| Name | 7-Methoxyrosmanol |
| Description | 7-Methoxyrosmanol (7-O-Methylrosmanol) can effectively suppress FSK-induced luciferase expression under the control of the CRE, PEPCK-C and G6Pase gene promoters, it may contribute to its antihyperglycemic activity. |
| In vitro | In order to find new effective HIV protease inhibitors, two diterpenes (carnosic acid and carnosol) were isolated from rosemary (Rosmarinus officinalis L.), and rosmanol and semisynthetic derivatives (7-Methoxyrosmanol 7-O-ethylrosmanol, and 11,12-O,O-dimethylcarnosol) were prepared. The inhibitory activity of all six compounds against HIV-1 protease was tested. The carnosic acid showed the strongest inhibitory effect (IC90 = 0.08 micrograms/ml). The same compound was also assayed against HIV-1 virus replication (IC90 = 0.32 micrograms/ml). |
| Storage | keep away from direct sunlight,keep away from moisture,The compound is unstable in solution. Please use soon | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (5.55 mM), Sonication is recommended. DMSO : 12 mg/mL (33.29 mM), Sonication is recommended.
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| Keywords | Inhibitor | inhibit | cAMP | 7-Methoxyrosmanol | 7Methoxyrosmanol | 7 Methoxyrosmanol |
| Inhibitors Related | UNC0006 | Bithionol | Eriocalyxin B | Adenosine receptor A1 antagonist 5 | HJC0350 | TDI-10229 | I942 | 8-Bromo-cAMP | GLP-1R modulator L7-028 | Torbafylline | 2-PCCA hydrochloride | GAT211 |
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