Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H8N2 |
| Molecular Weight | 144.1732 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=NC=CC2=C1C=CC=C2
InChI
InChIKey=OSILBMSORKFRTB-UHFFFAOYSA-N
InChI=1S/C9H8N2/c10-9-8-4-2-1-3-7(8)5-6-11-9/h1-6H,(H2,10,11)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Direct metalation of heteroaromatic esters and nitriles using a mixed lithium-cadmium base. Subsequent conversion to dipyridopyrimidinones. | 2010-02-05 |
|
| Sigma-1 ligands: Tic-hydantoin as a key pharmacophore. | 2010-01 |
|
| Selective inhibitors of the mutant B-Raf pathway: discovery of a potent and orally bioavailable aminoisoquinoline. | 2009-10-22 |
|
| Aggregation of imine-based metallo-supramolecular architectures through pi-pi interactions. | 2006-06-14 |
|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005-06 |
|
| Pathophysiological role of poly(ADP-ribose) polymerase (PARP) activation during acetaminophen-induced liver cell necrosis in mice. | 2005-03 |
|
| Structure-based design of novel guanidine/benzamidine mimics: potent and orally bioavailable factor Xa inhibitors as novel anticoagulants. | 2003-10-09 |
|
| Synthesis and pharmacological study of Rho-kinase inhibitors: pharmacomodulations on the lead compound Fasudil. | 2003-04 |
|
| Substituted acrylamides as factor Xa inhibitors: improving bioavailability by P1 modification. | 2002-08-05 |
|
| Chemistry of stable iminopropadienones, RN=C=C=C=O. | 2002-04-19 |
|
| The design of competitive, small-molecule inhibitors of coagulation factor Xa. | 2001-06 |
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| Code System | Code | Type | Description | ||
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73742
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DTXSID40165283
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216-243-2
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QUG12T52WZ
Created by
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1532-84-9
Created by
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C041545
Created by
admin on Mon Mar 31 19:14:18 GMT 2025 , Edited by admin on Mon Mar 31 19:14:18 GMT 2025
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SUBSTANCE RECORD
