10 Results for "

T-channel

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "T-channel" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-W032013
CAS No.: 111-87-5
Synonyms: Octanol
1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents . 1-Octanol is a highly attractive biofuel with diesel-like properties .
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1
1 Cited Publications
Cat. No.: HY-115681
CAS No.: 68682-01-9
Purity:  99.88%
Synonyms: 6-Prenylnaringenin; (±)-6-Prenylnaringenin
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

(2R/S)-6-PNG (6-Prenylnaringenin) is a potent and reversible Cav3.2 T-type Ca 2+ channels (T-channels) blocker. (2R/S)-6-PNG can penetrate the blood-brain barrier (BBB). (2R/S)-6-PNG suppresses neuropathic and visceral pain in mice .
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Cat. No.: HY-W032013S1
CAS No.: 78510-02-8
Synonyms: Octanol-d2
1-Octanol-d2 is the deuterium labeled 1-Octanol . 1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents . 1-Octanol is a highly attractive biofuel with diesel-like properties .
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Cat. No.: HY-W032013R
CAS No.: 111-87-5
Synonyms: Octanol (Standard)
1-Octanol (Standard) is the analytical standard of 1-Octanol. This product is intended for research and analytical applications. 1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents . 1-Octanol is a highly attractive biofuel with diesel-like properties .
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Cat. No.: HY-W032013S
CAS No.: 153336-13-1
Synonyms: Octanol-d17
1-Octanol-d17 is the deuterium labeled 1-Octanol . 1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents . 1-Octanol is a highly attractive biofuel with diesel-like properties .
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Cat. No.: HY-151451
CAS No.: 2878598-92-4
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Cav 3.2 inhibitor 2 is a Cav3.2 T-type Ca 2+ channels inhibitor with an IC50 of 0.09339 μM under -80mV holding potential. Cav 3.2 inhibitor 2 potently suppresses T-channel-dependent somatic and visceral pain in mice. Cav 3.2 inhibitor 2 can be used for the research of intractable pain .
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Cat. No.: HY-W032013S2
CAS No.: 1335435-64-7
Synonyms: Octanol-d2-1
1-Octanol-d2-1 is deuterated labeled 1-Octanol (HY-W032013). 1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents . 1-Octanol is a highly attractive biofuel with diesel-like properties .
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Cat. No.: HY-W032013S3
CAS No.: 3028869-76-0
Synonyms: Octanol-d5
1-Octanol-d5 is deuterated labeled 1-Octanol (HY-W032013). 1-Octanol (Octanol), a saturated fatty alcohol, is a T-type calcium channels (T-channels) inhibitor with an IC50 of 4 μM for native T-currents . 1-Octanol is a highly attractive biofuel with diesel-like properties .
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Cat. No.: HY-115681R
CAS No.: 68682-01-9
Synonyms: 6-Prenylnaringenin (Standard); (±)-6-Prenylnaringenin (Standard)
Research Areas:  

Neurological Disease

(2R/S)-6-PNG (Standard) is the analytical standard of (2R/S)-6-PNG. This product is intended for research and analytical applications. (2R/S)-6-PNG (6-Prenylnaringenin) is a potent and reversible Cav3.2 T-type Ca2+ channels (T-channels) blocker. (2R/S)-6-PNG can penetrate the blood-brain barrier (BBB). (2R/S)-6-PNG suppresses neuropathic and visceral pain in mice .
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Cat. No.: HY-B1167A
CAS No.: 4410-48-4
Synonyms: Cardiorythmine hydrochloride; (+)-Ajmaline hydrochloride
Ajmaline hydrochloride is a Class Ia antiarrhythmic agent. It inhibits HERG potassium channels with IC50s of 1.0 μmol/l and 42.3 μmol/l in HEK cells and moth spider oocytes respectively. The inhibitory effect of Ajmaline hydrochloride is rapid, reversible, and positive frequency dependent. It acts primarily on the open state of the HERG channel and may also be combined with the inactivated state. The inhibitory effect of ajmaline hydrochloride is dependent on aromatic residues in the S6 domain, and the sensitivity is significantly reduced in the inactivation-deficient HERG S620T channel. It can also slightly affect the activation voltage of HERG channels. Ajmaline hydrochloride's inhibitory effect on HERG channels may contribute to both its potent antiarrhythmic effects and its potential proarrhythmic risk.
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