2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline-d3

Product Name 2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline-d3
CAT No. CS-T-66733
CAS No. 1216791-04-6
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys CC1=NC2=C(N=C(N([2H])[2H])N3C)C3=C(C)C([2H])=C2N=C1C
Canonical Smiles CC1=CC2=NC(=C(N=C2C3=C1N(C(=N3)N)C)C)C
InchIKey MCFPPHKNJUOYBX-GKOSEXJESA-N
Inchl InChI=1S/C13H15N5/c1-6-5-9-10(16-8(3)7(2)15-9)11-12(6)18(4)13(14)17-11/h5H,1-4H3,(H2,14,17)/i4D3
IUPAC 4,7,8-trimethyl-3-(trideuteriomethyl)imidazo[4,5-f]quinoxalin-2-amine
Controlled No
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2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline-d3 is a deuterated form of the organic compound 2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline (ITQ). It is a heterocyclic compound with a fused quinoxaline-imidazole backbone. The compound has a molecular weight of 271.37 g/mol. ITQ is a potent inhibitor of the enzyme fibroblast growth factor receptor 1 (FGFR1), which is involved in the regulation of cell growth, differentiation, and survival. The inhibition of FGFR1 has been shown to have therapeutic potential in the treatment of various types of cancer, including lung cancer, breast cancer, and gastric cancer. The deuterated form of ITQ is used in research to study the pharmacokinetics and metabolic pathways of the compound in vivo. The chemical formula of 2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline-d3 is C11H10D3N3, and its chemical structure is similar to the non-deuterated form of ITQ. The compound is stable under normal conditions and can be stored at room temperature. It is soluble in organic solvents such as dimethyl sulfoxide (DMSO) and methanol. In conclusion, 2-Amino-3,4,7,8-tetramethyl-3H-imidazo[4,5-F]quinoxaline-d3 is a deuterated form of a potent inhibitor of FGFR1, which has potential therapeutic applications in cancer treatment. Its use in research can provide insight into the pharmacokinetics and metabolic pathways of the compound, which may aid in the development of more effective cancer therapies.

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