NCBI Taxonomy: 132437

Deguelia hatschbachii (ncbi_taxid: 132437)

found 55 associated metabolites at species taxonomy rank level.

Ancestor: Deguelia

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].

   

Osajin

4H,8H-Benzo(1,2-b:3,4-b)dipyran-4-one, 5-hydroxy-3-(p-hydroxyphenyl)-8,8-dimethyl-6-(3-methyl-2-butenyl)- (8CI)

C25H24O5 (404.1623654)


Osajin is a member of isoflavanones. Osajin is a natural product found in Deguelia hatschbachii, Euchresta japonica, and other organisms with data available. Origin: Plant, Pyrans Osajin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=482-53-1 (retrieved 2024-08-14) (CAS RN: 482-53-1). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

lupinifolin

(S) -7,8-Dihydro-5-hydroxy-8- (4-hydroxyphenyl) -2,2-dimethyl-10- (3-methyl-2-butenyl) -2H,6H-benzo [ 1,2-b:5,4-b ] dipyran-6-one

C25H26O5 (406.17801460000004)


   

Robustic acid

4-Hydroxy-5-methoxy-3- (4-methoxyphenyl) -8,8-dimethyl-2H,8H-benzo [ 1,2-b:5,4-b ] dipyran-2-one

C22H20O6 (380.125982)


   

Methyl robustate

Robustic acid methyl ether

C23H22O6 (394.1416312)


   

Scandenin

4-Hydroxy-3- (4-hydroxyphenyl) -5-methoxy-8,8-dimethyl-6- (3-methyl-2-butenyl) -2H,8H-benzo [ 1,2-b:3,4-b ] dipyran-2-one

C26H26O6 (434.17292960000003)


   

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].

   

6-[(4-Hydroxyphenyl)acetyl]-7-methoxy-2,2-dimethyl-8-(3-methyl-2-butenyl)-2H-1-benzopyran-5-ol

6-[(4-Hydroxyphenyl)acetyl]-7-methoxy-2,2-dimethyl-8-(3-methyl-2-butenyl)-2H-1-benzopyran-5-ol

C25H28O5 (408.1936638)


   
   

(2s)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

(2s)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C21H22O5 (354.1467162)


   

3a,5a,5b,8,8,11a,13b-heptamethyl-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-9-ol

3a,5a,5b,8,8,11a,13b-heptamethyl-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-9-ol

C31H52O (440.4017942)


   

(3s)-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-3-(2-oxopropyl)pyrano[2,3-f]chromene-2,4-dione

(3s)-3-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-6-(3-methylbut-2-en-1-yl)-3-(2-oxopropyl)pyrano[2,3-f]chromene-2,4-dione

C29H30O7 (490.199143)


   

(2s)-1-[5-hydroxy-7-methoxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-6-yl]-2-(4-hydroxyphenyl)pentane-1,4-dione

(2s)-1-[5-hydroxy-7-methoxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-6-yl]-2-(4-hydroxyphenyl)pentane-1,4-dione

C28H32O6 (464.2198772)


   

4-[(1e)-2-[3,5-dimethoxy-4-(3-methylbut-2-en-1-yl)phenyl]ethenyl]phenol

4-[(1e)-2-[3,5-dimethoxy-4-(3-methylbut-2-en-1-yl)phenyl]ethenyl]phenol

C21H24O3 (324.1725354)


   

(2s)-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one

(2s)-5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-10-(3-methylbut-2-en-1-yl)-2h,3h-pyrano[3,2-g]chromen-4-one

C25H26O5 (406.17801460000004)


   

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C21H22O5 (354.1467162)


   

(1s,3ar,5ar,5br,7ar,9s,11ar,11br,13as,13br)-3a,5a,5b,8,8,11a,13b-heptamethyl-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-9-ol

(1s,3ar,5ar,5br,7ar,9s,11ar,11br,13as,13br)-3a,5a,5b,8,8,11a,13b-heptamethyl-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-9-ol

C31H52O (440.4017942)


   

4-{2-[3,5-dimethoxy-4-(3-methylbut-2-en-1-yl)phenyl]ethenyl}phenol

4-{2-[3,5-dimethoxy-4-(3-methylbut-2-en-1-yl)phenyl]ethenyl}phenol

C21H24O3 (324.1725354)


   

1-[5-hydroxy-7-methoxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-6-yl]-2-(4-hydroxyphenyl)ethanone

1-[5-hydroxy-7-methoxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-6-yl]-2-(4-hydroxyphenyl)ethanone

C25H28O5 (408.1936638)


   

2-hydroxy-5-methoxy-3-(4-methoxyphenyl)-8,8-dimethylpyrano[3,2-g]chromen-4-one

2-hydroxy-5-methoxy-3-(4-methoxyphenyl)-8,8-dimethylpyrano[3,2-g]chromen-4-one

C22H20O6 (380.125982)


   

4-[(1e)-2-[5-methoxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-7-yl]ethenyl]phenol

4-[(1e)-2-[5-methoxy-2,2-dimethyl-8-(3-methylbut-2-en-1-yl)chromen-7-yl]ethenyl]phenol

C25H28O3 (376.2038338)


   

(2r)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

(2r)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)-2,3-dihydro-1-benzopyran-4-one

C21H22O5 (354.1467162)