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TAK-071

Chemical Structure : TAK-071

CAS No.: 1820812-16-5

TAK-071 (TAK071;TAK 071)

Catalog No.: PC-35576Not For Human Use, Lab Use Only.

TAK-071 (TAK071) is a potent, selective, low cooperativity (α-value) positive allosteric modulator of muscarinic M1 receptor with inflection point of 2.7 nM in Ca2+ flux assays in CHO-K1 cells.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

TAK-071 (TAK071) is a potent, selective, low cooperativity (α-value) positive allosteric modulator of muscarinic M1 receptor with inflection point of 2.7 nM in Ca2+ flux assays in CHO-K1 cells.
TAK-071 displays >370-fold M1R selectivity over other muscarinic receptors.
TAK-071 selectively induces afterdepolarization in prefrontal cortical pyramidal neurons significantly ameliorates scopolamine-induced cognitive deficits in rats combined with acetylcholinesterase inhibitor donepezil, with minimizing peripheral cholinergic side effects.

Physicochemical Properties

M.Wt 421.472
Formula C24H24FN3O3
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

4-fluoro-2-[(3S,4S)-4-hydroxytetrahydro-2H-pyran-3-yl]-5-methyl-6-[4-(1H-pyrazol-1-yl)benzyl]-2,3-dihydro-1H-isoindol-1-one

References

1. Sako Y, et al. Neuropsychopharmacology. 2018 Aug 1. doi: 10.1038/s41386-018-0168-8.

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