Exact Mass: 488.3290274
Exact Mass Matches: 488.3290274
Found 500 metabolites which its exact mass value is equals to given mass value 488.3290274,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Esculentic acid (Diplazium)
Asiatic acid is a pentacyclic triterpenoid that is ursane substituted by a carboxy group at position 28 and hydroxy groups at positions 2, 3 and 23 (the 2alpha,3beta stereoisomer). It is isolated from Symplocos lancifolia and Vateria indica and exhibits anti-angiogenic activity. It has a role as an angiogenesis modulating agent and a metabolite. It is a monocarboxylic acid, a triol and a pentacyclic triterpenoid. It derives from a hydride of an ursane. From Centella asiatica and other plants; shows a variety of bioactivities. Asiatic acid is a natural product found in Psidium guajava, Combretum fruticosum, and other organisms with data available. See also: Holy basil leaf (part of); Lagerstroemia speciosa leaf (part of); Centella asiatica flowering top (part of). Esculentic acid (Diplazium) is found in green vegetables. Esculentic acid (Diplazium) is a constituent of the edible fern Diplazium esculentum C1907 - Drug, Natural Product > C28269 - Phytochemical > C1905 - Triterpenoid Compound C274 - Antineoplastic Agent > C1931 - Antineoplastic Plant Product Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2]. Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2].
Euscaphic acid
Euscaphic acid is a pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 19 respectively (the 2alpha,3alpha-stereoisomer). It has been isolated from the leaves of Rosa laevigata. It has a role as a plant metabolite. It is a pentacyclic triterpenoid, a hydroxy monocarboxylic acid and a triol. It derives from a hydride of an ursane. Euscaphic acid is a natural product found in Ternstroemia gymnanthera, Rhaphiolepis deflexa, and other organisms with data available. A pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 19 respectively (the 2alpha,3alpha-stereoisomer). It has been isolated from the leaves of Rosa laevigata. Euscaphic acid is found in herbs and spices. Euscaphic acid is a constituent of Coleus amboinicus (Cuban oregano). Constituent of Coleus amboinicus (Cuban oregano). Euscaphic acid is found in loquat and herbs and spices. Euscaphic acid, a DNA polymerase inhibitor, is a triterpene from the root of the R. alceaefolius Poir. Euscaphic inhibits calf DNA polymerase α (pol α) and rat DNA polymerase β (pol β) with IC50 values of 61 and 108 μM[1]. Euscaphic acid induces apoptosis[2]. Euscaphic acid, a DNA polymerase inhibitor, is a triterpene from the root of the R. alceaefolius Poir. Euscaphic inhibits calf DNA polymerase α (pol α) and rat DNA polymerase β (pol β) with IC50 values of 61 and 108 μM[1]. Euscaphic acid induces apoptosis[2].
Cimigenol
Cimigenol is a triterpenoid. It derives from a hydride of a cycloartane. Cimigenol is a natural product found in Actaea pachypoda, Actaea dahurica, and other organisms with data available. See also: Black Cohosh (part of).
(3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid
(3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid is found in fruits. (3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid is isolated from leaves of Eriobotrya japonica (loquat).
Arjunolic acid
Arjunolic acid is found in fruits. Arjunolic acid is a constituent of Psidium guajava (guava) Constituent of Psidium guajava (guava). Arjunolic acid is found in fruits and guava.
16beta-Hydroxystellatogenin
16beta-Hydroxystellatogenin is found in fruits. 16beta-Hydroxystellatogenin is a constituent of Stenocereus stellatus (pitaya).
Pitheduloside I
Pitheduloside J is found in fruits. Pitheduloside J is a constituent of Pithecellobium dulce (manila tamarind). Constituent of Pithecellobium dulce (manila tamarino). Pitheduloside I is found in fruits.
Ananasic acid
Ananasic acid is a trihydroxytriterpenecarboxylic acid. Ananasic acid has been isolated from Ananas comosus (pineapple) stems. Constituent of pineapple stems
Glyyunnansapogenin B
Glyyunnansapogenin B is found in herbs and spices. Glyyunnansapogenin B is a constituent of roots of Glycyrrhiza glabra (licorice). Constituent of roots of Glycyrrhiza glabra (licorice). Glyyunnansapogenin B is found in tea and herbs and spices.
Camelliagenin B
Sapogenin from seeds of Camellia japonica and from Camellia sasanqua. Camelliagenin B is found in tea and fats and oils. Camelliagenin B is found in fats and oils. Sapogenin from seeds of Camellia japonica and from Camellia sasanqu
Ganoderiol D
Ganoderiol D is found in mushrooms. Ganoderiol D is a metabolite of Ganoderma lucidum (reishi). Metabolite of Ganoderma lucidum (reishi). Ganoderiol D is found in mushrooms.
Centellasapogenol A
Centellasapogenol A is found in green vegetables. Centellasapogenol A is a constituent of Centella asiatica (Asiatic pennywort) Constituent of Centella asiatica (Asiatic pennywort). Centellasapogenol A is found in green vegetables.
Hovenolactone
Sapogenin from Hovenia dulcis (raisin tree) Sapogenin from Hovenia dulcis (raisin tree
21beta-Hydroxyhederagenin
21beta-Hydroxyhederagenin is found in fruits. 21beta-Hydroxyhederagenin is a constituent of Luffa cylindrica (smooth luffa). Constituent of Luffa cylindrica (smooth luffa). 21beta-Hydroxyhederagenin is found in fruits.
Madasiatic acid
Constituent of Centella asiatica (Asiatic pennywort). Madasiatic acid is found in herbs and spices and green vegetables. Madasiatic acid is found in green vegetables. Madasiatic acid is a constituent of Centella asiatica (Asiatic pennywort)
7',8'-Dihydro-8'-hydroxycitraniaxanthin
7,8-Dihydro-8-hydroxycitraniaxanthin is found in citrus. 7,8-Dihydro-8-hydroxycitraniaxanthin is isolated from Sinton citrangequat. Isolated from Sinton citrangequat. 7,8-Dihydro-8-hydroxycitraniaxanthin is found in citrus.
