5-Amino-1H-imidazole-4-carboxamide hydrochloride
5-Amino-1H-imidazole-4-carboxamide hydrochloride structure
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Common Name | 5-Amino-1H-imidazole-4-carboxamide hydrochloride | ||
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| CAS Number | 72-40-2 | Molecular Weight | 162.58 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C4H7ClN4O | Melting Point | 250-252 °C (dec.)(lit.) | |
| MSDS | USA | Flash Point | 269.6ºC | |
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Astragaloside IV and cycloastragenol are equally effective in inhibition of endoplasmic reticulum stress-associated TXNIP/NLRP3 inflammasome activation in the endothelium.
J. Ethnopharmacol. 169 , 210-8, (2015) Astragaloside IV and cycloastragenol are present together in Astragalus membranaceus Moench (Fabaceae) and this study aims to simultaneously investigate their regulation of endothelial homeostasis in the setting of endoplasmic reticulum stress (ER stress).We ... |
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Pharmacological activation of AMPK ameliorates perivascular adipose/endothelial dysfunction in a manner interdependent on AMPK and SIRT1.
Pharmacol. Res. 89 , 19-28, (2014) Adipose and endothelial dysfunction is tightly associated with cardiovascular diseases in obesity and insulin resistance. Because perivascular adipose tissue (PVAT) surrounds vessels directly and influences vessel functions through paracrine effect, and AMP-a... |
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Quercetin oppositely regulates insulin-mediated glucose disposal in skeletal muscle under normal and inflammatory conditions: The dual roles of AMPK activation.
Mol. Nutr. Food. Res. 60 , 551-65, (2016) Quercetin is a dietary flavonoid whose role in the regulation of the activity of insulin remains controversial. Our study aimed to investigate how quercetin and its major metabolite quercetin-3-glucuronide (Q-3-G) regulate insulin-mediated glucose disposal in... |
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Synthesis of guanosine and its derivatives from 5-amino-1-beta-d-ribofuranoxyl-4-imidazolecarboxamide. I. Ring closure with benzoyl isothiocyanate.
J. Org. Chem. 32(6) , 1825-8, (1967)
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One-step protecting-group-free synthesis of azepinomycin in water.
Org. Biomol. Chem. 13(11) , 3378-81, (2015) We report an efficient, atom economical general acid-base catalyzed one-step multi-gram synthesis of azepinomycin from commercially available compounds in water. We propose that the described pH-dependent Amadori rearrangement, which couples an amino-imidazol... |
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J. Heterocycl. Chem. 30 , 593, (1993)
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J. Org. Chem. 56 , 2139, (1991)
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Heterocycles 34 , 1133, (1992)
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Electrochemical and molecular dynamics simulation studies on the corrosion inhibition of aluminum in molar hydrochloric acid using some imidazole derivatives. Khaled KF and Amin MA.
J. Appl. Electrochem. 39(12) , 2553-68, (2009)
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