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Filtered Search Results
Medchemexpress LLC B7-2/CD86 Human Bi 50ug | 50ug
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B7-2/CD86 protein negatively regulates T-cell activation by disrupting CD86 cluster formation modulating the T-cell response and influencing immune activation B7-2/CD86 Protein Human (Biotinylated HEK293 His-Avi) is the recombinant human-derived B7-2/CD86 protein expressed by HEK293 with C-Avi C-His labeled tag
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eMolecules 108-31-6 | Maleic anhydride | Oakwood Chemicals | MFCD00005518 | 98.057 | C4H2O3 | 99.000 | O=C1OC(=O)C=C1 | 5g | 480164068
Maleic anhydride | Oakwood Chemicals | 108-31-6 | MFCD00005518 | 98.057 | C4H2O3 | 99.000 | O=C1OC(=O)C=C1 | 5g | 480164068
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eMolecules 191606-78-7 | 1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole | Synthonix - Stock | MFCD06797466 | 439.154 | C17H31F3N2Sn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cc(nn1C)C(F)(F)F | 5g | 490913214
1-Methyl-5-(tributylstannyl)-3-(trifluoromethyl)-1H-pyrazole | Synthonix - Stock | 191606-78-7 | MFCD06797466 | 439.154 | C17H31F3N2Sn | 97.000 | CCCC[Sn](CCCC)(CCCC)c1cc(nn1C)C(F)(F)F | 5g | 490913214
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eMolecules 89980-69-8 | 3,4-Dimethoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | MFCD01311476 | 241.367 | C8H9BrMgO2 | 0.000 | [Br-].COc1ccc([Mg+])cc1OC | 500ml | 437237134
3,4-Dimethoxyphenylmagnesium bromide, 0.5 M in THF | Synthonix - Stock | 89980-69-8 | MFCD01311476 | 241.367 | C8H9BrMgO2 | 0.000 | [Br-].COc1ccc([Mg+])cc1OC | 500ml | 437237134
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Medchemexpress LLC Seproxetine hydrochloride | 127685-30-7 | MFCD06658520 | 93.1% | 331.76 g·mol⁻1 | C16H17ClF3NO | 100MG
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Seproxetine hydrochloride is the hydrochloride salt of seproxetine (S-norfluoxetine), a selective serotonin reuptake inhibitor (SSRI) and an active metabolite of fluoxetine. Intended for research use in biochemical and pharmacological studies, the compound is provided in multiple small-scale package sizes and is characterized by its molecular formula C16H17ClF3NO, molecular weight 331.76 g·mol⁻1, and CAS 127685-30-7.
- High enantiomeric excess and purity for research applications (97.6% ee; 93.1% purity).
- Available in multiple small package sizes to support screening and synthesis.
- Provided as the hydrochloride salt for improved handling and stability.
- Documented molecular formula and weight for accurate formulation and calculations.
- CAS number included for unambiguous chemical identification.
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eMolecules 13132-23-5 | 2,2-Dimethylpropylmagnesium chloride, 1.0 M in THF | Synthonix - Stock | MFCD00061550 | 130.900 | C5H11ClMg | 0.000 | [Cl-].CC(C)(C)C[Mg+] | 500ml | 437237090
2,2-Dimethylpropylmagnesium chloride, 1.0 M in THF | Synthonix - Stock | 13132-23-5 | MFCD00061550 | 130.900 | C5H11ClMg | 0.000 | [Cl-].CC(C)(C)C[Mg+] | 500ml | 437237090
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eMolecules 170793-00-7 | 4-Chloro-3-fluorophenylmagnesium bromide, 0.50 M in THF | Synthonix - Stock | MFCD02260213 | 233.750 | C6H3BrClFMg | 0.000 | [Br-].Fc1cc([Mg+])ccc1Cl | 50ml | 437237049
4-Chloro-3-fluorophenylmagnesium bromide, 0.50 M in THF | Synthonix - Stock | 170793-00-7 | MFCD02260213 | 233.750 | C6H3BrClFMg | 0.000 | [Br-].Fc1cc([Mg+])ccc1Cl | 50ml | 437237049
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Medchemexpress LLC Anpirtoline hydrochloride | 99201-87-3 | 99.9% | 265.21 | C10H14Cl2N2S | 100 MG
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Anpirtoline hydrochloride is a research-grade serotonergic compound that functions primarily as a 5-HT1B receptor agonist, with activity at 5-HT1A and 5-HT2 subtypes. It is supplied for laboratory research use only and is not for human or veterinary use. CAS: 99201-87-3; molecular weight: 265.21 g/mol.
