Dexibuprofen (Swedish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dexibuprofen" in Swedish language version.

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7doi.org

2^nd place

14^th place

6nih.gov

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17^th place

2worldcat.org

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9^th place

1fass.se

low place

112^th place

1chiralpedia.com

low place

chiralpedia.com

Kannappan, Valliappan. ”Dexibuprofen – Chiralpedia” (på amerikansk engelska). https://chiralpedia.com/blog/dexibuprofen/. Läst 27 augusti 2022.

doi.org

dx.doi.org

Cahn, R. S.; Ingold, Christopher; Prelog, V. (1966). ”Specification of Molecular Chirality”. Angewandte Chemie International Edition in English 5 (4): sid. 385–415. doi:10.1002/anie.196603851. ISSN 0570-0833. http://dx.doi.org/10.1002/anie.196603851.
Cahn, R. S.; Ingold, C. K.; Prelog, V. (1956). ”The specification of asymmetric configuration in organic chemistry”. Experientia 12 (3): sid. 81–94. doi:10.1007/bf02157171. ISSN 0014-4754. http://dx.doi.org/10.1007/bf02157171.
”The metabolic chiral inversion and dispositional enantioselectivity of the 2-arylpropionic acids and their biological consequences”. Biochemical Pharmacology 37 (1): sid. 105–14. January 1988. doi:10.1016/0006-2952(88)90762-9. PMID 3276314.
”The metabolic chiral inversion of 2-arylpropionic acids--a novel route with pharmacological consequences”. The Journal of Pharmacy and Pharmacology 35 (11): sid. 693–704. November 1983. doi:10.1111/j.2042-7158.1983.tb02874.x. PMID 6139449.
”Pharmacological differences between the optical isomers of ibuprofen: evidence for metabolic inversion of the (-)-isomer”. The Journal of Pharmacy and Pharmacology 28 (3): sid. 256–7. March 1976. doi:10.1111/j.2042-7158.1976.tb04144.x. PMID 6706.
”Enantioselective pharmacokinetics of ibuprofen and involved mechanisms”. Drug Metabolism Reviews 37 (1): sid. 215–34. 2005. doi:10.1081/dmr-200047999. PMID 15747501.
”On chiral drug action”. Medicinal Research Reviews 4 (3): sid. 359–413. 1984. doi:10.1002/med.2610040304. PMID 6087043.

fass.se

https://www.fass.se/LIF/product?userType=0&nplId=20001103000076. Hämtad 2022-11-04

nih.gov

ncbi.nlm.nih.gov

”Chiral non-steroidal anti-inflammatory drugs--a review”. Journal of the Indian Medical Association 106 (9): sid. 615–8, 622, 624. September 2008. PMID 19552094.
”The metabolic chiral inversion and dispositional enantioselectivity of the 2-arylpropionic acids and their biological consequences”. Biochemical Pharmacology 37 (1): sid. 105–14. January 1988. doi:10.1016/0006-2952(88)90762-9. PMID 3276314.
”The metabolic chiral inversion of 2-arylpropionic acids--a novel route with pharmacological consequences”. The Journal of Pharmacy and Pharmacology 35 (11): sid. 693–704. November 1983. doi:10.1111/j.2042-7158.1983.tb02874.x. PMID 6139449.
”Pharmacological differences between the optical isomers of ibuprofen: evidence for metabolic inversion of the (-)-isomer”. The Journal of Pharmacy and Pharmacology 28 (3): sid. 256–7. March 1976. doi:10.1111/j.2042-7158.1976.tb04144.x. PMID 6706.
”Enantioselective pharmacokinetics of ibuprofen and involved mechanisms”. Drug Metabolism Reviews 37 (1): sid. 215–34. 2005. doi:10.1081/dmr-200047999. PMID 15747501.
”On chiral drug action”. Medicinal Research Reviews 4 (3): sid. 359–413. 1984. doi:10.1002/med.2610040304. PMID 6087043.

worldcat.org

Cahn, R. S.; Ingold, Christopher; Prelog, V. (1966). ”Specification of Molecular Chirality”. Angewandte Chemie International Edition in English 5 (4): sid. 385–415. doi:10.1002/anie.196603851. ISSN 0570-0833. http://dx.doi.org/10.1002/anie.196603851.
Cahn, R. S.; Ingold, C. K.; Prelog, V. (1956). ”The specification of asymmetric configuration in organic chemistry”. Experientia 12 (3): sid. 81–94. doi:10.1007/bf02157171. ISSN 0014-4754. http://dx.doi.org/10.1007/bf02157171.