Flufenamic acid (English Wikipedia)

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

refsWebsite

Global rank English rank

19nih.gov

4^th place

15doi.org

2^nd place

4semanticscholar.org

11^th place

8^th place

3harvard.edu

18^th place

17^th place

2handle.net

102^nd place

76^th place

1ctdbase.org

low place

1worldcat.org

5^th place

1sciencedirect.com

149^th place

178^th place

1web.archive.org

1^st place

1drugs.com

399^th place

333^rd place

ctdbase.org

"Chemical–Gene Interaction Query: Flufenamic Acid (Homo sapiens)". Comparative Toxicogenomics Database. North Carolina State University. Retrieved July 4, 2015.

doi.org

Whitehouse MW (2005). "Drugs to treat inflammation: a historical introduction". Current Medicinal Chemistry. 12 (25): 2931–2942. doi:10.2174/092986705774462879. ISBN 9781608052073. PMID 16378496.
Serezhkin VN, Savchenkov AV (June 3, 2015). "Application of the Method of Molecular Voronoi–Dirichlet Polyhedra for Analysis of Noncovalent Interactions in Crystal Structures of Flufenamic Acid—The Current Record-Holder of the Number of Structurally Studied Polymorphs". Crystal Growth & Design. 15 (6): 2878–2882. doi:10.1021/acs.cgd.5b00326. ISSN 1528-7483. S2CID 100245760.
Mei H, Han J, White S, Graham DJ, Izawa K, Sato T, et al. (September 2020). "Tailor-Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern Pharmaceuticals". Chemistry. 26 (50): 11349–11390. doi:10.1002/chem.202000617. PMID 32359086. S2CID 218479815.
Khodov IA, Belov KV, Krestyaninov MA, Dyshin AA, Kiselev MG (February 2023). "Investigation of the Spatial Structure of Flufenamic Acid in Supercritical Carbon Dioxide Media via 2D NOESY". Materials. 16 (4): 1524. Bibcode:2023Mate...16.1524K. doi:10.3390/ma16041524. PMC 9961892. PMID 36837153.
Khodov IA, Belov KV, Huster D, Scheidt HA (June 2023). "Conformational State of Fenamates at the Membrane Interface: A MAS NOESY Study". Membranes. 13 (6): 607. doi:10.3390/membranes13060607. PMC 10300900. PMID 37367811.
Delaney SP, Smith TM, Korter TM (December 2014). "Conformational origins of polymorphism in two forms of flufenamic acid". Journal of Molecular Structure. 1078: 83–89. Bibcode:2014JMoSt1078...83D. doi:10.1016/j.molstruc.2014.02.001.
López-Mejías V, Kampf JW, Matzger AJ (June 2012). "Nonamorphism in flufenamic acid and a new record for a polymorphic compound with solved structures". Journal of the American Chemical Society. 134 (24): 9872–9875. Bibcode:2012JAChS.134.9872L. doi:10.1021/ja302601f. PMC 3634867. PMID 22690822.
Pippione AC, Carnovale IM, Bonanni D, Sini M, Goyal P, Marini E, et al. (April 2018). "Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid". European Journal of Medicinal Chemistry. 150: 930–945. doi:10.1016/j.ejmech.2018.03.040. hdl:10454/16082. PMID 29602039. S2CID 4690397.
Ojima I (July 2013). "Exploration of fluorine chemistry at the multidisciplinary interface of chemistry and biology". The Journal of Organic Chemistry. 78 (13): 6358–6383. doi:10.1021/jo400301u. PMC 3752428. PMID 23614876.
Altomonte S, Zanda M (November 2012). "Synthetic chemistry and biological activity of pentafluorosulphanyl (SF5) organic molecules". Journal of Fluorine Chemistry. 143: 57–93. doi:10.1016/j.jfluchem.2012.06.030. hdl:2164/2557.
Hendriks CM, Penning TM, Zang T, Wiemuth D, Gründer S, Sanhueza IA, et al. (October 2015). "Pentafluorosulfanyl-containing flufenamic acid analogs: Syntheses, properties and biological activities". Bioorganic & Medicinal Chemistry Letters. 25 (20): 4437–4440. doi:10.1016/j.bmcl.2015.09.012. PMC 4599580. PMID 26372652.
Nechipadappu SK, Tekuri V, Trivedi DR (May 2017). "Pharmaceutical Co-Crystal of Flufenamic Acid: Synthesis and Characterization of Two Novel Drug-Drug Co-Crystal". Journal of Pharmaceutical Sciences. 106 (5): 1384–1390. doi:10.1016/j.xphs.2017.01.033. PMID 28185907.
Maestrelli F, Rossi P, Paoli P, De Luca E, Mura P (February 2020). "The role of solid state properties on the dissolution performance of flufenamic acid". Journal of Pharmaceutical and Biomedical Analysis. 180: 113058. doi:10.1016/j.jpba.2019.113058. PMID 31881398. S2CID 209499101.
Wang Q, Han J, Sorochinsky A, Landa A, Butler G, Soloshonok VA (August 2022). "The Latest FDA-Approved Pharmaceuticals Containing Fragments of Tailor-Made Amino Acids and Fluorine". Pharmaceuticals. 15 (8): 999. doi:10.3390/ph15080999. PMC 9416721. PMID 36015147.
Aronson JK, ed. (2016). "Flufenamic acid and meclofenamic acid". Meyler's Side Effects of Drugs (16th ed.). Elsevier. p. 361. doi:10.1016/B978-0-444-53717-1.00755-1. ISBN 978-0-444-53716-4.

