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Filtered Search Results
![Medchemexpress LLC 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 25MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000232537.png-250.jpg)
Medchemexpress LLC 1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 25MG
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1-[3,5-bis(trifluoromethyl)benzoyl]-N-(4-chlorophenyl)-3-piperidinecarboxamide | 1207113-88-9 | 99.3% | 25MG
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![eMolecules 956697-53-3 | Erismodegib | Apollo Scientific485.507 | C26H26F3N3O3 | 0.000 | C[C@H]1CN(C[C@@H](C)O1)c1ccc(cn1)\N=C(/O)c1cccc(c1C)-c1ccc(OC(F)(F)F)cc1 | 50mg | 562455235](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502154998.JPG-250.jpg)
eMolecules 956697-53-3 | Erismodegib | Apollo Scientific485.507 | C26H26F3N3O3 | 0.000 | C[C@H]1CN(C[C@@H](C)O1)c1ccc(cn1)\N=C(/O)c1cccc(c1C)-c1ccc(OC(F)(F)F)cc1 | 50mg | 562455235
Erismodegib | Apollo Scientific | 956697-53-3485.507 | C26H26F3N3O3 | 0.000 | C[C@H]1CN(C[C@@H](C)O1)c1ccc(cn1)\N=C(/O)c1cccc(c1C)-c1ccc(OC(F)(F)F)cc1 | 50mg | 562455235
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eMolecules 122-99-6 | 2-Phenoxyethanol | Combi-Blocks | MFCD00002857 | 138.166 | C8H10O2 | 94.000 | OCCOc1ccccc1 | 25g | 342866165
2-Phenoxyethanol | Combi-Blocks | 122-99-6 | MFCD00002857 | 138.166 | C8H10O2 | 94.000 | OCCOc1ccccc1 | 25g | 342866165
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Medchemexpress LLC HY-B0664 100mg Medchemexpress, Ciprofibrate CAS:52214-84-3 Purity:>98%
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Medchemexpress, HY-B0664 100mg Ciprofibrate CAS:52214-84-3 Ciprofibrate (Win35833) is a potent peroxisome proliferator and increases the phosphorylation level of the PPARalpha. Ciprofibrate acts as an orally active hypolipidaemic agent and can be used for the research of primary hyperlipidaemias. 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 Azemiglitazone potassium | 1314533-27-1 | 99.5% | 409.50 | C19H16KNO5S | 10 MG
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Azemiglitazone potassium is the potassium salt of azemiglitazone, a thiazolidinedione-like insulin sensitizer that modulates the mitochondrial pyruvate carrier (MPC) with low PPARγ activation. It is provided as a high-purity research compound for in vitro and preclinical studies of metabolic disorders such as diabetes and nonalcoholic steatohepatitis (NASH).
- High purity suitable for research applications.
- Potassium salt form enhances handling and solubility in polar solvents.
- High DMSO solubility (250 mg/mL) with ultrasonic assistance.
- Recommended sealed storage away from moisture; solvent storage guidelines apply.
- Modulates mitochondrial pyruvate carrier and acts as an insulin sensitizer for metabolic research.
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Medchemexpress LLC SB-3CT | 292605-14-2 | MFCD09836266 | 50 mg
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SB-3CT | Purity: 99.24% | Mol Wt: 306.40 | 292605-14-2 | MFCD09836266 | 50 mg
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Medchemexpress LLC HY-101069 5mg Medchemexpress, Y-26763 CAS:127408-31-5 Purity:>98%
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Medchemexpress, HY-101069 5mg Y-26763 CAS:127408-31-5 Y-26763 is a K+ channel opener and active metabolite of Y-27152. Y-26763 is an ATP-sensitive K+ (KATP) channel activator. 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 5-methyl-7-methoxyisoflavone | 82517-12-2 | MFCD03093036 | 99.1% | 266.29 | C17H14O3 | 10 MG
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5-methyl-7-methoxyisoflavone is a non-steroidal isoflavone used in research for its aromatase inhibitory and antioxidant properties; it has reported remyelinating activity and NF-κB inhibitory effects and is supplied in solid and DMSO solution formats for biochemical and cellular studies.
- isoflavone scaffold with aromatase inhibitory activity.
- Orally active antioxidant with reported remyelinating properties.
- Shown to inhibit NF-κB signaling pathways.
- High listed purity (approximately 99.1%).
- Available as solid (10 mg-500 mg) and 10 mM DMSO solution formats for experimental flexibility.
