MEL-1 Activators
SEE ALSO...
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Methoxy-N-cyclopropanoyltryptamine | 139564-01-5 | sc-221033 | 5 mg | $80.00 | ||
5-Methoxy-N-cyclopropanoyltryptamine acts as a potent MEL-1, showcasing intriguing molecular interactions that enhance its reactivity profile. Its unique cyclopropanoyl moiety introduces strain, facilitating rapid electrophilic attacks on nucleophiles. This compound exhibits selective binding affinities, influencing downstream signaling pathways. The presence of the methoxy group further modulates electronic properties, optimizing its interaction dynamics in complex biochemical environments. | ||||||
N-Acetyltryptamine | 1016-47-3 | sc-202233 sc-202233A | 10 mg 50 mg | $117.00 $495.00 | ||
N-Acetyltryptamine functions as a notable MEL-1, characterized by its ability to engage in specific hydrogen bonding interactions that stabilize its conformation. The acetyl group enhances lipophilicity, promoting membrane permeability and influencing its kinetic behavior in biological systems. Its structural features allow for selective receptor binding, potentially altering downstream molecular cascades. Additionally, the compound's unique electronic distribution plays a crucial role in modulating its reactivity and interaction with various biomolecules. | ||||||
2-Iodomelatonin | 93515-00-5 | sc-203463 sc-203463A | 10 mg 50 mg | $72.00 $264.00 | 2 | |
2-Iodomelatonin, as a MEL-1, exhibits intriguing molecular interactions due to the presence of the iodine atom, which introduces unique steric and electronic effects. This halogen substitution enhances its lipophilic character, facilitating interactions with lipid membranes. The compound's distinct electronic configuration allows for specific binding affinities, influencing receptor dynamics and downstream signaling pathways. Its reactivity is further modulated by the iodine's polarizability, impacting its behavior in various chemical environments. | ||||||
GR 135531 | 190277-13-5 | sc-203981 sc-203981A | 10 mg 50 mg | $320.00 $1400.00 | ||
GR 135531, classified as a MEL-1, showcases remarkable reactivity as an acid halide, characterized by its ability to form stable acyl derivatives through nucleophilic acyl substitution. The presence of the halide enhances electrophilicity, promoting rapid reaction kinetics with amines and alcohols. Its unique steric profile allows for selective interactions, influencing the formation of specific reaction products. Additionally, the compound's solubility in organic solvents underscores its utility in diverse synthetic pathways. | ||||||