NCBI Taxonomy: 1933696

Salvia bracteata (ncbi_taxid: 1933696)

found 49 associated metabolites at species taxonomy rank level.

Ancestor: Salvia incertae sedis

Child Taxonomies: none taxonomy data.

Lupeol

(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol

C30H50O (426.386145)


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].

   

Sugiol

9(1H)-Phenanthrenone, 2,3,4,4a,10,10a-hexahydro-6-hydroxy-1,1,4a-trimethyl-7-(1-methylethyl)-, (4aS-trans)-

C20H28O2 (300.2089188)


Sugiol is an abietane diterpenoid that is ferruginol in which the methylene group para to the phenolic hydroxy group has been substituted by an oxo group. It has a role as a plant metabolite, an antiviral agent, an antineoplastic agent, an antioxidant and a radical scavenger. It is an abietane diterpenoid, a carbotricyclic compound, a meroterpenoid, a member of phenols and a cyclic terpene ketone. It is functionally related to a ferruginol. Sugiol is a natural product found in Austrocedrus chilensis, Libocedrus bidwillii, and other organisms with data available. An abietane diterpenoid that is ferruginol in which the methylene group para to the phenolic hydroxy group has been substituted by an oxo group.

   

Ferruginol

3-PHENANTHRENOL, 4B,5,6,7,8,8A,9,10-OCTAHYDRO-4B,8,8-TRIMETHYL-2-(1-METHYLETHYL)-, (4BS-TRANS)-

C20H30O (286.229653)


Ferruginol is an abietane diterpenoid that is abieta-8,11,13-triene substituted by a hydroxy group at positions 12. It has a role as an antineoplastic agent, an antibacterial agent, a protective agent and a plant metabolite. It is an abietane diterpenoid, a member of phenols, a carbotricyclic compound and a meroterpenoid. Ferruginol is a natural product found in Calocedrus macrolepis, Teucrium polium, and other organisms with data available. An abietane diterpenoid that is abieta-8,11,13-triene substituted by a hydroxy group at positions 12.

   

Sugiol

6-hydroxy-1,1,4a-trimethyl-7-(propan-2-yl)-1,2,3,4,4a,9,10,10a-octahydrophenanthren-9-one

C20H28O2 (300.2089188)


Sugiol is found in fruits. Sugiol is a constituent of Juniperus communis (juniper). Constituent of Juniperus communis (juniper). Sugiol is found in fruits.

   

Horminone

(4bS,10R)-3,10-dihydroxy-4b,8,8-trimethyl-2-(propan-2-yl)-1,4,4b,5,6,7,8,8a,9,10-decahydrophenanthrene-1,4-dione

C20H28O4 (332.19874880000003)


Horminone is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Horminone can be found in common sage, which makes horminone a potential biomarker for the consumption of this food product.

   

Horminone

1,4-Phenanthrenedione, 4b,5,6,7,8,8a,9,10-octahydro-3,10-dihydroxy-4b,8,8-trimethyl-2-(1-methylethyl)-, (4bS-(4balpha,8abeta,10beta))-

C20H28O4 (332.19874880000003)


Horminone is an abietane diterpenoid that is abieta-8,12-diene substituted by hydroxy groups at positions 7 and 12 and oxo groups at positions 11 and 14 (the 7alpha stereoisomer). It has a role as an antibacterial agent, an antineoplastic agent and a metabolite. It is an abietane diterpenoid, a secondary alcohol, a hydroxyquinone and a member of p-quinones. Horminone is a natural product found in Salvia tomentosa, Salvia virgata, and other organisms with data available. An abietane diterpenoid that is abieta-8,12-diene substituted by hydroxy groups at positions 7 and 12 and oxo groups at positions 11 and 14 (the 7alpha stereoisomer) .

   

Salvinolone

(4aS)-5,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4-dihydro-2H-phenanthren-9-one

C20H26O3 (314.1881846)


Salvinolone is a natural product found in Salvia bracteata, Salvia dichroantha, and other organisms with data available.

   

lupeol

Lup-20(29)-en-3.beta.-ol

C30H50O (426.386145)


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].

