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
Description
In Vitro
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.
In Vivo
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 |