vasorelaxant

(±)-Naringenin (Naringenine) is a natural product. It displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes.

Caroverine hydrochloride (Caroverine HCL) is a potent, competitive and reversible antagonist of NMDA and AMPA glutamate receptor. It is also an antioxidant and calcium-blocking agent that exhibits vasorelaxant action, and can be used for the research of inner ear tinnitus.

Vasorelaxant agent-1 (Compound 2j) is a vasodilator capable of crossing the blood-brain barrier. It exhibits remarkable vasodilatory activity with an EC50 of 0.02916 μM. Vasorelaxant agent-1 is non-carcinogenic and may be utilized in hypertension research.

Methyl cinnamate, a tyrosinase inhibitor and a flavoring compound, has antimicrobial, antiadipogenic, vasorelaxant, and anti-inflammatory effects.

Ethyl cinnamate has antifungal, and vasorelaxant effects. Ethyl cinnamate can lead to the damage of cell membrane system and metabolic disorder through inducing lipid peroxidation via initiating ROS overproduction. Ethyl cinnamate can inhibit the tonic contractions induced by high K+ and phenylephrine (PE) in a concentration-dependent manner, with respective IC50 values of 0.30 mM and 0.38 mM.

Harmalol hydrochloride (Harmidol hydrochloride) is a β-carboline alkaloid that can be extracted from the seeds of Peganum harmala L. Harmalol hydrochloride is the major metabolite of Harmaline and significantly inhibits dioxin-mediated induction of CYP1A1 at both transcriptional and post-translational levels. Harmalol hydrochloride showed vasorelaxant activity in isolated rat thoracic aortic preparations preconstricted with phenylephrine or KCl. Harmalol hydrochloride has antioxidant activity.

Win 58237 is an inhibitor of cyclic nucleotide phosphodiesterase (PDE) (Ki: 170 nM for PDE V), with vasorelaxant activity.

4-Octyl itaconate-Bn-S-NH2 (Compound 8b) functions as a vasorelaxant. It releases H₂S slowly and steadily, helping to reduce oxidative stress through antioxidant reactions that depend on Nrf2 activation. It also inhibits the generation of intracellular ROS and cytotoxicity caused by H₂O₂ damage and activates the potassium channel. This compound is applicable in hypertension research.

GS 389 is a novel tetrahydroisoquinoline analog with vasorelaxant properties. GS-389 significantly inhibited cGMP phosphodiesterase from the rabbit brain and increased cGMP levels in the rat aorta.

Quercetin 3,7-dimethyl ether is a flavonoid compound that exhibits pharmacological potential as a vasorelaxant and possesses anti-inflammatory and analgesic effects in inhibiting LPS-induced inflammation.

Euxanthone (1,7-Dihydroxyxanthone), an xanthone derivative extracted from the roots of Polygala tenuifolia Willd, has antitumour, neuroprotective and vasorelaxant activities, and attenuates Aβ1-42-induced oxidative stress and apoptosis by inducing autophagy.SB-674042 is used for the treatment of depression.SB-674042 is used for the treatment of depression.SB-674043 is used for the treatment of depression.SB-674044 is used for the treatment of depression.SB-674045 is used for the treatment of depression. 2A (BU-1) cell differentiation.

Isograndifoliol is a chemical compound that acts as a selective inhibitor of butyrylcholinesterase (BChE) with an IC50 value of 0.9 μM and exhibits moderate inhibition of acetylcholinesterase (AChE) with an IC50 value of 342.9 μM. Additionally, it demonstrates vasorelaxant and anti-tumor effects. This compound is utilized in research targeting dementia associated with neurodegenerative diseases.

(R)-IDHP, an isomer of IDHP and a metabolite of salvia, exhibits vasorelaxant properties by inhibiting calcium (Ca 2+) release and inward flow through both voltage-dependent and receptor-operated calcium channels in vascular smooth muscle cells. It is utilized in cardiovascular disease research [1].

ANP (1-30), frog, a peptide fragment sourced from atrial natriuretic peptide of frog origin, exhibits natriuretic, diuretic, and vasorelaxant properties.

Villocarine A, an indole alkaloid with natural vasorelaxant properties [1], is a chemical compound known for its ability to relax blood vessels.

(+)-Osbeckic acid, extracted from Tartary Buckwheat, acts as a vasorelaxant and demonstrates a significant vasorelaxant effect in Sprague-Dawley rat thoracic aorta rings, with an EC50 value of 887 μM [1].

Ethyl Cinnamate (Standard) is the certified analytical standard of Ethyl cinnamate intended for research and analytical applications, and Ethyl cinnamate is an orally active constituent of Kaempferia galanga rhizomes that exhibits anticancer, nematocidal, sedative, vasorelaxant, fragrance, and tissue-clearing properties, suppresses colorectal tumor growth via VEGFR2 pathway–mediated anti-angiogenesis, and inhibits high potassium- and phenylephrine-induced tonic contractions in rat aorta with IC50 values of 0.30 mM and 0.38 mM, respectively.

Uvaol (Standard) is a reference standard for research and analysis in studies involving Uvaol. Uvaol is present in olives and virgin olive oil with anti-inflammatory, anti-proliferative, and vasorelaxant activities.

(±)-Naringenin (Standard) is a reference standard for research and analysis in studies involving (±)-Naringenin. (±)-Naringenin (Naringenine) is a natural product. It displays vasorelaxant effect on endothelium-denuded vessels via the activation of BKCa channels in myocytes.

Evocarpine shows antimycobacterial, and vasorelaxant effects, it can inhibit Ca2+ influx through voltage-dependent calcium channels.

Ayanin has vasorelaxant activity, it also may have the potential for use in treating allergic asthma.The IC(50) value of Ayanin (quercetin-3,7,4'-O-trimethylether) is 2.2microM for inhibiting interleukin (IL)-4 production from purified basophils.

Cistanoside F is a natural phenylethanol glycoside exhibiting antioxidant activity, capable of scavenging superoxide anion radicals (O₂⁻).

Uvaol is present in olives and virgin olive oil with anti-inflammatory, anti-proliferative, and vasorelaxant activities.

ent-3-Acetoxy-labda-8(17),13-dien-15-oic acid have vasorelaxant and hypotensive actions, the mechanisms underlying the cardiovascular actions of the labdane involve the activation of the endothelial NO-cGMP pathway, the opening of K+ channels and the alteration on Ca2+ mobilization.