Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C13H17N3O5 |
Molecular Weight | 295.2912 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
N[C@@H](CC1=CC=C(O)C=C1)C(=O)NCC(=O)NCC(O)=O
InChI
InChIKey=HIINQLBHPIQYHN-JTQLQIEISA-N
InChI=1S/C13H17N3O5/c14-10(5-8-1-3-9(17)4-2-8)13(21)16-6-11(18)15-7-12(19)20/h1-4,10,17H,5-7,14H2,(H,15,18)(H,16,21)(H,19,20)/t10-/m0/s1
Molecular Formula | C13H17N3O5 |
Molecular Weight | 295.2912 |
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 |
---|---|---|
Analysis of peptides using partial (no discharge) atmospheric pressure chemical ionization conditions with ion trap mass spectrometry. | 2002 |
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Synthesis and intramolecular reactions of Tyr-Gly and Tyr-Gly-Gly related 6-O-glucopyranose esters. | 2004 Jan 2 |
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A novel accurate amplification created restriction site method for determination of the wild type and the precore mutant hepatitis B virus variants. | 2005 Jul |
|
Controllable distribution of single molecules and peptides within oligomer template investigated by STM. | 2006 Sep 27 |
|
On macromolecular refinement at subatomic resolution with interatomic scatterers. | 2007 Nov |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:02:30 GMT 2023
by
admin
on
Sat Dec 16 11:02:30 GMT 2023
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Record UNII |
DS6B3J0V03
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Record Status |
Validated (UNII)
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Record Version |
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-
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DS6B3J0V03
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123715
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74991
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admin on Sat Dec 16 11:02:30 GMT 2023 , Edited by admin on Sat Dec 16 11:02:30 GMT 2023
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