A6757
D-Arginine monohydrochloride
≥98% (TLC)
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About This Item
Formula empirica (notazione di Hill):
C6H14N4O2 · HCl
Numero CAS:
Peso molecolare:
210.66
Beilstein:
5773432
Numero CE:
Numero MDL:
Codice UNSPSC:
12352209
ID PubChem:
NACRES:
NA.77
Prodotti consigliati
Nome del prodotto
D-Arginine monohydrochloride, ≥98% (TLC)
Livello qualitativo
Saggio
≥98% (TLC)
Stato
powder
Colore
white
Punto di fusione
216-218 °C
applicazioni
cell analysis
peptide synthesis
Stringa SMILE
Cl.N[C@H](CCCNC(N)=N)C(O)=O
InChI
1S/C6H14N4O2.ClH/c7-4(5(11)12)2-1-3-10-6(8)9;/h4H,1-3,7H2,(H,11,12)(H4,8,9,10);1H/t4-;/m1./s1
KWTQSFXGGICVPE-PGMHMLKASA-N
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Applicazioni
D-arginine attenuates increased arginase expression, oxidative stress, endothelial dysfunction, and advanced glycation endproducts formation induced by methylgloxyl and high glucose. This attenuation by D-arginine is thought to occur through an endothelial NOS independent mechanism.
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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A simple method of preparing D-(minus)-arginine monohydrochloride from DL-arginine.
C P Berg et al.
Analytical biochemistry, 63(1), 68-72 (1975-01-01)
D-arginine attenuates methylglyoxal- and high glucose-induced endothelial dysfunction and oxidative stress by an eNOS-independent mechanism
Dahr, I., et al.
Journal of Pharmacology and Experimental Therapeutics, 63, 196-204 (2012)
Phuong V Tran et al.
Biochemical and biophysical research communications, 533(4), 965-970 (2020-10-04)
Central administration of L-arginine was reported to attenuate stress responses in neonatal chicks. The present study aimed to elucidate the differential effects of centrally administered L-arginine and its enantiomer, D-arginine, on the stress response in chicks and the associated mechanisms.
Ruo-Xiao Cheng et al.
Theranostics, 9(15), 4287-4307 (2019-07-10)
Methylglyoxal (MGO), an endogenous reactive carbonyl compound, plays a key role in the pathogenesis of diabetic neuropathy. The aim of this study is to investigate the role of MGO in diabetic itch and hypoalgesia, two common symptoms associated with diabetic
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