Exact Mass: 456.37155879999995
Exact Mass Matches: 456.37155879999995
Found 500 metabolites which its exact mass value is equals to given mass value 456.37155879999995,
within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error
0.01 dalton.
Ganodermatriol
Ganodermatriol is found in mushrooms. Ganodermatriol is a constituent of Ganoderma lucidum (reishi).
Ganoderic acid Z
Ganoderic acid Z is found in mushrooms. Ganoderic acid Z is isolated from Ganoderma lucidum (reishi). Isolated from Ganoderma lucidum (reishi). Ganoderic acid Z is found in mushrooms.
Oxyallobetulin
Oxyallobetulin is found in fruits. Oxyallobetulin is isolated from Diospyros lotus (date plum).
Katonic acid
Katonic acid is found in fruits. Katonic acid is a constituent of Sandoricum koetjape (santol) Constituent of Sandoricum koetjape (santol). Katonic acid is found in fruits.
3-Hydroxycycloart-24-en-21-oic acid
3-Hydroxycycloart-24-en-21-oic acid is found in fruits. 3-Hydroxycycloart-24-en-21-oic acid is a constituent of Lansium domesticum (langsat). Constituent of Lansium domesticum (langsat). 3-Hydroxycycloart-24-en-21-oic acid is found in fruits.
Lucidadiol
Lucidadiol is found in mushrooms. Lucidadiol is isolated from Ganoderma lucidum (reishi).
Epoxyganoderiol C
Epoxyganoderiol C is found in mushrooms. Epoxyganoderiol C is a metabolite of Ganoderma lucidum (reishi Metabolite of Ganoderma lucidum (reishi). Epoxyganoderiol C is found in mushrooms.
DG(12:0/12:0)
DG(12:0/12:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(12:0/12:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
3beta-Hydroxy-28,13-ursanolide
3beta-Hydroxy-28,13-ursanolide is found in herbs and spices. 3beta-Hydroxy-28,13-ursanolide is isolated from Helichrysum italicum (curry plant). Isolated from Helichrysum italicum (curry plant). Ursolic acid lactone is found in tea and herbs and spices.
Bryonolic acid
Constituent of Sandoricum indicum (santol). Bryonolic acid is found in many foods, some of which are olive, calabash, towel gourd, and fruits. Bryonolic acid is found in calabash. Bryonolic acid is a constituent of Sandoricum indicum (santol).
Ganodermanondiol
Ganodermanondiol is found in mushrooms. Ganodermanondiol is a constituent of Ganoderma lucidum (reishi). Constituent of Ganoderma lucidum (reishi). Ganodermanondiol is found in mushrooms.
Sandosapogenol
Sapogenin from French bean (Phaseolus vulgaris) seed. Sandosapogenol is found in pulses, yellow wax bean, and green bean. Sandosapogenol is found in pulses. Sapogenin from French bean (Phaseolus vulgaris) see
(+-)-Ethyl 3-hydroxy-2-methylbutyrate
(+-)-Ethyl 3-hydroxy-2-methylbutyrate is used as a food additive [EAFUS] ("EAFUS: Everything Added to Food in the United States. [http://www.eafus.com/]") It is used as a food additive .
3-Epikatonic acid
3-Epikatonic acid is found in pulses. 3-Epikatonic acid is a constituent of Cyamopsis tetragonoloba (guar) Constituent of Cyamopsis tetragonoloba (guar). 3-Epikatonic acid is found in pulses.
Trametenolic acid B
Trametenolic acid B is found in mushrooms. Trametenolic acid B is a metabolite of Ganoderma tsugae (red reishi Metabolite of Ganoderma tsugae (red reishi). Trametenolic acid B is found in mushrooms. Trametenolic acid is a lanostanol glycoside that isolated from the EtOH extract of the fruit bodies of Laetiporus versisporus[1]. Trametenolic acid is a lanostanol glycoside that isolated from the EtOH extract of the fruit bodies of Laetiporus versisporus[1].
11-Deoxoglycyrrhetinic acid
11-Deoxoglycyrrhetinic acid is found in herbs and spices. 11-Deoxoglycyrrhetinic acid is isolated from roots of Glycyrrhiza glabra (licorice Isolated from roots of Glycyrrhiza glabra (licorice). 11-Deoxoglycyrrhetinic acid is found in tea and herbs and spices.
Carissic acid
Ustiloxin E is found in cereals and cereal products. Ustiloxin E is isolated from the false smut balls caused by Ustilaginoidea virens on rice. Constituent of Carissa carandas (karanda). Carissic acid is found in beverages and fruits.
