NCBI Taxonomy: 387060

Dolichopentas longiflora (ncbi_taxid: 387060)

found 24 associated metabolites at species taxonomy rank level.

Ancestor: Dolichopentas

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).

   

Tectoquinone

2-methylanthracene-9,10-dione

C15H10O2 (222.06807600000002)


CONFIDENCE standard compound; INTERNAL_ID 1128; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9354; ORIGINAL_PRECURSOR_SCAN_NO 9353 CONFIDENCE standard compound; INTERNAL_ID 1128; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9397; ORIGINAL_PRECURSOR_SCAN_NO 9396 CONFIDENCE standard compound; INTERNAL_ID 1128; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9371; ORIGINAL_PRECURSOR_SCAN_NO 9370 CONFIDENCE standard compound; INTERNAL_ID 1128; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9424; ORIGINAL_PRECURSOR_SCAN_NO 9423 CONFIDENCE standard compound; INTERNAL_ID 1128; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9336; ORIGINAL_PRECURSOR_SCAN_NO 9335 CONFIDENCE standard compound; INTERNAL_ID 1128; DATASET 20200303_ENTACT_RP_MIX508; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 9398; ORIGINAL_PRECURSOR_SCAN_NO 9396 Tectoquinone (2-Methylanthraquinone) is a SARSCoV-2 main protease inhibitor against COVID-19. Tectoquinone exhibits strong mosquito larvicidal activity with the LC50 values of 3.3 and 5.4 μg/ml against A. aegypti and A. albopictus in 24 h, respectively[1][2]. Tectoquinone (2-Methylanthraquinone) is a SARSCoV-2 main protease inhibitor against COVID-19. Tectoquinone exhibits strong mosquito larvicidal activity with the LC50 values of 3.3 and 5.4 μg/ml against A. aegypti and A. albopictus in 24 h, respectively[1][2].

   

Mollugin

Methyl 6-hydroxy-2,2-dimethyl-2H-benzo[h]chromene-5-carboxylate

C17H16O4 (284.1048536)


   

mollugin

2H-Naphtho(1,2-b)pyran-5-carboxylic acid, 6-hydroxy-2,2-dimethyl-, methyl ester

C17H16O4 (284.1048536)


Rubimaillin is a benzochromene that is 2H-benzo[h]chromene which is substituted by two methyl groups at position 2, a methoxycarbonyl group at position 5, and a hydroxy group at position 6. Found in the Chinese medical plant Rubia cordifola, It has an anti-cancer effect by inhibition of TNF-alpha-induced NF-kappaB activation. It is also a dual inhibitor of acyl-CoA:cholesterol acyltransferase 1 and 2 (ACAT1 and ACAT2), but is more selective for the ACAT2 isozyme. It has a role as a plant metabolite, an acyl-CoA:cholesterol acyltransferase 2 inhibitor, a NF-kappaB inhibitor, an antineoplastic agent, an apoptosis inducer, a neuroprotective agent and an anti-inflammatory agent. It is a benzochromene, a methyl ester and a member of phenols. Mollugin is a natural product found in Rubia alata, Rubia argyi, and other organisms with data available. Mollugin is an orally active and potent NF-κB inhibitor. Mollugin induces S-phase arrest of HepG2 cells, and increased intracellular reactive oxygen species (ROS) levels. Mollugin induces DNA damage in HepG2 cells, as well as an increase in the expression of p-H2AX. Mollugin shows anti-cancer effect by inhibiting TNF-α-induced NF-κB activation. Mollugin enhances the osteogenic action of BMP-2 (bone morphogenetic protein 2) via the p38-Smad signaling pathway[1][2][3]. Mollugin is an orally active and potent NF-κB inhibitor. Mollugin induces S-phase arrest of HepG2 cells, and increased intracellular reactive oxygen species (ROS) levels. Mollugin induces DNA damage in HepG2 cells, as well as an increase in the expression of p-H2AX. Mollugin shows anti-cancer effect by inhibiting TNF-α-induced NF-κB activation. Mollugin enhances the osteogenic action of BMP-2 (bone morphogenetic protein 2) via the p38-Smad signaling pathway[1][2][3]. Mollugin is an orally active and potent NF-κB inhibitor. Mollugin induces S-phase arrest of HepG2 cells, and increased intracellular reactive oxygen species (ROS) levels. Mollugin induces DNA damage in HepG2 cells, as well as an increase in the expression of p-H2AX. Mollugin shows anti-cancer effect by inhibiting TNF-α-induced NF-κB activation. Mollugin enhances the osteogenic action of BMP-2 (bone morphogenetic protein 2) via the p38-Smad signaling pathway[1][2][3].

