616-04-6

N-Methylhydantoin Chemical Structure
616-04-6

Chemical Structure

N-Methylhydantoin

Synonym(s): 1-Methylhydantoin

  • CAS No.: 616-04-6
  • Formula:C4H6N2O2
  • Molecular Weight:114.10

IUPAC Name: 1-methylimidazolidine-2,4-dione

InChIKey: RHYBFKMFHLPQPH-UHFFFAOYSA-N

SMILES: O=C1NC(CN1C)=O

Biological Activity: N-Methylhydantoin is a creatinine degradation metabolite and non-substrate for microbial degradation.N-Methylhydantoin resists breakdown by most tested cytosine deaminase-forming microorganisms, which lack N-methylhydantoin amidohydrolase and N-carbamoylsarcosine amidohydrolase activity.N-Methylhydantoin forms as a product of creatinine hydrolysis by cytosine deaminase/creatinine deiminase in various microorganisms[1].

Cat. No. Product Name Purity Description Pricing
HY-113382
N-Methylhydantoin 99.81% N-Methylhydantoin is a creatinine degradation metabolite and non-substrate for microbial degradation.N-Methylhydantoin resists breakdown by most tested cytosine deaminase-forming microorganisms, which lack N-methylhydantoin amidohydrolase and N-carbamoylsarcosine amidohydrolase activity.N-Methylhydantoin forms as a product of creatinine hydrolysis by cytosine deaminase/creatinine deiminase in various microorganisms.
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HY-113382R
N-Methylhydantoin (Standard) ≥98% Delphinidin 3-glucoside (chloride) (Standard) is the analytical standard of Delphinidin 3-glucoside (chloride). This product is intended for research and analytical applications. Delphinidin 3-glucoside chloride (Delphinidin 3-O-glucoside chloride) is an active anthocyanin found in Hibiscus sabdariffa extract. Delphinidin 3-glucoside chloride induces a pro-apoptotic effect in B cell chronic lymphocytic leukaemia (B CLL). Delphinidin 3-glucoside chloride exerts phytoestrogen activity by binding to ERβ, with an IC50 of 9.7 μM. Delphinidin-3-O-glucoside chloride inhibits EGFR with an IC50 of 2.37 µM. Delphinidin 3-glucoside chloride exhibits antitumor effects through pAKT/IRF1/HOTAIR pathway. Delphinidin 3-glucoside chloride exhibits efficacy against oxidative stress, inhibits platelet activation and endothelial dysfunction.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References