- Potent 5-HT1B receptor agonist with activity at related 5-HT subtypes.
- High reported purity, suitable for pharmacological experiments.
- Available in multiple pack sizes to support screening or preparative work.
- Provided with documentation useful for research-grade handling and QC.
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eMolecules Synthonix - Stock (22-Difluoro-1-tributylstannylvinyl)-NN-diethylcarbamate 5g 525916187 D8449 143366-89-6 [null] 468.217 C19H37F2NO2Sn
Synthonix - Stock (22-Difluoro-1-tributylstannylvinyl)-NN-diethylcarbamate 5g 525916187 D8449 143366-89-6 [null] 468.217 C19H37F2NO2Sn
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Medchemexpress LLC BI-78D3 | 883065-90-5 | MFCD01313575 | >98.0% | 379.37 | C13H9N5O5S2 | 1 ML
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BI-78D3 (HY-10366) is a small-molecule substrate-competitive inhibitor of c-Jun N-terminal kinase (JNK) used in laboratory research. It inhibits JNK kinase activity with a reported IC50 of approximately 280 nM, and has molecular formula C13H9N5O5S2 and molecular weight 379.37 g/mol. The compound is supplied for research use only and is available in solid or solution formats.
- Substrate-competitive JNK inhibitor.
- Reported IC50 ≈ 280 nM against JNK.
- Molecular formula C13H9N5O5S2.
- Molecular weight 379.37 g/mol.
- Supplied for research use only (not for human or veterinary use).
- Available in solid or solution formats from distributors.
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TARGETMOL CHEMICALS INC BI-3812 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BI-3812 is an inhibitor of BCL6. Which inhibiting the BTB domain of BCL6 (IC50 3 nM). BI-3812 also has antitumor activity. purity: 99%
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eMolecules Synthonix Hept-6-enylmagnesium bromide 0.50 M in THF 50ml 702445919 H73638 154920-12-4 [null] 201.390 C7H13BrMg
Synthonix Hept-6-enylmagnesium bromide 0.50 M in THF 50ml 702445919 H73638 154920-12-4 [null] 201.390 C7H13BrMg
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Medchemexpress LLC Olanexidine (hydrochloride) | 146509-94-6 | MFCD32201949 | 96.3% | 408.80 g/mol | C17H28Cl3N5 | 100MG
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Olanexidine (hydrochloride) is a monobiguanide antibacterial small molecule for research use. It exhibits broad-spectrum bactericidal activity against both Gram-positive and Gram-negative bacteria and is supplied as the hydrochloride salt with characterized purity and molecular properties.
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eMolecules 34091-51-5 | 5-Iodo-1-methyl-1H-pyrazole | Ambeed | MFCD11109327 | 208.002 | C4H5IN2 | 97.000 | Cn1nccc1I | 100g | 632174004
5-Iodo-1-methyl-1H-pyrazole | Ambeed | 34091-51-5 | MFCD11109327 | 208.002 | C4H5IN2 | 97.000 | Cn1nccc1I | 100g | 632174004
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Medchemexpress LLC Mocravimod hydrochloride | 509088-69-1 | 99.99% | 480.45 | 25 MG
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Mocravimod hydrochloride is an orally active sphingosine-1-phosphate receptor (S1PR) modulator that blocks the signal T cells need to egress from lymph nodes and other lymphoid organs. It preferentially binds to S1PR1 and can be used for the study of acute myelogenous leukemia, diabetes, and Myocardial Ischemia-Reperfusion Injury (MIRI).
- Blocks T cell egress from lymph nodes
- Preferentially binds to S1PR1
- Lowers reactive oxygen species (ROS) concentration
- Prevents mitochondrial permeability transition pore opening
- Boosts mitochondrial membrane potential (MMP)
- Increases phosphorylation of AKT, EKR, GSK-3β, JAK2, and STAT3
- Retains T cell effector function
- Suitable for studying acute myelogenous leukemia, diabetes, and Myocardial Ischemia-Reperfusion Injury (MIRI)
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