drugs.com

"International listings for flufenamic acid". Drugs.com. Archived from the original on June 30, 2019. Retrieved July 3, 2015.

handle.net

hdl.handle.net

Pippione AC, Carnovale IM, Bonanni D, Sini M, Goyal P, Marini E, et al. (April 2018). "Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid". European Journal of Medicinal Chemistry. 150: 930–945. doi:10.1016/j.ejmech.2018.03.040. hdl:10454/16082. PMID 29602039. S2CID 4690397.
Altomonte S, Zanda M (November 2012). "Synthetic chemistry and biological activity of pentafluorosulphanyl (SF5) organic molecules". Journal of Fluorine Chemistry. 143: 57–93. doi:10.1016/j.jfluchem.2012.06.030. hdl:2164/2557.

harvard.edu

ui.adsabs.harvard.edu

Khodov IA, Belov KV, Krestyaninov MA, Dyshin AA, Kiselev MG (February 2023). "Investigation of the Spatial Structure of Flufenamic Acid in Supercritical Carbon Dioxide Media via 2D NOESY". Materials. 16 (4): 1524. Bibcode:2023Mate...16.1524K. doi:10.3390/ma16041524. PMC 9961892. PMID 36837153.
Delaney SP, Smith TM, Korter TM (December 2014). "Conformational origins of polymorphism in two forms of flufenamic acid". Journal of Molecular Structure. 1078: 83–89. Bibcode:2014JMoSt1078...83D. doi:10.1016/j.molstruc.2014.02.001.
López-Mejías V, Kampf JW, Matzger AJ (June 2012). "Nonamorphism in flufenamic acid and a new record for a polymorphic compound with solved structures". Journal of the American Chemical Society. 134 (24): 9872–9875. Bibcode:2012JAChS.134.9872L. doi:10.1021/ja302601f. PMC 3634867. PMID 22690822.

