NCBI Taxonomy: 2662166
Palicourea colorata (ncbi_taxid: 2662166)
found 19 associated metabolites at species taxonomy rank level.
Ancestor: Palicourea
Child Taxonomies: none taxonomy data.
(-)-Chimonanthine
(3aS,8bS)-8b-[(3aS,8bS)-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indol-8b-yl]-3-methyl-1,2,3a,4-tetrahydropyrrolo[2,3-b]indole
(-)-chimonanthine is the (3aS,3aS,8aS,8aS)-stereoisomer of chimonanthine. It is an enantiomer of a (+)-chimonanthine. (-)-Chimonanthine is a natural product found in Eumachia forsteriana, Chimonanthus praecox, and Idiospermum australiense with data available. meso-Chimonanthine is found in herbs and spices. meso-Chimonanthine is an alkaloid from Calycanthus floridus (Carolina allspice
Chimonanthine
Chimonanthine
A ring assembly that is 2,2,3,3,8,8,8a,8a-octahydro-1H,1H-3a,3a-bipyrrolo[2,3-b]indole substituted by methyl groups at positions 1 and 1.
(3as,8as)-7-[(3ar,8ar)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-3a-[(3ar,8ar)-7-[(3ar,8ar)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
(3as,8as)-7-[(3ar,8ar)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-3a-[(3ar,8ar)-7-[(3ar,8ar)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
(1r,13r)-10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,8,14,16,18,20-octaene
(1r,13r)-10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,8,14,16,18,20-octaene
10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,14,16,18-hexaene
10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,14,16,18-hexaene
10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,8,14,16,18,20-octaene
10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,8,14,16,18,20-octaene
(1r,9r,13r,21r)-10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,14,16,18-hexaene
(1r,9r,13r,21r)-10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,14,16,18-hexaene
1-methyl-7-{1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl}-3a-(1-methyl-3a-{1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl}-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-7-yl)-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
1-methyl-7-{1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl}-3a-(1-methyl-3a-{1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl}-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-7-yl)-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
(3ar)-7-[(3ar)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-3a-[(3as,8as)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
(3ar)-7-[(3ar)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-3a-[(3as,8as)-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl]-1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
(1r,9r,13s,21s)-10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,14,16,18-hexaene
(1r,9r,13s,21s)-10,22-dimethyl-8,10,20,22-tetraazahexacyclo[11.11.0.0¹,²¹.0²,⁷.0⁹,¹³.0¹⁴,¹⁹]tetracosa-2,4,6,14,16,18-hexaene
(1r,2s,10r,11s)-21,24-dimethyl-3,12,21,24-tetraazahexacyclo[9.7.3.3²,¹⁰.0¹,¹⁰.0⁴,⁹.0¹³,¹⁸]tetracosa-4,6,8,13,15,17-hexaene
(1r,2s,10r,11s)-21,24-dimethyl-3,12,21,24-tetraazahexacyclo[9.7.3.3²,¹⁰.0¹,¹⁰.0⁴,⁹.0¹³,¹⁸]tetracosa-4,6,8,13,15,17-hexaene
21,24-dimethyl-3,12,21,24-tetraazahexacyclo[9.7.3.3²,¹⁰.0¹,¹⁰.0⁴,⁹.0¹³,¹⁸]tetracosa-4,6,8,13,15,17-hexaene
21,24-dimethyl-3,12,21,24-tetraazahexacyclo[9.7.3.3²,¹⁰.0¹,¹⁰.0⁴,⁹.0¹³,¹⁸]tetracosa-4,6,8,13,15,17-hexaene
1-methyl-3a,7-bis({1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl})-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
1-methyl-3a,7-bis({1-methyl-2h,3h,8h,8ah-pyrrolo[2,3-b]indol-3a-yl})-2h,3h,8h,8ah-pyrrolo[2,3-b]indole
