Items 31 to 40 of 291 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Mestranol | 72-33-3 | sc-211802 | 10 mg | $233.00 | ||
Mestranol is a synthetic estrogen that exhibits unique molecular interactions through its ethynyl group, which enhances its binding affinity to estrogen receptors. This compound undergoes specific metabolic pathways, including hydroxylation and conjugation, which modulate its bioactivity. Its lipophilic nature allows for efficient membrane permeability, influencing its distribution and stability in biological systems. Mestranol's distinct structural characteristics contribute to its reactivity and interaction dynamics within cellular environments. | ||||||
Oleanolic Acid | 508-02-1 | sc-205775 sc-205775A | 100 mg 500 mg | $84.00 $296.00 | 8 | |
Oleanolic Acid is a pentacyclic triterpenoid that showcases unique interactions with cellular membranes due to its hydrophobic structure, facilitating its integration into lipid bilayers. It engages in specific signaling pathways, influencing gene expression through modulation of transcription factors. The compound exhibits antioxidant properties, which can alter reaction kinetics in oxidative stress scenarios. Its ability to form complexes with proteins enhances its functional versatility in various biochemical contexts. | ||||||
Fusidic acid sodium salt | 751-94-0 | sc-202164 | 50 mg | $32.00 | 2 | |
Fusidic acid sodium salt is a steroidal compound characterized by its unique ability to interact with protein synthesis pathways. It selectively binds to elongation factor G, inhibiting bacterial protein translation. This interaction alters the kinetics of ribosomal activity, leading to a disruption in cellular function. Additionally, its amphipathic nature allows it to influence membrane fluidity, potentially affecting cellular signaling and permeability in various biological systems. | ||||||
β-Estradiol 17-valerate | 979-32-8 | sc-239862 | 1 g | $135.00 | ||
β-Estradiol 17-valerate is a steroid that exhibits unique interactions with estrogen receptors, modulating gene expression through distinct signaling pathways. Its lipophilic nature enhances membrane permeability, facilitating rapid cellular uptake. The compound's esterification alters its pharmacokinetics, resulting in prolonged bioavailability and a gradual release profile. This behavior influences its affinity for target tissues, impacting downstream physiological responses and metabolic processes. | ||||||
20-Hydroxyecdysone | 5289-74-7 | sc-202407 sc-202407A sc-202407B | 5 mg 10 mg 50 mg | $92.00 $132.00 $500.00 | 6 | |
20-Hydroxyecdysone is a naturally occurring steroid that plays a crucial role in insect molting and development. It binds to ecdysteroid receptors, initiating a cascade of gene expression that regulates growth and metamorphosis. Its hydrophilic properties allow for effective solubility in biological systems, enhancing its bioactivity. The compound's unique structure facilitates specific molecular interactions, influencing various signaling pathways and metabolic processes in target organisms. | ||||||
Digitoxigenin | 143-62-4 | sc-255098 | 10 mg | $97.00 | 6 | |
Digitoxigenin is a steroidal compound characterized by its ability to interact with specific cellular receptors, influencing ion transport and cardiac function. Its unique steroid backbone allows for distinct conformational changes upon binding, which can modulate enzyme activity and cellular signaling pathways. The compound exhibits notable lipophilicity, enhancing its membrane permeability and facilitating rapid distribution within biological systems, thereby impacting physiological responses. | ||||||
Muristerone A | 38778-30-2 | sc-301176 | 1 mg | $147.00 | ||
Muristerone A is a steroid that exhibits unique interactions with nuclear receptors, particularly influencing gene expression through its binding affinity. Its structural configuration allows for selective modulation of transcriptional activity, impacting various metabolic pathways. The compound's hydrophobic nature enhances its solubility in lipid environments, promoting efficient cellular uptake. Additionally, Muristerone A can induce specific post-translational modifications, further diversifying its biological effects. | ||||||
Epibrassinolide | 78821-43-9 | sc-211419 | 10 mg | $353.00 | 3 | |
Epibrassinolide is a steroid that plays a crucial role in plant growth regulation by interacting with specific receptors to modulate signal transduction pathways. Its unique stereochemistry facilitates binding to brassinosteroid receptors, triggering a cascade of cellular responses that enhance stress tolerance and growth. The compound's lipophilic characteristics enable it to penetrate cellular membranes effectively, promoting rapid physiological changes. Furthermore, Epibrassinolide influences enzyme activity, contributing to the regulation of various metabolic processes. | ||||||
Prednisone Acetate | 125-10-0 | sc-394059 sc-394059A | 100 mg 1 g | $60.00 $240.00 | ||
Prednisone Acetate is a synthetic steroid characterized by its unique structural modifications that enhance its glucocorticoid activity. Its ability to selectively bind to glucocorticoid receptors initiates a series of genomic and non-genomic responses, influencing gene expression and cellular metabolism. The compound's hydrophobic nature allows for efficient membrane diffusion, facilitating rapid cellular uptake. Additionally, its interactions with various signaling pathways can modulate inflammatory responses and metabolic functions, showcasing its versatility in biological systems. | ||||||
2-Methoxyestradiol | 362-07-2 | sc-201371 sc-201371A | 10 mg 50 mg | $70.00 $282.00 | 6 | |
2-Methoxyestradiol is a naturally occurring estrogen metabolite that exhibits unique interactions with estrogen receptors, influencing cellular signaling pathways. Its distinct methoxy group enhances its solubility and alters its binding affinity, leading to varied biological effects. The compound is known to disrupt microtubule dynamics, affecting cell cycle progression and apoptosis. Additionally, its role in modulating angiogenesis highlights its complex behavior in cellular environments, showcasing its multifaceted nature. |