Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H12N2O4 |
Molecular Weight | 224.2133 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(CC(=O)C1=CC=CC(O)=C1N)C(O)=O
InChI
InChIKey=VCKPUUFAIGNJHC-UHFFFAOYSA-N
InChI=1S/C10H12N2O4/c11-6(10(15)16)4-8(14)5-2-1-3-7(13)9(5)12/h1-3,6,13H,4,11-12H2,(H,15,16)
Molecular Formula | C10H12N2O4 |
Molecular Weight | 224.2133 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:58:24 GMT 2023
by
admin
on
Sat Dec 16 11:58:24 GMT 2023
|
Record UNII |
27723548JL
|
Record Status |
Validated (UNII)
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Record Version |
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-
Download
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C275
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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Code System | Code | Type | Description | ||
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96400
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY | |||
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DTXSID00862009
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY | |||
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484-78-6
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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1547
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY | |||
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89
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY | |||
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3-Hydroxykynurenine
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY | |||
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27723548JL
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY | |||
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C63766
Created by
admin on Sat Dec 16 11:58:24 GMT 2023 , Edited by admin on Sat Dec 16 11:58:24 GMT 2023
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PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |