JTV-506
JTV-506 is a potent ATP-sensitive potassium channel opener. JTV-506 inhibits Histamine (HY-B1204)-induced contraction of tracheal smooth muscle by activation of KATP channels. JTV-506 attenuates pulmonary vascular tone through its direct action on vascular smooth muscle cells. JTV-506 can be used for pulmonary hypertension research.
For research use only. We do not sell to patients.
- CAS No.: 170148-29-5
- Formula: C19H22N4O5
- Molecular Weight:386.40
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
JTV-506 (1 nM-100 μM, 15 min) causes a concentration-dependent inhibition of Histamine-induced contraction in guinea-pig isolated tracheal smooth muscle, and is antagonized by Glibenclamide (HY-15206)[1].
JTV-506 (1 nM-100 μM) relaxes norepinephrine-preconstricted, endothelium-intact arteries from Monocrotaline (MCT) (HY-N0750)-treated and control rats[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 170148-29-5
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Molecular Weight 386.40
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Formula C19H22N4O5
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SMILES
N#CC1=CC=C2C([C@@H](NC(C=C3)=NN(C)C3=O)[C@H](O)C(COC)(COC)O2)=C1
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
[1]. Ando T, et al. Effects of JTV-506, a new K+ channel activator, on airway smooth muscle contraction and systemic blood pressure. Clin Exp Allergy. 1997 Jun;27(6):705-13. [Content Brief]
[2]. Tsutsumi Y, et al. JTV-506, a new K(ATP) channel opener, relaxes pulmonary artery isolated from monocrotaline-treated pulmonary hypertensive rats. J Anesth. 2004;18(3):210-5. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)