Naphthalenes

eMolecules​ 869893-91-4 | 3-Chloro-2-fluorobenzylzinc bromide, 0.50 M in THF | Synthonix288.850 | C7H5BrClFZn | 0.000 | [Br-].Fc1c(Cl)cccc1C[Zn+] | 25ml | 627353554

3-Chloro-2-fluorobenzylzinc bromide, 0.50 M in THF | Synthonix | 869893-91-4288.850 | C7H5BrClFZn | 0.000 | [Br-].Fc1c(Cl)cccc1C[Zn+] | 25ml | 627353554

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eMolecules​ 312692-98-1 | 3,5-Dimethylphenylzinc iodide, 0.50 M in THF | Synthonix297.440 | C8H9IZn | 0.000 | [I-].Cc1cc(C)cc([Zn+])c1 | 100ml | 532652791

3,5-Dimethylphenylzinc iodide, 0.50 M in THF | Synthonix | 312692-98-1297.440 | C8H9IZn | 0.000 | [I-].Cc1cc(C)cc([Zn+])c1 | 100ml | 532652791

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eMolecules​ 263355-05-1 | 3-Fluoro-2-methylphenyl magnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311483 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1c(F)cccc1[Mg+] | 50ml | 437237239

3-Fluoro-2-methylphenyl magnesium bromide, 0.5 M in THF | Synthonix - Stock | 263355-05-1 | MFCD01311483 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1c(F)cccc1[Mg+] | 50ml | 437237239

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eMolecules​ 4294-57-9 | 4-Methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD00000040 | 195.342 | C7H7BrMg | 98.000 | [Br-].Cc1ccc([Mg+])cc1 | 100ml | 437237323

4-Methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 4294-57-9 | MFCD00000040 | 195.342 | C7H7BrMg | 98.000 | [Br-].Cc1ccc([Mg+])cc1 | 100ml | 437237323

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Medchemexpress LLC 2-naphthol | 135-19-3 | MFCD00004067 | 99.9% | 144.17 g/mol | C10H8O | 500g

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2-Naphthol is a metabolite of naphthalene catalyzed by cytochrome P450 (CYP) isozymes (CYP 1A1 CYP 1A2 CYP 2A1 CYP 2E1 and CYP 2F2)

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eMolecules​ 460747-53-9 | 4-Chloro-3-methylphenylmagnesium bromide, 0.50 M in THF | Synthonix - Stock | MFCD02260216 | 229.780 | C7H6BrClMg | 0.000 | [Br-].Cc1cc([Mg+])ccc1Cl | 50ml | 437237040

4-Chloro-3-methylphenylmagnesium bromide, 0.50 M in THF | Synthonix - Stock | 460747-53-9 | MFCD02260216 | 229.780 | C7H6BrClMg | 0.000 | [Br-].Cc1cc([Mg+])ccc1Cl | 50ml | 437237040

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eMolecules​ 1204580-81-3 | 4-Methyl-3-(tributylstannyl)pyridine | Synthonix - Stock | MFCD11707000 | 382.179 | C18H33NSn | 96.000 | CCCC[Sn](CCCC)(CCCC)c1cnccc1C | 500mg | 525921305

4-Methyl-3-(tributylstannyl)pyridine | Synthonix - Stock | 1204580-81-3 | MFCD11707000 | 382.179 | C18H33NSn | 96.000 | CCCC[Sn](CCCC)(CCCC)c1cnccc1C | 500mg | 525921305

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Medchemexpress LLC Procaterol (hydrochloride hemihydrate) | 81262-93-3 | 99.8% | 25 MG

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Procaterol hydrochloride hemihydrate is an orally active β2 adrenoreceptor agonist primarily used for asthma research. It demonstrates significant biological activity in both in vitro and in vivo studies, including reducing rhinovirus infection, protecting cells from oxidative stress, and inhibiting inflammatory responses. This compound also alleviates cough in animal models, making it a valuable tool for related scientific investigations.

• Orally active β2 adrenoreceptor agonist
• Utilized for asthma research
• Decreases rhinovirus infection in human tracheal cells
• Inhibits IL-1β- and TNF-α-mediated eosinophil chemotactic activity
• Protects cells from H2O2-induced oxidative stress
• Inhibits histamine-induced airflow obstruction and microvascular leakage
• Abolishes Mch-induced cough in guinea pigs

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Medchemexpress LLC Pifusertib hydrochloride | 2930090-28-9 | 99.9% | 460.96 | 1 ML

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Pifusertib hydrochloride is a potent, selective, orally active allosteric Akt inhibitor that triggers anti-myeloma activities. It enhances fatal endoplasmic reticulum (ER) stress induced by proteasome inhibition, leading to apoptosis and autophagy.

• Potent, selective, orally active allosteric Akt inhibitor.
• Triggers anti-myeloma activities.
• Enhances fatal endoplasmic reticulum (ER) stress.
• Induces apoptosis and autophagy.
• Blocks basal phosphorylation of Akt and downstream targets in MM cells.
• Induces cytotoxicity in MM cells with high baseline Akt phosphorylation.
• Inhibits tumor growth in murine xenograft models.

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Medchemexpress LLC Flecainide hydrochloride | 57415-44-8 | 99.93% | 450.80 | 100 MG

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Flecainide hydrochloride is an orally active antiarrhythmic agent. It 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).

• In vitro: flecainide (hydrochloride) (500 nM) significantly reduces irregular Ca2+ release in single cardiomyocytes derived from ATS-iPSCs.
• In vivo: flecainide (hydrochloride) (20 mg/kg; intraperitoneal injection; single dose) completely inhibits catecholamine-induced ventricular arrhythmias in Casq2 knockout mice.

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eMolecules​ 1142219-89-3 | 4-Bromo-3-methylphenylzinc iodide, 0.50 M in THF | Synthonix362.310 | C7H6BrIZn | 0.000 | [I-].Cc1cc([Zn+])ccc1Br | 50ml | 532652628