NCBI Taxonomy: 39380

Swertia petiolata (ncbi_taxid: 39380)

found 21 associated metabolites at species taxonomy rank level.

Ancestor: Swertia

Child Taxonomies: none taxonomy data.

Ursolic acid

(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid

C30H48O3 (456.3603)


Ursolic acid is a ubiquitous triterpenoid in plant kingdom, medicinal herbs, and is an integral part of the human diet. During the last decade over 700 research articles have been published on triterpenoids research, reflecting tremendous interest and progress in our understanding of these compounds. This included the isolation and purification of these tritepernoids from various plants and herbs, the chemical modifications to make more effective and water soluble derivatives, the pharmacological research on their beneficial effects, the toxicity studies, and the clinical use of these triterpenoids in various diseases including anticancer chemotherapies. Ursolic acid (UA), a pentacyclic triterpene acid, has been isolated from many kinds of medicinal plants, such as Eriobotrya japonica, Rosmarinns officinalis, Melaleuca leucadendron, Ocimum sanctum and Glechoma hederaceae. UA has been reported to produce antitumor activities and antioxidant activity, and is reported to have an antioxidant activity. UA may play an important role in regulating the apoptosis induced by high glucose presumably through scavenging of ROS (reactive oxygen species). It has been found recently that ursolic acid treatment affects growth and apoptosis in cancer cells. (PMID: 15994040, 17516235, 17213663). Ursolic acid is a pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by a beta-hydroxy group at position 3. It has a role as a plant metabolite and a geroprotector. It is a pentacyclic triterpenoid and a hydroxy monocarboxylic acid. It derives from a hydride of an ursane. Ursolic acid is a natural product found in Gladiolus italicus, Freziera, and other organisms with data available. Ursolic Acid is a pentacyclic triterpenoid found in various fruits, vegetables and medicinal herbs, with a variety of potential pharmacologic activities including anti-inflammatory, antioxidative, antiviral, serum lipid-lowering, and antineoplastic activities. Upon administration, ursolic acid may promote apoptosis and inhibit cancer cell proliferation through multiple mechanisms. This may include the regulation of mitochondrial function through various pathways including the ROCK/PTEN and p53 pathways, the suppression of the nuclear factor-kappa B (NF-kB) pathways, and the increase in caspase-3, caspase-8 and caspase-9 activities. See also: Holy basil leaf (part of); Jujube fruit (part of); Lagerstroemia speciosa leaf (part of). D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors A pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by a beta-hydroxy group at position 3. C274 - Antineoplastic Agent > C129839 - Apoptotic Pathway-targeting Antineoplastic Agent Found in wax of apples, pears and other fruits. V. widely distributed in plants D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics C26170 - Protective Agent > C275 - Antioxidant D000893 - Anti-Inflammatory Agents D000890 - Anti-Infective Agents D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors 3-Epiursolic Acid is a triterpenoid that can be isolated from Eriobotrya japonica, acts as a competitive inhibitor of cathepsin L (IC50, 6.5 μM; Ki, 19.5 μM), with no obvious effect on cathepsin B[1]. 3-Epiursolic Acid is a triterpenoid that can be isolated from Eriobotrya japonica, acts as a competitive inhibitor of cathepsin L (IC50, 6.5 μM; Ki, 19.5 μM), with no obvious effect on cathepsin B[1]. Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy.

   

Gentisin

1,7-dihydroxy-3-methoxy-9H-xanthen-9-one

C14H10O5 (258.0528)


Gentisin is found in alcoholic beverages. Gentisin is a pigment from root of Gentiana lutea (yellow gentian

   

Isogentisin

9H-Xanthen-9-one, 1,3-dihydroxy-7-methoxy- (9ci)

C14H10O5 (258.0528)


Isogentisin is found in alcoholic beverages. Isogentisin is isolated from roots of Gentiana lutea (yellow gentian

   

Swerchirin

1,8-dihydroxy-3,5-dimethoxy-9H-xanthen-9-one

C15H12O6 (288.0634)


   

Gentisin

1,7-Dihydroxy-3-methoxyxanthone; 1,7-Dihydroxy-3-methoxyxanthen-9-one

C14H10O5 (258.0528)


Gentisin is a member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 7 and a methoxy group at position 3. It has a role as a plant metabolite. It is a member of xanthones, a polyphenol and an aromatic ether. Gentisin is a natural product found in Pterocarpus santalinus, Gentiana orbicularis, and other organisms with data available. See also: Menyanthes trifoliata leaf (part of). A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 7 and a methoxy group at position 3. Gentisin is found in alcoholic beverages. Gentisin is a pigment from root of Gentiana lutea (yellow gentian

   

Ursolic Acid

3-Hydroxy-12-ursen-28-oic acid

C30H48O3 (456.3603)


Origin: Plant; SubCategory_DNP: Triterpenoids relative retention time with respect to 9-anthracene Carboxylic Acid is 1.636 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.640 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.638 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.642 Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy.

