Exact Mass: 488.38385479999994
Exact Mass Matches: 488.38385479999994
Found 500 metabolites which its exact mass value is equals to given mass value 488.38385479999994,
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)
alpha-Tocopheryloxyacetic acid
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
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].
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
(20S,23E)-20,25-dihydroxy-3,4-secodammara-4(28),23-dienoic acid methyl ester
Harpullon = 15alpha,16alpha,22alpha,28-Tetrahydroxyolean-12-en-3-on
(20S,23E)-20,25-dihydroxy-3,4-secodammara-4(28),23-diene-3-carboxylic acid
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)
(20S,24S)-20,24-dihydroxy-3,4-secodammara-4(28),25-diene-3-carboxylic acid
3beta,23,28-trihydroxy-11alpha-methoxy-12-oleanene
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
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
7beta-methoxycucurbita-5,23(E)-diene-3beta,12beta,25-triol|cucurbalsaminol B
(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
(3beta,7beta,23E)-25-methoxycucurbita-5,23-diene-3,7,29-triol|balsaminagenin B
6alpha-hydroxy-3,12-dion-(20S),(24R)-epoxy-dammarane|panaxadione
3alpha,12beta,21beta,24-tetrahydroxyserrat-14-en-16-one|japonicumin B
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
3alpha,21beta,25-triol-tirucalla-21,24-epoxy-23-one
lamesticumin B
A triterpenoid of the class of onoceranoid-type terpenoids isolated from the twigs of Lansium domesticum.
(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
24-methylenecycloartane-3beta,6beta,7beta,16beta-tetraol
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
(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
methyl (20S,25)-epoxy-24alpha-hydroxy-3,4-secodammar-4(28)-en-3-oate
(25R) and (25S)-26-acetoxy-3beta,5alpha-dihydroxyergost-24(28)-en-6-one
25,26,27-trisnor-3beta-acetoxy-24-dimethoxycycloartane
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
(23R)-7beta-methoxycucurbita-5,24-diene-3beta,12beta,23-triol|cucurbalsaminol C
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
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
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
(3beta,5alpha)-Cholesta-8,24-dien-3-ol benzoate|O-Benzoyl-zymosterin|O-benzoyl-zymosterol|Zymosterylbenzoat
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.
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
1α-hydroxy-2β-(4-hydroxybutoxy)vitamin D3 / 1α-hydroxy-2β-(4-hydroxybutoxy)cholecalciferol
(5Z,7E)-(1S,2R,3R)-2-(4-hydroxybutyl)-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,20S)-20-methoxy-26,27-dimethyl-24a-homo-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,20R)-26,27-diethyl-24a-homo-22-oxa-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,22S)-26,27-dimethyl-24a,24b-dihomo-9,10-seco-5,7,10(19)-cholestatriene-1,3,22,25-tetrol
(5Z,7E)-(1S,3R,20S)-20-ethoxy-26,27-dimethyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,25-triol
(5Z,7E)-(1S,3R,20S)-26,27-diethyl-9,10-seco-5,7,10(19)-cholestatriene-1,3,20,25-tetrol
(5Z,7E)-(1S,3R,20R,22R)-26,27-dimethyl-24a,24b-dihomo-9,10-seco-5,7,10(19)-cholestatriene-1,3,22,25-tetrol
1α,25-dihydroxy-2β-butoxyvitamin D3 / 1α,25-dihydroxy-2β-butoxycholecalciferol
1α,25-Dihydroxyvitamin D3 25-trimethylsilyl ether
Pitheduloside I
Arjunolic acid
Camelliagenin B
madasiatic acid
Esculentic acid (Diplazium)
Hovenolactone
Centellasapogenol A
Liquiridiolic acid
(3beta,6alpha,19alpha)-3,6,19-Trihydroxy-12-ursen-28-oic acid
Ganoderiol D
Dotfc
16b-Hydroxystellatogenin
21b-Hydroxyhederagenin
bhas#38
An (omega-1)-hydroxy fatty acid ascaroside that is ascr#38 in which the pro-R hydrogen that is beta to the carboxy group is replaced by a hydroxy group. It is a metabolite of the nematode Caenorhabditis elegans.
bhos#38
An omega-hydroxy fatty acid ascaroside that is oscr#38 in which the pro-R hydrogen beta to the carboxy group is replaced by a hydroxy group. It is a metabolite of the nematode Caenorhabditis elegans.
