Target intelligence / Profile preview

Melanocortin 1 receptor (MC1R)

Target
MC1R
Molecular classification
G protein-coupled receptor, Receptor
01

Overview

The **Melanocortin 1 receptor** (MC1R) is a G protein-coupled receptor expressed primarily on the surface of melanocytes. It mediates the effects of melanocyte-stimulating hormones (MSH), especially α-MSH, by activating adenylate cyclase and increasing intracellular cAMP levels. This leads to enhanced melanin production—specifically promoting eumelanin over pheomelanin—and provides protection against UV-induced DNA damage. Variants in the MC1R gene are associated with differences in skin and hair color as well as susceptibility to melanoma. Several drugs targeting this pathway have been developed or approved for conditions involving pigmentation or photoprotection[2][4][5]. Note on correctness ("is_incorrect"): The query "Melanocyte activity" does not refer directly to a specific molecular target but rather describes a biological process. The canonical therapeutic target relevant here is the "Melanocortin 1 receptor" (MC1R). Therefore, "Melanocyte activity" is not itself a valid molecular target name; it should be mapped specifically to MC1R or another defined molecule involved in regulating this activity[2][5].

Other names
Melanocyte-stimulating hormone receptorMSH-RMSHRMelanocortin receptor 1MC1-R
02

Mechanism of action

Agonists stimulate cAMP signaling in melanocytes to increase eumelanin synthesis and photoprotection[2][5]

03

Biological functions

Regulation of melanogenesis (melanin production)Signal transduction via cAMP pathwayResponse to ultraviolet (UV) radiation
04

Disease associations

Skin cancer (melanoma risk modulation)Pigmentation disorders (e.g., red hair phenotype, fair skin)
05

Safety considerations

Potential for off-target effects due to broad GPCR family interactions; increased melanin may mask early melanoma detection in some cases[2][5]
06

Interacting drugs

Afamelanotide

2 more in the full profile.

07

Biomarkers

MC1R gene variants for melanoma risk and pigmentation phenotype[2]

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