arginine

Fructose-arginine is a non-saponin molecule from Korean Red Ginseng that attenuates AIM2 inflammatory vesicle activation.

Vitexin arginine is a natural c-glycosylated flavone isolated from various medicinal plants species,with anti-oxidant, anti-cancer, anti-inflammatory, anti-hyperalgesic, and neuroprotective effects.

Arginine glutamate is an agent of ammonia Detoxicant.

Levonadifloxacin, a broad-spectrum fluoroquinolone antibiotic, is used potentially for the treatment of staphylococci.

Amoxycillin arginine salt is a bioactive chemical.

Etrasimod arginine is used in the Treatment of Autoimmune and Inflammatory Diseases.

L-hydroxy Arginine is a substrate for nitric oxide synthase in the catabolism of L-arginine to form nitric oxide. It has been used as a biomarker for reduced nitric oxide formation in patients with cardiovascular disease and metabolic syndrome.

Nω-Propyl-L-arginine, a powerful and specific inhibitor of neuronal nitric oxide synthase (nNOS), effectively inhibits nNOS with a Ki of 57 nM. It exhibits a remarkable 149-fold selectivity for nNOS over endothelial NOS (eNOS).

Nω-allyl-L-arginine is a competitive and reversible inhibitor of bovine brain nitric oxide synthase (nNOS), inactivating nNOS efficiently over time. It also serves as a substrate, producing L-arginine, acrolein, and H2O.

L-Arginine-15N4 hydrochloride, the 15N-labeled variant of L-Arginine hydrochloride (T0670), serves as the nitrogen donor in the synthesis of nitric oxide. This potent vasodilator is crucial, especially during a sickle cell crisis where its levels are notably diminished.

Valyl-glycyl-arginine-4-nitroanilide is a tissue plasminogen activator.

Perindopril arginine is an angiotensin converting enzyme inhibitor, and amlodipine, a dihydropyridine calcium channel blocker, and is indicated for the treatment of hypertension, to lower blood pressure.

Hexa-D-arginine is an inhibitor of furin,blocks the activation of Pseudomonas aeruginosa exotoxin A in vivo.

Levonadifloxacin arginine ((S)-(-)-Nadifloxacin; WCK 771) is a broad-spectrum anti-staphylococcal agent. It exhibits antibacterial activity against both methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant Staphylococcus aureus. Additionally, it reduces monocyte THP-1 phagocytosis of MRSA and MSSA strains.

Hexa-D-arginine TFA (Furin Inhibitor II TFA) is a furin inhibitor with Ki values of 0.106 μM for furin, 0.58 μM for PACE4, and 13.2 μM for PC1.

Nor-N-omega-hydroxy-L-arginine-CoA (Nor-N-omega-hydroxy-L-arginine-coenzyme A) is a derivative of coenzyme A.

N-alpha-L-Acetyl-arginine-CoA (N-alpha-L-Acetyl-arginine-coenzyme A) is a derivative of coenzyme A.

N2-(Carboxyethyl)-L-arginine-CoA (N2-(Carboxyethyl)-L-arginine-coenzyme A) is a derivative of coenzyme A.

N-Omega-hydroxy-L-arginine-CoA (N-Omega-hydroxy-L-arginine-coenzyme A) is a derivative of coenzyme A.

L-Arginine-CoA (L-Arginine-coenzyme A) is a derivative of coenzyme A.

Dinor-Nω-Hydroxy-L-arginine-CoA (Dinor-Nω-Hydroxy-L-arginine-coenzyme A) is a derivative of coenzyme A.

α-(difluoromethyl)-DL-Arginine (RMI 71897) is an enzyma-activated, irreversible inhibitor of arginine decarboxylase for E. coli (Ki = 800 μM), Pseudomonas aeruginosa, and Klebsiella pneumoniae. At 0.01 mM, it has been shown to prevent osmotic stress-induced increases in arginine decarboxylase activity and putrescine synthesis in oat leaf cells. When combined with a variety of polyamine analogues, α-(difluoromethyl)-DL-Arginine inhibited the growth of Trypanosoma Crui in mammalian host cells at a minimum concentration of 10 mM and prevented the growth of Trypanosoma Crui in T-cell receptor alpha-deficient mouse models.

Nω-Hydroxy-nor-L-Arginine Dihydrochloride is a competitive and reversible inhibitor of arginase

L-Arginine hydrochloride serve as substrates and nitrogen donors for endothelial nitric oxide synthase (eNOS) to produce nitric oxide (NO). They are transported into vascular smooth muscle cells via cationic amino acid transporters, where they are metabolized into NO, polyamines, or L-proline. As effective vasodilators, they are commonly used to induce experimental acute pancreatitis models.