NCBI Taxonomy: 482952

Teclea (ncbi_taxid: 482952)

found 49 associated metabolites at genus taxonomy rank level.

Ancestor: Rutaceae incertae sedis

Child Taxonomies: Teclea pilosa, Teclea gerrardii, Teclea natalensis, Teclea hanangensis, Teclea trichocarpa, Teclea simplicifolia

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].

   

Skimmianine

4,7,8-trimethoxy-furo(2,3-b)quinoline

C14H13NO4 (259.0845)


Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   

Dictamnine

4-methoxyfuro(2,3-b)quinoline

C12H9NO2 (199.0633)


Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities. Dictamnine (Dictamine) exhibits cytotoxicity to human cervical and colon cancer cells and also has antibacterial and antifungal activities.

   

EVOXINE

2,3-Butanediol, 1-((4,8-dimethoxyfuro(2,3-b)quinolin-7-yl)oxy)-3-methyl-, (+)-

C18H21NO6 (347.1369)


   

Arborinine

9(10H)-Acridinone, 1-hydroxy-2,3-dimethoxy-10-methyl- (9ci)

C16H15NO4 (285.1001)


Arborinine is found in herbs and spices. Arborinine is an alkaloid from Ruta graveolens (rue

   

Flindersiamine

8-Methoxy-6,7-methylenedioxydictamnine

C14H11NO5 (273.0637)


   
   

1,3-dihydroxy-N-methylacridone

1,3-dihydroxy-10-methyl-9,10-dihydroacridin-9-one

C14H11NO3 (241.0739)


1,3-dihydroxy-n-methylacridone is a member of the class of compounds known as acridones. Acridones are acridines containing a ketone group attached to the C9 carbon atom of the acridine moiety. 1,3-dihydroxy-n-methylacridone is slightly soluble (in water) and a very weakly acidic compound (based on its pKa). 1,3-dihydroxy-n-methylacridone can be found in a number of food items such as canada blueberry, italian oregano, cashew nut, and pepper (c. annuum), which makes 1,3-dihydroxy-n-methylacridone a potential biomarker for the consumption of these food products.

   

Skimmianine

InChI=1/C14H13NO4/c1-16-10-5-4-8-11(13(10)18-3)15-14-9(6-7-19-14)12(8)17-2/h4-7H,1-3H

C14H13NO4 (259.0845)


Skimmianine is an organonitrogen heterocyclic compound, an organic heterotricyclic compound, an oxacycle and an alkaloid antibiotic. Skimmianine is a natural product found in Haplophyllum bucharicum, Haplophyllum cappadocicum, and other organisms with data available. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   

(S)-Edulinine

3-(2,3-dihydroxy-3-methylbutyl)-4-methoxy-1-methyl-1,2-dihydroquinolin-2-one

C16H21NO4 (291.1471)


(S)-Edulinine is found in pomes. (S)-Edulinine is an alkaloid from the bark of Casimiroa edulis (Mexican apple

   
   

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].

   
   

Skimmianine

Skimmianine

C14H13NO4 (259.0845)


Origin: Plant; SubCategory_DNP: Alkaloids derived from anthranilic acid, Quinoline alkaloids relative retention time with respect to 9-anthracene Carboxylic Acid is 1.053 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.048 Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   
   
   

edulinine

3-(2,3-dihydroxy-3-methylbutyl)-4-methoxy-1-methyl-1,2-dihydroquinolin-2-one

C16H21NO4 (291.1471)


   

Skimmianin

InChI=1\C14H13NO4\c1-16-10-5-4-8-11(13(10)18-3)15-14-9(6-7-19-14)12(8)17-2\h4-7H,1-3H

C14H13NO4 (259.0845)


Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1]. Skimmianine is a furoquinoline alkaloid present mainly in the Rutaceae family, with antispastic, anti-inflammatory activities and antiplatelet aggregation effect. Skimmianine exhibits cytotoxicity against a variety of cancer cell lines and genotoxicity[1].

