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Filtered Search Results
eMolecules 312692-85-6 | 3,4-Dichlorophenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01319864 | 338.270 | C6H3Cl2IZn | 0.000 | [I-].Clc1ccc([Zn+])cc1Cl | 25ml | 627353607
3,4-Dichlorophenylzinc iodide, 0.50 M in THF | Synthonix | 312692-85-6 | MFCD01319864 | 338.270 | C6H3Cl2IZn | 0.000 | [I-].Clc1ccc([Zn+])cc1Cl | 25ml | 627353607
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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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eMolecules 44767-62-6 | Hexylmagnesium chloride, 1.0 M in THF | Synthonix - Stock | MFCD06798087 | 144.930 | C6H13ClMg | 0.000 | [Cl-].CCCCCC[Mg+] | 100ml | 437237269
Hexylmagnesium chloride, 1.0 M in THF | Synthonix - Stock | 44767-62-6 | MFCD06798087 | 144.930 | C6H13ClMg | 0.000 | [Cl-].CCCCCC[Mg+] | 100ml | 437237269
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Medchemexpress LLC BI-2852 10MM/1ML
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BI-2852 10MM/1ML
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eMolecules 30897-90-6 | 4-Fluoro-2-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311469 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1cc(F)ccc1[Mg+] | 100ml | 437237230
4-Fluoro-2-methylphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 30897-90-6 | MFCD01311469 | 213.332 | C7H6BrFMg | 0.000 | [Br-].Cc1cc(F)ccc1[Mg+] | 100ml | 437237230
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LIFE CHEMICALS USA INC
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NC3952103 4 6-DICHLORO-N-NAPHTHALEN-1-Y
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eMolecules 186000-44-2 | 3-Bromophenylzinc iodide, 0.50 M in THF | Synthonix | MFCD01311440 | 348.290 | C6H4BrIZn | 0.000 | [I-].[Zn+]c1cccc(Br)c1 | 100ml | 532652621
3-Bromophenylzinc iodide, 0.50 M in THF | Synthonix | 186000-44-2 | MFCD01311440 | 348.290 | C6H4BrIZn | 0.000 | [I-].[Zn+]c1cccc(Br)c1 | 100ml | 532652621
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eMolecules 126403-68-7 | Cyclopropylzinc bromide, 0.50 M in THF | Synthonix | MFCD08741505 | 186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]C1CC1 | 100ml | 627353805
Cyclopropylzinc bromide, 0.50 M in THF | Synthonix | 126403-68-7 | MFCD08741505 | 186.360 | C3H5BrZn | 0.000 | [Br-].[Zn+]C1CC1 | 100ml | 627353805
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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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Medchemexpress LLC SPERMIDINE HYDROCHL 1G
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SPERMIDINE HYDROCHL 1G
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Medchemexpress LLC Higenamine hydrochloride | 11041-94-4 | 307.77 | 500 MG
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Higenamine hydrochloride is a selective inhibitor of LSD1 with an IC50 of 1.47 μM, naturally sourced from aconite. It exhibits anti-inflammatory and antibacterial properties and can mitigate IL-1β-induced apoptosis via the ROS-mediated PI3K/Akt signaling pathway. Additionally, it offers protective effects for brain cells against oxygen deprivation and stimulates bone formation in osteoporosis through the SMAD2/3 pathway. It is utilized in research for various conditions, including cancer, inflammation, and cardiorenal syndrome.
- Selective LSD1 inhibitor (IC50=1.47 μM)
- Derived from aconite
- Possesses anti-inflammatory activity
- Exhibits antibacterial activity
- Attenuates IL-1β-induced apoptosis
- Protects brain cells from oxygen deprivation
- Promotes bone formation in osteoporosis
- Relevant for studying cancer, inflammation, and cardiorenal syndrome
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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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eMolecules 109669-45-6 | Tributyl(5,6-dihydro-4H-pyran-2-yl)stannane | Synthonix - Stock373.168 | C17H34OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)C1=CCCCO1 | 5g | 525924751
Tributyl(5,6-dihydro-4H-pyran-2-yl)stannane | Synthonix - Stock | 109669-45-6373.168 | C17H34OSn | 95.000 | CCCC[Sn](CCCC)(CCCC)C1=CCCCO1 | 5g | 525924751
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Medchemexpress LLC (2S)-tert-butoxy[4-(2,3-dihydropyrano[4,3,2-de]quinolin-7-yl)-2-methylquinolin-3-yl]acetic acid | 1155419-89-8 | 99.7% | 442.51 g/mol | C27H26N2O4 | 10 MG
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BI 224436 is a research-grade small-molecule noncatalytic site integrase inhibitor for HIV-1, intended for in vitro antiviral and biochemical studies. It demonstrates potent activity against laboratory strains and is supplied as a solid with defined storage requirements.
- Potent noncatalytic site integrase inhibitor with EC50 <15 nM.
- High purity, 99.7%.
- Molecular weight 442.51 g/mol.
- Chemical formula C27H26N2O4.
- Solid, white to yellow appearance.
- Store at -20°C and protect from light.
- Suitable for in vitro antiviral and biochemical assays.
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Medchemexpress LLC CEVIMELINE HYDROCHL 25 mg
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CEVIMELINE HYDROCHL 25MG
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