Pyridines and derivatives
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- (1)
- (1)
- (39)
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Filtered Search Results
Medchemexpress LLC 3-[(3R,4R)-1-[(3S)-3-cyclohexyl-3-hydroxypropyl]-3,4-dimethylpiperidin-4-yl]phenol | 119193-09-8 | 98.0% | 345.52 g/mol | C22H35NO2 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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LY255582 is a pan-opioid receptor antagonist research compound used to study opioid receptor signaling, feeding behavior, and addiction. Supplied as a laboratory reagent for research use only (not for human or veterinary use).
- Pan-opioid antagonist active at mu, delta, and kappa receptors.
- Chemical formula C22H35NO2; molecular weight 345.52 g/mol.
- Supplied as a 5 mg solid with 98.0% purity (HPLC reported).
- Used in pharmacology studies of appetite, addiction, and receptor binding.
- Store desiccated at low temperature for stability.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Tandospirone | 87760-53-0 | MFCD00904852 | 99.4% | 383.49 g/mol | C21H29N5O2 | 5 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Tandospirone is a selective 5-HT1A receptor partial agonist used in preclinical pharmacology and neuroscience research. It is supplied with characterized purity and recommended storage conditions for laboratory use only; not for human consumption.
- Selective 5-HT1A receptor partial agonist.
- High purity: 99.4%.
- Cas number: 87760-53-0.
- Molecular formula: C21H29N5O2.
- Molecular weight: 383.49 g/mol.
- Available formats: solid powder and in solvent.
- Typical pack size: 5 MG.
- Recommended storage: powder -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (up to 2 years) or -20°C (up to 1 year).
- Intended for research use only; not for clinical or human use.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC Aβ42-IN-2 | 1914989-80-2 | 98.0% | 430.50 | 1 ML
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Aβ42-IN-2 is a γ-secretase modulator with an IC50 of 6.5 nM for Aβ42, making it suitable for Alzheimer's disease research. This product is for research use only.
- γ-Secretase modulator
- IC50 of 6.5 nM for Aβ42
- Used in Alzheimer's disease research
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Medchemexpress LLC VU0405601 25mg | 712325-30-9 | 357.20 | C17H13BrN2O2 | 25 MG
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VU0405601 is a potent KV11.1 (hERG) channel activator reported to protect cardiac tissue from dofetilide-induced ventricular tachycardia. It is supplied as a research-grade small molecule for electrophysiology and cardiac safety studies.
- Potent KV11.1 (hERG) channel activator suitable for electrophysiology studies.
- Reported to protect cardiac tissue from dofetilide-induced ventricular tachycardia in experimental models.
- High purity as listed by supplier (99.93%).
- Molecular formula C17H13BrN2O2; molecular weight 357.20 g/mol.
- Store solid at room temperature up to 3 years; in solvent, store at -80°C or -20°C per supplier guidance.
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eMolecules 75330-75-5 | Lovastatin | Key Organics/BIONET | MFCD00072164 | 404.547 | C24H36O5 | 97.000 | CC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@@H]12 | 2mg | 564361732
Lovastatin | Key Organics/BIONET | 75330-75-5 | MFCD00072164 | 404.547 | C24H36O5 | 97.000 | CC[C@H](C)C(=O)O[C@H]1C[C@@H](C)C=C2C=C[C@H](C)[C@H](CC[C@@H]3C[C@@H](O)CC(=O)O3)[C@@H]12 | 2mg | 564361732
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Medchemexpress LLC Immunoproteasome inhibitor 1 | 2755772-63-3 | 99.6% | 358.43 | C20H26N2O4 | 5 MG
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Immunoproteasome inhibitor 1 is a small-molecule, reversible immunoproteasome inhibitor supplied as a high-purity solid for biochemical and cellular research. It is intended for experimental use in studies of proteasome function and immune-related proteostasis, with recommended storage to preserve activity.
- High purity (>99.5%) suitable for analytical and biological assays.
- Supplied as a solid for flexible formulation and handling.
- Recommended storage conditions provided for stability and reproducibility.
- Defined molecular formula and molecular weight for accurate dosing.
- Provided with SMILES notation to support structure confirmation.
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Medchemexpress LLC Va-k-14 hydrochloride | 1171341-19-7 | 99.0% | 25 MG
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VA-K-14 hydrochloride is a research-grade small molecule that antagonizes the thyroid-stimulating hormone receptor (TSHR). It is supplied as the hydrochloride salt in solid form and is intended for laboratory research use only.
- Specific TSHR antagonist with reported IC50 = 12.3 μM.
- Hydrochloride salt and solid physical form.
- Molecular weight 341.86 g·mol⁻¹; formula C18H16ClN3S.
- High purity (~99.0%) suitable for in vitro studies.
- Available in small research pack sizes such as 25 mg.
- For laboratory research only; not for human or veterinary use.
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Medchemexpress LLC Piperitone | 89-81-6 | MFCD00045532 | 99.89% | 152.24 | 500 MG
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Piperitone is a powerful repellent and antiappetent agent that exhibits insecticidal activity. It is highly toxic to *Cymbopogon schoenanthus* adults, newly laid eggs, and neonate larvae. It has been shown to be more toxic than crude oil to *Callosobruchus maculatus* adults, inhibiting the development of newly laid eggs and neonate larvae.
- Powerful repellent and antiappetent agent
- Exhibits insecticidal activity
- Highly toxic to adults, newly laid eggs, and neonate larvae
- More toxic than crude oil to insect adults
- Inhibits development of newly laid eggs and neonate larvae
- Strong ovicidal activity, aborting all eggs at 6.7 μL/L
- Kills all neonate larvae at 10 μM
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Medchemexpress LLC JNJ-38877605 | 943540-75-8 | 100.0 % | C19H13F2N7 | 25 MG
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JNJ-38877605 is an orally active ATP-competitive inhibitor of c-Met with an IC50 of 4 nM, demonstrating 600-fold selectivity for c-Met over 200 other tyrosine and serine-threonine kinases. It inhibits c-Met phosphorylation and regulates lipid accumulation, making it suitable for research in tumor and metabolic diseases.
- Orally active ATP-competitive c-Met inhibitor
- IC50 of 4 nM for c-Met
- 600-fold selectivity for c-Met over 200 other kinases
- Inhibits c-Met phosphorylation
- Regulates lipid accumulation
- Suitable for tumor and metabolic disease research
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Medchemexpress LLC ACTH (1-16) (human) | 5576-42-1 | MFCD00133032 | 99.95% | 1937.23 | 1 MG
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This product is an adrenocorticotropic hormone fragment that has demonstrated the ability to improve cardiovascular function and survival in experimental hemorrhagic shock. It is intended for research use only.
- Improves cardiovascular function.
- Enhances survival in hemorrhagic shock models.
- Supplied as a solid, white to off-white appearance.
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Cayman Chemical JP104 Fatty Acids and Derivati
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An irreversible FAAH inhibitor of the carbamate class with an IC50 value of 7.3 nM for the human recombinant enzyme when tested using radiolabeled oleamide as the substrate; the alkyl derivative on JP104 reacts with azide-modified reporter tags, such as azido-rhodamine or azido-biotin, for visualization of JP104 bound to FAAH in vivo
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Medchemexpress LLC Recombinant human NUDC protein (His tag) | >95.0% | 5 UG
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Recombinant human NUDC protein expressed in HEK293 cells with a C-terminal His tag, supplied as a lyophilized powder (5 μg). Intended for research use in biochemical assays, antibody validation, and studies of mitotic spindle function; stored at -20 °C and reported to be >95.0% pure by reducing SDS-PAGE.
- HEK293-expressed to retain mammalian post-translational modifications.
- C-terminal His tag enables affinity purification and detection.
- High purity (>95.0%) as determined by reducing SDS-PAGE.
- Lyophilized format for stable storage at -20 °C.
- Supplied quantity suitable for small-scale experiments: 5 μg.
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Medchemexpress LLC Glutaminase-IN-3 | 1439399-45-7 | 99.9% | C19H19F3N6O2S | 25 MG
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Glutaminase-IN-3 (compound 657) is a potent glutaminase inhibitor with an IC50 of 0.24 μM for Glutaminase 1 (GLS1). It is extracted from patent WO2014089048A1, compound 657. This product is for research use only.
- Potent glutaminase inhibitor
- Inhibits Glutaminase 1 (GLS1) with an IC50 of 0.24 μM
- High purity of 99.9%
- Available as a white to yellow solid
- Suitable for research applications
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Medchemexpress LLC WAY-612453 | 300809-10-3 | 98.0% | C₉H₈Cl₂N₄S | 5 MG
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WAY-612453 is an active molecule, presented as a white to off-white solid. It is suitable for research in amyloid diseases and synucleinopathies. This product is intended for scientific research or drug registration application only and not for individual use.
- Active molecule for studying amyloid diseases
- Suitable for research in synucleinopathies
- Presented as a white to off-white solid
- For scientific research or drug registration application only
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Medchemexpress LLC Phosphoglucomutase, Rabbit muscle | 9001-81-4 | approximately 62,000 Daltons | 500 U
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Phosphoglucomutase, Rabbit muscle, is an enzyme frequently utilized in biochemical studies. This enzyme facilitates the transfer of a phosphate group on the α-D-glucose monomer, promoting the interconversion of glucose-1-phosphate and glucose-6-phosphate. It plays a significant role in glycolysis and gluconeogenesis, important in the metabolism of proteins, lipids, and nucleic acids.
- Optimum pH: 7.5-8.0, with activity maintained within the range of 4.5-8.5
- Activators include: Divalent cations (especially Mg2+), glucose-1,6-diphosphate, and glutathione
- Inhibitors include: High concentrations of chelating agents, gluconate-6-phosphate, nucleotides, and acetate
- Can be dissolved in water (1 mg/mL) or according to specific experimental requirements
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