   

1,3-dihydroxy-N-methylacridone

1,3-dihydroxy-N-methylacridone

C14H11NO3 (241.0739)


   

4,7-dimethoxyfuro[2,3-b]quinolin-8-ol

4,7-dimethoxyfuro[2,3-b]quinolin-8-ol

C13H11NO4 (245.0688)


   

(1r,2r,5s,6r,10r,13s,16s)-6-(furan-3-yl)-5,10,14,14-tetramethyl-15,19-dioxapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁵,⁹]icos-8-ene-11,18-dione

(1r,2r,5s,6r,10r,13s,16s)-6-(furan-3-yl)-5,10,14,14-tetramethyl-15,19-dioxapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁵,⁹]icos-8-ene-11,18-dione

C26H32O5 (424.225)


   

3-[(2r)-2,3-dihydroxy-3-methylbutyl]-4-methoxy-1-methylquinolin-2-one

3-[(2r)-2,3-dihydroxy-3-methylbutyl]-4-methoxy-1-methylquinolin-2-one

C16H21NO4 (291.1471)


   

11-methoxy-5-methyl-2h-[1,3]dioxolo[4,5-b]acridin-10-one

11-methoxy-5-methyl-2h-[1,3]dioxolo[4,5-b]acridin-10-one

C16H13NO4 (283.0845)


   

3-hydroxy-1-methoxy-10-methylacridin-9-one

3-hydroxy-1-methoxy-10-methylacridin-9-one

C15H13NO3 (255.0895)


   

15-(furan-3-yl)-10-hydroxy-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadeca-3,12-dien-5-one

15-(furan-3-yl)-10-hydroxy-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadeca-3,12-dien-5-one

C26H34O4 (410.2457)


   

1,3-dimethoxy-10-methylacridin-9-one

1,3-dimethoxy-10-methylacridin-9-one

C16H15NO3 (269.1052)


   

(1r,3br,4r,5ar,9ar,9br,11as)-1-(furan-3-yl)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

(1r,3br,4r,5ar,9ar,9br,11as)-1-(furan-3-yl)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

C26H34O3 (394.2508)


   

1-(furan-3-yl)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

1-(furan-3-yl)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

C26H34O3 (394.2508)


   

(1r,3br,4r,5as,9ar,9br,11as)-1-(furan-3-yl)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

(1r,3br,4r,5as,9ar,9br,11as)-1-(furan-3-yl)-4-hydroxy-3b,6,6,9a,11a-pentamethyl-1h,2h,4h,5h,5ah,9bh,10h,11h-cyclopenta[a]phenanthren-7-one

C26H34O3 (394.2508)


   

n-methyl-2-(2,4,6-trimethoxybenzoyl)aniline

n-methyl-2-(2,4,6-trimethoxybenzoyl)aniline

C17H19NO4 (301.1314)


   

4,7-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

4,7-dimethoxy-8-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

C18H19NO4 (313.1314)


   

1-hydroxy-2,3,4-trimethoxy-10-methylacridin-9-one

1-hydroxy-2,3,4-trimethoxy-10-methylacridin-9-one

C17H17NO5 (315.1107)


   

(2s)-1-({4,8-dimethoxyfuro[2,3-b]quinolin-7-yl}oxy)-3-methylbutane-2,3-diol

(2s)-1-({4,8-dimethoxyfuro[2,3-b]quinolin-7-yl}oxy)-3-methylbutane-2,3-diol

C18H21NO6 (347.1369)


   

2-(2-hydroxypropan-2-yl)-9-methyl-2h,3h-furo[2,3-b]quinolin-4-one

2-(2-hydroxypropan-2-yl)-9-methyl-2h,3h-furo[2,3-b]quinolin-4-one

C15H17NO3 (259.1208)


   

3-hydroxy-10-methyl-1-[(3-methylbut-2-en-1-yl)oxy]acridin-9-one

3-hydroxy-10-methyl-1-[(3-methylbut-2-en-1-yl)oxy]acridin-9-one

C19H19NO3 (309.1365)


   

(1r,2r,5s,10r,13r,16s)-6-(furan-3-yl)-5,10,14,14-tetramethyl-15,19-dioxapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁵,⁹]icos-8-ene-11,18-dione

