Items 181 to 190 of 201 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Prednisolone 21-acetate | 52-21-1 | sc-250775 sc-250775A sc-250775B sc-250775C sc-250775D | 1 g 5 g 10 g 100 g 500 g | $69.00 $345.00 $681.00 $3665.00 $8550.00 | 1 | |
Prednisolone 21-acetate is a synthetic glucocorticoid that exhibits a high affinity for glucocorticoid receptors, triggering a cascade of genomic and non-genomic responses. Its structural modifications enhance lipophilicity, allowing for efficient cellular uptake and prolonged action. The compound engages in specific protein interactions, modulating inflammatory pathways and influencing gene expression. Its unique metabolic profile ensures a balanced pharmacokinetic behavior, optimizing its biological effects. | ||||||
3,3′,5-Triiodo-L-thyronine sodium salt | 55-06-1 | sc-231968 sc-231968A sc-231968B | 100 mg 500 mg 1 g | $90.00 $245.00 $439.00 | ||
3,3',5-Triiodo-L-thyronine sodium salt is a potent thyroid hormone that plays a crucial role in regulating metabolic processes. It interacts with nuclear receptors, initiating transcriptional changes that influence energy metabolism and growth. The compound's unique iodine substitution enhances its binding affinity, leading to distinct physiological effects. Its rapid cellular uptake and specific receptor interactions facilitate a swift response in metabolic regulation, underscoring its significance in endocrine signaling pathways. | ||||||
Dydrogesterone | 152-62-5 | sc-214952 | 25 mg | $159.00 | 1 | |
Dydrogesterone is a synthetic progestogen that exhibits a high affinity for progesterone receptors, influencing gene expression and cellular signaling pathways. Its unique structure allows for selective binding, promoting distinct molecular interactions that modulate reproductive processes. The compound's stability and lipophilicity enhance its bioavailability, facilitating effective cellular uptake. Dydrogesterone's role in regulating hormonal balance underscores its importance in various physiological functions. | ||||||
Gibberellin A8 | 7044-72-6 | sc-490115 | 1 mg | $400.00 | ||
Gibberellin A8 is a plant hormone that plays a crucial role in regulating growth and development. It interacts with specific receptors to activate signaling pathways that promote stem elongation, seed germination, and flowering. Its unique molecular structure allows for precise binding, influencing gene expression related to growth processes. Gibberellin A8 also modulates enzyme activity, enhancing the breakdown of stored nutrients, which supports rapid growth in plants. | ||||||
cis-Zeatin | 32771-64-5 | sc-214743A sc-214743 | 1 mg 10 mg | $200.00 $849.00 | 1 | |
Cis-Zeatin is a cytokinin that significantly influences plant cell division and differentiation. It binds to specific receptors, triggering a cascade of signaling pathways that enhance shoot and root development. This hormone is known for its role in delaying leaf senescence, promoting chloroplast development, and regulating nutrient mobilization. Its unique structure allows for effective interaction with various enzymes, facilitating diverse physiological responses in plants. | ||||||
3,3′,5-Triiodo-L-thyronine-13C6 | sc-216565 | 5 mg | $8000.00 | |||
3,3',5-Triiodo-L-thyronine-13C6 is a potent thyroid hormone that plays a crucial role in regulating metabolic processes. Its unique isotopic labeling allows for precise tracking in metabolic studies. This compound interacts with nuclear receptors, modulating gene expression and influencing energy metabolism. Its distinct molecular structure enhances binding affinity, leading to varied physiological effects, including thermogenesis and lipid metabolism, making it a key player in endocrine signaling pathways. | ||||||
Diethylstilbestrol, mixture of cis and trans | 6898-97-1 | sc-234683 | 5 g | $78.00 | ||
Diethylstilbestrol, a synthetic estrogen, exhibits unique stereochemical properties due to its cis and trans isomeric forms, which influence its binding affinity to estrogen receptors. This compound engages in specific molecular interactions that modulate gene expression related to reproductive and developmental processes. Its distinct conformational flexibility allows for varied receptor activation, impacting cellular signaling pathways and influencing physiological responses. The compound's dual isomeric nature contributes to its complex biological behavior. | ||||||
Systemin | 137181-56-7 | sc-391333 sc-391333A | 0.5 mg 1 mg | $99.00 $268.00 | ||
Systemin is a plant peptide hormone that initiates defense responses against herbivory. It operates through a unique signaling pathway, activating jasmonic acid synthesis, which in turn regulates the expression of defense-related genes. This hormone's specific interactions with membrane receptors trigger a cascade of intracellular signaling events, enhancing the plant's resilience to stress. Its role in systemic acquired resistance highlights its importance in plant immunity and adaptation. | ||||||
3,5-Diiodothyropropionic acid | 1158-10-7 | sc-256593 | 50 mg | $184.00 | 4 | |
3,5-Diiodothyropropionic acid is a potent thyroid hormone analog that influences metabolic processes through its unique interactions with nuclear receptors. It modulates gene expression by binding to thyroid hormone receptors, altering transcriptional activity. This compound exhibits distinct kinetic properties, affecting the rate of metabolic reactions and energy expenditure. Its structural features allow for selective receptor engagement, impacting cellular signaling pathways and metabolic regulation. | ||||||
Estrone 3-sulfate potassium salt | 1240-04-6 | sc-234880 | 100 mg | $182.00 | ||
Estrone 3-sulfate potassium salt is a steroid hormone sulfate that plays a crucial role in regulating various biological processes. Its unique sulfate group enhances solubility and facilitates transport across cell membranes, allowing for efficient interaction with estrogen receptors. This compound exhibits distinct binding affinities, influencing gene transcription and cellular signaling pathways. Its stability in physiological conditions supports prolonged activity, making it a key player in endocrine regulation. | ||||||