Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H13N5O4S |
| Molecular Weight | 335.338 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC(C(O)=O)=C(\N=N\C2=CC=C(C=C2)S(N)(=O)=O)C(N)=C1
InChI
InChIKey=ZELCNSAUMHNSSU-ISLYRVAYSA-N
InChI=1S/C13H13N5O4S/c14-7-5-10(13(19)20)12(11(15)6-7)18-17-8-1-3-9(4-2-8)23(16,21)22/h1-6H,14-15H2,(H,19,20)(H2,16,21,22)/b18-17+
| Molecular Formula | C13H13N5O4S |
| Molecular Weight | 335.338 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/6707875
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6707875
Sulfachrysoidine is a sulfamylchrysoidine derivative and lipid-soluble azo dye with antibacterial activity.
Originator
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:18:42 GMT 2025
by
admin
on
Mon Mar 31 18:18:42 GMT 2025
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| Record UNII |
39O1389K38
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29739
Created by
admin on Mon Mar 31 18:18:42 GMT 2025 , Edited by admin on Mon Mar 31 18:18:42 GMT 2025
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| Code System | Code | Type | Description | ||
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DTXSID00871676
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236832
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100000083242
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8464
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CHEMBL2107474
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3559
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SUB10689MIG
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C72646
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739
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39O1389K38
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485-41-6
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207-617-6
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m10303
Created by
admin on Mon Mar 31 18:18:42 GMT 2025 , Edited by admin on Mon Mar 31 18:18:42 GMT 2025
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PRIMARY | Merck Index |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |