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A61603臭化水素酸塩

A61603臭化水素酸塩 price.
  • ¥28600 - ¥288000
  • 化学名: A61603臭化水素酸塩
  • 英語名: A 61603 HYDROBROMIDE
  • 別名:A61603臭化水素酸塩
  • CAS番号: 107756-30-9
  • 分子式: C14H20BrN3O3S
  • 分子量: 390.3
  • EINECS:
  • MDL Number:MFCD02262217
5物価
選択条件:
ブランド
  • 富士フイルム和光純薬株式会社(wako)
パッケージ
  • 5mg
  • 10mg
  • 50mg
  • 生産者富士フイルム和光純薬株式会社(wako)
  • 製品番号W01TRCA101090
  • 製品説明
  • 英語製品説明A 61603
  • 包装単位5mg
  • 価格¥28600
  • 更新しました2023-06-01
  • 購入
  • 生産者富士フイルム和光純薬株式会社(wako)
  • 製品番号W01TRCA101090
  • 製品説明
  • 英語製品説明A 61603
  • 包装単位10mg
  • 価格¥41300
  • 更新しました2023-06-01
  • 購入
  • 生産者富士フイルム和光純薬株式会社(wako)
  • 製品番号W01TOC1052
  • 製品説明A61603臭化水素酸塩
  • 英語製品説明A61603 Hydrobromide
  • 包装単位10mg
  • 価格¥69000
  • 更新しました2024-03-01
  • 購入
  • 生産者富士フイルム和光純薬株式会社(wako)
  • 製品番号W01TRCA101090
  • 製品説明
  • 英語製品説明A 61603
  • 包装単位50mg
  • 価格¥157900
  • 更新しました2023-06-01
  • 購入
  • 生産者富士フイルム和光純薬株式会社(wako)
  • 製品番号W01TOC1052
  • 製品説明A61603臭化水素酸塩
  • 英語製品説明A61603 Hydrobromide
  • 包装単位50mg
  • 価格¥288000
  • 更新しました2024-03-01
  • 購入
生産者 製品番号 製品説明 包装単位 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01TRCA101090
A 61603
5mg ¥28600 2023-06-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCA101090
A 61603
10mg ¥41300 2023-06-01 購入
富士フイルム和光純薬株式会社(wako) W01TOC1052 A61603臭化水素酸塩
A61603 Hydrobromide
10mg ¥69000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCA101090
A 61603
50mg ¥157900 2023-06-01 購入
富士フイルム和光純薬株式会社(wako) W01TOC1052 A61603臭化水素酸塩
A61603 Hydrobromide
50mg ¥288000 2024-03-01 購入

プロパティ

貯蔵温度  :Desiccate at +4°C
溶解性 :Soluble in H2O
外見  :crystalline solid
色 :White to off-white
水溶解度  :Soluble to 50 mM in water

安全情報

絵表示(GHS):
注意喚起語:
危険有害性情報:
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
注意書き:

説明

The α1-adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro (EC50 = 6.9 nM) much more potently than activation by phenylephrine adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro (EC50 = 6.9 nM) much more potently than activation by phenylephrine adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro (EC50 = 6.9 nM) much more potently than activation by phenylephrine adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro (EC50 = 6.9 nM) much more potently than activation by phenylephrine adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro (EC50 = 6.9 nM) much more potently than activation by phenylephrine adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the frequency of spontaneous Ca2+ transients in rat ventricular myocytes in vitro (EC50 = 6.9 nM) much more potently than activation by phenylephrine adrenergic receptors are Gq protein-coupled receptors that play a key role in the modulation of sympathetic nervous system activity and are the site of action for therapeutic agents, such as antihypertensive drugs. A-61603 is a selective α1A-adrenergic receptor agonist that is at least 35-fold more potent at α1A receptor sites than at α1B or α1D. Activation of the α1A-adrenergic receptor by A-61603 has been reported to increase the