GGT Substrates
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
L-Glutamic acid γ-(p-nitroanilide) hydrochloride | 67953-08-6 | sc-211703 sc-211703A sc-211703B sc-211703C | 500 mg 1 g 5 g 25 g | $72.00 $134.00 $458.00 $1572.00 | 4 | |
L-Glutamic acid γ-(p-nitroanilide) hydrochloride acts as a GGT by engaging in specific hydrogen bonding and hydrophobic interactions with the enzyme's active site. This compound's unique nitroaniline moiety enhances its reactivity, allowing for efficient substrate conversion. Its structural features promote distinct conformational changes in the enzyme, influencing reaction pathways and modulating kinetic parameters, ultimately affecting metabolic processes. | ||||||
L-Glutamic acid γ-(4-nitroanilide) | 7300-59-6 | sc-250219 | 1 g | $48.00 | ||
L-Glutamic acid γ-(4-nitroanilide) functions as a GGT through its ability to form stable complexes with the enzyme, driven by π-π stacking and electrostatic interactions. The presence of the nitro group introduces electron-withdrawing characteristics, which fine-tune the reactivity of the amine group. This compound's unique steric configuration facilitates selective binding, altering the enzyme's conformation and enhancing catalytic efficiency, thereby influencing metabolic flux. | ||||||
L-Glutamic acid gamma-(3-carboxy-4-nitroanilide) ammonium salt | 63699-78-5 | sc-207800 sc-207800A sc-207800B sc-207800C | 100 mg 1 g 10 g 100 g | $152.00 $589.00 $2919.00 $14052.00 | ||
L-Glutamic acid gamma-(3-carboxy-4-nitroanilide) ammonium salt acts as a GGT by engaging in specific hydrogen bonding and hydrophobic interactions with the enzyme's active site. The nitro substituent modulates electron density, impacting the compound's nucleophilicity. Its unique spatial arrangement promotes a favorable orientation for substrate binding, which can accelerate reaction rates and influence enzyme kinetics, ultimately affecting metabolic pathways. | ||||||