Naphthalenes

eMolecules​ 53429-23-5 | (2-isopropoxy-2-oxo-ethyl)zinc bromide, 0.50 M in THF | Synthonix246.410 | C5H9BrO2Zn | 0.000 | [Br-].CC(C)OC(=O)C[Zn+] | 100ml | 627353813

(2-isopropoxy-2-oxo-ethyl)zinc bromide, 0.50 M in THF | Synthonix | 53429-23-5246.410 | C5H9BrO2Zn | 0.000 | [Br-].CC(C)OC(=O)C[Zn+] | 100ml | 627353813

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eMolecules​ 186000-43-1 | 4-(Methoxycarbonyl)phenylzinc iodide, 0.50 M in THF | Synthonix327.430 | C8H7IO2Zn | 0.000 | [I-].COC(=O)c1ccc([Zn+])cc1 | 25ml | 627353701

4-(Methoxycarbonyl)phenylzinc iodide, 0.50 M in THF | Synthonix | 186000-43-1327.430 | C8H7IO2Zn | 0.000 | [I-].COC(=O)c1ccc([Zn+])cc1 | 25ml | 627353701

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Medchemexpress LLC 4-(2,3-dihydro-1,4-benzodioxin-6-yl)-3-[(5-nitro-1,3-thiazol-2-yl)sulfanyl]-1H-1,2,4-triazol-5-one | 883065-90-5 | >98.0% | 379.37 g/mol | C13H9N5O5S2 | 50 MG

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BI-78D3 is a small-molecule, substrate-competitive inhibitor of c-Jun N-terminal kinase (JNK) used as a research tool to probe JNK signaling. It inhibits JNK kinase activity with a reported IC50 of 280 nM. The compound has molecular formula C13H9N5O5S2, molecular weight 379.37 g/mol, and CAS 883065-90-5. Recommended storage: powder at -20°C (long term) or 4°C (short term); store solutions at -80°C or -20°C depending on duration.

• Substrate-competitive JNK inhibitor (IC50 280 nM).
• Suitable for biochemical and cell-based studies of JNK signaling.
• Molecular weight 379.37 g/mol; chemical formula C13H9N5O5S2.
• Powder form stable for long-term storage at -20°C.
• Available in small research pack sizes for assay development.

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eMolecules​ 308796-05-6 | 4-Pentylphenylzinc iodide, 0.50 M in THF | Synthonix339.530 | C11H15IZn | 0.000 | [I-].CCCCCc1ccc([Zn+])cc1 | 100ml | 532652955

4-Pentylphenylzinc iodide, 0.50 M in THF | Synthonix | 308796-05-6339.530 | C11H15IZn | 0.000 | [I-].CCCCCc1ccc([Zn+])cc1 | 100ml | 532652955

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eMolecules​ 1207760-37-9 | 4-Isoquinolinzinc bromide, 0.50 M in THF | Synthonix273.440 | C9H6BrNZn | 0.000 | [Br-].[Zn+]c1cncc2ccccc12 | 25ml | 627353669

4-Isoquinolinzinc bromide, 0.50 M in THF | Synthonix | 1207760-37-9273.440 | C9H6BrNZn | 0.000 | [Br-].[Zn+]c1cncc2ccccc12 | 25ml | 627353669

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eMolecules​ 132856-34-9 | 2,4,6-Trimethylbenzylmagnesium chloride, 0.25 M in 2-MeTHF | Synthonix - Stock192.970 | C10H13ClMg | 0.000 | [Cl-].Cc1cc(C)c(C[Mg+])c(C)c1 | 100ml | 507877784

2,4,6-Trimethylbenzylmagnesium chloride, 0.25 M in 2-MeTHF | Synthonix - Stock | 132856-34-9192.970 | C10H13ClMg | 0.000 | [Cl-].Cc1cc(C)c(C[Mg+])c(C)c1 | 100ml | 507877784

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eMolecules​ 117896-10-3 | 4-Methoxy-3-methylphenylmagnesium bromide, 0.5M in THF | Synthonix - Stock225.368 | C8H9BrMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1C | 50ml | 437237337

4-Methoxy-3-methylphenylmagnesium bromide, 0.5M in THF | Synthonix - Stock | 117896-10-3225.368 | C8H9BrMgO | 0.000 | [Br-].COc1ccc([Mg+])cc1C | 50ml | 437237337

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eMolecules​ 44767-62-6 | Hexylmagnesium chloride, 1.0 M in THF | Synthonix - Stock | MFCD06798087 | 144.930 | C6H13ClMg | 0.000 | [Cl-].CCCCCC[Mg+] | 500ml | 437237270

Hexylmagnesium chloride, 1.0 M in THF | Synthonix - Stock | 44767-62-6 | MFCD06798087 | 144.930 | C6H13ClMg | 0.000 | [Cl-].CCCCCC[Mg+] | 500ml | 437237270

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Apexbio Technology LLC BI-D1870 501437-28-1 10mM (in 1mL DMSO)

BI-D1870 (CAS 501437-28-1) is a cell-permeable small molecule inhibitor that selectively targets the p90 ribosomal S6 kinase (RSK) family comprising RSK1 RSK2 RSK3 and RSK4 It functions as an ATP-competitive inhibitor exhibiting IC50 values of 31 nM 24 nM 18 nM and 15 nM against RSK1 RSK2 RSK3 and RSK4 respectively BI-D1870 demonstrates over 500-fold greater selectivity for RSK isoforms compared to other AGC kinases In cellular assays such as with Rat-2 cells it has been shown to induce phosphorylation of ERK1/ERK2 and subsequent CREB phosphorylation BI-D1870 is widely utilized for investigating RSK-mediated signal transduction and downstream cellular processes in biomedical research

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TARGETMOL CHEMICALS INC BI-1408 5MG

Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. BI-1408 is a modulator potent of (gamma) secretase (IC50 0.04 uM for A(beta)42). purity: 98%

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Medchemexpress LLC BI-2852 5 mg

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