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Testosterone cypionate

Chemical compound


Chemical compound

FieldValue
IUPAC_name[(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-cyclopentylpropanoate
imageTestosterone cypionate.svg
image_classskin-invert-image
width250px
image2Testosterone cypionate molecule ball.png
image_class2bg-transparent
width2250px
tradenameDepo-Testosterone, others
pregnancy_AU
pregnancy_US
legal_AU
legal_CASchedule IV
legal_USSchedule III
routes_of_administrationIntramuscular injection
classAndrogen; Anabolic steroid; Androgen ester
bioavailabilityOral: very low
Intramuscular: very high
metabolismLiver
elimination_half-life~(7-8) days )
excretion90% Urine; 6% feces
CAS_number58-20-8
PubChem441404
DrugBankDB13943
ChemSpiderID390140
UNIIM0XW1UBI14
ChEMBL1201101
KEGGD00957
synonymsTC; TCPP; Testosterone cipionate; Testosterone cyclopentylpropionate; Testosterone cyclopentanepropionate; Testosterone 17β-cyclopentylpropionate
C27H=40O=3
SMILESC[C@]12CC[C@H]3C@HCCC5=CC(=O)CC[C@]35C
StdInChI1S/C27H40O3/c1-26-15-13-20(28)17-19(26)8-9-21-22-10-11-24(27(22,2)16-14-23(21)26)30-25(29)12-7-18-5-3-4-6-18/h17-18,21-24H,3-16H2,1-2H3/t21-,22-,23-,24-,26-,27-/m0/s1
StdInChIKeyHPFVBGJFAYZEBE-ZLQWOROUSA-N

Intramuscular: very high | elimination_half-life = ~(7-8) days )

Testosterone cypionate, sold under the brand name Depo-Testosterone among others, is an androgen and anabolic steroid (AAS) medication which is used mainly in the treatment of low testosterone levels in men, including hormone therapy for transgender men. It is given by injection into muscle or subcutaneously, once every one to four weeks, depending on clinical indication.

Side effects of testosterone cypionate include symptoms of masculinization like acne, increased hair growth, voice changes, and increased sexual desire. Testosterone supplementation is also known to reduce the threshold for aggressive behavior in men. The drug is a synthetic androgen and anabolic steroid and hence is an agonist of the androgen receptor (AR), the biological target of androgens like testosterone and dihydrotestosterone (DHT). Testosterone cypionate is converted by the body to testosterone that has both androgenic effects and anabolic effects, which make it useful for producing masculinization and suitable for androgen replacement therapy; still, the relative potency of these effects can depend on various factors and is a topic of ongoing research. Testosterone can either directly exert effects on target tissues or be metabolized by 5α-reductase into DHT or aromatized to estradiol (E2). Both testosterone and DHT bind to an androgen receptor(AR); however, DHT has a stronger binding affinity than testosterone and may have more androgenic effect in certain tissues at lower levels. Testosterone cypionate is a testosterone ester and a long-lasting prodrug of testosterone in the body. Because of this, it is considered to be a natural and bioidentical form of testosterone.

Testosterone cypionate was introduced for medical use in 1951. Along with testosterone enanthate, testosterone undecanoate, and testosterone propionate, it is one of the most commonly used testosterone esters. It is used mainly in the United States. In addition to its medical use, testosterone cypionate is used to improve physique and performance. The drug is a controlled substance in many countries and so non-medical use is generally illicit.

Medical uses

Testosterone cypionate is used primarily in androgen replacement therapy. It is currently FDA approved for the treatment of primary or hypogonadotropic hypogonadism (either congenital or acquired). The drug's safety in andropause (late-onset hypogonadism in men) has not yet been established, and there are concerns that it may escalate the risks of benign prostatic hyperplasia, prostate cancer and heart diseases. It is currently used off-label for breast cancer, breast disorders, delayed puberty in boys, oligospermia (low sperm count), transmasculine hormone replacement therapy in transgender men, and osteoporosis.

Side effects

Side effects of testosterone cypionate include virilization among others. Diminished sperm production is a common side-effect of testosterone replacement therapy because of the decreased intra-testicular concentration of testosterone and suppression of the hypothalamic-pituitary-gonadal axis.

Pharmacology

Pharmacodynamics

Testosterone cypionate is a prodrug of testosterone and is an androgen and anabolic–androgenic steroid (AAS). That is, it is an agonist of the androgen receptor (AR).

Testosterone cypionate is converted by the body to testosterone that has both androgenic effects and anabolic effects; still, the relative potency of these effects can depend on various factors and is a topic of ongoing research. Testosterone can either directly exert effects on target tissues or be metabolized by 5α-reductase into dihydrotestosterone (DHT) or aromatized to estradiol (E2). Both testosterone and DHT bind to an androgen receptor; however, DHT has a stronger binding affinity than testosterone and may have more androgenic effect in certain tissues at lower levels.

