Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

All progestins are not created equal.

Frank Z Stanczyk1

  • 1Departments of Obstetrics and Gynecology, and Preventive Medicine, University of Southern California Keck School of Medicine, Women's and Children's Hospital, 1240 N. Mission Road, Los Angeles, CA 90033, USA. gstanczk@socal.rr.com

Steroids
|December 12, 2003
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Efficacy and safety of estrogen therapy for prevention of osteoporosis in postmenopausal women.

Women's health (London, England)·2026
Same author

PrEP at the site of action in cisgender and transgender women: A pharmacology study of blood and rectal CD4<sup>+</sup> lymphocytes.

British journal of clinical pharmacology·2026
Same author

A detailed review of pharmacokinetics/pharmacodynamics of progestogens in oral contraception.

Frontiers in endocrinology·2026
Same author

Estrobolome: Is there a missing link?

The Journal of steroid biochemistry and molecular biology·2026
Same author

Sex steroid hormones, gonadotropins, and risk of testicular germ cell tumors: results from the STEED study.

Journal of the National Cancer Institute·2026
Same author

Long-term tamoxifen impacts the ovary but not preimplantation embryo development†.

Biology of reproduction·2025
Same journal

Steroidal alkaloids as multi-target therapeutics for the treatment of endometriosis.

Steroids·2026
Same journal

Emerging trends for therapeutic valuation of Cyclopamine: Structural features, mechanism of action, and formulation strategies.

Steroids·2026
Same journal

The antiproliferative and antimigratory properties of the 3-biotin-B-norcholesteryl benzimidazole derivative in MCF-7 cells are mediated through G1 phase arrest and apoptosis.

Steroids·2026
Same journal

Development and validation of an LC-MS method for quantification of sex steroid hormones in skeletal muscle.

Steroids·2026
Same journal

Circulating 4β-hydroxycholesterol as a biomarker of CYP3A4 activity: beyond drug development.

Steroids·2026
Same journal

Impact of glycosylation position on flavonoid isomers' inhibition of breast cancer-associated enzyme CYP1B1.

Steroids·2026
See all related articles

Progestins, used therapeutically, vary significantly in structure, metabolism, and potency. Understanding these differences is crucial for effective clinical application and avoiding misconceptions about their effects.

Area of Science:

  • Pharmacology
  • Endocrinology
  • Medicinal Chemistry

Background:

  • Progestins are vital therapeutic agents with diverse chemical structures.
  • Classification includes progesterone-related (pregnanes, 19-norpregnanes) and testosterone-related (17-ethinyl, non-17-ethinyl) compounds.
  • Oral progestins undergo extensive hepatic metabolism, often necessitating high therapeutic doses.

Purpose of the Study:

  • To review the classification and characteristics of therapeutic progestins.
  • To highlight the variability in progestin metabolism, pharmacokinetics, and potency.
  • To address misconceptions regarding progestin androgenicity.

Main Methods:

  • Literature review of progestin classification based on chemical structure.
  • Analysis of metabolic pathways, including hepatic first-pass metabolism.

Related Experiment Videos

  • Examination of pharmacokinetic data and potency assessment methods.
  • Review of studies comparing human and animal progestational activity and androgenicity.
  • Main Results:

    • Progestins are chemically diverse, categorized by structural relation to progesterone or testosterone.
    • 17-Ethinylated progestins include norethindrone and levonorgestrel families.
    • Significant inter-species differences exist in progestin activity, and rat data may not accurately predict human androgenicity.

    Conclusions:

    • Progestins exhibit wide variations in chemical structure, metabolism, pharmacokinetics, and potency.
    • Accurate assessment requires consideration of species-specific data.
    • Clinical use necessitates understanding these distinct progestin profiles.