(1r,2r,5s,10r,13r,16s)-6-(furan-3-yl)-5,10,14,14-tetramethyl-15,19-dioxapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁵,⁹]icos-8-ene-11,18-dione

C26H32O5 (424.225)


   

(1r,2r,8s,10r,11r,15r,16s)-15-(furan-3-yl)-10-hydroxy-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadeca-3,12-dien-5-one

(1r,2r,8s,10r,11r,15r,16s)-15-(furan-3-yl)-10-hydroxy-2,7,7,11,16-pentamethyl-6-oxatetracyclo[9.7.0.0²,⁸.0¹²,¹⁶]octadeca-3,12-dien-5-one

C26H34O4 (410.2457)


   

(2s)-2-(2-hydroxypropan-2-yl)-9-methyl-2h,3h-furo[2,3-b]quinolin-4-one

(2s)-2-(2-hydroxypropan-2-yl)-9-methyl-2h,3h-furo[2,3-b]quinolin-4-one

C15H17NO3 (259.1208)


   

6-{[(2r)-3,3-dimethyloxiran-2-yl]methoxy}-4,7-dimethoxyfuro[2,3-b]quinoline

6-{[(2r)-3,3-dimethyloxiran-2-yl]methoxy}-4,7-dimethoxyfuro[2,3-b]quinoline

C18H19NO5 (329.1263)


   

4,7-dimethoxy-6-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

4,7-dimethoxy-6-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

C18H19NO4 (313.1314)


   

6-[(3,3-dimethyloxiran-2-yl)methoxy]-4,7-dimethoxyfuro[2,3-b]quinoline

6-[(3,3-dimethyloxiran-2-yl)methoxy]-4,7-dimethoxyfuro[2,3-b]quinoline

C18H19NO5 (329.1263)


   

6-(furan-3-yl)-5,10,14,14-tetramethyl-15,19-dioxapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁵,⁹]icos-8-ene-11,18-dione

6-(furan-3-yl)-5,10,14,14-tetramethyl-15,19-dioxapentacyclo[11.7.0.0¹,¹⁶.0²,¹⁰.0⁵,⁹]icos-8-ene-11,18-dione

C26H32O5 (424.225)


   

4,8-dimethoxy-7-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

4,8-dimethoxy-7-[(3-methylbut-2-en-1-yl)oxy]furo[2,3-b]quinoline

C18H19NO4 (313.1314)


   

(3s)-3-hydroxy-2,2,10-trimethyl-3h,4h-pyrano[2,3-b]quinolin-5-one

(3s)-3-hydroxy-2,2,10-trimethyl-3h,4h-pyrano[2,3-b]quinolin-5-one

C15H17NO3 (259.1208)


   

(3r)-3-hydroxy-2,2,10-trimethyl-3h,4h-pyrano[2,3-b]quinolin-5-one

(3r)-3-hydroxy-2,2,10-trimethyl-3h,4h-pyrano[2,3-b]quinolin-5-one

C15H17NO3 (259.1208)


   

6,11-dimethoxy-5-methyl-2h-[1,3]dioxolo[4,5-b]acridin-10-one

6,11-dimethoxy-5-methyl-2h-[1,3]dioxolo[4,5-b]acridin-10-one

C17H15NO5 (313.095)


   

(2s)-1-({4,7-dimethoxyfuro[2,3-b]quinolin-6-yl}oxy)-3-methylbutane-2,3-diol

(2s)-1-({4,7-dimethoxyfuro[2,3-b]quinolin-6-yl}oxy)-3-methylbutane-2,3-diol

C18H21NO6 (347.1369)


   

3-hydroxy-2,2,10-trimethyl-3h,4h-pyrano[2,3-b]quinolin-5-one

3-hydroxy-2,2,10-trimethyl-3h,4h-pyrano[2,3-b]quinolin-5-one

C15H17NO3 (259.1208)


   

6,7,11-trimethoxy-5-methyl-2h-[1,3]dioxolo[4,5-b]acridin-10-one

6,7,11-trimethoxy-5-methyl-2h-[1,3]dioxolo[4,5-b]acridin-10-one

C18H17NO6 (343.1056)