Items 31 to 40 of 138 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Glucotropaeolin | 5115-71-9 | sc-285861 sc-285861A | 20 mg 50 mg | $1224.00 $2448.00 | 3 | |
Glucotropaeolin is a phytochemical characterized by its glucoside structure, which enables it to undergo hydrolysis to release isothiocyanates upon enzymatic action. This transformation is significant in plant defense, as the resulting compounds can deter herbivores and pathogens. The compound's solubility in water enhances its bioavailability, allowing for efficient transport within plant tissues. Additionally, its interactions with cellular signaling pathways may influence growth and stress responses in plants. | ||||||
8-Isopentenylnaringenin | 68682-02-0 | sc-221146 | 5 mg | $326.00 | ||
8-Isopentenylnaringenin is a phytochemical characterized by its unique structural features that enable specific interactions with plant signaling pathways. This compound is known to influence the expression of genes related to stress responses, enhancing the plant's ability to adapt to environmental challenges. Its distinct molecular configuration allows for effective binding to receptor sites, potentially modulating hormonal pathways. Additionally, its stability in various conditions contributes to its role in plant defense mechanisms. | ||||||
Brassinin | 105748-59-2 | sc-202978 sc-202978A sc-202978B sc-202978C | 50 mg 100 mg 250 mg 1 g | $240.00 $381.00 $900.00 $2700.00 | 2 | |
Brassinin is a phytochemical notable for its intricate molecular structure, which facilitates unique interactions with plant defense systems. This compound is involved in the regulation of secondary metabolite production, enhancing the plant's resilience against biotic stressors. Its ability to form complexes with specific proteins may influence signaling cascades, leading to altered gene expression. Furthermore, Brassinin exhibits remarkable stability, allowing it to persist in various environmental conditions, thereby reinforcing its role in plant protection. | ||||||
(−)-Huperzine A | 102518-79-6 | sc-200183 sc-200183A | 1 mg 5 mg | $140.00 $355.00 | 1 | |
(-)-Huperzine A is a phytochemical characterized by its ability to modulate neurotransmitter dynamics through selective inhibition of acetylcholinesterase. This compound engages in specific molecular interactions that enhance synaptic transmission, influencing cognitive pathways. Its unique stereochemistry contributes to its binding affinity, allowing for effective competition with substrates. Additionally, (-)-Huperzine A demonstrates notable solubility in polar solvents, facilitating its bioavailability in various biological systems. | ||||||
L(−)-Malic Acid | 97-67-6 | sc-218650 sc-218650A | 10 g 100 g | $31.00 $46.00 | ||
L(-)-Malic Acid is a naturally occurring dicarboxylic acid that plays a crucial role in the citric acid cycle, facilitating energy production in plants. Its unique structure allows it to participate in various biochemical pathways, enhancing the transport of nutrients and influencing cellular respiration. The compound exhibits chelating properties, enabling it to bind metal ions, which can affect enzyme activity and metabolic processes. Its ability to modulate pH levels also contributes to its role in plant metabolism. | ||||||
Plumbagin | 481-42-5 | sc-253283 sc-253283A | 100 mg 250 mg | $51.00 $61.00 | 6 | |
Plumbagin is a naphthoquinone that exhibits notable antioxidant properties, engaging in redox reactions that can scavenge free radicals. Its unique structure allows for strong interactions with cellular macromolecules, influencing signaling pathways and gene expression. Additionally, Plumbagin can form complexes with metal ions, which may alter their bioavailability and impact various metabolic processes. Its hydrophobic nature facilitates membrane penetration, enhancing its biological activity. | ||||||
Docosanoic acid | 112-85-6 | sc-205300 sc-205300A | 1 g 5 g | $34.00 $49.00 | ||
Docosanoic acid, a long-chain saturated fatty acid, exhibits unique properties that influence lipid metabolism and membrane fluidity in plant cells. Its hydrophobic nature allows it to integrate into lipid bilayers, affecting membrane permeability and stability. Additionally, it can participate in esterification reactions, forming complex lipids that play roles in energy storage and signaling. The compound's chain length contributes to its distinct physical characteristics, impacting its interactions with other biomolecules. | ||||||
Methyl Salicylate | 119-36-8 | sc-204802 sc-204802A | 250 ml 500 ml | $46.00 $69.00 | ||
Methyl Salicylate, a naturally occurring ester, is notable for its role in plant defense mechanisms. It interacts with various enzymes and proteins, influencing metabolic pathways related to stress responses. Its volatility allows for rapid diffusion through plant tissues, facilitating signaling processes. Additionally, Methyl Salicylate can form hydrogen bonds, enhancing its solubility in polar environments, which aids in its distribution and interaction with other phytochemicals. | ||||||
α-Linolenic Acid | 463-40-1 | sc-205545 sc-205545A | 50 mg 250 mg | $37.00 $113.00 | 2 | |
α-Linolenic Acid, a key omega-3 fatty acid, plays a crucial role in plant metabolism and cellular signaling. Its unique structure allows for the formation of lipid bilayers, influencing membrane fluidity and permeability. This fatty acid participates in the synthesis of signaling molecules, such as jasmonates, which mediate stress responses. Additionally, α-Linolenic Acid can undergo oxidation, generating reactive oxygen species that further modulate plant defense mechanisms. | ||||||
Bergenin monohydrate | 477-90-7 | sc-205601 sc-205601A | 1 mg 5 mg | $95.00 $216.00 | ||
Bergenin monohydrate is a phenolic compound known for its diverse interactions within plant systems. It exhibits strong antioxidant properties, scavenging free radicals and stabilizing cellular structures. This compound can influence secondary metabolite pathways, enhancing the synthesis of flavonoids and other phenolics. Its unique ability to form hydrogen bonds contributes to its solubility and stability in various environments, facilitating its role in plant defense and adaptation. | ||||||