Fmoc-Trp(Me)-OH bicin Hydrochloride InChi: InChI=1S/C38H59N13O8/c1-5-21(2)31(36(58)49-28(17-24-18-43-20-45-24)37(59)51-15-7-9-29(51)32(39)54)50-35(57)27(16-23-10-12-25(52)13-11-23)48-33(55)22(3)46-34(56)26(47-30(53)19-42-4)8-6-14-44-38(40)41/h10-13

InChi: InChI=1S/C38H59N13O8/c1-5-21(2)31(36(58)49-28(17-24-18-43-20-45-24)37(59)51-15-7-9-29(51)32(39)54)50-35(57)27(16-23-10-12-25(52)13-11-23)48-33(55)22(3)46-34(56)26(47-30(53)19-42-4)8-6-14-44-38(40)41/h10-13

Gliotoxin Induces Cofilin Phosphorylation to Promote Actin Cytoskeleton Dynamics and Internalization of Aspergillus fumigatus Into Type II Human Pneumocyte Cells

but without producing any reduction in muscle mass or anti-androgenic side effects

48 hours) in a concentration-dependent manner

Fmoc-Trp(Me)-OH bicin Hydrochloride InChi: InChI=1S/C38H59N13O8/c1-5-21(2)31(36(58)49-28(17-24-18-43-20-45-24)37(59)51-15-7-9-29(51)32(39)54)50-35(57)27(16-23-10-12-25(52)13-11-23)48-33(55)22(3)46-34(56)26(47-30(53)19-42-4)8-6-14-44-38(40)41/h10-13Fmoc Trp(Me) OH is synthesized by N (9 Fluorenylmethoxycarbonyloxy)succinimide (Fmoc ONSu) and 1 Methyl Ltrypthophan and can be used for protein or peptide synthesis. Product information CAS Number: 1334509 86 2 Molecular Weight: 440. 49 Formula: C27H24N2O4 Chemical Name: (2S) 2 ({[(9H fluoren 9 yl)methoxy]carbonyl}amino) 3 (1 methyl 1H indol 3 yl)propanoic acid Smiles: CN1C=C(C[C@H](NC(=O)OCC2C3=CC=CC=C3C3=CC=CC=C32)C(O)=O)C2=CC=CC=C12 InChiKey: