ブレタゼニル

ブレタゼニル 化学構造式
84379-13-5
CAS番号.
84379-13-5
化学名:
ブレタゼニル
别名:
ブレタゼニル;(13aS)-8-ブロモ-9-オキソ-11,12,13,13a-テトラヒドロ-9H-イミダゾ[1,5-a]ピロロ[2,1-c][1,4]ベンゾジアゼピン-1-カルボン酸tert-ブチル;(13aS)-8-ブロモ-11,12,13,13a-テトラヒドロ-9-オキソ-9H-イミダゾ[1,5-a]ピロロ[2,1-c][1,4]ベンゾジアゼピン-1-カルボン酸1,1-ジメチルエチル;tert-ブチル (7S)-14-ブロモ-12-オキソ-2,4,11-トリアザテトラシクロ[11.4.0.02,6.07,11]ヘプタデカ-1(17),3,5,13,15-ペンタエン-5-カルボキシラート;(4S)-6-オキソ-7-ブロモ-4α,5-プロパノ-5,6-ジヒドロ-4H-イミダゾ[1,5-a][1,4]ベンゾジアゼピン-3-カルボン酸tert-ブチル
英語名:
Bretazenil
英語别名:
BRETAZENIL;Brn 4765855;Bretazenilum;Unii-osz0E9dgoj;BRETAZENIL USP/EP/BP;Bretazenilum [inn-latin];9H-IMIDAZO(1,5-A)PYRROLO(2,1-C);1,1-dimethylethylester,(s)-13a-tetrahydro-8-bromo-9-oxo;9H-Imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid;9h-imidazo(1,5-a)pyrrolo(2,1-c)(1,4)benzodiazepine-1-carboxylicacid,11,12,13,
CBNumber:
CB6503200
化学式:
C19H20BrN3O3
分子量:
418.28
MOL File:
84379-13-5.mol

ブレタゼニル 物理性質

沸点 :
594.3±50.0 °C(Predicted)
比重(密度) :
1.56±0.1 g/cm3(Predicted)
貯蔵温度 :
2-8°C
溶解性:
DMSO: 24 mg/mL、可溶
外見 :
個体
酸解離定数(Pka):
0.78±0.20(Predicted)
色:
白い
InChI:
InChI=1S/C19H20BrN3O3/c1-19(2,3)26-18(25)15-16-13-8-5-9-22(13)17(24)14-11(20)6-4-7-12(14)23(16)10-21-15/h4,6-7,10,13H,5,8-9H2,1-3H3/t13-/m0/s1
InChIKey:
LWUDDYHYYNNIQI-ZDUSSCGKSA-N
SMILES:
N12C=NC(C(OC(C)(C)C)=O)=C1[C@]1([H])CCCN1C(=O)C1=C(Br)C=CC=C12

安全性情報

Sフレーズ  22-24/25
WGK Germany  3
RTECS 番号 NJ5899850

ブレタゼニル 価格 もっと(3)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01TOC3568
Bretazenil
84379-13-5 10mg ¥56000 2024-03-01 購入
Sigma-Aldrich Japan B6434 ブレタゼニル ≥96% (HPLC), solid
Bretazenil ≥96% (HPLC), solid
84379-13-5 5mg ¥32900 2024-03-01 購入
Sigma-Aldrich Japan B6434 ブレタゼニル ≥96% (HPLC), solid
Bretazenil ≥96% (HPLC), solid
84379-13-5 25mg ¥142000 2024-03-01 購入

ブレタゼニル 化学特性,用途語,生産方法

効能

抗不安薬

説明

Bretazenil is an imidazobenzodiazepine partial agonist and a potent anxiolytic. It is rapidly absorbed and has a half-life of 2.5 hours. Animal work has shown that, even after long-term administration of bretazenil, there are no changes in GABA receptor binding or function, and tolerance does not occur. Studies in humans have also suggested that bretazenil has a low abuse potential (Sellers et al. 1991). In terms of clinical effects, bretazenil has demonstrated anxiolytic efficacy in both generalized anxiety disorder and panic disorder (Katschnig et al. 1991), but no controlled study has compared bretazenil with a classic full agonist.

使用

Anti-anxiety agent.
Bretazenil potentiated GABA responses on α4β3γ2 cells.
Bretazenil is a partial benzodiazepine receptor agonist. Benzodiazepines, mainly diazepam, are commonly used as anticonvulsants in the treatment of organophosphate casualties. Bretazenil has been used to determine non-specific binding due to its affinity to bind to a variety of γ-aminobutyric acid type A (GABAA) receptor subtypes (α1-3;5). It has also been used as a GABAA receptor partial agonist in the subcutaneous Alzet minipumps to treat obese agouti related protein (AgRP) ablated and lean naive mice to study its effect on them.

