Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C5H10N2O3 |
| Molecular Weight | 146.1445 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](NC(=O)CN)C(O)=O
InChI
InChIKey=VPZXBVLAVMBEQI-VKHMYHEASA-N
InChI=1S/C5H10N2O3/c1-3(5(9)10)7-4(8)2-6/h3H,2,6H2,1H3,(H,7,8)(H,9,10)/t3-/m0/s1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Direct measurement indicates a slow cis/trans isomerization at the secondary amide peptide bond of glycylglycine. | 2001 Jul 4 |
|
| Hydrolysis of serine-containing peptides at neutral pH promoted by [MoO4]2- oxyanion. | 2011 Dec 5 |
|
| Hydrolytic activity of vanadate toward serine-containing peptides studied by kinetic experiments and DFT theory. | 2012 Aug 20 |
|
| Synthesis of C(2) -Symmetric Dimeric Re(I) Peptide Complexes. | 2013 Mar 1 |
|
| A supramolecular hydrogel as a carrier to deliver microRNA into the encapsulated cells. | 2014 Apr 11 |
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73855
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2M7GF488BL
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223-019-8
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1551643
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83246
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3695-73-6
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SUBSTANCE RECORD
