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Aliskiren





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(Redirected from Tekturna)
 


Aliskiren (brand names Tekturna and Rasilez) is the first in a class of drugs called direct renin inhibitors. It is used for essential (primary) hypertension.[2] While used for high blood pressure, other better studied medications are typically recommended due to concerns of higher side effects and less evidence of benefit.[3]

Aliskiren
Clinical data
Trade namesTekturna, Rasilez
AHFS/Drugs.comMonograph
MedlinePlusa607039
License data
  • US DailyMedAliskiren
  • US FDATekturna
  • Pregnancy
    category
    • C in first trimester
      D in second and third trimesters
    Routes of
    administration
    By mouth (tablets)
    ATC code
    Legal status
    Legal status
    • UK: POM (Prescription only)
  • US: WARNING[1]Rx-only
  • Pharmacokinetic data
    BioavailabilityLow (approximately 2.5%)
    MetabolismHepatic, CYP3A4-mediated
    Elimination half-life24 hours
    ExcretionRenal
    Identifiers
    • (2S,4S,5S,7S)-5-amino-N-(2-carbamoyl-2,2-dimethylethyl)-4-hydroxy-7-{[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl}-8-methyl-2-(propan-2-yl)nonanamide

    CAS Number
    PubChem CID
    IUPHAR/BPS
    DrugBank
    ChemSpider
    UNII
    KEGG
    ChEBI
    ChEMBL
    PDB ligand
    CompTox Dashboard (EPA)
    ECHA InfoCard100.127.451 Edit this at Wikidata
    Chemical and physical data
    FormulaC30H53N3O6
    Molar mass551.769 g·mol−1
    3D model (JSmol)
    • O=C(N)C(C)(C)CNC(=O)[C@H](C(C)C)C[C@H](O)[C@@H](N)C[C@@H](C(C)C)Cc1cc(OCCCOC)c(OC)cc1

    • InChI=1S/C30H53N3O6/c1-19(2)22(14-21-10-11-26(38-8)27(15-21)39-13-9-12-37-7)16-24(31)25(34)17-23(20(3)4)28(35)33-18-30(5,6)29(32)36/h10-11,15,19-20,22-25,34H,9,12-14,16-18,31H2,1-8H3,(H2,32,36)(H,33,35)/t22-,23-,24-,25-/m0/s1 ☒N

    • Key:UXOWGYHJODZGMF-QORCZRPOSA-N ☒N

     ☒NcheckY (what is this?)  (verify)

    In December 2011, Novartis halted a trial of the drug after discovering increased nonfatal stroke, kidney complications, high blood potassium, and low blood pressure in people with diabetes and kidney problems.[4][5]

    As a result, in 2012:

    Aliskiren was co-developed by the Swiss pharmaceutical companies Novartis and Speedel.[8][9]

    Medical uses

    edit

    While used for high blood pressure, other better-studied medications are typically recommended.[3] Prescrire has stated that aliskiren is potentially more harmful than beneficial and thus list it as a drug to avoid (as of 2014).[3]

    Adverse effects

    edit

    Contraindications

    edit

    Drug interactions

    edit

    Aliskiren is a minor inhibitor of substrate CYP3A4 and, more importantly, P-glycoprotein:

    Mechanism of action

    edit

    Aliskiren is an inhibitor of renin.[12] Renin, the first enzyme in the renin–angiotensin–aldosterone system, plays a role in blood pressure control. It cleaves angiotensinogentoangiotensin I, which is in turn converted by angiotensin-converting enzyme (ACE) to angiotensin II. Angiotensin II has both direct and indirect effects on blood pressure. It directly causes arterial smooth muscle to contract, leading to vasoconstriction and increased blood pressure. Angiotensin II also stimulates the production of aldosterone from the adrenal cortex, which causes the tubules of the kidneys to increase reabsorption of sodium, with water following, thereby increasing plasma volume, and thus blood pressure. Aliskiren binds to the S3bp binding site of renin, essential for its activity.[12] Binding to this pocket prevents the conversion of angiotensinogen to angiotensin I. Aliskiren is also available as combination therapy with hydrochlorothiazide.[13]

