Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C19H13IN5O2.Cl |
| Molecular Weight | 505.696 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Cl-].[O-][N+](=O)C1=CC=C(C=C1)N2N=C(N=[N+]2C3=CC=C(I)C=C3)C4=CC=CC=C4
InChI
InChIKey=JORABGDXCIBAFL-UHFFFAOYSA-M
InChI=1S/C19H13IN5O2.ClH/c20-15-6-8-16(9-7-15)23-21-19(14-4-2-1-3-5-14)22-24(23)17-10-12-18(13-11-17)25(26)27;/h1-13H;1H/q+1;/p-1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/8214593Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/5363023 | https://www.ncbi.nlm.nih.gov/pubmed/25991603 | https://www.ncbi.nlm.nih.gov/pubmed/15142801
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8214593
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/5363023 | https://www.ncbi.nlm.nih.gov/pubmed/25991603 | https://www.ncbi.nlm.nih.gov/pubmed/15142801
INT is a Tetrazolium derivative, that on reduction produces a red formazan dye that can be used for quantitative redox assays. INT have been used in cytology since the 1950s to detect reducing cell components and later to label metabolically active cells. Also, INT has been adapted in aquatic samples for the in vitro electron transport system (ETS) method, which allows the plankton respiration to be measured with higher sensitivity. INT have been shown to inhibit bacterial growth.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2366564 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8214593 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/25991603
The oxygen-dipping probe optode was also used for respiration toxicity tests of INT for unfiltered plankton communities, marine bacteria seawater cultures (0.8-μm filtered sea water fraction with no substrate addition), and V. harveyi cultures in the following way. Cultures were set up in a 125-ml glass bottle stoppered with a solid silicon stopper with the oxygen probe inserted and a port for INT addition. Incubations wereperformed in the dark, under agitation at 18 °C in a water bath. The cultures were allowed to respire for minutes to several hours after the oxygen equilibrium was established. Oxygen consumption was recorded continuously for less than 24 h with data acquisition periods between 30 s and 10 min. The effect of the addition of the tetrazolium salt was evaluated by quantifying the oxygen consumption rate of change after the different INT addition (0.05, 0.1, 0.25, and 0.5 mM).
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INT (chemical)
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DTXSID30932744
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75421
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89168
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XY3JA5594E
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205-676-2
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146-68-9
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64957
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SUBSTANCE RECORD