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TAK-915 

Cat. No. M28520

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TAK-915  Structure

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Quality Control & Documentation
Biological Activity

TAK-915 is a potent, selective, brain-penetrant and orally active phosphodiesterase 2A (PDE2A) inhibitor with an IC50 of 0.61 nM. TAK-915 is >4100-fold more selectivity for PDE2A than PDE1A. TAK-915 has the potential for neuropsychiatric and neurodegenerative disorders treatment.

Chemical Information
Molecular Weight 458.36
Formula C19H18F4N4O5
CAS Number 1476727-50-0
Form Solid
Solubility (25°C) DMSO 7.5 mg/mL (ultrasonic and warming and heat to 60°C)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Masato Nakashima, et al. Behav Brain Res. TAK-915, a phosphodiesterase 2A inhibitor, ameliorates the cognitive impairment associated with aging in rodent models

[2] Masato Nakashima, et al. J Pharmacol Exp Ther. Phosphodiesterase 2A Inhibitor TAK-915 Ameliorates Cognitive Impairments and Social Withdrawal in N-Methyl-d-Aspartate Receptor Antagonist-Induced Rat Models of Schizophrenia

[3] Satoshi Mikami, et al. Chem Pharm Bull (Tokyo). Discovery of a Novel Series of Pyrazolo[1,5-a]pyrimidine-Based Phosphodiesterase 2A Inhibitors Structurally Different from N-((1S)-1-(3-Fluoro-4-(trifluoromethoxy)phenyl)-2-methoxyethyl)-7-methoxy-2-oxo-2,3-dihydropyrido[2,3-b]pyrazine-4(1H)-carboxamide (䲧瘀Ỵ瘁㧀痿羹皘的얨څţڅĀ�皚

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  Catalog
Abmole Inhibitor Catalog




Keywords: TAK-915  supplier, PDE, inhibitors, activators

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