nih.gov

pubmed.ncbi.nlm.nih.gov

Whitehouse MW (2005). "Drugs to treat inflammation: a historical introduction". Current Medicinal Chemistry. 12 (25): 2931–2942. doi:10.2174/092986705774462879. ISBN 9781608052073. PMID 16378496.
"Mefenamic Acid". LiverTox Database. U.S. National Institutes of Health (NIH). June 23, 2015. PMID 31643176. Retrieved July 3, 2015. (fenamates generally not available in the United States, such as tolfenamic acid and flufenamic acid)
Mei H, Han J, White S, Graham DJ, Izawa K, Sato T, et al. (September 2020). "Tailor-Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern Pharmaceuticals". Chemistry. 26 (50): 11349–11390. doi:10.1002/chem.202000617. PMID 32359086. S2CID 218479815.
Khodov IA, Belov KV, Krestyaninov MA, Dyshin AA, Kiselev MG (February 2023). "Investigation of the Spatial Structure of Flufenamic Acid in Supercritical Carbon Dioxide Media via 2D NOESY". Materials. 16 (4): 1524. Bibcode:2023Mate...16.1524K. doi:10.3390/ma16041524. PMC 9961892. PMID 36837153.
Khodov IA, Belov KV, Huster D, Scheidt HA (June 2023). "Conformational State of Fenamates at the Membrane Interface: A MAS NOESY Study". Membranes. 13 (6): 607. doi:10.3390/membranes13060607. PMC 10300900. PMID 37367811.
López-Mejías V, Kampf JW, Matzger AJ (June 2012). "Nonamorphism in flufenamic acid and a new record for a polymorphic compound with solved structures". Journal of the American Chemical Society. 134 (24): 9872–9875. Bibcode:2012JAChS.134.9872L. doi:10.1021/ja302601f. PMC 3634867. PMID 22690822.
Pippione AC, Carnovale IM, Bonanni D, Sini M, Goyal P, Marini E, et al. (April 2018). "Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid". European Journal of Medicinal Chemistry. 150: 930–945. doi:10.1016/j.ejmech.2018.03.040. hdl:10454/16082. PMID 29602039. S2CID 4690397.
Ojima I (July 2013). "Exploration of fluorine chemistry at the multidisciplinary interface of chemistry and biology". The Journal of Organic Chemistry. 78 (13): 6358–6383. doi:10.1021/jo400301u. PMC 3752428. PMID 23614876.
Hendriks CM, Penning TM, Zang T, Wiemuth D, Gründer S, Sanhueza IA, et al. (October 2015). "Pentafluorosulfanyl-containing flufenamic acid analogs: Syntheses, properties and biological activities". Bioorganic & Medicinal Chemistry Letters. 25 (20): 4437–4440. doi:10.1016/j.bmcl.2015.09.012. PMC 4599580. PMID 26372652.
Nechipadappu SK, Tekuri V, Trivedi DR (May 2017). "Pharmaceutical Co-Crystal of Flufenamic Acid: Synthesis and Characterization of Two Novel Drug-Drug Co-Crystal". Journal of Pharmaceutical Sciences. 106 (5): 1384–1390. doi:10.1016/j.xphs.2017.01.033. PMID 28185907.
Maestrelli F, Rossi P, Paoli P, De Luca E, Mura P (February 2020). "The role of solid state properties on the dissolution performance of flufenamic acid". Journal of Pharmaceutical and Biomedical Analysis. 180: 113058. doi:10.1016/j.jpba.2019.113058. PMID 31881398. S2CID 209499101.
Wang Q, Han J, Sorochinsky A, Landa A, Butler G, Soloshonok VA (August 2022). "The Latest FDA-Approved Pharmaceuticals Containing Fragments of Tailor-Made Amino Acids and Fluorine". Pharmaceuticals. 15 (8): 999. doi:10.3390/ph15080999. PMC 9416721. PMID 36015147.

