TH9619
Based on 1 publication(s) in Google Scholar
TH9619 is a potent inhibitor of dehydrogenase and cyclohydrolase activities in both MTHFD1 and MTHFD2 with a IC50 value of 47 nM, and selectively kills cancer cells. TH9619 induces apoptosis by blocking the S phase. TH9619 has antitumor activity.
For research use only. We do not sell to patients.
- Purity: 99.33%
- CAS No.: 2379556-22-4
- Formula: C17H18FN7O7
- Molecular Weight:451.37
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Storage:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
Publications Citing Use of MedChemExpress (MCE) TH9619
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Biological Activity
TH9619 (7.8-1,000 nM, 420 s) displays high selectivity toward binding and stabilizing MTHFD2 over other common folate metabolism targets in intact HL-60 and LCL-889 cells[1].
TH9619 (1 nM-1 μM, 96 h) shows overall strong antiproliferative efficacy in AML cells and T-ALL Jurkat cells[1].
TH9619 (1-100 μM, 96 h) target MTHFD1(DC) but not mitochondrial MTHFD2 in SW620 cells[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Plasma concentration and pharmacokinetic (PK) evaluation of TH9619 following subcutaneous administration of 10 mg/kg in female NOG mice[1]
| Parameters | Cmax (μM) | Tmax (h) | AUC0-24 (μM*h) | AUC0-inf (uM*h) | λz range (h) | T1/2z (h) |
| TH9619 | 26.2 | 0.25 | 11.1 | 11.2 | 4-8 | 1.68 |