NCBI Taxonomy: 405316

Piper aequale (ncbi_taxid: 405316)

found 67 associated metabolites at species taxonomy rank level.

Ancestor: Piper

Child Taxonomies: none taxonomy data.

beta-Sitosterol 3-O-beta-D-galactopyranoside

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5R)-5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

C35H60O6 (576.4389659999999)


Daucosterol is a steroid saponin that is sitosterol attached to a beta-D-glucopyranosyl residue at position 3 via a glycosidic linkage. It has bee isolated from Panax japonicus var. major and Breynia fruticosa. It has a role as a plant metabolite. It is a steroid saponin, a beta-D-glucoside and a monosaccharide derivative. It is functionally related to a sitosterol. It derives from a hydride of a stigmastane. Sitogluside is a natural product found in Ophiopogon intermedius, Ophiopogon jaburan, and other organisms with data available. beta-Sitosterol 3-O-beta-D-galactopyranoside is found in herbs and spices. beta-Sitosterol 3-O-beta-D-galactopyranoside is a constituent of Hibiscus sabdariffa (roselle) leaves. C308 - Immunotherapeutic Agent Daucosterol is a natural sterol compound. Daucosterol is a natural sterol compound.

   

p-Anisic acid

4-Methoxy-benzoic Acid; 4-Anisic acid; Anisic acid pound>>p-Anisic acid pound>>p-Methoxybenzoic acid

C8H8O3 (152.0473418)


p-Anisic acid, also known as 4-anisate or draconic acid, belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group. p-Anisic acid is a drug. p-Anisic acid exists in all eukaryotes, ranging from yeast to humans. p-Anisic acid is a faint, sweet, and cadaverous tasting compound. Outside of the human body, p-anisic acid has been detected, but not quantified in several different foods, such as anises, cocoa beans, fennels, and german camomiles. This could make p-anisic acid a potential biomarker for the consumption of these foods. It is a white crystalline solid which is insoluble in water, highly soluble in alcohols and soluble in ether, and ethyl acetate. p-Anisic acid has antiseptic properties. It is also used as an intermediate in the preparation of more complex organic compounds. It is generally obtained by the oxidation of anethole or p-methoxyacetophenone. The term "anisic acid" often refers to this form specifically. p-Anisic acid is found naturally in anise. 4-methoxybenzoic acid is a methoxybenzoic acid substituted with a methoxy group at position C-4. It has a role as a plant metabolite. It is functionally related to a benzoic acid. It is a conjugate acid of a 4-methoxybenzoate. 4-Methoxybenzoic acid is a natural product found in Chaenomeles speciosa, Annona purpurea, and other organisms with data available. Anisic acid is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Stevia rebaudiuna Leaf (part of). Flavouring agent. Food additive listed in the EAFUS Food Additive Database (Jan. 2001) A methoxybenzoic acid substituted with a methoxy group at position C-4. COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS KEIO_ID A154 p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties[1]. p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties[1].

   

alpha-Terpineol

2-(4-Methylcyclohex-3-enyl)propan-2-ol (alpha-terpineol)

C10H18O (154.1357578)


alpha-Terpineol (CAS: 98-55-5) is a naturally occurring monoterpene alcohol that has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrain oil. There are three isomers of terpineol, alpha-, beta-, and gamma-terpineol, with the last two differing only by the location of the double bond. Terpineol is usually a mixture of these isomers with alpha-terpineol as the major constituent. Terpineol has a pleasant odour similar to lilac and is a common ingredient in perfumes, cosmetics, and flavours. alpha-Terpineol is occasionally found as a volatile component in urine. It is a water-soluble component of Melaleuca alternifolia Cheel, the tea tree oil (TTO). alpha-Terpineol is a likely mediator of the in vitro and in vivo activity of the TTO as an agent that could control C. albicans vaginal infections. Purified alpha-terpineol can suppress pro-inflammatory mediator production by activated human monocytes. alpha-Terpineol is able to impair the growth of human M14 melanoma cells and appear to be more effective on their resistant variants, which express high levels of P-glycoprotein in the plasma membrane, overcoming resistance to caspase-dependent apoptosis exerted by P-glycoprotein-positive tumour cells (PMID:5556886, 17083732, 11131302, 15009716). Terpineol is a naturally occurring monoterpene alcohol that has been isolated from a variety of sources such as cajuput oil, pine oil, and petitgrain oil. There are three isomers, alpha-, beta-, and gamma-terpineol, the last two differing only by the location of the double bond. Terpineol is usually a mixture of these isomers with alpha-terpineol as the major constituent. (R)-alpha-Terpineol is found in many foods, some of which are mentha (mint), sweet marjoram, lovage, and cardamom. α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2]. α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].