DG(8:0/16:0/0:0)
DG(8:0/16:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(8:0/16:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/16:0)
DG(8:0/0:0/16:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(8:0/i-16:0/0:0)
DG(8:0/i-16:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(8:0/i-16:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(8:0/0:0/i-16:0)
DG(8:0/0:0/i-16:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(10:0/14:0/0:0)
DG(10:0/14:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(10:0/14:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(10:0/0:0/14:0)
DG(10:0/0:0/14:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(10:0/i-14:0/0:0)
DG(10:0/i-14:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(10:0/i-14:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(10:0/0:0/i-14:0)
DG(10:0/0:0/i-14:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(12:0/0:0/12:0)
DG(12:0/0:0/12:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(i-12:0/12:0/0:0)
DG(i-12:0/12:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(i-12:0/12:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(i-12:0/0:0/12:0)
DG(i-12:0/0:0/12:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(i-12:0/i-12:0/0:0)
DG(i-12:0/i-12:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(i-12:0/i-12:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(i-12:0/0:0/i-12:0)
DG(i-12:0/0:0/i-12:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(12:0/i-12:0/0:0)
DG(12:0/i-12:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(12:0/i-12:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(12:0/0:0/i-12:0)
DG(12:0/0:0/i-12:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(14:0/10:0/0:0)
DG(14:0/10:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(14:0/10:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(14:0/0:0/10:0)
DG(14:0/0:0/10:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(i-14:0/10:0/0:0)
DG(i-14:0/10:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(i-14:0/10:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(i-14:0/0:0/10:0)
DG(i-14:0/0:0/10:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(16:0/8:0/0:0)
DG(16:0/8:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(16:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(16:0/0:0/8:0)
DG(16:0/0:0/8:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
DG(i-16:0/8:0/0:0)
DG(i-16:0/8:0/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(i-16:0/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
DG(i-16:0/0:0/8:0)
DG(i-16:0/0:0/8:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
Epibetulinic acid
Betulinic acid is a naturally occurring pentacyclic triterpenoid which has anti-retroviral, anti-malarial, and anti-inflammatory properties, as well as a more recently discovered potential as an anticancer agent, by inhibition of topoisomerase. It is found in the bark of several species of plants, principally the white birch (Betula pubescens) from which it gets its name, but also the Ber tree (Ziziphus mauritiana), the tropical carnivorous plants Triphyophyllum peltatum and Ancistrocladus heyneanus, Diospyros leucomelas a member of the persimmon family, Tetracera boiviniana, the jambul (Syzygium formosanum), flowering quince (Chaenomeles sinensis), Rosemary, and Pulsatilla chinensis.; Controversial is a role of p53 in betulinic acid-induced apoptosis. Fulda suggested p53-independent mechanism of the apoptosis, basing on fact of no accumulation of wild-type p53 detected upon treatment with the betulinic acid, whereas wild-type p53 protein strongly increased after treatment with doxorubicin. The suggestion is supported by study of Raisova. On the other hand Rieber suggested that betulinic acid exerts its inhibitory effect on human metastatic melanoma partly by increasing p53. Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4]. Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4].
b-Boswellic acid
Constituent of frankincense (Boswellia subspecies) and olibanum oil β-Boswellic acid is isolated from the gum resin of Boswellia serrata. β-Boswellic acid is a nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation[1]. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells[2]. β-Boswellic acid is isolated from the gum resin of Boswellia serrata. β-Boswellic acid is a nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation[1]. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells[2]. β-Boswellic acid is isolated from the gum resin of Boswellia serrata. β-Boswellic acid is a nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation[1]. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells[2].
Nandrolone laurate
Testosterone undecanoate
Xyloketal
alpha-Boswellic acid
alpha-Boswellic acid is a natural product found in Cyclocarya paliurus, Boswellia sacra, and other organisms with data available. alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpene compound from extracts of Frankincense, has anticonvulsant and anti-cancer properties[1]. alpha-Boswellic acid prevents and decreases the progression of Alzheimer’s hallmarks in vivo and can be used for Alzheimer’s disease research[2]. alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpene compound from extracts of Frankincense, has anticonvulsant and anti-cancer properties[1]. alpha-Boswellic acid prevents and decreases the progression of Alzheimer’s hallmarks in vivo and can be used for Alzheimer’s disease research[2]. alpha-Boswellic acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=471-66-9 (retrieved 2024-08-21) (CAS RN: 471-66-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Gadermandiol
Ganodermanondiol is a triterpenoid. (5R,10S,13R,14R,17R)-17-[(2R,5S)-5,6-dihydroxy-6-methylheptan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,12,15,16,17-octahydrocyclopenta[a]phenanthren-3-one is a natural product found in Ganoderma lucidum with data available.
Merotaine
3-Epiursolic acid is a natural product found in Pavetta indica, Conandron ramondioides, and other organisms with data available. 3-Epiursolic Acid is a triterpenoid that can be isolated from Eriobotrya japonica, acts as a competitive inhibitor of cathepsin L (IC50, 6.5 μM; Ki, 19.5 μM), with no obvious effect on cathepsin B[1]. 3-Epiursolic Acid is a triterpenoid that can be isolated from Eriobotrya japonica, acts as a competitive inhibitor of cathepsin L (IC50, 6.5 μM; Ki, 19.5 μM), with no obvious effect on cathepsin B[1].
α-Boswellic acid
alpha-Boswellic acid is a natural product found in Cyclocarya paliurus, Boswellia sacra, and other organisms with data available. alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpene compound from extracts of Frankincense, has anticonvulsant and anti-cancer properties[1]. alpha-Boswellic acid prevents and decreases the progression of Alzheimer’s hallmarks in vivo and can be used for Alzheimer’s disease research[2]. alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpene compound from extracts of Frankincense, has anticonvulsant and anti-cancer properties[1]. alpha-Boswellic acid prevents and decreases the progression of Alzheimer’s hallmarks in vivo and can be used for Alzheimer’s disease research[2].
α-boswellic acid
alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpene compound from extracts of Frankincense, has anticonvulsant and anti-cancer properties[1]. alpha-Boswellic acid prevents and decreases the progression of Alzheimer’s hallmarks in vivo and can be used for Alzheimer’s disease research[2]. alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpene compound from extracts of Frankincense, has anticonvulsant and anti-cancer properties[1]. alpha-Boswellic acid prevents and decreases the progression of Alzheimer’s hallmarks in vivo and can be used for Alzheimer’s disease research[2].
