a5IA

目录号: A14343

Benzodiazepine agonist

a5IA

a5IA Chemical Structure

CAS NO. 215874-86-5

a5IA is a nootropic drug invented in 2004 by a team working for Merck, Sharp and Dohme, which acts as a subtype-selective inverse agonist at the benzodiazepine binding site on the GABAA receptor.

库存: 现货

规格 价格 数量
10 mg
¥ 1,500.00
25 mg
¥ 3,000.00
50 mg
¥ 5,000.00
Warning 产品仅用于科学研究,不针对患者销售,望谅解.

详情

a5IA is a nootropic drug invented in 2004 by a team working for Merck, Sharp and Dohme, which acts as a subtype-selective inverse agonist at the benzodiazepine binding site on the GABAA receptor.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 27.6 mL 137.99 mL 275.98 mL
0.5 mM 5.52 mL 27.6 mL 55.2 mL
1 mM 2.76 mL 13.8 mL 27.6 mL
5 mM 0.55 mL 2.76 mL 5.52 mL

*The above data is based on the productmolecular weight 362.34546. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

目录号 A14343
MECHANISM OF ACTION Agonist
M. Wt 362.34546
Formula C17H14N8O2
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 215874-86-5
Synonyms N/A
SMILES CC1=CC(=NO1)C2=NN=C3N2N=C(C4=CC=CC=C43)OCC5=CN(N=N5)C

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