NOS Inhibitors
Items 31 to 34 of 34 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Calmidazolium chloride | 57265-65-3 | sc-201494 sc-201494A | 10 mg 50 mg | $153.00 $600.00 | 27 | |
Calmidazolium chloride functions as a nitric oxide synthase (NOS) inhibitor, characterized by its capacity to modulate calcium-dependent signaling pathways. Its unique molecular structure facilitates interactions with calmodulin, disrupting the enzyme's regulatory mechanisms. This interference alters the conformational dynamics of NOS, affecting substrate binding and product formation. The compound's ionic nature enhances solubility, promoting effective distribution and interaction with target proteins in various environments. | ||||||
Allicin | 539-86-6 | sc-202449 sc-202449A | 1 mg 5 mg | $460.00 $1428.00 | 7 | |
Allicin acts as a nitric oxide synthase (NOS) modulator, distinguished by its ability to form reactive sulfur species that influence redox signaling. Its unique thiosulfinate structure allows for selective interactions with cysteine residues in proteins, leading to post-translational modifications. This reactivity can alter enzyme activity and cellular signaling pathways. Additionally, allicin's lipophilic properties enhance membrane permeability, facilitating its bioactivity in diverse biological systems. | ||||||
S-Ethyl N-[4-Triflurormethyl)phenyl]isothiourea, Hydrochloride | 163490-78-6 | sc-208325 | 10 mg | $300.00 | ||
S-Ethyl N-[4-Trifluoromethyl)phenyl]isothiourea, Hydrochloride functions as a nitric oxide synthase (NOS) modulator, characterized by its ability to engage in specific hydrogen bonding interactions due to its isothiourea moiety. This compound exhibits unique electronic properties from the trifluoromethyl group, enhancing its reactivity and selectivity in biological systems. Its solubility in polar solvents facilitates rapid diffusion across membranes, influencing cellular signaling dynamics and enzyme interactions. | ||||||
NG-Monomethyl-L-homoarginine monoacetate | sc-222069 | 5 mg | $50.00 | |||
NG-Monomethyl-L-homoarginine monoacetate acts as a nitric oxide synthase (NOS) inhibitor, distinguished by its structural mimicry of L-arginine, which allows it to effectively compete for the active site of NOS. This compound's unique guanidinium group enhances its binding affinity, while its acetate moiety contributes to solubility and stability in aqueous environments. The compound's kinetic profile reveals a distinct inhibition mechanism, impacting nitric oxide production and downstream signaling pathways. | ||||||