IDRA 21

IDRA 21

제품명 IDRA 21
CAS 번호 22503-72-6
분자식 C8H10N2O2S
분자량 198.24 g/mol
외관 흰색에서 미백색의 결정성 분말
순수함 ≥98% (HPLC)
용해도 Soluble in DMSO, methanol; slightly soluble in water
저장 Store at -20°C, protected from light
패키지 10 mg, 50 mg, 100 mg, 500 mg, 1 g

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IDRA 21 Structure

동의어: IDRA 21, 7,8-dihydro-8-oxo-7-(2-hydroxyethyl)-9H-purine-6-carboxaldehyde, 7,8-dihydro-8-oxo-7-(2-hydroxyethyl)guanine, 8-oxo-7-(2-hydroxyethyl)guanine, 22503-72-6

IDRA 21 is a synthetic purine derivative that has garnered attention in neuropharmacology as a positive allosteric modulator of the AMPA receptor. Its chemical structure, featuring a 7,8-dihydro-8-oxo-purine core with a 2-hydroxyethyl side chain, distinguishes it from other AMPA receptor modulators and contributes to its unique pharmacological profile. While not a natural product, IDRA 21 is often studied alongside endogenous purines due to its structural similarity to guanine derivatives.

Initially identified through screening efforts aimed at finding cognitive enhancers, IDRA 21 has become a valuable tool compound for investigating glutamatergic signaling. Unlike direct AMPA receptor agonists, it modulates receptor activity by slowing desensitization, thereby enhancing synaptic responses without inducing excitotoxicity. This mechanism has positioned it as a candidate for addressing cognitive deficits in neurological disorders.

In research settings, IDRA 21 is primarily used to probe the role of AMPA receptors in learning and memory processes. Its ability to cross the blood-brain barrier and its favorable pharmacokinetic profile in animal models make it a subject of interest for preclinical studies. While not yet approved for clinical use, IDRA 21 continues to be a reference compound in the development of next-generation cognitive enhancers.

Function

  • AMPA receptor potentiation: Enhances glutamate-induced currents by reducing receptor desensitization.
  • Cognitive enhancement: Improves performance in various animal models of learning and memory.
  • 신경 보호: May protect against excitotoxic damage under certain conditions.
  • Synaptic plasticity modulation: Influences long-term potentiation (LTP) and long-term depression (LTD).
  • Research tool: Widely used to study glutamatergic transmission in vitro and in vivo.

Source & Standardization

  • Source: Synthetic chemical synthesis
  • Extraction: Not applicable (synthetic)
  • Standardization: ≥98% purity by HPLC
  • Forms: Crystalline powder
  • 응용 분야: Neuropharmacology research, cognitive enhancement studies, AMPA receptor research

사양

매개변수 사양
분석법 (HPLC) ≥98.0%
식별 NMR, MS conform to structure
건조 손실 ≤0.5%
소각 잔류물 ≤0.1%
중금속 ≤10 ppm
Microbial Limits Total aerobic count ≤1000 CFU/g

Documentation & Supply

  • Monthly capacity: 10 kg
  • 리드 타임: 3-5 business days (stock items)
  • 문서: COA, MSDS, TDS available upon request
  • 포장: Amber glass vials or aluminum foil bags

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