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Fimasartan

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Fimasartan
Clinical data
Trade namesKanarb
ATC code
Identifiers
  • 2-(2-Butyl-4-methyl-6-oxo-1-{[2'-(1H-tetrazol-5-yl)-4-biphenylyl]methyl}-1,6-dihydro-5-pyrimidinyl)-N,N-dimethylethanethioamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC27H31N7OS
Molar mass501.646 g/mol g·mol−1
3D model (JSmol)
  • CCCCC1=NC(=C(C(=O)N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NN=NN4)CC(=S)N(C)C)C
  • InChI=1S/C27H31N7OS/c1-5-6-11-24-28-18(2)23(16-25(36)33(3)4)27(35)34(24)17-19-12-14-20(15-13-19)21-9-7-8-10-22(21)26-29-31-32-30-26/h7-10,12-15H,5-6,11,16-17H2,1-4H3,(H,29,30,31,32)
  • Key:AMEROGPZOLAFBN-UHFFFAOYSA-N

Fimasartan is a non-peptide angiotensin II receptor antagonist (ARB) used for the treatment of hypertension and heart failure.[1] Through oral administration, fimasartan blocks angiotensin II receptor type 1 (AT1 receptors), reducing pro-hypertensive actions of angiotensin II, such as systemic vasoconstriction and water retention by the kidneys.[2] Concurrent administration of fimasartan with diuretic hydrochlorothiazide has shown to be safe in clinical trials.[3] Fimasartan was approved for use in South Korea in September 9, 2010 and is available under the brand name Kanarb through Boryung Pharmaceuticals, who are presently seeking worldwide partnership.[4]

Mechanism of action

Fimasartan acts on the kidney’s rennin-angiotensin cascade, which begins when renin release from the kidney causes the breakdown of angiotensinogen into angiotensin I. Angiotensin-converting enzyme (ACE) then catalyzes the reaction that forms angiotensin II, which acts on AT1 receptors on the blood vessels, heart, and kidneys.[5] On blood vessels, the AT1 receptor is coupled to an intracellular pathway that causes smooth muscle contraction (vasoconstriction) of blood vessels.[6] In blocking the AT1 receptor, fimasartan inhibits vasoconstriction, favouring vasodilation. At the kidney and adrenal gland, AT1 blockage and prevention of aldosterone formation increase excretion of water and salt by the kidneys, which decreases overall blood volume.[7] At the heart, AT1 blockage decreases contractility and the stimulatory effects of the sympathetic nervous system.[4] Collectively, fimasartain leads to a reduction in blood pressure and alleviation of hypertensive symptoms. ARBs like fimasartan have also shown to be protective against stroke, myocardial infarction, and heart failure.[8] Fimasartan has been shown to reduce cardiac hypertrophy, fibrosis, remodelling, and unnecessary cell proliferation via blockage of AT1 activation [4][9] conceivably through decreased Endothelin 1 production, a result of AT1 activation.[10] Fimastartan can also block TGF-β1 production (also AT1 dependent), which contributes to fibrosis and ventricular damage post-infarct.[11] After ARB administration, mice showed improved prognosis after a myocardial infarcation,[9] though further studies still need to be done to assess fimasartan’s specific effects on decreasing cardiovascular damage.

Side effects

Side effects In clinical trials, fimasartan was well tolerated in all patients. However, higher dosing (360 mg/day) was accompanied by increased dizziness (most likely due to the momentary decrease in blood pressure) and headaches in a low number of patients.[1] Other side effects such as diarrhea, syncope, and cold feet were also experienced in a low number of subjects, which all resolved without medical intervention.[1]