Pharmacokinetics

The pharmacokinetics of testosterone cypionate via depot intramuscular injection, including its elimination half-life and duration of action, are said to be extremely comparable to and hence essentially the same as those of testosterone enanthate. As such, testosterone cypionate and testosterone enanthate are considered to be "functionally interchangeable" as medications. For reference, testosterone enanthate has an elimination half-life of 4.5 days and a mean residence time of 8.5 days and requires frequent administration of approximately once per week. Large fluctuations in testosterone levels result with it, with levels initially being elevated and supraphysiological. The pharmacokinetics of testosterone cypionate have been studied and reported.

Chemistry

Testosterone cypionate, or testosterone 17β-cyclopentylpropionate, is a synthetic androstane steroid and a derivative of testosterone. It is an androgen ester; specifically, it is the C17β cyclopentylpropionate (cypionate) ester of testosterone.

History

Testosterone cypionate was first synthesized in 1951 and was introduced for medical use in the United States the same year under the brand name Depo-Testosterone.

Society and culture

Generic names

Testosterone cypionate is the generic name of the drug and its .

Brand names

Testosterone cypionate is or has been marketed under a variety of brand names, including:

  • Andro Cyp
  • Andronaq LA
  • Andronate
  • Dep Andro
  • Dep Test
  • Deposteron
  • Depostomead
  • Depotest
  • Depo-Testosterone
  • Depovirin
  • Durandro
  • Duratest
  • Jectatest
  • Malogen CYP
  • Pertestis
  • Testa-C
  • Testadiate Depo
  • Testex Elmu Prolongatum
  • Testoject LA
  • Virilon

Availability

Testosterone cypionate is marketed in the United States. It is not widely available outside of the United States, though it has been marketed in Canada, Australia, Spain, Brazil, and South Africa.

Testosterone cypionate, along with other AAS, is a schedule III controlled substance in the United States under the Controlled Substances Act and a schedule IV controlled substance in Canada under the Controlled Drugs and Substances Act.

References

References

  1. (26 July 2012). "Testosterone: Action, Deficiency, Substitution". Cambridge University Press.
  2. (13 January 2010). "Andrology: Male Reproductive Health and Dysfunction". Springer Science & Business Media.
  3. (2011). "Anabolics". Molecular Nutrition Llc.
  4. (May 2018). "Recommendations for the Use of Testosterone in Male Transgender". Revista Brasileira de Ginecologia e Obstetricia.
  5. (April 2017). "Testosterone therapy for transgender men". The Lancet. Diabetes & Endocrinology.
  6. (2001). "Principles and Practice of Endocrinology and Metabolism". Lippincott Williams & Wilkins.
  7. (2000). "Lexicon of Psychiatry, Neurology, and the Neurosciences". Lippincott Williams & Wilkins.
  8. (November 2017). "Endocrine Treatment of Gender-Dysphoric/Gender-Incongruent Persons: An Endocrine Society Clinical Practice Guideline". The Journal of Clinical Endocrinology and Metabolism.
  9. (2020). "Is testosterone linked to human aggression? A meta-analytic examination of the relationship between baseline, dynamic and manipulated testosterone on human aggression.". Hormones and Behavior.
  10. (June 2008). "Pharmacology of anabolic steroids". British Journal of Pharmacology.
  11. (2017). "Thyroid Diseases".
  12. (2002). "Anabolic steroids". Recent Prog Horm Res.
  13. (April 2016). "Compounded Bioidentical Hormones in Endocrinology Practice: An Endocrine Society Scientific Statement". The Journal of Clinical Endocrinology and Metabolism.
  14. (19 July 2016). "What is Testosterone Cypionate". HRTGuru corp..
  15. (December 2022). "Testosterone treatment of late-onset hypogonadism - benefits and risks". Rev Endocr Metab Disord.
  16. "Testosterone cypionate - Pfizer". Springer Nature Switzerland AG.
  17. "Depo-Testosterone; testosterone cypionate injection, USP". U.S. Food and Drug Administration.
  18. (January 2019). "Testosterone Is a Contraceptive and Should Not Be Used in Men Who Desire Fertility". The World Journal of Men's Health.
  19. (28 October 2007). "The Leydig Cell in Health and Disease". Springer Science & Business Media.
  20. (June 1987). "Hormone kinetics after intramuscular testosterone cypionate". Fertility and Sterility.
  21. (14 November 2014). "The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies". Springer.
  22. (January 2000). "Index Nominum 2000: International Drug Directory". Taylor & Francis.
  23. (September 1953). "Testosterone phenyl propionate (TPP): biological trials with a new androgen". British Journal of Pharmacology and Chemotherapy.
  24. (22 October 2013). "Pharmaceutical Manufacturing Encyclopedia, 3rd Edition". William Andrew Publishing.
  25. (21 February 2005). "Testosterone Dreams: Rejuvenation, Aphrodisia, Doping". University of California Press.
  26. (6 December 2012). "Concise Dictionary of Pharmacological Agents: Properties and Synonyms". Springer Science & Business Media.
  27. "Testosterone". Drugs.com International.
  28. (21 December 2006). "Drug Abuse Handbook, Second Edition". CRC Press.
  29. (5 August 2016). "Pharmacology for Canadian Health Care Practice". Elsevier Health Sciences.
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