319 Results for "

Calcium/Sodium Channel Blocker

" in MedChemExpress (MCE) Product Catalog:
Products (319)

319 Results for "Calcium/Sodium Channel Blocker" in MCE Product Catalog:

91
91 Publications Verification
Cat. No.: HY-A0064
CAS No.: 152-11-4
Synonyms: (±)-Verapamil hydrochloride; CP-16533-1 hydrochloride
Verapamil hydrochloride ((±)-Verapamil hydrochloride) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil hydrochloride also inhibits CYP3A4. Verapamil hydrochloride has the potential for high blood pressure, heart arrhythmias and angina research .
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91
91 Publications Verification
Cat. No.: HY-14275
CAS No.: 52-53-9
Purity:  98.96%
Synonyms: (±)-Verapamil; CP-16533-1
Verapamil ((±)-Verapamil) is a calcium channel blocker and a potent and orally active first-generation P-glycoprotein (P-gp) inhibitor. Verapamil also inhibits CYP3A4. Verapamil has the potential for high blood pressure, heart arrhythmias and angina research .
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30
30 Cited Publications
Cat. No.: HY-13519
CAS No.: 289905-88-0
Purity:  99.73%
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

TRAM-34 is a highly selective blocker of intermediate-conductance calcium-activated K + channel (IKCa1) (Kd=20 nM).
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29
29 Cited Publications
Cat. No.: HY-B0284
CAS No.: 21829-25-4
Synonyms: BAY-a-1040
Research Areas:  

Cardiovascular Disease Cancer

Nifedipine (BAY-a-1040) is a potent calcium channel blocker and agent of choice for cardiac insufficiencies.
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27
27 Cited Publications
Cat. No.: HY-13750
CAS No.: 60940-34-3
Purity:  99.58%
Synonyms: SPI-1005; PZ-51; CCG-39161
Ebselen (SPI-1005), a glutathione peroxidase mimetic, is a potent voltage-dependent calcium channel (VDCC) blocker . Ebselen potently inhibits M pro (IC50=0.67 μM) and COVID-19 virus (EC50=4.67 μM) .Ebselen is an inhibitor of HIV-1 capsid CTD dimerization. Ebselen, an organoselenium compound, can permeate the blood-brain barrier and has anti-inflammatory, antioxidant and anticancer activity .
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15
15 Cited Publications
Cat. No.: HY-B0317
CAS No.: 88150-42-9
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Cancer

Amlodipine, an antianginal agent and an orally active dihydropyridine calcium channel blocker, works by blocking the voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium. Amlodipine can be used for the research of high blood pressure and cancer .
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15
15 Cited Publications
Cat. No.: HY-B0317B
CAS No.: 111470-99-6
Synonyms: Amlodipine benzenesulfonate
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Cancer

Amlodipine besylate (Amlodipine benzenesulfonate), an antianginal agent and an orally active dihydropyridine calcium channel blocker, works by blocking the voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium. Amlodipine besylate can be used for the research of high blood pressure and cancer .
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15
15 Cited Publications
Cat. No.: HY-B0317A
CAS No.: 88150-47-4
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Cancer

Amlodipine maleate is a dihydropyridine calcium channel blocker, acts as an orally active antianginal agent. Amlodipine maleate blocks the voltage-dependent L-type calcium channels, thereby inhibiting the initial influx of calcium. Amlodipine maleate can be used for the research of high blood pressure and cancer .
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14
14 Cited Publications
Cat. No.: HY-15553A
CAS No.: 116666-63-8
Synonyms: Ro 40-5967 dihydrochloride
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Cancer

Mibefradil dihydrochloride (Ro 40-5967 dihydrochloride) is a calcium channel blocker with moderate selectivity for T-type Ca 2+ channels (IC50s of 2.7 μM and 18.6 μM for T-type and L-type currents, respectively) .
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10
10 Cited Publications
Cat. No.: HY-14656
CAS No.: 33286-22-5
Purity:  99.47%
Synonyms: CRD-401
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease Cancer

Diltiazem hydrochloride is a Ca 2+ influx inhibitor (slow channel blocker or calcium antagonist).
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10
10 Cited Publications
Cat. No.: HY-B1357
CAS No.: 71-63-6
Digitoxin is an anti-cancer agent. Digitoxin induces apoptosis, inhibits influenza cytokine storm, causes DNA double-stranded breaks (DSBs) and blocks the cell cycle at the G2/M phase. Digitoxin induces calcium uptake into cells by forming transmembrane calcium channels and can be used for research of heart failure .
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9
9 Cited Publications
Cat. No.: HY-103315
CAS No.: 68099-86-5
Purity:  99.98%
Synonyms: CERM 1978
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

