| 词条 | Oxendolone |
| 释义 |
| Verifiedfields = | Watchedfields = | verifiedrevid = | IUPAC_name = (9S,14S,17S)-16-ethyl-17-hydroxy-13-methyl-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-one | image = Oxendolone.svg | width = 225px | tradename = Prostetin, Roxenone | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = Intramuscular injection[1][2][3][4] | class = Steroidal antiandrogen; Progestin; Progestogen | bioavailability = Oral: Very low (1% in dogs)[5] | protein_bound = | metabolism = | elimination_half-life = {{abbrlink|IM|Intramuscular injection}}: 5.0–6.6 days.[4][1] | excretion = | CAS_number_Ref = | CAS_number = 33765-68-3 | CAS_supplemental = | ATC_prefix = | ATC_suffix = | PubChem = 36592 | DrugBank_Ref = | DrugBank = | ChemSpiderID_Ref = | ChemSpiderID = 392001 | synonyms = TSAA-291; 16β-Ethyl-19-nortestosterone; 16β-Ethylestr-4-en-17β-ol-3-one | C=20 | H=30 | O=2 | molecular_weight = 302.451 g/mol | SMILES = CCC1CC2C3CCC4=CC(=O)CCC4C3CCC2(C1O)C | StdInChI_Ref = | StdInChI = 1S/C20H30O2/c1-3-12-11-18-17-6-4-13-10-14(21)5-7-15(13)16(17)8-9-20(18,2)19(12)22/h10,12,15-19,22H,3-9,11H2,1-2H3/t12?,15?,16-,17?,18+,19+,20?/m1/s1 | StdInChIKey_Ref = | StdInChIKey = FCKLFGKATYPJPG-LNRSQMQGSA-N }}Oxendolone, sold under the brand names Prostetin and Roxenone, is an antiandrogen and progestin medication which is used in Japan in the treatment of enlarged prostate.[2][3][4][5][6] However, this use is controversial due to concerns about its clinical efficacy.[6] Oxendolone is not effective by mouth and must be given by injection into muscle.[5][1][2][3][4] Oxendolone is an antiandrogen, and hence is an antagonist of the androgen receptor, the biological target of androgens like testosterone and dihydrotestosterone.[19][20][21][22][1] It is also a progestin, or a synthetic progestogen, and hence is an agonist of the progesterone receptor, the biological target of progestogens like progesterone.[19][20][21][22] Due to its progestogenic activity, oxendolone has antigonadotropic effects.[28][29] Oxendolone has no other important hormonal activity. Oxendolone was introduced for medical use in 1981.[3] It is used only in Japan.[3][6] Medical usesOxendolone is used in the treatment of benign prostatic hyperplasia (BPH) in Japan.[3][6] It has been used at a dosage of 200 mg once every 2 weeks via intramuscular injection.[7] Although it is approved for the treatment of BPH in Japan, concerns have been raised about its use for this condition due to poor efficacy seen in clinical trials.[6] Side effects{{See also|Antiandrogen#Side effects|Progestin#Side effects}}PharmacologyPharmacodynamicsOxendolone binds to the androgen receptor (Ki = 320 nM) and progesterone receptor (Ki = 20 nM) and acts as a weak but clinically relevant inhibitor of 5α-reductase ({{abbrlink|IC50|half-maximal inhibitory concentration}} = 1.4 μM).[8][9][10][11] The relative binding affinity of oxendolone for the androgen receptor is 0.8 to 3.6% of that of metribolone.[12][13] Oxendolone is not a silent antagonist of the androgen receptor but is rather predominantly antagonistic with weak agonistic activity;[9] for this reason, it has been described as a selective androgen receptor modulator.[14] The medication has potent antigonadotropic effects via its progestogenic activity.[15] It has been found to suppress luteinizing hormone and testosterone levels to an equivalent extent as allylestrenol and chlormadinone acetate, which are two progestins that are similarly used at high doses to treat BPH.[7] PharmacokineticsThe oral bioavailability of oxendolone in dogs is extremely low, 1% at most.[16] Due to its low oral bioavailability, oxendolone is administered by intramuscular injection in humans.[17][18][19][20] Its elimination half-life via this route is 5.0 to 6.6 days.[20] Chemistry{{See also|List of progestogens|Steroidal antiandrogen|List of steroidal antiandrogens}}Oxendolone, also known as 16β-ethyl-19-nortestosterone or 16β-ethylestr-4-en-17β-ol-3-one, is a synthetic estrane steroid and a derivative of testosterone and 19-nortestosterone (nandrolone).[2][3] The acetate ester of oxendolone is known as TSAA-328, while the caproate ester of oxendolone is known as TSAA-330.