Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-007811 |
CAS: 1216997-87-3 |
Molecular Formula: C12H10D3N5 |
Molecular Weight: 230.28 |
Chemical Structure |
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Description | 2-Amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline is a mutagenic/carcinogenic heterocyclic amine formation found in fried beef steak. |
Synonyms | 3-(D3)methyl-4,8-dimethyl-3H-imidazo[4,5-f]quinoxalin-2-amine |
IUPAC Name | 4,8-dimethyl-3-(trideuteriomethyl)imidazo[4,5-f]quinoxalin-2-amine |
Related CAS | 95896-78-9 (unlabelled) |
Canonical SMILES | CC1=CC2=NC=C(N=C2C3=C1N(C(=N3)N)C)C |
InChI | InChI=1S/C12H13N5/c1-6-4-8-9(15-7(2)5-14-8)10-11(6)17(3)12(13)16-10/h4-5H,1-3H3,(H2,13,16)/i3D3 |
InChI Key | LAZSIJHHPMHKQI-HPRDVNIFSA-N |
Melting Point | >260°C |
Purity | >98% |
Solubility | Soluble in DMSO, Methanol |
Appearance | Green Solid |
Storage | Store at -20°C |
2-Amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline-[d3] is a specialized compound utilized in various scientific applications. Here are some key applications of this compound:
Cancer Research: This compound is used in cancer research to investigate its effects on cellular processes related to carcinogenesis. By studying its interactions with DNA and cellular pathways, researchers can assess its potential as a chemotherapeutic agent. It may help in understanding molecular mechanisms involved in tumor progression and drug resistance.
Pharmacokinetic Studies: In drug development, this compound serves as a tracer in pharmacokinetic studies due to its stable isotopic labeling with deuterium. Researchers use it to track the absorption, distribution, metabolism, and excretion of pharmaceuticals. This information is essential for optimizing dosage regimens and ensuring drug safety and efficacy.
Chemical Synthesis: 2-Amino-3,4,8-trimethyl-3H-imidazo[4,5-f]quinoxaline-[d3] can be used as an intermediate in the synthesis of more complex compounds. Its unique structure allows chemists to explore new synthetic pathways leading to the discovery of novel molecules. This application is particularly valuable in the development of new drugs and materials.
Environmental Testing: In environmental science, this compound can be employed to study the degradation and persistence of quinoxaline derivatives in ecosystems. By using isotopically labeled versions, scientists can accurately trace and model their behavior in soil and water. These insights are crucial for assessing environmental impact and establishing regulations for chemical contaminants.
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