684-93-5

N-Nitroso-N-methylurea Chemical Structure
684-93-5

Chemical Structure

N-Nitroso-N-methylurea

  • CAS No.: 684-93-5
  • Formula:C2H5N3O2
  • Molecular Weight:103.08

IUPAC Name: 1-methyl-1-nitrosourea

InChIKey: ZRKWMRDKSOPRRS-UHFFFAOYSA-N

SMILES: O=C(N)N(C)N=O

Biological Activity: N-Nitroso-N-methylurea (NMU;MNU;NMH) is a potent carcinogen, mutagen and teratogenand. N-Nitroso-N-methylurea is a direct-acting alkylating agent that interacts with DNA. N-Nitroso-N-methylurea targets multiple animal organs to cause various cancer and/or degenerative disease. N-Nitroso-N-methylurea is also a precursor in the synthesis of diazomethane[1][2][3][4].

Cat. No. Product Name Purity Description Pricing
HY-34758
N-Nitroso-N-methylurea 99.74% N-Nitroso-N-methylurea (NMU;MNU;NMH) is a potent carcinogen, mutagen and teratogenand. N-Nitroso-N-methylurea is a direct-acting alkylating agent that interacts with DNA. N-Nitroso-N-methylurea targets multiple animal organs to cause various cancer and/or degenerative disease. N-Nitroso-N-methylurea is also a precursor in the synthesis of diazomethane.
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HY-W717139
N-Nitroso-N-methylurea-d5 N-Nitroso-N-methylurea-d5 is the deuterium labeled N-Nitroso-N-methylurea (HY-34758). N-Nitroso-N-methylurea (NMU;MNU;NMH) is a potent carcinogen, mutagen and teratogenand. N-Nitroso-N-methylurea is a direct-acting alkylating agent that interacts with DNA. N-Nitroso-N-methylurea targets multiple animal organs to cause various cancer and/or degenerative disease. N-Nitroso-N-methylurea is also a precursor in the synthesis of diazomethane.
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HY-101002
Sarcosinamide chloroethylnitrosourea Sarcosinamide chloroethylnitrosourea is an orally active alkylating agent. Sarcosinamide chloroethylnitrosourea can induce apoptosis by promoting DNA alkylation. Sarcosinamide chloroethylnitrosourea can be used in cancer-related research.
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HY-128612
Methylnitronitrosoguanidine 99.97% Methylnitronitrosoguanidine (MNNG) is an orally active alkylating agent with toxic and mutagenic effects. Methylnitronitrosoguanidine can as a carcinogen and mutagen. 50% water content, specifications are based on dry weight.
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HY-W015972
Propionamide 99.73% Propionamide is a saturated amide small molecule compound. Propionamide can be used to assist in the mechanistic research of BTK covalent inhibitors.
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HY-W019815
N-Ethyl-N-nitrosourea 99.94% N-Ethyl-N-nitrosourea (ENU) is a DNA alkylating agent. N-Ethyl-N-nitrosourea induces leukemia by alkylating nucleobases, disrupting DNA, and resulting in bone marrow suppression and the formation of leukemic cells. N-Ethyl-N-nitrosourea is teratogenic in vivo, inducing tumor formation and paw malformations in pregnant rats. N-Ethyl-N-nitrosourea cause central nervous system (CNS) tumors and genetic disorders.
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HY-W175543
Methoxyurea Methoxyurea (Compound 3) is a potential regulator of nitric oxide (NO) donors that acts on hemoglobins such as oxy-hemoglobin (OxyHb) and met-hemoglobin (MetHb). Methoxyurea is promising for research of sickle cell disease (SCD).
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HY-W188178
N-Mitrososarcosine N-Nitrososarcosine is a nitrosation product of Sarcosine (HY-101037) and can be found in cured meat products. N-Nitrososarcosine (225 mg/kg) induces the formation of metastatic liver carcinomas in mice.
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HY-W540767R
N-nitroso-n-methylurethane (Standard) ≥98% N-nitroso-n-methylurethane (Standard) is the analytical standard of N-nitroso-n-methylurethane. This product is intended for research and analytical applications.
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HY-W665796
N-Methyl-N-nitroso-2-propanamine N-Methyl-N-nitroso-2-propanamine is an N-nitrosamine, which induces tumor formation in mice.
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HY-W719784
Dimethynur Dimethynur is an anti-tumor agent. Dimethynur exerts anti-tumor effects in solid sarcoma mouse models. Dimethynur can be used in cancer research.
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HY-W738465
N,N-Dimethylamidino Urea 98.78% N,N-Dimethylamidino Urea (N-Carbonylguanidine) is an intermediate in the electrochemical oxidation of Metformin (HY-B0627). Metformin can be used in the study of type 2 diabetes. N,N-Dimethylamidino Urea can be used as a marker to study the metabolic pathway of metformin in vivo.
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References