IMDNQ1
IMDNQ1 is a Trypanosoma cruzi inhibitor derived from 1,4-naphthoquinone substituted with cyclic imide. IMDNQ1 effectively inhibits the proliferation of Trypanosoma cruzi epimastigotes, while also reducing the viability of mouse fibroblasts. The selectivity index between the antiproliferative activity and cytotoxicity of IMDNQ1 is 60.25, indicating a certain level of safety. IMDNQ1 can be widely used in studies related to Chagas disease.
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- CAS No.: 623163-52-0
- 화학식: C14H8ClNO4
- 분자량:289.67
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Parasite Isoforms
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Biological Activity
제품 설명
In Vitro
IMDNQ1 (0.39-100 μM; 48 h) exhibits low cytotoxicity to Balb/C 3T3 mouse fibroblasts with an IC50 of 165.9 μM, resulting in a selectivity index of 60.25 that is significantly higher than Nifurtimox (HY-W040073)[1].
IMDNQ1 (0.39-100 µM; 48 h) potently inhibits the proliferation of Trypanosoma cruzi epimastigotes (Tulahuen CL98 strain) with an IC50 of 2.77 µM, showing significantly greater activity than Nifurtimox (HY-W040073)[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:Balb/C 3T3 mouse fibroblasts (clone A31)
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Concentration:0.39-100 µM
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Incubation Time:48 h
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Result:Reduced the viability of Balb/C 3T3 mouse fibroblasts with an IC50 of 165.9 µM.
Exhibited significantly less cytotoxicity than nifurtimox (IC50=114.0 µM).
Achieved a selectivity index of 60.25, which is significantly higher than the selectivity index of nifurtimox.
Chemical Information
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CAS No. 623163-52-0
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분자량 289.67
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화학식 C14H8ClNO4
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SMILES
O=C1C(Cl)=C(C(=O)C=2C=CC=CC12)N3C(=O)CCC3=O
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)