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Alfatradiol
Medication
Medication
| Field | Value | ||
|---|---|---|---|
| Watchedfields | changed | ||
| verifiedrevid | 458276229 | ||
| IUPAC_name | (8R,9S,13S,14S,17R)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,17-diol | ||
| image | Alfatradiol skeletal.svg | ||
| image_class | skin-invert-image | ||
| alt | Skeletal formula of alfatradiol | ||
| width | 225px | ||
| image2 | Alfatradiol 3D ball.png | ||
| image_class2 | bg-transparent | ||
| alt2 | Ball-and-stick model of the alfatradiol molecule | ||
| width2 | 225px | ||
| tradename | Avicis, Avixis, Ell-Cranell Alpha, Pantostin | ||
| Drugs.com | |||
| pregnancy_AU | |||
| pregnancy_US | C | ||
| pregnancy_category | No studies | ||
| legal_AU | |||
| legal_CA | |||
| legal_UK | |||
| legal_US | Rx-only | ||
| routes_of_administration | Topical | ||
| class | Estrogen; 5α-Reductase inhibitor | ||
| CAS_number_Ref | |||
| CAS_number | 57-91-0 | ||
| ATC_prefix | None | ||
| ChEMBL_Ref | |||
| ChEMBL | 286452 | ||
| ChEBI_Ref | |||
| ChEBI | 17160 | ||
| PubChem | 68570 | ||
| ChemSpiderID_Ref | |||
| ChemSpiderID | 61840 | ||
| UNII_Ref | |||
| UNII | 3VQ38D63M7 | ||
| synonyms | 17α-Estradiol; 17-Epiestradiol; MX-4509; Estra-1,3,5(10)-triene-3,17α-diol; β-Estradiol (obsolete, misleading) | ||
| C | 18 | H=24 | O=2 |
| SMILES | OC1CCC3C1(C)CCC(c2cc4)C3CCc2cc4O | ||
| StdInChI_Ref | |||
| StdInChI | 1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17-,18+/m1/s1 | ||
| StdInChIKey_Ref | |||
| StdInChIKey | VOXZDWNPVJITMN-SFFUCWETSA-N |
17α-estradiol as a medication
| Drugs.com =
| elimination_half-life =
Alfatradiol, also known as 17α-estradiol and sold under the brand names Avicis, Avixis, Ell-Cranell Alpha, and Pantostin, is a weak estrogen and 5α-reductase inhibitor medication which is used topically in the treatment of pattern hair loss (androgenic alopecia or pattern baldness) in men and women. It is a stereoisomer of the endogenous steroid hormone and estrogen 17β-estradiol (or simply estradiol).
Medical uses
Alfatradiol is used in form of an ethanolic solution for topical application on the scalp. Similarly to other drugs against alopecia, topical or oral, it has to be applied continuously to prevent further hair loss. Regrowth of hair that was already lost is only possible to a limited extent. In general, advanced alopecia does not respond well to medical treatment, which has historically been thought to be a consequence of the hair roots being lost.
A university-led study (including several authors who are advisors to companies such as Pfizer) in 103 women comparing alfatradiol to minoxidil, another topical hair loss treatment, found the latter to be more effective. In contrast to minoxidil, alfatradiol did not result in an increase of hair density or thickness, but only in slowing down or stabilization of hair loss in this study. In an earlier study, no systemic side effects were noted, and 17α-estradiol was found to reduce androgenic hair loss, though it was not effective at growing new hair.
Other efforts of alfatradiol had been directed at neurodegenerative diseases including Parkinson's.
Other hair loss medications include ketoconazole, finasteride, and dutasteride.
Contraindications
Nothing is known about the use of alfatradiol during pregnancy or lactation, or in patients under 18 years of age. The package leaflet recommends against using it under these circumstances.
Side effects
Local burning or itching is not an effect of alfatradiol, but of the ethanol in the solvent. The solution can stimulate sebum production.
