m-PEG5-phosphonic acid enoside Rb3 InChi: InChI=1S/C20H21N7O3/c1-12-5-6-16(30-12)17-18-19(24-20(21)23-17)27(26-25-18)9-13-3-2-4-14(22-13)10-29-15-7-8-28-11-15/h2-6

InChi: InChI=1S/C20H21N7O3/c1-12-5-6-16(30-12)17-18-19(24-20(21)23-17)27(26-25-18)9-13-3-2-4-14(22-13)10-29-15-7-8-28-11-15/h2-6

Smiles: O=C1[C@H]2[C@H]([C@H]3C[C@@H]2CC3)C(=O)N1CCCCN1CCN(CC1)C1N=CC=CN=1

Urolithin C treatment actively increases the lactate dehydrogenase (LDH) release and lipid peroxidation malondialdehyde (MDA)

3-dione(CNQX) in the hippocampus in vitro

2019 Nov 15

m-PEG5-phosphonic acid enoside Rb3 InChi: InChI=1S/C20H21N7O3/c1-12-5-6-16(30-12)17-18-19(24-20(21)23-17)27(26-25-18)9-13-3-2-4-14(22-13)10-29-15-7-8-28-11-15/h2-6m PEG5 phosphonic acid is a PEG based PROTAC linker that can be used in the synthesis of PROTACs. Product information CAS Number: 1807512 39 5 Molecular Weight: 316. 29 Formula: C11H25O8P Chemical Name: (2,5,8,11,14 pentaoxahexadecan 16 yl)phosphonic acid Smiles: COCCOCCOCCOCCOCCP(O)(O)=O InChiKey: RCTDZLSRRJVKHJ UHFFFAOYSA N InChi: InChI=1S C11H25O8P c1 15 2 3 16 4 5 17 6 7 18 8 9 19 10 11 20(12,13)14 h2 11H2,1H3,(H2,12,13,14) Technical Data