Items 71 to 80 of 201 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Medroxyprogesterone 17-Acetate | 71-58-9 | sc-205744 sc-205744A | 500 mg 1 g | $67.00 $99.00 | ||
Medroxyprogesterone 17-Acetate is a synthetic progestin characterized by its acetate ester, which enhances its lipophilicity and stability. This modification allows for prolonged action and selective receptor binding, influencing gene expression related to reproductive functions. Its unique structure facilitates specific interactions with nuclear receptors, modulating transcriptional activity. Additionally, it undergoes metabolic transformations that yield various active metabolites, contributing to its biological effects. | ||||||
Dichlorisone acetate | 79-61-8 | sc-234576 sc-234576B | 5 mg 500 mg | $215.00 $500.00 | 1 | |
Dichlorisone acetate is a synthetic compound featuring a dichlorinated structure that enhances its reactivity and specificity in biological systems. Its unique halogen substituents facilitate strong interactions with target proteins, influencing signaling pathways. The compound exhibits distinct kinetic properties, allowing for rapid binding and dissociation from receptors. This dynamic behavior, combined with its lipophilic nature, promotes effective cellular uptake and modulation of gene expression, impacting various physiological processes. | ||||||
Hexestrol | 84-16-2 | sc-205713 sc-205713A | 1 g 5 g | $97.00 $291.00 | 1 | |
Hexestrol is a synthetic nonsteroidal estrogen characterized by its unique phenolic structure, which allows for selective binding to estrogen receptors. This compound exhibits a high affinity for these receptors, leading to distinct conformational changes that activate specific gene transcription pathways. Its stability in biological systems is enhanced by its ability to form hydrogen bonds, influencing downstream signaling cascades. Additionally, Hexestrol's lipophilicity aids in its membrane permeability, facilitating cellular interactions. | ||||||
Gibberellin A4 | 468-44-0 | sc-235248 | 5 mg | $151.00 | 3 | |
Gibberellin A4 is a plant hormone that plays a crucial role in regulating growth and development. It interacts with specific receptors to trigger signal transduction pathways that promote cell elongation and seed germination. This compound influences gene expression by modulating transcription factors, leading to enhanced enzyme activity in metabolic processes. Its unique ability to promote stem elongation and flowering is linked to its dynamic molecular interactions within plant tissues, facilitating adaptive growth responses. | ||||||
Triamcinolone | 124-94-7 | sc-204924 sc-204924A | 50 mg 250 mg | $36.00 $89.00 | 3 | |
Triamcinolone is a synthetic glucocorticoid distinguished by its potent anti-inflammatory properties and unique structural features that enhance its interaction with glucocorticoid receptors. This compound undergoes specific conformational changes upon binding, modulating gene expression related to immune response and metabolism. Its lipophilic nature promotes efficient cellular uptake, while its ability to form stable complexes with proteins influences its pharmacokinetics and distribution within biological systems. | ||||||
Indole-3-butyric Acid | 133-32-4 | sc-279212 sc-279212A sc-279212B sc-279212C sc-279212D | 5 g 25 g 100 g 250 g 1 kg | $38.00 $110.00 $260.00 $520.00 $1457.00 | 1 | |
Indole-3-butyric Acid is a key plant hormone that influences root development and growth. It enhances cell division and elongation by binding to specific receptors, initiating a cascade of biochemical reactions. This compound modulates auxin transport and distribution, leading to differential growth responses in plant tissues. Its unique interactions with cellular components promote adventitious root formation, showcasing its pivotal role in plant morphology and adaptation. | ||||||
Betamethasone 21-phosphate sodium salt | 151-73-5 | sc-204648 sc-204648A | 250 mg 1 g | $115.00 $351.00 | ||
Betamethasone 21-phosphate sodium salt is a synthetic corticosteroid that exhibits potent anti-inflammatory properties through its interaction with glucocorticoid receptors. Upon binding, it activates gene transcription pathways that regulate immune responses and cellular metabolism. This compound also influences ion transport mechanisms, enhancing cellular stability and resilience. Its solubility in aqueous environments facilitates rapid cellular uptake, allowing for swift modulation of physiological processes. | ||||||
2-hydroxy Estradiol | 362-05-0 | sc-205085 sc-205085-CW sc-205085A sc-205085B sc-205085C | 1 mg 1 mg 5 mg 10 mg 25 mg | $96.00 $132.00 $353.00 $598.00 $1189.00 | ||
2-Hydroxy Estradiol is a naturally occurring estrogen that plays a crucial role in modulating various physiological processes. It exhibits unique binding affinity to estrogen receptors, influencing gene expression and cellular signaling pathways. This compound is involved in the regulation of reproductive functions and bone metabolism. Its distinct hydroxyl group enhances its solubility and reactivity, facilitating interactions with other biomolecules and contributing to its biological activity. | ||||||
5a-Pregnane-3,20-dione | 566-65-4 | sc-206068 sc-206068A | 500 mg 1 g | $113.00 $203.00 | 1 | |
5a-Pregnane-3,20-dione is a steroid hormone characterized by its role in the regulation of metabolic processes and reproductive functions. It interacts with specific nuclear receptors, triggering a cascade of gene expression changes that influence cellular behavior. This compound is notable for its hydrophobic nature, which affects its transport and bioavailability in biological systems. Its unique structural features allow for selective enzymatic transformations, impacting various metabolic pathways. | ||||||
Asterric acid | 577-64-0 | sc-202474 | 1 mg | $196.00 | ||
Asterric acid is a unique acid halide that plays a pivotal role in cellular signaling and metabolic regulation. Its structure facilitates specific interactions with protein receptors, leading to the modulation of gene expression. The compound exhibits distinct reactivity patterns, particularly in acylation reactions, which influence its stability and interaction with other biomolecules. Its lipophilic characteristics enhance membrane permeability, allowing for efficient cellular uptake and signaling. | ||||||