IDRA 21

IDRA 21 Structure
CAS No.
22503-72-6
Chemical Name:
IDRA 21
Synonyms
AMPAKINE;IDRA 21;IDRA 21,98%;S-18986 IDRA-21 AMPAKINE;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-...;7-CHLORO-3-METHYL-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE S,S-DIOXIDE;7-CHLORO-3-METHYL-3,4-DIHYDRO-2H-1,2,4-BENZOTHIADIAZINE 1,1-DIOXIDE;7-Chloro-3,4-dihydro-3-methyl-2H-1,2,4-benzothiadiazine 1,1-dioxide;IDRA 21 Benzothiadiazine,7-chloro- 3,4-dihydro-3-methyl-,1,1- dioxide
CBNumber:
CB3468324
Molecular Formula:
C8H9ClN2O2S
Molecular Weight:
232.69
MOL File:
22503-72-6.mol
MSDS File:
SDS
Modify Date:
2024/6/15 22:11:33

IDRA 21 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

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
Safety Statements  24/25
WGK Germany  3

IDRA 21 price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) I5773 IDRA 21 ≥98% 22503-72-6 5MG ₹24183.05 2022-06-14 Buy
Product number Packaging Price Buy
I5773 5MG ₹24183.05 Buy

IDRA 21 Chemical Properties,Uses,Production

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.

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 ).

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IDRA 21 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 2H-1,2,4-Benzothiadiazine,7-chloro-3,4-dihydro-3-Methyl-, 1,1-dioxide 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 1,1-... IDRA 21 Benzothiadiazine,7-chloro- 3,4-dihydro-3-methyl-,1,1- dioxide AMPAKINE S-18986 IDRA-21 AMPAKINE 22503-72-6 Ligand-Gated Ion Channels Ion Channels Ionotropic Glutamate Receptor Modulators Cell Signaling and Neuroscience Cell Biology BioChemical API