Weight | 286.331 g/mol |
---|---|
Formula | C16H18N2O3 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Levcromakalim (94470-67-4, 94535-50-9)
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- SINGLE-CHANNEL AND WHOLE-CELL K-CURRENTS EVOKED BY LEVCROMAKALIM IN SMOOTH-MUSCLE CELLS FROM THE RABBIT PORTAL-VEIN (British Journal of Pharmacology, 1993)
- Differential effects of acetylcholine, nitric oxide and levcromakalim on smooth muscle membrane potential and tone in the rabbit basilar artery (British Journal of Pharmacology, 1993)
- Activation by levcromakalim and metabolic inhibition of glibenclamide-sensitive K channels in smooth muscle cells of pig proximal urethra. (British Journal of Pharmacology, 1996)
- Potassium channel modulation in rat portal vein by ATP depletion: a comparison with the effects of levcromakalim (BRL 38227) (British Journal of Pharmacology, 1992)
- BRL 38227 (levcromakalim)-induced hyperpolarization reduces the sensitivity to Ca2+ of contractile elements in canine coronary artery (Naunyn-schmiedebergs Archives of Pharmacology, 1993)
- Levcromakalim may induce a voltage-independent K-current in rat portal veins by modifying the gating properties of the delayed rectifier (British Journal of Pharmacology, 1993)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1(C(C(C2=C(O1)C=CC(=C2)C#N)N3CCCC3=O)O)C
-
InChIKeyTVZCRIROJQEVOT-UHFFFAOYSA-N
- Pubchem - Levcromakalim
- Wikipedia - Cromakalim
Cromakalim (INN) is a potassium channel-opening vasodilator. The active isomer is levcromakalim. It acts on ATP-sensitive potassium channels and so causes membrane hyperpolarization.
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