NCBI Taxonomy: 85202

Euclea natalensis (ncbi_taxid: 85202)

found 37 associated metabolites at species taxonomy rank level.

Ancestor: Euclea

Child Taxonomies: Euclea natalensis subsp. obovata, Euclea natalensis subsp. natalensis, Euclea natalensis subsp. angustifolia, Euclea natalensis subsp. rotundifolia

Juglone

InChI=1/C10H6O3/c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12/h1-5,12

C10H6O3 (174.0317)


Juglone is a hydroxy-1,4-naphthoquinone that is 1,4-naphthoquinone in which the hydrogen at position 5 has been replaced by a hydroxy group. A plant-derived 1,4-naphthoquinone with confirmed antibacterial and antitumor activities. It has a role as a herbicide, a reactive oxygen species generator and a geroprotector. Juglone is a natural product found in Talaromyces diversus, Carya alba, and other organisms with data available. Occurs in Juglans subspecies and pecan nuts (Carya illinoensis). Juglone is found in many foods, some of which are common walnut, liquor, black walnut, and nuts. Juglone is found in black walnut. Juglone occurs in Juglans species and pecan nuts (Carya illinoensis D000074385 - Food Ingredients > D005503 - Food Additives > D005520 - Food Preservatives D009676 - Noxae > D003603 - Cytotoxins D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

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 (426.3861)


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].

   

Betulin

(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-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

C30H50O2 (442.3811)


Betulin is found in black elderberry. Betulin is a constituent of Corylus avellana (filbert) and Vicia faba. Betulin (lup-20(29)-ene-3 ,28-diol) is an abundant naturally occurring triterpene. It is commonly isolated from the bark of birch trees and forms up to 30\\\\\% of the dry weight of the extractive. The purpose of the compound in the bark is not known. It can be converted to betulinic acid (the alcohol group replaced by a carboxylic acid group), which is biologically more active than betulin itself. Chemically, betulin is a triterpenoid of lupane structure. It has a pentacyclic ring structure, and hydroxyl groups in positions C3 and C28 Betulin is a pentacyclic triterpenoid that is lupane having a double bond at position 20(29) as well as 3beta-hydroxy and 28-hydroxymethyl substituents. It has a role as a metabolite, an antiviral agent, an analgesic, an anti-inflammatory agent and an antineoplastic agent. It is a pentacyclic triterpenoid and a diol. It derives from a hydride of a lupane. Betulin is a natural product found in Diospyros morrisiana, Euonymus carnosus, and other organisms with data available. A pentacyclic triterpenoid that is lupane having a double bond at position 20(29) as well as 3beta-hydroxy and 28-hydroxymethyl substituents. Constituent of Corylus avellana (filbert) and Vicia faba Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line.

   

Diospyrin

[2,2-Binaphthalene]-1,4,5,8-tetrone,1,5-dihydroxy-3,7-dimethyl-

C22H14O6 (374.079)


   

Isodiospyrin

[1,2-Binaphthalene]-5,5,8,8-tetrone, 1,4-dihydroxy-2,3-dimethyl-, (R)- (8CI); (1R)-1,4-Dihydroxy-2,3-dimethyl[1,2-binaphthalene]-5,5,8,8-tetrone; (-)-Isodiospyrin

C22H14O6 (374.079)


Isodiospyrin is a member of biphenyls. Isodiospyrin is a natural product found in Diospyros morrisiana, Diospyros verrucosa, and other organisms with data available. Isodiospyrin, a natural dimeric naphthoquinone, is a human DNA topoisomerase I (Topoisomerase) inhibitor. Isodiospyrin can prevent both DNA relaxation and kinase activities of human topoisomerase I. Isodiospyrin shows anticancer, antibacterial and antifungal activities[1][2][3]. Isodiospyrin, a natural dimeric naphthoquinone, is a human DNA topoisomerase I (Topoisomerase) inhibitor. Isodiospyrin can prevent both DNA relaxation and kinase activities of human topoisomerase I. Isodiospyrin shows anticancer, antibacterial and antifungal activities[1][2][3].