   

Corbisterol

Stigmasta-5,7,22E-trien-3beta-ol

C29H46O (410.3548466)


   

(4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a-tetrahydrophenanthrene-1,4-dione

(4bs,8as)-3-hydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a-tetrahydrophenanthrene-1,4-dione

C20H26O3 (314.1881846)


   

(1s,8s,10s)-5-isopropyl-4-methoxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.0¹,¹⁰.0²,⁷]hexadeca-2(7),3,5-trien-14-one

(1s,8s,10s)-5-isopropyl-4-methoxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.0¹,¹⁰.0²,⁷]hexadeca-2(7),3,5-trien-14-one

C21H28O3 (328.2038338)


   

(4br,8ar)-1-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydro-5h-phenanthrene-3,4-dione

(4br,8ar)-1-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydro-5h-phenanthrene-3,4-dione

C21H28O4 (344.19874880000003)


   

2-isopropyl-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-3-yl acetate

2-isopropyl-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-3-yl acetate

C22H30O4 (358.214398)


   

3,10-dihydroxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione

3,10-dihydroxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione

C20H26O4 (330.18309960000005)


   

(4as,9r,10as)-6-hydroxy-7-isopropyl-1,1,4a-trimethyl-5,8-dioxo-2,3,4,9,10,10a-hexahydrophenanthren-9-yl acetate

(4as,9r,10as)-6-hydroxy-7-isopropyl-1,1,4a-trimethyl-5,8-dioxo-2,3,4,9,10,10a-hexahydrophenanthren-9-yl acetate

C22H30O5 (374.209313)


   

2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol

2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol

C20H30O (286.229653)


   

3-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydro-5h-phenanthrene-1,4-dione

3-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydro-5h-phenanthrene-1,4-dione

C21H28O4 (344.19874880000003)


   

(4bs)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol

(4bs)-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-3-ol

C20H30O (286.229653)


   

(4as,10as)-7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene

(4as,10as)-7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene

C21H32O (300.24530219999997)


   

1-(5-ethyl-6-methylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol

1-(5-ethyl-6-methylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol

C29H46O (410.3548466)


   

(4bs,8as)-2-isopropyl-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-3-yl acetate

(4bs,8as)-2-isopropyl-4b,8,8-trimethyl-1,4-dioxo-5,6,7,8a,9,10-hexahydrophenanthren-3-yl acetate

C22H30O4 (358.214398)


   

5-isopropyl-4-methoxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.0¹,¹⁰.0²,⁷]hexadeca-2(7),3,5-trien-14-one

5-isopropyl-4-methoxy-11,11-dimethyl-16-oxatetracyclo[6.6.2.0¹,¹⁰.0²,⁷]hexadeca-2(7),3,5-trien-14-one

C21H28O3 (328.2038338)


   

(4as)-5,6-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4-dihydro-2h-phenanthren-9-one

(4as)-5,6-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4-dihydro-2h-phenanthren-9-one

C20H26O3 (314.1881846)


   

(4br,8ar)-3,8a-dimethoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydrophenanthrene-1,4,5-trione

(4br,8ar)-3,8a-dimethoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydrophenanthrene-1,4,5-trione

C22H28O5 (372.1936638)


   

7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene

7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthrene

C21H32O (300.24530219999997)


   

(4br,8ar)-3-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydro-5h-phenanthrene-1,4-dione

(4br,8ar)-3-hydroxy-8a-methoxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-6,7,9,10-tetrahydro-5h-phenanthrene-1,4-dione

C21H28O4 (344.19874880000003)


   

5,6-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4-dihydro-2h-phenanthren-9-one

5,6-dihydroxy-7-isopropyl-1,1,4a-trimethyl-3,4-dihydro-2h-phenanthren-9-one

C20H26O3 (314.1881846)


   

1,10-dihydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione

1,10-dihydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione

C20H28O4 (332.19874880000003)


   

3-hydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a-tetrahydrophenanthrene-1,4-dione

3-hydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a-tetrahydrophenanthrene-1,4-dione

C20H26O3 (314.1881846)


   

(4bs,8as,10s)-3,10-dihydroxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione

(4bs,8as,10s)-3,10-dihydroxy-4b,8,8-trimethyl-2-(prop-1-en-2-yl)-5,6,7,8a,9,10-hexahydrophenanthrene-1,4-dione

C20H26O4 (330.18309960000005)


   

δ7-stigmasterol

δ7-stigmasterol

C29H46O (410.3548466)


   

(4bs,8as,10r)-1,10-dihydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione

(4bs,8as,10r)-1,10-dihydroxy-2-isopropyl-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthrene-3,4-dione

C20H28O4 (332.19874880000003)