DXR-IN-2
DXR-IN-2 is a 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR) inhibitor and an antimalarial agent (IC50: 0.1062 μM for Plasmodium falciparum DXR and 0.369 μM for Plasmodium falciparum). DXR-IN-2 inhibits Plasmodium falciparum growth by suppressing the methyl erythritol phosphate (MEP) pathway via DXR.
For research use only. We do not sell to patients.
- CAS No.: 2260608-07-7
- Formula: C10H12NO5P
- Molecular Weight:257.18
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
All Parasite Isoforms
More
Biological Activity
Description
In Vitro
DXR-IN-2 (Compound 11a) (0.10-100 μg/mL, 24 h) shows negligible cytotoxicity against HepG2, with an IC50 of >50 μM[1].
DXR-IN-2 (0.5 ng/mL-100 μg/mL, 3 days) inhibits Plasmodium falciparum 3D7 growth by inhibiting the MEP pathway via DXR[1].
DXR-IN-2 (1 μM) remains stable in mouse liver microsomes for more than 1 h[1].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only. Further protocols information, click here.
Chemical Information
-
CAS No. 2260608-07-7
-
Molecular Weight 257.18
-
Formula C10H12NO5P
-
SMILES
O=C(C1=CC=CC=C1)N(C/C=C/P(O)(O)=O)O
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
-
Cell Cytotoxicity Assay
Cytotoxicity assays are usually based on the assessment of cell membrane damage, which can also be indirectly detected by measuring cell viability. Detection methods include MTT assay, CKK-8 assay, LDH assay and ATP assay, etc.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)