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Organic compounds that consists entirely of hydrogen and carbon elements usually organized in a chain; some may have a cyclic structure. Includes hydrocarbons that have additional functional groups such as aromatic rings.
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Dynole 2-24 is an indole-based dynamin GTPase inhibitor with an IC₅₀ of 0.56 μM for dynamin I. This compound is non-toxic and demonstrates increased potency against dynamin I and II both in vitro and within cells, with an IC₅₀ (CME) of 1.9 μM. It exhibits a 4.4-fold selectivity for dynamin I. Dynole 2-24 acts as an active in-cell inhibitor of clathrin-mediated endocytosis (CME).
Indole-based dynamin GTPase inhibitor.
IC₅₀ of 0.56 μM for dynamin I.
Nontoxic.
Increased potency against dynamin I and II in vitro and in cells (IC₅₀(CME)=1.9 μM).
Shows 4.4-fold selectivity for dynamin I.
Active in-cell inhibitor of clathrin-mediated endocytosis.
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Pentadecane is a floral volatile antimalarial agent with anti-inflammatory, analgesic, and antipyretic activities. It is a colorless to off-white liquid that can inhibit the growth of parasites such as Leishmania and avoid infection of macrophages. Store this product at room temperature for up to 3 years.
Inhibits growth of parasites such as Leishmania
Avoids infection of macrophages
Possesses anti-inflammatory, analgesic, and antipyretic activities
Ships at room temperature
Store at room temperature for 3 years
Store in solvent at -80°C for 2 years, or -20°C for 1 year
Keep container tightly sealed in a cool, well-ventilated area
Keep away from direct sunlight and sources of ignition
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I-287 is an orally active, selective protease-activated receptor 2 (PAR2) inhibitor used in research to modulate Gαq and Gα12/13-mediated signaling. It is supplied as a high-purity small-molecule compound characterized for pharmacology studies in cellular and animal models.
Selective PAR2 inhibitor.
Orally active small molecule.
Acts as a negative allosteric regulator of Gαq and Gα12/13.
Characterized for modulation of downstream signaling pathways.
High purity (~99.4%) suitable for research applications.
Available in research-scale quantities, such as 10 mg.
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TPI-287 is a brain-penetrant taxane-class microtubule stabilizer intended for preclinical oncology research. It stabilizes microtubules, shows antineoplastic activity in models of metastatic breast cancer to the brain, and is supplied as a research-grade small molecule for laboratory investigation.
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Dynole 2-24 is an indole-based dynamin GTPase inhibitor. It is nontoxic and demonstrates increased potency against dynamin I and II both in vitro and within cells. This compound also exhibits selective inhibition of dynamin I and is an active in-cell inhibitor of clathrin-mediated endocytosis.
Indole-based dynamin GTPase inhibitor.
Has an IC50 of 0.56 μM for dynamin I.
Nontoxic.
Shows increased potency against dynamin I and II in vitro and in cells (IC₅₀(CME)=1.9 μM).
Displays 4.4-fold selectivity for dynamin I.
Functions as an active in-cell inhibitor of clathrin-mediated endocytosis.
Encompass Procurement Services Non-distribution item offered as a customer accommodation; additional freight charges may apply. Learn More
Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
18-Azido-stearic acid is a versatile click chemistry reagent featuring an azide group. It functions as a hydrophobic bioconjugation linker, particularly when utilized with N-Myristoyltransferase, allowing for further modifications via Click-chemistry. It effectively participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules and ring strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups.
Contains an azide group for click chemistry applications
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Stearic acid is a long-chain dietary saturated fatty acid that significantly reduces visceral fat by inducing apoptosis of preadipocytes. This compound is valuable for research into cardiovascular and metabolic diseases.
Significantly reduces visceral fat
Induces apoptosis of preadipocytes
Used in cardiovascular and metabolic disease studies
Increases apoptosis of 3T3L1 preadipocytes
Decreases expression of cIAP2 and Bcl2
Can reduce bone mineral density
Can reduce abdominal fat content
Can reduce serum glucose concentration
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