Amino-PEG5-Boc 2743 Smiles: C[C@]12C=C(O)C(=O)C(C)=C1C[C@H]1OC(=O)[C@H](OC(=O)CC(C)C)[C@H]3[C@@]4(OC[C@]13[C@@H]2[C@@H](O)[C@@H]4O)C(=O)OC

Smiles: C[C@]12C=C(O)C(=O)C(C)=C1C[C@H]1OC(=O)[C@H](OC(=O)CC(C)C)[C@H]3[C@@]4(OC[C@]13[C@@H]2[C@@H](O)[C@@H]4O)C(=O)OC

The mechanism of action by which salinomycin kills cancer stem cells specifically remains unknown

Smiles: CCCCCCCCCCCCCCCCOC[C@H](COP(O)(=O)OCCN)OC(C)=O

phospholipid synthesis

Inhibition of mitotic microtubules correlates with antitumor activity

Amino-PEG5-Boc 2743 Smiles: C[C@]12C=C(O)C(=O)C(C)=C1C[C@H]1OC(=O)[C@H](OC(=O)CC(C)C)[C@H]3[C@@]4(OC[C@]13[C@@H]2[C@@H](O)[C@@H]4O)C(=O)OCAmino PEG5 Boc is a PEG based PROTAC linker that can be used in the synthesis of PROTACs. Product information CAS Number: 1446282 18 3 Molecular Weight: 365. 46 Formula: C17H35NO7 Chemical Name: tert butyl 1 amino 3,6,9,12,15 pentaoxaoctadecan 18 oate Smiles: CC(C)(C)OC(=O)CCOCCOCCOCCOCCOCCN InChiKey: XSTIRQZQKAJSIM UHFFFAOYSA N InChi: InChI=1S C17H35NO7 c1 17(2,3)25 16(19)4 6 20 8 10 22 12 14 24 15 13 23 11 9 21 7 5 18 h4 15,18H2,1 3H3 Technical Data