   

Isogentisin

1,3-Dihydroxy-7-methoxyxanthone

C14H10O5 (258.0528)


A member of the class of xanthones that is 9H-xanthen-9-one substituted by hydroxy groups at positions 1 and 3 and a methoxy group at position 7.

   

Urson

(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid

C30H48O3 (456.3603)


D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors C274 - Antineoplastic Agent > C129839 - Apoptotic Pathway-targeting Antineoplastic Agent D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics C26170 - Protective Agent > C275 - Antioxidant D000893 - Anti-Inflammatory Agents D000890 - Anti-Infective Agents D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy.

   

Gentisin

5-18-04-00497 (Beilstein Handbook Reference)

C14H10O5 (258.0528)


   

Swerchirin

9H-Xanthen-9-one, 1,8-dihydroxy-3,5-dimethoxy- (9CI)

C15H12O6 (288.0634)


A member of the class of xanthones that is the 5-O-methyl derivative of bellidifolin. Isolated from Centaurium erythraea and Swertia chirayita, it exhibits hypoglycemic activity.

   

(1s,3ar,5as,5br,7ar,9s,11ar,11br)-1-isopropyl-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-cyclopenta[a]chrysen-9-ol

(1s,3ar,5as,5br,7ar,9s,11ar,11br)-1-isopropyl-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-cyclopenta[a]chrysen-9-ol

C30H50O (426.3861)


   

(1s,3as,5as,5br,7ar,9s,11ar,11br,13br)-9-hydroxy-1-isopropyl-5a,5b,8,8,11a-pentamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysene-3a-carboxylic acid

(1s,3as,5as,5br,7ar,9s,11ar,11br,13br)-9-hydroxy-1-isopropyl-5a,5b,8,8,11a-pentamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysene-3a-carboxylic acid

C30H48O3 (456.3603)


   

2-hydroxy-3,5-dimethylbenzene-1,4-dicarboxylic acid

2-hydroxy-3,5-dimethylbenzene-1,4-dicarboxylic acid

C10H10O5 (210.0528)


   

(1s,2r,3s,6s,7r,10r,14r,15r,18r,20s)-10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-11-en-22-one

(1s,2r,3s,6s,7r,10r,14r,15r,18r,20s)-10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-11-en-22-one

C30H46O3 (454.3447)


   

10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-10-en-22-one

10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-10-en-22-one

C30H46O3 (454.3447)


   

10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-11-en-22-one

10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-11-en-22-one

C30H46O3 (454.3447)


   

3-hydroxy-5,8-dimethoxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}xanthen-9-one

3-hydroxy-5,8-dimethoxy-1-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}xanthen-9-one

C21H22O11 (450.1162)


   

1-isopropyl-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-cyclopenta[a]chrysen-9-ol

1-isopropyl-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-cyclopenta[a]chrysen-9-ol

C30H50O (426.3861)


   

3-hydroxy-5,8-dimethoxy-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}xanthen-9-one

3-hydroxy-5,8-dimethoxy-1-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}xanthen-9-one

C21H22O11 (450.1162)


   

(1s,2r,3s,6s,7r,14r,15r,18r,20s)-10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-10-en-22-one

(1s,2r,3s,6s,7r,14r,15r,18r,20s)-10-isopropyl-2,7,14,15,19,19-hexamethyl-21,23-dioxahexacyclo[18.2.1.0²,¹⁸.0³,¹⁵.0⁶,¹⁴.0⁷,¹¹]tricos-10-en-22-one

C30H46O3 (454.3447)


   

9-hydroxy-1-isopropyl-5a,5b,8,8,11a-pentamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysene-3a-carboxylic acid

9-hydroxy-1-isopropyl-5a,5b,8,8,11a-pentamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysene-3a-carboxylic acid

C30H48O3 (456.3603)