Formulation: A solid
Formal Name: N-[3-[(3,4-dihydro-2,4-dioxo-3-propylthieno[3,2-d]pyrimidin-1(2H)-yl)methyl]phenyl]-benzeneacetamide
Purity: ≥98%
Formula Markup: C24H23N3O3S
Formula Weight: 433,5
Shelf life (days): 1460
CAS Number: 2098776-03-3
Notes: SC-13 is an inhibitor of flap endonuclease 1 (FEN1; IC50 = 4.2 nM) and an activator of stimulator of interferon genes (STING).{69691,69692} It increases the levels of γ histone H2AX (γH2AX) in MCF-7 and MDA-MB-231 breast cancer cells when used at a concentration of 40 µM.{69691} SC13 (20 or 50 µM) induces chromosomal aberrations in MCF-7 cells. It potentiates the proliferation inhibition induced by cisplatin (Item No. 13119), 5-fluorouracil (Item No. 14416), or temozolomide (Item No. 14163) in MCF-7 cells when used at a concentration of 20 µM. SC-13 (20 µM) increases levels of cyclic GMP-AMP (cGAMP) synthase (cGAS), phosphorylated STING, chemokine (C-C motif) ligand 5 (CCL5), and CCL10 in HeLa cervical cancer and MCF-7 cells.{69692} In vivo, SC-13 (5 mg/kg every other day), in combination with T cells expressing chimeric antigen receptors (CARs), reduces tumor volume and weight without affecting body weight, as well as increases the number of CD8+ T cell tumor infiltrates, in a HeLa mouse xenograft model.