Items 11 to 17 of 17 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Pyrrophenone | 341973-06-6 | sc-296161 sc-296161A | 500 µg 1 mg | $194.00 $369.00 | 3 | |
Pyrrophenone, as a phospholipase activating peptide, exhibits a remarkable ability to induce conformational changes in membrane proteins. Its unique structure facilitates specific interactions with lipid headgroups, enhancing the accessibility of phospholipases to their substrates. This activation accelerates lipid hydrolysis, influencing signaling pathways and cellular responses. Additionally, Pyrrophenone's distinct charge distribution plays a pivotal role in modulating membrane curvature, impacting cellular morphology and function. | ||||||
FTY720 (R)-Phosphate | 402616-23-3 | sc-221638 sc-221638A | 500 µg 1 mg | $75.00 $190.00 | ||
FTY720 (R)-Phosphate functions as a phospholipase activating peptide by engaging in selective binding with membrane-associated proteins, promoting their activation. Its unique stereochemistry allows for enhanced affinity towards phospholipid bilayers, leading to increased enzymatic activity. The compound's dynamic interactions with lipid environments facilitate rapid lipid turnover, influencing cellular signaling cascades. Furthermore, its hydrophilic and hydrophobic regions contribute to membrane fluidity, affecting cellular dynamics and organization. | ||||||
Halopemide | 59831-65-1 | sc-221704 sc-221704A | 5 mg 25 mg | $123.00 $371.00 | ||
Halopemide acts as a phospholipase activating peptide by modulating lipid bilayer properties through specific interactions with membrane proteins. Its unique structural features enable it to stabilize transient protein-lipid complexes, enhancing enzymatic efficiency. The compound's ability to alter membrane curvature and fluidity plays a crucial role in facilitating lipid metabolism. Additionally, Halopemide's influence on intracellular signaling pathways underscores its importance in cellular communication and response mechanisms. | ||||||
PAF C-18 | 74389-69-8 | sc-205421 sc-205421A | 5 mg 10 mg | $100.00 $190.00 | 1 | |
PAF C-18 functions as a phospholipase activating peptide by engaging in selective interactions with lipid membranes, promoting the formation of lipid-protein complexes. Its unique amphipathic structure allows it to integrate into lipid bilayers, influencing membrane dynamics and enhancing enzymatic activity. This compound also plays a pivotal role in modulating cellular signaling cascades, thereby affecting various physiological processes through its impact on membrane integrity and fluidity. | ||||||
Pyrrolidino PAF C-16 | 91021-63-5 | sc-205479 sc-205479A | 1 mg 5 mg | $45.00 $205.00 | ||
Pyrrolidino PAF C-16 acts as a phospholipase activating peptide by selectively binding to phospholipid membranes, facilitating the activation of phospholipases through its unique structural conformation. Its hydrophobic and hydrophilic regions enable it to disrupt membrane stability, leading to altered lipid organization. This interaction enhances the kinetics of enzymatic reactions, influencing lipid metabolism and cellular signaling pathways, ultimately affecting membrane composition and cellular responses. | ||||||
2-thio PAF | 96801-55-7 | sc-205093 sc-205093A | 5 mg 10 mg | $290.00 $410.00 | ||
2-thio PAF functions as a phospholipase activating peptide by engaging in specific interactions with lipid bilayers, promoting the activation of phospholipases. Its unique thiol group enhances reactivity, allowing for the formation of disulfide bonds that stabilize transient protein-lipid complexes. This modulation of membrane dynamics influences the kinetics of enzymatic activity, thereby impacting lipid turnover and cellular signaling cascades, ultimately reshaping membrane architecture and functionality. | ||||||
Hexanolamino PAF C-16 | 137566-83-7 | sc-205342 sc-205342A | 1 mg 10 mg | $21.00 $170.00 | ||
Hexanolamino PAF C-16 acts as a phospholipase activating peptide by facilitating the interaction between phospholipases and membrane lipids. Its unique hexanolamino structure enhances hydrophobic interactions, promoting the formation of lipid-protein complexes. This peptide influences the conformational dynamics of membrane proteins, accelerating enzymatic reactions and altering lipid metabolism. The resulting changes in membrane fluidity and composition can significantly affect cellular signaling pathways and membrane integrity. | ||||||