Chemical category
Gelsemium alkaloids
Description
Alkaloids with a structure that is based on the tetracyclic gelsemium skeleton. These alkaloids contain an oxindole function and a cage-like, hydroaromatic residue which is believed to arise from an intermediate related to anhydrovobasinediol by formation of a 6,20 bond and rearrangement to an oxindole. The major alkaloids in this group are related to Gelsemine; however, a smaller group, characterized by Gelsedine, lack the 6,20 bond, and have also lost C-21.
Ancestors
Below are a few examples of gelsemium alkaloids found in the ClassyFire database.
Example Entities
ID | Structure | Formula | Mass | |
---|---|---|---|---|
8532375 | C26H34Cl3IN2O5Si | 715.91 | Show | |
8532395 | C26H34Cl3N2O5Si | 589.0 | Show | |
8556427 | C20H26N2O4 | 358.438 | Show | |
8871429 | C20H24N2O4 | 356.422 | Show | |
8891964 | C19H24N2O3 | 328.412 | Show | |
8894717 | C20H26N2O5 | 374.437 | Show | |
9002076 | C26H34Cl3IN2O5Si | 715.91 | Show | |
9002097 | C26H34Cl3N2O5Si | 589.0 | Show | |
9383879 | C20H24N2O4 | 356.422 | Show | |
9459621 | C20H26N2O4 | 358.438 | Show | |
9480313 | C19H24N2O3 | 328.412 | Show | |
9502076 | C20H26N2O4 | 358.438 | Show | |
9514728 | C20H26N2O5 | 374.437 | Show | |
16413559 | C21H26N2O5 | 386.448 | Show | |
16392149 | C20H24N2O3 | 340.423 | Show | |
23393533 | C21H28N2O5 | 388.464 | Show | |
23409681 | C23H25Cl3N2O5 | 515.81 | Show | |
23411345 | C20H24N2O3 | 340.423 | Show | |
23411348 | C27H28N2O5 | 460.53 | Show | |
23799993 | C22H28N2O4 | 384.476 | Show | |
23909434 | C20H22N2O2 | 322.408 | Show | |
33806599 | C19H20N2O3 | 324.38 | Show | |
33806598 | C20H21N3O3 | 351.406 | Show | |
45339470 | C35H43N5O4 | 597.76 | Show | |
45794850 | C20H22N2O2 | 322.408 | Show |