NCBI Taxonomy: 487037

Juniperus barbadensis var. lucayana (ncbi_taxid: 487037)

found 24 associated metabolites at varietas taxonomy rank level.

Ancestor: Juniperus barbadensis

Child Taxonomies: none taxonomy data.

Cedrol

(3R-(3.ALPHA.,3A.BETA.,6.ALPHA.,7.BETA.,8A.ALPHA.))-OCTAHYDRO-3,6,8,8-TETRAMETHYL-1H-3A,7-METHANOAZULEN-6-OL

C15H26O (222.1983546)


Cedrol is a cedrane sesquiterpenoid and a tertiary alcohol. Cedrol is a natural product found in Xylopia aromatica, Widdringtonia whytei, and other organisms with data available. Cedrol is a bioactive sesquiterpene, a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes[1]. Cedrol is found in cedar essential oil and poetesses anti-septic, anti-inflammatory, anti-spasmodic, tonic, astringent, diuretic, insecticidal, and anti-fungal activities[2]. Cedrol is a bioactive sesquiterpene, a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes[1]. Cedrol is found in cedar essential oil and poetesses anti-septic, anti-inflammatory, anti-spasmodic, tonic, astringent, diuretic, insecticidal, and anti-fungal activities[2].

   

alpha-Bisabolol

6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol

C15H26O (222.1983546)


alpha-Bisabolol is a nontoxic sesquiterpene alcohol present in natural essential oil, with anticancer activity. alpha-Bisabolol exerts selective anticancer effect on A549 NSCLC cells (IC50=15 μM) via induction of cell cycle arrest, mitochondrial apoptosis and inhibition of PI3K/Akt signalling pathways. alpha-Bisabolol also strongly induces apoptosis in glioma cells[1][2]. alpha-Bisabolol is a nontoxic sesquiterpene alcohol present in natural essential oil, with anticancer activity. alpha-Bisabolol exerts selective anticancer effect on A549 NSCLC cells (IC50=15 μM) via induction of cell cycle arrest, mitochondrial apoptosis and inhibition of PI3K/Akt signalling pathways. alpha-Bisabolol also strongly induces apoptosis in glioma cells[1][2].

   

Cedrol

2,6,6,8-tetramethyltricyclo[5.3.1.0¹,⁵]undecan-8-ol

C15H26O (222.1983546)


Cedrol is a member of the class of compounds known as cedrane and isocedrane sesquiterpenoids. Cedrane and isocedrane sesquiterpenoids are sesquiternoids with a structure based on the cedrane or the isocedrane skeleton. Cedrane is a tricyclic molecules a 3,6,8,8-tetramethyl-1H-3a,7-methano-azulene moiety. Isocedrane is a rearranged cedrane arising from the migration of methyl group moved from the 6-position to the 4-position. Cedrol is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Cedrol is a sweet, cedarwood, and dry tasting compound found in ginger, pepper (spice), and peppermint, which makes cedrol a potential biomarker for the consumption of these food products. Cedrol is a sesquiterpene alcohol found in the essential oil of conifers (cedar oil), especially in the genera Cupressus (cypress) and Juniperus (juniper). It has also been identified in Origanum onites, a plant related to oregano. Its main uses are in the chemistry of aroma compounds. It makes up about 19\\\\% of cedarwood oil Texas and 15.8\\\\% of cedarwood oil Virginia . Cedrol is a bioactive sesquiterpene, a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes[1]. Cedrol is found in cedar essential oil and poetesses anti-septic, anti-inflammatory, anti-spasmodic, tonic, astringent, diuretic, insecticidal, and anti-fungal activities[2]. Cedrol is a bioactive sesquiterpene, a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes. Cedrol inhibits CYP2B6-mediated bupropion hydroxylase and CYP3A4-mediated midazolam hydroxylation with Ki of 0.9 μM and 3.4 μM, respectively. Cedrol also has weak inhibitory effect on CYP2C8, CYP2C9, and CYP2C19 enzymes[1]. Cedrol is found in cedar essential oil and poetesses anti-septic, anti-inflammatory, anti-spasmodic, tonic, astringent, diuretic, insecticidal, and anti-fungal activities[2].

   
   

(1r,2r,5r,7r,8s)-7-(hydroxymethyl)-2,6,6-trimethyltricyclo[5.2.2.0¹,⁵]undecan-8-ol

(1r,2r,5r,7r,8s)-7-(hydroxymethyl)-2,6,6-trimethyltricyclo[5.2.2.0¹,⁵]undecan-8-ol

C15H26O2 (238.1932696)


   

(6s)-7,7-dimethyl-11-methylidenespiro[5.5]undec-2-ene-3-carboxylic acid

(6s)-7,7-dimethyl-11-methylidenespiro[5.5]undec-2-ene-3-carboxylic acid

C15H22O2 (234.1619712)


   

(4as,6r,7s)-4,4,4a,7-tetramethyl-1,2,3,5,6,8-hexahydrobenzo[7]annulene-6,7-diol

(4as,6r,7s)-4,4,4a,7-tetramethyl-1,2,3,5,6,8-hexahydrobenzo[7]annulene-6,7-diol

C15H26O2 (238.1932696)


   

(2s,3r)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

(2s,3r)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzopyran-4-one

C15H12O6 (288.06338519999997)


   

(1r,2r,5r,7r,8s)-2,6,6,7-tetramethyltricyclo[5.2.2.0¹,⁵]undecan-8-ol

(1r,2r,5r,7r,8s)-2,6,6,7-tetramethyltricyclo[5.2.2.0¹,⁵]undecan-8-ol

C15H26O (222.1983546)


   

(4as,7s)-7-(hydroxymethyl)-1,1,4a-trimethyl-2,3,4,5,6,8-hexahydrobenzo[7]annulen-7-ol

(4as,7s)-7-(hydroxymethyl)-1,1,4a-trimethyl-2,3,4,5,6,8-hexahydrobenzo[7]annulen-7-ol

C15H26O2 (238.1932696)


   

(7s)-1,1,4a,7-tetramethyl-2,3,4,5,6,8-hexahydrobenzo[7]annulen-7-ol

(7s)-1,1,4a,7-tetramethyl-2,3,4,5,6,8-hexahydrobenzo[7]annulen-7-ol

C15H26O (222.1983546)