N-Eicosapentaenoyl Tryptophan
C31H40N2O3 (488.30387700000006)
N-eicosapentaenoyl tryptophan belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is an Eicosapentaenoic acid amide of Tryptophan. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Eicosapentaenoyl Tryptophan is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Eicosapentaenoyl Tryptophan is therefore classified as a long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.
Antcin K
Cimiaserin B
Jacarandic acid
Rotundic acid
Rotundic acid, also known as rotundate, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Rotundic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Rotundic acid can be found in olive, which makes rotundic acid a potential biomarker for the consumption of this food product. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1].
4,10,16,22,27,32-Hexaoxa-1,7,13,19-tetraazatricyclo(11.11.5.57,19)tetratriacontane
C24H48N4O6 (488.35736679999997)
(8S,9S,10S,11S,13S,14S,17R)-11,17-Dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-9-nonyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
polygalic acid
Polygalic acid is a 12alpha-hydroxy steroid. Polygalic acid is a natural product found in Bellis perennis with data available. Polygalic acid, a triterpenoid saponin, is considered one of the major active constituents of Polygala tenuifolia[1]. Polygalic acid, a triterpenoid saponin, is considered one of the major active constituents of Polygala tenuifolia[1].
Tormentic_acid
Tormentic acid is a triterpenoid. It has a role as a metabolite. Tormentic acid is a natural product found in Debregeasia saeneb, Chaenomeles speciosa, and other organisms with data available. A natural product found in Euscaphis japonica. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2]. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2]. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2].
Rotundicacid
Rotundic acid is a triterpenoid. It has a role as a metabolite. Rotundic acid is a natural product found in Ilex chinensis, Ilex excelsa, and other organisms with data available. A natural product found in Euscaphis japonica. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1].
Bayogenin
Bayogenin is a pentacyclic triterpenoid. It derives from a hydride of an oleanane. Bayogenin is a natural product found in Castanospermum australe, Phytolacca dodecandra, and other organisms with data available. Bayogenin is an alfalfa saponin, shows moderate potency of glycogen phosphorylase inhibition[1][2].
alisol F
See also: Alisma plantago-aquatica subsp. orientale root (part of). Alisol F is a triterpene isolated from Alisma orinentale, has immunosuppressive and anti-virus functions. Alisol F exhibits inhibitory activity in vitro on hepatitis B virus (HBV) surface antigen (HBsAg) secretion of the HepG2.2.15 cell line with an IC50 of 0.6 μM[1]. Alisol F is a triterpene isolated from Alisma orinentale, has immunosuppressive and anti-virus functions. Alisol F exhibits inhibitory activity in vitro on hepatitis B virus (HBV) surface antigen (HBsAg) secretion of the HepG2.2.15 cell line with an IC50 of 0.6 μM[1].
Polygalic
Polygalic acid is a 12alpha-hydroxy steroid. Polygalic acid is a natural product found in Bellis perennis with data available. Polygalic acid, a triterpenoid saponin, is considered one of the major active constituents of Polygala tenuifolia[1]. Polygalic acid, a triterpenoid saponin, is considered one of the major active constituents of Polygala tenuifolia[1].
Eudesmagnolol
Fomitopinic acid A
A tetracyclic triterpenoid that is lanost-8-ene substituted by hydroxy groups at positions 24 and 25 , a carboxylic acid at position 21 and an oxo grouo at position 3 (the 24S stereoisomer). Isolated from the fruit bodies of Fomitopsis pinicola, it exhibits antiinflammatory activity against cylooxygenase-1 (COX-1) and cylooxygenase-2 (COX-2).
Asiatic Acid
Esculentic acid (diplazium) is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Esculentic acid (diplazium) is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Esculentic acid (diplazium) can be found in green vegetables, which makes esculentic acid (diplazium) a potential biomarker for the consumption of this food product. C1907 - Drug, Natural Product > C28269 - Phytochemical > C1905 - Triterpenoid Compound C274 - Antineoplastic Agent > C1931 - Antineoplastic Plant Product relative retention time with respect to 9-anthracene Carboxylic Acid is 1.377 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.378 Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2]. Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2].
Tormentic acid
Tormentic acid, also known as tormentate, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Tormentic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Tormentic acid can be found in loquat and olive, which makes tormentic acid a potential biomarker for the consumption of these food products. Tormentic acid is a bio-active isolate of Luehea divaricata and Agrimonia eupatoria. Tormentic acid derivatives have been synthesized and researched . Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2]. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2]. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2].
Spathodic acid
A pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 3, 19 and 24 (the 3beta,19alpha stereoisomer). It has been isolated from the roots of Rubia yunnanensis.
