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Filtered Search Results
Medchemexpress LLC 1-(5-chloronaphthalen-1-yl)sulfonyl-1,4-diazepane hydrochloride | 105637-50-1 | MFCD00065525 | 99.9% | 361.29 g/mol | C15H18Cl2N2O2S | 100 MG
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ML-9 is a small-molecule research inhibitor of Akt kinase that also inhibits myosin light-chain kinase (MLCK) and STIM1. It shows reported Ki values of 4 μM (MLCK), 32 μM (PKA), and 54 μM (PKC), and can induce autophagy by stimulating autophagosome formation. Intended for laboratory research use; handle and store under dry, sealed conditions.
- Inhibits Akt kinase, MLCK, and STIM1.
- Induces autophagy by stimulating autophagosome formation.
- High purity: 99.86%.
- Molecular weight: 361.29 g/mol.
- Chemical formula: C15H18Cl2N2O2S.
- Available as solids (including 100 mg) and 10 mM solutions in DMSO.
- Storage: solid at 4°C; in solvent -80°C (up to 6 months) or -20°C (up to 1 month).
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eMolecules Medchem Express / Ospemifene / 10mg / 446273207 / HY-B0723 / / 128607-22-7 / MFCD00871890 / 378.900 / C24H23ClO2
Medchem Express / Ospemifene / 10mg / 446273207 / HY-B0723 / / 128607-22-7 / MFCD00871890 / 378.900 / C24H23ClO2
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Medchemexpress LLC Ipriflavone | 35212-22-7 | MFCD00221719 | >98.0% | 280.32 | 500 MG
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Ipriflavone is a synthetic isoflavone derivative used to suppress bone resorption. It is intended for research and analytical applications.
- Targets cytochrome P450.
- Relevant to research in metabolic disease.
- Relevant to research in cancer.
- Functions to suppress bone resorption.
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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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eMolecules Medchem Express / Suplatast (Tosilate) / 100mg / 446268103 / HY-17002 / / 94055-76-2 / MFCD00867604 / 499.640 / C23H33NO7S2
Medchem Express / Suplatast (Tosilate) / 100mg / 446268103 / HY-17002 / / 94055-76-2 / MFCD00867604 / 499.640 / C23H33NO7S2
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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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eMolecules ChemScene / 5-(Cyclopropylmethoxy)-1H-pyrazol-3-amine / 100mg / 632319307 / CS-0119828 / 0.000 / 852443-66-4 / MFCD20724093 / 153.185 / C7H11N3O
ChemScene / 5-(Cyclopropylmethoxy)-1H-pyrazol-3-amine / 100mg / 632319307 / CS-0119828 / 0.000 / 852443-66-4 / MFCD20724093 / 153.185 / C7H11N3O
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eMolecules Medchem Express / RX 801077 (hydrochloride) / 5mg / 788477976 / HY-100904 / / 89196-95-2 / MFCD00672666 / 222.670 / C11H11ClN2O
Medchem Express / RX 801077 (hydrochloride) / 5mg / 788477976 / HY-100904 / / 89196-95-2 / MFCD00672666 / 222.670 / C11H11ClN2O
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Selleck Chemical LLC ONO-4059 analogue
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ONO-4059 analogue (ONO-WG-307) is an analogue of ONO-4059 which is a highly potent and selective oral BTK inhibitor with IC50 of 23 9 nM Phase 1
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Selleck Chemical LLC Genz-123346 free base
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Genz-123346 is an inhibitor of GL1 synthase that blocks the conversion of ceramide to GL1 the first step in the biosynthesis of gangliosides and other glycosphingolipids
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Selleck Chemical LLC Aripiprazole-50mg
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Aripiprazole (OPC-14597) is a novel atypical antipsychotic drug that is reported to be a high-affinity 5-HT receptor partial agonist.
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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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eMolecules Medchem Express / Tracazolate (hydrochloride) / 5mg / 761506663 / HY-B1803A / / 1135210-68-2 / MFCD03791317 / 340.850 / C16H25ClN4O2
Medchem Express / Tracazolate (hydrochloride) / 5mg / 761506663 / HY-B1803A / / 1135210-68-2 / MFCD03791317 / 340.850 / C16H25ClN4O2
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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 / Phenothrin / 5mg / 716993901 / HY-B1072 / / 26002-80-2 / MFCD00078716 / 350.458 / C23H26O3
Medchem Express / Phenothrin / 5mg / 716993901 / HY-B1072 / / 26002-80-2 / MFCD00078716 / 350.458 / C23H26O3
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