NCBI Taxonomy: 72901
Blumea (ncbi_taxid: 72901)
found 34 associated metabolites at genus taxonomy rank level.
Ancestor: Inulinae
Child Taxonomies: Blumea lacera, Blumea virens, Blumea mollis, Blumea adamsii, Blumea diffusa, Blumea clarkei, Blumea sinuata, Blumea riparia, Blumea tenella, Blumea procera, Blumea brevipes, Blumea axillaris, Blumea saxatilis, Blumea formosana, Blumea arfakiana, Blumea aromatica, Blumea fistulosa, Blumea napifolia, Blumea oxyodonta, Blumea laciniata, Blumea bifoliata, Blumea sagittata, Blumea sylvatica, Blumea canalensis, Blumea densiflora, Blumea paniculata, Blumea martiniana, Blumea balsamifera, Blumea lanceolaria, Blumea megacephala, Blumea macrophylla, Blumea integrifolia, Blumea sessiliflora, unclassified Blumea, Blumea oblongifolia, Blumea benguetensis, Blumea hieraciifolia, Blumea arnakidophora, Blumea saussureoides, Blumea cf. canalensis Bernardi 9667
Pachypodol
Pachypodol is a trimethoxyflavone that is quercetin in which the hydroxy groups at position 3, 7 and 3 are replaced by methoxy groups. It has been isolated from Combretum quadrangulare and Euodia elleryana. It has a role as a plant metabolite and an antiemetic. It is a dihydroxyflavone and a trimethoxyflavone. It is functionally related to a quercetin. Pachypodol is a natural product found in Larrea cuneifolia, Macaranga triloba, and other organisms with data available. A trimethoxyflavone that is quercetin in which the hydroxy groups at position 3, 7 and 3 are replaced by methoxy groups. It has been isolated from Combretum quadrangulare and Euodia elleryana. Pachypodol exerts antioxidant and cytoprotective effects in HepG2 cells[1].Pachypodol inhibits the growth of CaCo 2 colon cancer cell line in vitro(IC50 = 185.6 mM)[2]. Pachypodol exerts antioxidant and cytoprotective effects in HepG2 cells[1].Pachypodol inhibits the growth of CaCo 2 colon cancer cell line in vitro(IC50 = 185.6 mM)[2].
Germacrene D
Germacrene d, also known as germacrene d, (s-(e,e))-isomer, is a member of the class of compounds known as germacrane sesquiterpenoids. Germacrane sesquiterpenoids are sesquiterpenoids having the germacrane skeleton, with a structure characterized by a cyclodecane ring substituted with an isopropyl and two methyl groups. Germacrene d can be found in a number of food items such as peppermint, roman camomile, hyssop, and common walnut, which makes germacrene d a potential biomarker for the consumption of these food products.
Carvotanacetone
Carvotanacetone belongs to the family of Monocyclic Monoterpenes. These are monoterpenes containing 1 ring in the isoprene chain
Velutin
Velutin is a dimethoxyflavone that is luteolin in which the hydroxy groups at positions 7 and 3 are replaced by methoxy groups. It has a role as an anti-inflammatory agent, a plant metabolite, a melanin synthesis inhibitor, an antibacterial agent, an antioxidant and an anti-allergic agent. It is a dimethoxyflavone and a dihydroxyflavone. It is functionally related to a 4,5,7-trihydroxy-3-methoxyflavone. Velutin is a natural product found in Avicennia officinalis, Lantana montevidensis, and other organisms with data available. See also: Acai (part of). A dimethoxyflavone that is luteolin in which the hydroxy groups at positions 7 and 3 are replaced by methoxy groups. [Raw Data] CB095_Velutin_neg_50eV_000026.txt [Raw Data] CB095_Velutin_neg_40eV_000026.txt [Raw Data] CB095_Velutin_neg_30eV_000026.txt [Raw Data] CB095_Velutin_neg_20eV_000026.txt [Raw Data] CB095_Velutin_neg_10eV_000026.txt [Raw Data] CB095_Velutin_pos_50eV_CB000040.txt [Raw Data] CB095_Velutin_pos_40eV_CB000040.txt [Raw Data] CB095_Velutin_pos_30eV_CB000040.txt [Raw Data] CB095_Velutin_pos_20eV_CB000040.txt [Raw Data] CB095_Velutin_pos_10eV_CB000040.txt Velutin is an aglycone extracted from Flammulina velutipes, with inhibitory activity against melanin biosynthesis. Velutin reduces osteoclast differentiation and down-regulates HIF-1α through the NF-κB pathway[1][2]. Velutin is an aglycone extracted from Flammulina velutipes, with inhibitory activity against melanin biosynthesis. Velutin reduces osteoclast differentiation and down-regulates HIF-1α through the NF-κB pathway[1][2]. Velutin is an aglycone extracted from Flammulina velutipes, with inhibitory activity against melanin biosynthesis. Velutin reduces osteoclast differentiation and down-regulates HIF-1α through the NF-κB pathway[1][2].
