11 Results for "

neuronal depolarization

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "neuronal depolarization" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-B0517
CAS No.: 96-88-8
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization .
loading...
    loading...
1
1 Cited Publications
Cat. No.: HY-B0517A
CAS No.: 1722-62-9
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

Mepivacaine hydrochloride binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization .
loading...
    loading...
Cat. No.: HY-101765
CAS No.: 1092502-33-4
Purity:  99.91%
GW 833972A is a selective CB₂ receptor agonist with pEC₅₀ of the human CB₂ receptor for GW 833972A of 7.3, and its selectivity for the CB₂ receptor is approximately 1000 times higher than that for the CB₁ receptor. GW 833972A inhibits induced neuronal depolarization and suppresses coughing caused by citric acid in guinea pig models. GW 833972A can be used for the study of chronic cough .
loading...
    loading...
Cat. No.: HY-178963
CAS No.: 7469-49-0
Research Areas:  

Neurological Disease

Nav1.2-IN-2 is a Nav1.2 inhibitor with a human IC50 of 0.18 μM. Nav1.2-IN-2 preferentially binds to the inactivated state of Nav1.2, reduces window current, suppresses neuronal depolarization and action potential generation. Nav1.2-IN-2 suppresses Veratridine (HY-N6691)-induced Ca 2+ influx. Nav1.2-IN-2 can be used for the research of epilepsy .
loading...
    loading...
Cat. No.: HY-119961
CAS No.: 24358-84-7
Purity:  99.72%
Synonyms: Dexivacaine; (S)-Mepivacaine
Target:  

Sodium Channel

Research Areas:  

Cardiovascular Disease

(+)-Mepivacaine is a racemic isomer of Mepivacaine (HY-B0517), which has analgesic and vasoconstrictive activity. Mepivacaine is an amide type agent that temporarily causes local loss of consciousness. Mepivacaine binds to specific voltage-gated sodium channels on neuronal cell membranes, inhibiting sodium influx and membrane depolarization .
loading...
    loading...
Cat. No.: HY-B0517S
CAS No.: 1346597-90-7
Mepivacaine-d3 is the deuterium labeled Mepivacaine. Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization .
loading...
    loading...
Cat. No.: HY-B0517R
CAS No.: 96-88-8
Research Areas:  

Neurological Disease

Mepivacaine (Standard) is the analytical standard of Mepivacaine. This product is intended for research and analytical applications. Mepivacaine is an amide-type local anesthetic agent. Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization .
loading...
    loading...
Cat. No.: HY-135131
CAS No.: 301-15-5
Target:  

iGluR

Research Areas:  

Neurological Disease

Synthalin hydrochloride is a K+ channel blocker with neuronal excitability modulating activity. Synthalin hydrochloride has an effect on NMDA-mediated depolarization, possibly through receptor-mediated modulation of L-glutamate and serotonin (5-HT). The use of Synthalin hydrochloride can enhance the understanding of changes in membrane potential of different neurons and help study the role of polyamines in neuronal excitability .
loading...
    loading...
Cat. No.: HY-B0517AR
CAS No.: 1722-62-9
Research Areas:  

Neurological Disease

Mepivacaine (hydrochloride) (Standard) is the analytical standard of Mepivacaine (hydrochloride). This product is intended for research and analytical applications. Mepivacaine hydrochloride binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization .
loading...
    loading...
Cat. No.: HY-180365
CAS No.: 667905-37-5
GW 833972A free base is a selective CB₂ receptor agonist with pEC₅₀ of the human CB₂ receptor for GW 833972A free base of 7.3, and its selectivity for the CB₂ receptor is approximately 1000 times higher than that for the CB₁ receptor. GW 833972A free base inhibits induced neuronal depolarization and suppresses coughing caused by citric acid in guinea pig models. GW 833972A free base can be used for the study of chronic cough .
loading...
    loading...
Cat. No.: HY-101765R
CAS No.: 1092502-33-4
GW 833972A (Standard) is the analytical standard of GW 833972A (HY-101765). This product is intended for research and analytical applications. GW 833972A is a selective CB₂ receptor agonist with pEC₅₀ of the human CB₂ receptor for GW 833972A of 7.3, and its selectivity for the CB₂ receptor is approximately 1000 times higher than that for the CB₁ receptor. GW 833972A inhibits induced neuronal depolarization and suppresses coughing caused by citric acid in guinea pig models. GW 833972A can be used for the study of chronic cough .
loading...
    loading...
  • 1