Tetrahydrofuran
Medchemexpress LLC MPT0B392 | 1346169-92-3 | MFCD32174244 | 99.6% | 404.44 | C19H20N2O6S | 50 MG
MPT0B392 is an orally active quinoline-derived microtubule-depolymerizing agent that inhibits tubulin polymerization, activates c-Jun N-terminal kinase (JNK), and induces apoptosis. It is used in cellular assays and preclinical models to study microtubule dynamics and apoptosis signaling pathways.
- Inhibits tubulin polymerization and induces mitotic arrest.
- Activates c-Jun N-terminal kinase (JNK) and promotes apoptosis.
- High purity (99.6%) for reliable experimental results.
- Soluble in DMSO (≈100 mg/mL) for convenient formulation.
- Solid, light yellow appearance for easy inspection.
- Stable as powder at -20°C for up to 3 years.
Medchemexpress LLC MPT0B392 | 1346169-92-3 | 99.6% | 404.44 g/mol | C19H20N2O6S | 100 MG
MPT0B392 is an orally active quinoline-derived microtubule-depolymerizing agent that activates c-Jun N-terminal kinase (JNK) and induces apoptosis. It inhibits tubulin polymerization and causes mitotic arrest, making it useful in cell biology and oncology research investigating microtubule dynamics and drug resistance mechanisms.
- High purity (≈99.6%) suitable for research assays.
- Solid powder, light yellow to yellow appearance.
- Well-characterized molecular properties (C19H20N2O6S, 404.44 g/mol).
- Documented storage stability in powder and solution.
- Biological activity: tubulin depolymerizer, JNK activator, apoptosis inducer.
- Includes CAS number for unambiguous identification.
Medchemexpress LLC Rifalazil 100mg | 129791-92-0 | 100MG
Rifalazil (KRM-1648 ABI-1648) a rifamycin derivative inhibits the bacterial DNA-dependent RNA polymerase and kills bacterial cells by blocking off the -subunit in RNA polymerase[1 Rifalazil (KRM-1648 ABI-1648) is an antibiotic exhibits high potency against mycobacteria gram-positive bacteria Helicobacter pylori C pneumoniae and C trachomatis with MIC values from 0 00025 to 0 0025 g/ml[3 Rifalazil (KRM-1648 ABI-1648) has the potential for the treatment of Chlamydia infection Clostridium difficile associated diarrhea (CDAD) and tuberculosis (TB)[2
Medchemexpress LLC N'-(4-(diethylamino)-2-hydroxybenzylidene)isonicotinohydrazide | 140405-36-3 | MFCD00542031 | 99.7% | 312.37 g/mol | C17H20N4O2 | 10 MG
RSVA405 (CAS 140405-36-3) is a small-molecule activator of AMP-activated protein kinase (AMPK) used in cellular and biochemical research. It promotes CaMKKβ-dependent AMPK activation, inhibits mTOR signaling, and can induce autophagy; supplied at high purity for research applications.
- Potent AMPK activator; reported EC50 = 1 μM.
- High purity (~99.7%).
- Molecular formula C17H20N4O2; molecular weight 312.37 g/mol.
- Soluble in DMSO; available as solid or DMSO solution.
- For research use only; not for human consumption.
AARON CHEMICALS LLC DIMETHYL ISOSORBIDE, 500G
Dimethyl Isosorbide | Purity: 97% | Mol Wt: 174.1944 | 5306-85-4 | MFCD00064828 | 500g
Sigma Aldrich Fine Chemicals Biosciences Tetrahydrofuran ACS reagent, >=99.0%, contains 250 ppm BHT as inhibitor | 109-99-9 | MFCD00005356 | 4L
Tetrahydrofuran ACS reagent, >=99.0%, contains 250 ppm BHT as inhibitor | Purity: >=99.0% | Mol Wt: 72.11 | 109-99-9 | MFCD00005356 | 4L
Medchemexpress LLC Ceftaroline 100mg | 189345-04-8 | 100MG
T-91825 (PPI-0903M) an N-phosphono-type cephalosporin is the active form of TAK-599 T-91825 is active against both gram-positive and gram-negative bacteria[1 [2
eMolecules Medchem Express / Broflanilide / 5mg / 559839407 / HY-108689 / / 1207727-04-5 / [null] / 663.285 / C25H14BrF11N2O2
Medchem Express / Broflanilide / 5mg / 559839407 / HY-108689 / / 1207727-04-5 / [null] / 663.285 / C25H14BrF11N2O2