亮丙瑞林(Leuprorelin、leuprolide),商品名柳菩林(Lupron),[10]是一种人工合成的激素,用于治疗前列腺癌乳癌子宮內膜異位症子宮肌瘤性早熟英语Precocious puberty[10] [11]。可以肌肉皮下注射[10]

亮丙瑞林
臨床資料
商品名英语Drug nomenclatureLupron, Eligard, Lucrin, Lupaneta, others
其他名稱leuprolide, leuprolidine, A-43818, Abbott-43818, DC-2-269, TAP-144
AHFS/Drugs.comMonograph
MedlinePlusa685040
核准狀況
懷孕分級
  • : D
给药途径植入物皮下注射肌肉注射
藥物類別英语Drug class促性腺素釋素相似劑英语GnRH analogue; 促性腺素釋素刺激劑英语GnRH agonist; 抗促性腺素英语Antigonadotropin
ATC碼
法律規範狀態
法律規範
藥物動力學數據
生物半衰期3小時
排泄途徑
识别信息
  • N-[1-[[1-[[1-[[1-[[1-[[1-[[5-(diaminomethylideneamino)-1-
    [2-(ethylcarbamoyl)pyrrolidin-1-yl]-1-oxo-pentan-2-
    yl]carbamoyl]-3-methyl-butyl]carbamoyl]-3-methyl-
    butyl]carbamoyl]-2-(4-hydroxyphenyl)ethyl]
    carbamoyl]-2-hydroxy-ethyl]carbamoyl]-2-(1H-indol-3-
    yl)ethyl]carbamoyl]-2-(3H-imidazol-4-yl)ethyl]-5-oxo-
    pyrrolidine-2-carboxamide
CAS号53714-56-0
74381-53-6 (乙酸盐))  checkY
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard英语CompTox Chemicals Dashboard (EPA)
ECHA InfoCard100.161.466 編輯維基數據鏈接
化学信息
化学式C59H84N16O12
摩尔质量1,209.42 g·mol−1
3D模型(JSmol英语JSmol
  • CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CC(C)C)NC(=O)[C@H](Cc2ccc(cc2)O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc3c[nH]c4c3cccc4)NC(=O)[C@H](Cc5c[nH]cn5)NC(=O)[C@@H]6CCC(=O)N6
  • InChI=1S/C59H84N16O12/c1-6-63-57(86)48-14-10-22-75(48)58(87)41(13-9-21-64-59(60)61)68-51(80)42(23-32(2)3)69-52(81)43(24-33(4)5)70-53(82)44(25-34-15-17-37(77)18-16-34)71-56(85)47(30-76)74-54(83)45(26-35-28-65-39-12-8-7-11-38(35)39)72-55(84)46(27-36-29-62-31-66-36)73-50(79)40-19-20-49(78)67-40/h7-8,11-12,15-18,28-29,31-33,40-48,65,76-77H,6,9-10,13-14,19-27,30H2,1-5H3,(H,62,66)(H,63,86)(H,67,78)(H,68,80)(H,69,81)(H,70,82)(H,71,85)(H,72,84)(H,73,79)(H,74,83)(H4,60,61,64)/t40-,41-,42-,43 ,44-,45-,46-,47-,48-/m0/s1 ☒N
  • Key:GFIJNRVAKGFPGQ-LIJARHBVSA-N ☒N

常见副作用包括潮熱、情绪不稳定、失眠頭痛和注射部位疼痛[10]。其他副作用包括可能高血糖过敏腦下垂體中風英语Pituitary apoplexy[10]怀孕期使用可能会伤害婴儿[10]。它属于促性腺素釋素調節劑英语Gonadotropin-releasing hormone modulator家族, [10]可降低促性腺激素,而降低睾酮雌二醇[10]

亮丙瑞林于 1973 年获得专利,于 1985 年取得美国的醫療使用許可[10] [12]。名列世界卫生组织基本药物清单[13]

参考文獻

编辑
  1. ^ ELIGARD (Mundipharma Pty Ltd) Department of Health and Aged Care. Retrieved 30 March 2023
  2. ^ Product monograph brand safety updates. Health Canada. February 2024 [24 March 2024]. 
  3. ^ Regulatory Decision Summary for Eligard. Drug and Health Products Portal. 21 September 2023 [2 April 2024]. 
  4. ^ Lupron- leuprolide acetate lupron- leuprolide acetate injection, solution. DailyMed. [27 May 2021]. (原始内容存档于27 May 2021). 
  5. ^ Eligard- leuprolide acetate kit. DailyMed. 26 March 2020 [20 August 2020]. (原始内容存档于10 August 2020). 
  6. ^ Fensolvi- leuprolide acetate kit. DailyMed. 3 June 2020 [20 August 2020]. (原始内容存档于26 October 2020). 
  7. ^ Viadur- leuprolide acetate. DailyMed. [26 May 2021]. (原始内容存档于27 May 2021). 
  8. ^ Lupron Depot- leuprolide acetate kit. DailyMed. [27 May 2021]. (原始内容存档于27 May 2021). 
  9. ^ Camcevi EPAR. European Medicines Agency (EMA). 22 March 2022 [21 June 2022]. 
  10. ^ 10.0 10.1 10.2 10.3 10.4 10.5 10.6 10.7 10.8 Leuprolide Acetate. The American Society of Health-System Pharmacists. [8 December 2016]. (原始内容存档于23 December 2016). "Leuprolide Acetate". The American Society of Health-System Pharmacists. Archived from the original on 23 December 2016. Retrieved 8 December 2016.
  11. ^ 19th WHO Model List of Essential Medicines (April 2015) (PDF). WHO. April 2015 [May 10, 2015]. (原始内容存档 (PDF)于May 13, 2015). 
  12. ^ Fischer, Jnos; Ganellin, C. Robin. Analogue-based Drug Discovery. John Wiley & Sons. 2006: 514 [2019-03-02]. ISBN 9783527607495. (原始内容存档于2019-03-06) (英语). 
  13. ^ World Health Organization. World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. 2019. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO. 

延伸閱讀

编辑
  • Shajnfeld A, Krueger RB. Reforming (Purportedly) Non-Punitive Responses to Sexual Offending. Developments in Mental Health Law. July 2006, 25: 81. SSRN 1077282 .