Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Wy 49051 is an orally active antagonist of H1 receptor(IC50 of 44 nM).
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
1 mg | 在庫あり | ¥ 58,000 |
5 mg | 在庫あり | ¥ 114,000 |
10 mg | 在庫あり | ¥ 166,000 |
25 mg | 在庫あり | ¥ 259,500 |
50 mg | 在庫あり | ¥ 349,000 |
100 mg | 在庫あり | ¥ 454,500 |
500 mg | 在庫あり | ¥ 911,500 |
1 mL * 10 mM (in DMSO) | 在庫あり | ¥ 151,000 |
説明 | Wy 49051 is an orally active antagonist of H1 receptor(IC50 of 44 nM). |
ターゲット&IC50 | H1 receptor:44 nM |
In vitro | Wy 49051 showed a great inhibitory effect on H1. At a concentration of 100 nM, it produced 92% inhibition of histamine-induced guinea pig ileal contraction. Wy 49051 is the most effective compound, with 700 times the potency of astemizole and 470 times the potency of hydroquinone. Wy 49051 also has high affinity for α1 receptor with IC50 of 8 nM[1]. |
In vivo | Wy 49051 demonstrates efficacy in counteracting histamine-induced lethality in guinea pigs, with effective doses (ED50) of 1.91 mg/kg orally (po), 0.70 mg/kg intraperitoneally (ip), and 0.01 mg/kg intravenously (iv). Additionally, the compound maintains its oral efficacy without any reduction for up to 18 hours posttreatment[1]. |
別名 | Wy-49051 |
分子量 | 487.59 |
分子式 | C28H33N5O3 |
CAS No. | 113418-56-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 45 mg/mL (92.29 mM)
You can also refer to dose conversion for different animals. 詳細
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Wy 49051 113418-56-7 GPCR/G Protein Immunology/Inflammation Neuroscience Histamine Receptor Wy-49051 Inhibitor inhibitor inhibit