2-(2-(4-Bromophenoxy)ethyl)-5-ethylpyridine-d4 832rtapenem sodium O[C@]12CC3=C(NC4[C@@H]5OC6C7=C(C[C@H]8N(CC9CC9)CC[C@]75[C@@]8(O)CC3=4)C=CC=6O)[C@@H]3OC4C5=C(C[C@H]1N(CC1CC1)CC[C@]253)C=CC=4O

O[C@]12CC3=C(NC4[C@@H]5OC6C7=C(C[C@H]8N(CC9CC9)CC[C@]75[C@@]8(O)CC3=4)C=CC=6O)[C@@H]3OC4C5=C(C[C@H]1N(CC1CC1)CC[C@]253)C=CC=4O

BAPTA-AM inhibits neuronal Ca2+-activated K+ channel currents

and its profile enables further study of PARP14 biology and disease association both in vitro and in vivo

InChiKey: ZAPXLIGWCAZCNY-BEYSDYMESA-N

InChiKey: FQXVWSGUAKXSLO-CKLOPMIDSA-N

2-(2-(4-Bromophenoxy)ethyl)-5-ethylpyridine-d4 832rtapenem sodium O[C@]12CC3=C(NC4[C@@H]5OC6C7=C(C[C@H]8N(CC9CC9)CC[C@]75[C@@]8(O)CC3=4)C=CC=6O)[C@@H]3OC4C5=C(C[C@H]1N(CC1CC1)CC[C@]253)C=CC=4OProduct information CAS Number: 1346598 69 3 Molecular Weight: 310. 22 Formula: C15H16BrNO Chemical Name: 2 {2 [4 bromo(2,3,5,6 H)phenoxy]ethyl} 5 ethylpyridine Smiles: [2H]C1=C(Br)C([2H])=C([2H])C(OCCC2=CC=C(CC)C=N2)=C1[2H] InChiKey: DOZJKXJBAFQCPO YBNXMSKUSA N InChi: InChI=1S C15H16BrNO c1 2 12 3 6 14(17 11 12)9 10 18 15 7 4 13(16)5 8 15 h3 8,11H,2,9 10H2,1H3 i4D,5D,7D,8D Technical Data Appearance: Solid Power Purity: 98% (or refer to the