Basic information Safety Supplier Related

imidazenil

Basic information Safety Supplier Related

imidazenil Basic information

Product Name:
imidazenil
Synonyms:
  • imidazenil
  • 6-(2-Bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxamide
  • 4H-Imidazo[1,5-a][1,4]benzodiazepine-3-carboxamide,6-(2-bromophenyl)-8-fluoro-
CAS:
151271-08-8
MF:
C18H12BrFN4O
MW:
399.22
Mol File:
151271-08-8.mol
More
Less

imidazenil Chemical Properties

Boiling point:
587.0±50.0 °C(Predicted)
Density 
1.67±0.1 g/cm3(Predicted)
pka
15.37±0.40(Predicted)
More
Less

imidazenil Usage And Synthesis

Description

Imidazenil is an imidazobenzodiazepine with the profile of a partial agonist. Animal studies have shown that it does not produce sedation or ataxia in rats nor does it potentiate the effects of alcohol (Guisti et al. 1993). Imidazenil has a low intrinsic activity at the GABAA receptor and therefore causes only slight enhancement of GABA-ergic tone. Its efficacy may, however, be increased when GABA tone is reduced, which could lead to its being active only in conditions where GABA tone is altered. This may well make it an ideal treatment for anxiety and epilepsy.

Uses

Imidazenil, a new anxiolytic and anticonvulsant drug, attenuates a benzodiazepine-induced cognition deficit in monkeys.

Side effects

When taken by mouth: Ostarine is possibly unsafe. It might cause liver damage and other serious side effects such as heart attack.

Synthesis

The synthesis of imidazenil is as follows:
A mixture of 3 g (7.5 mmol) of 6-(2-bromophenyl)-8-fluoro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylic acid, 300 mL of methylene chloride and 2.25 g (10.8 mmol) of phosphorus pentachloride was stirred at room temperature for 2 hours. Ammonia gas was then introduced until the mixture was basic. After layering with 20 mL of concentrated aqueous ammonia, the mixture was stirred for 15 minutes. The methylene chloride was washed with water, dried and evaporated. The residue was crystallized from ethanol/water to yield 2.4 g of product having the above formula. A second crop of 0.4 g was obtained from the mother liquor for a total yield of 2.8 g. For analysis, a sample of the product was recrystallized from methylene chloride/ethanol and had m.p. 298°-299° C.

imidazenilSupplier

Shanghai Lollane Biological Technology Co.,Ltd.
Tel
021-52996696,15000506266 15000506266
Pharmacodia (Beijing) Co.,Ltd
Tel
+86-400-851-9921
Email
sales@pharmacodia.com
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Email
info@efebio.com
Shanghai Rechem science Co., Ltd.
Tel
21-31433387 15618786686
Email
sales@rechemscience.com
Amadis Chemical Company Limited
Tel
571-89925085
Email
sales@amadischem.com