88 Results for "

Ca2++influx

" in MedChemExpress (MCE) Product Catalog:
Products (88)

88 Results for "Ca2++influx" in MCE Product Catalog:

Cat. No.: HY-111527
CAS No.: 896203-18-2
Purity:  99.92%
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

PPZ2 is a diacylglycerol (DAG)-activated TRPC3/TRPC6/TRPC7 channel activator with activity in promoting neuronal development and survival. PPZ2 activates recombinant TRPC3/TRPC6/TRPC7 channels in a dose-dependent manner without affecting other TRPC channels. PPZ2 elicits cation currents and calcium ion (Ca(2+)) influx in cultured central neurons. PPZ2 is able to induce BDNF-like neurite outgrowth and neuroprotection, an effect that disappears after TRPC3/TRPC6/TRPC7 knockdown or inhibition. PPZ2 also increases the activation of the calcium-dependent transcription factor cAMP response element binding protein. The effects of PPZ2 suggest that calcium signaling mediated by activation of DAG-activated TRPC channels plays an important role in its neurotrophic effects .
Cat. No.: HY-12962
CAS No.: 700878-19-9
Purity:  98.98%
Target:  

iGluR

Research Areas:  

Neurological Disease

NMDA-IN-1 is a potent and NR2B-selective NMDA antagonist with Ki of 0.85 nM; NR2B Ca2+ influx IC50 is 9.7 nM; no activities on NR2A, NR2C, NR2D, hERG-channel and α1-adrenergic receptor.
Cat. No.: HY-113037AS
CAS No.: 895550-58-0
Synonyms: Farnesyl diphosphate-d6
Farnesyl pyrophosphate-d6 (Farnesyl diphosphate-d6) is a deuterium labeled Farnesyl pyrophosphate (HY-113037B). Farnesyl pyrophosphate is a metabolic intermediate in the mevalonate (MVA) pathway. It is a TRP channel (TRPM2) agonist that triggers Ca2+ influx and cell death. Farnesyl pyrophosphate is a key branch substrate for cholesterol synthesis, ubiquinone synthesis, protein farnesylation, and geranylgeranyl pyrophosphate (GGPP) synthesis. Farnesyl pyrophosphate is used in research on cerebral ischemia, neurodegenerative diseases, pancreatic cancer, inflammation, and autoimmune diseases.
Cat. No.: HY-N3729
CAS No.: 87402-88-8
Synonyms: Denudatin B
(-)-Denudatin B is an antiplatelet agent. (-)-Denudatin B relaxed vascular smooth muscle by inhibiting the Ca2+ influx through voltage-gated and receptor-operated Ca2+ channels . And (-)-Denudatin B has nonspecific antiplatelet action
Cat. No.: HY-101015
CAS No.: 221632-26-4
Target:  

Phospholipase Apoptosis

Research Areas:  

Inflammation/Immunology

(2E)-OBAA is a potent phospholipase A2 (PLA2) inhibitor, with an IC50 of 70 nM. (2E)-OBAA induces apoptosis of HUVEC cells. (2E)-OBAA blocks Melittin-induced Ca 2+ influx in Trypanosoma brucei, with an IC50 of 0.4 μM [2] .
Cat. No.: HY-N15737
CAS No.: 50982-40-6
Fukinolic acid is a benzyltartaric acid ester, is a vasodilator with antiviral activity against enterovirus A71 (EV-A71) replication. Fukinolic acid is a receptor-operated Ca 2+ channels (ROC) inhibitor, suppressing extracellular Ca 2+ influx through ROC activated by Norepinephrine (HY-13715) without affecting voltage-dependent Ca 2+ channels [2].
Cat. No.: HY-133168R
CAS No.: 1094250-15-3
Englerin A (Standard) is the analytical standard of Englerin A. This product is intended for research and analytical applications. Englerin A is a potent and selective activator of TRPC4 and TRPC5 channels, with EC50s of 11.2 and 7.6 nM, respectively. Englerin A can induce renal carcinoma cells death by elevated Ca2+ influx and Ca2+ cell overload [2] .
Cat. No.: HY-129088
CAS No.: 312747-21-0
Purity:  99.68%
Research Areas:  

