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Filtered Search Results
Medchemexpress LLC Benzocaine hydrochloride | 23239-88-5 | MFCD00012999 | 201.65 | C9H12ClNO2 | 500mg
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Benzocaine (hydrochloride) is an orally active local agent that can suppress or relieve pain that acts on voltage-gated Na channels at a common receptor with an IC50 value of 0 8 mM at 30 mV Additionally Benzocaine (hydrochloride) non-competitively inhibits Ca-ATPase binding with Ca2 with an IC50 of 47 1 mM Benzocaine (hydrochloride) can be used in research within the field of neuromuscular regulation[1][2][3]
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Medchemexpress LLC Flecainide hydrochloride | 57415-44-8 | 99.93% | 450.80 | 1 ML
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Flecainide hydrochloride is an orally active antiarrhythmic agent that blocks sodium channels and inhibits calcium ion release mediated by the cardiac ryanodine receptor (RyR2). It can be used in the research of diseases such as catecholaminergic polymorphic ventricular tachycardia (CPVT).
- Significantly reduces irregular Ca2+ release in single cardiomyocytes derived from ATS-iPSCs.
- Completely inhibits catecholamine-induced ventricular arrhythmias in Casq2 knockout mice.
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eMolecules 100045-83-8 | Tributyl[(methoxymethoxy)methyl]stannane | Synthonix - Stock | MFCD03412101 | 365.145 | C15H34O2Sn | 97.000 | CCCC[Sn](CCCC)(CCCC)COCOC | 5g | 525924159
Tributyl[(methoxymethoxy)methyl]stannane | Synthonix - Stock | 100045-83-8 | MFCD03412101 | 365.145 | C15H34O2Sn | 97.000 | CCCC[Sn](CCCC)(CCCC)COCOC | 5g | 525924159
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Medchemexpress LLC Lurasidone hydrochloride | 367514-88-3 | 99.86% | C28H37ClN4O2S | 100 MG
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Lurasidone hydrochloride is a chemical reagent from MedChemExpress that functions as an antagonist for both dopamine D2 and 5-HT7 receptors. It also acts as a partial agonist of the 5-HT1A receptor.
- Antagonist of dopamine D2 and 5-HT7 receptors
- Partial agonist of 5-HT1A receptor
- Suitable for neurological disease research
- Stable under recommended storage conditions
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eMolecules 7608-06-2 | Heptylzinc bromide, 0.50 M in THF | Synthonix | MFCD02260126 | 244.480 | C7H15BrZn | 0.000 | [Br-].CCCCCCC[Zn+] | 25ml | 627353661
Heptylzinc bromide, 0.50 M in THF | Synthonix | 7608-06-2 | MFCD02260126 | 244.480 | C7H15BrZn | 0.000 | [Br-].CCCCCCC[Zn+] | 25ml | 627353661
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Medchemexpress LLC Gabapentin hydrochloride | 60142-95-2 | 98.0% | C9H18ClNO2 | 1 ML
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Gabapentin hydrochloride is a potent, orally active P/Q type Ca2+ channel blocker. It inhibits neuronal Ca2+ influx and reduces neurotransmitter release. This GABA analog can be used to relieve neuropathic pain.
- Potent, orally active P/Q type Ca2+ channel blocker
- Inhibits neuronal Ca2+ influx
- Reduces neurotransmitter release
- GABA analog for neuropathic pain relief
- Improves spatial and emotional cognitive performance (in mice)
- Exhibits analgesic effect and reduces writhing (in mice)
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eMolecules 518989-99-6 | 4-Chloro-2-fluorophenylzinc iodide, 0.50 M in THF | Synthonix | MFCD02260161 | 321.820 | C6H3ClFIZn | 0.000 | [I-].Fc1cc(Cl)ccc1[Zn+] | 50ml | 532652698
4-Chloro-2-fluorophenylzinc iodide, 0.50 M in THF | Synthonix | 518989-99-6 | MFCD02260161 | 321.820 | C6H3ClFIZn | 0.000 | [I-].Fc1cc(Cl)ccc1[Zn+] | 50ml | 532652698
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eMolecules 251635-59-3 | 4-Methyl-2-(tributylstannyl)thiazole | Synthonix - Stock | MFCD09025808 | 388.200 | C16H31NSSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1nc(C)cs1 | 500mg | 525920530
4-Methyl-2-(tributylstannyl)thiazole | Synthonix - Stock | 251635-59-3 | MFCD09025808 | 388.200 | C16H31NSSn | 95.000 | CCCC[Sn](CCCC)(CCCC)c1nc(C)cs1 | 500mg | 525920530