   

Ramentaceone

1,4-Naphthalenedione,5-hydroxy-7-methyl-

C11H8O3 (188.0473)


   

Neodiospyrin

8-hydroxy-2-(4-hydroxy-2-methyl-5,8-dioxo-5,8-dihydronaphthalen-1-yl)-6-methyl-1,4-dihydronaphthalene-1,4-dione

C22H14O6 (374.079)


Neodiospyrin is found in fruits. Neodiospyrin is isolated from roots of Diospyros kaki (Japanese persimmon

   

(R)-Shinanolone

4,8-dihydroxy-6-methyl-1,2,3,4-tetrahydronaphthalen-1-one

C11H12O3 (192.0786)


(R)-Shinanolone is found in fruits. (R)-Shinanolone is isolated from Diospyros kaki (Japanese persimmon

   

lupeol

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

C30H50O (426.3861)


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].

   

Neodiospyrin

8-hydroxy-5-(8-hydroxy-6-methyl-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-6-methyl-1,4-dihydronaphthalene-1,4-dione

C22H14O6 (374.079)


   

Betulin

NCGC00168803-04_C30H50O2_Lup-20(29)-ene-3,28-diol, (3beta)-

C30H50O2 (442.3811)


Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line. Betulin (Trochol), is a sterol regulatory element-binding protein (SREBP) inhibitor with an IC50 of 14.5 μM in K562 cell line.

   

(R)-Shinanolone

4,8-dihydroxy-6-methyl-1,2,3,4-tetrahydronaphthalen-1-one

C11H12O3 (192.0786)


   

Nucin

InChI=1\C10H6O3\c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12\h1-5,12

C10H6O3 (174.0317)


D000074385 - Food Ingredients > D005503 - Food Additives > D005520 - Food Preservatives D009676 - Noxae > D003603 - Cytotoxins D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors

   

(1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20s)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl acetate

(1s,4s,5r,8r,10s,13s,14r,17s,18r,19s,20s)-4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl acetate

C32H48O4 (496.3552)


   
   

(1r,2r,5'r)-1,1',5',8-tetrahydroxy-3',6-dimethyl-2,3,6',7'-tetrahydro-1h,5'h-[2,2'-binaphthalene]-4,8'-dione

(1r,2r,5'r)-1,1',5',8-tetrahydroxy-3',6-dimethyl-2,3,6',7'-tetrahydro-1h,5'h-[2,2'-binaphthalene]-4,8'-dione

C22H22O6 (382.1416)


   

(1s,4s,5r,8s,10s,13s,14r,17s,18r,19s,20s)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-23-one

(1s,4s,5r,8s,10s,13s,14r,17s,18r,19s,20s)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-23-one

C30H46O3 (454.3447)


   

8,12,17-trihydroxy-6,15-dimethylpentacyclo[10.7.1.0²,¹¹.0⁴,⁹.0¹³,¹⁸]icosa-2(11),4,6,8,13,15,17-heptaene-3,10,19-trione

8,12,17-trihydroxy-6,15-dimethylpentacyclo[10.7.1.0²,¹¹.0⁴,⁹.0¹³,¹⁸]icosa-2(11),4,6,8,13,15,17-heptaene-3,10,19-trione

C22H16O6 (376.0947)


   

3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-ol

3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-ol

C30H50O2 (442.3811)


   

4,5'-dihydroxy-2,7'-dimethyl-[1,2'-binaphthalene]-1',4',5,8-tetrone

4,5'-dihydroxy-2,7'-dimethyl-[1,2'-binaphthalene]-1',4',5,8-tetrone

C22H14O6 (374.079)


   

(1r,3ar,3br,7s,9ar,9br,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol

(1r,3ar,3br,7s,9ar,9br,11ar)-1-[(2r,5r)-5-ethyl-6-methylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-ol

C29H50O (414.3861)


   

4,8'-dihydroxy-2,6'-dimethyl-[1,2'-binaphthalene]-1',4',5,8-tetrone

4,8'-dihydroxy-2,6'-dimethyl-[1,2'-binaphthalene]-1',4',5,8-tetrone

C22H14O6 (374.079)


   

(4r,4'r)-8,8'-dihydroxy-4,4'-dimethoxy-6,6'-dimethyl-4h,4'h-[2,2'-binaphthalene]-1,1'-dione