Esclentic acid
Origin: Plant; SubCategory_DNP: Triterpenoids
(3S,16S,20R,22R,24S)-16,24:20,24-diepoxycholest-5-ene-3,22,25-triol 3-acetate|suberoretisteroid A
Harpullon = 15alpha,16alpha,22alpha,28-Tetrahydroxyolean-12-en-3-on
12alpha,16alpha-diacetoxy-20,24-dimethyl-25-norscalaran-24-one
3beta.5.6beta-trihydroxy-ursen-(12)-oic acid-(28)|3beta.5.6beta-Trihydroxy-ursen-(12)-saeure-(28)
24(R)-methylcholesta-5,22-diene-1alpha,3beta,11alpha,18-tetrol 18-acetate
3alpha,11alpha,23-trihydroxy-lup-20(29)-en-28-oic acid|3alpha,11alpha,23-Trihydroxy-lup-20(29)-en-28-saeure|3alpha-,11alpha,23-trihydroxy-lup-20(29)-en-28-oic acid|sapogenol
(3alpha,7alpha,11alpha,22S,25R)-3,7,11-trihydroxy-22,26-epoxylanost-8-en-26-one|artabotryol E
3alpha,20beta,21beta-trihydroxyserrat-14-en-24-oic acid
25R-antcin K|3alpha,4beta,7beta-trihydroxy-4alpha-methylergosta-8,24(28)-dien-11-on-25R-26-oic acid|3alpha,4beta,7beta-trihydroxy-4alpha-methylergosta-8,24(28)-dien-11-on-26-oic acid|antcin K
3,4-secocycloarta-4-hydroxy-24(Z)-en-3,26-dioic acid|lancifoic acid A
(3beta,21beta,22alpha)-3,21,22-Trihydroxy-12-oleanen-28-oic acid
(20R,24S)-6alpha,16beta,25-trihydroxy-20,24-epoxycycloartan-3-one|20(R),24(S)-epoxy-6alpha,16beta,25-trihydroxycycloartan-3-one|20R,24S-epoxycycloartan-6alpha,16beta,25-triol-3-one|3-oxocycloastragenol|6alpha,16beta,25-trihydroxy-20R,24S-epoxycycloartane-3-one|cyclopycanthogenin|cyclopycnanthogenin
(2alpha,3alpha,22beta)-2,3,22-trihydroxy-21-oxo-29-norfriedelan-24,2beta-olide|triflora lactone
6alpha-hydroxy-3,12-dion-(20S),(24R)-epoxy-dammarane|panaxadione
3alpha,12beta,21beta,24-tetrahydroxyserrat-14-en-16-one|japonicumin B
{(E)-3-(chloromethylene)-2,3-dihydrobenzo[b]oxepin-7-yl}methyl stearate
29-hydroxyhederagenin|3beta,23,29-trihydroxy-olean-12-en-28-oic acid|3beta,23,29-trihydroxyolean-12-en-28-oic acid|nipponogenin E
24-methylenecholest-5-en-1alpha,3beta,11alpha,18-tetrol 18-acetate|24-methylenecholest-5-ene-1alpha,3beta,11alpha,18-tetrol 18-acetate
4(R),23-epoxy-2alpha,3alpha,19alpha-trihydroxy-24-norurs-12-en-28-oic acid|4(R),23-Epoxy-2??,3??,19??-trihydroxy-24-norurs-12-en-28-oic acid
3alpha,21beta,25-triol-tirucalla-21,24-epoxy-23-one
(3beta,7beta,15beta,23E)-3,7,15,25-tetrahydroxycucurbita-5,23-dien-19-al|(3beta,7beta,9beta,10alpha,15beta,23E)-3,7,15,25-tetrahydroxy-19-norlanosta-5,23-diene-9-carboxaldehyde
24(S),25-dihydroxy-3-oxocycloartan-30-oic acid|glaucartanoic acid A
(3beta,7beta)-3,7,22,23-tetrahydroxycucurbita-5,24-dien-19-al|(3beta,7beta,9beta,10alpha)-3,7,22,23-tetrahydroxy-19-norlanosta-5,24-diene-9-carboxaldehyde
13beta-28-epoxy-3beta,22alpha,23-trihydroxyolean-16-one
(17alpha,20beta,24alpha)-21,24-cyclopenta-1alpha,3beta,21alpha,25,28-pentahydroxy-5alpha-lanosta-7,9(11)-diene|inonotusol C
(3beta,7beta)-3,7,23,24-tetrahydroxycucurbita-5,25-dien-19-al|(3beta,7beta,9beta,10alpha)-3,7,23,24-tetrahydroxy-19-norlanosta-5,25-diene-9-carboxaldehyde
(3alpha,13alpha,14beta,17alpha,20S,23R,24R)-21,23-epoxy-3,24,25-trihydroxylanost-7-en-21-one|meliasenin X
(?)-(3R,10S,11R,17S,20R,21S,24R)-21,24-cyclopenta-3,11,21,25-tetrahydroxylanosta-8-en-7-one|inonotusol E
2alpha,3beta,6beta-trihydroxylolean-12-en-28-oic acid|6beta-hydroxymaslinic acid
3alpha,21beta,24,29-tetrahydroxy-16-oxoserrat-14-en
(1beta,3beta,19beta)-1,3,19-trihydroxyolean-12-en-28-oic acid
3,4-seco-4,23-dihydroxyolean-12-en-22-one-3-carboxylic acid
2beta-hydroxy-2,3-secotirucalla-2,29-epoxy-7-ene-23-oxo-3-oic acid|aphanamgrandin C
(23R,24S)-23,24,25-trihydroxytirucall-8-ene-3,7-dione|brumollisol A
3beta,11alpha,12,15alpha-tetrahydroxyurs-12-en-24-al
2alpha,3beta,21alpha-trihydroxy-urs-12-en-28-oic acid
Gardenoin J
(3S,8S,9R,10R,13R,14S,16R,17R,21S,23S)-16,23-epoxy-3,20,25-trihydroxycucurbit-5-en-11-one|elaeocarpucin F
(2E,6E,10E)-12,14,15-trihydroxy-1-(2,5-dimethoxy-3-methylphenyl)-3,7,11,15-tetramethylhexadeca-2,6,10-trien-5-one|cystoazorol B
(22E,24S)-11alpha-acetoxy-ergostane-22,25-dien-3beta,5alpha,6beta-triol
(23R,24S)-23,24,25-trihydroxytirucall-7-ene-3,6-dione
16beta,21beta,22alpha,23,28-pentahydroxyolean-12-en-3-one
(25R) and (25S)-26-acetoxy-3beta,5alpha-dihydroxyergost-24(28)-en-6-one
24-nor-3alpha,11alpha-dihydroxy-lup-20(29)-en-23,28-dioic acid
2-norolean-12-en-1,3,30-trioic acid|dysoxyhainic acid F
3,6,23-trihydroxyurs-12-en-28-oic acid|3beta,6beta,23-trihydroxyurs-12-en-28-oic acid
2alpha,3beta,13beta-trihydroxyurs-11-en-28-oic acid
