Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C4H9NO3 |
| Molecular Weight | 119.1192 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](O)[C@@H](N)C(O)=O
InChI
InChIKey=AYFVYJQAPQTCCC-PWNYCUMCSA-N
InChI=1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3-/m1/s1
| Molecular Formula | C4H9NO3 |
| Molecular Weight | 119.1192 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Solid-phase synthesis and configurational reassigment of callipeltin E. Implications for the structures of callipeltins A and B. | 2006 Aug 18 |
|
| Solid-phase total synthesis and structure proof of callipeltin B. | 2006 Dec 6 |
|
| Application of two different kinds of sera against the Proteus penneri lipopolysaccharide core region in search of epitopes determining cross-reactions with antibodies. | 2008 Mar-Apr |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:30:15 GMT 2023
by
admin
on
Sat Dec 16 08:30:15 GMT 2023
|
| Record UNII |
0756UWA0SA
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| Record Status |
Validated (UNII)
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| Record Version |
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90624
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206267
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58645
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246-488-0
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32826
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DTXSID40179542
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0756UWA0SA
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24830-94-2
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| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
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ENANTIOMER -> ENANTIOMER |
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