Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H12N2O |
| Molecular Weight | 116.1616 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)[C@H](N)C(N)=O
InChI
InChIKey=XDEHMKQLKPZERH-BYPYZUCNSA-N
InChI=1S/C5H12N2O/c1-3(2)4(6)5(7)8/h3-4H,6H2,1-2H3,(H2,7,8)/t4-/m0/s1
| Molecular Formula | C5H12N2O |
| Molecular Weight | 116.1616 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [Isolation of the ergot (Claviceps purpurea (Fr.) Tul., strain VKM-F-366D), producing the lactamic alkaloid ergocornam]. | 2002 Nov-Dec |
|
| Design of chiral monochloro-s-triazine reagents for the liquid chromatographic separation of amino acid enantiomers. | 2003 May 23 |
|
| Concurrent induction and mechanism-based inactivation of CYP3A4 by an L-valinamide derivative. | 2003 Sep |
|
| Adducts of N-terminal valines in hemoglobin with isoprene diepoxide, a metabolite of isoprene. | 2004 |
|
| Clinical outcomes and management of mechanism-based inhibition of cytochrome P450 3A4. | 2005 Mar |
|
| Formation of three N-acetyl-L-cysteine monoadducts and one diadduct by the reaction of S-(1,2-dichlorovinyl)-L-cysteine sulfoxide with N-acetyl-L-cysteine at physiological conditions: chemical mechanisms and toxicological implications. | 2007 Oct |
|
| HPLC Method for Determination of Enantiomeric Purity of a Novel Respiratory Fluoroquinolone: WCK 1152. | 2008 May-Jun |
|
| Mass spectral analyses of hydroxymethylvinyl ketone-hemoglobin adducts formed after in vivo exposure of Sprague-Dawley rats to 3-butene-1,2-diol. | 2009 Jun |
|
| Formation of mono- and bis-Michael adducts by the reaction of nucleophilic amino acids with hydroxymethylvinyl ketone, a reactive metabolite of 1,3-butadiene. | 2009 May |
|
| Specificity of a prodrug-activating enzyme hVACVase: the leaving group effect. | 2010 Dec 6 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:20:30 GMT 2023
by
admin
on
Sat Dec 16 08:20:30 GMT 2023
|
| Record UNII |
JCM10841JE
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| Record Status |
Validated (UNII)
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| Record Version |
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4540-60-7
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DTXSID90196502
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admin on Sat Dec 16 08:20:30 GMT 2023 , Edited by admin on Sat Dec 16 08:20:30 GMT 2023
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