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Volumn 446, Issue 3, 2014, Pages 782-785

One step synthesis of 6-oxo-cholestan-3β,5α-diol

Author keywords

Cancer; Cholestanetriol; OCDO; Oxysterols; Radiolabelled

Indexed keywords

CARBON 14; CHOLESTANE DERIVATIVE; CHOLESTEROL DERIVATIVE; IODINE DERIVATIVE; PERIODATE; STEROL DERIVATIVE;

EID: 84898797442     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2014.01.138     Document Type: Article
Times cited : (11)

References (23)
  • 1
    • 84884230660 scopus 로고    scopus 로고
    • The oxysterol-CXCR2 axis plays a key role in the recruitment of tumor-promoting neutrophils
    • L. Raccosta, R. Fontana, D. Maggioni, C. Lanterna, E.J. Villablanca, and A. Paniccia et al. The oxysterol-CXCR2 axis plays a key role in the recruitment of tumor-promoting neutrophils J. Exp. Med. 210 2013 1711 1728
    • (2013) J. Exp. Med. , vol.210 , pp. 1711-1728
    • Raccosta, L.1    Fontana, R.2    Maggioni, D.3    Lanterna, C.4    Villablanca, E.J.5    Paniccia, A.6
  • 2
    • 84884336501 scopus 로고    scopus 로고
    • Oxysterols and related sterols: Implications in pharmacology and pathophysiology
    • M. Poirot, and S. Silvente-Poirot Oxysterols and related sterols: implications in pharmacology and pathophysiology Biochem. Pharmacol. 86 2013 1 2
    • (2013) Biochem. Pharmacol. , vol.86 , pp. 1-2
    • Poirot, M.1    Silvente-Poirot, S.2
  • 3
    • 84888791736 scopus 로고    scopus 로고
    • 27-Hydroxycholesterol links hypercholesterolemia and breast cancer pathophysiology
    • E.R. Nelson, S.E. Wardell, J.S. Jasper, S. Park, S. Suchindran, and M.K. Howe et al. 27-Hydroxycholesterol links hypercholesterolemia and breast cancer pathophysiology Science 342 2013 1094 1098
    • (2013) Science , vol.342 , pp. 1094-1098
    • Nelson, E.R.1    Wardell, S.E.2    Jasper, J.S.3    Park, S.4    Suchindran, S.5    Howe, M.K.6
  • 4
    • 84878557557 scopus 로고    scopus 로고
    • Dendrogenin A arises from cholesterol and histamine metabolism and shows cell differentiation and anti-tumour properties
    • P. de Medina, M.R. Paillasse, G. Segala, M. Voisin, L. Mhamdi, and F. Dalenc et al. Dendrogenin A arises from cholesterol and histamine metabolism and shows cell differentiation and anti-tumour properties Nat. Commun. 4 2013 1840
    • (2013) Nat. Commun. , vol.4 , pp. 1840
    • De Medina, P.1    Paillasse, M.R.2    Segala, G.3    Voisin, M.4    Mhamdi, L.5    Dalenc, F.6
  • 5
    • 84870511070 scopus 로고    scopus 로고
    • Cholesterol metabolism and cancer: The good, the bad and the ugly
    • S. Silvente-Poirot, and M. Poirot Cholesterol metabolism and cancer: the good, the bad and the ugly Curr. Opin. Pharmacol. 12 2012 673 676
    • (2012) Curr. Opin. Pharmacol. , vol.12 , pp. 673-676
    • Silvente-Poirot, S.1    Poirot, M.2
  • 6
    • 84872869007 scopus 로고    scopus 로고
    • Targeting C4-demethylating genes in the cholesterol pathway sensitizes cancer cells to EGF receptor inhibitors via increased EGF receptor degradation
    • A. Sukhanova, A. Gorin, I.G. Serebriiskii, L. Gabitova, H. Zheng, and D. Restifo et al. Targeting C4-demethylating genes in the cholesterol pathway sensitizes cancer cells to EGF receptor inhibitors via increased EGF receptor degradation Cancer Discov. 3 2013 96 111
    • (2013) Cancer Discov. , vol.3 , pp. 96-111
    • Sukhanova, A.1    Gorin, A.2    Serebriiskii, I.G.3    Gabitova, L.4    Zheng, H.5    Restifo, D.6
  • 7
    • 84892170909 scopus 로고    scopus 로고
    • Molecular pathways: Sterols and receptor signaling in cancer
    • L. Gabitova, A. Gorin, and I. Astsaturov Molecular pathways: sterols and receptor signaling in cancer Clin. Cancer Res. 20 2014 28 34
    • (2014) Clin. Cancer Res. , vol.20 , pp. 28-34
    • Gabitova, L.1    Gorin, A.2    Astsaturov, I.3
  • 8
    • 77955799773 scopus 로고    scopus 로고
    • Identification and pharmacological characterization of cholesterol-5,6-epoxide hydrolase as a target for tamoxifen and AEBS ligands
    • P. de Medina, M.R. Paillasse, G. Segala, M. Poirot, and S. Silvente-Poirot Identification and pharmacological characterization of cholesterol-5,6-epoxide hydrolase as a target for tamoxifen and AEBS ligands Proc. Natl. Acad. Sci. USA 107 2010 13520 13525
