Fatty Acid Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
(2S,3R,4E)-2-Amino-4-tetradecene-1,3-diol | 24558-60-9 | sc-391392 | 10 mg | $360.00 | ||
(2S,3R,4E)-2-Amino-4-tetradecene-1,3-diol exhibits unique properties as a fatty acid, characterized by its dual functional groups that enable versatile interactions with lipid membranes. Its elongated hydrocarbon chain enhances hydrophobic interactions, promoting integration into lipid bilayers. The compound's ability to form hydrogen bonds with polar head groups facilitates membrane fluidity and stability, while its reactivity allows for selective modifications in lipid metabolism pathways, influencing cellular signaling and energy homeostasis. | ||||||
(+)-trans-C75 | 1234694-20-2 | sc-500786 sc-500786A | 1 mg 5 mg | $141.00 $849.00 | 1 | |
(+)-trans-C75 is a distinctive fatty acid known for its unique stereochemistry, which influences its interaction with biological membranes. The compound's trans configuration enhances its packing efficiency within lipid bilayers, contributing to altered membrane dynamics. Its hydrophobic tail promotes strong van der Waals forces, while the presence of functional groups allows for specific binding to proteins involved in lipid metabolism. This interplay can modulate enzymatic activity and cellular signaling pathways, impacting overall lipid homeostasis. | ||||||
Methyl 15-Hydroxypentadecanoate, (C15) | 76529-42-5 | sc-280962A sc-280962 | 1 mg 5 mg | $38.00 $75.00 | ||
Methyl 15-Hydroxypentadecanoate is a long-chain fatty acid derivative characterized by its unique hydroxyl group, which facilitates hydrogen bonding and enhances solubility in polar environments. This compound exhibits distinct reactivity patterns, particularly in esterification and transesterification reactions, where the hydroxyl group can act as a nucleophile. Its hydrophobic tail contributes to unique micelle formation, influencing lipid bilayer dynamics and membrane interactions. The compound's structural features also allow for specific interactions with other lipids, potentially affecting phase behavior in lipid mixtures. | ||||||
JP104 | 887264-45-1 | sc-221782 sc-221782A | 5 mg 10 mg | $70.00 $135.00 | ||
JP104 is a notable fatty acid characterized by its unique carbon chain length and branching, which significantly affects its solubility and reactivity. The compound exhibits distinct intermolecular forces, leading to enhanced micelle formation in aqueous environments. Its ability to participate in esterification reactions is influenced by its functional groups, facilitating interactions with various substrates. This reactivity can alter lipid profiles and influence metabolic pathways, showcasing its role in biochemical processes. | ||||||