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Aromatic organic heterocyclic compounds that consist of a six-membered ring with four carbon atoms and two nitrogen atoms at opposite positions of the ring, making this ring symmetrical.
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3-Methyl-2-quinoxalinone (3-methyl-1H-quinoxalin-2-one) is a heterocyclic small-molecule synthetic intermediate commonly used in medicinal and pharmaceutical synthesis. It is supplied as a high-purity solid for research and organic synthesis applications.
High purity (99.6%) for research and synthesis.
Molecular formula C9H8N2O and molecular weight 160.17 g/mol.
Suitable as a building block in pharmaceutical and organic chemistry.
Available in laboratory quantities, including 10 G packaging.
Solid form for convenient handling and storage.
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A deuterated Piezo1 agonist supplied for laboratory research use. It activates Piezo1 channels and is provided with analytical and safety documentation to support experimental reproducibility and handling.
Deuterated Piezo1 agonist suitable for research applications.
High purity (99.8%) for experimental consistency.
Supplied with datasheet, certificate of analysis, HNMR, and RP-HPLC documentation.
Available in multiple small pack sizes for dose-ranging studies.
Powder stable at -20°C for up to 3 years; aliquots in solvent require -80°C for long-term storage.
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Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. DPTIP is an effective inhibitor of neutral sphingomyelinase 2 with an IC50 value of 30 nM. purity: 98%
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SET 2 is an antagonist of transient receptor potential vanilloid type 2(TRPV2) with an IC50 of 0.46 uM. SET 2 shows selectivity over TRPV1 TRPV3 and TRPV4. purity: 98%
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Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Droxinostat (NS 41080) is a selective inhibitor of HDAC mostly for HDACs 6 and 8 with IC50 of 2.47 uM and 1.46 uM greater than 8-fold selective against HDAC3 and no inhibition to HDAC1 2 4 5 7 9 and 10. purity: 99%
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Also available in 1 mg 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. UNC1999 is a orally bioavailable effective and specific inhibitor of EZH2 (IC50=2 nM) and EZH1 (IC50=45). purity: 99%
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Also available in 2 mg 5 mg 10 mg 25 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Pimasertib (AS703026) is an orally bioavailable small-molecule inhibitor of MEK1 and MEK2 (MEK1/2) with potential antineoplastic activity. purity: 98%
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SHMT-IN-2 (compound 2) is a specific human SHMT1/2 small molecule inhibitor that acts on SHMT1 (IC50 13 nM) and SHMT2 (IC50 66 nM). SHMT-IN-2 inhibits the growth of many human cancer cells and is sensitive to B-cell lymphoma. purity: 98%
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. PDE4B-IN-2 (A 33) is an orally active and selective PDE4B inhibitor with an IC50 of 15 nM. PDE4B-IN-2 inhibits PDE4D (IC50=1.7 µM). PDE4B-IN-2 exhibits potent anti-inflammatory effects. purity: 99%
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Also available in 10 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. APNEA ((2R3R4S5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-34-diol) is a non-selective agonist of adenosine A3 receptor. purity: 99%
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Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. ISCK03 is a selective SCF/c-Kit inhibitor. purity: 98%
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. A(beta)42-IN-2 is a (gamma)-secretase modulator. A(beta)42-IN-2 has an IC 50 of 6.5 nM for (alpha)(beta) 42. A(beta)42-IN-2 can be used for the Alzheimer's disease research[1]. purity: 99%
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