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Salvinorinas A (Lithuanian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Salvinorinas A" in Lithuanian language version.

refsWebsite
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9nih.gov
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8doi.org
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1worldcat.org
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1cyjack.com
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1google.co.uk
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1web.archive.org
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1sagewisdom.org
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doi.org

  • Prisinzano TE (2005). „Psychopharmacology of the hallucinogenic sage Salvia divinorum“. Life Sci. 78 (5): 527–31. doi:10.1016/j.lfs.2005.09.008. PMID 16213533.
  • Harding, Wayne W.; Schmidt, Matthew; Tidgewell, Kevin; Kannan, Pavitra; Holden, Kenneth G.; Gilmour, Brian; Navarro, Hernan; Rothman, Richard B.; Prisinzano, Thomas E. (2006-01-01). „Synthetic Studies of Neoclerodane Diterpenes from Salvia d ivinorum : Semisynthesis of Salvinicins A and B and Other Chemical Transformations of Salvinorin A“. Journal of Natural Products. 69 (1): 107–112. doi:10.1021/np050398i. ISSN 0163-3864. PMC 2544632. PMID 16441078.
  • Imanshahidi M, Hosseinzadeh H (2006). „The pharmacological effects of Salvia species on the central nervous system“. Phytother Res. 20 (6): 427–37. doi:10.1002/ptr.1898. PMID 16619340.
  • Zhang Y, Butelman ER, Schlussman SD, Ho A, Kreek MJ (2005). „Effects of the plant-derived hallucinogen salvinorin A on basal dopamine levels in the caudate putamen and in a conditioned place aversion assay in mice: agonist actions at kappa opioid receptors“. Psychopharmacology (Berl.). 179 (3): 551–8. doi:10.1007/s00213-004-2087-0. PMID 15682306.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)
  • Bigham AK, Munro TA, Rizzacasa MA, Robins-Browne RM (2003). „Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorum“. J. Nat. Prod. 66 (9): 1242–4. doi:10.1021/np030313i. PMID 14510607.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)
  • Munro TA, Rizzacasa MA (2003). „Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin A“. J. Nat. Prod. 66 (5): 703–5. doi:10.1021/np0205699. PMID 12762813.
  • Lingham AR, Hügel HM, Rook TJ (2006). „Studies Towards the Synthesis of Salvinorin A“. Aust. J. Chem. 59 (5): 340–348. doi:10.1071/CH05338.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)
  • Scheerer JR, Lawrence JF, Wang GC, Evans DA (2007). „Asymmetric synthesis of salvinorin A, a potent kappa opioid receptor agonist“. J. Am. Chem. Soc. 129 (29): 8968–9. doi:10.1021/ja073590a. PMID 17602636.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)

google.co.uk

scholar.google.co.uk

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Prisinzano TE (2005). „Psychopharmacology of the hallucinogenic sage Salvia divinorum“. Life Sci. 78 (5): 527–31. doi:10.1016/j.lfs.2005.09.008. PMID 16213533.
  • Harding, Wayne W.; Schmidt, Matthew; Tidgewell, Kevin; Kannan, Pavitra; Holden, Kenneth G.; Gilmour, Brian; Navarro, Hernan; Rothman, Richard B.; Prisinzano, Thomas E. (2006-01-01). „Synthetic Studies of Neoclerodane Diterpenes from Salvia d ivinorum : Semisynthesis of Salvinicins A and B and Other Chemical Transformations of Salvinorin A“. Journal of Natural Products. 69 (1): 107–112. doi:10.1021/np050398i. ISSN 0163-3864. PMC 2544632. PMID 16441078.
  • Imanshahidi M, Hosseinzadeh H (2006). „The pharmacological effects of Salvia species on the central nervous system“. Phytother Res. 20 (6): 427–37. doi:10.1002/ptr.1898. PMID 16619340.
  • Zhang Y, Butelman ER, Schlussman SD, Ho A, Kreek MJ (2005). „Effects of the plant-derived hallucinogen salvinorin A on basal dopamine levels in the caudate putamen and in a conditioned place aversion assay in mice: agonist actions at kappa opioid receptors“. Psychopharmacology (Berl.). 179 (3): 551–8. doi:10.1007/s00213-004-2087-0. PMID 15682306.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)
  • Mowry M, Mosher M, Briner W (2003). „Acute physiologic and chronic histologic changes in rats and mice exposed to the unique hallucinogen salvinorin A“ (PDF). J Psychoactive Drugs. 35 (3): 379–82. PMID 14621136.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)
  • Bigham AK, Munro TA, Rizzacasa MA, Robins-Browne RM (2003). „Divinatorins A-C, new neoclerodane diterpenoids from the controlled sage Salvia divinorum“. J. Nat. Prod. 66 (9): 1242–4. doi:10.1021/np030313i. PMID 14510607.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)
  • Munro TA, Rizzacasa MA (2003). „Salvinorins D-F, new neoclerodane diterpenoids from Salvia divinorum, and an improved method for the isolation of salvinorin A“. J. Nat. Prod. 66 (5): 703–5. doi:10.1021/np0205699. PMID 12762813.
  • Scheerer JR, Lawrence JF, Wang GC, Evans DA (2007). „Asymmetric synthesis of salvinorin A, a potent kappa opioid receptor agonist“. J. Am. Chem. Soc. 129 (29): 8968–9. doi:10.1021/ja073590a. PMID 17602636.{{cite journal}}: CS1 priežiūra: multiple names: authors list (link)

ncbi.nlm.nih.gov

sagewisdom.org

web.archive.org

worldcat.org