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Filtered Search Results
Medchemexpress LLC N-(3-((3-(5-chlorothiophene-2-sulfonamido)-4-methoxyindazol-1-yl)methyl)benzyl)-2-hydroxy-2-methylpropanamide | 1240516-71-5 | 99.8% | 549.06 | C24H25ClN4O5S2 | 25 MG
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GSK2239633A is a small-molecule CC-chemokine receptor 4 (CCR4) antagonist supplied for research use. It inhibits [125I]-TARC binding to human CCR4 with a reported pIC50 of 7.96 and shows activity in human CD4+ CCR4+ T-cells. The compound is provided as a solid with high reported purity and defined molecular formula and weight, suitable for in vitro pharmacology and analytical studies.
- Allosteric CCR4 antagonist with reported pIC50 ~7.96.
- Validated in vitro activity on human CD4+ CCR4+ T-cells.
- High reported purity suitable for research assays.
- Solid form, stable for analytical use.
- Contains defined molecular formula and molecular weight for characterization.
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Selleck Chemical LLC AST-487
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AST-487 (NVP-AST487) a N N -diphenyl urea is an ATP competitive inhibitor of Flt3 with ki of 0 12 M Besides FLT3 AST487 also inhibits RET KDR c-KIT and c-ABL kinase with IC50 values below 1 M
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Sigma Aldrich Fine Chemicals Biosciences Clofibrate liquid | 637-07-0 | MFCD00000615 | 5G
Clofibrate liquid | Mol Wt: 242.7 | 637-07-0 | MFCD00000615 | 5G
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eMolecules Medchem Express / RS 17053 hydrochloride / 5mg / 441681764 / HY-101336 / / 169505-93-5 / MFCD09971032 / 449.420 / C24H30Cl2N2O2
Medchem Express / RS 17053 hydrochloride / 5mg / 441681764 / HY-101336 / / 169505-93-5 / MFCD09971032 / 449.420 / C24H30Cl2N2O2
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Medchemexpress LLC Lesogaberan hydrochloride | 2925644-17-1 | 98.0% | 177.54 | C3H10ClFNO2P | 25 MG
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Lesogaberan hydrochloride is a research-grade GABAB receptor agonist (hydrochloride salt) used as a pharmacological tool to study GABAB-mediated signaling and peripheral effects on lower esophageal sphincter relaxation. It is supplied as a solid reagent with supporting analytical documentation for laboratory research use only; not for human or veterinary use.
- Potent, selective GABAB receptor agonist with EC50 of 8.6 nM.
- High reported purity (98.0%).
- Provided with datasheet, COA, and SDS for analytical verification.
- Recommended storage: solid at 4°C under inert atmosphere to minimize degradation.
- Suitable for in vitro pharmacology and biochemical assays.
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Enzo Life Sciences SB-366791 (25 mg). CAS: 472981-92-3
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A potent and selective vanilloid receptor (TRPV1) antagonist. An effective antagonist of hTRPV1 when stimulated by capsaicin, acid, or noxious heat. Purity: ≥98% (TLC). Solubility: Soluble in DMSO (25mg/ml) or 100% ethanol (10mg/ml with warming). Long Term Storage: Ambient.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431508 HKOCL-4M 5MG
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Enzo Life Sciences Suberoyl bis-hydroxamic acid (100mg). CAS: 38937-66-5
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Induces cellular differentiation. Inhibits histone deacetylation. Purity: ≥95% (TLC). Solubility: Soluble in DMSO. Long Term Storage: Ambient.
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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NC3976866 ERDAFITINIB 10MM 1ML IN DMSO
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Medchemexpress LLC Trifarotene | 895542-09-3 | 99.1% | 459.58 g/mol | C29H33NO4 | 100 MG
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Trifarotene is a selective retinoic acid receptor γ (RARγ) agonist supplied as a white to off-white solid for research use. It is intended for in vitro and in vivo studies of RAR/RXR signaling and related pathways and is not for human therapeutic use.
- High purity (≈99.1% by LCMS)
- Chemical formula C29H33NO4, molecular weight 459.58 g/mol
- Soluble in DMSO (≈250 mg/mL) and formulatable for in vivo dosing
- Stable under recommended powder and solution storage conditions
- Suitable for receptor pharmacology and preclinical studies
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![Medchemexpress LLC N-[[3-[[3-[(5-chlorothiophen-2-yl)sulfonylamino]-4-methoxyindazol-1-yl]methyl]phenyl]methyl]-2-hydrox | 1240516-71-5 | MFCD30533311 | 99.8% | 549.06 g/mol | C24H25ClN4O5S2 | 100 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000215478.png-250.jpg)
Medchemexpress LLC N-[[3-[[3-[(5-chlorothiophen-2-yl)sulfonylamino]-4-methoxyindazol-1-yl]methyl]phenyl]methyl]-2-hydrox | 1240516-71-5 | MFCD30533311 | 99.8% | 549.06 g/mol | C24H25ClN4O5S2 | 100 MG
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GSK2239633A is a small-molecule CCR4 antagonist used in research to inhibit [125I]-TARC binding to human CCR4 (reported pIC50 7.96). It is supplied as a high-purity solid with defined storage recommendations and high solubility in DMSO for assay preparation.
- High purity suitable for research assays.
- Selective CCR4 antagonistic activity (pIC50 7.96).
- Solid form with recommended freezer storage.
- High solubility in DMSO for stock preparation.
- Molecular weight 549.06 g/mol and formula C24H25ClN4O5S2.
- For research use only; not for human or diagnostic use.
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eMolecules Medchem Express / CP-466722 / 5mg / 446259735 / HY-11002 / / 1080622-86-1 / MFCD17392566 / 349.354 / C17H15N7O2
Medchem Express / CP-466722 / 5mg / 446259735 / HY-11002 / / 1080622-86-1 / MFCD17392566 / 349.354 / C17H15N7O2
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Medchemexpress LLC Darifenacin | 133099-04-4 | 99.8% | C28H30N2O2 | 5 MG
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Darifenacin is a selective and orally active M3 muscarinic receptor (M3R) antagonist. It is primarily used in the study of urinary incontinence and symptoms of overactive bladder. Additionally, it has demonstrated potential anti-tumor effects by inhibiting tumor growth in colorectal cancer cells.
- Selective M3 muscarinic receptor antagonist (pKi of 8.9).
- Binds >20-fold more specifically to M3R.
- Inhibits tumor growth in colorectal cancer cells.
- Used in studies for urinary incontinence and overactive bladder.
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Selleck Chemical LLC Apabetalone
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Apabetalone (RVX-208 RVX-000222) is a potent BET bromodomain inhibitor with IC50 of 0 510 M for BD2 in a cell-free assay about 170-fold selectivity over BD1 Phase 2
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Medchemexpress LLC Flecainide | 54143-55-4 | 414.34 | 50 MG
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Flecainide (Standard) is the analytical standard of Flecainide, intended for research and analytical applications. Flecainide is an orally active antiarrhythmic agent that 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).
- Analytical standard for research and analytical applications
- Orally active antiarrhythmic agent
- Blocks sodium channels
- Inhibits calcium ion release mediated by the cardiac ryanodine receptor (RyR2)
- Useful in research of diseases like catecholaminergic polymorphic ventricular tachycardia (CPVT)
- Reference standard for qualitative, quantitative, and methodological research experiments in HPLC, GC, and MS
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