| Weight | 74.083 g/mol |
|---|---|
| Formula | C2H6N2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
METHYLUREA (598-50-5)
Score:
#2171 in Physics
,
#2720 in Biochemistry
,
#6730 in Chemistry
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- Direct mutagenesis of Ha-ras-1 oncogenes by N-nitroso-N-methylurea during initiation of mammary carcinogenesis in rats. (Nature, 1985)
- Induction of mammary carcinomas in rats by nitroso-methylurea involves malignant activation of H-ras-1 locus by single point mutations (Nature, 1983)
- Jack bean urease (EC 3.5.1.5). V. On the mechanism of action of urease on urea, formamide, acetamide, N-methylurea, and related compounds (Biochemistry and Cell Biology, 1980)
- N-nitroso-N-methylurea-induced rat mammary tumors arise from cells with preexisting oncogenic Hras1 gene mutations. (Proceedings of the National Academy of Sciences of the United States of America, 1994)
- Pineal melatonin inhibition of tumor promotion in the N-nitroso-N-methylurea model of mammary carcinogenesis : potential involvement of antiestrogenic mechanisms in vivo (Journal of Cancer Research and Clinical Oncology, 1991)
- Chemoprevention of N-Nitroso-N-methylurea-Induced Mammary Cancers by Pretreatment with 17-Estradiol and Progesterone (Journal of the National Cancer Institute, 1985)
-
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SMILESCNC(=O)N
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InChIKeyXGEGHDBEHXKFPX-UHFFFAOYSA-N
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Similar Compounds
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(563-41-7)
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3 suppliers
tert-Butylurea
(1118-12-3)
1 alternate name
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(592-31-4)
1 alternate name
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1 alternate name
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N-METHYLACETAMIDE
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1 alternate name
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formamide
(75-12-7)
1 alternate name
2 safety hazards
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(22033-10-9)
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(1801-72-5)
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15438-70-7
(15438-70-7)
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1852-17-1
(1852-17-1)
1 alternate name
3 suppliers
cyclopropylurea
(19757-64-3)
1 alternate name
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1,3-Di-tert-butylurea
(5336-24-3)
1 alternate name
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n-allylformamide
(16250-37-6)
1 alternate name
3 suppliers
1,3-Dibutylurea
(1792-17-2)
1 alternate name
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N-Octadecylurea
(2158-08-9)
1 alternate name
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N-METHYLTHIOUREA
(598-52-7)
1 alternate name
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N-(3-methoxypropyl)urea
(1119-61-5)
1 alternate name
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N-ETHYLACETAMIDE
(625-50-3)
1 alternate name
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N-(Hydroxymethyl)acetamide
(625-51-4)
1 alternate name
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101074-13-9
(101074-13-9)
1 alternate name
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1,3-bis(ethoxymethyl)urea
(13201-92-8)
1 alternate name
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(462-60-2)
1 alternate name
3 suppliers
N,N-DIMETHYLACETAMIDE
(127-19-5)
1 alternate name
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DIMETHYLCARBAMOYL CHLORIDE
(79-44-7)
1 alternate name
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3 suppliers
Chloroacetylurea
(4791-21-3)
1 alternate name
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N-methoxyurea
(3272-27-3)
1 alternate name
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52338-87-1
(52338-87-1)
1 alternate name
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(110-21-4)
1 alternate name
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(624-84-0)
1 alternate name
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2-amino-N-methylacetamide hydrochloride
(49755-94-4)
1 alternate name
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1,3-Dimethylthiourea
(61805-96-7, 534-13-4)
1 alternate name
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2-Amino-N-methylacetamide
(22356-89-4)
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(52696-91-0)
1 alternate name
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(591-08-2)
1 alternate name
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(28408-65-3, 5202-78-8)
1 alternate name
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(513-80-4)
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(21520-79-6)
1 alternate name
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(1704-79-6)
1 alternate name
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(694-32-6)
1 alternate name
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(96-30-0)
1 alternate name
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(1111-78-0)
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(59138-84-0)
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1,1-dimethylguanidine hydrochloride
(22583-29-5)
1 alternate name
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(6145-42-2)
1 alternate name
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2-hydroxy-n-methylacetamide
(5415-94-1)
1 alternate name
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2-bromo-N-methylacetamide
(34680-81-4)
1 alternate name
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(4814-80-6)
1 alternate name
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(124-40-3, 6912-12-5)
1 alternate name
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(6972-05-0)
1 alternate name
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53170-19-7
(53170-19-7)
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(1001-53-2)
1 alternate name
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(80-73-9)
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(2609-10-1)
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azetidin-2-one
(930-21-2)
1 alternate name
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(461-72-3)
1 alternate name
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1 alternate name
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pyrrolidine-1-carboxamide
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(1852-18-2)
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(44565-47-1)
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(1448-98-2)
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(626-36-8)
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(541-53-7)
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(10166-54-8)
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(5468-77-9)
1 alternate name
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N-(2-Hydroxyethyl)acetamide
(142-26-7)
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108-74-7
(108-74-7)
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METHYLUREA
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