말톨 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "말톨" in Korean language version.

refsWebsite

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6doi.org

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4nih.gov

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2archive.org

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archive.org

N. Kaneko, H. Yasui, J. Takada, K. Suzuki, H. Sakurai (2004). “Orally administrated aluminum-maltolate complex enhances oxidative stress in the organs of mice”. 《J. Inorg. Biochem.》 98 (12): 2022–2031. doi:10.1016/j.jinorgbio.2004.09.008. PMID 15541491. CS1 관리 - 여러 이름 (링크)
Amatori, I.Bagaloni; Macedi, M.Formica; Giorgi, V.Fusi (2010). “Malten, a new synthetic molecule showing in vitro antiproliferative activity against tumour cells and induction of complex DNA structural alterations”. 《Br. J. Cancer》 103 (2): 239–48. doi:10.1038/sj.bjc.6605745.

doi.org

dx.doi.org

B. D. Liboiron, K. H. Thompson, G. R. Hanson, E. Lam, N. Aebischer, C. Orvig (2005). “New Insights into the Interactions of Serum Proteins with Bis(maltolato)oxovanadium(IV): Transport and Biotransformation of Insulin-Enhancing Vanadium Pharmaceuticals”. 《J. Am. Chem. Soc.》 127 (14): 5104–5115. doi:10.1021/ja043944n. PMID 15810845. CS1 관리 - 여러 이름 (링크)
N. Kaneko, H. Yasui, J. Takada, K. Suzuki, H. Sakurai (2004). “Orally administrated aluminum-maltolate complex enhances oxidative stress in the organs of mice”. 《J. Inorg. Biochem.》 98 (12): 2022–2031. doi:10.1016/j.jinorgbio.2004.09.008. PMID 15541491. CS1 관리 - 여러 이름 (링크)
L. R. Bernstein, T. Tanner, C. Godfrey, B. Noll (2000). “Chemistry and pharmacokinetics of gallium maltolate, a compound with high oral gallium bioavailability”. 《Metal Based Drugs》 7 (1): 33–48. doi:10.1155/MBD.2000.33. PMC 2365198. PMID 18475921. CS1 관리 - 여러 이름 (링크)
D.M. Reffitt, T.J. Burden, P.T. Seed, J. Wood J, R.P. Thompson, J.J. Powell (2000). “Assessment of iron absorption from ferric trimaltol”. 《Ann. Clin. Biochem.》 37 (4): 457–66. doi:10.1258/0004563001899645. PMID 10902861. CS1 관리 - 여러 이름 (링크)
Amatori, G.Ambrosi; Fanelli, M.Formica; Fusi, L.Giorgi; Macedi, M.Micheloni; Paoli, R.Pontellini (2012). “Synthesis, basicity, structural characterization, and biochemical properties of two [(3-hydroxy-4-pyron-2-yl)methyl]amine derivatives showing antineoplastic features”. 《J. Org. Chem.》 77 (5): 2207–18. doi:10.1021/jo202270j.
Amatori, I.Bagaloni; Macedi, M.Formica; Giorgi, V.Fusi (2010). “Malten, a new synthetic molecule showing in vitro antiproliferative activity against tumour cells and induction of complex DNA structural alterations”. 《Br. J. Cancer》 103 (2): 239–48. doi:10.1038/sj.bjc.6605745.

nih.gov

ncbi.nlm.nih.gov

B. D. Liboiron, K. H. Thompson, G. R. Hanson, E. Lam, N. Aebischer, C. Orvig (2005). “New Insights into the Interactions of Serum Proteins with Bis(maltolato)oxovanadium(IV): Transport and Biotransformation of Insulin-Enhancing Vanadium Pharmaceuticals”. 《J. Am. Chem. Soc.》 127 (14): 5104–5115. doi:10.1021/ja043944n. PMID 15810845. CS1 관리 - 여러 이름 (링크)
N. Kaneko, H. Yasui, J. Takada, K. Suzuki, H. Sakurai (2004). “Orally administrated aluminum-maltolate complex enhances oxidative stress in the organs of mice”. 《J. Inorg. Biochem.》 98 (12): 2022–2031. doi:10.1016/j.jinorgbio.2004.09.008. PMID 15541491. CS1 관리 - 여러 이름 (링크)
L. R. Bernstein, T. Tanner, C. Godfrey, B. Noll (2000). “Chemistry and pharmacokinetics of gallium maltolate, a compound with high oral gallium bioavailability”. 《Metal Based Drugs》 7 (1): 33–48. doi:10.1155/MBD.2000.33. PMC 2365198. PMID 18475921. CS1 관리 - 여러 이름 (링크)
D.M. Reffitt, T.J. Burden, P.T. Seed, J. Wood J, R.P. Thompson, J.J. Powell (2000). “Assessment of iron absorption from ferric trimaltol”. 《Ann. Clin. Biochem.》 37 (4): 457–66. doi:10.1258/0004563001899645. PMID 10902861. CS1 관리 - 여러 이름 (링크)