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Journal Abstract Search

90 related items for PubMed ID: 8786367

  • 1. Halistanol disulfate B, a novel sulfated sterol from the sponge Pachastrella sp.: inhibitor of endothelin converting enzyme.
    Patil AD, Freyer AJ, Breen A, Carte B, Johnson RK.
    J Nat Prod; 1996 Jun; 59(6):606-8. PubMed ID: 8786367
    [Abstract] [Full Text] [Related]

  • 2. Clathsterol, a novel anti-HIV-1 RT sulfated sterol from the sponge Clathria species.
    Rudi A, Yosief T, Loya S, Hizi A, Schleyer M, Kashman Y.
    J Nat Prod; 2001 Nov; 64(11):1451-3. PubMed ID: 11720531
    [Abstract] [Full Text] [Related]

  • 3. Daleformis, a new phytoalexin from the roots fo Dalea filiciformis: an inhibitor of endothelin converting enzyme.
    Patil AD, Freyer AJ, Eggleston DS, Haltiwanger RC, Tomcowicz B, Breen A, Johnson RK.
    J Nat Prod; 1997 Mar; 60(3):306-8. PubMed ID: 9157193
    [Abstract] [Full Text] [Related]

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  • 5. A new sterol sulfate, Sch 572423, from a marine sponge, Topsentia sp.
    Yang SW, Buivich A, Chan TM, Smith M, Lachowicz J, Pomponi SA, Wright AE, Mierzwa R, Patel M, Gullo V, Chu M.
    Bioorg Med Chem Lett; 2003 May 19; 13(10):1791-4. PubMed ID: 12729666
    [Abstract] [Full Text] [Related]

  • 6. TMC-66, a new endothelin converting enzyme inhibitor produced by Streptomyces sp. A5008.
    Asai Y, Nonaka N, Suzuki S, Nishio M, Takahashi K, Shima H, Ohmori K, Ohnuki T, Komatsubara S.
    J Antibiot (Tokyo); 1999 Jul 19; 52(7):607-12. PubMed ID: 10513839
    [Abstract] [Full Text] [Related]

  • 7. Halistanol sulfates I and J, new SIRT1-3 inhibitory steroid sulfates from a marine sponge of the genus Halichondria.
    Nakamura F, Kudo N, Tomachi Y, Nakata A, Takemoto M, Ito A, Tabei H, Arai D, de Voogd N, Yoshida M, Nakao Y, Fusetani N.
    J Antibiot (Tokyo); 2018 Feb 19; 71(2):273-278. PubMed ID: 29184120
    [Abstract] [Full Text] [Related]

  • 8. Novel HIV-inhibitory halistanol sulfates F-H from a marine sponge, Pseudoaxinissa digitata.
    Bifulco G, Bruno I, Minale L, Riccio R.
    J Nat Prod; 1994 Jan 19; 57(1):164-7. PubMed ID: 8158159
    [Abstract] [Full Text] [Related]

  • 9. WS75624 A and B, new endothelin converting enzyme inhibitors isolated from Saccharothrix sp. No. 75624. II. Structure elucidation of WS75624 A and B.
    Yoshimura S, Tsurumi Y, Takase S, Okuhara M.
    J Antibiot (Tokyo); 1995 Oct 19; 48(10):1073-5. PubMed ID: 7490209
    [Abstract] [Full Text] [Related]

  • 10. Biemnasterol, a new cytotoxic sterol with the rare 22,25-diene side chain, isolated from the marine sponge Biemna sp.
    Zeng CM, Ishibashi M, Kobayashi J.
    J Nat Prod; 1993 Nov 19; 56(11):2016-8. PubMed ID: 8289069
    [Abstract] [Full Text] [Related]

  • 11. 5,6:8,9-diepoxy and other cytotoxic sterols from the marine sponge Homaxinella sp.
    Mansoor TA, Lee YM, Hong J, Lee CO, Im KS, Jung JH.
    J Nat Prod; 2006 Jan 19; 69(1):131-4. PubMed ID: 16441084
    [Abstract] [Full Text] [Related]

