NCBI Taxonomy: 1333960

Euphorbia wallichii (ncbi_taxid: 1333960)

found 16 associated metabolites at species taxonomy rank level.

Ancestor: Euphorbia sect. Holophyllum

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 (576.439)


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.

   

Tirucallol

(3S,5R,10S,13S,14S,17S)-4,4,10,13,14-pentamethyl-17-((S)-6-methylhept-5-en-2-yl)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol

C30H50O (426.3861)


Tirucallol is a triterpenoid. Tirucallol is a natural product found in Euphorbia oxyphylla, Euphorbia caducifolia, and other organisms with data available. Constituent of gum mastic and pistachio nut resin. Tirucallol is found in many foods, some of which are soy bean, tea, cucumber, and muskmelon. Tirucallol is found in cucumber. Tirucallol is a constituent of gum mastic and pistachio nut resin. Tirucallol, a tetracyclic triterpene, is isolated from Euphorbia lacteal latex. Tirucallol has topical anti-inflammatory effect. Tirucallol can suppress ear edema in the mouse model and inhibit nitrite production in lipopolysaccharide-stimulated macrophages[1]. Tirucallol, a tetracyclic triterpene, is isolated from Euphorbia lacteal latex. Tirucallol has topical anti-inflammatory effect. Tirucallol can suppress ear edema in the mouse model and inhibit nitrite production in lipopolysaccharide-stimulated macrophages[1].

   

(+)-Tirucallol

(20S)-(+)-triucalla-8,24-diene-3beta-ol

C30H50O (426.3861)


   

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 (576.439)


   

ST 29:1;O;Hex

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

C35H60O6 (576.439)


   

Lanster

(3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol

C30H50O (426.3861)


COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

   

2,5-dihydroxy-4,4,4'a,6',6',7a,8'a,10'a-octamethyl-tetradecahydrospiro[indene-1,2'-phenanthren]-1'-one

2,5-dihydroxy-4,4,4'a,6',6',7a,8'a,10'a-octamethyl-tetradecahydrospiro[indene-1,2'-phenanthren]-1'-one

C30H50O3 (458.376)


   

(1s,4s,6s,9s,10r,12r,13s,15r)-6,13-dihydroxy-5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecan-7-one

(1s,4s,6s,9s,10r,12r,13s,15r)-6,13-dihydroxy-5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecan-7-one

C20H30O3 (318.2195)


   

6,13-dihydroxy-5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecan-7-one

6,13-dihydroxy-5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecan-7-one

C20H30O3 (318.2195)


   

(1s,2s,3ar,4'as,4'bs,5s,7as,8'ar,10'as)-2,5-dihydroxy-4,4,4'a,6',6',7a,8'a,10'a-octamethyl-tetradecahydrospiro[indene-1,2'-phenanthren]-1'-one

(1s,2s,3ar,4'as,4'bs,5s,7as,8'ar,10'as)-2,5-dihydroxy-4,4,4'a,6',6',7a,8'a,10'a-octamethyl-tetradecahydrospiro[indene-1,2'-phenanthren]-1'-one

C30H50O3 (458.376)


   

(1s,3as,5ar,7s,9as,11as)-3a,6,6,9a,11a-pentamethyl-1-[(2r)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol

(1s,3as,5ar,7s,9as,11as)-3a,6,6,9a,11a-pentamethyl-1-[(2r)-6-methyl-5-methylideneheptan-2-yl]-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol

C31H52O (440.4018)


   

5,5,9-trimethyl-6-oxopentacyclo[11.2.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁴]hexadecane-13-carboxylic acid

5,5,9-trimethyl-6-oxopentacyclo[11.2.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁴]hexadecane-13-carboxylic acid

C20H28O3 (316.2038)


   

3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylideneheptan-2-yl)-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol

3a,6,6,9a,11a-pentamethyl-1-(6-methyl-5-methylideneheptan-2-yl)-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-ol

C31H52O (440.4018)


   

(1s,4s,6r,9s,10r,12r,13s,15r)-5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecane-6,13-diol

(1s,4s,6r,9s,10r,12r,13s,15r)-5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecane-6,13-diol

C20H32O2 (304.2402)


   

5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecane-6,13-diol

5,5,9-trimethylpentacyclo[11.3.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁵]heptadecane-6,13-diol

C20H32O2 (304.2402)


   

(1s,4s,9s,10r,12r,13s,14s)-5,5,9-trimethyl-6-oxopentacyclo[11.2.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁴]hexadecane-13-carboxylic acid

(1s,4s,9s,10r,12r,13s,14s)-5,5,9-trimethyl-6-oxopentacyclo[11.2.1.0¹,¹⁰.0⁴,⁹.0¹²,¹⁴]hexadecane-13-carboxylic acid

C20H28O3 (316.2038)