Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H11N3O2 |
| Molecular Weight | 145.1597 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCN(N=O)C(N)=O
InChI
InChIKey=LSWOCDLIYSKTRX-UHFFFAOYSA-N
InChI=1S/C5H11N3O2/c1-2-3-4-8(7-10)5(6)9/h2-4H2,1H3,(H2,6,9)
| Molecular Formula | C5H11N3O2 |
| Molecular Weight | 145.1597 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| A new model of pre-B acute lymphoblastic leukemia chemically induced in rats. | 2005-10 |
|
| Immunity against mouse thymus-leukemia antigen (TL) protects against development of lymphomas induced by a chemical carcinogen, N-butyl-N-nitrosourea. | 2004-11 |
|
| Effects of 2,4,5-trichlorophenoxyacetic acid, pentachlorophenol, methylprednisolone, and Freund's adjuvant on 2-hydroxyethylnitrosourea carcinogenesis in MRC-Wistar rats. | 1991-01 |
|
| Induction of hepatic tumors by diethylstilbestrol in N-nitrosobutylurea-initiated female rats. | 1987-02 |
|
| Inhibitory effect of antiestrogen on hepatic tumorigenesis in WF rats treated with diethylstilbestrol alone or in combination with N-nitrosobutylurea. | 1984-04 |
|
| Induction of hepatic tumors by diethylstilbestrol alone or in synergism with n-nitrosobutylurea in castrated male WF rats. | 1983-05 |
|
| Synergism of diethylstilbestrol and other carcinogens in concurrent development of hepatic, mammary, and pituitary tumors in castrated male rats. | 1980-07 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:27:09 GMT 2025
by
admin
on
Mon Mar 31 19:27:09 GMT 2025
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| Record UNII |
77IB43T49K
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| Record Status |
Validated (UNII)
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| Record Version |
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