1alpha,11alpha-dihydroxygorgosterol-13-carboxylic acid
11-acetoxy-3beta,6alpha-dihydroxy-24-methylene-9,11-seco-5alpha-cholest-7-en-9-one
2alpha,3beta,23-trihydroxylup-20(29)-en-28-oic acid|Hovenic acid
3beta-(2-O-acetyl-alpha-L-fucopyranosyloxy)pregna-5,20-diene|3beta-(2?-O-acetyl-alpha-l-fucopyranosyloxy)pregna-20-ene|sclerosteroid I|ximaosteroid D
3,15,16-trihydroxy-(3beta,15alpha,16alpha)-olean-12-en-28-oic acid|3beta,15alpha,16alpha-trihydroxy-18beta-olean-12-en-28-oic acid|3beta,15alpha,16alpha-trihydroxy-olean-12-en-28-oic acid|3beta,15alpha,16alpha-Trihydroxy-olean-12-en-28-saeure|Entagen-saeure <3beta.15alpha.16alpha-Trihydroxy-oleanen-(12)-carbonaaeure(28)>|entagenic acid|Entagensaeure
3-oxo-11beta,23-dihydroxy-24,24-dimethyl-26,27-dinorprotost-13(17)-en-25-oic acid|alisol O
(2beta,3beta,4alpha,16beta)-2,3,16-trihydroxy-15-oxo-28-norolean-12-en-23-oic acid
16beta-hydroxy-2,3-seco-lup-20(29)-ene-2,3-dioic acid
16alpha,21alpha-Epoxy-olean-12-en-3beta,22alpha,24,28-tetraol|16alpha,21alpha-epoxy-olean-12-ene-3beta,22alpha,24,28-tetraol|aescigenin
(2alpha,3beta)-2,3,30-Trihydroxy-12-oleanen-28-oic acid
(6S)-hydroxy-(24xi)-hydroperoxy-29-nor-3,4-seco-cycloart-4(30),25-dien-3-oic acid methyl ester|Anticancer Triterpene PMV70P691-043
16-keto-cycloastragenol|20(R),24(S)-epoxy-3beta,6alpha,25-trihydroxycycloartan-16-one|20R,24S-epoxycycloartan-3beta,6alpha,25-triol-16-one|cycloasalgenin
3alpha,9beta,13alpha-trihydroxy-11(12),15(17)-trinervitadiene-3,9,13-tripropionate|3alpha,9beta,13alpha-tripropionoxy-1beta,8beta-trinervita-11,15(17)-diene
2-oxo-3beta,19alpha,22alpha-trihydroxy-24-nor-urs-12-en-28-oic acid
(3S,16S,20R,22R,24S)-16,24:20,24-diepoxycholest-5-ene-3,22,25-triol 22-acetate|suberoretisteroid B
9-sec-butyl-6-isobutyl-15,17-dimethoxy-12-methylamino-4,7,10-triaza-bicyclo[12.3.1]octadeca-1(18),2,14,16-tetraene-5,8,11-trione|Mucronin-E|Mucronine E
C26H40N4O5 (488.29985500000004)
Ser Val Lys Arg
Esculentic acid (Diplazium)
10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid is a natural product found in Psidium, Punica, and other organisms with data available. Esculentic acid (Diplazium) is found in green vegetables. Esculentic acid (Diplazium) is a constituent of the edible fern Diplazium esculentum Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2]. Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2].
Isoarjunolic acid
2alpha,3alpha,23-trihydroxyolean-12-en-28-oic acid is a pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 23 respectively (the 2alpha,3alpha-stereoisomer). It has been isolated from the leaves of Rosa laevigata. It has a role as a plant metabolite and an anti-inflammatory agent. It is a hydroxy monocarboxylic acid, a triol and a pentacyclic triterpenoid. It derives from a hydride of an oleanane. 2alpha,3alpha,23-Trihydroxyolean-12-en-28-oic acid is a natural product found in Salvia virgata and Rosa laevigata with data available. A pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 23 respectively (the 2alpha,3alpha-stereoisomer). It has been isolated from the leaves of Rosa laevigata.
2,3,24-Trihydroxyolean-12-en-28-oicacid
2,3,24-Trihydroxyolean-12-en-28-oic acid is a natural product found in Vitex negundo var. cannabifolia, Actinidia chinensis, and Prunella vulgaris with data available.
I1exo1ic acid
Rotundic acid is a triterpenoid. It has a role as a metabolite. Rotundic acid is a natural product found in Ilex chinensis, Ilex excelsa, and other organisms with data available. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1].
Arjunolicacid
Arjunolic acid is a pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 23 (the 2alpha,3beta stereoisomer). Isolated from Symplocos lancifolia and Juglans sinensis, it exhibits antioxidant and antimicrobial activities. It has a role as a metabolite, an antibacterial agent, an antifungal agent and an antioxidant. It is a pentacyclic triterpenoid and a hydroxy monocarboxylic acid. It derives from a hydride of an oleanane. Arjunolic acid is a natural product found in Musanga cecropioides, Akebia quinata, and other organisms with data available. A pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 23 (the 2alpha,3beta stereoisomer). Isolated from Symplocos lancifolia and Juglans sinensis, it exhibits antioxidant and antimicrobial activities.
Caulophyllogenin
Caulophyllogenin is a triterpenoid.
MLS001076292-01!11BETA,17ALPHA,21-TRIHYDROXY-4-PREGNENE-3,20-DIONE 21-CAPRYLATE
C30H48O5_Olean-12-en-28-oic acid, 2,3,19-trihydroxy-, (2alpha,3beta,5xi,9xi,19alpha)
C30H48O5_(2alpha,3alpha,5xi,9xi,18xi)-2,3,19-Trihydroxyurs-12-en-28-oic acid
C30H48O5_(5xi,8alpha,9beta,11beta,14beta,16beta,23S,24R)-11,24,25-Trihydroxy-16,23-epoxydammar-13(17)-en-3-one
C30H48O5_Urs-12-en-28-oic acid, 2,3,23-trihydroxy-, (2alpha,3beta,5xi,9xi,18xi)
(1S,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
(1R,2R,4aS,6aS,6bR,10S,12aR,14bS)-1,8,10-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
(1S,4aR,6aS,6bR,10R,11R,12aR,14bS)-1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
(4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
(1S,4aR,6aS,6bR,10R,11R,12aR,14bS)-1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid_major
(4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid_major
(1S,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid_minor
(1S,2R,4aS,6aS,6bR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid_major
Phe Ile Ile Pro
C26H40N4O5 (488.29985500000004)
Phe Ile Leu Pro
C26H40N4O5 (488.29985500000004)
Phe Ile Pro Ile
C26H40N4O5 (488.29985500000004)
Phe Ile Pro Leu
C26H40N4O5 (488.29985500000004)
Phe Leu Ile Pro
C26H40N4O5 (488.29985500000004)
Phe Leu Leu Pro
C26H40N4O5 (488.29985500000004)
Phe Leu Pro Ile
C26H40N4O5 (488.29985500000004)
Phe Leu Pro Leu
C26H40N4O5 (488.29985500000004)
Phe Pro Ile Ile
C26H40N4O5 (488.29985500000004)
Phe Pro Ile Leu
C26H40N4O5 (488.29985500000004)
Phe Pro Leu Ile
C26H40N4O5 (488.29985500000004)
Phe Pro Leu Leu
C26H40N4O5 (488.29985500000004)
Ile Phe Ile Pro
C26H40N4O5 (488.29985500000004)
Ile Phe Leu Pro
C26H40N4O5 (488.29985500000004)
Ile Phe Pro Ile
C26H40N4O5 (488.29985500000004)
Ile Phe Pro Leu
C26H40N4O5 (488.29985500000004)
Ile Ile Phe Pro
C26H40N4O5 (488.29985500000004)
Ile Ile Ile Met
C23H44N4O5S (488.30322540000003)
Ile Ile Leu Met
C23H44N4O5S (488.30322540000003)
Ile Ile Met Ile
C23H44N4O5S (488.30322540000003)
Ile Ile Met Leu
C23H44N4O5S (488.30322540000003)
Ile Ile Pro Phe
C26H40N4O5 (488.29985500000004)
Ile Lys Lys Thr
Ile Lys Thr Lys
Ile Leu Phe Pro
C26H40N4O5 (488.29985500000004)
Ile Leu Ile Met
C23H44N4O5S (488.30322540000003)
Ile Leu Leu Met
C23H44N4O5S (488.30322540000003)
Ile Leu Met Ile
C23H44N4O5S (488.30322540000003)
Ile Leu Met Leu
C23H44N4O5S (488.30322540000003)
Ile Leu Pro Phe
C26H40N4O5 (488.29985500000004)
Ile Met Ile Ile
C23H44N4O5S (488.30322540000003)
Ile Met Ile Leu
C23H44N4O5S (488.30322540000003)
Ile Met Leu Ile
C23H44N4O5S (488.30322540000003)
Ile Met Leu Leu
C23H44N4O5S (488.30322540000003)
Ile Pro Phe Ile
C26H40N4O5 (488.29985500000004)
Ile Pro Phe Leu
C26H40N4O5 (488.29985500000004)
Ile Pro Ile Phe
C26H40N4O5 (488.29985500000004)
Ile Pro Leu Phe
C26H40N4O5 (488.29985500000004)
Ile Thr Lys Lys
Lys Ile Lys Thr
Lys Ile Thr Lys
Lys Lys Ile Thr
Lys Lys Leu Thr
Lys Lys Thr Ile
Lys Lys Thr Leu
Lys Leu Lys Thr
Lys Leu Thr Lys
Lys Arg Ser Val
Lys Arg Val Ser
Lys Ser Arg Val
Lys Ser Val Arg
Lys Thr Ile Lys
Lys Thr Lys Ile
Lys Thr Lys Leu
Lys Thr Leu Lys
Lys Val Arg Ser
Lys Val Ser Arg
Leu Phe Ile Pro
C26H40N4O5 (488.29985500000004)
Leu Phe Leu Pro
C26H40N4O5 (488.29985500000004)
Leu Phe Pro Ile
C26H40N4O5 (488.29985500000004)
Leu Phe Pro Leu
C26H40N4O5 (488.29985500000004)
Leu Ile Phe Pro
C26H40N4O5 (488.29985500000004)
Leu Ile Ile Met
C23H44N4O5S (488.30322540000003)
Leu Ile Leu Met
C23H44N4O5S (488.30322540000003)
Leu Ile Met Ile
C23H44N4O5S (488.30322540000003)
Leu Ile Met Leu
C23H44N4O5S (488.30322540000003)
Leu Ile Pro Phe
C26H40N4O5 (488.29985500000004)
Leu Lys Lys Thr
Leu Lys Thr Lys
Leu Leu Phe Pro
C26H40N4O5 (488.29985500000004)
Leu Leu Ile Met
C23H44N4O5S (488.30322540000003)
Leu Leu Leu Met
C23H44N4O5S (488.30322540000003)
Leu Leu Met Ile
C23H44N4O5S (488.30322540000003)
Leu Leu Met Leu
