Nootropics Powder CAS 22503-72-6 Idra 21 Improve Memory API Smart Drug

Product Details:

Place of Origin: China
Brand Name: Changland
Certification: GMP&ISO
Model Number: 22503-72-6

Payment & Shipping Terms:

Price: usd 340 per 100 gram;usd 2900 per 1 kg
Packaging Details: 1KG per foil bag, 25KG per drum.
Delivery Time: 5 working days
Payment Terms: MoneyGram, Western Union, T/T, D/P, D/A, L/C

Description

Nootropics Powder CAS 22503-72-6 Idra 21 Improve Memory API Smart Drug

Description

Cas: 22503-72-6 MF: C8H9ClN2O2S
MW: 232.69 Origin: China
Density: 1.394±0.06 G/cm3(Predicted) EINECS NO.: 200-184-4
Melting Point: 209 °C(Solv: Acetic Acid (64-19-7)) Boiling Point: 405.1±55.0 °C(Predicted)
High Light:

Nootropics Powder CAS 22503-72-6

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Idra 21 Nootropics Powder

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Improve Memory API Nootropics Powder

 

Factory Supplies Nootropics Powder CAS 22503-72-6 Idra 21 Improve Memory API Smart Drug

Product introduction

Product name Idra 21
CAS No. 22503-72-6
MF C8H9ClN2O2S
MW 232.69
Origin China
Appearance White powder
Sample Available
Boiling Point 405.1±55.0 °C(Predicted)

 

What is IDRA-21?
IDRA-21 is a relatively new nootropic compound. It works as an ampakine stimulant drug and is currently being researched in regards to its effects in memory improvement, cognitive enhancement, stimulation, and reversing cognitive deficits.

IDRA-21 Benefits
1. Increases in cognitive ability.
2. Increased accuracy when completing tasks.
3. Increases in short term memory.
4. IDRA-21 can potentially treat schizophrenia.
5. IDRA-21 can possibly be a treatment for depression.
6. IDRA-21 has a neuroprotective effect, so it can protect the brain from age-related cognitive defects.
7. Increased alertness and wakefulness.

IDRA-21 Mode of Action
IDRA-21 shows nootropic effects in animal studies, significantly improving learning and memory. It is around 10-30 times more potent than aniracetam in reversing cognitive deficits induced by orscopolamine,and produces sustained effects lasting for up to 48 hours after a single dose.The mechanism for this action is thought to be through promoting the induction of long-term potentiation between synapses in the brain.

IDRA-21 does not produce neurotoxicity under normal conditions,although it may worsen neuronal damage following global ischemia after stroke or seizures.

In comparison to the benzoylpiperidine derived ampakine drugs, IDRA-21 was more potent than CX-516, but less potent than CX-546. Newer benzothiadiazide derivatives with greatly increased potency compared to IDRA-21 have been developed,but these have not been researched to the same extent, with the benzoylpiperidine and benzoylpyrrolidine CX-series of drugs being favoured for clinical development, most likely due to more favourable toxicity profiles at high doses.

IDRA-21 Dosage
Although there are currently no published clinical studies that focus on the dosage for human consumption, there are several peer-review online sites that suggest positive experiences when IDRA-21 is taken orally. The suggested to promote cognitive function are at 5-25mg.