Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H11NO |
| Molecular Weight | 197.2325 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=CN(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=DCNUQRBLZWSGAV-UHFFFAOYSA-N
InChI=1S/C13H11NO/c15-11-14(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-11H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and characterization of modified nucleotides in the 970 hairpin loop of Escherichia coli 16S ribosomal RNA. | 2009-08-15 |
|
| Metabolism investigation leading to novel drug design 2: orally active prostacyclin mimetics. Part 5. | 2006-09-01 |
|
| A novel method for the synthesis of dinucleoside boranophosphates by a boranophosphotriester method. | 2004-08-06 |
|
| Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies. | 2003-08-05 |
|
| A versatile approach towards regioselective platinated DNA sequences. | 2003-04-14 |
|
| Quadruplex and pentaplex self-assemblies of oligonucleotides containing short runs of 8-aza-7-deaza-2'-deoxyisoguanosine or 2'-deoxyisoguanosine. | 2001-11-22 |
Patents
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| Code System | Code | Type | Description | ||
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607-00-1
Created by
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69081
Created by
admin on Mon Mar 31 21:05:18 GMT 2025 , Edited by admin on Mon Mar 31 21:05:18 GMT 2025
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210-129-6
Created by
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FF0X003442
Created by
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3864
Created by
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DTXSID9022077
Created by
admin on Mon Mar 31 21:05:18 GMT 2025 , Edited by admin on Mon Mar 31 21:05:18 GMT 2025
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PRIMARY |
SUBSTANCE RECORD