Powder: -20°C for 3 years | In solvent: -80°C for 1 year
G15 is a cell-permeable non-steroidal antagonist of GPER (Ki = 20 nM)
パッケージサイズ | 在庫状況 | 単価(税別) | |||
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サンプルについてお問い合わせ | |||||
1 mg | 在庫あり | ¥ 7,500 | |||
5 mg | 在庫あり | ¥ 17,500 | |||
10 mg | 在庫あり | ¥ 29,000 | |||
25 mg | 在庫あり | ¥ 52,500 | |||
50 mg | 在庫あり | ¥ 89,500 | |||
100 mg | 在庫あり | ¥ 134,500 | |||
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 19,000 |
説明 | G15 is a cell-permeable non-steroidal antagonist of GPER (Ki = 20 nM) |
ターゲット&IC50 | GPER:20 nM(Ki) |
In vivo | G-15 antagonizes the anti-depressive effects of estrogen in vivo[1]. |
動物実験 | G15 and G1 were first dissolved in DMSO and diluted with saline; the final concentration in DMSO was 1 mM. Desipramine and E2 (cyclodextrin-encapsulated, 4-5.5% E2) were dissolved in saline solution and DMSO was added to a final concentration of 1 mM. An appropriate vehicle-treated group (saline with 1 mM DMSO) was included as a control (sham). All solutions were freshly prepared before each experimental series. Independent groups of mice (n=12-16) were treated with two consecutive intraperitoneal injections as follows: vehicle solution + vehicle solution (sham group); vehicle + G-1 (indicated amount in nmol); vehicle + desipramine (10mg/kg); G15 (10nmol/mouse) + desipramine (10mg/kg); G15 (10nmol/mouse) + G-1 (1nmol/mouse); vehicle + G15 (10nmol/mouse); vehicle + soluble E2 (5 mg/kg); G15 (25nmol/mouse) + soluble E2 (5 mg/kg). The second compound was injected 15 min (7 min for E2) after the first injection and the tail suspension test performed 30 min after the second injection[1]. |
分子量 | 370.24 |
分子式 | C19H16BrNO2 |
CAS No. | 1161002-05-6 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 41.67 mg/mL (112.55 mM)
You can also refer to dose conversion for different animals. 詳細
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G15 1161002-05-6 Endocrinology/Hormones Estrogen Receptor/ERR Inhibitor inhibit G-15 G 15 inhibitor