메뉴 건너뛰기




Volumn 68, Issue 2, 2003, Pages 125-132

Synthesis and antiviral activity of sulfated and acetylated derivatives of 2β,3α-dihydroxy-5α-cholestane

Author keywords

Antiviral activity; Sulfated steroids; Synthesis

Indexed keywords

ANTIVIRUS AGENT; CHOLESTANE DERIVATIVE; DISODIUM 2BETA,3ALPHA DIHYDROXY 5ALPHA CHOLESTANE DISULFATE; N,N DIMETHYLFORMAMIDE; SODIUM 2BETA ACETOXY 3ALPHA HYDROXY 5ALPHA CHOLESTANE 3 SULFATE; SODIUM 2BETA,3ALPHA DIHYDROXY 5ALPHA CHOLESTANE 2 SULFATE; SODIUM 2BETA,3ALPHA DIHYDROXY 5ALPHA CHOLESTANE 3 SULFATE; SODIUM 3ALPHA ACETOXY 2BETA HYDROXY 5ALPHA CHOLESTANE 2 SULFATE; STEROID; SULFUR DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037326222     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0039-128X(02)00166-6     Document Type: Article
Times cited : (31)

References (20)
  • 2
    • 0001229636 scopus 로고
    • Polyoxygenated steroids of marine origin
    • D'Auria M.V., Minale L., Riccio R. Polyoxygenated steroids of marine origin. Chem. Rev. 93:1993;1839-1895.
    • (1993) Chem. Rev. , vol.93 , pp. 1839-1895
    • D'Auria, M.V.1    Minale, L.2    Riccio, R.3
  • 3
    • 0028268008 scopus 로고
    • HIV-inhibitory natural products. 11. Comparative studies of sulfated sterols from marine invertebrates
    • McKee T.C., Cardellina J.H., Riccio R., D'Auria M.V., Iorizzi M., Minale L.et al. HIV-inhibitory natural products. 11. Comparative studies of sulfated sterols from marine invertebrates. J. Med. Chem. 37:1994;793-797.
    • (1994) J. Med. Chem. , vol.37 , pp. 793-797
    • McKee, T.C.1    Cardellina, J.H.2    Riccio, R.3    D'Auria, M.V.4    Iorizzi, M.5    Minale, L.6
  • 6
    • 0031954017 scopus 로고    scopus 로고
    • New sulfated polyhydroxysteroids from the antarctic ophiuroid Astrotoma agassizii
    • Roccatagliata A.J., Maier M.S., Seldes A.M. New sulfated polyhydroxysteroids from the antarctic ophiuroid Astrotoma agassizii. J. Nat. Prod. 61:1998;370-374.
    • (1998) J. Nat. Prod. , vol.61 , pp. 370-374
    • Roccatagliata, A.J.1    Maier, M.S.2    Seldes, A.M.3
  • 7
    • 0033021691 scopus 로고    scopus 로고
    • Evaluation of the antiviral activity of natural sulfated polyhydroxysteroids and their synthetic derivatives and analogs
    • Comin M.J., Maier M.S., Roccatagliata A.J., Pujol C.A., Damonte E.B. Evaluation of the antiviral activity of natural sulfated polyhydroxysteroids and their synthetic derivatives and analogs. Steroids. 64:1999;335-340.
    • (1999) Steroids , vol.64 , pp. 335-340
    • Comin, M.J.1    Maier, M.S.2    Roccatagliata, A.J.3    Pujol, C.A.4    Damonte, E.B.5
  • 8
    • 0001587276 scopus 로고
    • A convenient procedure for the preparation of triethylamine-sulfur trioxide
    • Nair V., Bernstein S. A convenient procedure for the preparation of triethylamine-sulfur trioxide. Oppi Briefs. 19:1987;466-467.
    • (1987) Oppi Briefs , vol.19 , pp. 466-467
    • Nair, V.1    Bernstein, S.2
  • 10
    • 0023107627 scopus 로고
    • Synthesis of homodolichosterone and related 2-deoxysteroids
    • Takatsuto S., Ikekawa N. Synthesis of homodolichosterone and related 2-deoxysteroids. Chem. Pharm. Bull. 35:1987;829-832.
    • (1987) Chem. Pharm. Bull. , vol.35 , pp. 829-832