ST 30:3;O5
1alpha-hydroxy-2beta-(4-hydroxybutoxy)vitamin D3
1alpha,25-dihydroxy-2beta-(4-hydroxybutyl)vitamin D3
(20S)-1alpha,25-dihydroxy-20-methoxy-26,27-dimethyl-24a-homovitamin D3
(20S)-1alpha,25-dihydroxy-20-ethoxy-26,27-dimethylvitamin D3
(20S)-1alpha,20,25-trihydroxy-26,27-diethylvitamin D3
(22R)-1alpha,22,25-trihydroxy-26,27-dimethyl-24a,24b-dihomo-20-epivitamin D3
1alpha,25-dihydroxy-2beta-butoxyvitamin D3
1alpha,25-Dihydroxyvitamin D3 25-trimethylsilyl ether
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
25-O-methyl-12beta, 20S-dihydroxydammar-23-en-3-one
Hexadecanamide, N-[(1R,2R)-2-hydroxy-2-(4-methoxyphenyl)-1-(1-pyrrolidinylmethyl)ethyl]-
C30H52N2O3 (488.39777219999996)
(2b,3a,5a,16b,17b)-17-Acetoxy-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane
4,10,16,22,27,32-Hexaoxa-1,7,13,19-tetraazatricyclo(11.11.5.57,19)tetratriacontane
C24H48N4O6 (488.35736679999997)
alpha-Tocopheryloxyacetic acid
C308 - Immunotherapeutic Agent > C129820 - Antineoplastic Immunomodulating Agent D020011 - Protective Agents > D000975 - Antioxidants > D024505 - Tocopherols C274 - Antineoplastic Agent
(3R)-21-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]-3-hydroxyhenicosanoic acid
Rubiyunnanol C
A pentacyclic triterpenoid of the class of arborinane-type terpenoids isolated from the roots of Rubia yunnanensis.
(3R,20R)-20-[(3,6-dideoxy-alpha-L-arabino-hexopyranosyl)oxy]-3-hydroxyheneicosanoic acid
(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].
1,2-Bis(trimethylsilyloxy)-3-octadecyloxypropane
C27H60O3Si2 (488.40807699999993)
(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
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.
(2α,3α)-2,3,24-Trihydroxyurs-12-en-28-oic acid
[1-hydroxy-3-[(5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenoxy]propan-2-yl] octanoate
[1-[(7Z,10Z,13Z,16Z,19Z)-docosa-7,10,13,16,19-pentaenoxy]-3-hydroxypropan-2-yl] hexanoate
[1-hydroxy-3-[(9Z,12Z,15Z,18Z,21Z)-tetracosa-9,12,15,18,21-pentaenoxy]propan-2-yl] butanoate
[1-[(11Z,14Z,17Z,20Z,23Z)-hexacosa-11,14,17,20,23-pentaenoxy]-3-hydroxypropan-2-yl] acetate
(1-hydroxy-3-octoxypropan-2-yl) (5Z,8Z,11Z,14Z,17Z)-icosa-5,8,11,14,17-pentaenoate
(1-decoxy-3-hydroxypropan-2-yl) (3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoate
[1-hydroxy-3-[(3Z,6Z,9Z,12Z,15Z)-octadeca-3,6,9,12,15-pentaenoxy]propan-2-yl] decanoate
[3-carboxy-2-[(8E,11E,14E,17E,20E)-tricosa-8,11,14,17,20-pentaenoyl]oxypropyl]-trimethylazanium
C30H50NO4+ (488.37396400000006)
(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
[1-Carboxy-3-(3-heptadecanoyloxy-2-hydroxypropoxy)propyl]-trimethylazanium
[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
[1-Carboxy-3-(3-propanoyloxy-2-tridecanoyloxypropoxy)propyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
[3-(3-Butanoyloxy-2-dodecanoyloxypropoxy)-1-carboxypropyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
[1-Carboxy-3-(3-pentanoyloxy-2-undecanoyloxypropoxy)propyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
[3-(3-Acetyloxy-2-tetradecanoyloxypropoxy)-1-carboxypropyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
[1-Carboxy-3-(2-decanoyloxy-3-hexanoyloxypropoxy)propyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
[1-Carboxy-3-(3-heptanoyloxy-2-nonanoyloxypropoxy)propyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
[1-Carboxy-3-[2,3-di(octanoyloxy)propoxy]propyl]-trimethylazanium
C26H50NO7+ (488.35870900000003)
2-[carboxy-[3-[(Z)-hexadec-9-enoyl]oxy-2-hydroxypropoxy]methoxy]ethyl-trimethylazanium
C26H50NO7+ (488.35870900000003)
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.