Germacrene D
(-)-germacrene D is a germacrene D. It is an enantiomer of a (+)-germacrene D. (-)-Germacrene D is a natural product found in Teucrium montanum, Stachys obliqua, and other organisms with data available. See also: Clary Sage Oil (part of).
(3-hydroxy-4-isopropyl-6-oxocyclohex-1-en-1-yl)methyl 2-methylbut-2-enoate
8-(acetyloxy)-7-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-6-yl 3-methylbutanoate
1,12-dihydroxy-2,11-dimethyl-7-methylidene-6-oxo-5,14-dioxatricyclo[9.2.1.0⁴,⁸]tetradecan-9-yl 2-methylpropanoate
2-(2,5-dihydroxyphenyl)-6-hydroxy-3,5,7-trimethoxychromen-4-one
[5'-(but-3-en-1-yn-1-yl)-[2,2'-bithiophen]-5-yl]methyl acetate
(1s,2r,3r,5r,9r,10r,11r)-10-hydroxy-5,9-dimethyl-14-methylidene-13-oxo-4,12-dioxatricyclo[9.3.0.0³,⁵]tetradecan-2-yl (2z)-2-methylbut-2-enoate
8-(acetyloxy)-6-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-7-yl 3-methylbutanoate
3-{2,3-dimethoxy-4-[(2-methylbut-2-enoyl)oxy]phenyl}prop-2-en-1-yl 2-methylbut-2-enoate
(1r,4r,6s,10s)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.0⁴,⁶]dodecane
(2s,3r,4s,5r)-2-[4-hydroxy-2-isopropyl-5-(3-methylbut-2-en-1-yl)phenoxy]oxane-3,4,5-triol
(3r,3as,4s,8as)-3-hydroxy-3-isopropyl-6,8a-dimethyl-1,2,3a,4,5,8-hexahydroazulen-4-yl 4-hydroxybenzoate
(1r,2s,3s,4r,4as,8as)-3,4a,8,8-tetramethyl-4-[(2z)-3-methylpenta-2,4-dien-1-yl]-hexahydro-1h-naphthalene-1,2,3-triol
(1's,3r,3'r,5s,6'r,7'r)-5-(furan-3-yl)-3',6',7'-trimethyl-9'-oxaspiro[oxolane-3,2'-tricyclo[5.2.2.0¹,⁶]undecane]-2,8'-dione
(3ar,4ar,6r,8s,8ar,9ar)-8-hydroxy-8a-methyl-3,5-dimethylidene-2-oxo-octahydronaphtho[2,3-b]furan-6-yl 3-methylbutanoate
2-(ethoxymethyl)-4-hydroxy-5-isopropylcyclohex-2-en-1-one
(2r)-2-hydroxy-4-{5'-methyl-[2,2'-bithiophen]-5-yl}but-3-yn-1-yl 3-methylbutanoate
C18H20O3S2 (348.08538100000004)