Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C7H13NO4 |
| Molecular Weight | 175.1824 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)CC[C@H](N)C(=O)OC
InChI
InChIKey=YEJSPQZHMWGIGP-YFKPBYRVSA-N
InChI=1S/C7H13NO4/c1-11-6(9)4-3-5(8)7(10)12-2/h5H,3-4,8H2,1-2H3/t5-/m0/s1
| Molecular Formula | C7H13NO4 |
| Molecular Weight | 175.1824 |
| 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 |
|---|---|---|
| Glutamatergic and serotonergic mechanisms in the dorsal facial area for common carotid artery blood flow control in the cat. | 2002 Oct 31 |
|
| Carbohydrate and amino acid metabolism in Tuber borchii mycelium during glucose utilization: a (13)C NMR study. | 2003 Jul |
|
| Preparation of hydrophilic polyhydroxyalkyl glutamine crosslinked films and its biodegradability. | 2007 Sep |
|
| Role of plant glyoxylate reductases during stress: a hypothesis. | 2009 Sep 14 |
|
| Identification of transcriptome induced in roots of maize seedlings at the late stage of waterlogging. | 2010 Aug 25 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:45:57 GMT 2023
by
admin
on
Fri Dec 15 19:45:57 GMT 2023
|
| Record UNII |
3K9BK9LB73
|
| Record Status |
Validated (UNII)
|
| Record Version |
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3K9BK9LB73
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93032
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6525-53-7
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DTXSID40215570
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229-414-1
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admin on Fri Dec 15 19:45:57 GMT 2023 , Edited by admin on Fri Dec 15 19:45:57 GMT 2023
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| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