C23H44N4O5S (488.30322540000003)
Leu Leu Pro Phe
C26H40N4O5 (488.29985500000004)
Leu Met Ile Ile
C23H44N4O5S (488.30322540000003)
Leu Met Ile Leu
C23H44N4O5S (488.30322540000003)
Leu Met Leu Ile
C23H44N4O5S (488.30322540000003)
Leu Met Leu Leu
C23H44N4O5S (488.30322540000003)
Leu Pro Phe Ile
C26H40N4O5 (488.29985500000004)
Leu Pro Phe Leu
C26H40N4O5 (488.29985500000004)
Leu Pro Ile Phe
C26H40N4O5 (488.29985500000004)
Leu Pro Leu Phe
C26H40N4O5 (488.29985500000004)
Leu Thr Lys Lys
Met Ile Ile Ile
C23H44N4O5S (488.30322540000003)
Met Ile Ile Leu
C23H44N4O5S (488.30322540000003)
Met Ile Leu Ile
C23H44N4O5S (488.30322540000003)
Met Ile Leu Leu
C23H44N4O5S (488.30322540000003)
Met Leu Ile Ile
C23H44N4O5S (488.30322540000003)
Met Leu Ile Leu
C23H44N4O5S (488.30322540000003)
Met Leu Leu Ile
C23H44N4O5S (488.30322540000003)
Met Leu Leu Leu
C23H44N4O5S (488.30322540000003)
Pro Phe Ile Ile
C26H40N4O5 (488.29985500000004)
Pro Phe Ile Leu
C26H40N4O5 (488.29985500000004)
Pro Phe Leu Ile
C26H40N4O5 (488.29985500000004)
Pro Phe Leu Leu
C26H40N4O5 (488.29985500000004)
Pro Ile Phe Ile
C26H40N4O5 (488.29985500000004)
Pro Ile Phe Leu
C26H40N4O5 (488.29985500000004)
Pro Ile Ile Phe
C26H40N4O5 (488.29985500000004)
Pro Ile Leu Phe
C26H40N4O5 (488.29985500000004)
Pro Leu Phe Ile
C26H40N4O5 (488.29985500000004)
Pro Leu Phe Leu
C26H40N4O5 (488.29985500000004)
Pro Leu Ile Phe
C26H40N4O5 (488.29985500000004)
Pro Leu Leu Phe
C26H40N4O5 (488.29985500000004)
Arg Lys Ser Val
Arg Lys Val Ser
Arg Ser Lys Val
Arg Ser Val Lys
Arg Val Lys Ser
Arg Val Ser Lys
Ser Lys Arg Val
Ser Lys Val Arg
Ser Arg Lys Val
Ser Arg Val Lys
Ser Val Arg Lys
Thr Ile Lys Lys
Thr Lys Ile Lys
Thr Lys Lys Ile
Thr Lys Lys Leu
Thr Lys Leu Lys
Thr Leu Lys Lys
Val Lys Arg Ser
Val Lys Ser Arg
Val Arg Lys Ser
Val Arg Ser Lys
Val Ser Lys Arg
Val Ser Arg Lys
Pitheduloside I
Arjunolic acid
Camelliagenin B
madasiatic acid
Esculentic acid (Diplazium)
Hovenolactone
Centellasapogenol A
Liquiridiolic acid
7',8'-Dihydro-8'-hydroxycitraniaxanthin
(3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid
Ganoderiol D
Dotfc
16b-Hydroxystellatogenin
21b-Hydroxyhederagenin
ST 30:3;O5
Ganocasurarin A
Acacic acid
A pentacyclic triterpenoid that is olean-12-ene substituted by carboxy group at position 28 and hydroxy groups at positions 3, 16 and 21 (the 3beta,16alpha,21beta stereoisomer).
3beta,6beta,19alpha-trihydroxy-urs-12-en-28-oic acid
Cortisol octanoate
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones
tridecylbenzenesulphonic acid, compound with 2,2,2-nitrilotriethanol (1:1)
C25H46NO6S (488.30456760000004)
[(2R,3R,4R)-3,4-bis[[tert-butyl(dimethyl)silyl]oxy]-3,4-dihydro-2H-pyran-2-yl]methoxy-tert-butyl-dimethylsilane
C24H52O4Si3 (488.31732320000003)
4,10,16,22,27,32-Hexaoxa-1,7,13,19-tetraazatricyclo(11.11.5.57,19)tetratriacontane
C24H48N4O6 (488.35736679999997)
23-Acetoxy-12-epi-deoxoscalarin
A scalarane sesterterpenoid that is 12-epi-deoxoscalarin with an additional acetoxy group at position 23. It has been isolated from the sponge, Hyattella species.
Rubiyunnanol C
A pentacyclic triterpenoid of the class of arborinane-type terpenoids isolated from the roots of Rubia yunnanensis.
(2S,3R,4aS,6aR,6aS,6bR,9S,10S,12aR,14bS)-3,10-dihydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid
Euscaphic acid
Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2]. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2]. Tormentic acid, a triterpene isolated from Rosa rugosa, exerts anti-inflammatory, antihyperlipidemic, and anti-atherogenic properties[1][2].
465-00-9
Rotundic acid
Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1]. Rotundic acid, a triterpenoid obtained from Ilex rotunda Thunb., induces DNA damage and cell apoptosis in hepatocellular carcinoma through AKT/mTOR and MAPK Pathways. Rotundic acid possesses anti-inflammatory and cardio-protective abilities[1].
