Items 11 to 20 of 138 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
L-Methionine | 63-68-3 | sc-394076 sc-394076A sc-394076B sc-394076C sc-394076D sc-394076E | 25 g 100 g 250 g 1 kg 5 kg 10 kg | $33.00 $36.00 $56.00 $148.00 $566.00 $1081.00 | ||
L-Methionine is an essential amino acid characterized by its sulfur-containing side chain, which plays a crucial role in various biochemical processes. Its unique structure allows it to participate in methylation reactions, serving as a precursor for important biomolecules like cysteine and taurine. This amino acid also influences antioxidant pathways, contributing to the regulation of oxidative stress. Furthermore, L-Methionine's ability to form disulfide bonds enhances protein stability and functionality, impacting cellular metabolism and growth. | ||||||
Horseradish peroxidase (HRP), RZ 1.0 | 9003-99-0 | sc-280786 sc-280786A | 100 mg 250 mg | $149.00 $281.00 | 6 | |
Horseradish peroxidase (HRP) is a versatile enzyme known for its ability to catalyze the reduction of hydrogen peroxide, facilitating electron transfer reactions. Its unique heme group enables specific interactions with various substrates, leading to distinct reaction kinetics. HRP exhibits remarkable stability and activity across a range of pH levels, making it an effective biocatalyst. Additionally, its role in oxidative stress responses highlights its importance in plant defense mechanisms. | ||||||
Ginsenoside Rg1 | 22427-39-0 | sc-205708 sc-205708A | 5 mg 10 mg | $260.00 $476.00 | ||
Ginsenoside Rg1 is a bioactive saponin derived from ginseng, characterized by its unique glycosylation pattern that influences its solubility and interaction with cellular membranes. This compound engages in specific molecular interactions with receptors, modulating signaling pathways and enhancing cellular responses. Its structural complexity allows for diverse biological activities, while its stability under physiological conditions supports its role in various biochemical processes. | ||||||
trans-4-Hydroxy-L-proline | 51-35-4 | sc-208462 sc-208462A | 25 g 100 g | $69.00 $222.00 | 1 | |
Trans-4-Hydroxy-L-proline is a naturally occurring amino acid that plays a significant role in plant metabolism. Its unique stereochemistry allows it to participate in the stabilization of collagen structures, influencing plant cell wall integrity. This compound can modulate enzymatic activities and is involved in the biosynthesis of secondary metabolites, contributing to the plant's defense mechanisms. Its presence can also affect the overall growth and development of plant tissues. | ||||||
Xylitol | 87-99-0 | sc-280193 sc-280193A | 100 g 500 g | $30.00 $100.00 | ||
Xylitol is a sugar alcohol that exhibits unique interactions with biological systems, particularly in its role as a competitive inhibitor of certain enzymes involved in carbohydrate metabolism. Its five-carbon structure allows it to participate in various metabolic pathways, influencing energy balance in cells. Additionally, xylitol's hydrophilic nature enhances its solubility in aqueous environments, facilitating its transport and uptake in plant tissues, which can impact osmotic regulation and cellular hydration. | ||||||
Thaxtomin A | 122380-18-1 | sc-358702 sc-358702A | 1 mg 5 mg | $241.00 $979.00 | 1 | |
Thaxtomin A is a phytochemical known for its role in plant defense mechanisms, particularly against pathogens. It disrupts cellulose synthesis by inhibiting specific enzymes, leading to altered cell wall integrity. This compound interacts with plant signaling pathways, triggering stress responses and enhancing resistance. Its unique structural features allow for selective binding to target proteins, influencing reaction kinetics and modulating plant growth and development under stress conditions. | ||||||
L-Carnitine hydrochloride | 6645-46-1 | sc-204782 sc-204782A | 1 g 5 g | $56.00 $97.00 | ||
L-Carnitine hydrochloride is a phytochemical that plays a crucial role in cellular energy metabolism. It facilitates the transport of fatty acids into mitochondria, where they undergo β-oxidation. This compound exhibits unique interactions with mitochondrial membranes, enhancing permeability and influencing metabolic pathways. Its presence can modulate reactive oxygen species levels, impacting cellular signaling and energy homeostasis. Additionally, L-Carnitine hydrochloride's solubility properties allow for efficient bioavailability in various biological systems. | ||||||
(1R)-(−)-Fenchone | 7787-20-4 | sc-237829 | 50 g | $35.00 | ||
(1R)-(-)-Fenchone is a phytochemical characterized by its distinctive bicyclic structure, which enables it to engage in specific molecular interactions with various biological receptors. Its unique stereochemistry contributes to its ability to influence enzymatic pathways, potentially altering metabolic processes. The compound exhibits notable volatility and solubility, facilitating its diffusion through plant tissues and enhancing its role in ecological signaling. Additionally, (1R)-(-)-Fenchone's reactivity with nucleophiles can lead to diverse chemical transformations, underscoring its dynamic behavior in phytochemical contexts. | ||||||
Galangin | 548-83-4 | sc-235240 | 25 mg | $133.00 | 5 | |
Galangin is a flavonoid known for its unique ability to form hydrogen bonds, which enhances its interaction with cellular membranes and proteins. This property allows it to modulate various signaling pathways, influencing cellular responses. Its planar structure contributes to effective π-π stacking interactions, promoting stability in complex formations. Additionally, Galangin's antioxidant properties stem from its capacity to scavenge free radicals, showcasing its role in plant defense mechanisms. | ||||||
Linamarin | 554-35-8 | sc-203439 | 50 mg | $262.00 | 5 | |
Linamarin is a cyanogenic glycoside that exhibits intriguing molecular interactions, particularly through its ability to release hydrogen cyanide upon enzymatic hydrolysis. This process occurs via specific enzymatic pathways, highlighting its role in plant defense against herbivores. The compound's structural features facilitate interactions with various enzymes, influencing reaction kinetics and stability. Linamarin's solubility in water further enhances its bioavailability, allowing for diverse ecological interactions. | ||||||