NCBI Taxonomy: 2743252

Esenbeckia almawillia (ncbi_taxid: 2743252)

found 31 associated metabolites at species taxonomy rank level.

Ancestor: Esenbeckia

Child Taxonomies: none taxonomy data.

Isopimpinellin

InChI=1/C13H10O5/c1-15-10-7-3-4-9(14)18-12(7)13(16-2)11-8(10)5-6-17-11/h3-6H,1-2H3

C13H10O5 (246.052821)


Isopimpinellin is a member of psoralens. Isopimpinellin is a natural product found in Zanthoxylum mayu, Zanthoxylum ovalifolium, and other organisms with data available. Isopimpinellin is found in angelica. Isopimpinellin is present in the seeds of Pastinaca sativa (parsnip) Isopimpinellin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. See also: Angelica keiskei top (part of). Present in the seeds of Pastinaca sativa (parsnip). Isopimpinellin is found in many foods, some of which are carrot, anise, celery stalks, and fennel. Isopimpinellin is found in angelica. Isopimpinellin is present in the seeds of Pastinaca sativa (parsnip D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1]. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1].

   

Chalepin

Heliettin

C19H22O4 (314.1518012)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

Flindersiamine

8-Methoxy-6,7-methylenedioxydictamnine

C14H11NO5 (273.0637196)


   

Maculosidine

Furo(2,3-b)quinoline, 4,6,8-trimethoxy-

C14H13NO4 (259.0844538)


   

1-Methyl-8-methoxy-2-pentylquinolin-4(1H)-one

1-Methyl-8-methoxy-2-pentylquinolin-4(1H)-one

C16H21NO2 (259.1572206)


   
   

1-Methyl-8-methoxy-2-heptylquinolin-4(1H)-one

1-Methyl-8-methoxy-2-heptylquinolin-4(1H)-one

C18H25NO2 (287.188519)


   

Isopimpinellin

Isopimpinellin

C13H10O5 (246.052821)


Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1]. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1].

   

Isopimpinellin

7H-Furo(3,2-g)(1)benzopyran-7-one, 4,9-dimethoxy- (8CI)(9CI)

C13H10O5 (246.052821)


Isopimpinellin is found in angelica. Isopimpinellin is present in the seeds of Pastinaca sativa (parsnip) Isopimpinellin belongs to the family of Furanocoumarins. These are polycyclic aromatic compounds containing a furan ring fused to a coumarin moeity. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1]. Isopimpinellin, an orally active compound isolated from Glomerella cingulata. Isopimpinellin blocks DNA adduct formation and skin tumor initiation by 7,12-dimethylbenz[a]anthracene. Isopimpinellin possesses anti-leishmania effect[1].

   

Chalepin

Chalepin

C19H22O4 (314.1518012)


D011838 - Radiation-Sensitizing Agents > D017319 - Photosensitizing Agents > D011564 - Furocoumarins

   

1-methyl-3,3-bis(3-methylbut-2-en-1-yl)quinoline-2,4-dione

1-methyl-3,3-bis(3-methylbut-2-en-1-yl)quinoline-2,4-dione

C20H25NO2 (311.188519)


   

8-methoxy-2-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-methylquinolin-4-one

8-methoxy-2-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-methylquinolin-4-one

C19H17NO5 (339.1106672)


   

8-methoxy-1-methyl-2-pentylquinolin-4-one

8-methoxy-1-methyl-2-pentylquinolin-4-one

C16H21NO2 (259.1572206)


   

methyl (2e)-3-(7-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enoate

methyl (2e)-3-(7-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enoate

C12H12O5 (236.06847019999998)


   

(+)-rutamarin alcohol

(+)-rutamarin alcohol

C19H22O4 (314.1518012)


   

(2e)-3-(6-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enal

(2e)-3-(6-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enal

C11H10O4 (206.057906)


   

methyl 3-(7-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enoate

methyl 3-(7-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enoate

C12H12O5 (236.06847019999998)


   

3-(6-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enal

3-(6-methoxy-2h-1,3-benzodioxol-5-yl)prop-2-enal

C11H10O4 (206.057906)


   

2-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-methylquinolin-4-one

2-(7-methoxy-2h-1,3-benzodioxol-5-yl)-1-methylquinolin-4-one

C18H15NO4 (309.100103)


   

2-heptyl-8-methoxy-1-methylquinolin-4-one

2-heptyl-8-methoxy-1-methylquinolin-4-one

C18H25NO2 (287.188519)


   

2-hexyl-8-methoxy-1-methylquinolin-4-one

2-hexyl-8-methoxy-1-methylquinolin-4-one

C17H23NO2 (273.1728698)