Pharmacology

Fimasartan is rapidly absorbed and has minimal accumulation in the body 7 days after administration.[1] Fimasartan possesses a half-life of 9 to 16 hours,[3] appropriate for daily dosing. Fimasartan was found to be effective in fasted or fed states, with a variety of dosing regimens. In trials, the maximum effects of the drug occurred slightly after the maximum plasma concentration (T-max) was achieved,[1] which occurs 30 minutes to 3 hours after dosing.[12] Fimasartan was found mostly in unmetabolized form in the plasma and in bile excretions. Urinary elimination of the drug was low, at less than 3% 24 hours after administration, entailing that the fimasartan does not undergo renal excretion.[1]

References

  1. ^ a b c d e f Chi, Y., Lee, H., Paik, S., Lee, J.H., Yoo, B.W., Kim, S.L., Hyun, K.T., and Kim, S.L. Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Fimasartan Following Single and Repeated Oral Administration in the Fasted and Fed States in Healthy Subjects. (2011). American Journal Cardiovascular Drugs.11(5): 335-46.
  2. ^ DeMello, W.C., and Frohlich, E.D. "Systemic Versus Local Renin Angiotensin Systems. An Overview." Renin Angiotensin System and Cardiovascular Disease. New York, NY: Humana, 2009.
  3. ^ a b Jeon, H., Soo Lim, K., Shin, K., Kim, J.W., Hyun Yoon, S., Cho, J., Shin, S., Jang, I., and Yu, K. (2012) "Assessment of the Drug-Drug Interactions between Fimasartan and Hydrochlorothiazide in Healthy Volunteers." Journal of Cardiovascular Pharmacology. 59(1): 84-91.
  4. ^ a b c “Fimasartan.” (2011) American Journal Cardiovascular Drugs. 11(4): 249-252
  5. ^ Burnier, M. Angiotensin ll Type 1 Receptor Blockers. (2001). Circulation. 103: 904-912.
  6. ^ Soo Shin, B., Kim, T.H., Paik, S., Chi, Y., Joo, H., Tan, H., Choi, Y., Kim, M., and Yoo, S. Simultaneous Determination of Fimasartan, a Novel Antihypertensive Agent, and Its Active Metabolite in Rat Plasma by Liquid Chromatography–tandem Mass Spectrometry."(2011) Biomedical Chromatography. 25:1208-214.
  7. ^ Klabunde, Richard E. Angiotensin Receptor Blockers (ARBs).CV Pharmacology. N.p., 15 Mar. 2007. Web. 28 Feb. 2013. <http://cvpharmacology.com/vasodilator/ARB.htm>
  8. ^ Neal, B., MacMahon, S., Chapman, N. Effects of ACE inhibitors, calcium antagonists, and other blood-pressure- lowering drugs: results of prospectively designed overviews of randomised trials. (2000) Blood Pressure Lowering Treatment Trialists’ Collaboration. 356:1955–1964.
  9. ^ a b Harada, K., Sugaya, T., Murakami, K., Yazaki, Y., and Komuro, I. Remodeling and Improved Survival After Myocardial Infarction Angiotensin II Type 1A Receptor Knockout Mice Display Less Left Ventricular. (1991).Circulation. 100: 2093-2099.
  10. ^ Phillips, PA. Interaction between endothelin and angiotensin II. (1999). Clinical and Experimental Pharmacology and Physiology. 26(7): 517-518.
  11. ^ Sun, Y., Zhang, J.Q., Zhang, J., Ramires, F.J. Angiotensin II, transforming growth factor-beta1 and repair in the infarcted heart. (1998). Journal of Molecular and Cellular Cardiology. 30: 1559-1569.
  12. ^ Gu, N., Kim, B., Kyoung, S.L., Kim, S.E., Nam, W.S., Yoon, S.H., Cho, J., Shin, S., Jang, I., Yu, K. The Effect of Fimasartan, an Angiotensin Receptor Type 1 Blocker, on the Pharmacokinetics and Pharmacodynamics of Warfarin in Healthy Korean Male Volunteers: A One- Sequence, Two-Period Crossover Clinical Trial. (2012). Clinical Therapeutics. 34(7): 1592-1600.
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