User:Mr. Ibrahem/Abiraterone acetate

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Mr. Ibrahem/Abiraterone acetate
Clinical data
Pronunciationa" bir a' ter one
Trade namesZytiga, Yonsa, others
Other namesCB-7630; JNJ-212082; 17-(3-Pyridinyl)androsta-5,16-dien-3β-ol acetate, abiraterone (BAN UK), abiraterone acetate (JAN JP), abiraterone acetate (USAN US)
AHFS/Drugs.comMonograph
MedlinePlusa611046
License data
Pregnancy
category
Routes of
administration		By mouth (tablets)[2][3]
Drug classAntineoplastic
Legal status
Legal status
Pharmacokinetic data
BioavailabilityUnknown, but may be 50% at most on empty stomach[6]
Protein bindingAbiraterone: ~99.8% (to albumin and α1-AGpTooltip alpha-1 acid glycoprotein)[6][2][7]
MetabolismEsterases, CYP3A4, SULT2A1[7]
MetabolitesAbiraterone, others[2][6]
Elimination half-lifeAbiraterone: 12–24 hours[2][6][3]
ExcretionFeces: 88%[2][7]
Urine: 5%[2][7][3]
Identifiers
  • [(3S,8R,9S,10R,13S,14S)-10,13-dimethyl-17-pyridin-3-yl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
Chemical and physical data
FormulaC26H33NO2
Molar mass391.555 g·mol−1
3D model (JSmol)
Melting point144 to 145 °C (291 to 293 °F) [8]
  • CC(=O)O[C@H]1CC[C@@]2([C@H]3CC[C@]4([C@H]([C@@H]3CC=C2C1)CC=C4C5=CN=CC=C5)C)C
  • InChI=1S/C26H33NO2/c1-17(28)29-20-10-12-25(2)19(15-20)6-7-21-23-9-8-22(18-5-4-14-27-16-18)26(23,3)13-11-24(21)25/h4-6,8,14,16,20-21,23-24H,7,9-13,15H2,1-3H3/t20-,21-,23-,24-,25-,26+/m0/s1 checkY
  • Key:UVIQSJCZCSLXRZ-UBUQANBQSA-N checkY
  (verify)

Abiraterone acetate, sold under the brand name Zytiga among others, is a medication used to treat prostate cancer.[9] Specifically it is used together with a corticosteroid for metastatic castration-resistant prostate cancer (mCRPC) and metastatic high-risk castration-sensitive prostate cancer (mCSPC).[2][3] It should either be used following removal of the testicles or along with a gonadotropin-releasing hormone (GnRH) analog.[2] It is taken by mouth.[9]

Common side effects include tiredness, vomiting, headache, joint pain, high blood pressure, swelling, low blood potassium, high blood sugar, hot flashes, diarrhea, and cough.[9][2] Other severe side effects may include liver failure and adrenocortical insufficiency.[2] In males whose partners can become pregnant, birth control is recommended.[2] Supplied as abiraterone acetate it is converted in the body to abiraterone.[2] Abiraterone acetate works by suppressing the production of androgens – specifically it inhibits CYP17A1 – and thereby decreases the production of testosterone.[9] In doing so, it prevents the effects of these hormones in prostate cancer.[9]

Abiraterone acetate was described in 1995, and approved for medical use in the United States and Europe in 2011.[11][2] It is on the World Health Organization's List of Essential Medicines.[12] In the United Kingdom it costs the NHS £2,700 a month as of 2018.[13] In the United States this amount costs US$3,300 as of 2019.[14] The medication is marketed widely throughout the world.[15]

References[edit]

  1. ^ a b "Abiraterone Use During Pregnancy". Drugs.com. 13 March 2020. Archived from the original on 25 November 2020. Retrieved 8 June 2020.
  2. ^ a b c d e f g h i j k l m n "Zytiga- abiraterone acetate tablet, film coated". DailyMed. 13 June 2019. Archived from the original on 13 November 2014. Retrieved 15 November 2019.
  3. ^ a b c d "Yonsa- abiraterone acetate tablet". DailyMed. 5 June 2018. Archived from the original on 13 August 2020. Retrieved 15 November 2019.
  4. ^ "Zytiga abiraterone acetate product information" (PDF). TGA eBusiness Services. Janssen-Cilag Pty Ltd. 1 March 2012. Archived from the original on 24 November 2020. Retrieved 24 January 2014.
  5. ^ "Zytiga 500 mg film-coated tablets - Summary of Product Characteristics (SmPC)". electronic medicines compendium (emc). Datapharm. 4 March 2019. Archived from the original on 15 November 2019. Retrieved 15 November 2019.
  6. ^ a b c d Benoist GE, Hendriks RJ, Mulders PF, Gerritsen WR, Somford DM, Schalken JA, van Oort IM, Burger DM, van Erp NP (November 2016). "Pharmacokinetic Aspects of the Two Novel Oral Drugs Used for Metastatic Castration-Resistant Prostate Cancer: Abiraterone Acetate and Enzalutamide". Clin Pharmacokinet. 55 (11): 1369–1380. doi:10.1007/s40262-016-0403-6. PMC 5069300. PMID 27106175.
  7. ^ a b c d "Meeting Library - Meeting Library". meetinglibrary.asco.org. Archived from the original on 20 September 2016. Retrieved 9 September 2016.
  8. ^ Potter, Gerard A.; Barrie, S. Elaine; Jarman, Michael; Rowlands, Martin G. (1995). "Novel Steroidal Inhibitors of Human Cytochrome P45017 alpha (17.alpha.-Hydroxylase-C17,20-lyase): Potential Agents for the Treatment of Prostatic Cancer". Journal of Medicinal Chemistry. 38 (13): 2463–2471. doi:10.1021/jm00013a022. ISSN 0022-2623. PMID 7608911.
  9. ^ a b c d e f g "Abiraterone Acetate Monograph for Professionals". Drugs.com. Archived from the original on 6 May 2012. Retrieved 15 November 2019.
  10. ^ "WHOCC - ATC/DDD Index". www.whocc.no. Archived from the original on 1 July 2021. Retrieved 10 September 2020.
  11. ^ Scowcroft H (21 September 2011). "Where did abiraterone come from?". Cancer Research UK. Archived from the original on 25 September 2011. Retrieved 28 September 2011.
  12. ^ World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  13. ^ British national formulary : BNF 76 (76 ed.). Pharmaceutical Press. 2018. p. 921. ISBN 9780857113382.
  14. ^ "Abiraterone Prices, Coupons & Patient Assistance Programs". Drugs.com. Archived from the original on 9 October 2019. Retrieved 15 November 2019.
  15. ^ "Abiraterone". Drugs.com. Archived from the original on 30 November 2014. Retrieved 14 April 2018.
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