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MT-2 (Melanotan II)

Melanogenesis research

A synthetic analog of α-MSH studied as a non-selective melanocortin receptor agonist in pigmentation and sexual-function research.

$34.99per vial · research use

Quantity

Up to 50%
  • Melanogenesis models
  • MC receptor pharmacology
  • Photoprotection research
Women's research
For research use only. Not for human consumption.

Women's research notes

What researchers study MT-2 (Melanotan II) for in women

MT-2 research intersects with female-specific endpoints in dermatology and sexual-function studies, including HSDD (hypoactive sexual desire disorder) — its analog bremelanotide is FDA-approved in premenopausal women.

Pigmentation & photoprotection

Pre-clinical research has measured eumelanin density and UV-response endpoints following melanocortin agonist administration in female models.

Female sexual-function research

MC4R agonism is the mechanism underlying bremelanotide, FDA-approved for premenopausal HSDD — MT-2 is the structural parent compound studied in that research lineage.

Appetite & energy balance

Female pre-clinical models have examined melanocortin agonist effects on food intake and energy expenditure endpoints.

Selected literature

  • Dorr RT, et al. Life Sci 1996 — Melanotan II pharmacology
  • Kingsberg SA, et al. Obstet Gynecol 2019 — Bremelanotide for HSDD
Information below summarizes published pre-clinical and clinical research. It is provided for educational purposes for qualified researchers and is not medical advice, a treatment recommendation, or a claim of efficacy. Products are sold for research use only.