   

alpha-Terpineol acetate

2-(4-methylcyclohex-3-en-1-yl)propan-2-yl acetate

C12H20O2 (196.14632200000003)


alpha-Terpineol acetate, also known as a-terpineol acetic acid or p-menth-1-en-8-yl acetate, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. alpha-Terpineol acetate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2]. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2].

   

Conocarpan

(+)-Conocarpan

C18H18O2 (266.1306728)


   

Terpenol

3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, sodium salt, (1S)-

C10H18O (154.1357578)


Alpha-terpineol is a terpineol that is propan-2-ol substituted by a 4-methylcyclohex-3-en-1-yl group at position 2. It has a role as a plant metabolite. alpha-TERPINEOL is a natural product found in Nepeta nepetella, Xylopia aromatica, and other organisms with data available. 2-(4-Methyl-3-cyclohexen-1-yl)-2-propanol is a metabolite found in or produced by Saccharomyces cerevisiae. See also: Coriander Oil (part of); Cannabis sativa subsp. indica top (part of); Peumus boldus leaf (part of). A terpineol that is propan-2-ol substituted by a 4-methylcyclohex-3-en-1-yl group at position 2. (-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1]. (-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1]. (-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1]. (-)-α-Terpineol ((S)-α-Terpineol), a monoterpene compound, is one of compounds in Melaleuca alternifolia[1]. α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2]. α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].

   

alpha-Terpineol acetate

(+/-)-alpha-Terpinyl acetate, predominantly alpha-isomer, technical, >=90\\% (GC)

C12H20O2 (196.14632200000003)


alpha-Terpineol acetate, also known as a-terpineol acetic acid or p-menth-1-en-8-yl acetate, belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes. alpha-Terpineol acetate is a very hydrophobic molecule, practically insoluble in water, and relatively neutral. Alpha-Terpinyl acetate is a p-menthane monoterpenoid. alpha-Terpinyl acetate is a natural product found in Xylopia sericea, Elettaria cardamomum, and other organisms with data available. Terpinyl acetate is a metabolite found in or produced by Saccharomyces cerevisiae. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2]. α-Terpinyl acetate is a monoterpene ester isolated from Laurus nobilis L. essential oil. α-Terpinyl acetate is a competitive P450 2B6 substrate which binding to the active site of P450 2B6 with a Kd value of 5.4?μM[1][2].

   

beta-Sitosterol 3-O-beta-D-galactopyranoside

2-{[14-(5-ethyl-6-methylheptan-2-yl)-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C35H60O6 (576.4389659999999)


   

ST 29:1;O;Hex

stigmast-5-en-3beta-yl beta-D-galactopyranoside

C35H60O6 (576.4389659999999)


   

alpha-terpineol

alpha-terpineol

C10H18O (154.1357578)


α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2]. α-Terpineol is isolated from Eucalyptus globulus Labill, exhibits strong antimicrobial activity against periodontopathic and cariogenic bacteria[1]. α-Terpineol possesses antifungal activity against T. mentagrophytes, and the activity might lead to irreversible cellular disruption[2].

