Thebaine (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Thebaine" in English language version.

refsWebsite

Global rank English rank

7web.archive.org

1^st place

3doi.org

2^nd place

3nih.gov

4^th place

3incb.org

low place

9,618^th place

1unodc.org

2,494^th place

2,269^th place

1usdoj.gov

2,755^th place

1,753^rd place

1justice.gc.ca

2,540^th place

1,620^th place

1brocku.ca

low place

1psu.edu

207^th place

136^th place

1washingtonpost.com

34^th place

27^th place

1canberratimes.com.au

4,198^th place

2,356^th place

1foodstandards.gov.au

low place

1sciencedaily.com

993^rd place

920^th place

brocku.ca

Novak, B.; Hudlicky, T.; Reed, J.; Mulzer, J.; Trauner, D. (2000). "Morphine Synthesis and Biosynthesis-An Update" (PDF). Current Organic Chemistry. 4 (3): 343–62. CiteSeerX 10.1.1.515.9096. doi:10.2174/1385272003376292. Archived (PDF) from the original on 2012-06-19.

canberratimes.com.au

"DEA Diversion Control Division". Archived (PDF) from the original on 2014-06-11. Retrieved 2014-07-12.

doi.org

Mikus, G.; Somogyi, A. A.; Bochner, F.; Eichelbaum, M. (1991). "Thebaine O-demethylation to oripavine: Genetic differences between two rat strains". Xenobiotica. 21 (11): 1501–9. doi:10.3109/00498259109044400. PMID 1763524.
Aceto, M. D.; Harris, L. S.; Abood, M. E.; Rice, K. C. (1999). "Stereoselective μ- and δ-opioid receptor-related antinociception and binding with (+)-thebaine". European Journal of Pharmacology. 365 (2–3): 143–7. doi:10.1016/S0014-2999(98)00862-0. PMID 9988096.
Novak, B.; Hudlicky, T.; Reed, J.; Mulzer, J.; Trauner, D. (2000). "Morphine Synthesis and Biosynthesis-An Update" (PDF). Current Organic Chemistry. 4 (3): 343–62. CiteSeerX 10.1.1.515.9096. doi:10.2174/1385272003376292. Archived (PDF) from the original on 2012-06-19.

foodstandards.gov.au

"National Recall of Poppy Seeds". Food Standards Australia New Zealand. Food Standards Australia New Zealand (FSANZ). Retrieved 21 November 2022.

incb.org

Narcotic Drugs 2014 (PDF). INTERNATIONAL NARCOTICS CONTROL BOARD. 2015. p. 21. ISBN 9789210481571. Archived (PDF) from the original on 2015-06-02.
"International Narcotics Control Board Narcotic Drugs 2018" (PDF). INCB.org.
"Narcotic Drugs: Estimated World Requirements for 2015; Statistics for 2013" (PDF). International Narcotics Control Board. United Nations International Narcotics Control Board. 2015. p. 151 ff. Archived (PDF) from the original on June 2, 2015. Retrieved January 7, 2016.

justice.gc.ca

laws-lois.justice.gc.ca

"Controlled Drugs and Substances Act". Justice Laws Website. Government of Canada. 2012-11-06. Archived from the original on 2013-11-22. Retrieved 2014-01-12.

nih.gov

pubmed.ncbi.nlm.nih.gov

Mikus, G.; Somogyi, A. A.; Bochner, F.; Eichelbaum, M. (1991). "Thebaine O-demethylation to oripavine: Genetic differences between two rat strains". Xenobiotica. 21 (11): 1501–9. doi:10.3109/00498259109044400. PMID 1763524.
WHO Advisory Group (1980). "The dependence potential of thebaine". Bulletin on Narcotics. 32 (1): 45–54. PMID 6778542. Archived from the original on 2014-05-12.
Aceto, M. D.; Harris, L. S.; Abood, M. E.; Rice, K. C. (1999). "Stereoselective μ- and δ-opioid receptor-related antinociception and binding with (+)-thebaine". European Journal of Pharmacology. 365 (2–3): 143–7. doi:10.1016/S0014-2999(98)00862-0. PMID 9988096.

psu.edu

citeseerx.ist.psu.edu

Novak, B.; Hudlicky, T.; Reed, J.; Mulzer, J.; Trauner, D. (2000). "Morphine Synthesis and Biosynthesis-An Update" (PDF). Current Organic Chemistry. 4 (3): 343–62. CiteSeerX 10.1.1.515.9096. doi:10.2174/1385272003376292. Archived (PDF) from the original on 2012-06-19.

sciencedaily.com

"Genetically modified E. coli pump out morphine precursor: Bacteria yield 300 times more opiates than yeast". ScienceDaily.

unodc.org

WHO Advisory Group (1980). "The dependence potential of thebaine". Bulletin on Narcotics. 32 (1): 45–54. PMID 6778542. Archived from the original on 2014-05-12.

usdoj.gov

deadiversion.usdoj.gov

"DEA Diversion Control Division" (PDF). Archived (PDF) from the original on 2014-06-11. Retrieved 2014-07-12.

washingtonpost.com

Whoriskey, Peter. "Johnson & Johnson companies used a super poppy to make narcotics for popular opioid pills - Washington Post". Washington Post. Retrieved 27 March 2020.

web.archive.org

WHO Advisory Group (1980). "The dependence potential of thebaine". Bulletin on Narcotics. 32 (1): 45–54. PMID 6778542. Archived from the original on 2014-05-12.
"DEA Diversion Control Division" (PDF). Archived (PDF) from the original on 2014-06-11. Retrieved 2014-07-12.
"Controlled Drugs and Substances Act". Justice Laws Website. Government of Canada. 2012-11-06. Archived from the original on 2013-11-22. Retrieved 2014-01-12.
Novak, B.; Hudlicky, T.; Reed, J.; Mulzer, J.; Trauner, D. (2000). "Morphine Synthesis and Biosynthesis-An Update" (PDF). Current Organic Chemistry. 4 (3): 343–62. CiteSeerX 10.1.1.515.9096. doi:10.2174/1385272003376292. Archived (PDF) from the original on 2012-06-19.
Narcotic Drugs 2014 (PDF). INTERNATIONAL NARCOTICS CONTROL BOARD. 2015. p. 21. ISBN 9789210481571. Archived (PDF) from the original on 2015-06-02.
"Narcotic Drugs: Estimated World Requirements for 2015; Statistics for 2013" (PDF). International Narcotics Control Board. United Nations International Narcotics Control Board. 2015. p. 151 ff. Archived (PDF) from the original on June 2, 2015. Retrieved January 7, 2016.
"DEA Diversion Control Division". Archived (PDF) from the original on 2014-06-11. Retrieved 2014-07-12.