DG(28:5)
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methyl 3-[(3s,3ar,5as,6s,7s,9ar,9br)-3-[(2s,4e)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
(1s,6r,8s,9r,11r,12s,15s,16r,19r,20s,21r)-8,9,19-trihydroxy-20-(hydroxymethyl)-1,7,7,11,16,20-hexamethylpentacyclo[13.8.0.0³,¹².0⁶,¹¹.0¹⁶,²¹]tricos-3-en-5-one
(1s,2r,4as,6as,6br,8ar,9s,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid
8,10-dihydroxy-9-(hydroxymethyl)-2,2,4a,6b,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-6a-carboxylic acid
(1r,3s,6ar,6bs,7s,8ar,11r,12s,12ar,14r,14bs)-14-methoxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1h-picene-1,3,7-triol
(1s,3as,5ar,9ar,9br,11as)-1-[(2r,3s,5r)-5-[(1r)-1,2-dihydroxy-2-methylpropyl]-2-hydroxyoxolan-3-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(4as,6as,6br,10s,12ar)-10-hydroxy-9,9-bis(hydroxymethyl)-2,2,6a,6b,12a-pentamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
(2z,6r)-6-[(3r,3ar,6s,7r,9br)-6-(2-carboxyethyl)-7-(2-hydroxypropan-2-yl)-3a,6,9b-trimethyl-1h,2h,3h,4h,5h,7h,8h,9h-cyclopenta[a]naphthalen-3-yl]-2-methylhept-2-enoic acid
(1s,2r,4as,6as,6br,8ar,9r,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid
methyl 3-[(3s,3ar,5ar,6s,7s,9ar,9br)-3-[(2r,5s)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
(9e)-2,29-diaminotriaconta-5,9,11,14,17,20-hexaene-3,8,28-triol
C30H52N2O3 (488.39777219999996)
3-methyl-6-(1-{4,7,10-trihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl}ethyl)oxan-2-one
methyl (2s)-2-[(3s,3as,5ar,5br,7ar,9s,11ar,11bs,13ar,13bs)-9-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl]-2-hydroxypropanoate
(1s,3as,5ar,6s,9r,9ar,9bs,11as)-1-[(2s,4r)-4-[(2s)-3,3-dimethyloxiran-2-yl]-4-hydroxybutan-2-yl]-9-hydroxy-6-(hydroxymethyl)-3a,6,9a,11a-tetramethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(1s,2r,4ar,6as,6br,8r,8ar,10s,12ar,12br,14bs)-8,10,14b-trihydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-1,2,3,4,5,6,7,8,8a,10,11,12,12b,13-tetradecahydropicene-2-carboxylic acid
(4as,6as,6br,8ar,9r,12ar,12br,14bs)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid
(1s,3as,5ar,9ar,11as)-3a,6,6,9a,11a-pentamethyl-1-[(2s,5s,6r)-5,6,7-trihydroxy-6-methylheptan-2-yl]-1h,2h,3h,5h,5ah,8h,9h,10h,11h-cyclopenta[a]phenanthrene-4,7-dione
(1s,3s,4s,6s,7s,8r,11s,12s,15r,16r)-4,6-dihydroxy-15-[(2r,5r)-5-hydroxy-6-methylhept-6-en-2-yl]-7,12,16-trimethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane-7-carboxylic acid
methyl 3-[(3s,3ar,5ar,6s,7s,9ar,9br)-3-[(2s,4e)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
(1s,2r,8r,12s,14s)-6-[(1r)-1,2-dihydroxy-2-methylpropyl]-12-hydroxy-1,2,8,14,18,18-hexamethyl-5-oxapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁴,¹⁹]henicos-9-en-17-one
(1r,2s,3as,3bs,4r,7s,9ar,9bs,10s,11as)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-4,7,10-trihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-2-yl acetate
1-[5-(1,2-dihydroxy-2-methylpropyl)-2-hydroxyoxolan-3-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(1r,3as,3bs,7r,9s,9ar,9bs,10r,11as)-7,9,10-trihydroxy-9a-methyl-1-[(1r)-1-[(1s,2r)-2-methyl-2-[(2r)-3-methylbutan-2-yl]cyclopropyl]ethyl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthrene-11a-carboxylic acid
5-hydroxy-1-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-3a,3b,6,6,9a-pentamethyl-decahydro-1h-cyclopenta[a]phenanthrene-7,11-dione
