Protopine alkaloids
Protopine alkaloids are a class of structurally unique indoloquinoline alkaloids, distinguished by their distinctive nitrogen-containing heterocyclic ring system. Found primarily in the plant family Rubiaceae, protopine derivatives exhibit a wide range of biological activities. Notably, these compounds have shown potential as therapeutic agents for various conditions due to their anti-inflammatory, antifungal, and analgesic properties. Structurally, protopine alkaloids feature an indolequinoline ring system with additional functional groups that contribute to their diverse pharmacological effects. Research into protopine alkaloids continues, driven by the interest in developing new drugs from natural sources. Their complex structure and promising biological activities make them a focal point for both academic and industrial studies in medicinal chemistry.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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protopine | 130-86-9 | C20H19NO5 |
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Bis[1,3]benzodioxolo[4,5-c:5',6'-g]azecin-13(5H)-one,4,6,7,14-tetrahydro-5-methyl-, hydrochloride (1:1) | 6164-47-2 | C20H20ClNO5 |
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Benzo[c][1,3]benzodioxolo[5,6-g]azecin-14(6H)-one,5,7,8,15-tetrahydro-3-hydroxy-4-methoxy-6-methyl- | 22047-92-3 | C20H21NO5 |
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Allocryptopine | 485-91-6 | C21H23NO5 |
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Hunnemanine | 490-52-8 | C20H21NO5 |
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7,16-dimethyl-6,8,9,16-tetrahydrobis[1,3]benzodioxolo[4,5-c:5'',6''-g]azecin-15(7H)-one | 521-87-9 | C21H21NO5 |
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Dibenz[c,g]azecin-13(14H)-one,3,10-dihydroxy-, (5E,7Z)- | 196086-14-3 | C17H13NO3 |
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Allocryptopine | 24240-04-8 | C21H23NO5 |
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1-Methoxy-13-oxoallocryptopine | 20194-55-2 | C22H23NO7 |
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6020-20-8 | C22H26ClNO5 |
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