Bretazenil

Bretazenil Struktur
84379-13-5
CAS-Nr.
84379-13-5
Englisch Name:
Bretazenil
Synonyma:
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
Summenformel:
C19H20BrN3O3
Molgewicht:
418.28
MOL-Datei:
84379-13-5.mol

Bretazenil Eigenschaften

Siedepunkt:
594.3±50.0 °C(Predicted)
Dichte
1.56±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
Löslichkeit
DMSO: 24 mg/mL, soluble
Aggregatzustand
solid
pka
0.78±0.20(Predicted)
Farbe
white
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

Sicherheit

S-Sätze: 22-24/25
WGK Germany  3
RTECS-Nr. NJ5899850

Bretazenil Chemische Eigenschaften,Einsatz,Produktion Methoden

S-Sätze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Beschreibung

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.

Verwenden

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.

Biologische Aktivität

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.

Pharmakologie

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.

Bretazenil Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Bretazenil Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 86)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shanghai Synchem Pharma Co., Ltd
+86-61984905-1 +86-18016477331
synchempharma@aliyun.com China 95 58
Zhejiang J&C Biological Technology Co.,Limited
+1-2135480471 +1-2135480471
sales@sarms4muscle.com China 10523 58
Henan Bao Enluo International TradeCo.,LTD
+86-17331933971 +86-17331933971
deasea125996@gmail.com China 2503 58
Hebei Yanxi Chemical Co., Ltd.
+8617531190177
peter@yan-xi.com China 5993 58
Dorne Chemical Technology co. LTD
+86-13583358881 +86-18560316533
Ethan@dornechem.com China 294 58
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+8613043004613
Sara@xmwonderfulbio.com China 305 58
Shandong Huisheng Import & Export Co., Ltd.
+86-13176845580 +86-13176845580
da@zhongda-biotech.com China 248 58
Anhui Ruihan Technology Co., Ltd
+8617756083858
daisy@anhuiruihan.com China 994 58
Shandong Hanjiang Chemical Co., Ltd
+86-0533-2066820 +8618369939125
hanson@sdhanjiang.com China 1527 58
CONTIDE BIOTECH CO.,LTD
+85253358525
xena@healthtide-api.com China 499 58

84379-13-5()Verwandte Suche:


  • 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
  • 84379-13-5
  • C19H20N3O3Br
  • 84379-13-5
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