2,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14-tetradecahydropicene-4a-carboxylic acid
8-acetyl-9-(acetyloxy)-1-ethyl-1,4a,6a,10b-tetramethyl-tetradecahydrochrysen-6-yl acetate
(1s,2r,4as,6as,6br,8as,10r,11s,12r,12ar,12bs,14bs)-10,11,12-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid
5,10-dihydroxy-4a-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-2-carboxylic acid
(1s,3r,6s,8r,11s,12s,15r,16r)-15-[(2r)-5,5-dimethoxypentan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl acetate
2-[(3r,3ar,3br,5ar,6r,7r,9ar,9br,11s,11as)-6-(carboxymethyl)-11-hydroxy-6,9a,9b,11a-tetramethyl-3-(prop-1-en-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-7-yl]-2-methylpropanoic acid
(1s,4s,5r,6s,9s,10r,12r,14r)-4-(decyloxy)-5,6-dihydroxy-7-(hydroxymethyl)-3,11,11,14-tetramethyltetracyclo[7.5.1.0¹,⁵.0¹⁰,¹²]pentadeca-2,7-dien-15-one
methyl 3-[(1s,4r,5r,8s,9s,11s,12s,13r)-12-ethenyl-5-[(2r,5r)-5-hydroperoxy-6-methylhept-6-en-2-yl]-11-hydroxy-4,8-dimethyltetracyclo[7.5.0.0¹,¹³.0⁴,⁸]tetradecan-13-yl]propanoate
(1s,1's,2r,4r,9'r,10'r,15's)-4-(2-hydroxypropan-2-yl)-1,9',10',14',14'-pentamethyl-3,7,16'-trioxaspiro[bicyclo[2.2.1]heptane-2,6'-pentacyclo[13.2.2.0¹,¹³.0²,¹⁰.0⁵,⁹]nonadecan]-15'-ol
7,10-dihydroxy-1-(2-hydroxy-6-methyl-4-oxohept-5-en-2-yl)-3a,3b,6,6,9a-pentamethyl-dodecahydrocyclopenta[a]phenanthren-8-one
methyl 3-[(3s,3ar,5as,6s,7s,9ar,9br)-3-[(2s,5s)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
(1s,4s,5r,8r,10s,11r,13r,14r,16r,17s,18r,19s,20r)-10,11,16-trihydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosan-23-one
(2r,5z)-2-[(1r,3s,3ar,5ar,7s,9as,11ar)-3,7-dihydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-7-hydroxy-6-methylhept-5-enoic acid
(1s,2r,4as,6as,6br,8ar,9r,10r,11r,12ar,14bs)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid
(2r,4ar,6as,6br,8ar,10s,11r,12ar,12br,14bs)-10,11-dihydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
(3s,4r,4ar,6ar,6bs,8as,12as,14r,14ar,14bs)-4,8a-bis(hydroxymethyl)-14-methoxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol
(3s,5r)-5-[(1s,3ar,3bs,5ar,9as,9bs,10s)-10-hydroxy-3a,3b,6,6,9a-pentamethyl-7-oxo-1h,2h,3h,4h,5h,5ah,8h,9h,9bh,10h-cyclopenta[a]phenanthren-1-yl]-3-hydroxy-2,2-dimethylhexanoic acid
(1s,2r,4s,6s,8r,12s,13s,14s,19r)-6-[(1r)-1,2-dihydroxy-2-methylpropyl]-12-hydroxy-1,2,8,14,18,18-hexamethyl-5-oxapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁴,¹⁹]henicos-9-en-17-one
(1s,4s,5r,8s,11r,13r,14s,17r,18s,20r,21r,24r)-20,21-dihydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosane-11-carboxylic acid
(1r,3ar,5r,7s,9ar,9br,11ar)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-5a,7,9b-trihydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,5h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-5-yl acetate
(2s)-2-[(3r,3as,5as,5br,7ar,9r,10s,11ar,11br,13br)-3,9,10-trihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1h,2h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysen-3-yl]propanoic acid
8,10-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-4a-carboxylic acid
5,10-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
(1s,3as,5ar,9ar,9br,11as)-1-[(2r,3s,5r)-5-[(1s)-1,2-dihydroxy-2-methylpropyl]-2-hydroxyoxolan-3-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(1r,4as,6as,6br,8as,12ar,12bs,14br)-1,8,10-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
1,10-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
