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Product Details

BML-288 | PDE2 inhibitor

BML-288 (851-55-3) is a potent and selective inhibitor of phosphodiesterase PDE2, IC50 = 40 nM. More potent than EHNA, another commonly used PDE2 inhibitor. Displays no effect on a panel of over 80 receptors, ion channels and enzymes.1 Cell permeable.

References/Citations

1) Chambers et al. (2006), A new chemical tool for exploring the physiological function of the PDE2 isozyme; Bioorg. Med. Chem. Lett., 16 307

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Focus Biomolecules cell signaling reagent supplier, chemical structure of BML-288 | PDE2 inhibitor | CAS 851-55-3

Catalog#  10-1319

$55.00
Quantity
Please note that we do not sell to individuals and that all orders placed by non-research organizations will incur a $20 restocking/refund fee.
 
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CAS:
851-55-3
Catalog Number:
10-1319
Activity:
PDE2 inhibitor
Chemical Name:
6,7-Dihydro-5-methyl-6-oxo-N-(1,3,4-thiadiazol-2-yl)-5H-furo[2,3-f]indole-7-carboxamide
Molecular Weight:
314.32
Molecular Formula:
C14H10N4O3S
Solubility:
Soluble in DMSO (up to 25 mg/ml)
Physical Properties:
Off-white solid
Purity:
98% by TLC
NMR (Conforms)
Storage Temperature:
-20°C (des.)
Stability:
Stable for 1 year as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
Shipping Code:
RT
Materials provided by Focus Biomolecules are for laboratory research use only and are not intended for human or veterinary applications.

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