Classification Term: 1653
Atisane diterpenoids (ontology term: CHEMONTID:0002738)
Diterpenoids with a structure based on the atisane skeleton, which is a tetracyclic compound containing the [2,2,2]bicyc1ic ring system with the C15-C16 bridge attached at C12." [ISBN:9780080526980, ISBN:9780124695597]
found 4 associated metabolites at family metabolite taxonomy ontology rank level.
Ancestor: Villanovane, atisane, trachylobane or helvifulvane diterpenoids
Child Taxonomies: Atisine-type diterpenoid alkaloids, Hetidine-type diterpenoid alkaloids, Hetisine-type diterpenoid alkaloids, Danudatine-type diterpenoid alkaloids, Isoatisine-type diterpenoid alkaloids
Yucalexin A19
Yucalexin A19 is found in root vegetables. Yucalexin A19 is a constituent of cassava roots (Manihot esculenta). Constituent of cassava roots (Manihot esculenta). Yucalexin A19 is found in root vegetables.
Yucalexin A16
Yucalexin A16 is found in root vegetables. Yucalexin A16 is a stress metabolite of cassava root (Manihot esculenta). Stress metabolite of cassava root (Manihot esculenta). Yucalexin A16 is found in root vegetables.
Guan-fu base A
Guanfu base A is an antiarrhythmic alkaloid isolated from Aconitum coreanum and is a potent noncompetitive CYP2D6 inhibitor, with a Ki of 1.20 μM in human liver microsomes (HLMs) and a Ki of 0.37 μM for the human recombinant form (rCYP2D6). Guanfu base A is also a potent competitive inhibitor of CYP2D in monkey (Ki of 0.38 μM) and dog (Ki of 2.4 μM) microsomes[1]. Guanfu base A also inhibits HERG channel current[2]. Guanfu base A is an antiarrhythmic alkaloid isolated from Aconitum coreanum and is a potent noncompetitive CYP2D6 inhibitor, with a Ki of 1.20 μM in human liver microsomes (HLMs) and a Ki of 0.37 μM for the human recombinant form (rCYP2D6). Guanfu base A is also a potent competitive inhibitor of CYP2D in monkey (Ki of 0.38 μM) and dog (Ki of 2.4 μM) microsomes[1]. Guanfu base A also inhibits HERG channel current[2].
serofendic acid
C21H34O4S (382.21776840000007)