BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

262 related articles for article (PubMed ID: 17580847)

  • 1. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: preparation and opioid receptor activity of salvinicin analogues.
    Simpson DS; Katavic PL; Lozama A; Harding WW; Parrish D; Deschamps JR; Dersch CM; Partilla JS; Rothman RB; Navarro H; Prisinzano TE
    J Med Chem; 2007 Jul; 50(15):3596-603. PubMed ID: 17580847
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neoclerodane diterpenes as a novel scaffold for mu opioid receptor ligands.
    Harding WW; Tidgewell K; Byrd N; Cobb H; Dersch CM; Butelman ER; Rothman RB; Prisinzano TE
    J Med Chem; 2005 Jul; 48(15):4765-71. PubMed ID: 16033256
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: semisynthesis of salvinicins A and B and other chemical transformations of salvinorin A.
    Harding WW; Schmidt M; Tidgewell K; Kannan P; Holden KG; Gilmour B; Navarro H; Rothman RB; Prisinzano TE
    J Nat Prod; 2006 Jan; 69(1):107-12. PubMed ID: 16441078
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: exploration of the 1-position.
    Holden KG; Tidgewell K; Marquam A; Rothman RB; Navarro H; Prisinzano TE
    Bioorg Med Chem Lett; 2007 Nov; 17(22):6111-5. PubMed ID: 17904842
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: role of the furan in affinity for opioid receptors.
    Simpson DS; Lovell KM; Lozama A; Han N; Day VW; Dersch CM; Rothman RB; Prisinzano TE
    Org Biomol Chem; 2009 Sep; 7(18):3748-56. PubMed ID: 19707679
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Synthesis and κ-opioid receptor activity of furan-substituted salvinorin A analogues.
    Riley AP; Groer CE; Young D; Ewald AW; Kivell BM; Prisinzano TE
    J Med Chem; 2014 Dec; 57(24):10464-75. PubMed ID: 25426797
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synthetic studies of neoclerodane diterpenes from Salvia divinorum: selective modification of the furan ring.
    Harding WW; Schmidt M; Tidgewell K; Kannan P; Holden KG; Dersch CM; Rothman RB; Prisinzano TE
    Bioorg Med Chem Lett; 2006 Jun; 16(12):3170-4. PubMed ID: 16621556
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New neoclerodane diterpenoids isolated from the leaves of Salvia divinorum and their binding affinities for human kappa opioid receptors.
    Lee DY; Ma Z; Liu-Chen LY; Wang Y; Chen Y; Carlezon WA; Cohen B
    Bioorg Med Chem; 2005 Oct; 13(19):5635-9. PubMed ID: 16084728
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Isolation and chemical modification of clerodane diterpenoids from Salvia species as potential agonists at the kappa-opioid receptor.
    Li Y; Husbands SM; Mahon MF; Traynor JR; Rowan MG
    Chem Biodivers; 2007 Jul; 4(7):1586-93. PubMed ID: 17638340
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Salvinicins A and B, new neoclerodane diterpenes from Salvia divinorum.
    Harding WW; Tidgewell K; Schmidt M; Shah K; Dersch CM; Snyder J; Parrish D; Deschamps JR; Rothman RB; Prisinzano TE
    Org Lett; 2005 Jul; 7(14):3017-20. PubMed ID: 15987194
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Synthesis of salvinorin A analogues as opioid receptor probes.
    Tidgewell K; Harding WW; Lozama A; Cobb H; Shah K; Kannan P; Dersch CM; Parrish D; Deschamps JR; Rothman RB; Prisinzano TE
    J Nat Prod; 2006 Jun; 69(6):914-8. PubMed ID: 16792410
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Opioid receptor probes derived from cycloaddition of the hallucinogen natural product salvinorin A.
    Lozama A; Cunningham CW; Caspers MJ; Douglas JT; Dersch CM; Rothman RB; Prisinzano TE
    J Nat Prod; 2011 Apr; 74(4):718-26. PubMed ID: 21338114
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Salvinorin A, an active component of the hallucinogenic sage salvia divinorum is a highly efficacious kappa-opioid receptor agonist: structural and functional considerations.
    Chavkin C; Sud S; Jin W; Stewart J; Zjawiony JK; Siebert DJ; Toth BA; Hufeisen SJ; Roth BL
    J Pharmacol Exp Ther; 2004 Mar; 308(3):1197-203. PubMed ID: 14718611
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synthesis and in vitro pharmacological studies of new C(4)-modified salvinorin A analogues.
    Lee DY; He M; Liu-Chen LY; Wang Y; Li JG; Xu W; Ma Z; Carlezon WA; Cohen B
    Bioorg Med Chem Lett; 2006 Nov; 16(21):5498-502. PubMed ID: 16945525
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Selective natural kappa opioid and cannabinoid receptor agonists with a potential role in the treatment of gastrointestinal dysfunction.
    Fichna J; Schicho R; Janecka A; Zjawiony JK; Storr M
    Drug News Perspect; 2009 Sep; 22(7):383-92. PubMed ID: 19890495
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Kappa-opioid receptor-selective dicarboxylic ester-derived salvinorin A ligands.
    Polepally PR; White K; Vardy E; Roth BL; Ferreira D; Zjawiony JK
    Bioorg Med Chem Lett; 2013 May; 23(10):2860-2. PubMed ID: 23587424
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A unique natural selective kappa-opioid receptor agonist, salvinorin A, and its roles in human therapeutics.
    Cruz A; Domingos S; Gallardo E; Martinho A
    Phytochemistry; 2017 May; 137():9-14. PubMed ID: 28190678
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Salvinorins J from Salvia divinorum: mutarotation in the neoclerodane system.
    Kutrzeba LM; Ferreira D; Zjawiony JK
    J Nat Prod; 2009 Jul; 72(7):1361-3. PubMed ID: 19473009
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Total synthesis of the hallucinogenic neoclerodane diterpenoid salvinorin A.
    Nozawa M; Suka Y; Hoshi T; Suzuki T; Hagiwara H
    Org Lett; 2008 Apr; 10(7):1365-8. PubMed ID: 18311991
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Salvinorin A: from natural product to human therapeutics.
    Vortherms TA; Roth BL
    Mol Interv; 2006 Oct; 6(5):257-65. PubMed ID: 17035666
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.