Cardiovascular Disease

HUP30 is a vasodilating agent. HUP30 stimulates soluble guanylyl cyclase, activate K + channels, and blocks extracellular Ca 2+ influx .
Cat. No.: HY-121966
CAS No.: 112356-54-4
Purity:  98.00%
Synonyms: Riparin III
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Riparin is a nonspecific smooth muscle relaxant. Riparin exerts spasmolytic effect by inhibiting Ca 2+ influx and inhibiting the release of intracellular calcium ion stores .
Cat. No.: HY-14656R
CAS No.: 33286-22-5
Synonyms: CRD-401 (Standard)
Diltiazem (hydrochloride) (Standard) is the analytical standard of Diltiazem (hydrochloride). This product is intended for research and analytical applications. Diltiazem hydrochloride is a Ca 2+ influx inhibitor (slow channel blocker or calcium antagonist).
Cat. No.: HY-14656S1
CAS No.: 1217860-13-3
Diltiazem-(acetoxy-d3) (hydrochloride) is the deuterium labeled Diltiazem hydrochloride. Diltiazem hydrochloride is a Ca2+ influx inhibitor (slow channel blocker or calcium antagonist)[1][2].
Cat. No.: HY-14656S2
CAS No.: 1309283-34-8
Synonyms: CRD-401-d6 hydrochloride
Diltiazem-d6 (hydrochloride) (CRD-401-d6 (hydrochloride)) is deuterium labeled Diltiazem (hydrochloride). Diltiazem hydrochloride is a Ca 2+ influx inhibitor (slow channel blocker or calcium antagonist).
Cat. No.: HY-P5796
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

FS-2 is a potent and specific L-type CaV channel inhibitor. FS-2 inhibits high K + or glucose induced L-type Ca 2+ influx in RIN beta cells .
Cat. No.: HY-N0081A
CAS No.: 14017-71-1
(-)-Praeruptorin A is a nature product that could be isolated from the roots of Peucedanum praeruptorum Dunn. (-)-Praeruptorin A relaxes ileum and tracheal smooth muscles by activating NO/cGMP signaling pathway. (-)-Praeruptorin A has dramatically therapeutic effects on hypertension mainly through acting as a Ca 2+-influx blocker .
Cat. No.: HY-120820
CAS No.: 182633-59-6
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

LY320954 is a selective 5-HT2A receptor antagonist, with a Ki of 96 nM. LY320954 potently inhibits Ca 2+ influx in the functional assay (EC50 of 35.5 nM). LY320954 inhibits 5-HT-induced paw swelling in rats, with ED50 of 4.8 mg/kg .
Cat. No.: HY-176021
Research Areas:  

Cardiovascular Disease

U-44069 serinol amide is a derivative of U-44069 (HY-121825). U-44069 serinol amide is a stable analog of the endoperoxide prostaglandin H2 (HY-136500). U-44069 serinol amide is a vasoconstrictor that can induce preglomerular Ca 2+ influx .
Cat. No.: HY-A0057R
CAS No.: 60142-96-3
Gabapentin (Standard) is the analytical standard of Gabapentin. This product is intended for research and analytical applications. Gabapentin is a potent, orally active P/Q type Ca2+ channel blocker. Gabapentin inhibits neuronal Ca2+ influx and reduction of neurotransmitter release. Gabapentin is a GABA analog that can be used to relieve neuropathic pain [2] .
Cat. No.: HY-W721517
CAS No.: 1126623-20-8
Gabapentin-d10 is the deuterium labeled Gabapentin (HY-A0057). Gabapentin is a potent, orally active P/Q type Ca2+ channel blocker. Gabapentin inhibits neuronal Ca2+ influx and reduction of neurotransmitter release. Gabapentin is a GABA analog that can be used to relieve neuropathic pain [2] .
Cat. No.: HY-N0724R
CAS No.: 2752-64-9
Mesaconitine (Standard) is the analytical standard of Mesaconitine. This product is intended for research and analytical applications. Mesaconitine is a nitric oxide synthase activator. Mesaconitine drives extracellular Na + and Ca 2+ influx into endothelial cells, increases intracellular Na + and Ca 2+ concentrations, and triggers nitric oxide release. Mesaconitine is applicable for pain-related research [2] .
Cat. No.: HY-169845
CAS No.: 687568-35-0
Target:  

Calcium Channel

Research Areas:  

Neurological Disease

Calcium Channel antagonist 6 (Compound 328) is a highly selective antagonist of voltage-gated calcium channel CaV2.2 with an IC50 value of 0.37 μM. Calcium Channel antagonist 6 inhibits of neuron depolarization-induced Ca 2+ influx. Calcium Channel antagonist 6 is promising for research of neuropathic pain .