  • 12. Antibacterial activity and cytotoxicity analysis of halistanol trisulphate from marine sponge Petromica citrina.
    Marinho PR, Simas NK, Kuster RM, Duarte RS, Fracalanzza SE, Ferreira DF, Romanos MT, Muricy G, Giambiagi-Demarval M, Laport MS.
    J Antimicrob Chemother; 2012 Oct 19; 67(10):2396-400. PubMed ID: 22729926
    [Abstract] [Full Text] [Related]

  • 13. A new C29-sterol with a cyclopropane ring at C-25 and 26 from the Vietnamese marine sponge lanthella sp.
    Tung NH, Van Minh C, Van Kiem P, Huong HT, Ha TT, Dat NT, Nhiem NX, Cuong NX, Hyun JH, Kang HK, Kim YH.
    Arch Pharm Res; 2009 Dec 19; 32(12):1695-8. PubMed ID: 20162396
    [Abstract] [Full Text] [Related]

  • 14. Cytotoxic sterol derivatives from a marine sponge Homaxinella sp.
    Mansoor TA, Hong J, Lee CO, Bae SJ, Im KS, Jung JH.
    J Nat Prod; 2005 Mar 19; 68(3):331-6. PubMed ID: 15787431
    [Abstract] [Full Text] [Related]

  • 15. Design and synthesis of potent, selective inhibitors of endothelin-converting enzyme.
    Wallace EM, Moliterni JA, Moskal MA, Neubert AD, Marcopulos N, Stamford LB, Trapani AJ, Savage P, Chou M, Jeng AY.
    J Med Chem; 1998 Apr 23; 41(9):1513-23. PubMed ID: 9554884
    [Abstract] [Full Text] [Related]

  • 16. Novel, selective indole-based ECE inhibitors: lead optimization via solid-phase and classical synthesis.
    Brands M, Ergüden JK, Hashimoto K, Heimbach D, Schröder C, Siegel S, Stasch JP, Weigand S.
    Bioorg Med Chem Lett; 2005 Oct 01; 15(19):4201-5. PubMed ID: 16085415
    [Abstract] [Full Text] [Related]

  • 17. Novel selective quinazoline inhibitors of endothelin converting enzyme-1.
    Ahn K, Sisneros AM, Herman SB, Pan SM, Hupe D, Lee C, Nikam S, Cheng XM, Doherty AM, Schroeder RL, Haleen SJ, Kaw S, Emoto N, Yanagisawa M.
    Biochem Biophys Res Commun; 1998 Feb 04; 243(1):184-90. PubMed ID: 9473502
    [Abstract] [Full Text] [Related]

  • 18. WS79089A, B and C, new endothelin converting enzyme inhibitors isolated from Streptosporangium roseum. No. 79089. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities.
    Tsurumi Y, Ohhata N, Iwamoto T, Shigematsu N, Sakamoto K, Nishikawa M, Kiyoto S, Okuhara M.
    J Antibiot (Tokyo); 1994 Jun 04; 47(6):619-30. PubMed ID: 8040066
    [Abstract] [Full Text] [Related]

  • 19. A rapid and selective endothelin-converting enzyme assay: characterization of a phosphoramidon-sensitive enzyme from guinea pig lung membrane.
    Fawzi AB, Cleven RM, Wright DL.
    Anal Biochem; 1994 Nov 01; 222(2):342-50. PubMed ID: 7864357
    [Abstract] [Full Text] [Related]

  • 20. Synthesis of novel substituted pyridines as inhibitors of endothelin converting enzyme-1 (ECE-1).
    Massa MA, Patt WC, Ahn K, Sisneros AM, Herman SB, Doherty A.
    Bioorg Med Chem Lett; 1998 Aug 18; 8(16):2117-22. PubMed ID: 9873497
    [Abstract] [Full Text] [Related]

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