(4r,4'r)-8,8'-dihydroxy-4,4'-dimethoxy-6,6'-dimethyl-4h,4'h-[2,2'-binaphthalene]-1,1'-dione

C24H22O6 (406.1416)


   

(1r,3ar,5ar,5br,7ar,9s,11as,11br,13ar,13bs)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl (2e)-3-(4-methoxy-3-methylphenyl)prop-2-enoate

(1r,3ar,5ar,5br,7ar,9s,11as,11br,13ar,13bs)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl (2e)-3-(4-methoxy-3-methylphenyl)prop-2-enoate

C41H60O3 (600.4542)


   

10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-23-one

10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-23-one

C30H46O3 (454.3447)


   

(1s,2r)-1,1',5',8-tetrahydroxy-3',6-dimethyl-2,3,6',7'-tetrahydro-1h,5'h-[2,2'-binaphthalene]-4,8'-dione

(1s,2r)-1,1',5',8-tetrahydroxy-3',6-dimethyl-2,3,6',7'-tetrahydro-1h,5'h-[2,2'-binaphthalene]-4,8'-dione

C22H22O6 (382.1416)


   

5,8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,1',4,4'-tetrone

5,8,8'-trihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,1',4,4'-tetrone

C22H14O7 (390.0739)


   

8,8'-dihydroxy-4,4'-dimethoxy-6,6'-dimethyl-4h,4'h-[2,2'-binaphthalene]-1,1'-dione

8,8'-dihydroxy-4,4'-dimethoxy-6,6'-dimethyl-4h,4'h-[2,2'-binaphthalene]-1,1'-dione

C24H22O6 (406.1416)


   

(1s,12r)-8,12,17-trihydroxy-6,15-dimethylpentacyclo[10.7.1.0²,¹¹.0⁴,⁹.0¹³,¹⁸]icosa-2(11),4,6,8,13,15,17-heptaene-3,10,19-trione

(1s,12r)-8,12,17-trihydroxy-6,15-dimethylpentacyclo[10.7.1.0²,¹¹.0⁴,⁹.0¹³,¹⁸]icosa-2(11),4,6,8,13,15,17-heptaene-3,10,19-trione

C22H16O6 (376.0947)


   

(3ar,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl (2e)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate

(3ar,5ar,5br,7ar,9s,11ar,11br,13ar,13br)-3a,5a,5b,8,8,11a-hexamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysen-9-yl (2e)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate

C40H58O4 (602.4335)


   

4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl acetate

4,5,9,9,13,19,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracos-15-en-10-yl acetate

C32H48O4 (496.3552)


   

stigmast-5-en-3-ol, (3β)-

stigmast-5-en-3-ol, (3β)-

C29H50O (414.3861)


   

1',4-dihydroxy-7'-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-2,3'-dimethyl-[1,2'-binaphthalene]-5,5',8,8'-tetrone

1',4-dihydroxy-7'-(8-hydroxy-6-methyl-1,4-dioxonaphthalen-2-yl)-2,3'-dimethyl-[1,2'-binaphthalene]-5,5',8,8'-tetrone

C33H20O9 (560.1107)


   

(4r)-4,8-dihydroxy-6-methyl-3,4-dihydro-2h-naphthalen-1-one

(4r)-4,8-dihydroxy-6-methyl-3,4-dihydro-2h-naphthalen-1-one

C11H12O3 (192.0786)


   

5-hydroxy-7-methyl-2,3-dihydronaphthalene-1,4-dione

5-hydroxy-7-methyl-2,3-dihydronaphthalene-1,4-dione

C11H10O3 (190.063)


   

(1s,2r,5's)-1,1',5',8-tetrahydroxy-3',6-dimethyl-2,3,6',7'-tetrahydro-1h,5'h-[2,2'-binaphthalene]-4,8'-dione

(1s,2r,5's)-1,1',5',8-tetrahydroxy-3',6-dimethyl-2,3,6',7'-tetrahydro-1h,5'h-[2,2'-binaphthalene]-4,8'-dione

C22H22O6 (382.1416)


   

8,8'-dihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,1',4,4'-tetrone

8,8'-dihydroxy-6,6'-dimethyl-[2,2'-binaphthalene]-1,1',4,4'-tetrone

C22H14O6 (374.079)