   

2-Methoxy-3-methylanthracene-9,10-dione

2-Methoxy-3-methylanthracene-9,10-dione

C16H12O3 (252.0786402)


   

1H-Naphtho[2,3-c]pyran-5,10-dione

1H-Naphtho[2,3-c]pyran-5,10-dione

C13H8O3 (212.0473418)


   

2-Methylanthraquinone

InChI=1/C15H10O2/c1-9-6-7-12-13(8-9)15(17)11-5-3-2-4-10(11)14(12)16/h2-8H,1H

C15H10O2 (222.06807600000002)


2-methylanthraquinone is an anthraquinone that is 9,10-anthraquinone in which the hydrogen at position 2 is substituted by a methyl group. It is functionally related to a 9,10-anthraquinone. 2-Methylanthraquinone is a natural product found in Clausena heptaphylla, Ophiorrhiza pumila, and other organisms with data available. Tectoquinone (2-Methylanthraquinone) is a SARSCoV-2 main protease inhibitor against COVID-19. Tectoquinone exhibits strong mosquito larvicidal activity with the LC50 values of 3.3 and 5.4 μg/ml against A. aegypti and A. albopictus in 24 h, respectively[1][2]. Tectoquinone (2-Methylanthraquinone) is a SARSCoV-2 main protease inhibitor against COVID-19. Tectoquinone exhibits strong mosquito larvicidal activity with the LC50 values of 3.3 and 5.4 μg/ml against A. aegypti and A. albopictus in 24 h, respectively[1][2].

   

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).

   

Tectochinon

InChI=1\C15H10O2\c1-9-6-7-12-13(8-9)15(17)11-5-3-2-4-10(11)14(12)16\h2-8H,1H

C15H10O2 (222.06807600000002)


Tectoquinone (2-Methylanthraquinone) is a SARSCoV-2 main protease inhibitor against COVID-19. Tectoquinone exhibits strong mosquito larvicidal activity with the LC50 values of 3.3 and 5.4 μg/ml against A. aegypti and A. albopictus in 24 h, respectively[1][2]. Tectoquinone (2-Methylanthraquinone) is a SARSCoV-2 main protease inhibitor against COVID-19. Tectoquinone exhibits strong mosquito larvicidal activity with the LC50 values of 3.3 and 5.4 μg/ml against A. aegypti and A. albopictus in 24 h, respectively[1][2].

   

methyl (3r,4s)-3,4,6-trihydroxy-2,2-dimethyl-3h,4h-naphtho[1,2-b]pyran-5-carboxylate

methyl (3r,4s)-3,4,6-trihydroxy-2,2-dimethyl-3h,4h-naphtho[1,2-b]pyran-5-carboxylate

C17H18O6 (318.11033280000004)


   

13-methyl-14,16-dioxatetracyclo[11.2.1.0²,¹¹.0⁴,⁹]hexadeca-2(11),4,6,8-tetraene-3,10-dione

13-methyl-14,16-dioxatetracyclo[11.2.1.0²,¹¹.0⁴,⁹]hexadeca-2(11),4,6,8-tetraene-3,10-dione

C15H12O4 (256.0735552)


