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Filtered Search Results
eMolecules (2,6-Dibromophenyl)methanol | 1013031-65-6 | MFCD13185492 | 1g
Ambeed | (2,6-Dibromophenyl)methanol | 1g | 552652668 | A214973 | | 1013031-65-6 | MFCD13185492 | 265.932 | C7H6Br2O
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Medchemexpress LLC HY-101420 5mg Medchemexpress, VUF10460 CAS:1028327-66-3 Purity:>98%
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Medchemexpress, HY-101420 5mg VUF10460 CAS:1028327-66-3 VUF10460 is a non-imidazole histamine H4 receptor agonist; binds to rat H4 receptor with a pK i of 7.46. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC PKI-166 10mg | 187724-61-4 | 330.38 | C20H18N4O | 10 MG
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PKI-166 is a potent, selective, and orally bioavailable epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor with a reported IC50 of 0.7 nM. It is provided for research use only and has molecular formula C20H18N4O and high purity by HPLC.
- Potent EGFR kinase inhibition (IC50 ≈ 0.7 nM).
- High chemical purity (≥98% by HPLC).
- Suitable for in vitro and in vivo research applications.
- Orally bioavailable in preclinical studies.
- Well-characterized molecular properties for experimental reproducibility.
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Medchemexpress LLC mTOR inhibitor-8 | 2489196-70-3 | 98.1% | C24H19ClN4OS | 10MG
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mTOR inhibitor-8 is a small-molecule inhibitor of the mechanistic target of rapamycin (mTOR) that acts via FKBP12 to inhibit mTOR activity and induces autophagy in A549 human lung cancer cells. It is provided as a solid research reagent and is available in multiple sizes and solution formats for use in cell-based assays.
- Inhibits mTOR activity via FKBP12.
- Induces autophagy in A549 human lung cancer cells.
- Supplied as a solid and as a 10 mM solution in DMSO for assay flexibility.
- High purity (98.1%) suitable for research applications.
- Defined chemical formula (C24H19ClN4OS) and molecular weight for accurate identification.
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![Medchemexpress LLC Methyl-4-(6-{4-[(methoxycarbonyl)amino]phenyl}-4-morpholin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-1-yl) | 1062169-56-5 | 98.0% | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/VN00132390-HY-12034-5MG.JPG-250.jpg)
Medchemexpress LLC Methyl-4-(6-{4-[(methoxycarbonyl)amino]phenyl}-4-morpholin-4-yl-1H-pyrazolo[3,4-d]pyrimidin-1-yl) | 1062169-56-5 | 98.0% | 5 MG
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WYE-354 is an ATP-competitive mTOR inhibitor used in research to block mTORC1 and mTORC2 signaling and to study PI3K/mTOR pathway modulation in vitro. It is supplied as a high-purity small molecule in solid form or as a ready-to-use DMSO solution for laboratory assays.
- ATP-competitive mTOR inhibitor with IC50 ≈ 5 nM.
- High purity suitable for biochemical and cell-based assays.
- Available as solid and as a 10 mM solution in DMSO for convenience.
- Molecular weight 495.53 g·mol⁻¹ and formula C24H29N7O5.
- Commonly used for pathway, signaling, and autophagy research in vitro.
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Apexbio Technology LLC BAY 61-3606 732983-37-8 5mg
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BAY 61-3606 (CAS 732983-37-8) is a selective orally bioavailable inhibitor of spleen tyrosine kinase (SYK) displaying an IC50 of 10 nM and a Ki of 7 5 nM for SYK by competitively binding ATP This compound shows minimal activity against other tyrosine kinases such as Src Fyn Lyn Btk and Itk at concentrations up to 4 7 M BAY 61-3606 suppresses Fc RI-mediated degranulation and mediator release in mast cells and basophils as well as Fc R-driven responses in macrophages and neutrophils In preclinical models BAY 61-3606 attenuates inflammatory cell functions and reduces allergic and asthmatic responses supporting its utility in investigating SYK-mediated signaling and inflammation
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Selleck Chemical LLC WYE-125132 (WYE-132) S2661-5mg
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WYE-125132 (WYE-132) is a highly potent ATP-competitive mTOR inhibitor with IC50 of 0 19 nM highly selective for mTOR versus PI3Ks or PI3K-related kinases hSMG1 and ATR
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eMolecules Medchem Express / TH287 / 5mg / 446267994 / HY-16965 / / 1609960-30-6 / MFCD29035111 / 269.130 / C11H10Cl2N4
Medchem Express / TH287 / 5mg / 446267994 / HY-16965 / / 1609960-30-6 / MFCD29035111 / 269.130 / C11H10Cl2N4
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Medchemexpress LLC Phenyl 6-(3-methoxy-2-(4-(trifluoromethyl)phenyl)benzoylamino)-3,4-dihydroisoquinoline-2-carboxylate | 913541-47-6 | MFCD28502203 | 99.0% | 546.54 | C31H25F3N2O4 | 50 MG
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SLX-4090 is an orally active, enterocytic-specific microsomal triglyceride transfer protein (MTP) inhibitor (IC50 8.0 nM) used as a research reagent in dyslipidemia and lipid metabolism studies. It is supplied as a purified solid and is available in solution formats suitable for in vitro and in vivo assays.
