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Fluoxymesterone

产品号 DB01185 公司名称 DrugBank
CAS号 76-43-7 公司网站 http://www.ualberta.ca/
分子式 C20H29FO3 电 话 (780) 492-3111
分子量 336.4408632 传 真
纯 度 电子邮件 david.wishart@ualberta.ca
保 存 Chembase数据库ID: 1056

产品价格信息

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产品别名

标题
Fluoxymesterone
IUPAC标准名
(1R,2S,10S,11S,14S,15S,17S)-1-fluoro-14,17-dihydroxy-2,14,15-trimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one
IUPAC传统名
fluoxymesterone
商标名
Flutestos
Oratestin
Fluosterone
Anadroid-F
Neo-Ormonal
Ora Testryl
Testoral
Ultandrene
Android-f
Androsterolo
Fluotestin
Flusteron
Halotestin
Ora-testryl
Oralsterone
Ultandren
别名
Androfluorone
Fluoximesteronum
Fluoxymesteronum [INN-Latin]
Fluossimesterone [DCIT]
Fluoximesterona [INN-Spanish]
Fluoximesterone
Fluoxymestrone
FXM
Androfluorene

产品登记号

PubChem SID 46508867
PubChem CID 6446
CAS号 76-43-7

产品性质

疏水性(logP) 2
溶解度 67.5 mg/L

产品详细信息

详细说明 (English)
Item Information
Drug Groups illicit; approved
Description An anabolic steroid that has been used in the treatment of male hypogonadism, delayed puberty in males, and in the treatment of breast neoplasms in women. [PubChem]
Indication In males, used as replacement therapy in conditions associated with symptoms of deficiency or absence of endogenous testosterone. In females, for palliation of androgenresponsive recurrent mammary cancer in women who are more than one year but less than five years postmenopausal.
Pharmacology Fluoxymesterone is a synthetic androgen, or male hormone, similar to testosterone. Fluoxymesterone works by attaching itself to androgen receptors; this causes it to interact with the parts of the cell involved in the making of proteins. It may cause an increase in the synthesis of some proteins or a decrease in the synthesis of others. These proteins have a variety of effects, including blocking the growth of some types of breast cancer cells, stimulating cells that cause male sexual characteristics, and stimulating the production of red blood cells.
Toxicity Side effects include virilization (masculine traits in women), acne, fluid retention, and hypercalcemia.
Affected Organisms
Humans and other mammals
Biotransformation Presence of 17-alpha alkyl group reduces susceptibility to hepatic enzyme degradation, which slows metabolism and allows oral administration. Inactivation of testosterone occurs primarily in the liver
Absorption Oral absorption is less than 44%.
Half Life 9.2 hours
Protein Binding Very high (99%) with 80% to sex hormone binding globulin, 19% to albumin.
References
Miner JN, Chang W, Chapman MS, Finn PD, Hong MH, Lopez FJ, Marschke KB, Rosen J, Schrader W, Turner R, van Oeveren A, Viveros H, Zhi L, Negro-Vilar A: An orally active selective androgen receptor modulator is efficacious on bone, muscle, and sex function with reduced impact on prostate. Endocrinology. 2007 Jan;148(1):363-73. Epub 2006 Oct 5. [Pubmed]
External Links
Wikipedia
RxList
Drugs.com

参考文献

  • Miner JN, Chang W, Chapman MS, Finn PD, Hong MH, Lopez FJ, Marschke KB, Rosen J, Schrader W, Turner R, van Oeveren A, Viveros H, Zhi L, Negro-Vilar A: An orally active selective androgen receptor modulator is efficacious on bone, muscle, and sex function with reduced impact on prostate. Endocrinology. 2007 Jan;148(1):363-73. Epub 2006 Oct 5. Pubmed