Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C5H12N2O2 |
| Molecular Weight | 132.161 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCCCC(N)C(O)=O
InChI
InChIKey=AHLPHDHHMVZTML-UHFFFAOYSA-N
InChI=1S/C5H12N2O2/c6-3-1-2-4(7)5(8)9/h4H,1-3,6-7H2,(H,8,9)
| Molecular Formula | C5H12N2O2 |
| Molecular Weight | 132.161 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL1869 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10623504 |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Effects of agrin on the expression and distribution of the water channel protein aquaporin-4 and volume regulation in cultured astrocytes. | 2007-10 |
|
| Synthesis of metal-chelating lipids to sensitize lanthanide ions. | 2003-05-16 |
|
| Improved polygalacturonase production from Bacillus sp. MG-cp-2 under submerged (SmF) and solid state (SSF) fermentation. | 2002 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 22:21:23 GMT 2025
by
admin
on
Mon Mar 31 22:21:23 GMT 2025
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| Record UNII |
2381769MQC
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| Record Status |
Validated (UNII)
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| Record Version |
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m8239
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616-07-9
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