Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H7N5O2 |
| Molecular Weight | 193.1628 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1N=CN=C2C(=O)N(C)C(=O)N=C12
InChI
InChIKey=SLGRAIAQIAUZAQ-UHFFFAOYSA-N
InChI=1S/C7H7N5O2/c1-11-6(13)4-5(10-7(11)14)12(2)9-3-8-4/h3H,1-2H3
| Molecular Formula | C7H7N5O2 |
| Molecular Weight | 193.1628 |
| 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 |
|---|---|---|
| AiiA-mediated quorum quenching does not affect virulence or toxoflavin expression in Burkholderia glumae SL2376. | 2010-12 |
|
| Methods for genetic manipulation of Burkholderia gladioli pathovar cocovenenans. | 2010-11-16 |
|
| Proteomic analysis of quorum sensing-dependent proteins in Burkholderia glumae. | 2010-06-04 |
|
| Inhibition of inducible nitric oxide synthase expression by a novel small molecule activator of the unfolded protein response. | 2008-09-27 |
|
| Proteomic analysis of the proteins regulated by HrpB from the plant pathogenic bacterium Burkholderia glumae. | 2008-01 |
|
| Plastic architecture of bacterial genome revealed by comparative genomics of Photorhabdus variants. | 2008 |
|
| The complete genome sequence of Yersinia pseudotuberculosis IP31758, the causative agent of Far East scarlet-like fever. | 2007-08 |
|
| Study on glycosylated prodrugs of toxoflavins for antibody-directed enzyme tumor therapy. | 2007-07-02 |
|
| Regulation of polar flagellum genes is mediated by quorum sensing and FlhDC in Burkholderia glumae. | 2007-04 |
|
| Quorum sensing and the LysR-type transcriptional activator ToxR regulate toxoflavin biosynthesis and transport in Burkholderia glumae. | 2004-11 |
|
| Syntheses of 3-substituted 1-methyl-6-phenylpyrimido[5,4-e]-1,2,4-triazine-5,7(1H,6H)-diones (6-phenyl analogs of toxoflavin) and their 4-oxides, and evaluation of antimicrobial activity of toxoflavins and their analogs. | 1993-02 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:02:51 GMT 2025
by
admin
on
Mon Mar 31 23:02:51 GMT 2025
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| Record UNII |
5N5YI4IP1P
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| Record Status |
Validated (UNII)
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| Record Version |
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66541
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m10988
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80729
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5N5YI4IP1P
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67078
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84-82-2
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Toxoflavin
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DTXSID00861658
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