(1S,2R,4aS,6aS,6bR,9R,10S,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
(8S,9S,10S,11S,13S,14S,17R)-11,17-Dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-9-nonyl-1,2,6,7,8,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-one
[3-carboxy-2-[(4E,7E,10E,13E,15E,19E)-17-hydroxydocosa-4,7,10,13,15,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,11E,13E,16E,19E)-10-hydroxydocosa-4,7,11,13,16,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,9E,13E,16E,19E)-11-hydroxydocosa-4,7,9,13,16,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,10E,14E,16E,19E)-13-hydroxydocosa-4,7,10,14,16,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,10E,13E,17E,19E)-16-hydroxydocosa-4,7,10,13,17,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,10E,13E,16E,18E)-20-hydroxydocosa-4,7,10,13,16,18-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(5E,7E,10E,13E,16E,19E)-4-hydroxydocosa-5,7,10,13,16,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,8E,10E,13E,16E,19E)-7-hydroxydocosa-4,8,10,13,16,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,6E,10E,13E,16E,19E)-8-hydroxydocosa-4,6,10,13,16,19-hexaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,10E,13E,16E)-18-(3-ethyloxiran-2-yl)octadeca-4,7,10,13,16-pentaenoyl]oxypropyl]-trimethylazanium
[3-carboxy-2-[(4E,7E,10E,13E)-15-[3-[(E)-pent-2-enyl]oxiran-2-yl]pentadeca-4,7,10,13-tetraenoyl]oxypropyl]-trimethylazanium
Nipponogenin E
A pentacyclic triterpenoid that is olean-12-en-28-oic acid substituted by hydroxy groups at positions 3, 23 and 29. It has been isolated from the stem bark of Kalopanax pictus.
salvin A
A pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 5 (the 2alpha,3beta stereoisomer). Isolated from Salvia santolinifolia, it exhibits inhibitory activity against cholinesterase.
(3S)-3-hydroxy-5-[(3R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-(2-hydroxypropan-2-yl)oxan-2-one
2alpha,3beta,23-Trihydroxylup-20(29)-en-28-oic acid
A pentacyclic triterpenoid that is lup-20(29)-en-28-oic acid substituted by hydroxy groups at positions 2, 3 and 23 respectively (the 2alpha,3beta-stereoisomer). It has been isolated from the leaves of Rosa laevigata.
salvin B
A pentacyclic triterpenoid that is urs-12-en-28-oic acid substituted by hydroxy groups at positions 3, 6 and 24 (the 3alpha,6alpha stereoisomer). Isolated from Salvia santolinifolia, it exhibits inhibitory activity against cholinesterase.
(5S,6R,9R)-14-acetamido-N-cyclohexyl-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(3S,6aS,8R,10aS)-8-[2-[[(3R)-1-benzylpyrrolidin-3-yl]amino]-2-oxoethyl]-3-hydroxy-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(5S,6R,9R)-8-(cyclopentylmethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
(5R,6S,9R)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propyl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5R,6R,9S)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propyl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5R,6R,9R)-14-(cyclobutanecarbonylamino)-5-methoxy-3,6,9-trimethyl-2-oxo-N-propyl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5S,6S,9S)-14-(cyclobutanecarbonylamino)-5-methoxy-3,6,9-trimethyl-2-oxo-N-propyl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(3R,6aR,8R,10aR)-8-[2-[[(3S)-1-benzylpyrrolidin-3-yl]amino]-2-oxoethyl]-3-hydroxy-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3R,6aS,8S,10aS)-3-hydroxy-8-[2-oxo-2-[[(3R)-1-(phenylmethyl)-3-pyrrolidinyl]amino]ethyl]-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3R,6aR,8S,10aR)-3-hydroxy-8-[2-oxo-2-[[(3S)-1-(phenylmethyl)-3-pyrrolidinyl]amino]ethyl]-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(5S,6R,9S)-14-(cyclobutanecarbonylamino)-5-methoxy-3,6,9-trimethyl-2-oxo-N-propyl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(4S,7S,8R)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(4R,7R,8R)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
(5S,6S,9R)-14-(cyclobutanecarbonylamino)-5-methoxy-3,6,9-trimethyl-2-oxo-N-propyl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(4S,7R,8R)-5-(cyclobutanecarbonyl)-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
(3S,6aR,8R,10aR)-3-hydroxy-8-[2-oxo-2-[[(3S)-1-(phenylmethyl)-3-pyrrolidinyl]amino]ethyl]-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3S,6aS,8S,10aS)-8-[2-[[(3R)-1-benzylpyrrolidin-3-yl]amino]-2-oxoethyl]-3-hydroxy-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3S,6aR,8S,10aR)-8-[2-[[(3S)-1-benzylpyrrolidin-3-yl]amino]-2-oxoethyl]-3-hydroxy-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3R,6aR,8S,10aR)-8-[2-[[(3R)-1-benzylpyrrolidin-3-yl]amino]-2-oxoethyl]-3-hydroxy-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(4R,7R,8S)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5R,6R,9S)-8-(cyclopentylmethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(5S,6S,9S)-8-(cyclopentylmethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(5R,6S,9R)-8-(cyclopentylmethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(5S,6R,9S)-8-(cyclopentylmethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(5R,6S,9R)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5R,6R,9S)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
N-[(5R,6R,9R)-8-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclobutanecarboxamide
C26H40N4O5 (488.29985500000004)
N-[(5R,6R,9S)-8-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclobutanecarboxamide
C26H40N4O5 (488.29985500000004)
N-[(5R,6S,9R)-8-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclobutanecarboxamide
C26H40N4O5 (488.29985500000004)
(5S,6S,9S)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5S,6S,9R)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5R,6S,9R)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(4S,7S,8S)-5-acetyl-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-cyclohexylurea
C26H40N4O5 (488.29985500000004)
1-[(4R,7S,8S)-5-acetyl-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-cyclohexylurea
C26H40N4O5 (488.29985500000004)
1-[(4R,7R,8S)-5-acetyl-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-cyclohexylurea
C26H40N4O5 (488.29985500000004)
(3S,6aS,8S,10aS)-3-hydroxy-8-[2-oxo-2-[[(3S)-1-(phenylmethyl)-3-pyrrolidinyl]amino]ethyl]-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3R,6aS,8R,10aS)-3-hydroxy-8-[2-oxo-2-[[(3R)-1-(phenylmethyl)-3-pyrrolidinyl]amino]ethyl]-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
(3R,6aS,8R,10aS)-3-hydroxy-8-[2-oxo-2-[[(3S)-1-(phenylmethyl)-3-pyrrolidinyl]amino]ethyl]-N-propyl-3,4,6,6a,8,9,10,10a-octahydro-2H-pyrano[2,3-c][1,5]oxazocine-1-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(4R,7S,8R)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(4R,7S,8S)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(4S,7R,8S)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(4S,7S,8S)-5-[cyclobutyl(oxo)methyl]-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5R,6R,9R)-8-(cyclopentylmethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propylurea
1-[(5S,6S,9S)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5S,6S,9R)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5R,6R,9R)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5S,6R,9R)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
1-[(5S,6R,9S)-8-(2-cyclopropyl-1-oxoethyl)-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-propan-2-ylurea
C26H40N4O5 (488.29985500000004)
N-[(5S,6S,9S)-8-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclobutanecarboxamide
C26H40N4O5 (488.29985500000004)
N-[(5S,6S,9R)-8-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclobutanecarboxamide
C26H40N4O5 (488.29985500000004)
N-[(5S,6R,9S)-8-[2-(dimethylamino)-1-oxoethyl]-5-methoxy-3,6,9-trimethyl-2-oxo-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]cyclobutanecarboxamide
C26H40N4O5 (488.29985500000004)
(5R,6R,9R)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5R,6R,9S)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5S,6R,9R)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
(5S,6R,9S)-14-[[cyclobutyl(oxo)methyl]amino]-5-methoxy-3,6,9-trimethyl-2-oxo-N-propan-2-yl-11-oxa-3,8-diazabicyclo[10.4.0]hexadeca-1(12),13,15-triene-8-carboxamide
C26H40N4O5 (488.29985500000004)
1-[(4R,7R,8R)-5-acetyl-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-cyclohexylurea
C26H40N4O5 (488.29985500000004)
1-[(4S,7R,8R)-5-acetyl-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-cyclohexylurea
C26H40N4O5 (488.29985500000004)
1-[(4S,7S,8R)-5-acetyl-8-methoxy-4,7,10-trimethyl-11-oxo-2-oxa-5,10-diazabicyclo[10.4.0]hexadeca-1(12),13,15-trien-14-yl]-3-cyclohexylurea
C26H40N4O5 (488.29985500000004)
(2α,3α)-2,3,24-Trihydroxyurs-12-en-28-oic acid
[(4E,8E,12E)-2-(butanoylamino)-3-hydroxypentadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-3-hydroxy-2-(propanoylamino)hexadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-2-acetamido-3-hydroxyheptadeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
[(4E,8E,12E)-3-hydroxy-2-(pentanoylamino)tetradeca-4,8,12-trienyl] 2-(trimethylazaniumyl)ethyl phosphate
(1-heptanoyloxy-3-hydroxypropan-2-yl) (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenoate
(1-hydroxy-3-nonanoyloxypropan-2-yl) (3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoate
(1-hydroxy-3-pentanoyloxypropan-2-yl) (7Z,10Z,13Z,16Z,19Z)-docosa-7,10,13,16,19-pentaenoate
[3-hydroxy-2-[(E)-undec-4-enoyl]oxypropyl] (7E,9E,11E,13E)-hexadeca-7,9,11,13-tetraenoate
(3-hydroxy-2-undecanoyloxypropyl) (5E,7E,9E,11E,13E)-hexadeca-5,7,9,11,13-pentaenoate
Asiatic
Asiatic acid is a pentacyclic triterpenoid that is ursane substituted by a carboxy group at position 28 and hydroxy groups at positions 2, 3 and 23 (the 2alpha,3beta stereoisomer). It is isolated from Symplocos lancifolia and Vateria indica and exhibits anti-angiogenic activity. It has a role as an angiogenesis modulating agent and a metabolite. It is a monocarboxylic acid, a triol and a pentacyclic triterpenoid. It derives from a hydride of an ursane. From Centella asiatica and other plants; shows a variety of bioactivities. Asiatic acid is a natural product found in Psidium guajava, Combretum fruticosum, and other organisms with data available. See also: Holy basil leaf (part of); Lagerstroemia speciosa leaf (part of); Centella asiatica flowering top (part of). A pentacyclic triterpenoid that is ursane substituted by a carboxy group at position 28 and hydroxy groups at positions 2, 3 and 23 (the 2alpha,3beta stereoisomer). It is isolated from Symplocos lancifolia and Vateria indica and exhibits anti-angiogenic activity. C1907 - Drug, Natural Product > C28269 - Phytochemical > C1905 - Triterpenoid Compound C274 - Antineoplastic Agent > C1931 - Antineoplastic Plant Product Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2]. Asiatic acid, a pentacyclic triterpene found in Centella asiatica, induces apoptosis in melanoma cells. Asiatic acid has the potential for skin cancer treatment[1]. Asiatic acid also has anti-inflammatory activities[2].
4,4,10,13,14-pentamethyl-17-(5,6,7-trihydroxy-6-methylheptan-2-yl)-2,5,6,11,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,7-dione
11-acetoxy-3beta,6alpha-dihydroxy-24-methylene-9,11-seco-5alpha-cholesta-7,22E-dien-9-one.
11-acetoxy-3beta,6alpha-dihydroxy-24-methyl-9,11-seco-5alpha-cholesta-7,22Z-dien-9-one.
2alpha,3alpha,23-trihydroxyurs-12-en-28-oic acid
A pentacyclic triterpenoid that is urs-12-ene substituted by a carboxy group at position 28 and hydroxy groups at positions 2, 3 and 23 (the 2alpha,3alpha stereoisomer). It has been isolated from Juglans sinensis.
3beta,6beta,23-trihydroxyolean-12-en-28-oic acid
A pentacyclic triterpenoid that is oleanolic acid substituted by additional hydroxy groups at positions 6 and 23. It has been isolated from Kalopanax pictus.
TG(26:5)
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