Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Leelamine hydrochloride, a tricyclic diterpene extracted from pine tree bark, inhibits the transcriptional activity of the androgen receptor, known to regulate fatty acid synthesis [2,3]. This compound acts as a cannabinoid receptor type 1 (CB1) agonist and suppresses SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, irrespective of androgen receptor status.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
2 mg | 5 days | $ 98.00 |
Description | Leelamine hydrochloride, a tricyclic diterpene extracted from pine tree bark, inhibits the transcriptional activity of the androgen receptor, known to regulate fatty acid synthesis [2,3]. This compound acts as a cannabinoid receptor type 1 (CB1) agonist and suppresses SREBP1-regulated fatty acid/lipid synthesis in prostate cancer cells, irrespective of androgen receptor status. |
Molecular Weight | 321.93 |
Formula | C20H32ClN |
CAS No. | 16496-99-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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Leelamine hydrochloride 16496-99-4 Others Leelamine Hydrochloride inhibitor inhibit