    • (2010) Proc. Natl. Acad. Sci. USA , vol.107 , pp. 13520-13525
    • De Medina, P.1    Paillasse, M.R.2    Segala, G.3    Poirot, M.4    Silvente-Poirot, S.5
  • 10
    • 72249094961 scopus 로고    scopus 로고
    • Synthesis of new alkylaminooxysterols with potent cell differentiating activities: Identification of leads for the treatment of cancer and neurodegenerative diseases
    • P. de Medina, M.R. Paillasse, B. Payre, S. Silvente-Poirot, and M. Poirot Synthesis of new alkylaminooxysterols with potent cell differentiating activities: identification of leads for the treatment of cancer and neurodegenerative diseases J. Med. Chem. 52 2009 7765 7777
    • (2009) J. Med. Chem. , vol.52 , pp. 7765-7777
    • De Medina, P.1    Paillasse, M.R.2    Payre, B.3    Silvente-Poirot, S.4    Poirot, M.5
  • 11
  • 12
    • 84880836872 scopus 로고    scopus 로고
    • Antiestrogen-binding site ligands induce autophagy in myeloma cells that proceeds through alteration of cholesterol metabolism
    • B. Sola, M. Poirot, P. de Medina, S. Bustany, V. Marsaud, and S. Sivente-Poirot et al. Antiestrogen-binding site ligands induce autophagy in myeloma cells that proceeds through alteration of cholesterol metabolism Oncotarget 4 2013 911 922
    • (2013) Oncotarget , vol.4 , pp. 911-922
    • Sola, B.1    Poirot, M.2    De Medina, P.3    Bustany, S.4    Marsaud, V.5    Sivente-Poirot, S.6
  • 13
    • 84884324369 scopus 로고    scopus 로고
    • 5,6-Epoxy-cholesterols contribute to the anticancer pharmacology of tamoxifen in breast cancer cells
    • G. Segala, P. de Medina, L. Iuliano, C. Zerbinati, M.R. Paillasse, and E. Noguer et al. 5,6-Epoxy-cholesterols contribute to the anticancer pharmacology of tamoxifen in breast cancer cells Biochem. Pharmacol. 86 2013 175 189
    • (2013) Biochem. Pharmacol. , vol.86 , pp. 175-189
    • Segala, G.1    De Medina, P.2    Iuliano, L.3    Zerbinati, C.4    Paillasse, M.R.5    Noguer, E.6
  • 14
    • 84884314618 scopus 로고    scopus 로고
    • Oxysterols in cancer cell proliferation and death
    • J. de Weille, C. Fabre, and N. Bakalara Oxysterols in cancer cell proliferation and death Biochem. Pharmacol. 86 2013 154 160
    • (2013) Biochem. Pharmacol. , vol.86 , pp. 154-160
    • De Weille, J.1    Fabre, C.2    Bakalara, N.3
  • 16
    • 13844255073 scopus 로고    scopus 로고
    • Cholesterol-3-beta, 5-alpha, 6-beta-triol induced genotoxicity through reactive oxygen species formation
    • Y.W. Cheng, J.J. Kang, Y.L. Shih, Y.L. Lo, and C.F. Wang Cholesterol-3-beta, 5-alpha, 6-beta-triol induced genotoxicity through reactive oxygen species formation Food Chem. Toxicol. 43 2005 617 622
    • (2005) Food Chem. Toxicol. , vol.43 , pp. 617-622
    • Cheng, Y.W.1    Kang, J.J.2    Shih, Y.L.3    Lo, Y.L.4    Wang, C.F.5
  • 19
    • 0018598647 scopus 로고
    • Inhibition of human lymphocyte E-rosette formation by oxygenated sterols
    • R.A. Streuli, J. Chung, A.M. Scanu, and S. Yachnin Inhibition of human lymphocyte E-rosette formation by oxygenated sterols J. Immunol. 123 1979 2897 2902
    • (1979) J. Immunol. , vol.123 , pp. 2897-2902
    • Streuli, R.A.1    Chung, J.2    Scanu, A.M.3    Yachnin, S.4
  • 22
    • 33845933692 scopus 로고    scopus 로고
    • 4,5-Epoxycholestane-3,6-diols: Templates for generating the full set of eight cholestane-3,5,6-triol stereoisomers in multigram scales, but not for a cholestane-3,4,6-triol
    • K. Zhao, Y. Wang, and L. Han 4,5-Epoxycholestane-3,6-diols: templates for generating the full set of eight cholestane-3,5,6-triol stereoisomers in multigram scales, but not for a cholestane-3,4,6-triol Steroids 72 2007 95 104
    • (2007) Steroids , vol.72 , pp. 95-104
    • Zhao, K.1    Wang, Y.2    Han, L.3
  • 23
    • 0000110990 scopus 로고
    • Selective oxidation with N-Bromosuccinimide. II. Cholestane-3beta,5alpha, 6beta-triol
    • L.F. Fieser, and S. Rajagopalan Selective oxidation with N-Bromosuccinimide. II. Cholestane-3beta,5alpha,6beta-triol J. Am. Chem. Soc. 71 1949 3938 3941
    • (1949) J. Am. Chem. Soc. , vol.71 , pp. 3938-3941
    • Fieser, L.F.1    Rajagopalan, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.