DRA-21 is a positive allosteric modulator of the AMPA receptor and a benzothiadiazine derivative. It is a chiral molecule, with-IDRA-21 being the active form. IDRA-21 shows nootropic effects in animal studies, significantly improving learning and memory .
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 alprazolam or scopolamine, and produces sustained effects lasting for up to 48 hours after a single dose.
Investigational New Drug , Most distributors or contact manufacturers import from Chinese pharmaceutical factory or agent as an API.
White to off-white solid powder.
IDRA-21’s primary benefit is a dramatic improvement in learning and memory. It significantly outperformed aniracetam and is approximately 10-30x more potent at reversing cognitive deficits caused by scopolamine and alprazolam. In addition, IDRA-21 benefits last for up to three days after just one dose.
IDRA-21 is also thought to induce long-term potentiation (LTP). LTP is a long-lasting enhancement in how neurons communicate within the brain. It is vital for improving synaptic plasticity, which strengthens synapses within the brain. As synapses are largely responsible for memories, enhancing their strength and function is vital to improving overall cognition.
Dosage and Stack
One dose of IDRA-21 may last up to 3 days. It is difficult to say what doses are suitable for humans. However, nootropics advise consumers to take a maximum of 5-25 mg.
Dosage form application
- Pure powder form without excipients for research use.
- Tablet or capsule for prescription use.
IDRA-21 should not be taken with other ampakine medicines, such as aniracetam. Nootropics that increase glutamate levels should be avoided in conjunction with IDRA-21.
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