Tham khảo Paroxypropione

  1. 1 2 J. Elks (14 tháng 11 năm 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. tr. 662–. ISBN 978-1-4757-2085-3. 
  2. ↑ Index Nominum 2000: International Drug Directory. Taylor & Francis. Tháng 1 năm 2000. tr. 796–. ISBN 978-3-88763-075-1. 
  3. 1 2 Paulsen, C. Alvin; Mortimore, Glenn E.; Heller, Carl G. (1951). “THE PITUITARY ACTION AND ESTROGENIC EFFECT OF PARAHYDROXYPROPIOPHENONE”. The Journal of Clinical Endocrinology & Metabolism 11 (8): 892–894. ISSN 0021-972X. doi:10.1210/jcem-11-8-892. 
  4. 1 2 Mombelli, E. (2012). “Evaluation of the OECD (Q)SAR Application Toolbox for the profiling of estrogen receptor binding affinities”. SAR and QSAR in Environmental Research 23 (1-2): 37–57. ISSN 1062-936X. doi:10.1080/1062936X.2011.623325. 
  5. ↑ Buu-Hoi, Ng. Ph.; Xuong, Ng. D.; Lavit, Denise (1953). “Fluorine-containing analogs of 4-hydroxypropiophenone”. The Journal of Organic Chemistry 18 (8): 910–915. ISSN 0022-3263. doi:10.1021/jo50014a002. 
  6. ↑ P.L. Chambers; P. Günzel (12 tháng 3 năm 2013). Mechanism of Toxic Action on Some Target Organs: Drugs and Other Substances. Springer Science & Business Media. tr. 276–. ISBN 978-3-642-67265-1. 
  7. ↑ Gottschlich, Regina; Metzler, Manfred (1979). “High-pressure, reverse-phase partition chromatography separation of diethylstilbestrol metabolites and analogs”. Analytical Biochemistry 92 (1): 199–202. ISSN 0003-2697. doi:10.1016/0003-2697(79)90645-6. 
  8. ↑ Richard E. Jones; Kristin H. Lopez (28 tháng 9 năm 2013). Human Reproductive Biology. Academic Press. tr. 46–. ISBN 978-0-12-382185-0. 
  9. ↑ Pugazhendhi D, Pope GS, Darbre PD (2005). “Oestrogenic activity of p-hydroxybenzoic acid (common metabolite of paraben esters) and methylparaben in human breast cancer cell lines”. J Appl Toxicol 25 (4): 301–9. PMID 16021681. doi:10.1002/jat.1066. 
  10. ↑ De Vega Ruiz, T (1955). “Protein breakdown before and after operations. Influence of growth hormone and of inhibitors of the pituitary adrenal system.”. Cirug., Ginecol. Urol. 9: 289–326. 
  11. ↑ Bussolati C, de Carneri I, Castellino S, Marinoni V, Sperzani GL (1967). “Treatment of Experimental and Clinical Schistosomiasis with Hormonal Inhibitors of Ovulation”. Am. J. Trop. Med. Hyg. 16 (4): 497–9. PMID 5006470. 
  12. ↑ Scott, Charles C.; Kroc, Robert L.; Stasilli, Neil R. (1952). “METABOLIC AND TOXICITY STUDIES ON PARA-HYDROXYPROPIOPHENONE”. Endocrinology 50 (6): 607–611. ISSN 0013-7227. doi:10.1210/endo-50-6-607. 
  13. ↑ Vafiadis, Anastasios P.; Bakalbassis, Evangelos G. (2003). “A computational study of the structure-activity relationships of some p-hydroxybenzoic acid antioxidants”. Journal of the American Oil Chemists' Society 80 (12): 1217–1223. ISSN 0003-021X. doi:10.1007/s11746-003-0845-3. 
  14. ↑ Kiresee Saghana, PR; Hemalatha, S. “Free Radical Scavenging Activity of 4-Hydroxypropiophenone by In Vitro Assays” (PDF). World Journal of Pharmacy and Pharmaceutical Sciences 4 (12): 935–950. ISSN 2278-4357. 
  15. ↑ Murashige, Ryo; Hayashi, Yuka; Ohmori, Syo; Torii, Ayuko; Aizu, Yoko; Muto, Yasuyuki; Murai, Yuta; Oda, Yuji; Hashimoto, Makoto Tetrahedron, 2011, vol. 67, # 3 p. 641 - 649.
  16. ↑ Walter H Hartung, Bằng sáng chế Hoa Kỳ số 1.995.709 (1935 to Sharp & Dohme Inc)

Tài liệu tham khảo

WikiPedia: Paroxypropione http://www.chemspider.com/Chemical-Structure.6035.... http://www.google.com/patents?vid=1995709 http://www.wjpps.com/download/article/1448873223.p... //www.ncbi.nlm.nih.gov/pubmed/13579130 //www.ncbi.nlm.nih.gov/pubmed/16021681 //www.ncbi.nlm.nih.gov/pubmed/5006470 http://www.ajtmh.org/content/16/4/497.extract http://www.cabdirect.org/abstracts/19561404674.htm... http://www.commonchemistry.org/ChemicalDetail.aspx... //dx.doi.org/10.1002%2Fjat.1066