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Postion:Product Catalog >API>Hormones and the Endocrine System>Estrogen and progestin drugs>ethinyloestradiol;ethinyl estradiol;Ethinylestradiol
ethinyloestradiol;ethinyl estradiol;Ethinylestradiol
  • ethinyloestradiol;ethinyl estradiol;Ethinylestradiol
  • ethinyloestradiol;ethinyl estradiol;Ethinylestradiol
  • ethinyloestradiol;ethinyl estradiol;Ethinylestradiol
  • ethinyloestradiol;ethinyl estradiol;Ethinylestradiol
  • ethinyloestradiol;ethinyl estradiol;Ethinylestradiol

ethinyloestradiol;ethinyl estradiol;Ethinylestradiol

Price $2
Package 1KG
Min. Order: 1G
Supply Ability: 6000g/day
Update Time: 2018-09-26

Product Details

Product Name: ethinyloestradiol;ethinyl estradiol;Ethinylestradiol CAS No.: 57-63-6
Min. Order: 1G Purity: 98% ada@tuskwei.com sky;17197824028 whapp;+008617197824028
Supply Ability: 6000g/day Release date: 2018/09/26

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The images only for reference

Ethinylestradiol (EE) is an estrogen medication which is used widely in birth control pills in combination with progestins.[9] It is also occasionally used as a component of menopausal hormone therapy for the treatment of menopausal symptoms in combination with progestins.[9] In the past, EE was widely used alone for various indications such as the treatment of gynecological disorders and prostate cancer, but this is no longer the case. It is usually taken by mouth.[9]

The general side effects of EE include breast tenderness and enlargement, headache, fluid retention, and nausea among others.In men, EE can additionally cause breast development, feminization in general, hypogonadism, and sexual dysfunction. Rare but serious side effects include blood clots, liver damage, and cancer of the uterus.

EE is an estrogen, or an agonist of the estrogen receptors.It is a synthetic derivative of the natural estrogen estradiol, and differs from estradiol in various ways.Compared to estradiol, EE has greatly improved bioavailability when taken by mouth, is more resistant to metabolism, and shows relatively increased effects in certain parts of the body like the liver and uterus.These differences make EE more favorable for use in birth control pills than estradiol, though also result in an increased risk of blood clots and certain other rare adverse effects.

EE was developed in the 1930s and was introduced for medical use in 1943.The drug started being used in birth control pills in the 1960s.Today, EE is found in almost all combined forms of birth control pills and is nearly the exclusive estrogen used for this purpose, making it one of if not the most widely used estrogens.

Ethinylestradiol
Article illustration
Article illustration
Clinical data
Pronunciation /??θ?n?l?i?str??da?.?l/
Trade names Numerous
Synonyms 17α-Ethynylestradiol; 17α-Ethynylestra-1,3,5(10)-triene-3,17β-diol; NSC-10973
Pharmacokinetic data
Bioavailability 38–48%[3][4]
Protein binding 97–98% (to albumin;[5] is not bound to SHBG)[6]
Metabolism Liver (primarily CYP3A4)[2]
Biological half-life 7–36 hours[7][3][2][8]
Excretion Feces: 62%[7]
Urine: 38%[7]
Identifiers
IUPAC name[show]
CAS Number
  • 57-63-6 Article illustration
PubChem CID
  • 5991
IUPHAR/BPS
  • 7071
DrugBank
  • DB00977 Article illustration
ChemSpider
  • 5770 Article illustration
UNII
  • 423D2T571U
KEGG
  • D00554 Article illustration
ChEBI
  • CHEBI:4903 Article illustration
ChEMBL
  • CHEMBL691 Article illustration
ECHA InfoCard 100.000.311
Chemical and physical data
Formula C20H24O2
Molar mass 296.403 g/mol
 

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