NCBI Taxonomy: 129110
Pseudocyphellaria (ncbi_taxid: 129110)
found 100 associated metabolites at genus taxonomy rank level.
Ancestor: Lobariaceae
Child Taxonomies: Pseudocyphellaria dubia, Pseudocyphellaria glabra, Pseudocyphellaria aurata, Pseudocyphellaria divulsa, Pseudocyphellaria biliana, Pseudocyphellaria confusa, Pseudocyphellaria allanii, Pseudocyphellaria hirsuta, Pseudocyphellaria mallota, Pseudocyphellaria hookeri, Pseudocyphellaria murrayi, Pseudocyphellaria crocata, Pseudocyphellaria citrina, Pseudocyphellaria dozyana, Pseudocyphellaria lacerata, Pseudocyphellaria coriacea, Pseudocyphellaria lechleri, Pseudocyphellaria coronata, Pseudocyphellaria obvoluta, Pseudocyphellaria scabrosa, Pseudocyphellaria knightii, Pseudocyphellaria lindsayi, Pseudocyphellaria maculata, Pseudocyphellaria neglecta, Pseudocyphellaria perpetua, Pseudocyphellaria punctata, Pseudocyphellaria carpoloma, Pseudocyphellaria argyracea, Pseudocyphellaria montagnei, Pseudocyphellaria berberina, Pseudocyphellaria pubescens, Pseudocyphellaria clathrata, Pseudocyphellaria corbettii, Pseudocyphellaria norvegica, Pseudocyphellaria episticta, Pseudocyphellaria pilosella, Pseudocyphellaria faveolata, Pseudocyphellaria intricata, Pseudocyphellaria multifida, Pseudocyphellaria wilkinsii, Pseudocyphellaria philipiana, Pseudocyphellaria coriifolia, Pseudocyphellaria cinnamomea, Pseudocyphellaria dissimilis, Pseudocyphellaria anthraspis, Pseudocyphellaria holarctica, Pseudocyphellaria gallowayana, Pseudocyphellaria pomaikaiana, Pseudocyphellaria freycinetii, Pseudocyphellaria endochrysea, Pseudocyphellaria lividofusca, Pseudocyphellaria hawaiiensis, Pseudocyphellaria guilleminii, Pseudocyphellaria xanthosticta, unclassified Pseudocyphellaria, Pseudocyphellaria homoeophylla, Pseudocyphellaria rainierensis, Pseudocyphellaria epiflavoides, Pseudocyphellaria sandwicensis, Pseudocyphellaria desfontainii, Pseudocyphellaria macroisidiata, Pseudocyphellaria piloselloides, Pseudocyphellaria aff. lacerata, Pseudocyphellaria fimbriatoides, Pseudocyphellaria rufovirescens, Pseudocyphellaria cf. intricata FH-2008, Pseudocyphellaria aff. crocata Luecking sn, Pseudocyphellaria aff. crocata Moncada 5621, Pseudocyphellaria aff. crocata Moncada 5665, Pseudocyphellaria aff. crocata Galloway 7313a, Pseudocyphellaria aff. crocata Luecking 34807, Pseudocyphellaria aff. crocata Scharnagl KS02, Pseudocyphellaria aff. intricata Weerakoon 165
Lupeol
Lupeol is a pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in many edible fruits and vegetables. It has a role as an anti-inflammatory drug and a plant metabolite. It is a secondary alcohol and a pentacyclic triterpenoid. It derives from a hydride of a lupane. Lupeol has been investigated for the treatment of Acne. Lupeol is a natural product found in Ficus auriculata, Ficus septica, and other organisms with data available. See also: Calendula Officinalis Flower (part of). A pentacyclic triterpenoid that is lupane in which the hydrogen at the 3beta position is substituted by a hydroxy group. It occurs in the skin of lupin seeds, as well as in the latex of fig trees and of rubber plants. It is also found in many edible fruits and vegetables. D000893 - Anti-Inflammatory Agents Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1]. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1].
Lupeyl acetate
Lupeol acetate is an organic molecular entity. It has a role as a metabolite. Lupeol acetate is a natural product found in Euphorbia dracunculoides, Euphorbia larica, and other organisms with data available. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].
Ergosterol peroxide
Ergosterol peroxide is found in fruits. Ergosterol peroxide is obtained from leaves of Ananas comosus (pineapple obtained from leaves of Ananas comosus (pineapple). Ergosterol peroxide is found in pineapple and fruits.
Lupeol acetate
Vulgarol
Vulgarol, also known as 2,5-dihydroxy-3,6-diphenyl-1,4-benzoquinone, is a member of the class of compounds known as P-benzoquinones. P-benzoquinones are benzoquinones where the two C=O groups are attached at the 1- and 4-positions, respectively. Vulgarol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Vulgarol can be found in mugwort, which makes vulgarol a potential biomarker for the consumption of this food product.
vulpinic acid
Vulpinic acid, a lichen metabolite, decreases H2O2-induced ROS production, oxidative stress and oxidative stress-related damages in human umbilical vein endothelial cells (HUVEC). Vulpinic acid is active against staphylococci, enterococci, and anaerobic bacteria.Vulpinic acid has?the?potential?for?atherosclerosis?research[1][2].
Lupeol acetate
Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].
lupeol
D000893 - Anti-Inflammatory Agents Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1]. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC)[1].
4-(2,4-Dihydroxy-3,6-dimethyl-benzoyloxy)-2-hydroxy-6-methyl-benzoesaeure|4-(2,4-dihydroxy-3,6-dimethyl-benzoyloxy)-2-hydroxy-6-methyl-benzoic acid|Norobtusatic acid|Norobtusatsaeure
4-(2,4-dihydroxy-3,6-dimethylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid
Lupeol acetate
Lupeyl acetate, also known as lupeyl acetic acid, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Lupeyl acetate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Lupeyl acetate can be found in burdock, date, and fig, which makes lupeyl acetate a potential biomarker for the consumption of these food products. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1]. Lupeol acetate, a derivative of Lupeol, suppresses the progression of rheumatoid arthritis (RA) by inhibiting the activation of macrophages and osteoclastogenesis through downregulations of TNF-α, IL-1β, MCP-1, COX-2, VEGF and granzyme B[1].
