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Lupeol (Clerodol; Monogynol B; Fagarasterol (Fagarasterol) is an active pentacyclic triterpenoid with antioxidant, anti-tumor and anti-inflammatory activities. Lupeol is a potent androgen receptor inhibitor that can be used in cancer research, especially in prostate cancer with androgen-dependent phenotypes (ADPC) and castration-resistant phenotypes (CRPC).
| Molecular Weight | 426.72 |
| Formula | C30H50O |
| CAS Number | 545-47-1 |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
[1] Donghai Li, et al. Lupeol Accumulation Correlates with Auxin in the Epidermis of Castor
[4] Fan-Shiu Tsai, et al. Lupeol and Its Role in Chronic Diseases
| Related Androgen Receptor Products |
|---|
| LGD-3303
LGD-3303 is a nonsteroidal, nonaromatizable selective androgen receptor ligand that binds to the androgen receptor with high affinity in a radiolabeled to competitive binding assay (Ki=0.9 nM). |
| Ar-V7-IN-1
Ar-V7-IN-1 is a potent inhibitor of Ar-V7. AR-V7 is a hormone-independent splice variant of the androgen receptor. Ar-V7-IN-1 has the potential for the research of various indications such as prostate cancer. |
| SC912
SC912 is a potent and selective AR-V7 inhibitor with IC50 of 0.36 μM. SC912 binds directly to AR-FL and AR-V7 proteins, inhibites nuclear localization and chromatin binding capabilities. SC912 exerts anticancer activity through inhibition of proliferation, induction of cell cycle arrest and apoptosis. |
| A4B17
A4B17 is an androgen receptor N-terminal inhibitor, which can be used for the research of androgen-responsive prostate cancer. |
| AZ'3137
AZ‘3137 is an orally active PROTAC-type androgen receptor (AR) degrader, with a DC50 value of 22 nM. |
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