Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H5N3O5 |
Molecular Weight | 211.1317 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
NC(=O)C1=CC(=CC(=C1)[N+]([O-])=O)[N+]([O-])=O
InChI
InChIKey=UUKWKUSGGZNXGA-UHFFFAOYSA-N
InChI=1S/C7H5N3O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H,(H2,8,11)
Molecular Formula | C7H5N3O5 |
Molecular Weight | 211.1317 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL612854 Sources: https://www.ncbi.nlm.nih.gov/pubmed/4744839 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | UNISTAT-2 Approved UseIndications for use. As an aid in the
prevention of coccidiosis caused by
Eimeria tenella, E. necatrix, and E. acervulina. |
PubMed
Title | Date | PubMed |
---|---|---|
Efficacy of 101 antimicrobials and other agents on the development of Cryptosporidium parvum in vitro. | 1996 Dec |
|
Solid-phase synthesis of chiral stationary phases based on 2,4,5,6-tetrachloro-1,3-dicyanobenzene derivatives spaced from N-3,5-dinitrobenzoyl alpha-amino acids: comparative study of their resolution efficacy. | 2001 Jun |
|
Elucidation of the chiral recognition mechanism of cinchona alkaloid carbamate-type receptors for 3,5-dinitrobenzoyl amino acids. | 2002 Jul 24 |
|
PnrA, a new nitroreductase-family enzyme in the TNT-degrading strain Pseudomonas putida JLR11. | 2005 Aug |
|
Determination of enantiomeric composition by negative-ion electrospray ionization-mass spectrometry using deprotonated N-(3,5-dinitrobenzoyl)amino acids as chiral selectors. | 2005 Oct |
|
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation. | 2007 |
|
A comprehensive chemoselective and enantioselective 2D-HPLC set-up for fast enantiomer analysis of a multicomponent mixture of derivatized amino acids. | 2007 Aug |
|
Discrimination of enantiomers of alpha-amino acids by chiral derivatizing reagents from trans-1,2-diaminocyclohexane. | 2008 Mar |
|
Continuous separation of racemic 3,5-dinitrobenzoyl-amino acids in a centrifugal contact separator with the aid of cinchona-based chiral host compounds. | 2009 |
|
Charge-transfer interaction between poly(9-vinylcarbazole) and 3,5-dinitrobenzamido group or 3-nitrobenzamido group. | 2010 Mar 2 |
Sample Use Guides
Chickens: 227 grams per ton
nitromide (0.025 percent) and 272 grams
per ton sulfanitran (0.03 percent).
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4744839
Nitromide was active against Eimeria tenella at 100 ug/ml.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:26:53 GMT 2023
by
admin
on
Fri Dec 15 15:26:53 GMT 2023
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Record UNII |
9DUJ3CMK8S
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Record Status |
Validated (UNII)
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Record Version |
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-
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CHEMBL1437065
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C72599
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