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Merck

SML0439

Sigma-Aldrich

MBCQ

≥98% (HPLC)

Sinónimos:

4-((3,4-Methylenedioxybenzyl)amino)-6-chloroquinazoline

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About This Item

Fórmula empírica (notación de Hill):
C16H12ClN3O2
Número de CAS:
Peso molecular:
313.74
MDL number:
UNSPSC Code:
41106305
PubChem Substance ID:
NACRES:
NA.77

Quality Level

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 5 mg/mL (clear solution)

storage temp.

2-8°C

SMILES string

Clc1ccc2ncnc(NCc3ccc4OCOc4c3)c2c1

InChI

1S/C16H12ClN3O2/c17-11-2-3-13-12(6-11)16(20-8-19-13)18-7-10-1-4-14-15(5-10)22-9-21-14/h1-6,8H,7,9H2,(H,18,19,20)

InChI key

CNODHOSDWZLJGA-UHFFFAOYSA-N

Biochem/physiol Actions

MBCQ is selective inhibitor of cGMP-specific phosphodiesterase PDE V; IC50=19 nM.

Features and Benefits

This compound is a featured product for Cyclic Nucleotide research. Click here to discover more featured Cyclic Nucleotide products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Phosphodiesterases page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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American journal of physiology. Cell physiology, 309(5), C332-C347 (2015-06-26)
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Artículos

Cyclic nucleotide phosphodiesterases (PDEs) catalyze the hydrolysis of cAMP and/or cGMP. There are 11 different mammalian PDE families.

Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.

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