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eMolecules 171860-68-7 | Cyclopentylzinc bromide, 0.50 M in THF | Synthonix214.410 | C5H9BrZn | 97.000 | [Br-].[Zn+]C1CCCC1 | 100ml | 532652731
Cyclopentylzinc bromide, 0.50 M in THF | Synthonix | 171860-68-7214.410 | C5H9BrZn | 97.000 | [Br-].[Zn+]C1CCCC1 | 100ml | 532652731
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eMolecules 15890-72-9 | n-Dodecylmagnesium bromide, 0.50 M in THF | Synthonix | MFCD00075165 | 273.541 | C12H25BrMg | 0.000 | [Br-].CCCCCCCCCCCC[Mg+] | 50ml | 702445884
n-Dodecylmagnesium bromide, 0.50 M in THF | Synthonix | 15890-72-9 | MFCD00075165 | 273.541 | C12H25BrMg | 0.000 | [Br-].CCCCCCCCCCCC[Mg+] | 50ml | 702445884
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Medchemexpress LLC G4RGDSP, integrin-binding peptide | 774577-43-4 | 99.6% | 758.74 | 25 MG
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G4RGDSP, Integrin-binding peptide is a cell integrin-binding peptide that targets integrin receptors. It is coupled to alginate to increase the viability of cells in the scaffold. It can be used as an extrudable carrier for chondrocyte delivery for the study of 3D printing technology.
- Targets integrin receptors.
- Can be coupled to alginate to increase cell viability in scaffolds.
- Usable as an extrudable carrier for chondrocyte delivery for 3D printing technology.
- Can increase the expression of aggregin, collagen type II, and sox9 genes in HAC cells.
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eMolecules 160732-56-9 | 1-Azido-1,2-benziodoxol-3(1H)-one, 40% in diatomaceous earth | Synthonix - Stock | MFCD04038996 | 289.032 | C7H4IN3O2 | 95.000 | [N-]=[N+]=N[I]1OC(=O)c2ccccc12 | 5g | 525906036
1-Azido-1,2-benziodoxol-3(1H)-one, 40% in diatomaceous earth | Synthonix - Stock | 160732-56-9 | MFCD04038996 | 289.032 | C7H4IN3O2 | 95.000 | [N-]=[N+]=N[I]1OC(=O)c2ccccc12 | 5g | 525906036
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Medchemexpress LLC Fenspiride hydrochloride | 5053-08-7 | 99.1% | C15H21ClN2O2 | 1 ML
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Fenspiride hydrochloride is an orally active, non-steroidal anti-inflammatory agent that acts as an antagonist of the H1-histamine receptor. It inhibits phosphodiesterase 3 (PDE3), phosphodiesterase 4 (PDE4), and phosphodiesterase 5 (PDE5) activities. This compound can be used for research related to respiratory diseases.
- Antagonist of the H1-histamine receptor
- Inhibits phosphodiesterase 3, phosphodiesterase 4, and phosphodiesterase 5 activities
- Useful for research on respiratory diseases
- Inhibits histamine-induced contraction of isolated guinea pig trachea (in vitro)
- Reduces lipopolysaccharide-induced tumor necrosis factor concentrations (in vivo)
- Reduces primed stimulation of alveolar macrophages (in vivo)
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eMolecules 308796-27-2 | 4-(Methylthio)phenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01863641 | 315.480 | C7H7ISZn | 95.000 | [I-].CSc1ccc([Zn+])cc1 | 100ml | 721997568
4-(Methylthio)phenylzinc iodide, 0.50 M in THF | Synthonix | 308796-27-2 | MFCD01863641 | 315.480 | C7H7ISZn | 95.000 | [I-].CSc1ccc([Zn+])cc1 | 100ml | 721997568
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Apexbio Technology LLC BI-847325 1207293-36-4 5mg
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BI-847325 (CAS 1207293-36-4) is a dual inhibitor targeting MEK1/2 and Aurora kinases with reported IC50 values of 25 nM and 4 nM against MEK1 and MEK2 and 3 nM 25 nM and 15 nM against Aurora A B and C respectively By inhibiting these kinases BI-847325 disrupts the MAPK/ERK and cell cycle signaling pathways that regulate cell proliferation and survival In cellular assays it demonstrates nanomolar EC50 values for inhibition of pERK and pHH3 in KRAS- and BRAF-mutant cancer cell lines and potently suppresses proliferation across a wide range of tumor cell models In xenograft studies it fully blocks tumor growth in BRAF- and KRAS-mutant cancer models This compound is utilized in research on kinase-targeted cancer therapies
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