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Testolactone
Chemical compound
Chemical compound
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Testolactone (, ) (brand name Teslac) is a non-selective, irreversible, steroidal aromatase inhibitor which is used as an antineoplastic drug to treat advanced-stage breast cancer. The drug was discontinued in 2008 and is no longer available for medical use.
Medical uses
Testolactone is mainly used for treating various types of breast cancer in women who have been through menopause or whose ovaries no longer function. It works by blocking the production of estrogens, which helps prevent the growth of breast cancers that are stimulated by estrogens. It may also prevent tumor cells from being activated by other hormones. In addition, it has been used in the treatment of gynecomastia.
Testolactone is used to treat breast cancer at a dosage of 250 mg four times per day by mouth or 100 mg three times per week by intramuscular injection.
Available forms
Testolactone has been provided in the form of 50 mg and 250 mg oral tablets.
Side effects
The most common side effects include:
-
Abnormal skin sensations
-
Aches of the legs and arms
-
General body discomfort
-
Hair loss
-
Loss of appetite
-
Nausea
-
Redness of the tongue
-
Vomiting
Rare but serious side effects include:
- Allergic reactions
- New breast lumps
- Bone pain
- Menstrual changes, abnormal vaginal bleeding, abnormal vaginal discharge, pelvic pain or pressure
- Excessive nausea, vomiting, or thirst
- Glossitis
- Edema
- Paresthesia
- Erythema
- Alopecia
Pharmacology
The principal action of testolactone is reported to be inhibition of aromatase activity and the reduction in estrogen synthesis that follows. Androstenedione, a 19-carbon steroid hormone produced in the adrenal glands and the gonads, is where estrone synthesis originates and is the source of estrogen in postmenopausal women. In vitro studies report that the aromatase inhibition may be noncompetitive and irreversible, and could possibly account for the persistence of this drug's effect on estrogen synthesis after drug withdrawal. This reduction is substantially less than with second- and third-generation aromatase inhibitors.
In addition to its activity as an aromatase inhibitor, testolactone also reportedly possesses some anabolic activity and weak androgenic activity via binding to and activation of the androgen receptor (AR). However, its affinity for the AR is very low; in one study, it showed 0.0029% of the affinity of the anabolic steroid metribolone (100%) for the human AR (Ki = 41 μM and 1.18 nM, respectively). In accordance, androgenic side effects such as hirsutism, acne, and voice changes have been reported in no women in clinical trials with testolactone.
Chemistry
Testolactone, also known as 13-hydroxy-3-oxo-13,17-secoandrosta-1,4-dien-17-oic acid δ-lactone, is a synthetic 18-oxasteroid and a D-homo-18-oxo analogue of androstenedione (androst-4-en-3,17-dione), with a six-membered lactone ring in place of the five-membered carbocyclic D-ring.
History
Testolactone was first approved for medical use in the United States in 1970.
References
References
- (8 May 2018). "Drugs: Synonyms and Properties: Synonyms and Properties". Taylor & Francis.
- [http://www.drugbank.ca/cgi-bin/getCard.cgi?CARD=DB00894.txt Testolactone] at DrugBank.ca
- (July 2006). "Use of aromatase inhibitors to increase final height". Molecular and Cellular Endocrinology.
- (2022-03-19). "Testolactone Advanced Patient Information".
- [https://www.drugs.com/cdi/testolactone.html Testolactone facts and comparisons at Drugs.com]
- (2004). "Precocious puberty and statural growth". Human Reproduction Update.
- (2001). "Principles and Practice of Endocrinology and Metabolism". Lippincott Williams & Wilkins.
- (9 September 2009). "The Breast E-Book: Comprehensive Management of Benign and Malignant Diseases". Elsevier Health Sciences.
- (24 October 1990). "Hormones and Vitamins in Cancer Treatment". CRC Press.
- Medical Economics. (February 1983). "Physicians Desk Reference". PDR Network, LLC.
- (1989-05-06). "Treatment of men with idiopathic oligozoospermic infertility using the aromatase inhibitor, testolactone. Results of a double-blinded, randomized, placebo-controlled trial with crossover". Journal of Andrology.
- "Testolactone Uses, Side Effects & Warnings".
- "Testolactone Side Effects: Common, Severe, Long Term".
- (2011). "Anabolics". Molecular Nutrition Llc.
- (24 January 2012). "Foye's Principles of Medicinal Chemistry". Lippincott Williams & Wilkins.
- (July 1984). "The use of human skin fibroblasts to obtain potency estimates of drug binding to androgen receptors". The Journal of Clinical Endocrinology and Metabolism.
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