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Medchemexpress LLC HY-18850 5mg Medchemexpress, MAPK13-IN-1 CAS:229002-10-2 Purity:>98%
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Medchemexpress, HY-18850 5mg MAPK13-IN-1 CAS:229002-10-2 MPAK13-IN-1 is a MAPK13 (p38δ) inhibitor, with an IC50 of 620 nM. 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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eMolecules 1146963-51-0 | Medchem Express | J-147 | 5mg | 446263489 | HY-13779 | MFCD25976644 | 350.341 | C18H17F3N2O2
Medchem Express | FPL64176 | 5mg | 742367493 | HY-103307 | 120934-96-5 | MFCD00274043 | 347.414 | C22H21NO3
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eMolecules 39905-57-2 | 4-(Hexyloxy)aniline | ChemScene | MFCD00007868 | 193.290 | C12H19NO | 98.000 | CCCCCCOc1ccc(N)cc1 | 5g | 712787493
4-(Hexyloxy)aniline | ChemScene | 39905-57-2 | MFCD00007868 | 193.290 | C12H19NO | 98.000 | CCCCCCOc1ccc(N)cc1 | 5g | 712787493
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Medchemexpress LLC Mps1-IN-3 hydrochloride | 2989453-29-2 | 98.0% | 574.09 g/mol | C26H32ClN7O4S | 50MG
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Mps1-IN-3 hydrochloride is a potent, selective Mps1 (TTK) kinase inhibitor (IC50 = 50 nM) supplied as a hydrochloride salt for research use. The compound is provided as a solid with high purity and suitable solubility in DMSO for in vitro and in vivo studies.
- Molecular formula: C26H32ClN7O4S.
- Molecular weight: 574.09 g/mol.
- Purity: 98.0%.
- Appearance: Light yellow to green yellow solid.
- Solubility: DMSO ≥ 20 mg/mL.
- Storage: Store sealed at -20°C; in solution, -80°C up to 6 months or -20°C up to 1 month.
- Applications: Suitable for cellular assays and xenograft studies, including sensitization experiments.
- Packaging: Available in multiple milligram-scale quantities.
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Medchemexpress LLC (S)-UFR2709 hydrochloride | 2934318-93-9 | 98.1% | 255.74 | 50 MG
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(S)-UFR2709 hydrochloride is a competitive nAChR antagonist that shows higher affinity for α4β2 nAChRs than for α7 nAChRs. It has been observed to decrease anxiety and reduce ethanol consumption and preference in alcohol-preferring rats. It acts as an anxiolytic agent and can be used for the study of nicotine addiction.
- Competitive nAChR antagonist with higher affinity for α4β2 nAChRs than α7 nAChRs
- Decreases anxiety
- Reduces ethanol consumption and ethanol preference in alcohol-preferring rats
- Acts as an anxiolytic agent
- Can be used for the study of nicotine addiction
- Inhibits nicotine reward
- Decreases nicotine-evoked mRNA expression of α4 nACh receptor subunit in the brain of adult zebrafish
- Does not affect the weight or locomotor activity of rats at effective doses for reducing alcohol consumption
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Medchemexpress LLC Galanthamine N-Oxide | 134332-50-6 | 1 MG
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Galanthamine N-Oxide is an alkaloid derived from the bulbs of *Zephyranthes concolor*. This compound acts as an inhibitor of electric eel acetylcholinesterase (AChE) and is recognized for its role in inhibiting substrate accommodation within the active site of *Torpedo californica* AChE (TcAChE), human AChE (hAChE), and human BChE (hBChE) enzymes. It is intended for research use only.
- Derived from *Zephyranthes concolor* bulbs
- Inhibits electric eel acetylcholinesterase (AChE)
- Prominent inhibitor of substrate accommodation in AChE and BChE enzymes
- Target: Cholinesterase (ChE)
- Pathway: Neuronal Signaling
- Appears as a white to off-white solid
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Medchemexpress LLC 1,4-dimethoxybenzene | 150-78-7 | MFCD00008401 | 100.0% | 138.16 g/mol | C8H10O2 | 25 MG
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1,4-Dimethoxybenzene (CAS 150-78-7) analytical standard supplied as a high-purity reference material for research and analytical applications. Offered in small-scale quantities suitable for method development, calibration, and qualitative or quantitative analysis.
- High purity 99.99% for accurate analytical results.
- Available in small quantities, including 25 mg, for lab-scale use.
- Supplied as a solid reference standard for chromatography and spectroscopy.
- Molecular weight 138.16 g/mol and chemical formula C8H10O2 for documentation.
- SMILES provided to support informatics and structure confirmation.
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