12-oleanene-3,11,16,23,28-pentol; (3β,11α,16β)-form,11-ketone
{"Ingredient_id": "HBIN000933","Ingredient_name": "12-oleanene-3,11,16,23,28-pentol; (3\u03b2,11\u03b1,16\u03b2)-form,11-ketone","Alias": "NA","Ingredient_formula": "C30H48O5","Ingredient_Smile": "NA","Ingredient_weight": "488.7","OB_score": "NA","CAS_id": "75027-36-0","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "9356","PubChem_id": "NA","DrugBank_id": "NA"}
15α-hydroxymollic acid
{"Ingredient_id": "HBIN001615","Ingredient_name": "15\u03b1-hydroxymollic acid","Alias": "NA","Ingredient_formula": "C30H48O5","Ingredient_Smile": "CC(CCC=C(C)C)C1CC(C2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "39031","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
16α-hydroxymollic acid
{"Ingredient_id": "HBIN001807","Ingredient_name": "16\u03b1-hydroxymollic acid","Alias": "NA","Ingredient_formula": "C30H48O5","Ingredient_Smile": "CC(CCC=C(C)C)C1C(CC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C(=O)O)O)O)C)C)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "39030","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
(20s)-3β-acetoxy-20-hydroperoxy-30-norlupane
{"Ingredient_id": "HBIN003493","Ingredient_name": "(20s)-3\u03b2-acetoxy-20-hydroperoxy-30-norlupane","Alias": "NA","Ingredient_formula": "C31H52O4","Ingredient_Smile": "Not Available","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "202","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
2,3,24-trihydroxy-12-oleanen-28-oic acid; (2α,3α)-form
{"Ingredient_id": "HBIN003824","Ingredient_name": "2,3,24-trihydroxy-12-oleanen-28-oic acid; (2\u03b1,3\u03b1)-form","Alias": "NA","Ingredient_formula": "C30H48O5","Ingredient_Smile": "NA","Ingredient_weight": "488.7","OB_score": "NA","CAS_id": "88586-19-0","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "9001","PubChem_id": "NA","DrugBank_id": "NA"}
15-(5,5-dimethoxypentan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-yl acetate
methyl 3-[3-(2,6-dihydroxy-6-methylhept-4-en-2-yl)-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
methyl (1s,2r,4as,6ar,6br,8ar,9r,10s,12ar,12br,14ar,14bs)-10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-hexadecahydro-1h-picene-4a-carboxylate
(1r,9s,10r,16r)-16-methyl-4-[(1r,2r,5s,7r,9s,10r,16r)-16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadecan-5-yl]-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadeca-2,4,6-triene
methyl 5-hydroxy-6-{7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl}-2-methylheptanoate
methyl 2-hydroxy-2-{9-hydroxy-5a,5b,8,8,11a,13b-hexamethyl-hexadecahydrocyclopenta[a]chrysen-3-yl}propanoate
1-(4,5-dihydroxy-6-methoxy-6-methylheptan-2-yl)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl hexadecanoate
methyl 3-[(3s,3ar,5ar,6s,7s,9ar,9br)-3-[(2s,5r)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
(1r,3as,5ar,9ar,9bs,11as)-1-(4,5-dihydroxy-6-methoxy-6-methylheptan-2-yl)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
3-[4-hydroxy-3-(2-hydroxy-6-methyl-5-methylideneheptan-2-yl)-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
n-[(6s,8r,11r,12s,15s,16r)-15-[(1s)-1-(dimethylamino)ethyl]-7,7,12,16-tetramethyltetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-6-yl]benzenecarboximidic acid
C33H48N2O (488.37664379999995)
henicosyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
(1r,3s,6ar,6bs,8as,11r,12s,12as,14r,14bs)-8a-(hydroxymethyl)-14-methoxy-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1h-picene-1,3-diol