Ursolic acid lactone
Ursolic Acid
Origin: Plant; SubCategory_DNP: Triterpenoids relative retention time with respect to 9-anthracene Carboxylic Acid is 1.636 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.640 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.638 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.642 Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy.
Niloticin
CC12CCC(O)C(C)(C)C1CCC(C1(C)CC3=O)(C)C2CCC11OCC32CCC(C)(C)CC21
Secaubryenol
Bacosine
[Raw Data] CBA75_Bacosine_neg_50eV.txt [Raw Data] CBA75_Bacosine_neg_40eV.txt [Raw Data] CBA75_Bacosine_neg_30eV.txt [Raw Data] CBA75_Bacosine_neg_20eV.txt [Raw Data] CBA75_Bacosine_neg_10eV.txt
Lansiolic acid
A triterpenoid of the class of onoceranoid-type terpenoids isolated from the twigs of Lansium domesticum.
Ganodermanondiol
14beta,15beta-Epoxy-21beta-hydroxyserratan-3-one
Anwuweizic acid
Isomangiferolic acid
3-Hydroxycycloart-24-en-21-oic acid
(23Xi)-3alpha,23-dihydroxy-tirucalla-7,24-dien-21-al
(12beta,23E)-12,20-dihydroxydammara-23,25-dien-3-one|cylindrictone A
4,4-Dimethyl-24-methylenecholesta-8,14-diene-3,11,12-triol
(24Z)-3a-oxa-3a-homo-27-hydroxy-7,24-tirucalladien-3-one
(22R)-22-hydroxy-24-methylene-3-norlanost-8-en-28-oic acid|gilvsin D
3alpha-hydroxy-bauer-7-en-28-oic acid|Myrtifolsaeure
D:A-Friedooleanane-1,3-dione, 7-hydroxy-, (7.alpha.)-
3beta-hydroxylup-20(29)-en-30-oic acid|betulinic acid
(4aR,6aR,6aR,6bR,8aR,10S,12aR,14bR)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid
(22alpha,20?鈥?-form-20,29-Epoxy-22-hydroxy-3-lupanone
(3beta)-3-hydroxy-18(13->12beta)-abeo-lanosta-13(17),24-dien-18-oic acid|(3beta,5alpha,12beta)-17-[(1R)-1,5-dimethylhex-4-en-1-yl]-3-hydroxy-4,4,10,14-tetramethylgon-13(17)-ene-12-carboxylic acid|fornicatin C
D:A-friedo-3-oxo-oleanane-27-carboxylic acid|Trichadonic acid
20(R)-21,24-Cyclo-3??,25-dihydroxyldammar-23(24)-en-21-one
21beta-hydroxy-3,4-seco-lupa-4(23),20(29)-dien-3-oic acid|lippiolic acid
3-[(3S,3aR,5aR,6S,7S,9aR,9bR)-6,9a,9b-trimethyl-3-[(2S,5S)-2-methyl-5-prop-1-en-2-yloxolan-2-yl]-7-prop-1-en-2-yl-1,2,3,3a,4,5,5a,7,8,9-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
28,30-dihydroxy-3-oxolup-20(29)-ene|28,30-dihydroxylup-20(29)-en-3-one|28,30-dihydroxylup-20(29)-ene-3-one
3beta-hydroxy-D:A-friedo-oleanan-27,16alpha-lactone
3beta,11alpha-dihydroxy-4alpha,14alpha-dimethyl-5alpha-ergosta-8,24(28)-dien-7-one
3beta,24-dihydroxyolean-12-en-21-one|Soyasapogenol-E
(22R)-3beta,22-dihydroxylanosta-8,24-dien-11-one|3beta,22-dihydroxylanosta-8,24-dien-11-one|inonotsuoxodiol A
3,4-seco-cycloart-4(29),25-dien-24-hydroxy-3-oic acid|coccinetane F
3-oxo-D:A-friedooleanan-28-oic acid|3-oxofriedelan-28-oic acid|7beta-hydroxy-3-oxofriedelan-28-oic acid|canophyllic acid|Friedelin-28-saeure|oxocanophyllic acid
26-hydroxy-1,3-friedelanedione|26-hydroxyfriedelane-1,3-dione
(14beta,21beta)-14,26-Epoxy-21-hydroxy-3-serratanone|21beta-hydroxy-14beta,26-epoxy-serratane-3-one
3beta,7alpha-dihydroxy-4alpha,14alpha-dimethyl-5alpha-ergosta-8,24(28)-dien-11-one
(6Z)-5-(23-Cyano-23-hydroxy-6-tricosenyl)pyrrole-2-carboxaldehyde|(Z)-5-(23-Cyano-23-hydroxy-6-tricosenyl)-2-pyrrolecarboxaldehyde
C29H48N2O2 (456.37155879999995)
3-beta-28-Carboxylic acid-12-Lupen-3,28-diol|3beta-3-Hydroxy-12-lupen-28-oic acid
12,13-dihydromicromeric acid|18betaH-urs-20(30)-en-3beta-ol-28-oic acd
1alpha,3beta-dihydroxy-5alpha-cycloart-24-en-23-one|thailandiol
(23R,25R)-3alpha-Hydroxy-9,19-cyclo-9beta-lanostan-26,23-olide
(+)-lanosta-7,9(11),24-trien-3beta,15alpha,21-triol|pinicolol B
Buxaminol-E-(N-isopropylidenderivat)|Buxaminol-E-
C29H48N2O2 (456.37155879999995)
(3beta,23R)-cucurbita-5,24-dien-7-one-3,23-diol|balsaminol E
(3beta,22beta)-3,22-Dihydroxy-13(18)-oleanen-11-one|Abrisapogenol J
betulinic acid
Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4]. Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4].
