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Dihydroeponemycin covalently modifies a subset of catalytic proteasomal subunits
InChi: InChI=1S/C25H24O6/c1-13(2)5-6-16-22(29)21-19(28)11-14(26)12-20(21)30-23(16)17-7-8-18(27)15-9-10-25(3
13±0 and 58±9 nM for JAK1
3)24(31-23(33)15-17-11-12-21(34-4)22(14-17)35-5)32-25(29-16-27)30-20-10-6-9-19-18(20)8-7-13-28-19/h6-14
11-trioxatricyclo[7
DL-Laudanosine ciclovir Hydrochloride Dihydroeponemycin covalently modifies a subsetDL Laudanosine, an Atracurium and Cisatracurium metabolite, crosses the bloodbrain barrier and may cause excitement and seizure activity. Product information CAS Number: 1699 51 0 Molecular Weight: 357. 44 Formula: C21H27NO4 Chemical Name: 1 [(3,4 dimethoxyphenyl)methyl] 6,7 dimethoxy 2 methyl 1,2,3,4 tetrahydroisoquinoline Smiles: CN1CCC2=CC(OC)=C(C=C2C1CC1=CC(OC)=C(C=C1)OC)OC InChiKey: KGPAYJZAMGEDIQ UHFFFAOYSA N InChi: InChI=1S C21H27NO4 c1 22 9 8
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