[21] They were never marketed.[21] HistoryOxendolone has been marketed in Japan by Takeda since 1981.[3] Society and cultureGeneric namesOxendolone is the generic name of the drug and its {{abbrlink|INN|International Nonproprietary Name}}, {{abbrlink|USAN|United States Adopted Name}}, and {{abbrlink|JAN|Japanese Accepted Name}}.[2][22] It is also known by its developmental code name TSAA-291.[2][22]Brand namesOxendolone is or has been sold under the brand names Prostetin and Roxenone.[2][22] AvailabilityOxendolone is marketed only in Japan.[22] References1. ^1 {{cite journal|last1=Gao|first1=Wenqing|last2=Bohl|first2=Casey E.|last3=Dalton|first3=James T.|title=Chemistry and Structural Biology of Androgen Receptor|journal=Chemical Reviews|volume=105|issue=9|year=2005|pages=3352–3370|issn=0009-2665|doi=10.1021/cr020456u|pmid=16159155|pmc=2096617}} {{Navboxes2. ^1 2 3 4 {{cite book|author=J. Elks|title=The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies|url=https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA914|date=14 November 2014|publisher=Springer|isbn=978-1-4757-2085-3|pages=914–}} 3. ^1 2 3 4 5 {{cite book|author=William Andrew Publishing|title=Pharmaceutical Manufacturing Encyclopedia, 3rd Edition|url=https://books.google.com/books?id=_J2ti4EkYpkC&pg=PA2935-IA129|date=22 October 2013|publisher=Elsevier|isbn=978-0-8155-1856-3|pages=2935–}} 4. ^{{cite book|author1=Martin Negwer|author2=Hans-Georg Scharnow|title=Organic-chemical drugs and their synonyms: (an international survey)|url=https://books.google.com/books?id=zmpqAAAAMAAJ|year=2001|publisher=Wiley-VCH|isbn=978-3-527-30247-5|page=2023}} 5. ^{{cite journal|last1=Tan|first1=MH Eileen|last2=Li|first2=Jun|last3=Xu|first3=H Eric|last4=Melcher|first4=Karsten|last5=Yong|first5=Eu-leong|title=Androgen receptor: structure, role in prostate cancer and drug discovery|journal=Acta Pharmacologica Sinica|volume=36|issue=1|year=2014|pages=3–23|issn=1671-4083|doi=10.1038/aps.2014.18|pmid=24909511|pmc=4571323}} 6. ^1 2 3 4 {{cite journal|last1=Ishizuka|first1=Osamu|last2=Nishizawa|first2=Osamu|last3=Hirao|first3=Yoshihiko|last4=Ohshima|first4=Shinichi|title=Evidence-based meta-analysis of pharmacotherapy for benign prostatic hypertrophy|journal=International Journal of Urology|volume=9|issue=11|year=2002|pages=607–612|issn=0919-8172|doi=10.1046/j.1442-2042.2002.00539.x|pmid=12534901}} 7. ^1 2 {{cite journal | vauthors = Katayama T, Umeda K, Kazama T | title = [Hormonal environment and antiandrogenic treatment in benign prostatic hypertrophy] | language = Japanese | journal = Hinyokika Kiyo | volume = 32 | issue = 11 | pages = 1584–9 | date = November 1986 | pmid = 2435122 | doi = | url = }} 8. ^1 2 {{cite book|title=Annual Reports in Medicinal Chemistry|url=https://books.google.com/books?id=HrALiG-4t7UC&pg=PA199|date=8 September 1989|publisher=Academic Press|isbn=978-0-08-058368-6|pages=199–}} 9. ^1 2 3 {{cite book|title=Annual report of Shionogi Research Laboratories|url=https://books.google.com/books?id=kR40AAAAIAAJ|year=1991|pages=76–77}} 10. ^1 2 {{cite journal|last1=Kirby|first1=RogerS.|last2=Christmas|first2=Timothy|title=The potential value of 5-alpha-reductase inhibition in the treatment of bladder outflow obstruction due to benign prostatic hyperplasia|journal=World Journal of Urology|volume=9|issue=1|year=1991|issn=0724-4983|doi=10.1007/BF00184713}} 11. ^1 2 {{cite journal|last1=Bashirelahi|first1=N.|last2=Ganesan|first2=S.|last3=Ekiko|first3=D.B.|last4=Young|first4=J.D.|last5=Shida|first5=K.|last6=Yamanaka|first6=H.|last7=Takahashi|first7=E.|title=Effect of 16β-ethyl-17β-hydroxy-4-estren-3-one (tsaa-291) on the binding of promegestone (r5020) and methyltrienolone (r1881) to hyperplastic and neoplastic human prostate|journal=Journal of Steroid Biochemistry|volume=25|issue=3|year=1986|pages=367–374|issn=0022-4731|doi=10.1016/0022-4731(86)90249-9}} 12. ^{{cite journal|last1=Dalton|first1=James T.