NCBI Taxonomy: 553653
Goniothalamus gardneri (ncbi_taxid: 553653)
found 94 associated metabolites at species taxonomy rank level.
Ancestor: Goniothalamus
Child Taxonomies: none taxonomy data.
Asitrilobin B
Annonacin is a natural product found in Xylopia aromatica, Asimina triloba, and other organisms with data available. Asitrilobin B is found in fruits. Asitrilobin B is a constituent of the seeds of Asimina triloba (pawpaw). Constituent of the seeds of Asimina triloba (pawpaw). Asitrilobin B is found in fruits.
2'-Hydroxy-4,4',6'-trimethoxychalcone
Flavokawain A is a member of chalcones. 2-Hydroxy-4,4,6-trimethoxychalcone is a natural product found in Dahlia tenuicaulis, Piper methysticum, and other organisms with data available. See also: Piper methysticum root (part of). 2-Hydroxy-4,4,6-trimethoxychalcone is found in beverages. 2-Hydroxy-4,4,6-trimethoxychalcone is found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damage (2002). Found in kava (Piper methysticum). FDA advises against use of kava in food due to potential risk of severe liver damage (2002) (E)-Flavokawain A, a chalcone extracted from Kava, has anticarcinogenic effect. (E)-Flavokawain A induces apoptosis in bladder cancer cells by involvement of bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice[1]. (E)-Flavokawain A, a chalcone extracted from Kava, has anticarcinogenic effect. (E)-Flavokawain A induces apoptosis in bladder cancer cells by involvement of bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice[1]. Flavokawain A, a proming anticarcinogenic agent, is a chalcone from kava extract with anti-tumor activity. Flavokawain A induces cell apoptosis by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway. Flavokawain A has the potential for the study of bladder cancer[1]. Flavokawain A, a proming anticarcinogenic agent, is a chalcone from kava extract with anti-tumor activity. Flavokawain A induces cell apoptosis by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway. Flavokawain A has the potential for the study of bladder cancer[1].
Isoannonacin A
Isoannonacin is found in fruits. Isoannonacin is isolated from Annona muricata (soursop) and Asimina triloba (pawpaw). Isolated from Annona muricata (soursop) and Asimina triloba (pawpaw). Isoannonacin is found in fruits.
Annonacin
cis-Annonacin is found in fruits. cis-Annonacin is a constituent of Annona muricata (soursop). Constituent of Annona muricata (soursop). cis-Annonacin is found in fruits.
2,4-Dihydroxy-4,6-dimethoxydihydrochalcone
Flavokawin A
(E)-Flavokawain A, a chalcone extracted from Kava, has anticarcinogenic effect. (E)-Flavokawain A induces apoptosis in bladder cancer cells by involvement of bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice[1]. (E)-Flavokawain A, a chalcone extracted from Kava, has anticarcinogenic effect. (E)-Flavokawain A induces apoptosis in bladder cancer cells by involvement of bax protein-dependent and mitochondria-dependent apoptotic pathway and suppresses tumor growth in mice[1]. Flavokawain A, a proming anticarcinogenic agent, is a chalcone from kava extract with anti-tumor activity. Flavokawain A induces cell apoptosis by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway. Flavokawain A has the potential for the study of bladder cancer[1]. Flavokawain A, a proming anticarcinogenic agent, is a chalcone from kava extract with anti-tumor activity. Flavokawain A induces cell apoptosis by involvement of Bax protein-dependent and mitochondria-dependent apoptotic pathway. Flavokawain A has the potential for the study of bladder cancer[1].
Annonacin
Isoannonacin A
5-(hydroxymethyl)-3-(icos-19-en-11-yn-1-yl)oxolan-2-one
(2r)-7-hydroxy-5-methoxy-2-(4-methoxyphenyl)-2,3-dihydro-1-benzopyran-4-one
3-[(2r,8r)-2,8-dihydroxy-9-[(2s,5s)-5-[(1s)-1,4,5-trihydroxyheptadecyl]oxolan-2-yl]nonyl]-5-hydroxy-5-methylfuran-2-one
5-methyl-3-(2,8,15,16-tetrahydroxytriacontyl)-5h-furan-2-one
(2s)-7-hydroxy-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydro-1-benzopyran-4-one
(5s)-3-[(2r,6s,13r,14s,17r,18s)-2,6,13,14,17,18-hexahydroxytriacontyl]-5-methyl-5h-furan-2-one
5-methyl-3-[(2r)-2,8,15,16-tetrahydroxytriacontyl]-5h-furan-2-one
4-[(1s,2s,3r,4r)-2-(2,4-dihydroxy-6-methoxybenzoyl)-3,4-bis(4-methoxyphenyl)cyclobutanecarbonyl]-5-methoxybenzene-1,3-diol
(5s)-5-methyl-3-[(2r)-2,8,15,16-tetrahydroxytriacontyl]-5h-furan-2-one
(3r,5s)-5-(hydroxymethyl)-3-(icos-19-en-11-yn-1-yl)oxolan-2-one
(5s)-3-[(2r)-2,6,13,14,17,18-hexahydroxytriacontyl]-5-methyl-5h-furan-2-one
(5s)-5-methyl-3-[(2r,8r,11r)-2,8,11-trihydroxy-11-[(2r,5r)-5-[(1r)-1-hydroxypentadecyl]oxolan-2-yl]undecyl]-5h-furan-2-one
(5s)-3-[(2r,6s,13r,14s,17s,18r)-2,6,13,14,17,18-hexahydroxytriacontyl]-5-methyl-5h-furan-2-one
[(1s,14r,15z)-15-ethylidene-6-methoxy-3,17-diazapentacyclo[12.3.1.0²,¹⁰.0⁴,⁹.0¹²,¹⁷]octadeca-2(10),4,6,8-tetraen-13-yl]methanol
C20H24N2O2 (324.18376839999996)