24-(E)-3-oxo-dammara-6-beta-hydroxy-20,24-dien-26-ol
(20R)-28-hydroxy-3-oxolupan-30-al|(20R)-28-hydroxylupan-30-al-3-one
5alpha,8alpha-epidioxy-24(xi)-methylcholesta-6,22-diene-3beta-ol
(3beta,11beta)-3,11-dihydroxylanosta-8,24-dien-7-one
(13alpha,14beta,17alpha,20S,23R,24R)-l23,24-dihydroxyanosta-7,25-dien-3-one|23,24-Dihydroxy-9alpha-tirucall-7,25-dien-3-on|23,24-Dihydroxy-9alpha-tirucall-7,25-dien-3-on, Bourjotinolon B|bourjotinolone B
3beta-Hydroxy-lanost-8-en-7,11-dion|3beta-hydroxy-lanost-8-ene-7,11-dione|3beta-Hydroxy-lanosten-(8)-dion-(7.11)|7,11-dioxolanost-8-en-3beta-ol
(1beta,11alpha)-1,11-Dihydroxy-20(29)-lupen-3-one|(1beta,11alpha)-dihydroxy-lup-20(29)-en-3-one|1beta,11alpha-dihydroxylup-20(29)-en-3-one
24R-hydroxy-3,4-seco-9betaH-lanost-4(28),7,25(26)-trien-3-oic acid|seco-coccinic acid E
(3beta,21R,24S)-21,24-cyclolanosta-7,9(11)-diene-3,21,25-triol|(3beta,5alpha,17beta)-17-[(1R,2R,3S)-2-hydroxy-3-(1-hydroxy-1-methylethyl)cyclopentyl]-4,4,14-trimethylandrosta-7,9(11)-dien-3-ol|inonotsutriol C
(3beta,22alpha)-3,22-dihydroxytaraxast-20-en-30-al|3beta, 22alpha-dihydroxytaraxaster-20-en-30-al
11beta,21beta-dihydroxy-beta-amyrinone|11beta,21beta-dihydroxy-olean-12-en-3-one
23-oxo-8betaH-lanost-9(11)-en-3,4-olide|coccinilactone A
(16S,23S,24R)-23,24-epoxycycloartan-3-one-16,25-diol
3beta-3-Hydroxy-13(18)-oleanen-28-oic acid|3beta-hydroxy-olean-13(18)-en-28-oic acid|3beta-Hydroxy-olean-13(18)-en-28-saeure
(21RS,23R)-21,23-Epoxy-5alpha-cycloart-24-ene-3beta,21-diol
25-Hydroxy-friedelan-3,21-dion|25-hydroxy-friedelane-3,21-dione|25-hydroxyfriedelane-3,21-dione
6beta-6,28-Dihydroxy-20(29)-lupen-3-one|6beta-form-6,28-Dihydroxy-20(29)-lupen-3-one
23-oxo-3,4-seco-9betaH-lanost-4(28),7-dien-3-oic acid|seco-coccinic acid A
(3beta, 22R)-3, 22-Dihydroxylanosta-8, 24-dien-7-one
(22R)-cycloart-20,25-dien-2alpha,3beta,22alpha-triol
(21R,24R)-21,25-Dihydroxy-21,24-cyclo-5alpha-cycloartan-3-one
(24Z)-3beta,27-dihydroxy-7,24-tirucalladien-21-al|(24Z)-3??,27-Dihydroxy-7,24-tirucalladien-21-al
25-hydroxy-3-oxo-D:A-friedooleanan-28-al|3,28-dioxo-D:A-friedo-oleanan-25-ol
3beta-hydroxy-18alpha,19alpha-urs-20-en-28-oic acid|heterobetulinic acid
(22R)-cycloart-20,25-diene-2alpha,3beta,22alpha-triol
5alpha-[3(15),7(14),11(13)-trien]pentadecanyloxydihydroarteannuin B
4alpha-carboxy,4beta,14alpha-dimethyl-9beta,19-cyclo-5alpha-cholest-24-en-3beta-ol
betulic acid
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- is a natural product found in Euphorbia polygonifolia, Ternstroemia gymnanthera, and other organisms with data available. A lupane-type triterpene derivative of betulin which was originally isolated from BETULA or birch tree. It has anti-inflammatory, anti-HIV and antineoplastic activities. Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4]. Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4]. Epibetulinic acid exhibits potent inhibitory effects on NO and prostaglandin E2 (PGE2) production in mouse macrophages (RAW 264.7) stimulated with bacterial endotoxin with IC50s of 0.7 and 0.6 μM, respectively. Anti-inflammatory activity[1].
J7YR6A878I
20-epi-bryonolic acid is a pentacyclic triterpenoid of D:C-friedooleanane-type triterpenoids isolated from the stems of Lagenaria siceraria and roots of Coriaria intermedia and has been found to exhibit antineoplastic activity. It has a role as a metabolite and an antineoplastic agent. It is a pentacyclic triterpenoid and a hydroxy monocarboxylic acid. (2s,4As,6as,8ar,10s,12as,14as,14br)-10-hydroxy-2,4a,6a,9,9,12a,14a-heptamethyl-1,2,3,4,4a,5,6,6a,7,8,8a,9,10,11,12,12a,13,14,14a,14b-icosahydropicene-2-carboxylic acid is a natural product found in Benincasa hispida, Macaranga conifera, and other organisms with data available. A pentacyclic triterpenoid of D:C-friedooleanane-type triterpenoids isolated from the stems of Lagenaria siceraria and roots of Coriaria intermedia and has been found to exhibit antineoplastic activity.
