-2002
    • Otrubova, K.1    McGuire, K.L.2    McAlpine, S.R.3
  • 11
    • 33645329115 scopus 로고    scopus 로고
    • Plant Cyclopeptides
    • Tan, N. H. & Zhou, J. Plant Cyclopeptides. Chem. Rev. 106, 840-895 (2006).
    • (2006) Chem. Rev. , vol.106 , pp. 840-895
    • Tan, N.H.1    Zhou, J.2
  • 12
    • 53149144247 scopus 로고    scopus 로고
    • Design and synthesis of cyclo[-Arg-Gly-Asp-c(triazole)-Gly-Xaa-] peptide analogues by click chemistry
    • Liu, Y. Q. et al. Design and synthesis of cyclo[-Arg-Gly-Asp-c(triazole)- Gly-Xaa-] peptide analogues by click chemistry. Tetrahedron 47, 10728-10734 (2008).
    • (2008) Tetrahedron , vol.47 , pp. 10728-10734
    • Liu, Y.Q.1
  • 13
    • 52049109838 scopus 로고    scopus 로고
    • Natural products in drug discovery
    • Harvey, A. L. Natural products in drug discovery. Drug Discov. Today 13, 895-901 (2008).
    • (2008) Drug Discov. Today , vol.13 , pp. 895-901
    • Harvey, A.L.1
  • 14
    • 39149096281 scopus 로고    scopus 로고
    • Comprehensive study of sansalvamide A derivatives and their structure-activity relationships against drug-resistant colon cancer cell lines
    • Otrubova, K., Lushington, G., McGuire, K. L. & McAlpine, S. R. Comprehensive study of sansalvamide A derivatives and their structure-activity relationships against drug-resistant colon cancer cell lines. J. Med. Chem. 3, 530-544 (2008).
    • (2008) J. Med. Chem. , vol.3 , pp. 530-544
    • Otrubova, K.1    Lushington, G.2    McGuire, K.L.3    McAlpine, S.R.4
  • 15
    • 38749144034 scopus 로고    scopus 로고
    • Synthesis and cytotoxicity of a new class of potent decapeptide macrocycles
    • Davis, M. R. et al. Synthesis and cytotoxicity of a new class of potent decapeptide macrocycles. Org. Lett. 2, 177-180 (2008).
    • (2008) Org. Lett. , vol.2 , pp. 177-180
    • Davis, M.R.1
  • 16
    • 34547855100 scopus 로고    scopus 로고
    • Identification of Sansalvamide A analog potent against pancreatic cancer cell lines
    • Pan, P. S., McGuire, K. L. & McAlpine, S. R. Identification of Sansalvamide A analog potent against pancreatic cancer cell lines. Bioorg. Med. Chem. Lett. 18, 5072-5077 (2007).
    • (2007) Bioorg. Med. Chem. Lett. , vol.18 , pp. 5072-5077
    • Pan, P.S.1    McGuire, K.L.2    McAlpine, S.R.3
  • 17
    • 33947246678 scopus 로고    scopus 로고
    • Synthesis of second-generation sansalvamide A derivatives: Novel templates as potential antitumor agents
    • Rodriguez, R. A. et al. Synthesis of second-generation sansalvamide A derivatives: novel templates as potential antitumor agents. J. Org. Chem. 6, 1980-2002 (2007).
    • (2007) J. Org. Chem. , vol.6 , pp. 1980-2002
    • Rodriguez, R.A.1
  • 18
    • 33745592766 scopus 로고    scopus 로고
    • Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-2
    • Styers, T. J. et al. Synthesis of Sansalvamide A derivatives and their cytotoxicity in the MSS colon cancer cell line HT-2. Bioorg. Med. Chem. 16, 5625-5631 (2006).
    • (2006) Bioorg. Med. Chem. , vol.16 , pp. 5625-5631
    • Styers, T.J.1
  • 19
    • 33244483270 scopus 로고    scopus 로고
    • Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives
    • Otrubova, K. et al. Synthesis and novel structure-activity relationships of potent sansalvamide A derivatives. Chem. Commun. 9, 1033-1034 (2006).
    • (2006) Chem. Commun. , vol.9 , pp. 1033-1034
    • Otrubova, K.1
  • 20
    • 30544431590 scopus 로고    scopus 로고
    • A novel peptide sansalvamide analogue inhibits pancreatic cancer cell growth through G0/G1 cell-cycle arrest
    • Ujiki, M. B. et al. A novel peptide sansalvamide analogue inhibits pancreatic cancer cell growth through G0/G1 cell-cycle arrest. Biochem. Biophys. Res. Commun. 4, 1224-1228 (2006).
    • (2006) Biochem. Biophys. Res. Commun. , vol.4 , pp. 1224-1228
    • Ujiki, M.B.1
  • 21
    • 0034127813 scopus 로고    scopus 로고
    • Human oesophageal adenocarcinoma cell lines JROECL 47 and JROECL 50 are admixtures of the human colon carcinoma cell line HCT 11
    • Wijnhoven, B. P. et al. Human oesophageal adenocarcinoma cell lines JROECL 47 and JROECL 50 are admixtures of the human colon carcinoma cell line HCT 11. Br. J. Cancer. 9, 1510-1512 (2000).
    • (2000) Br. J. Cancer. , vol.9 , pp. 1510-1512
    • Wijnhoven, B.P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.