CAS 509-17-1

Fórmula: C34H48N2O9

InChI: InChI=1S/C34H48N2O9/c1-7-36-16-31(17-45-29(38)19-10-8-9-11-22(19)35-18(2)37)13-12-24(42-4)33-21-14-20-23(41-3)15-32(39,25(21)26(20)43-5)34(40,30(33)36)28(44-6)27(31)33/h8-11,20-21,23-28,30,39-40H,7,12-17H2,1-6H3,(H,35,37)/t20-,21-,23+,24+,25-,26+,27-,28+,30+,31+,32-,33+,34-/m1/s1

Clave InChI: NUXFDCYXMLVOFU-AYBRVATOSA-N

SMILES: CCN1C[C@@]2(CC[C@@H]([C@@]34[C@@H]2[C@@H]([C@@]([C@H]31)([C@]5(C[C@@H]([C@H]6C[C@@H]4[C@@H]5[C@H]6OC)OC)O)O)OC)OC)COC(=O)C7=CC=CC=C7NC(=O)C

Ajacine

Producto controlado

CAS: 509-17-1

Ajacine is a diterpenoid alkaloid that has been isolated from the genus Aconitum. It has been shown to have epileptiform activity and to be neurotoxic at high concentrations. Ajacine inhibits neurotransmission by blocking the postsynaptic potential, which leads to an increase in extracellular potassium. This is thought to be due to the hydroxyl group on ajacine that can form hydrogen bonds with water molecules, leading to increased membrane permeability. Ajacine also inhibits virus replication by interfering with viral neuraminidase and is active against a wide range of infectious diseases including HIV and herpes simplex virus.

Fórmula: C₃₄H₄₈N₂O₉

Pureza: Min. 95%

Peso molecular: 628.8 g/mol

Ref: 3D-AAA50917