Quinolines and derivatives
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Filtered Search Results
Apexbio Technology LLC Taurochenodeoxycholic acid sodium salt 6009-98-9 200mg
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Taurochenodeoxycholic acid sodium salt (CAS 6009-98-9) is an animal-derived bile acid derivative that modulates cell signaling pathways involved in apoptosis thereby influencing cellular growth and survival Research indicates that it also participates in the regulation of inflammatory responses and immune-related signaling mechanisms This compound is frequently utilized in cellular and animal models to investigate bile acid receptor-mediated physiological and pathological processes including its roles in metabolic disorders inflammatory diseases and immune-mediated conditions
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eMolecules AstaTech / 6-HYDROXYQUINOLINE-5-CARBALDEHYDE / 0.1g / 633668236 / 31374 / 98.000 / 77717-71-6 / MFCD11869102 / 173.171 / C10H7NO2
AstaTech / 6-HYDROXYQUINOLINE-5-CARBALDEHYDE / 0.1g / 633668236 / 31374 / 98.000 / 77717-71-6 / MFCD11869102 / 173.171 / C10H7NO2
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000422023 7 4 -DI-O-METHYLAPIG 25MG
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000422055 31-NORLANOSTENOL 25MG
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TARGETMOL CHEMICALS INC 3-Methyladenine 200MG
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Also available in 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. 3-Methyladenine (3-MA) is a PI3K inhibitor that selectively inhibits class IB PI3Kgamma (IC50 = 60 uM) and class III VPS34 (IC50 = 25 uM). 3-Methyladenine inhibits autophagy. Purity 99.51%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000427441 BETULIN 200MG
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Medchemexpress LLC Tropifexor | 1383816-29-2 | MFCD31693060 | 99.4% | 603.6 g/mol | C29H25F4N3O5S | 200 MG
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Tropifexor is a non-bile-acid, small-molecule agonist of the farnesoid X receptor (FXR) with reported biochemical potency around EC50 ≈ 0.2 nM. Identified in medicinal chemistry studies and advanced into clinical development, it is used in research on cholestatic liver diseases and nonalcoholic steatohepatitis (NASH). Available as a research reagent with reported high purity and defined analytical properties.
- Highly potent FXR agonist (EC50 ≈ 0.2 nM).
- Non-bile-acid small molecule suitable for biochemical and cellular assays.
- Reported high purity for research applications.
- Well characterized chemical properties for analytical workflows.
- Supported by published discovery and clinical development literature.
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TARGETMOL CHEMICALS INC Levosimendan 200MG
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Also available in 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Levosimendan (OR1259) is a calcium sensitizer used in the management of acutely decompensated congestive heart failure. It increases the sensitivity of the heart to calcium, thus increasing cardiac contractility without a rise in intracellular calcium. Levosimendan exerts its effect by increasing calcium sensitivity of myocytes by binding to cardiac troponin C in a calcium-dependent manner. Purity 99.7%
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Medchemexpress LLC 4-(2-(4-nitro-1H-imidazol-1-yl)ethyl)morpholine | 6497-78-5 | MFCD02029312 | >98.0% | 226.24 g/mol | C9H14N4O3 | 25 MG
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RGW-611 (4-(2-(4-nitro-1H-imidazol-1-yl)ethyl)morpholine) is a morpholine-derived research compound reported to sensitize hypoxic cells to radiation and to stimulate fatty acid synthesis. Supplied as a solid for laboratory research use.
- Enhances radiation-induced cell death in hypoxic V79-379A cells.
- Stimulates fatty acid synthesis in cellular assays.
- High purity suitable for research (>98.0% by HPLC).
- Molecular formula C9H14N4O3; molecular weight 226.24 g/mol.
- Store protected from light; use cold storage for stock solutions.
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Medchemexpress LLC RGW-611 50mg | 6497-78-5 | 50MG
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RGW 611 is a morpholine derivative that enhances radiation-induced cell death of hypoxic V79-379A cells RGW 611 also stimulates fatty acid synthesis[1 [2
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Medchemexpress LLC TLR7/8 agonist 1 dihydrochloride | 1620278-72-9 | MFCD31657341, MFCD26793840 | 99.7% | 432.39 | C22H27Cl2N5 | 50 MG
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TLR7/8 agonist 1 dihydrochloride is an imidazoquinoline-based small molecule that functions as a dual agonist of Toll-like receptors 7 and 8. Supplied as a dihydrochloride salt in solid form, it is intended for research use in immunostimulation and TLR signaling studies and includes recommended solubility and storage guidance.
- Dual TLR7/TLR8 agonist activity suitable for immunostimulation studies.
- Dihydrochloride salt form improves solubility and handling.
- High purity (99.7%) for reproducible experimental results.
- Solid, off-white to light yellow appearance for easy visual inspection.
- Highly soluble in DMSO; in vitro and in vivo formulation protocols provided.
- Recommended storage: solid at 4°C; in solution -80°C (6 months) or -20°C (1 month).
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TARGETMOL CHEMICALS INC Dactolisib 200MG
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Also available in 25 mg, 50 mg, 100 mg and bulk. Please contact Fisher for quotes. Dactolisib (BEZ235) is an orally bioavailable inhibitor of PI3K and mTOR, with IC50 values of 4 nM for p110alpha, 5 nM for p110gamma, 7 nM for p110delta, 75 nM for p110beta, and 20.7 nM for mTOR. Purity 99.71%
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000447108 DBCO-AMINE GMP 50MG
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eMolecules 2-QUINOLINECARBOXALDEHYDE 10G
5000165056 2-QUINOLINECARBOXALDEHYDE 10G
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TARGETMOL CHEMICALS INC Monocrotaline 200MG
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Also available in 1 g, 1 mL, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Monocrotaline (Crotaline) is a pyrrolizidine alkaloid extracted from the seeds of the Crotalaria plant. Monocrotaline has certain cellular activity against HepG2 cells and can induce pulmonary hypertension in rodents. Purity 99.59%
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