|last2=Gao|first2=Wenqing|title=Androgen Receptor|year=2010|pages=143–182|doi=10.1007/978-90-481-3303-1_6}} 13. ^{{cite journal | vauthors = Wakeling AE, Furr BJ, Glen AT, Hughes LR | title = Receptor binding and biological activity of steroidal and nonsteroidal antiandrogens | journal = J. Steroid Biochem. | volume = 15 | issue = | pages = 355–9 | date = December 1981 | pmid = 7339263 | doi = 10.1016/0022-4731(81)90297-1 | url = }} 14. ^{{cite journal|last1=Hikichi|first1=Yukiko|last2=Yamaoka|first2=Masuo|last3=Kusaka|first3=Masami|last4=Hara|first4=Takahito|title=Selective androgen receptor modulator activity of a steroidal antiandrogen TSAA-291 and its cofactor recruitment profile|journal=European Journal of Pharmacology|volume=765|year=2015|pages=322–331|issn=0014-2999|doi=10.1016/j.ejphar.2015.08.052|pmid=26335395}} 15. ^1 {{cite journal|last1=Sudo|first1=K.|last2=Yamazaki|first2=I.|last3=Masuoka|first3=M.|last4=Nakayama|first4=R.|title=IV. EFFECTS OF THE ANTI-ANDROGEN TSAA-291 (16 -ETHYL-17 -HYDROXY-4-OESTREN-3-ONE) ON THE SECRETION OF GONADOTROPHINS|journal=European Journal of Endocrinology|volume=92|issue=3 Supplb|year=1979|pages=S53–S66|issn=0804-4643|doi=10.1530/acta.0.092S053}} 16. ^1 2 {{cite book|author1=Michael J. Rathbone|author2=Jonathan Hadgraft|author3=Michael S. Roberts|title=Modified-Release Drug Delivery Technology|url=https://books.google.com/books?id=mw9W82MLYZ8C&pg=PA368|date=7 November 2002|publisher=CRC Press|isbn=978-0-8247-0869-6|pages=368–}} 17. ^1 2 {{cite journal | vauthors = Henkler G, Klotzbach M, Koch H, Müller W, Richter J | title = [Progress in the area of drug development. 15] | language = German | journal = Pharmazie | volume = 37 | issue = 11 | pages = 753–65 | year = 1982 | pmid = 6131442 | doi = | url = | quote = [Oxendolone] has been clinically tested in Japan (weekly intramuscular injection of 200-400 mg) in prostatic hypertrophy.}} 18. ^1 2 {{cite journal | vauthors = Hikichi Y, Yamaoka M, Kusaka M, Hara T | title = Selective androgen receptor modulator activity of a steroidal antiandrogen TSAA-291 and its cofactor recruitment profile | journal = Eur. J. Pharmacol. | volume = 765 | issue = | pages = 322–31 | year = 2015 | pmid = 26335395 | doi = 10.1016/j.ejphar.2015.08.052 | url = | quote = According to the clinical data of TSAA-291, the plasma level of TSAA-291 after weekly intramuscular administration at 400 mg/kg for 12 weeks is approximately 100 nM (Drug Information).}} 19. ^1 2 {{cite journal | vauthors = Ostri P, Swartz R, Meyhoff HH, Petersen JH, Lindgård G, Frimodt-Møller C, Andersson T, Nielsen MS | title = Antiandrogenic treatment of benign prostatic hyperplasia: a placebo controlled trial | journal = Urol. Res. | volume = 17 | issue = 1 | pages = 29–33 | year = 1989 | pmid = 2466359 | doi = 10.1007/bf00261046| url = | quote = Thirty patients were treated with weekly injections of oxendolone 200 mg during a 3 months' period, and 30 patients were allocated to placebo treatment.}} 20. ^1 2 3 4 {{cite journal | vauthors = Midgley I, Fowkes AG, Darragh A, Lambe R, Chasseaud LF, Taylor T | title = The metabolic fate of the anti-androgenic agent, oxendolone, in man | journal = Steroids | volume = 41 | issue = 4 | pages = 521–36 | year = 1983 | pmid = 6419414 | doi = 10.1016/0039-128x(83)90092-2| url = | quote = After intramuscular administration of 16β-ethyl-17β-hydroxy-4-[4-14C] estren-3-one (14C-oxendolone; 300 mg) to 3 human subjects, [...]}} 21. ^1 {{cite journal | vauthors = Masuoka M, Masaki T, Yamazaki I, Hori T, Nakayama R | title = Anti-androgen TSAA-291. III. Hormonal spectra of anti-androgen TSAA-291 (16 beta-ethyl-17 beta-hydroxy-4-oestren-3-one) and its derivatives | journal = Acta Endocrinol Suppl (Copenh) | volume = 229 | issue = | pages = 36–52 | year = 1979 | pmid = 294106 | doi = | url = }} 22. ^1 2 3 https://www.drugs.com/international/oxendolone.html | title = Medical uses | titlestyle = background:#ccccff | list1 ={{Androgens and antiandrogens}}{{Progestogens and antiprogestogens}}{{Drugs used in benign prostatic hypertrophy}} }}{{Navboxes | title = Pharmacodynamics | titlestyle = background:#ccccff | list1 ={{Androgen receptor modulators}}{{Progesterone receptor modulators}} }} 8 : 5α-Reductase inhibitors|Alcohols|Antigonadotropins|Drugs for benign prostatic hyperplasia|Estranes|Ketones|Progestogens|Steroidal antiandrogens |
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