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BSO treatment reduced GSH concentration in mouse fetuses by 55% and 70% at 2 mM and 20 mM BSO doses
This component also displays affinity for 5-HT1A and 5-HT2B receptors with IC50 of 62
K858 does not inhibit the ATPase activity of the mitotic kinesins CENP-E and MKLP1
Solubility: DMSO : 60 mg/mL (158
a Highly Potent and Selective Inhibitor of RIP2 Kinase
Dihydroartemisinin-d3 Size:Contact [email protected] for quotation BSO treatment reduced GSH concentrationProduct information CAS Number: 176774 98 4 Molecular Weight: 287. 37 Formula: C15H24O5 Chemical Name: (1R,4S,5R,8S,9R,10S,12R,13R) 9 (H)methyl 1,5 dimethyl 11,14,15,16 tetraoxatetracyclo[10. 3. 1. 0,. 0,]hexadecan 10 ol Smiles: [2H]C([2H])([2H])[C@H]1[C@@H](O)O[C@@H]2O[C@@]3(C)CC[C@H]4[C@H](C)CC[C@@H]1[C@@]24OO3 InChiKey: BJDCWCLMFKKGEE MPBQXAAISA N InChi: InChI=1S C15H24O5 c1 8 4 5 11 9(2)12(16)17 13 15(11)10(8)6 7 14(3,18 13)19 20 15 h8 13,16H,4
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