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Merck

116850

Adenylyl Cyclase Type V Inhibitor, NKY80

The Adenylyl Cyclase Type V Inhibitor, NKY80, also referenced under CAS 299442-43-6, controls the biological activity of Adenylyl Cyclase Type V. This small molecule/inhibitor is primarily used for Cell Signaling applications.

別名:

Adenylyl Cyclase Type V Inhibitor, NKY80, 2-Amino-7-(furanyl)-7,8-dihydro-5(6H)-quinazolinone

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この商品について

実験式(ヒル表記法):
C12H11N3O2
CAS番号:
分子量:
229.23
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
Assay:
≥97% (HPLC)
Form:
solid
Storage condition:
OK to freeze, protect from light
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Quality Segment

assay

≥97% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

pale orange

solubility

DMSO: 200 mg/mL, methanol: 5 mg/mL

shipped in

wet ice

storage temp.

−20°C

SMILES string

Nc1nc2c(cn1)C(=O)CC(C2)c3[o]ccc3

InChI

1S/C12H11N3O2/c13-12-14-6-8-9(15-12)4-7(5-10(8)16)11-2-1-3-17-11/h1-3,6-7H,4-5H2,(H2,13,14,15)

InChI key

SOJUSNIBPPMLCC-UHFFFAOYSA-N

General description

A cell-permeable quinazolinone containing a non-nucleoside compound that acts as a potent, selective inhibitor of adenylyl cyclase (AC) type V isoform (IC50 = 8.3 µM, 132 µM and 1.7 mM for type V, III and II, respectively) in the presence of Gsα GTPγS-Forskolin. Displays ~210-fold greater selectivity for type V over the type II isoform. The inhibition is non-competitive with respect to ATP and Forskolin. Regulates the AC catalytic activity in heart and lung tissues.
A cell-permeable, non-nucleoside compound that acts as a potent, and selective inhibitor of adenylyl cyclase (AC) type V (IC50 = 8.3 µM, 132 µM and 1.7 mM for type V, III and II, respectively) in the presence of G5α GTPγS-Forskolin. Displays ~210-fold greater selectivity for type V over the type II isoform. The inhibition is non-competitive with respect to ATP and Forskolin. Reported to regulate AC catalytic activity in heart and lung tissues.

Biochem/physiol Actions

Cell permeable: yes
Primary Target
Adenylate cyclase (AC) type V isoform
Product does not compete with ATP.
Reversible: no
Target IC50: 8.3 µM, 132 µM and 1.7 mM for type V, III and II, of adenylyl cyclase (AC), respectively, in the presence of Gsα GTPγS-Forskolin

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.

Other Notes

Onda, T., et al. 2001. J. Biol. Chem.276, 47785.

Legal Information

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

Disclaimer

Toxicity: Standard Handling (A)


ピクトグラム

Exclamation mark

注意喚起語

Warning

ハザードコード

Hazard Classifications

Acute Tox. 4 Oral

保管分類

11 - Combustible Solids

WGK

WGK 3

引火点 (F)

Not applicable

引火点(°C)

Not applicable



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