NCBI Taxonomy: 4382

Lobelia (ncbi_taxid: 4382)

found 14 associated metabolites at genus taxonomy rank level.

Ancestor: Campanulaceae

Child Taxonomies: Lobelia erinus, Lobelia laxa, Lobelia nana, Lobelia tupa, Lobelia fugax, Lobelia urens, Lobelia sancta, Lobelia aguana, Lobelia anceps, Lobelia patula, Lobelia kalmii, Lobelia comosa, Lobelia aurita, Lobelia blanda, Lobelia gruina, Lobelia carens, Lobelia dunnii, Lobelia alanae, Lobelia amoena, Lobelia tenera, Lobelia canbyi, Lobelia montana, Lobelia kraussi, Lobelia fervens, Lobelia roughii, Lobelia stricta, Lobelia goetzei, Lobelia inflata, Lobelia tenuior, Lobelia anatina, Lobelia excelsa, Lobelia gibbosa, Lobelia villosa, Lobelia feayana, Lobelia burttii, Lobelia clavata, Lobelia davidii, Lobelia doniana, Lobelia holstii, Lobelia telekii, Lobelia spicata, Lobelia neglecta, Lobelia aquatica, Lobelia paludosa, Lobelia galpinii, Lobelia sartorii, Lobelia linearis, Lobelia depressa, Lobelia sinaloae, Lobelia hongiana, Lobelia exaltata, Lobelia martagon, Lobelia puberula, Lobelia boivinii, Lobelia minutula, Lobelia vivaldii, Lobelia flexuosa, Lobelia colorata, Lobelia heyneana, Lobelia ionantha, Lobelia giberroa, Lobelia melliana, Lobelia nubigena, Lobelia boykinii, Lobelia deckenii, Lobelia seguinii, Lobelia macrodon, Lobelia acrochila, Lobelia hederacea, Lobelia muscoides, Lobelia fenshamii, Lobelia chinensis, Lobelia baumannii, Lobelia tomentosa, Lobelia assurgens, Lobelia dortmanna, Lobelia thermalis, Lobelia fistulosa, Lobelia comptonii, Lobelia lasiantha, Lobelia oahuensis, Lobelia pteropoda, Lobelia rarifolia, Lobelia wilmsiana, Lobelia hartwegii, Lobelia volcanica, Lobelia mcvaughii, Lobelia laxiflora, Lobelia sumatrana, Lobelia rubescens, Lobelia fatiscens, Lobelia hypoleuca, Lobelia kauaensis, Lobelia schimperi, Lobelia petiolata, Lobelia yuccoides, Lobelia bambuseti, Lobelia proctorii, Lobelia taliensis, Lobelia bridgesii, Lobelia zeylanica, Lobelia nuttallii, Lobelia bequaertii, Lobelia alsinoides, Lobelia boninensis, Lobelia cardinalis, Lobelia hartlaubii, Lobelia malowensis, Lobelia xalapensis, Lobelia dasyphylla, Lobelia pratioides, Lobelia cordifolia, Lobelia knoblochii, Lobelia brevifolia, Lobelia polyphylla, Lobelia sonderiana, Lobelia thuliniana, Lobelia gregoriana, Lobelia irasuensis, Lobelia divaricata, Lobelia columnaris, Lobelia aberdarica, Lobelia lindblomii, Lobelia organensis, Lobelia glandulosa, Lobelia iteophylla, Lobelia pleotricha, Lobelia thapsoidea, Lobelia arnhemiaca, Lobelia glaberrima, Lobelia gattingeri, Lobelia mildbraedii, Lobelia stuhlmannii, Lobelia wollastonii, Lobelia graniticola, Lobelia jasionoides, Lobelia inconspicua, Lobelia rhombifolia, Lobelia winifrediae, Lobelia jaliscensis, Lobelia fenestralis, Lobelia longisepala, Lobelia pyramidalis, Lobelia niihauensis, Lobelia lammersiana, Lobelia siphilitica, Lobelia linnaeoides, Lobelia viridiflora, Lobelia ritabeaniana, Lobelia udzungwensis, Lobelia rotundifolia, Lobelia heterophylla, Lobelia vanreenensis, unclassified Lobelia, Lobelia erlangeriana, Lobelia erectiuscula, Lobelia sessilifolia, Lobelia loochooensis, Lobelia cliffortiana, Lobelia persicifolia, Lobelia capillifolia, Lobelia digitalifolia, Lobelia coronopifolia, Lobelia stricklandiae, Lobelia laurentioides, Lobelia rhytidosperma, Lobelia trigonocaulis, Lobelia portoricensis, Lobelia morogoroensis, Lobelia gloria-montis, Lobelia appendiculata, Lobelia lukwangulensis, Lobelia nicotianifolia, Lobelia simplicicaulis, Lobelia chamaedryfolia, Lobelia cymbalarioides, Lobelia rhynchopetalum, Lobelia leschenaultiana, Lobelia cleistogamoides

Diosmin

5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C28H32O15 (608.1741122)


