Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C3H8N2O |
| Molecular Weight | 88.1084 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCNC(N)=O
InChI
InChIKey=RYECOJGRJDOGPP-UHFFFAOYSA-N
InChI=1S/C3H8N2O/c1-2-5-3(4)6/h2H2,1H3,(H3,4,5,6)
| Molecular Formula | C3H8N2O |
| Molecular Weight | 88.1084 |
| 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 |
|---|---|---|
| Inhibition of HIV-1 infection by alkylureas. | 1991 Dec |
|
| Interactions of the neurotoxin vipoxin in solution studied by dynamic light scattering. | 2004 Jan |
|
| Selective alkylation of beta(II)-tubulin and thioredoxin-1 by structurally related subsets of aryl chloroethylureas leading to either anti-microtubules or redox modulating agents. | 2008 Aug 1 |
|
| N-4-iodophenyl-N'-2-chloroethylurea, a novel potential anticancer agent with colon-specific accumulation: radioiodination and comparative in vivo biodistribution profiles. | 2010 Apr |
|
| PU/PTFE-stimulated monocyte-derived soluble factors induced inflammatory activation in endothelial cells. | 2010 Mar |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:12:41 GMT 2023
by
admin
on
Fri Dec 15 17:12:41 GMT 2023
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| Record UNII |
7K14B03X18
|
| Record Status |
Validated (UNII)
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| Record Version |
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625-52-5
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7K14B03X18
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2047170
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210-898-8
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