14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one
methyl 6-hydroxy-2-{7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl}-6-methylheptanoate
(1r,3ar,5ar,5br,7ar,9r,11ar,11br,13ar,13bs)-1-[(1s)-1-hydroperoxyethyl]-3a,5a,5b,8,8,11a-hexamethyl-hexadecahydrocyclopenta[a]chrysen-9-yl acetate
16-methyl-4-{16-methyl-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadecan-5-yl}-6,14-diazatetracyclo[7.5.3.0¹,¹⁰.0²,⁷]heptadeca-2,4,6-triene
3-[(3s,3ar,4r,5ar,6s,7s,9ar,9br)-4-hydroxy-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
4-carbamimidamidobutyl (1r,6r,10s)-10-heptyl-6-pentyl-7,9,12-triazatricyclo[6.3.1.0⁴,¹²]dodeca-4,8-diene-5-carboxylate
C27H48N6O2 (488.38385479999994)
methyl 10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-hexadecahydro-1h-picene-4a-carboxylate
6-(hydroxymethyl)-1-(6-methoxy-6-methylhept-4-en-2-yl)-3a,6,9b,11a-tetramethyl-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthrene-4,7-diol
(1s,3r,8r,11s,12s,14s,15r,16r)-15-(4,5-dihydroxy-5,6-dimethylheptan-2-yl)-14-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-one
(1s,3s,4r,8s,9r,11s,12r)-6,6,9-trimethyl-2,13-dioxapentacyclo[9.3.0.0¹,³.0⁴,⁸.0⁹,¹¹]tetradecan-12-yl hexadecanoate
(2s,3r,5z,8r,9e,11z,14z,17z,20z,28r,29s)-2,29-diaminotriaconta-5,9,11,14,17,20-hexaene-3,8,28-triol
C30H52N2O3 (488.39777219999996)
methyl (2s)-2-[(1s,3as,5ar,7r,9as,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-6-hydroxy-6-methylheptanoate
(1s,3as,5ar,9ar,9br,11as)-1-[(2s,4r,5s)-4,5-dihydroxy-6-methoxy-6-methylheptan-2-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
4-carbamimidamidobutyl (6r,10s)-10-heptyl-6-pentyl-7,9,12-triazatricyclo[6.3.1.0⁴,¹²]dodeca-4,8-diene-5-carboxylate
C27H48N6O2 (488.38385479999994)
methyl 3-[(3s,3ar,5as,6s,7s,9ar,9br)-3-[(2s,5r)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoate
4,8a-bis(hydroxymethyl)-14-methoxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol
(1s,2s,4ar,9ar)-1-hydroxy-2,6,6,9a-tetramethyl-1-{2-[(1r,4r,5s,6s,9r)-4,5,10,10-tetramethyl-11,12-dioxatricyclo[7.2.1.0¹,⁶]dodecan-5-yl]ethyl}-hexahydro-2h-benzo[7]annulen-7-one
(2r,3s,5z,9e,11z,14z,17z,20z,28s,29r)-2,29-diaminotriaconta-5,9,11,14,17,20-hexaene-3,8,28-triol
C30H52N2O3 (488.39777219999996)
methyl (2r,5s,6s)-6-[(1r,3ar,5ar,7r,9as,11ar)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl]-5-hydroxy-2-methylheptanoate
(1r,3s,4r,7s,9r,12s,14s,17s,19r,22s)-14,19-dihydroxy-7-methoxy-4,8,8,12,18,18,22-heptamethylpentacyclo[12.9.0.0³,¹².0⁴,⁹.0¹⁷,²²]tricosan-23-one
3-[(3s,3as,4r,5ar,6s,7s,9ar,9br)-4-hydroxy-3-[(2s)-2-hydroxy-6-methyl-5-methylideneheptan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
(1r,3as,3br,4s,6s,7s,9as,9bs,11ar)-6-(hydroxymethyl)-1-[(2r,4e)-6-methoxy-6-methylhept-4-en-2-yl]-3a,6,9b,11a-tetramethyl-1h,2h,3h,3bh,4h,7h,8h,9h,9ah,10h,11h-cyclopenta[a]phenanthrene-4,7-diol
henicosyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate
methyl 3-{3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-6,9a,9b-trimethyl-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl}propanoate
n-{15-[1-(dimethylamino)ethyl]-7,7,12,16-tetramethyltetracyclo[9.7.0.0³,⁸.0¹²,¹⁶]octadeca-1(18),2-dien-6-yl}benzenecarboximidic acid
C33H48N2O (488.37664379999995)
(2r,3s,4z,7s,8e,11z,14z,17z,20z,28s,29r)-2,29-diaminotriaconta-4,8,11,14,17,20-hexaene-3,7,28-triol
C30H52N2O3 (488.39777219999996)