Oleanic acid
relative retention time with respect to 9-anthracene Carboxylic Acid is 1.635 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.631 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.630 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.633 Oleanolic acid (Caryophyllin) is a natural compound from plants with anti-tumor activities. Oleanolic acid (Caryophyllin) is a natural compound from plants with anti-tumor activities.
b-Boswellic acid
β-Boswellic acid is isolated from the gum resin of Boswellia serrata. β-Boswellic acid is a nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation[1]. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells[2]. β-Boswellic acid is isolated from the gum resin of Boswellia serrata. β-Boswellic acid is a nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation[1]. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells[2]. β-Boswellic acid is isolated from the gum resin of Boswellia serrata. β-Boswellic acid is a nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation[1]. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells[2].
(1S,2R,4aS,6aS,6bR,10S,12aR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
(4aS,6aS,6bR,10S,12aR)-10-hydroxy-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
3-Hydroxy-12-oleanen-28-oic acid
Origin: Plant; SubCategory_DNP: Triterpenoids
(1S,2R,4aS,6aS,6bR,10S,12aR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid_59.3\\%
(1S,2R,4aS,6aS,6bR,10S,12aR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid_major
(1S,2R,4aS,6aS,6bR,10S,12aR)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid_64.2\\%
(4aS,6aS,6bR,10S,12aR)-10-hydroxy-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,10S,12aR)-10-hydroxy-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_minor
Testosterone Undecanoate
D006730 - Hormones, Hormone Substitutes, and Hormone Antagonists > D006728 - Hormones > D000728 - Androgens C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C1636 - Therapeutic Steroid Hormone C147908 - Hormone Therapy Agent > C548 - Therapeutic Hormone > C2360 - Anabolic Steroid
(5Z,7E,22E)-(1S,3R)-24a,24b,24c-trihomo-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,25-triol
(5Z,7E,22E)-(1S,3R)-26,27-dimethyl-24a-homo-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,25-triol
(5Z,7E,22E)-(1S,3R,20S)-26,27-dimethyl-24a-homo-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,25-triol
(5Z,7E,22Z)-(1S,3R,20S)-26,27-dimethyl-24a-homo-9,10-seco-5,7,10(19),22-cholestatetraene-1,3,25-triol
(5Z,7E)-(1S,3S)-1-hydroxymethyl-26,27-dimethyl-9,10-seco-5,7,10(19),16-cholestatetraene-3,25-diol
(5Z,7E)-(1R,3R)-1-hydroxymethyl-26,27-dimethyl-9,10-seco-5,7,10(19),16-cholestatetraene-3,25-diol
(5Z,7E,)-(1S,3R,20S)-20-butyl-21-nor-9,10-seco-5,7,10(19),16-cholestatetraene-1,3,25-triol
Sandosapogenol
(+-)-Ethyl 3-hydroxy-2-methylbutyrate
Katonic acid
Epikatonic acid
elemolic acid
3alpha-3-Hydroxytirucalla-7,24-dien-21-oic acid
Oxyallobetulin
Ganodermatriol
Epoxyganoderiol C
Trametenolic acid
Trametenolic acid is a lanostanol glycoside that isolated from the EtOH extract of the fruit bodies of Laetiporus versisporus[1]. Trametenolic acid is a lanostanol glycoside that isolated from the EtOH extract of the fruit bodies of Laetiporus versisporus[1].
Anaphalisoleanenoic acid
Bryonolic acid
Epi-Oleanolic Acid
3-Epioleanolic acid is an active component of Verbena officinalis Linn, with anti-inflammatory activity[1]. 3-Epioleanolic acid is an active component of Verbena officinalis Linn, with anti-inflammatory activity[1].
Carissic acid
Lucidadiol
3-Hydroxy-28,13-lupanolide
3-Epimasticadienolic acid
Combretanone C
A pentacyclic triterpenoid that is 9beta,19-cyclolanost-23-ene substituted by an oxo group at position 3 and hydroxy groups at positions 7 and 25. It has been isolated from the leaves of Combretum quadrangulare.
Combretanone D
A pentacyclic triterpenoid that is 9beta,19-cyclolanost-24-ene substituted by an oxo group at position 3 and hydroxy groups at positions 7 and 23. It has been isolated from the leaves of Combretum quadrangulare.
1alpha,25-dihydroxy-22,23-didehydro-24a,24b,24c-trihomovitamin D3
(22E)-1alpha,25-dihydroxy-26,27-dimethyl-22,23-didehydro-24a-homo-20-epivitamin D3
(22Z)-1alpha,25-dihydroxy-26,27-dimethyl-22,23-didehydro-24a-homo-20-epivitamin D3
(20S)-20-butyl-1alpha,25-dihydroxy-16,17-didehydro-21-norvitamin D3
11-Deoxoglycyrrhetinic acid
Maprounic acid
A pentacyclic triterpenoid isolated from Maprounea africana and has been shown to exhibit inhibitory activity against HIV-1 reverse transcriptase.
