Atovaquone-d5 l)amine It less potently activates IGF1R

It less potently activates IGF1R and EGFR (EC50s = 100 µM for both)

76 uM for Jarid1c) against H3K4me3/2/1 demethylases

In vivo: Animal study showed that after administration of 2-hydroxyestradiol

Tempo induces DNA-strand breakage

Hexythiazox is harmless to mammals and has no effect on beneficial insects and predators of mites

Atovaquone-d5 l)amine It less potently activates IGF1RProduct information CAS Number: 1329792 63 3 Molecular Weight: 371. 87 Formula: C22H19ClO3 Chemical Name: 3 [4 (4 chlorophenyl)(1,2,2,6,6 H)cyclohexyl] 4 hydroxy 1,2 dihydronaphthalene 1,2 dione Smiles: [2H]C1(C2=C(O)C3=CC=CC=C3C(=O)C2=O)C([2H])([2H])CC(CC1([2H])[2H])C1C=CC(Cl)=CC=1 InChiKey: BSJMWHQBCZFXBR YNUDWXFUSA N InChi: InChI=1S C22H19ClO3 c23 16 11 9 14(10 12 16)13 5 7 15(8 6 13)19 20(24)17 3 1 2 4 18(17)21(25)22(19)26 h1 4,9 13,15,24H,5 8H2