IDRA 21
IDRA 21 Basic information
- Product Name:
- IDRA 21
- Synonyms:
-
- IDRA 21
- IDRA 21,7-Chloro-3-methyl-3,4-dihydro-2H-1,2,4-benzothiadiazineS,S-dioxide
- 7-CHLORO-3-METHYL-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE
- 7-CHLORO-3-METHYL-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE 1,1-DIOXIDE
- 7-CHLORO-3-METHYL-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE S,S-DIOXIDE
- IDRA 21,98%
- 7-chloro-3-methyl-3,4-dihydro-2H-benzo[e][1,2,4]thiadiazine 1,1-dioxide
- 7-Chloro-3,4-dihydro-3-methyl-2H-1,2,4-benzothiadiazine 1,1-dioxide
- CAS:
- 22503-72-6
- MF:
- C8H9ClN2O2S
- MW:
- 232.69
- EINECS:
- 1592732-453-0
- Product Categories:
-
- API
- Mol File:
- 22503-72-6.mol
IDRA 21 Chemical Properties
- Melting point:
- 209 °C(Solv: acetic acid (64-19-7))
- Boiling point:
- 405.1±55.0 °C(Predicted)
- Density
- 1.394±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- DMSO (Slightly), Methanol (Slightly, Sonicated)
- form
- Solid
- pka
- 9.78±0.40(Predicted)
- color
- Off-White to Pale Yellow
- InChIKey
- VZRNTCHTJRLTMU-UHFFFAOYSA-N
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
IDRA 21 Usage And Synthesis
Chemical Properties
white to off-white crystalline powder
Uses
IDRA-21 is a benzothiadiazine derivative and a positive allosteric modulator of glutamate AMPA receptors (1,2,3,4). It is able to increase excitatory synaptic strength by inhibiting AMPA receptor desensitization. IDRA 21 may exhibit therapeutic effects to ameliorate memory deficits in patients with cognitive impairments such as Alzheimer''s disease.
Uses
IDRA-21 inhibits AMPA receptor desensitization and enhances cognition by a related mechanism. IDRA-21 is more able to cross the blood-brain barrier than Cyclothiazide (C988960).
Definition
ChEBI: 7-chloro-3-methyl-3,4-dihydro-2H-1$l^{6},2,4-benzothiadiazine 1,1-dioxide is a benzothiadiazine.
Biological Activity
Inhibits AMPA receptor desensitization and enhances cognition by a related mechanism. More able to cross the blood-brain barrier than cyclothiazide (6-Chloro-3,4-dihydro-3-(5-norbornen-2-yl)-2H-1,2,4-benzothiazidiazine-7-sulfonamide-1,1-dioxide ).
storage
Room temperature
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