| Systematic (IUPAC) name | |
|---|---|
| 19-Nor-17α-pregna-1,3,5(10)-trien-20-yne-3,17-diol | |
| Clinical data | |
| AHFS/Drugs.com | International Drug Names |
| MedlinePlus | a604032 |
| Pregnancy cat. | X (USA) |
| Legal status | Rx-only (U.S.) |
| Routes | Oral, transdermal |
| Pharmacokinetic data | |
| Bioavailability | 97% is bound |
| Metabolism | Liver |
| Half-life | 36±13 hours |
| Excretion | Feces and Urine |
| Identifiers | |
| CAS number | 57-63-6 |
| ATC code | G03CA01 L02AA03 |
| PubChem | CID 5991 |
| DrugBank | APRD00691 |
| ChemSpider | 5770 |
| UNII | 423D2T571U |
| KEGG | D00554 |
| ChEBI | CHEBI:4903 |
| ChEMBL | CHEMBL1078384 |
| Chemical data | |
| Formula | C20H24O2 |
| Mol. mass | 296.403 |
| SMILES | eMolecules & PubChem |
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Ethynylestradiol ( /ˌɛθɨnɨlˌiːstrəˈdaɪ.əl/), also ethynyl estradiol (EE), is a derivative of estradiol. Ethynyl estradiol is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills. It is one of the most commonly used medications.
The same contraindications and precautions apply for EE as with other estrogen medications.
Estinyl was a preparation of EE alone that was used for the management of menopausal symptoms and female hypogonadism.[1]
EE is released into the environment as a xenoestrogen from the urine and feces of people who take it as a medication.
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The first orally active semisynthetic steroidal estrogen, ethinylestradiol (17α-ethynylestradiol), the 17α-ethynyl analog of estradiol, was synthesized in 1938 by Hans Herloff Inhoffen and Walter Hohlweg at Schering AG in Berlin.[2][3][4][5][6]
Ethinyl estradiol was approved by the FDA in the U.S. on June 25, 1943 and marketed by Schering as Estinyl.[7] The FDA withdrew approval of Estinyl effective June 4, 2004 at the request of Schering, who had discontinued marketing Estinyl.[8]
While estradiol is readily absorbed when taken orally, it is also quickly inactivated by the liver. Substitution at C17 of the estrane steroid with an ethinyl group proved to provide an estrogen that is much more resistant to degradation and paved the way for the development of oral contraceptives.
EE is absorbed in the small intestine and reaches a serum peak about 2 hours later. It undergoes extensive metabolism in the liver involving the cytochrome P450 3A4 isoenzyme. EE and its metabolites are excreted with the bile. Due to the effect of enterohepatic circulation a second peak is seen several hours later. Individually, wide variations exist in the overall absorption process, and can be further modified by drugs (i.e. antibiotics) that affect the enterohepatic circulation or liver enzymes. In circulation EE is almost fully bound to plasma albumin. It is metabolized by hydroxylation of the aromatic ring and excreted in both feces and urine, in part as glucuronide and sulfate conjugate.
EE is hormonally effective by activating the estrogen receptor and thus is an estrogen. It finds its most common use in the estrogen-progestin combination preparations of oral contraceptives. Over time, formulations have decreased the EE dose from as high as 100 μg to as low as 10 μg in LoLoestrin Fe.[9]
Depends on needs and age, see Consumer Information for more information.
Ethinylestradiol is prepared from estron in one step by ethinylation with ethine, sodium and sodium amide.[10]
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