Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H12N4 |
| Molecular Weight | 212.2505 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC(N)=C(C=C1)\N=N\C2=CC=CC=C2
InChI
InChIKey=IWRVPXDHSLTIOC-FOCLMDBBSA-N
InChI=1S/C12H12N4/c13-9-6-7-12(11(14)8-9)16-15-10-4-2-1-3-5-10/h1-8H,13-14H2/b16-15+
| Molecular Formula | C12H12N4 |
| Molecular Weight | 212.2505 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Adsorption of Chrysoidine R by using fly ash in batch process. | 2007 Jun 25 |
|
| Chelating compound, chrysoidine, is more effective in both antiprion activity and brain endothelial permeability than quinacrine. | 2007 May |
|
| Removal and recovery of Chrysoidine Y from aqueous solutions by waste materials. | 2010 Apr 15 |
|
| Large impact of the apoplast on somatic embryogenesis in Cyclamen persicum offers possibilities for improved developmental control in vitro. | 2010 Apr 28 |
|
| Investigation on the toxic interaction of chrysoidine hydrochloride-CTMAB combined contamination with calf thymus DNA. | 2010 Jan |
|
| Rapid method for the confirmatory analysis of chrysoidine in aquaculture products by ultra-performance liquid chromatography-tandem mass spectrometry. | 2010 Sep |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:09:42 GMT 2023
by
admin
on
Sat Dec 16 02:09:42 GMT 2023
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| Record UNII |
IP3X2567YP
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| Record Status |
Validated (UNII)
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| Record Version |
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m3531
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