Androstan-17-one, 3-hydroxy-2,16-di-1-piperidinyl-,(2,3,5,16)-(9CI)
C29H48N2O2 (456.37155879999995)
Mairin
C308 - Immunotherapeutic Agent > C2139 - Immunostimulant Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4]. Betulinic acid is a natural pentacyclic triterpenoid, acts as a eukaryotic topoisomerase I inhibitor, with an IC50 of 5 μM, and possesses anti-HIV, anti-malarial, anti-inflammatory and anti-tumor properties[1][2][3][4].
Caryophyllin
Oleanolic acid (Caryophyllin) is a natural compound from plants with anti-tumor activities. Oleanolic acid (Caryophyllin) is a natural compound from plants with anti-tumor activities.
Urson
D018501 - Antirheumatic Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D016861 - Cyclooxygenase Inhibitors C274 - Antineoplastic Agent > C129839 - Apoptotic Pathway-targeting Antineoplastic Agent D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D002491 - Central Nervous System Agents > D000700 - Analgesics C26170 - Protective Agent > C275 - Antioxidant D000893 - Anti-Inflammatory Agents D000890 - Anti-Infective Agents D000970 - Antineoplastic Agents D004791 - Enzyme Inhibitors Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy. Ursolic acid (Prunol) is a natural pentacyclic triterpenoid carboxylic acid, exerts anti-tumor effects and is an effective compound for cancer prevention and therapy.
AIDS-085920
Masticadielic acid
Isolated from terebinth (Pistacia terebinthus). Masticadienolic acid is found in fruits.
Epiursolic acid
Carissic acid, also known as carissate, is a member of the class of compounds known as triterpenoids. Triterpenoids are terpene molecules containing six isoprene units. Carissic acid is practically insoluble (in water) and a weakly acidic compound (based on its pKa). Carissic acid can be found in beverages and fruits, which makes carissic acid a potential biomarker for the consumption of these food products. 3-Epiursolic Acid is a triterpenoid that can be isolated from Eriobotrya japonica, acts as a competitive inhibitor of cathepsin L (IC50, 6.5 μM; Ki, 19.5 μM), with no obvious effect on cathepsin B[1]. 3-Epiursolic Acid is a triterpenoid that can be isolated from Eriobotrya japonica, acts as a competitive inhibitor of cathepsin L (IC50, 6.5 μM; Ki, 19.5 μM), with no obvious effect on cathepsin B[1].
3-hydroxy-17-[(E)-7-hydroxy-6-methylhept-5-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-7-one
(2S,4aS,6aS,6bR,10S,12aS)-10-hydroxy-2-(hydroxymethyl)-2,4a,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,14b-dodecahydro-1H-picen-13-one
8,8,11,14,15,19,19-Heptamethyl-21-oxahexacyclo[18.2.2.01,18.02,15.05,14.06,11]tetracos-4-ene-9,20-diol
(3S,4S,10S,13R)-3-hydroxy-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-4-carboxylic acid
3beta,22S-dihydroxytirucalla-7,24-dien-23-one
A tirucallane triterpenoid that is tirucalla-7,24-diene substituted by hydroxy groups at positions 3 and 22 and an oxo group at position 23. It has been isolated from Dysoxylum lenticellatum.
(20r)-28-Hydroxylupen-30-al-3-one
A pentacyclic triterpenoid that is lupan-30-al with a hydroxy substituent at position 28 and an oxo group at position 3 (the 20R stereoisomer) . Isolated from Acacia mellifera, it exhibits cytotoxicity activity against the NSCLC-N6 cell line, derived from a human non-small-cell bronchopulmonary carcinoma.
3beta-Hydroxyurs-20-en-28-oic acid
A pentacyclic triterpenoid that is urs-20-ene substituted by a carboxy group at position 28 and a beta-hydroxy group at position 3. It has been isolated from Juglans sinensis.
(3beta,24E)-3-Hydroxylanosta-8,24-dien-26-oic acid
3beta-Hydroxy-9beta-9,19-cyclolanost-24-en-28-oic acid
(3S,5R,10S,13R,14S,15S,17R)-3,15-dihydroxy-4,4,10,13-tetramethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-14-carbaldehyde
2-(Octanoyloxy)-1-((octyloxy)methyl)ethyl octanoate
(1-Hexanoyloxy-3-hydroxypropan-2-yl) octadecanoate
(1-Hydroxy-3-octanoyloxypropan-2-yl) hexadecanoate
(2R,6aS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid
(1-Hydroxy-3-nonanoyloxypropan-2-yl) pentadecanoate
(1-Hydroxy-3-undecanoyloxypropan-2-yl) tridecanoate
(1-Decanoyloxy-3-hydroxypropan-2-yl) tetradecanoate
[(2S)-1-hydroxy-3-undecanoyloxypropan-2-yl] tridecanoate
[(2S)-3-hydroxy-2-undecanoyloxypropyl] tridecanoate
(1-Hydroxy-3-pentanoyloxypropan-2-yl) nonadecanoate
(1-Hydroxy-3-propanoyloxypropan-2-yl) henicosanoate
(1-Heptanoyloxy-3-hydroxypropan-2-yl) heptadecanoate
[(2R)-3-decanoyloxy-2-hydroxypropyl] tetradecanoate
Polpunonic acid
A natural product found in Maytenus diversifolia and Gymnosporia emarginata.
2,3-didodecanoyl-sn-glycerol
A 2,3-diacyl-sn-glycerol in which both acyl groups are specified as lauroyl (dodecanoyl).
didodecanoylglycerol
A diglyceride that is glycerol in which any two of the hydroxy groups have undergone formal esterification by condensation with dodecanoic (lauric) acid. Formula C27H52O5. For the structure shown, either R1 = H and R2 = dodecanoyl or R1 = dodecanoyl and R2 = H.
diacylglycerol 24:0
Any diglyceride that is glycerol in which any two of the hydroxy groups have been acylated by saturated fatty acids which together contain a total of 24 carbon atoms.
