Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H7N3O3 |
| Molecular Weight | 181.1488 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)NC1=CC=C(C=C1)[N+]([O-])=O
InChI
InChIKey=LXXTVGKSGJADFU-UHFFFAOYSA-N
InChI=1S/C7H7N3O3/c8-7(11)9-5-1-3-6(4-2-5)10(12)13/h1-4H,(H3,8,9,11)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Structure-activity relationships in cholapod anion carriers: enhanced transmembrane chloride transport through substituent tuning. | 2008 |
|
| Novel stationary phases for high-performance liquid chromatography analysis of cyclodextrin derivatives. | 2006-05-26 |
|
| Potent and selective inhibitors of platelet-derived growth factor receptor phosphorylation. 1. Synthesis, structure-activity relationship, and biological effects of a new class of quinazoline derivatives. | 2002-07-04 |
|
| Inhibition of guinea-pig complement by derivatives of benzamidine. I. Effect of p-nitrophenylureido derivative of m-(m-phenoxypropoxy)benzamidine on guinea-pig complement component haemolytic activity. | 1974-04 |
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227938
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556-10-5
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DTXSID40310514
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313520
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DY0F0348GL
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m7983
Created by
admin on Mon Mar 31 22:42:24 GMT 2025 , Edited by admin on Mon Mar 31 22:42:24 GMT 2025
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PRIMARY | Merck Index |
SUBSTANCE RECORD