ncbi.nlm.nih.gov

Khodov IA, Belov KV, Krestyaninov MA, Dyshin AA, Kiselev MG (February 2023). "Investigation of the Spatial Structure of Flufenamic Acid in Supercritical Carbon Dioxide Media via 2D NOESY". Materials. 16 (4): 1524. Bibcode:2023Mate...16.1524K. doi:10.3390/ma16041524. PMC 9961892. PMID 36837153.
Khodov IA, Belov KV, Huster D, Scheidt HA (June 2023). "Conformational State of Fenamates at the Membrane Interface: A MAS NOESY Study". Membranes. 13 (6): 607. doi:10.3390/membranes13060607. PMC 10300900. PMID 37367811.
López-Mejías V, Kampf JW, Matzger AJ (June 2012). "Nonamorphism in flufenamic acid and a new record for a polymorphic compound with solved structures". Journal of the American Chemical Society. 134 (24): 9872–9875. Bibcode:2012JAChS.134.9872L. doi:10.1021/ja302601f. PMC 3634867. PMID 22690822.
Ojima I (July 2013). "Exploration of fluorine chemistry at the multidisciplinary interface of chemistry and biology". The Journal of Organic Chemistry. 78 (13): 6358–6383. doi:10.1021/jo400301u. PMC 3752428. PMID 23614876.
Hendriks CM, Penning TM, Zang T, Wiemuth D, Gründer S, Sanhueza IA, et al. (October 2015). "Pentafluorosulfanyl-containing flufenamic acid analogs: Syntheses, properties and biological activities". Bioorganic & Medicinal Chemistry Letters. 25 (20): 4437–4440. doi:10.1016/j.bmcl.2015.09.012. PMC 4599580. PMID 26372652.
Wang Q, Han J, Sorochinsky A, Landa A, Butler G, Soloshonok VA (August 2022). "The Latest FDA-Approved Pharmaceuticals Containing Fragments of Tailor-Made Amino Acids and Fluorine". Pharmaceuticals. 15 (8): 999. doi:10.3390/ph15080999. PMC 9416721. PMID 36015147.

livertox.nih.gov

"Mefenamic Acid". LiverTox Database. U.S. National Institutes of Health (NIH). June 23, 2015. PMID 31643176. Retrieved July 3, 2015. (fenamates generally not available in the United States, such as tolfenamic acid and flufenamic acid)

sciencedirect.com

Aronson JK, ed. (2016). "Flufenamic acid and meclofenamic acid". Meyler's Side Effects of Drugs (16th ed.). Elsevier. p. 361. doi:10.1016/B978-0-444-53717-1.00755-1. ISBN 978-0-444-53716-4.

semanticscholar.org

api.semanticscholar.org

Serezhkin VN, Savchenkov AV (June 3, 2015). "Application of the Method of Molecular Voronoi–Dirichlet Polyhedra for Analysis of Noncovalent Interactions in Crystal Structures of Flufenamic Acid—The Current Record-Holder of the Number of Structurally Studied Polymorphs". Crystal Growth & Design. 15 (6): 2878–2882. doi:10.1021/acs.cgd.5b00326. ISSN 1528-7483. S2CID 100245760.
Mei H, Han J, White S, Graham DJ, Izawa K, Sato T, et al. (September 2020). "Tailor-Made Amino Acids and Fluorinated Motifs as Prominent Traits in Modern Pharmaceuticals". Chemistry. 26 (50): 11349–11390. doi:10.1002/chem.202000617. PMID 32359086. S2CID 218479815.
Pippione AC, Carnovale IM, Bonanni D, Sini M, Goyal P, Marini E, et al. (April 2018). "Potent and selective aldo-keto reductase 1C3 (AKR1C3) inhibitors based on the benzoisoxazole moiety: application of a bioisosteric scaffold hopping approach to flufenamic acid". European Journal of Medicinal Chemistry. 150: 930–945. doi:10.1016/j.ejmech.2018.03.040. hdl:10454/16082. PMID 29602039. S2CID 4690397.
Maestrelli F, Rossi P, Paoli P, De Luca E, Mura P (February 2020). "The role of solid state properties on the dissolution performance of flufenamic acid". Journal of Pharmaceutical and Biomedical Analysis. 180: 113058. doi:10.1016/j.jpba.2019.113058. PMID 31881398. S2CID 209499101.

web.archive.org

"International listings for flufenamic acid". Drugs.com. Archived from the original on June 30, 2019. Retrieved July 3, 2015.

worldcat.org

search.worldcat.org

Serezhkin VN, Savchenkov AV (June 3, 2015). "Application of the Method of Molecular Voronoi–Dirichlet Polyhedra for Analysis of Noncovalent Interactions in Crystal Structures of Flufenamic Acid—The Current Record-Holder of the Number of Structurally Studied Polymorphs". Crystal Growth & Design. 15 (6): 2878–2882. doi:10.1021/acs.cgd.5b00326. ISSN 1528-7483. S2CID 100245760.