TG(24:0)
Provides by LipidSearch Vendor. © Copyright 2006-2024 Thermo Fisher Scientific Inc. All rights reserved
17-hydroxy-5,5,9,14,18,18-hexamethyl-23-oxahexacyclo[20.2.1.0¹,¹⁰.0⁴,⁹.0¹³,²².0¹⁴,¹⁹]pentacosan-6-one
10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-1-carboxylic acid
10-hydroxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-6a-carboxylic acid
10-hydroxy-2,2,6a,8a,9,9,12a-heptamethyl-1,3,4,5,6,6b,7,8,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
(1r,3as,3br,5ar,9as)-1-[(2r,5s)-5,6-dihydroxy-6-methylheptan-2-yl]-3a,3b,6,6,9a-pentamethyl-1h,2h,3h,4h,5h,5ah,8h,9h-cyclopenta[a]phenanthren-7-one
(3s,4ar,6ar,6bs,8r,8as,14ar,14bs)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicene-3,8-diol
(2e,6r)-6-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-methylhept-2-enoic acid
4,10-dihydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1h-picen-13-one
3-[3-(5-hydroxy-6-methylhept-6-en-2-yl)-3a,6,9b-trimethyl-7-(prop-1-en-2-yl)-1h,2h,3h,4h,5h,5ah,7h,8h-cyclopenta[a]naphthalen-6-yl]propanoic acid
(1r,4as,6ar,6br,8ar,10s,12ar,12br,14ar,14bs)-10-hydroxy-1,6a,6b,9,9,12a-hexamethyl-2-methylidene-hexadecahydropicene-4a-carboxylic acid
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-methylhept-2-enal
4a-(hydroxymethyl)-4,6b,8a,11,11,12b,14a-heptamethyl-tetradecahydropicene-1,3-dione
(1r,4ar,6ar,6bs,8ar,11s,12r,12ar,14r,14as,14bs)-1,14-dihydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydropicen-3-one
(4ar,6ar,6br,10s,12ar,12br,14br)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-6a-carboxylic acid
10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14-tetradecahydropicene-4a-carboxylic acid
10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,7,8,8a,10,11,12,12b,13,14,14a-tetradecahydro-2h-picene-4a-carboxylic acid
3-[(1s,4r,5r,8s,9s,12s,13r)-5-[(2r,4e)-6-hydroxy-6-methylhept-4-en-2-yl]-4,8-dimethyl-12-(prop-1-en-2-yl)tetracyclo[7.5.0.0¹,¹³.0⁴,⁸]tetradecan-13-yl]propanoic acid
(4r,4as,6as,6br,8ar,12ar,12bs,13s,14as,14bs)-13-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydropicene-3,7-dione
(1r,3as,5ar,5bs,7as,9s,11as,11bs,13ar,13br)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid
9-hydroxy-3a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-5a-carboxylic acid
(1s,2s,4ar,6ar,6br,8ar,10r,12ar,12br,14bs)-10-hydroxy-1,2,4a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-6a-carboxylic acid
6-hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethyl-tetradecahydropicene-1,3-dione
[1-isopropyl-3b,6,9b,11a-tetramethyl-7-(2-methyl-1-oxopropan-2-yl)-1h,2h,3h,3ah,4h,5h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-6-yl]acetic acid
(4as,6ar,6br,8ar,10s,12ar,12br,14as)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,7,8,8a,10,11,12,12b,13,14,14a-tetradecahydropicene-4a-carboxylic acid
(4r,4ar,6as,6br,8as,10r,12as,12bs,14bs)-4,10-dihydroxy-2,2,4a,6a,6b,9,9-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-12a-carbaldehyde
6-(2-hydroxypropan-2-yl)-2,9,11,15,19,19-hexamethyl-5-oxapentacyclo[12.8.0.0²,¹¹.0⁴,¹⁰.0¹⁵,²⁰]docos-1(14)-en-18-one
2-{7-hydroxy-6,6,9a,11a-tetramethyl-1h,2h,3h,3ah,4h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-1-yl}-6-methyl-5-methylideneheptanoic acid
6-{7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl}-2-methylhept-3-ene-2,5-diol
6-{7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl}-2-methylhept-2-enoic acid
(1s,3as,5ar,9ar,9br,11as)-1-[(2r,3r,4e)-3,6-dihydroxy-6-methylhept-4-en-2-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
3-[(1s,2r,4as,4br,6ar,10ar)-2-(2-hydroxypropan-2-yl)-1,4a,4b,6a,9,9-hexamethyl-3,4,5,6,7,8,10,10a-octahydro-2h-chrysen-1-yl]propanoic acid
3-[2-hydroxy-6,9a,9b,11a-tetramethyl-3,7-bis(prop-1-en-2-yl)-dodecahydro-1h-cyclopenta[a]phenanthren-6-yl]propanoic acid
(4r,4ar,6as,6br,8ar,10s,12as,12br)-4,10-dihydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1h-picen-13-one
(1s,4ar,6ar,6br,8ar,10s,12ar,12br,14ar,14br)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-4,5,6,7,8,8a,10,11,12,12b,13,14,14a,14b-tetradecahydro-1h-picene-4a-carboxylic acid
(4as,6as,6br,8ar,10s,12ar,12br)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14-tetradecahydropicene-4a-carboxylic acid
1-(4,7-dihydroxy-6-methylhept-5-en-2-yl)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-one