- High potency MTP inhibition (IC50 ~8.0 nM).
- Enterocytic-specific activity useful for targeted lipid studies.
- High purity (about 98.97%) for reproducible results.
- Available as solid and DMSO solution formats for assay flexibility.
- Suitable for dyslipidemia and lipid metabolism research models.
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eMolecules 2-(2-Methylphenyl)pyrimidine-5-carbaldehyde | 876710-73-5 | 1G
Chem-Impex | 2-(2-Methylphenyl)pyrimidine-5-carbaldehyde | 1G | 876710-73-5 | MFCD08272865 | MW:195.22
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eMolecules 1-(2,5-Dibromophenyl)thiourea | 854890-84-9 | MFCD14673413 | 1g
Combi-Blocks | 1-(2,5-Dibromophenyl)thiourea | 1g | 117531798 | HC-3368 | 98.000 | 854890-84-9 | MFCD14673413 | 310.010 | C7H6Br2N2S
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eMolecules tert-butyl 5-bromo-4-formyl-7-methyl-indole-1-carboxylate | 1628640-26-5 | | 1g
Pharmablock | tert-butyl 5-bromo-4-formyl-7-methyl-indole-1-carboxylate | 1g | 596622786 | PBW0760 | | 1628640-26-5 | | 338.201 | C15H16BrNO3
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eMolecules Ambeed / Potassium trifluoro(5-formylfuran-2-yl)borate / 1g / 672523275 / A446781 / / 907604-62-0 / MFCD11052668 / 201.980 / C5H3BF3KO2
Ambeed / Potassium trifluoro(5-formylfuran-2-yl)borate / 1g / 672523275 / A446781 / / 907604-62-0 / MFCD11052668 / 201.980 / C5H3BF3KO2
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![Medchemexpress LLC Anthra[1,2-c]thiadiazole-6,11-dione | 4219-52-7 | 98.0% | 5 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000231892.png-250.jpg)
Medchemexpress LLC Anthra[1,2-c]thiadiazole-6,11-dione | 4219-52-7 | 98.0% | 5 MG
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NSC745885 is a small-molecule anti-tumor agent reported to down-regulate EZH2 through proteasome-mediated degradation. It has demonstrated selective cytotoxicity against multiple cancer cell lines and is used in preclinical cellular research of bladder and oral squamous cell carcinoma.
- Down-regulates EZH2 via proteasome-mediated degradation.
- Exhibits selective cytotoxicity toward malignant cell lines.
- Supplied as a solid with high purity suitable for research.
- Stable when stored at low temperatures according to handling guidance.
- Available in small research quantities for laboratory studies.
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![eMolecules Ambeed / Methyl 7-formylbenzofuran-2-carboxylate / 100mg / 600830271 / A1372484 / / 1780084-52-7 / [null] / 204.181 / C11H8O4](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461244.JPG-250.jpg)
eMolecules Ambeed / Methyl 7-formylbenzofuran-2-carboxylate / 100mg / 600830271 / A1372484 / / 1780084-52-7 / [null] / 204.181 / C11H8O4
Ambeed / Methyl 7-formylbenzofuran-2-carboxylate / 100mg / 600830271 / A1372484 / / 1780084-52-7 / [null] / 204.181 / C11H8O4
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