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.

• Szinonimák: Adenylyl Cyclase Type V Inhibitor, NKY80, 2-Amino-7-(furanyl)-7,8-dihydro-5(6H)-quinazolinone
• Tapasztalati képlet (Hill-képlet): C₁₂H₁₁N₃O₂
• CAS-szám: 299442-43-6
• Molekulatömeg: 229.23
• UNSPSC Code: 12352200
• NACRES: NA.77
• MDL number: MFCD02026323

Tulajdonságok

• Termék neve: 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.
• Quality Level: 100
• 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
• 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

Leírás

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

Disclaimer

Toxicity: Standard Handling (A)

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 G_sα 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.

Other Notes

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

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

Biztonsági adatok

• pictograms: GHS07
• signalword: Warning
• hcodes: H302
• pcodes: P264 - P270 - P301 + P312 - P501
• Hazard Classifications: Acute Tox. 4 Oral
• Tárolási osztály: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable