MSG606 is a selective antagonist of the melanocortin 1 receptor (MC1R), known for its ability to negate the neuroprotective effects of MC1R agonists. This compound effectively inhibits cancer cell proliferation and disrupts the transition from the G1 to S phase of the cell cycle. Additionally, MSG606 has demonstrated potential in delaying pain hypersensitivity and reducing cholesterol levels. It is valuable for research applications related to cancer, inflammation, neurological disorders, and metabolic diseases, including breast cancer and subarachnoid hemorrhage.
MSG606 is a selective antagonist of the melanocortin 1 receptor (MC1R), known for its ability to negate the neuroprotective effects of MC1R agonists. This compound effectively inhibits cancer cell proliferation and disrupts the transition from the G1 to S phase of the cell cycle. Additionally, MSG606 has demonstrated potential in delaying pain hypersensitivity and reducing cholesterol levels. It is valuable for research applications related to cancer, inflammation, neurological disorders, and metabolic diseases, including breast cancer and subarachnoid hemorrhage.
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