Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C4H9N3O2 |
| Molecular Weight | 131.1332 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H](CC(N)=O)C(N)=O
InChI
InChIKey=DSLBDPPHINVUID-REOHCLBHSA-N
InChI=1S/C4H9N3O2/c5-2(4(7)9)1-3(6)8/h2H,1,5H2,(H2,6,8)(H2,7,9)/t2-/m0/s1
| Molecular Formula | C4H9N3O2 |
| Molecular Weight | 131.1332 |
| 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 |
|---|---|---|
| Design of inhibitors of scytalone dehydratase: probing interactions with an asparagine carboxamide. | 2002 Dec |
|
| Structural basis of the water-assisted asparagine recognition by asparaginyl-tRNA synthetase. | 2006 Jul 7 |
|
| Nitrogen metabolism of asparagine and glutamate in Vero cells studied by (1)H/ (15)N NMR spectroscopy. | 2007 Nov |
|
| Amide inequivalence in the fibrillar assembly of islet amyloid polypeptide. | 2008 Mar |
|
| Deamidation of asparagine residues: direct hydrolysis versus succinimide-mediated deamidation mechanisms. | 2009 Feb 12 |
Patents
| 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 |
P342G15XO5
|
| Record Status |
Validated (UNII)
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| Record Version |
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P342G15XO5
Created by
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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447212
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DTXSID40168294
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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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16748-73-5
Created by
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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