1176316-99-6
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- CAS号:
- 1176316-99-6
- 英文名:
- AgoMelatine (hydrochloride)
- 英文别名:
- S-20098 HYDROCHLORIDE;AgoMelatine (hydrochloride);Agomelatine hydrochloride (S-20098 HCl);Agomelatine hydrochloride
(S-20098 hydrochloride)
- 中文名:
- 1176316-99-6
- 中文别名:
- 盐酸阿戈美拉汀
- CBNumber:
- CB42677042
- 分子式:
- C15H18ClNO2
- 分子量:
- 279.76
- MOL File:
- 1176316-99-6.mol
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1176316-99-6化学性质
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储存条件:
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Store at -20°C
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溶解度:
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DMSO: ≥ 100 mg/mL (357.45 mM)
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形态:
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Powder
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颜色:
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White to off-white
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1176316-99-6性质、用途与生产工艺
Agomelatine hydrochloride (S-20098 hydrochloride) 是一种 MT1 和 MT2 受体的特异性激动剂，对 CHO-hMT1，HEK-hMT1，CHO-hMT2，HEK-hMT2 的 Ki 分别为 0.1，0.06，0.12 和 0.27 nM。Agomelatine hydrochloride 还是一种选择性的 5-HT2C 受体拮抗剂，在天然 (猪) 和克隆的人 5-HT2C 受体中 pKi 分别为 6.4 和 6.2。
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5-HT
2C
Receptor
6.4 (pKi, native porcine)
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5-HT
2C
Receptor
6.2 (pKi, human)
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hMT1
0.1 (Ki, CHO Cells)
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hMT1
0.06 (Ki, HEK Cells)
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hMT2
0.12 (Ki, CHO Cells)
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hMT2
0.27 (Ki, HEK Cells)
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Agomelatine (S 20098) acts as a full agonist of MT1 and MT2 receptors with EC
50
s of 1.6±0.4, 0.10±0.04 nM for CHO hMT1 CHO-hMT2 (hΜΤ1 and hΜΤ2 receptors expressed in CHO or HEK cell membranes).
Agomelatine (S20098) also interacts with h5-HT2B receptors (6.6), whereas it shows low affinity at native (rat)/cloned, human 5-HT2A (<5.0/5.3) and 5-HT1A (<5.0/5.2) receptors, and negligible (<5.0) affinity for other 5-HT receptors.
Agomelatine (25, 50, or 75 mg/kg; i.p.) has antioxidant activity in Strychnine (75 mg/kg, i.p.) or Pilocarpine (400 mg/kg, i.p.) induced seizure models in mice. Agomelatine dose not have any antioxidant effects on parameters of oxidative stress produced by Pentylenetetrazole (PTZ) or Picrotoxin (PTX) induced seizure models when compared to controls.
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Animal Model:
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Female Swiss mice (20-30 g) were administered PTZ (85 mg/kg, i.p.), PTX (7 mg/kg, i.p.), strychnine (75 mg/kg, i.p.), Pilocarpine (400 mg/kg, i.p.), respectively
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Dosage:
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25, 50, or 75 mg/kg
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Administration:
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Administered intraperitoneally (i.p.)
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Result:
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All dosages showed a significant decrease in thiobarbituric acid reactive substances (TBARS) levels and nitrite content in all brain areas when compared to controls in the Pilocarpine induced seizure model.
All dosages decreased TBARS levels in all brain areas, and at low doses (25 or 50 mg/kg) decreased nitrite contents, but only at 25 or 50 mg/kg showed a significant increase in catalase activity in three brain areas when compared to controls in the Strychnine-induced seizure model.
Did not have any antioxidant effects on parameters of oxidative stress produced by PTX- or PTZ-induced seizure models when compared to controls.
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1176316-99-6
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| 更新日期 | 产品编号 | 产品名称 | CAS编号 | 包装 | 价格 |
|---|
| 2024/04/30 | HY-17038A | 1176316-99-6
Agomelatine hydrochloride | 1176316-99-6 | 5mg | 460元 |
| 2024/04/30 | HY-17038A | 1176316-99-6
Agomelatine hydrochloride | 1176316-99-6 | 10mM * 1mLin DMSO | 506元 |
1176316-99-6, 1176316-99-6 相关搜索:
- 盐酸阿戈美拉汀
- 1176316-99-6
- Agomelatine hydrochloride (S-20098 HCl)
- S-20098 HYDROCHLORIDE
- Agomelatine hydrochloride
(S-20098 hydrochloride)
- AgoMelatine (hydrochloride)