NCBI Taxonomy: 316917

Givotia madagascariensis (ncbi_taxid: 316917)

found 34 associated metabolites at species taxonomy rank level.

Ancestor: Givotia

Child Taxonomies: none taxonomy data.

Scopoletin

7-hydroxy-6-methoxy-2H-chromen-2-one

C10H8O4 (192.0422568)


Scopoletin is a hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. It has a role as a plant growth regulator and a plant metabolite. It is functionally related to an umbelliferone. Scopoletin is a natural product found in Ficus auriculata, Haplophyllum cappadocicum, and other organisms with data available. Scopoletin is a coumarin compound found in several plants including those in the genus Scopolia and the genus Brunfelsia, as well as chicory (Cichorium), redstem wormwood (Artemisia scoparia), stinging nettle (Urtica dioica), passion flower (Passiflora), noni (Morinda citrifolia fruit) and European black nightshade (Solanum nigrum) that is comprised of umbelliferone with a methoxy group substituent at position 6. Scopoletin is used to standardize and establish pharmacokinetic properties for products derived from the plants that produce it, such as noni extract. Although the mechanism(s) of action have not yet been established, this agent has potential antineoplastic, antidopaminergic, antioxidant, anti-inflammatory and anticholinesterase effects. Plant growth factor derived from the root of Scopolia carniolica or Scopolia japonica. See also: Arnica montana Flower (part of); Lycium barbarum fruit (part of); Viburnum opulus root (part of). Isolated from Angelica acutiloba (Dong Dang Gui). Scopoletin is found in many foods, some of which are lambsquarters, lemon, sunflower, and sherry. Scopoletin is found in anise. Scopoletin is isolated from Angelica acutiloba (Dong Dang Gui A hydroxycoumarin that is umbelliferone bearing a methoxy substituent at position 6. Acquisition and generation of the data is financially supported in part by CREST/JST. [Raw Data] CBA72_Scopoletin_pos_20eV.txt [Raw Data] CBA72_Scopoletin_pos_40eV.txt [Raw Data] CBA72_Scopoletin_neg_30eV.txt [Raw Data] CBA72_Scopoletin_neg_50eV.txt [Raw Data] CBA72_Scopoletin_pos_50eV.txt [Raw Data] CBA72_Scopoletin_pos_10eV.txt [Raw Data] CBA72_Scopoletin_neg_40eV.txt [Raw Data] CBA72_Scopoletin_neg_10eV.txt [Raw Data] CBA72_Scopoletin_pos_30eV.txt [Raw Data] CBA72_Scopoletin_neg_20eV.txt Scopoletin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=92-61-5 (retrieved 2024-07-12) (CAS RN: 92-61-5). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0). Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Spruceanol

(-)-8,11,13,15-cleistanthatetraene-3,12-diol

C20H28O2 (300.2089188)


   

Scopoletin

Scopoletin

C10H8O4 (192.0422568)


relative retention time with respect to 9-anthracene Carboxylic Acid is 0.636 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.637 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.629 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.631 IPB_RECORD: 1582; CONFIDENCE confident structure Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

Scopoletol

2H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy- (9CI)

C10H8O4 (192.0422568)


Scopoletin is an inhibitor of acetylcholinesterase (AChE). Scopoletin is an inhibitor of acetylcholinesterase (AChE).

   

(11r,13r,14r)-6,12,12,14-tetramethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraene-5,13-diol

(11r,13r,14r)-6,12,12,14-tetramethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraene-5,13-diol

C19H26O2 (286.1932696)


   

(2r,4as,4br,7r,8ar,10as)-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthren-2-ol

(2r,4as,4br,7r,8ar,10as)-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthren-2-ol

C20H32O (288.24530219999997)


   

15-formyl-14-hydroxy-6-methoxy-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4-carboxylic acid

15-formyl-14-hydroxy-6-methoxy-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-4-carboxylic acid

C18H14O8 (358.0688644)


   

7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthren-2-ol

7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthren-2-ol

C20H32O (288.24530219999997)


   

8-ethenyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol

8-ethenyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,6-diol

C20H28O2 (300.2089188)


   

6,12,12,14-tetramethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraene-5,13-diol

6,12,12,14-tetramethyltricyclo[9.4.0.0³,⁸]pentadeca-1,3(8),4,6-tetraene-5,13-diol

C19H26O2 (286.1932696)


   

(2r,4as,4br,6s,7r,8ar,10as)-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthrene-2,6-diol

(2r,4as,4br,6s,7r,8ar,10as)-7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthrene-2,6-diol

C20H32O2 (304.24021719999996)


   

(2s,3r,4ar,10as)-8-ethenyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,3,6-triol

(2s,3r,4ar,10as)-8-ethenyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,3,6-triol

C20H28O3 (316.2038338)


   

8-ethenyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,3,6-triol

8-ethenyl-1,1,4a,7-tetramethyl-2,3,4,9,10,10a-hexahydrophenanthrene-2,3,6-triol

C20H28O3 (316.2038338)


   

7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthrene-2,6-diol

7-ethenyl-4b,7,10a-trimethyl-1-methylidene-decahydrophenanthrene-2,6-diol

C20H32O2 (304.24021719999996)