Chemical category
Homoaporphines
Description
Alkaloids derived from phenethylisoquinoline precursors by direct intramolecular oxidative coupling. They incorporate a nucleus A and are always pentaoxygenated at C- 1, -2, - 10, - 11, and - 12. The nitrogen function in ring B is usually N-methylated, but it may also be secondary.
Ancestors
Below are a few examples of homoaporphines found in the ClassyFire database.
Example Entities
ID | Structure | Formula | Mass | |
---|---|---|---|---|
41801278 | C23H27NO6 | 413.47 | Show | |
41801695 | C23H24F3NO6 | 467.441 | Show | |
41809114 | C23H25NO8 | 443.452 | Show | |
65433687 | C21H20F3NO5 | 423.388 | Show | |
2541774 | C22H28INO5 | 513.372 | Show | |
2541799 | C22H28NO5 | 386.467 | Show | |
41801053 | C22H27NO7S | 449.52 | Show | |
41801569 | C22H25NO6 | 399.443 | Show | |
41802004 | C22H22F3NO8S | 517.47 | Show | |
41802079 | C29H29NO8 | 519.55 | Show | |
41802188 | C22H25NO9S | 479.5 | Show | |
41808950 | C22H24F3NO7S | 503.49 | Show | |
44476830 | C18H19NO2 | 281.355 | Show | |
55912286 | C18H19NO2 | 281.355 | Show | |
64637418 | C20H21NO4 | 339.391 | Show | |
64832376 | C22H27NO6 | 401.459 | Show | |
64832403 | C23H29NO6 | 415.486 | Show | |
64832435 | C21H25NO6 | 387.432 | Show | |
65201350 | C21H25NO5 | 371.433 | Show | |
65307324 | C22H27NO4 | 369.461 | Show | |
9766518 | C23H29NO5 | 399.487 | Show | |
65769866 | C23H29NO5 | 399.487 | Show | |
11036545 | C22H27NO5 | 385.46 | Show | |
11231981 | C22H27NO5 | 385.46 | Show | |
10545691 | C21H25NO5 | 371.433 | Show |