Bepridil hydrochloride (CERM 1978) is a calcium channel blocker, with antianginal activity.
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9
9 Cited Publications
Cat. No.: HY-16952
CAS No.: 64706-54-3
Synonyms: (±)-Bepridil; Org 5730
Bepridil ((±)-Bepridil) is a calcium channel blocking agent used as antiarrhythmic agent. Bepridil inhibits both calcium and sodium currents, has research potential in certain ischemia-induced ventricular arrhythmias. Bepridil also has strong inhibition of SARS-CoV-2 from entry and replication inside Vero E6 and A549 cells .
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9
9 Cited Publications
Cat. No.: HY-139426
CAS No.: 891016-02-7
Purity:  99.91%
Synonyms: ML-SI3 (cis/trans mix)
ML-SI3 is a mixture of cis/trans ML-SI3 (HY-139426A), which is a TRPML1/2 channel inhibitor with IC50s of 4.7 μM and 1.7 μM, respectively. ML-SI3 also inhibits lysosomal calcium efflux and blocks downstream TRPML1-mediated autophagy. The cis/trans ML-SI3 (HY-139426A) components of ML-SI3 are TRPML2 activators with EC50s of 3.3 μM and 9.4 μM, respectively .
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8
8 Cited Publications
Cat. No.: HY-118628
CAS No.: 110683-10-8
Purity:  99.63%
Synonyms: N-(p-Amylcinnamoyl) anthranilic acid; ACA
Research Areas:  

Cardiovascular Disease

(E/Z)-BML264 (N-(p-amylcinnamoyl) Anthranilic Acid) is a broad spectrum Phospholipase A2 (PLA2) inhibitor and TRP channel blocker . (E/Z)-BML264 is a SLC13A3 inhibitor. (E/Z)-BML264 (N-(p-amylcinnamoyl) Anthranilic Acid) is also an effective reversible inhibitor of calcium-activated chloride channels, has potential to treat arrhythmia .
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6
6 Cited Publications
Cat. No.: HY-12515
CAS No.: 55985-32-5
Purity:  99.09%
Synonyms: YC-93 free base
Nicardipine (YC-93 free base) is a calcium channel blocker with an IC50 of 1 μM for blocking cardiac calcium channels. Nicardipine acts as an agent for chronic stable angina and for controlling blood pressure .
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6
6 Cited Publications
Cat. No.: HY-12515A
CAS No.: 54527-84-3
Purity:  99.73%
Synonyms: YC-93
Nicardipine hydrochloride (YC-93) is a calcium channel blocker with an IC50 of 1 μM for blocking cardiac calcium channels. Nicardipine hydrochloride acts as an agent for chronic stable angina and for controlling blood pressure .
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6
6 Cited Publications
Cat. No.: HY-B0493
CAS No.: 4394-00-7
Target:  

Chloride Channel COX

Research Areas:  

Inflammation/Immunology Cancer

Niflumic acid is a calcium-activated chloride channel blocker and COX-2 inhibitor with the IC50 value of 100 nM. Niflumic acid induces apoptosis through caspase-8/Bid/Bax pathway in lung cancer cells. Niflumic acide exhibits anti-tumor activity by affecting the expression of ERK1/2 and the activity of MMP2 and MMP9. Niflumic acid has orally bioactivity. Niflumic acid acts on rheumatoid arthritis .
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5
5 Cited Publications
Cat. No.: HY-113618A
CAS No.: 1219927-22-6
Research Areas:  

Cardiovascular Disease

RO2959 hydrochloride is a potent and selective CRAC channel inhibitor with an IC50 of 402 nM. RO2959 hydrochloride is a potent blocker of store operated calcium entry (SOCE) mediated by Orai1/Stim1 channels with an IC50 of 25 nM. RO2959 hydrochloride is also a potent inhibitor of human IL-2 production, and potently blocks T cell receptor triggered gene expression and T cell functional pathways .
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5
5 Cited Publications
Cat. No.: HY-111613
CAS No.: 53251-94-8
Purity:  99.73%
Target:  

Calcium Channel

Research Areas:  

Cancer

Pinaverium bromide is an L-type calcium channel blocker with selectivity for the gastrointestinal tract, effectively relieves pain, diarrhea and intestinal discomfort, provides good therapeutic efficacies without significant adverse effects on Irritable bowel syndrome (IBS) patients .
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