Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H9NO3S |
| Molecular Weight | 223.248 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC=CC2=CC=CC(=C12)S(O)(=O)=O
InChI
InChIKey=CYJJLCDCWVZEDZ-UHFFFAOYSA-N
InChI=1S/C10H9NO3S/c11-8-5-1-3-7-4-2-6-9(10(7)8)15(12,13)14/h1-6H,11H2,(H,12,13,14)
| Molecular Formula | C10H9NO3S |
| Molecular Weight | 223.248 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Characterization of large peptide fragments derived from the N-terminal domain of the ribosomal protein L9: definition of the minimum folding motif and characterization of local electrostatic interactions. | 2002 Nov 12 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005 Jun |
|
| The design, synthesis, and characterization of the first cavitand-based de novo hetero-template-assembled synthetic proteins (Hetero-TASPs). | 2007 Nov 21 |
|
| Effects of acrylamide on the activity and structure of human brain creatine kinase. | 2009 Nov 20 |
|
| Amyloid oligomers: spectroscopic characterization of amyloidogenic protein states. | 2010 Mar |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:17:21 GMT 2023
by
admin
on
Sat Dec 16 04:17:21 GMT 2023
|
| Record UNII |
0D93Y3MXV4
|
| Record Status |
Validated (UNII)
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| Record Version |
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