Isolated from parsley. Diosmetin 7-rutinoside is found in many foods, some of which are sweet orange, spearmint, rosemary, and peppermint. C - Cardiovascular system > C05 - Vasoprotectives > C05C - Capillary stabilizing agents > C05CA - Bioflavonoids Diosmin is found in green vegetables. Diosmin is isolated from parsle C26170 - Protective Agent > C275 - Antioxidant > C306 - Bioflavonoid Diosmin is a disaccharide derivative that consists of diosmetin substituted by a 6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. It has a role as an antioxidant and an anti-inflammatory agent. It is a glycosyloxyflavone, a rutinoside, a disaccharide derivative, a monomethoxyflavone and a dihydroxyflavanone. It is functionally related to a diosmetin. Chronic venous insufficiency is a common condition the western population. Compression and pharmacotherapy are frequently used to manage chronic venous insufficiency, improving circulation and symptoms of venous disease. Diosmin is a bioflavonoid isolated from various plants or synthesized from [hesperidin]. It is used for the improvement of capillary fragility or venous insufficiency, including chronic venous insufficiency (CVI) and hemorrhoids. Diosmin is widely available over-the-counter and demonstrates a favourable a favorable safety profile. Diosmin is a natural product found in Asyneuma argutum, Citrus hystrix, and other organisms with data available. A bioflavonoid that strengthens vascular walls. See also: Agathosma betulina leaf (part of). [Raw Data] CBA89_Diosmin_neg_50eV.txt [Raw Data] CBA89_Diosmin_pos_10eV.txt [Raw Data] CBA89_Diosmin_neg_20eV.txt [Raw Data] CBA89_Diosmin_pos_50eV.txt [Raw Data] CBA89_Diosmin_neg_30eV.txt [Raw Data] CBA89_Diosmin_neg_40eV.txt [Raw Data] CBA89_Diosmin_pos_30eV.txt [Raw Data] CBA89_Diosmin_neg_10eV.txt [Raw Data] CBA89_Diosmin_pos_20eV.txt [Raw Data] CBA89_Diosmin_pos_40eV.txt Diosmin is a flavonoid found in a variety of citrus fruits and also an agonist of the aryl hydrocarbon receptor (AhR). Diosmin is a flavonoid found in a variety of citrus fruits and also an agonist of the aryl hydrocarbon receptor (AhR).

   

Tomentin

2- (3,4-Dihydroxyphenyl) -5,6-dihydroxy-3,7-dimethoxy-4H-1-benzopyran-4-one

C17H14O8 (346.0688644)


   

Isorhoifolin

5-Hydroxy-2-(4-hydroxyphenyl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one

C27H30O14 (578.163548)


Isorhoifolin is a natural product found in Astragalus onobrychis, Phillyrea latifolia, and other organisms with data available. Isorhoifolin is found in citrus. Isorhoifolin is isolated from leaves of Citrus paradisi (grapefruit) and other plant species. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2]. Isorhoifolin is a flavonoid glycoside from Hemistepta lyrata. Isorhoifolin displays an anti-leakage effect[1][2].

   

beta-Amyrin palmitate

4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl hexadecanoate

C46H80O2 (664.615798)


Beta-amyrin palmitate, also known as B-amyrin palmitic acid, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Beta-amyrin palmitate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Beta-amyrin palmitate can be found in black elderberry, which makes beta-amyrin palmitate a potential biomarker for the consumption of this food product.

   

Luteolin 7-rutinoside

Luteolin-7-O-beta-D-rutinoside

C27H30O15 (594.158463)


Luteolin-7-rutinoside has both anti-arthritic and antifungal activities, can result in a combination therapy for the treatment of fungal arthritis due to C. albicans infection.

   

5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one

5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one

C28H32O15 (608.1741122)


   

1-[(2r)-1-methylpiperidin-2-yl]pentan-2-one

1-[(2r)-1-methylpiperidin-2-yl]pentan-2-one

C11H21NO (183.1623056)


   

2-[(2r,6s)-6-[(2s)-2-hydroxybutyl]-1-methyl-3,6-dihydro-2h-pyridin-2-yl]-1-phenylethanone

2-[(2r,6s)-6-[(2s)-2-hydroxybutyl]-1-methyl-3,6-dihydro-2h-pyridin-2-yl]-1-phenylethanone

C18H25NO2 (287.188519)


   

(2r,3r,4s,5s,6r)-2-{[(4e,12e)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy}-6-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxane-3,4,5-triol

(2r,3r,4s,5s,6r)-2-{[(4e,12e)-1,7-dihydroxytetradeca-4,12-dien-8,10-diyn-6-yl]oxy}-6-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxane-3,4,5-triol

C26H38O12 (542.2363148)


   

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

2-(3,4-dihydroxyphenyl)-5-hydroxy-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-4-one

C27H30O15 (594.158463)


   

1-(1-methylpiperidin-2-yl)butan-2-one

1-(1-methylpiperidin-2-yl)butan-2-one

C10H19NO (169.14665639999998)