Phytochemicals
Items 91 to 100 of 138 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
2-Phenylethanol | 60-12-8 | sc-238198 | 250 ml | $68.00 | ||
2-Phenylethanol, a phenolic compound, exhibits intriguing interactions within plant systems, particularly in the modulation of aromatic profiles. Its ability to form hydrogen bonds enhances its solubility in various solvents, facilitating its role in biosynthetic pathways. This compound can influence the expression of genes related to stress responses, while its hydrophobic characteristics allow it to integrate into lipid membranes, potentially affecting membrane fluidity and signaling cascades. | ||||||
o-Xylene | 95-47-6 | sc-397231 sc-397231A sc-397231B | 250 ml 1 L 2.5 L | $67.00 $173.00 $367.00 | ||
o-Xylene, a dimethyl-substituted aromatic hydrocarbon, plays a notable role in plant metabolism, particularly in the synthesis of secondary metabolites. Its unique structure allows for effective π-π stacking interactions, which can stabilize complex formations with other phytochemicals. This compound can influence enzymatic activity by modulating the active sites of certain enzymes, thereby affecting metabolic pathways. Additionally, its hydrophobic nature aids in membrane penetration, impacting cellular signaling and transport processes. | ||||||
2-Methylbutyraldehyde | 96-17-3 | sc-238148 | 50 g | $100.00 | ||
2-Methylbutyraldehyde, a branched-chain aldehyde, exhibits intriguing interactions within plant systems, particularly in the realm of volatile organic compounds. Its unique carbon skeleton facilitates specific hydrogen bonding and dipole-dipole interactions, enhancing its reactivity in various biochemical pathways. This compound can influence the biosynthesis of terpenes and other secondary metabolites, potentially altering plant defense mechanisms. Its moderate polarity allows for effective solubility in diverse organic matrices, impacting its distribution and bioavailability in plant tissues. | ||||||
Chlorophyll, oil soluble | 1406-65-1 | sc-337628 | 100 g | $209.00 | ||
Chlorophyll, an oil-soluble phytochemical, plays a pivotal role in photosynthesis by facilitating light absorption through its unique porphyrin structure. This compound exhibits strong π-π stacking interactions, enhancing its stability and efficiency in capturing photons. Its hydrophobic tail allows for integration into thylakoid membranes, optimizing energy transfer processes. Additionally, chlorophyll's ability to form complexes with metal ions can influence electron transport dynamics, impacting overall plant metabolism. | ||||||
2-Phenylethylamine hydrochloride | 156-28-5 | sc-254290 | 25 g | $60.00 | ||
2-Phenylethylamine hydrochloride, a notable phytochemical, is characterized by its ability to modulate neurotransmitter activity through specific receptor interactions. Its aromatic structure allows for effective π-π interactions, enhancing binding affinity to various biological targets. This compound also participates in unique metabolic pathways, influencing the synthesis of biogenic amines. Furthermore, its solubility properties facilitate its role in plant signaling, contributing to stress response mechanisms. | ||||||
1,4-Diaminobutane | 110-60-1 | sc-255938 sc-255938A | 25 g 100 g | $37.00 $92.00 | ||
1,4-Diaminobutane, a versatile phytochemical, exhibits unique properties through its ability to form hydrogen bonds, enhancing its interaction with biological macromolecules. This compound plays a role in polyamine biosynthesis, influencing cellular growth and differentiation. Its linear structure allows for effective chain interactions, promoting stability in various environments. Additionally, it participates in redox reactions, contributing to cellular signaling and stress response pathways in plants. | ||||||
Umbelliferone | 93-35-6 | sc-208477 sc-208477A sc-208477B sc-208477C | 25 g 100 g 250 g 1 kg | $86.00 $273.00 $398.00 $1581.00 | ||
Umbelliferone, a coumarin derivative, is notable for its ability to absorb UV light, which aids in protecting plants from photodamage. Its structure allows for intramolecular hydrogen bonding, influencing its solubility and reactivity. This compound participates in various metabolic pathways, including the biosynthesis of flavonoids, and exhibits antioxidant properties by scavenging free radicals. Its unique interactions with enzymes can modulate biochemical processes, enhancing plant resilience. | ||||||
Ginkgolic acid C17:1 | 111047-30-4 | sc-228252 sc-228252A sc-228252B | 5 mg 10 mg 20 mg | $279.00 $452.00 $834.00 | 2 | |
Ginkgolic acid C17:1, a phytochemical derived from Ginkgo biloba, exhibits unique properties due to its unsaturated fatty acid structure. It interacts with cellular membranes, potentially altering fluidity and permeability. This compound can influence lipid metabolism and has been shown to modulate signaling pathways related to stress responses in plants. Its ability to form complexes with metal ions may also play a role in protecting against oxidative stress, enhancing plant vitality. | ||||||
(+)cis,trans-Abscisic Acid-d6 | 721948-65-8 | sc-217922 sc-217922A | 1 mg 10 mg | $554.00 $3723.00 | 37 | |
(+)cis,trans-Abscisic Acid-d6 is a stable isotopic variant of abscisic acid, a key plant hormone involved in stress responses. Its deuterated form allows for precise tracking in metabolic studies, revealing insights into its role in stomatal closure and seed dormancy. This compound participates in intricate signaling cascades, influencing gene expression and enzyme activity. Its unique isotopic labeling enhances the understanding of its biosynthetic pathways and interactions with other phytohormones. | ||||||
trans-3-Hydroxycinnamic acid | 14755-02-3 | sc-251274 sc-251274A | 5 g 25 g | $20.00 $64.00 | ||
Trans-3-Hydroxycinnamic acid is a notable phytochemical recognized for its role in plant defense mechanisms and stress responses. Its unique structure enables it to participate in the phenylpropanoid pathway, influencing the synthesis of lignin and flavonoids. This compound exhibits antioxidant properties, scavenging free radicals and stabilizing cellular components. Additionally, it can form complexes with metal ions, potentially affecting nutrient availability and transport within plant tissues. | ||||||