L-Arginine (hydrochloride)


CAS No. : 1119-34-2

(Synonyms: (S)-(+)-Arginine hydrochloride)

1119-34-2
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Cat. No. : HY-N0455A
M.Wt: 210.66
Formula: C6H15ClN4O2
Purity: >98 %
Solubility: DMSO : < 1 mg/mL (ultrasonic;warming;heat to 80°C);H2O : 100 mg/mL (ultrasonic)
Introduction of 1119-34-2 :

L-Arginine ((S)-(+)-Arginine) is the substrate for the endothelial nitric oxide synthase (eNOS) to generate NO. L-Arginine is transported into vascular smooth muscle cells by the cationic amino acid transporter family of proteins where it is metabolized to nitric oxide (NO), polyamines, or L-proline. L-Arginine is a potent vasodilator, and can be used to induce experimental acute pancreatitis[1][2][3][4][5]. In Vitro:Arginine is an α-amino acid. The L-form is one of the 20 most common natural amino acids. At the level of molecular genetics, in the structure of the messenger ribonucleic acid mRNA, CGU, CGC, CGA, CGG, AGA, and AGG, are the triplets of nucleotide bases or codons that code for arginine during protein synthesis. In mammals, arginine is classified as a semiessential or conditionally essential amino acid, depending on the developmental stage and health status of the individual[1].
L-Arginine is associated with a decrease in cardiac index. L-Arginine (450 mg/kg during a 15-minute period) amplifies and sustains the hyperemia (38%) and increases absolute brain blood flow after eNOS upregulation by chronic Simvastatin (HY-17502) (2 mg/kg; sc; daily for 14 days) in SV-129 mice[2][3].
In Vivo:Note:
Please do not refer to only one article to determine the experimental conditions. It is recommended to determine the optimal experimental conditions (animal strain, age, dosage, frequency and cycle, detection time and indicators, etc.) through preliminary experiments before the formal experiment.

L-Arginine hydrochloride has been widely accepted as a method to induce experimental acute pancreatitis[4][5].
Dose reference for L-Arginine hydrochloride induction[4][5]:
(1) Model animal: Male Wistar albino rats
Acute pancreatitis: single i.p. injection of 500 mg of L-arginine/100 g body weight
(2) Model animal: Male ICR mice
Acute pancreatitis: i.p. with 2.25 g/kg body weight of L-Arginine hourly for 2 hours
Dissolution method of L-Arginine hydrochloride[5]:
L-arginine solution was prepared by dissolving L-arginine powder in 0.9% normal saline and adjusting the pH to 7 with 5 N HCl.
Induction of Experimental Acute Pancreatitis[4][5]
Background
L-Arginine hydrochloride is a substrate for endothelial nitric oxide synthase (eNOS) to produce NO, which can be metabolized into nitric oxide (NO), polyamines or L-proline, stimulating inflammatory responses. L-Arginine hydrochloride can also selectively destroy pancreatic acinar cells, leading to acute necrotizing pancreatitis.
Specific Modeling Methods
Rat[4]: Wistar albino rats • Male • 150 g
Administration: 250 mg, 500 mg, 750 mg every 100 g body weight (L-Arginine) • ip • single dose • starved for 15 hours
Mice[5]: ICT mouse • Male • 4-week-old • 25-30 g
Administration: 450 mg/100 g body weight (L-Arginine) • ip • twice dosages • sacrificed at 72 hours
Note
(1) When the dose exceeds 500 mg/100 g body weight, most rats will die within a few hours after injection; When the dose is less than 250 mg, the induced symptoms of pancreatic disease will be mild[4].
(2) Dissolution method in Reference: L-Arginine solution was prepared by dissolving L-Arginine powder in 0.9% normal saline and adjusting pH to 7 with 5N hydrochloric acid[5].
Modeling Indicators
Phenotypic changes: weight loss, lower activity, softer hair.
Tissue morphology: pancreatic edema, damage, atrophy, granulation tissue contraction and chalky spots (location of fat necrosis).
Cellular changes: basophils decrease and vesicles, cell pyknosis, nuclear fragmentation. Pancreatic albino cells disappear and die, and pancreatic tissue is replaced by monocytes and fibroblasts.
Molecular changes: serum amylase levels increase, and fat necrosis is obvious.
Correlated Product(s): Curcumin (HY-N0005)

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