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-santonin (CAS No 481-06-1) is a sesquiterpene lactone commonly studied in the field of biomedical research for its bioactive properties It is derived from Artemisia species particularly Artemisia maritima -santonin is known to influence biochemical pathways by interacting with specific cellular targets including enzymes and receptors that modulate inflammation and apoptosis Its in vitro activity often falls within the nanomolar to low micromolar range indicating significant potency This compound is frequently used in cell models and animal studies to explore its potential as an anti-inflammatory and antiparasitic agent as well as in drug screening programs to identify novel therapeutic candidates Experimental concentrations typically depend on the specific research design
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-santonin (CAS No 481-06-1) is a sesquiterpene lactone commonly studied in the field of biomedical research for its bioactive properties It is derived from Artemisia species particularly Artemisia maritima -santonin is known to influence biochemical pathways by interacting with specific cellular targets including enzymes and receptors that modulate inflammation and apoptosis Its in vitro activity often falls within the nanomolar to low micromolar range indicating significant potency This compound is frequently used in cell models and animal studies to explore its potential as an anti-inflammatory and antiparasitic agent as well as in drug screening programs to identify novel therapeutic candidates Experimental concentrations typically depend on the specific research design
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
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Alantolactone is a sesquiterpene lactone used in research as a selective STAT3 inhibitor with potent anticancer activity; it induces apoptosis in cancer cells and is supplied as a solid with characterized purity, solubility, and storage recommendations suitable for in vitro and in vivo studies.
Selective STAT3 inhibitor suitable for cancer biology research.
High purity (≈99.9%) supports reproducible results.
Soluble in DMSO at high concentrations for in vitro assays.
Available in small pack sizes (including 10 MG) for pilot studies.
Recommended storage conditions provided for long-term stability.
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Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Alantolactone (Inula camphor)(Alant camphor) a sesquiterpene lactone has potential activity against triple-negative breast Y MDA-MB-231 cells by suppressing the signal transducer and activator of transcription 3 (STAT3) signaling pathway. purity: 99%
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Alantolactone a naturally occurring eudesmane-type sesquiterpene lactone (SL) could induce activin/SMAD3 signaling and disrupt Cripto-1/activin receptor type II A interaction
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Medchemexpress, HY-N0038 5mg Alantolactone CAS:546-43-0 Alantolactone is a selective STAT3 inhibitor, with potent anticancer activity. 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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Alantolactone a naturally occurring eudesmane-type sesquiterpene lactone (SL) could induce activin/SMAD3 signaling and disrupt Cripto-1/activin receptor type II A interaction
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DL-alpha-tocopherol methoxypolyethylene glycol succinate is a polyethylene glycol succinate derivative of DL-alpha-tocopherol used as a solubilizer and surfactant in biological and pharmaceutical formulations. It is supplied as a solution and characterized for solubility, storage, and purity.
provides amphiphilic solubilization for hydrophobic compounds
forms clear aqueous solutions: water ≥ 50 mg/mL
soluble in PBS at 25 mg/mL with ultrasonic treatment and warming
high purity by HPLC (98.0%)
polymeric chemical formula (C2H4O)nC34H56O5; reported molecular weight approximately 605 g/mol
store as solution at -20 °C for up to 2 years
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CY 208-243 is a selective dopamine D1 receptor agonist that demonstrates antiparkinsonian activity. It is intended for research purposes only. In vivo studies show that pretreatment with CY 208-243 prevents the increase of dopamine (DA) release and metabolism induced by the D-1 antagonist, SCH 23390.
Selective dopamine D1 receptor agonist
Exhibits antiparkinsonian activity
Prevents increase of DA release and metabolism
For research use only
Appearance: Solid, white to off-white
Solubility (in vitro): DMSO: 50 mg/mL
Storage (powder): -20°C for 3 years, 4°C for 2 years
Storage (in solvent): -80°C for 6 months, -20°C for 1 month
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