    Chemistry

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    The chemical name for aliskiren is (2 S,4S,5S,7S)-5-amino-N-(2-carbamoyl-2-methylpropyl)-4-hydroxy-2-isopropyl-7-[ 4-methoxy-3-(3-methoxypropoxy)benzyl]-8-methylnonanamide.[14]

    Rationale for design

    edit

    Many drugs control blood pressure by interfering with angiotensin or aldosterone. However, when these drugs are used chronically, the body increases renin production, which drives blood pressure up again. Therefore, pharmacologists have been looking for a drug to inhibit renin directly. Aliskiren is the first drug to do so.[15][16]

    References

    edit
    1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.
  • ^ "First Hypertension Drug to Inhibit Kidney Enzyme Approved". CBC. 2007-03-06. Archived from the original on 2007-03-22. Retrieved 2007-03-14.
  • ^ a b c "Towards better patient care: drugs to avoid in 2014". Prescrire International. 23 (150): 161–5. June 2014. PMID 25121155.
  • ^ Healthzone.ca: Blood-pressure drug reviewed amid dangerous side effects
  • ^ a b Parving HH, Brenner BM, McMurray JJ, de Zeeuw D, Haffner SM, Solomon SD, et al. (December 2012). "Cardiorenal end points in a trial of aliskiren for type 2 diabetes" (PDF). The New England Journal of Medicine. 367 (23): 2204–13. doi:10.1056/NEJMoa1208799. PMID 23121378.
  • ^ a b "FDA Drug Safety Communication: New Warning and Contraindication for blood pressure medicines containing aliskiren (Tekturna)". U.S. Food and Drug Administration (FDA). 19 January 2016. Retrieved 12 February 2020.
  • ^ "Aliskiren Information". U.S. Food and Drug Administration. 8 July 2015. Retrieved 12 February 2020.
  • ^ Gradman AH, Schmieder RE, Lins RL, Nussberger J, Chiang Y, Bedigian MP (March 2005). "Aliskiren, a novel orally effective renin inhibitor, provides dose-dependent antihypertensive efficacy and placebo-like tolerability in hypertensive patients". Circulation. 111 (8): 1012–8. doi:10.1161/01.CIR.0000156466.02908.ED. PMID 15723979.
  • ^ Staessen JA, Li Y, Richart T (October 2006). "Oral renin inhibitors". Lancet. 368 (9545): 1449–56. doi:10.1016/S0140-6736(06)69442-7. PMID 17055947. S2CID 20729350.
  • ^ a b Drugs.com: Tekturna
  • ^ EMA (2018-09-17). "European Medicines Agency recommends new contraindications and warnings for aliskiren-containing medicines". European Medicines Agency. Retrieved 2023-11-05.
  • ^ a b Rahuel J, Rasetti V, Maibaum J, Rüeger H, Göschke R, Cohen NC, et al. (July 2000). "Structure-based drug design: the discovery of novel nonpeptide orally active inhibitors of human renin". Chemistry & Biology. 7 (7): 493–504. doi:10.1016/S1074-5521(00)00134-4. PMID 10903938.
  • ^ Baldwin CM, Plosker GL (2009). "Aliskiren/hydrochlorothiazide combination: in mild to moderate hypertension". Drugs. 69 (7): 833–41. doi:10.2165/00003495-200969070-00004. PMID 19441870. S2CID 26512682.
  • ^ "Recommended INN List 45" (PDF). WHO Drug Information. 15 (1). 2001.
  • ^ Ingelfinger JR (June 2008). "Aliskiren and dual therapy in type 2 diabetes mellitus". The New England Journal of Medicine. 358 (23): 2503–5. doi:10.1056/NEJMe0803375. PMID 18525047.
  • ^ PharmaXChange: Direct Renin Inhibitors as Antihypertensive Drugs Archived 2010-12-07 at the Wayback Machine
  • edit

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Aliskiren&oldid=1227051138"
     



    Last edited on 3 June 2024, at 11:22  





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    This page was last edited on 3 June 2024, at 11:22 (UTC).

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