    • Takatsuto, S.1    Ikekawa, N.2
  • 11
    • 26544458075 scopus 로고
    • Synthesis of 2,24-diepicastasterone and its 22S,23S-isomer: Novel brassinosteroids with a trans-2,3-diol function
    • Levinson EE, Kuznetsova NA, Podkhalyuzina NY, Traven VF. Synthesis of 2,24-diepicastasterone and its 22S,23S-isomer: novel brassinosteroids with a trans-2,3-diol function. Mendeleev Commun 1994;96-9.
    • (1994) Mendeleev Commun , pp. 96-99
    • Levinson, E.E.1    Kuznetsova, N.A.2    Podkhalyuzina, N.Y.3    Traven, V.F.4
  • 12
    • 0014305416 scopus 로고
    • Steroid conjugates. IV. The preparation of steroid sulfate with triethylamine-sulfur trioxide
    • Dusza J.P., Joseph J.P., Bernstein S. Steroid conjugates. IV. The preparation of steroid sulfate with triethylamine-sulfur trioxide. Steroids. 9:1968;49-61.
    • (1968) Steroids , vol.9 , pp. 49-61
    • Dusza, J.P.1    Joseph, J.P.2    Bernstein, S.3
  • 13
    • 0026031093 scopus 로고
    • New antiviral sterol disulfate ortho esters from the marine sponge Petrosia weinbergi
    • Koehn F.E., Gunasekera M., Cross S.S. New antiviral sterol disulfate ortho esters from the marine sponge Petrosia weinbergi. J. Org. Chem. 56:1991;1322-1325.
    • (1991) J. Org. Chem. , vol.56 , pp. 1322-1325
    • Koehn, F.E.1    Gunasekera, M.2    Cross, S.S.3
  • 14
    • 0028914454 scopus 로고
    • Mild deprotection of steroid esters by bis(tributyltin)oxide
    • Pérez M.G., Maier M.S. Mild deprotection of steroid esters by bis(tributyltin)oxide. Tetrahedron Lett. 36:1995;3311-3314.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 3311-3314
    • Pérez, M.G.1    Maier, M.S.2
  • 15
    • 0002032217 scopus 로고
    • The epidemiology and clinical manifestations of herpes simplex virus infections
    • Roizman B, Whitley RJ, López C, editors. New York: Raven Press [chapter 3]
    • Whitley RJ, Gnann JW. The epidemiology and clinical manifestations of herpes simplex virus infections. In: Roizman B, Whitley RJ, López C, editors. The human herpes virus. New York: Raven Press; 1993. p. 69-105 [chapter 3].
    • (1993) The Human Herpes Virus , pp. 69-105
    • Whitley, R.J.1    Gnann, J.W.2
  • 19
    • 0026022980 scopus 로고
    • Weinbersterol disulfates A and B, antiviral steroid sulfates from the sponge Petrosia weinbergi
    • Sun H.H., Cross S.S., Gunasekera M., Koehn F.E. Weinbersterol disulfates A and B, antiviral steroid sulfates from the sponge Petrosia weinbergi. Tetrahedron. 47:1991;1185-1190.
    • (1991) Tetrahedron , vol.47 , pp. 1185-1190
    • Sun, H.H.1    Cross, S.S.2    Gunasekera, M.3    Koehn, F.E.4
  • 20
    • 0029950814 scopus 로고    scopus 로고
    • Halistanol disulfate B, a novel sulfated sterol from the sponge Pachastrella sp.: Inhibitor of endothelin converting enzyme
    • Patil A.D., Freyer A.J., Breen A., Carte B., Johnson R.K. Halistanol disulfate B, a novel sulfated sterol from the sponge Pachastrella sp.: inhibitor of endothelin converting enzyme. J. Nat. Prod. 59:1996;606-608.
    • (1996) J. Nat. Prod. , vol.59 , pp. 606-608
    • Patil, A.D.1    Freyer, A.J.2    Breen, A.3    Carte, B.4    Johnson, R.K.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.