生物活性

Bretazenil is a positive allosteric modulator of GABAA receptors with anticonvulsant and anxiolytic activity. It potentiates GABA-gated chloride currents in rat cortical neurons and in HEK293 cells expressing α1β1γ2 subunit-containing GABAA receptors (EC50s = 60 and 10 nM, respectively). Bretazenil inhibits binding of the benzodiazepine diazepam to rat cerebral cortex homogenates (IC50 = 2.2 nM). It inhibits tonic convulsions induced by pentylenetetrazol (PTZ; Item No. 18682) and maximal electroshock (MES) in rats (ED50s = 0.07 and 0.48 mg/kg, respectively). Bretazenil (5-30 mg/kg) increases the number of open arm entries and percentage of time spent in the open arms of the elevated plus maze in mice, indicating anxiolytic-like activity.

薬理学

Bretazenil exhibits an ticonflflict and anticonvulsant properties. Only mild sedation appears at doses needed to produce anticonvulsant or anxiolytic effects, and potentiation of ethanol-induced sedation is less pronounced than with diazepam.

ブレタゼニル 上流と下流の製品情報

原材料

準備製品


ブレタゼニル 生産企業

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84379-13-5(ブレタゼニル)キーワード:


  • 84379-13-5
  • 1,1-dimethylethylester,(s)-13a-tetrahydro-8-bromo-9-oxo
  • 9h-imidazo(1,5-a)pyrrolo(2,1-c)(1,4)benzodiazepine-1-carboxylicacid,11,12,13,
  • (13aS)-8-Bromo-9-oxo-11,12,13,13a-tetrahydro-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid tert-butyl ester
  • 9H-Imidazo(1,5-A)pyrrolo(2,1-C)(1,4)benzodiazepine-1-carboxylic acid, 8-bromo-11,12,13,13A-tetrahydro-9-oxo-, 1,1-dimethylethyl ester, (S)-
  • Bretazenilum
  • Bretazenilum [inn-latin]
  • Brn 4765855
  • Unii-osz0E9dgoj
  • (13aS)-8-Bromo-11,12,13,13a-tetrahydro-9-oxo-9H-imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylicacid1,1-dimethylethylester
  • 9H-Imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid
  • Ro 16-6028, 9H-Imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid
  • BRETAZENIL
  • 9H-IMIDAZO(1,5-A)PYRROLO(2,1-C)(1,4)BENZODIAZEPINE-1-CARBOXYLIC ACID,11,12,13,13A-TTRRRAHYDRO-8-BROMO-9-OXO-,1,1-DIMETHYLETHYL ESTER,(S)-
  • 9H-Imidazo[1,5-a]pyrrolo[2,1-c][1,4]benzodiazepine-1-carboxylic acid, 8-bromo-11,12,13,13a-tetrahydro-9-oxo-, 1,1-dimethylethyl ester, (13aS)-
  • BRETAZENIL USP/EP/BP
  • 9H-IMIDAZO(1,5-A)PYRROLO(2,1-C)
  • Inhibitor,site,Bretazenil,inhibit,γ-Aminobutyric acid Receptor,function,benzodiazepine,Gamma-aminobutyric acid Receptor,GABA Receptor,motoric,Ro 16-6028,anticonvulsant
  • (S)-tert-butyl 8-bromo-9-oxo-11,12,13,13a-tetrahydro-9H-benzo[e]imidazo[5,1-c]pyrrolo[1,2-a][1,4]diazepine-1-carboxylate
  • ブレタゼニル
  • (13aS)-8-ブロモ-9-オキソ-11,12,13,13a-テトラヒドロ-9H-イミダゾ[1,5-a]ピロロ[2,1-c][1,4]ベンゾジアゼピン-1-カルボン酸tert-ブチル
  • (13aS)-8-ブロモ-11,12,13,13a-テトラヒドロ-9-オキソ-9H-イミダゾ[1,5-a]ピロロ[2,1-c][1,4]ベンゾジアゼピン-1-カルボン酸1,1-ジメチルエチル
  • tert-ブチル (7S)-14-ブロモ-12-オキソ-2,4,11-トリアザテトラシクロ[11.4.0.02,6.07,11]ヘプタデカ-1(17),3,5,13,15-ペンタエン-5-カルボキシラート
  • (4S)-6-オキソ-7-ブロモ-4α,5-プロパノ-5,6-ジヒドロ-4H-イミダゾ[1,5-a][1,4]ベンゾジアゼピン-3-カルボン酸tert-ブチル
  • ベンゾジアゼピン系抗不安薬
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