222 Results for "

depolarize

" in MedChemExpress (MCE) Product Catalog:
Products (222)

222 Results for "depolarize" in MCE Product Catalog:

Cat. No.: HY-B1532
CAS No.: 494-52-0
Synonyms: (S)-Anabasine; (+)-Anabasine
Anabasine ((S)-Anabasine) is an alkaloid that found as a minor component in tobacco (Nicotiana). Anabasine is a botanical pesticide nicotine, acts as a full agonist of nicotinic acetylcholine receptors (nAChRs). Anabasine induces depolarization of TE671 cells endogenously expressing human fetal muscle-type nAChRs (EC50=0.7 μM) .
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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 .
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Cat. No.: HY-136909
CAS No.: 121345-64-0
Purity:  99.78%
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

SR33805 is a potent Ca 2+ channel antagonist, with EC50s of 4.1 nM and 33 nM in depolarized and polarized conditions, respectively. SR33805 blocks L-type but not T-type Ca 2+ channels. SR33805 can be used for the research of acute or chronic failing hearts .
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Cat. No.: HY-114410
CAS No.: 292053-42-0
Purity:  99.87%
Research Areas:  

Cancer

CCI-006 is a selective inhibitor and chemosensitizer of MLL-rearranged leukemia cells, by inhibits mitochondrial respiration resulting in insurmountable mitochondrial depolarization and a pro-apoptotic unfolded protein response (UPR) in a subset of MLL-r leukemia cells .
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Cat. No.: HY-111014
CAS No.: 955371-66-1
Purity:  99.63%
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

VK-II-36 is a carvedilol analog that suppresses sarcoplasmic reticulum Ca 2+release but does not block the β-receptor.VK-II-36 inhibits triggered activities evoked by both early and delayed after depolarizations .
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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 .
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Cat. No.: HY-136980
CAS No.: 6157-06-8
Purity:  99.79%
Synonyms: Asp-Glu
Target:  

Endogenous Metabolite

Research Areas:  

Neurological Disease

Aspartylglutamate (Asp-Glu) is a dipeptide that exhibits excitatory activity, as it has been shown to depolarize CA1 pyramidal neurons and increase conductance in response to stimulation. Aspartylglutamate selectively binds to certain glutamate receptors and demonstrates potent effects in specific regions of the hippocampus, particularly in the stratum radiatum where it enhances excitatory neurotransmission.
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Cat. No.: HY-W748509
CAS No.: 88660-10-0
Pipernonaline is a piperine derivative with antiprostate cancer activity. Pipernonaline inhibits the proliferation of androgen-dependent/independent LNCaP/PC-3 prostate cells. Pipernonaline activates caspase-3 and promotes procaspase-3/PARP cleavage. Pipernonaline also mediates reactive oxygen species (ROS) production, increased intracellular Ca(2+), and mitochondrial membrane depolarization .
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Cat. No.: HY-17033
CAS No.: 143558-00-3
Synonyms: Org-9426
Target:  

nAChR

Research Areas:  

Neurological Disease Cancer

Rocuronium (Org-9426) is an aminosteroid non-depolarizing neuromuscular blocker or muscle relaxant used in modern anaesthesia.
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Cat. No.: HY-16423
CAS No.: 156137-99-4
Synonyms: Org 9487
Target:  

mAChR

Research Areas:  

Neurological Disease

Rapacuronium bromide (Org 9487), a non-depolarizing neuromuscular blocker, is an allosteric modulator of muscarinic acetylcholine receptor (mAChR) .
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Cat. No.: HY-100823
CAS No.: 111900-32-4
Target:  

mGluR

Research Areas:  

Neurological Disease

(1S,3R)-ACPD is a mGluR agonist that can depolarize pyramidal cells .
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Cat. No.: HY-P3775
CAS No.: 87549-54-0
Target:  

Inhibitory Antibodies

Research Areas:  

Neurological Disease

a-Bag Cell Peptide (1-7) is a NH2-terminal fragment α-bag cell peptide. α-bag cell peptide can inhibit the left upper quadrant (LUQ) neurons and the depolarization of the bag cells . α-Bag Cell Peptide Fragment
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Cat. No.: HY-B0615AS
CAS No.: 2300178-76-9
Synonyms: EN 313-d8; Ethmozin-d8; Moracizine-d8
Moricizine-d8 Hydrochloride is the deuterium labeled Moricizine Hydrochloride (HY-B0615A). Moricizine Hydrochloride is an orally active Class I antiarrhythmic agent. Moricizine Hydrochloride decreases the maximum rate of phase 0 depolarization; increases rates of phase 2 and 3 repolarization, decreases action potential duration, and decreases effective refractory period .
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Cat. No.: HY-114372
CAS No.: 466-61-5
Research Areas:  

Cancer

Lycopodine, a pharmacologically important bioactive component derived from Lycopodium clavatumspores, triggers apoptosis by modulating 5-lipoxygenase, and depolarizing mitochondrial membrane potential in refractory prostate cancer cells without modulating p53 activity . Lycopodine inhibits proliferation of HeLa cells through induction of apoptosis via caspase-3 activation .
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Cat. No.: HY-A0258A
CAS No.: 7601-55-0
Synonyms: Metocurine iodide; Dimethylchondrocurarine iodide
Target:  

nAChR

Research Areas:  

Neurological Disease

Metubine (Metocurine iodide) is a non-depolarizing muscle relaxant. Metubine has neuromuscular blocking activities .
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Cat. No.: HY-N6882
CAS No.: 66026-80-0
Synonyms: G8CG
Genistein 8-c-glucoside (G8CG) is a glucoside. Genistein 8-c-glucoside induces mitochondrial membrane depolarization and induces apoptosis .
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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 .
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Cat. No.: HY-178450
CAS No.: 2766757-56-4
Target:  

P2X Receptor

Research Areas:  

Neurological Disease

HW091077 is a highly selective P2X3 receptor antagonist with an IC50 of 17 nM. HW091077 blocks ATP-induced calcium influx and cell depolarization to inhibit cough reflex pathways. HW091077 is promising for research of chronic cough .
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Cat. No.: HY-14764
CAS No.: 333963-42-1
Synonyms: SPI 8811
Cobiprostone (SPI 8811) is a type-2 chloride channel activator. Cobiprostone protects against Indomethacin (HY-14397)-induced depolarization of mitochondrial membrane potential and reverses the loss of mitochondrial membrane potential. Cobiprostone protects against NSAID-induced cellular damage .
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Cat. No.: HY-N1306
CAS No.: 3122-87-0
Sideroxylin is a C-methylated flavone isolated from Callistemon lanceolatus and exerts antimicrobial activity against Staphylococcus aureus. Sideroxylin inhibits ovarian cancer cell proliferation and induces apoptosis, causing DNA fragmentation, depolarization of the mitochondrial membrane, the generation of reactive oxygen species (ROS) .
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