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Merck

5.08957

PDE5 Inhibitor, Cpd7a

Synonym(s):

PDE5 Inhibitor, Cpd7a

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About This Item

Empirical Formula (Hill Notation):
C22H20ClN3O2
CAS Number:
Molecular Weight:
393.87
MDL number:
NACRES:
NA.77
UNSPSC Code:
12352200
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assay

≥98% (HPLC)

form

solid

potency

270 pM IC50

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

color

cream

solubility

DMSO: 100 mg/mL

storage temp.

2-8°C

Quality Level

Biochem/physiol Actions

Primary Target
PDE5
Reversible: yes

Disclaimer

Toxicity: Standard Handling (A)

General description

A cell-permeable, brain permeant, quinoline-based compound that acts as a highly potent and selective inhibitor of phosphodiesterase 5 (PDEV; IC50 = 270 pM). Exhibits over 10,000 fold greater selectivity over various other phosphodiestrases and trivial activity against PDE VI (IC50 = 339 nM). Shown to increase cGMP levels in mouse hippocampus and attenuates long term potentiation and memory defects in mice with elevated levels of oligomeric Aβ42. It is rapidly absorbed with peak plasma concentration observed at 30 min. Displays desirable pharmacokinetic properties with plasma t1/2 = 1.33 h and brain t1/2 = 1.04 h.

Please note that the molecular weight for this compound is batch-specific due to variable water content.

Other Notes

Fiorito, J., et al. 2013. Eur. J. Med. Chem.60, 285.

Packaging

Packaged under inert gas

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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