Pharmacology
Pharmacodynamics
Alfatradiol (17α-estradiol) is distinguished from estradiol (17β-estradiol), the predominant sex hormone in females, only by the stereochemistry of the carbon atom 17. In contrast to 17β-estradiol, 17α-estradiol, while it still binds to the estrogen receptor, has less or no feminizing estrogenic activity depending on its dosage and the tissue it is affecting. Alfatradiol acts as an inhibitor of the enzyme 5α-reductase, which is responsible for the activation of testosterone to dihydrotestosterone, and which plays a role in regulating hair growth. 17α-Estradiol has been studied as a therapeutic with potential to treat Alzheimer's and Parkinson's disease and other patients with neurodegenerative diseases. 17α-Estradiol (as the sodium salt of its sulfated form) is a minor component (
Alfatradiol binds to the ERα and ERβ with 58% and 11% of the relative binding affinity of 17β-estradiol. However, it has 100-fold lower estrogenic activity relative to estradiol. On the other hand, alfatradiol has been found to bind to and activate the brain-expressed ER-X with a greater potency than estradiol, indicating that it may be the predominant endogenous ligand for the receptor. In contrast to estradiol, alfatradiol is not a ligand of the G protein-coupled estrogen receptor (affinity 10 μM).
Society and culture
Generic names
Alfatradiol is the generic name of the drug and its . It is also known as 17α-estradiol.
Brand names
Alfatradiol is marketed under the brand names Avicis, Avixis, Ell-Cranell Alpha, and Pantostin.
Availability
Alfatradiol is available in Germany and several Latin American countries, including Argentina, Brazil, and Mexico.
Research
Alfatradiol administered systemically improved metabolic function, reduced insulin resistance, decreased intra-abdominal fat, and decreased inflammation in old male mice without inducing feminization, suggesting potential usefulness in the treatment of type 2 diabetes.
References
References
- J. Elks. (14 November 2014). "The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies". Springer.
- "Alfatradiol". Drugs.com International.
- (May 2007). "Comparison of the efficacy and safety of topical minoxidil and topical alfatradiol in the treatment of androgenetic alopecia in women". Journal der Deutschen Dermatologischen Gesellschaft.
- (1980). "[Local therapy of androgenetic alopecia with 17 alpha-estradiol. A controlled, randomized double-blind study (author's transl)]". Dermatologica.
- "Alfatradiol". Adis Insight.
- (2008). "17α-Estradiol: A Less-Feminizing Estrogen". Drug Development Research.
- (June 2005). "Development of 17alpha-estradiol as a neuroprotective therapeutic agent: rationale and results from a phase I clinical study". Annals of the New York Academy of Sciences.
- (2009). "Review of the Effects of 17α-Estradiol in Humans: A Less Feminizing Estrogen with Neuroprotective Potential". Drug Development Research.
- (March 1997). "Comparison of the ligand binding specificity and transcript tissue distribution of estrogen receptors alpha and beta". Endocrinology.
- (13 February 2014). "Male Alopecia: Guide to Successful Management". Springer Science & Business Media.
- (September 2005). "17alpha-estradiol: a brain-active estrogen?". Endocrinology.
- (July 2015). "International Union of Basic and Clinical Pharmacology. XCVII. G Protein-Coupled Estrogen Receptor and Its Pharmacologic Modulators". Pharmacol. Rev..
- (January 2017). "17α-Estradiol Alleviates Age-related Metabolic and Inflammatory Dysfunction in Male Mice Without Inducing Feminization". The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences.
- (2001). "Recommended International Nonproprietary Names (rec. Inn): List 46". WHO Drug Information.
- (2005). "Rote Liste". Editio Cantor Verlag.
- (2007). "Austria-Codex". Österreichischer Apothekerverlag.
- (1998). "Hunnius Pharmazeutisches Wörterbuch". Walter de Gruyter Verlag.
- (2001). "Arzneimittelwirkungen". Wissenschaftliche Verlagsgesellschaft.
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