达那唑
临床资料 | |
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商品名 | Danatrol, Danocrine, Danol, Danoval, others |
其他名称 | WIN-17757; 2,3-Isoxazolethisterone; 2,3-Isoxazol-17α-ethynyltestosterone; 17α-Ethynyl-17β-hydroxyandrost-4-en-[2,3-d]isoxazole |
AHFS/Drugs.com | Monograph |
MedlinePlus | a682599 |
怀孕分级 |
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给药途径 | 口服给药 |
药物类别 | 雄激素、同化类固醇、黄体制剂、孕激素、抗促性腺激素、固醇类合成抑制剂、抗动情素药物 |
ATC码 | |
法律规范状态 | |
法律规范 |
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药物动力学数据 | |
生物利用度 | Saturable with dosage, higher with food intake[1] |
血浆蛋白结合率 | 会与白蛋白、SHBG, CBG结合[2][3][4] |
药物代谢 | 肝脏(CYP3A4)[8][5][9][1][6] |
代谢产物 | • 2-OHM-Ethisterone[5] • Ethisterone[6][7] |
生物半衰期 | Acute: 3–10 hours[8][1] Chronic: 24–26 hours[8] |
排泄途径 | 尿、粪便[8][1] |
识别信息 | |
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CAS号 | 17230-88-5 |
PubChem CID | |
IUPHAR/BPS | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.037.503 |
化学信息 | |
化学式 | C22H27NO2 |
摩尔质量 | 337.463 g/mol |
3D模型(JSmol) | |
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达那唑(Danazol)为一种用于治疗子宫内膜异位症、乳腺小叶增生、遗传性血管性水肿及其他疾病的药物[8][1][10][11][12],主要经口服给药[1]。
达那唑具有雄性化的副作用,使其用途大受限制。常见不良反应包含痤疮、多毛症,以及声音变低沉[1][13]。达那唑的作用机转复杂,同时具有弱雄激素、弱同化类固醇、弱孕激素,弱抗促性腺激素、弱固醇类合成抑制剂,以及功能性抗动情素药物[4][9][14][9][14][15]。
达那唑发现于1963年,并于1971年应用于医学[9][16][17][18]。随著副作用更少的性腺激素释放素类似物应用逐渐广泛,达那唑在治疗子宫内膜异位症的角色已被前者所取代[3]。
参考文献
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- ^ 3.0 3.1 Eberhard Nieschlag; Hermann M. Behre; Susan Nieschlag. Andrology: Male Reproductive Health and Dysfunction. Springer Science & Business Media. 13 January 2010: 426–428. ISBN 978-3-540-78355-8.
- ^ 4.0 4.1 Eric J. Thomas; John Rock. Modern Approaches to Endometriosis. Springer Science & Business Media. 6 December 2012: 239–256 [2019-10-09]. ISBN 978-94-011-3864-2. (原始内容存档于2020-01-10).
- ^ 5.0 5.1 Thomas L. Lemke; David A. Williams. Foye's Principles of Medicinal Chemistry. Lippincott Williams & Wilkins. 24 January 2012: 1361– [2019-10-09]. ISBN 978-1-60913-345-0. (原始内容存档于2020-01-10).
- ^ 6.0 6.1 Florencio Zaragoza Dörwald. Lead Optimization for Medicinal Chemists: Pharmacokinetic Properties of Functional Groups and Organic Compounds. John Wiley & Sons. 4 February 2013: 485– [2019-10-09]. ISBN 978-3-527-64565-7. (原始内容存档于2020-01-09).
- ^ Robert J. Kurman. Blaustein's Pathology of the Female Genital Tract. Springer Science & Business Media. 17 April 2013: 390– [2019-10-09]. ISBN 978-1-4757-3889-6. (原始内容存档于2020-01-10).
- ^ 8.0 8.1 8.2 8.3 8.4 Brayfield, A (编). Danazol. Martindale: The Complete Drug Reference. Pharmaceutical Press. 30 October 2013 [1 April 2014]. (原始内容存档于2021-08-28).
- ^ 9.0 9.1 9.2 9.3 Howard W. Jones; John A. Rock. Te Linde's Operative Gynecology. Wolters Kluwer Health. 10 July 2015: 1327–1330 [2019-10-09]. ISBN 978-1-4963-1521-2. (原始内容存档于2020-01-10). 引用错误:带有name属性“JonesRock2015”的
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- ^ 14.0 14.1 Aurel Lupulescu. Hormones and Vitamins in Cancer Treatment. CRC Press. 24 October 1990: 103– [2019-10-09]. ISBN 978-0-8493-5973-6. (原始内容存档于2020-01-10).
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- ^ G.P. Ellis and G.B. Ellis, doi:10.1016/S0079-6468(08)70187-5 (1979), pp. 126, note 158, 130, notes 1513, 2369, citing doi:10.1021/jm00299a034
- ^ Alan N. Elias; Grant Gwinup. Hirsutism. Praeger. 1 January 1983: 70 [2019-10-09]. (原始内容存档于2017-03-28).
- ^ Dmowski WP, Scholer HF, Mahesh VB, Greenblatt RB. Danazol--a synthetic steroid derivative with interesting physiologic properties. Fertil. Steril. 1971, 22 (1): 9–18. PMID 5538758. doi:10.1016/S0015-0282(16)37981-X.
延伸阅读
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- Jenkin G. Review: The mechanism of action of danazol, a novel steroid derivative. Aust N Z J Obstet Gynaecol. May 1980, 20 (2): 113–8. PMID 6998453. doi:10.1111/j.1479-828X.1980.tb00107.x.
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- Beaumont H, Augood C, Duckitt K, Lethaby A. Danazol for heavy menstrual bleeding. Cochrane Database Syst Rev. July 2007, (3): CD001017. PMID 17636649. doi:10.1002/14651858.CD001017.pub2.
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