   

ANISIC ACID

InChI=1\C8H8O3\c1-11-7-4-2-6(3-5-7)8(9)10\h2-5H,1H3,(H,9,10

C8H8O3 (152.0473418)


COVID info from PDB, Protein Data Bank Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties[1]. p-Anisic acid (4-Methoxybenzoic acid) is one of the isomers of anisic acid, with anti-bacterial and antiseptic properties[1].

   

(+)-Conocarpan

(+)-Conocarpan

C18H18O2 (266.1306728)


A member of the class of benzofurans that is 2,3-dihydro-1-benzofuran substituted by a methyl group at position 3, a prop-1-en-1-yl group at position 5 and a 4-hydroxyphenyl group at position 2. It is a lignan derivative isolated from the roots of Krameria lappacea.

   

rataniaphenol II

rataniaphenol II

C18H16O2 (264.1150236)


A member of the class of benzofurans that is 1-benzofuran substituted by a 4-hydroxyphenyl group at position 2, a methyl group at position 3 and a prop-1-en-1-yl group at position 5. It is a lignan derivative isolated from the roots of Krameria lappacea.

   

4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}-2-(3-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenoxy)phenol

4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}-2-(3-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenoxy)phenol

C36H30O4 (526.214398)


   

4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C18H18O2 (266.1306728)


   

2-methoxy-4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

2-methoxy-4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

C19H18O3 (294.1255878)


   

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]-2-{4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenoxy}phenol

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]-2-{4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenoxy}phenol

C36H30O4 (526.214398)


   

4-[(2r,3r)-5-methoxy-3-methyl-7-(prop-2-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[(2r,3r)-5-methoxy-3-methyl-7-(prop-2-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

2-methoxy-4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

2-methoxy-4-[(2r,3r)-3-methyl-5-[(1e)-prop-1-en-1-yl]-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

5-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}-2h-1,3-benzodioxole

5-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}-2h-1,3-benzodioxole

C19H16O3 (292.10993859999996)


   

3-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol

3-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol

C20H20O4 (324.13615200000004)


   

4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}-2-(4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenoxy)phenol

4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}-2-(4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenoxy)phenol

C36H30O4 (526.214398)


   

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenol

C18H16O2 (264.1150236)


   

1-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]propan-2-one

1-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]propan-2-one

C19H16O4 (308.1048536)


   

(2r,3r)-2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde

(2r,3r)-2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde

C16H14O3 (254.0942894)


   

4-[5-methoxy-3-methyl-7-(prop-2-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[5-methoxy-3-methyl-7-(prop-2-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde

2-(4-hydroxyphenyl)-3-methyl-2,3-dihydro-1-benzofuran-5-carbaldehyde

C16H14O3 (254.0942894)


   

2-methoxy-4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

2-methoxy-4-{3-methyl-5-[(1e)-prop-1-en-1-yl]-1-benzofuran-2-yl}phenol

C19H18O3 (294.1255878)


   

5-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]-2h-1,3-benzodioxole

5-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]-2h-1,3-benzodioxole

C19H16O3 (292.10993859999996)


   

2-methoxy-4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

2-methoxy-4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C19H20O3 (296.14123700000005)


   

(2s,3r)-3-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol

(2s,3r)-3-[2-(2h-1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]butan-2-ol

C20H20O4 (324.13615200000004)


   

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]-2-{3-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenoxy}phenol

4-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]-2-{3-[3-methyl-5-(prop-1-en-1-yl)-1-benzofuran-2-yl]phenoxy}phenol

C36H30O4 (526.214398)


   

4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

4-[3-methyl-5-(prop-1-en-1-yl)-2,3-dihydro-1-benzofuran-2-yl]phenol

C18H18O2 (266.1306728)


   

(4s,8r,9r)-8-[(1s)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione

(4s,8r,9r)-8-[(1s)-1,2-dihydroxyethyl]-9-hydroxy-4-(4-hydroxyphenyl)-1,7-dioxaspiro[4.4]nonane-2,6-dione

C15H16O8 (324.0845136)