   

methyl (1as,7ar)-7a-(3-methylbut-2-en-1-yl)-2,7-dioxonaphtho[2,3-b]oxirene-1a-carboxylate

methyl (1as,7ar)-7a-(3-methylbut-2-en-1-yl)-2,7-dioxonaphtho[2,3-b]oxirene-1a-carboxylate

C17H16O5 (300.0997686)


   

methyl 3,4,6-trihydroxy-2,2-dimethyl-3h,4h-naphtho[1,2-b]pyran-5-carboxylate

methyl 3,4,6-trihydroxy-2,2-dimethyl-3h,4h-naphtho[1,2-b]pyran-5-carboxylate

C17H18O6 (318.11033280000004)


   

(1s,13r)-13-methyl-14,16-dioxatetracyclo[11.2.1.0²,¹¹.0⁴,⁹]hexadeca-2(11),4,6,8-tetraene-3,10-dione

(1s,13r)-13-methyl-14,16-dioxatetracyclo[11.2.1.0²,¹¹.0⁴,⁹]hexadeca-2(11),4,6,8-tetraene-3,10-dione

C15H12O4 (256.0735552)


   

methyl (3s,4s)-3,4,6-trihydroxy-2,2-dimethyl-3h,4h-naphtho[1,2-b]pyran-5-carboxylate

methyl (3s,4s)-3,4,6-trihydroxy-2,2-dimethyl-3h,4h-naphtho[1,2-b]pyran-5-carboxylate

C17H18O6 (318.11033280000004)


   

methyl 6-hydroxy-3-methoxy-2,2-dimethylbenzo[h]chromene-5-carboxylate

methyl 6-hydroxy-3-methoxy-2,2-dimethylbenzo[h]chromene-5-carboxylate

C18H18O5 (314.1154178)


   

methyl 3,6-dihydroxy-2,2-dimethylbenzo[h]chromene-5-carboxylate

methyl 3,6-dihydroxy-2,2-dimethylbenzo[h]chromene-5-carboxylate

C17H16O5 (300.0997686)


   

methyl 7a-(3-methylbut-2-en-1-yl)-2,7-dioxonaphtho[2,3-b]oxirene-1a-carboxylate

methyl 7a-(3-methylbut-2-en-1-yl)-2,7-dioxonaphtho[2,3-b]oxirene-1a-carboxylate

C17H16O5 (300.0997686)


   

1h-benzo[g]isochromene-5,10-dione

1h-benzo[g]isochromene-5,10-dione

C13H8O3 (212.0473418)


   

(3s,4s)-3-methoxy-4-[(3s,4s)-3-methoxy-5,10-dioxo-1h,3h,4h-naphtho[2,3-c]pyran-4-yl]-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione

(3s,4s)-3-methoxy-4-[(3s,4s)-3-methoxy-5,10-dioxo-1h,3h,4h-naphtho[2,3-c]pyran-4-yl]-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione

C28H22O8 (486.1314612)


   

5,10-dioxo-1h,3h,4h-naphtho[2,3-c]pyran-3-yl acetate

5,10-dioxo-1h,3h,4h-naphtho[2,3-c]pyran-3-yl acetate

C15H12O5 (272.0684702)


   

3-methoxy-4-{3-methoxy-5,10-dioxo-1h,3h,4h-naphtho[2,3-c]pyran-4-yl}-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione

3-methoxy-4-{3-methoxy-5,10-dioxo-1h,3h,4h-naphtho[2,3-c]pyran-4-yl}-1h,3h,4h-naphtho[2,3-c]pyran-5,10-dione

C28H22O8 (486.1314612)


   

(1r,13s)-13-methyl-14,16-dioxatetracyclo[11.2.1.0²,¹¹.0⁴,⁹]hexadeca-2(11),4,6,8-tetraene-3,10-dione

(1r,13s)-13-methyl-14,16-dioxatetracyclo[11.2.1.0²,¹¹.0⁴,⁹]hexadeca-2(11),4,6,8-tetraene-3,10-dione

C15H12O4 (256.0735552)