Tham khảo Moexipril

  1. ↑ Hochadel, Maryanne biên tập (2006). The AARP Guide to Pills. Sterling Publishing Company. tr. 640. ISBN 978-1-4027-1740-6. Truy cập ngày 9 tháng 10 năm 2009.
  2. 1 2 Belal, F.F, K.M. Metwaly, and S.M. Amer. "Development of Membrane Electrodes for the Specific Determination of Moexipril Hydrochloride in Dosage Forms and Biological Fluids." Portugaliae Electrochimica Acta. 27.4 (2009): 463-475.
  3. 1 2 3 Rodgers, Katie, Michael C Vinson, and Marvin W Davis. "Breakthroughs: New drug approvals of 1995 -- part 1." Advanstar Communications, Inc. 140.3 (1996): 84.
  4. ↑ Fischer, Jnos; Ganellin, C. Robin (2006). Analogue-based Drug Discovery (bằng tiếng Anh). John Wiley & Sons. tr. 468. ISBN 9783527607495.
  5. ↑ Dart, Richard C. (2004). Medical toxicology. Lippincott Williams & Wilkins. tr. 647. ISBN 978-0-7817-2845-4. Truy cập ngày 9 tháng 10 năm 2009.
  6. 1 2 White, W. B.; Stimpel, M (1995). “Long-term safety and efficacy of moexipril alone and in combination with hydrochlorothiazide in elderly patients with hypertension”. Journal of Human Hypertension. 9 (11): 879–884. PMID 8583466.
  7. ↑ Rosendorff, C (1996). “The renin-angiotensin system and vascular hypertrophy”. Journal of the American College of Cardiology. 28 (4): 803–812. doi:10.1016/s0735-1097(96)00251-3. PMID 8837552.
  8. 1 2 3 Chrysant, S. G. (1998). “Vascular remodeling: The role of angiotensin-converting enzyme inhibitors”. American Heart Journal. 135 (2 Pt 2): 21–30. doi:10.1053/hj.1998.v135.86971. PMID 9488609.
  9. 1 2 3 Hartman, J.C. "The role of bradykinin and nitric oxide in the cardioprotective action of ACE inhibitors." The Annals of Thoracic Surgery. 60.3 (1995): 789-792.
  10. ↑ Jaiswal N, Diz DI, Chappell MC, Khosia MC, Ferrario CM (1992). “Stimulation of endothelial cell prostaglandin production by angiotensin peptides. Characterization of receptors”. Hypertension. 19 (2): 49–55. doi:10.1161/01.hyp.19.2_suppl.ii49.
  11. ↑ Phillips, PA. "Interaction between endothelin and angiotensin II." Clinical and Experimental Pharmacology and Physiology. 26.7. (1999): 517-518.
  12. ↑ Youn, T. J.; Kim, H. S.; Oh, B. H. (1999). “Ventricular remodeling and transforming growth factor-beta 1 mRNA expression after nontransmural myocardial infarction in rats: Effects of angiotensin converting enzyme inhibition and angiotensin II type 1 receptor blockade”. Basic research in cardiology. 94 (4): 246–253. doi:10.1007/s003950050149. PMID 10505424.
  13. ↑ Kalász, H; Petroianu, G; Tekes, K; Klebovich, I; Ludányi, K; Gulyás, Z (2007). “Metabolism of moexipril to moexiprilat: Determination of in vitro metabolism using HPLC-ES-MS”. Medicinal Chemistry. 3 (1): 101–106. doi:10.2174/157340607779317490. PMID 17266629.
  14. ↑ Chrysant, George S, PK Nguyen. "Moexipril and left ventricular hypertrophy." Vascular Health Risk Management. 3.1 (2007): 23-30.
  15. 1 2 Cawello, W; Boekens, H; Waitzinger, J; Miller, U (2002). “Moexipril shows a long duration of action related to an extended pharmacokinetic half-life and prolonged ACE inhibition”. International journal of clinical pharmacology and therapeutics. 40 (1): 9–17. doi:10.5414/cpp40009. PMID 11837383.
  16. ↑ Cameron, RT; Coleman, RG; Day, JP; Yalla, KC; Houslay, MD; Adams, DR; Shoichet, BK; Baillie, GS (tháng 5 năm 2013). “Chemical informatics uncovers a new role for moexipril as a novel inhibitor of cAMP phosphodiesterase-4 (PDE4)”. Biochemical Pharmacology. 85 (9): 1297–1305. doi:10.1016/j.bcp.2013.02.026. PMC 3625111. PMID 23473803.
  17. ↑ M. L. Hoefle, S. Klutchko, Đăng ký phát minh {{{country}}} {{{number}}}, "{{{title}}}", trao vào [[{{{gdate}}}]] ; eidem, Bằng sáng chế Hoa Kỳ số 4.344.949 (both 1982 to Warner-Lambert).
  18. ↑ Klutchko, Sylvester; Blankley, C. John; Fleming, Robert W.; Hinkley, Jack M.; Werner, Ann E.; Nordin, Ivan; Holmes, Ann; Hoefle, Milton L.; Cohen, David M. (1986). “Synthesis of novel angiotensin converting enzyme inhibitor quinapril and related compounds. A divergence of structure-activity relationships for non-sulfhydryl and sulfhydryl types”. Journal of Medicinal Chemistry. 29 (10): 1953–61. doi:10.1021/jm00160a026. PMID 3020249.
  19. ↑ Kaltenbronn, James S.; Dejohn, Dana; Krolls, Uldis (2009). “SYNTHESIS OF [S-(R∗,R∗)] – ETHYL α–[(1–CARBOXYETHYL) AMINO]–BENEZENEBUTANOATE, AN IMPORTANT INTERMEDIATE IN THE SYNTHESIS OF ANGIOTENSIN CONVERTING ENZYME INHIBITORS”. Organic Preparations and Procedures International. 15: 35. doi:10.1080/00304948309355428.