O1918
Based on 1 publication(s) in Google Scholar
O1918 is a selective non-CB1 receptor and GPR18 antagonist.
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研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- 純度: 98.71%
- CAS 番号: 536697-79-7
- 分子式: C19H26O2
- 分子量:286.41
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保管条件:
Solution, -20°C, 2 years
MedChemExpress(MCE)の使用を引用している文献 O1918
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生物活性
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
化学情報
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CAS 番号 536697-79-7
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性状 Liquid
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分子量 286.41
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分子式 C19H26O2
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Color Colorless to light yellow
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SMILES
C=C([C@@H]1CCC(C)=C[C@H]1C2=C(OC)C=C(C)C=C2OC)C
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Solution, -20°C, 2 years
Publications (1)
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Journal Impact Factor
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Most Recent
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J Neurochem
2024 Nov;168(11):3715-3726. PMID: 37987505
プロトコル
Rats[1]
In order to examine the influence of different receptor antagonists on the changes in cardiovascular parameters induced by anandamide or methanandamide (both in anaesthetized and pithed rats), the particular agonist is injected twice (S1 and S2, 20 min apart). Methanandamide is administered at 0.5 µmol/kg. S1 is applied 5 min after injection of saline solution or ruthenium red 3 (µmol/kg in pithed rats anaesthetized with urethane). Cannabidiol or O1918 (3 µmol/kg) or their solvents are administered 10 min before S2. AM 251, cannabidiol or O1918 (3 µmol/kg, each) are administered simultaneously with pancuronium[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
純度とドキュメンテーション
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データシート (275 KB)
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SDS (394 KB)
- English - EN (394 KB)
- Français - FR (394 KB)
- Deutsch - DE (394 KB)
- Norwegian - NO (394 KB)
- Español - ES (394 KB)
- Swedish - SV (394 KB)
- Italian - IT (394 KB)
- Korean - KR (394 KB)
- Portuguese - PT (394 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Agnieszka Zakrzeska, et al. A cannabinoid receptor, sensitive to O-1918, is involved in the delayed hypotension induced by anandamide in anaesthetized rats. Br J Pharmacol. 2010 Jun; 160(3): 574–584. [Content Brief]
[2]. Matouk AI, et al. Abnormal cannabidiol confers cardioprotection in diabetic rats independent of glycemic control. Eur J Pharmacol. 2018 Feb 5;820:256-264. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)