(1r,4ar,6ar,6br,8ar,12bs,14r,14as,14bs)-1,14-dihydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12b,13,14,14a-dodecahydro-1h-picen-3-one
10-hydroxy-2,2,6a,9,9,12b,14a-heptamethyl-1,3,4,5,6,6b,7,10,11,12,12a,13,14,14b-tetradecahydropicene-4a-carboxylic acid
(1s,2r,4as,6ar,6br,8ar,10s,12ar,12br,14br)-10-hydroxy-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
(1r,2s,3as,3bs,7s,9ar,9bs,11as)-1-[(2r,3e,5r)-5,6-dimethylhept-3-en-2-yl]-7-hydroxy-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-2-yl acetate
(1s,3ar,5as,5br,7ar,9r,11ar,11br,13as,13bs)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid
(1r,2r,4ar,6as,6br,8ar,10s,12ar,12br,14br)-10-hydroxy-1,4a,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydro-1h-picene-2-carboxylic acid
(3r,3ar,5as,7as,9s,11as,12s,13as,13br)-9,12-dihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,7h,7ah,9h,10h,11h,12h,13h,13bh-cyclopenta[a]chrysen-6-one
(1s,3as,5ar,7s,9as,11as)-7-hydroxy-1-[(2r,5s)-5-hydroxy-6-methylhept-6-en-2-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-4-one
3-[(3s,3ar,5ar,6r,7s,9ar,9br)-6,9a,9b-trimethyl-3-[(2s,5s)-2-methyl-5-(prop-1-en-2-yl)oxolan-2-yl]-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
(2z,6s)-6-[(1s,3as,5ar,7s,9ar,9br,11as)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-1-yl]-2-methylhept-2-enoic acid
(4ar,6ar,6br,8ar,10r,12ar,12bs,14br)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-6a-carboxylic acid
(4r,4ar,6as,6br,8ar,10s,12as,12bs)-4,10-dihydroxy-2,2,4a,6a,6b,9,9,12a-octamethyl-3,4,5,6,7,8,8a,10,11,12,12b,14-dodecahydro-1h-picen-13-one
(4as,6ar,6bs,8r,8as,9r,12as,12br,14as,14br)-8-hydroxy-2,2,4a,6a,8a,9,12b,14a-octamethyl-tetradecahydropicene-3,10-dione
2-{3a,5a,5b,8,8,11a-hexamethyl-9-oxo-tetradecahydro-1h-cyclopenta[a]chrysen-1-yl}propanoic acid
(1r,3as,5ar,5br,7ar,8s,11ar,11br,13ar,13br)-3a,8-bis(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-(prop-1-en-2-yl)-tetradecahydro-1h-cyclopenta[a]chrysen-9-one
2-[9-hydroxy-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-hexadecahydrocyclopenta[a]chrysen-1-yl]prop-2-enal
(1r,4r,5s,8s,10s,13r,14r,16r,17r,18s,19r,20s)-10-hydroxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[14.6.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosan-23-one
(2r,4ar,6ar,6br,8as,12bs,14ar,14br)-2-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,9,10,12b,13,14,14a-dodecahydro-1h-picen-3-one
1,6-dihydroxy-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-1h,2h,3h,4h,5h,5bh,6h,7h,7ah,10h,11h,13h,13bh-cyclopenta[a]chrysen-9-one
(1r,3as,5as,5br,7ar,9r,11ar,11bs,13ar,13bs)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-(prop-1-en-2-yl)-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid
(5s,6s)-5-hydroxy-6-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-2-methylhept-2-en-4-one
6b-(hydroxymethyl)-4,4a,8a,11,11,12b,14a-heptamethyl-tetradecahydropicene-1,3-dione
(4as,6ar,6br,8ar,10r,12ar,12br,14as)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,7,8,8a,10,11,12,12b,13,14,14a-tetradecahydropicene-4a-carboxylic acid
(1r,3ar,5ar,9as,11ar)-1-[(2s,3s,5e)-3,7-dihydroxy-6-methylhept-5-en-2-yl]-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,4h,5h,5ah,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-one
3-[(3s,3ar,5as,6s,7s,9ar,9br)-6,9a,9b-trimethyl-3-[(2s,5s)-2-methyl-5-(prop-1-en-2-yl)oxolan-2-yl]-7-(prop-1-en-2-yl)-decahydrocyclopenta[a]naphthalen-6-yl]propanoic acid
7-hydroxy-1-(6-hydroxy-6-methylhept-4-en-2-yl)-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-4-one
(2e,6r)-6-[(1r,3ar,7s,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]-2-methylhept-2-enoic acid
15-[2-hydroxy-3-(2-hydroxypropan-2-yl)cyclopentyl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-6-one
(2r,4as,6as,6br,8ar,10s,12ar,12br,14bs)-10-hydroxy-2,4a,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-2-carboxylic acid
(2r)-2-[(1s,3r,6s,8r,11s,12s,15r,16r)-6-hydroxy-7,7,12,16-tetramethylpentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan-15-yl]-6-methylhept-5-enoic acid
(1s,4r,5r,8r,10s,13r,14r,17r,18s,19s)-10-hydroxy-4,5,9,9,13,20,20-heptamethyl-21-oxahexacyclo[17.3.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosan-22-one
(1r,4r,9r,10r,13r,14s,17s,19r,22s)-17-hydroxy-5,5,9,14,18,18-hexamethyl-23-oxahexacyclo[20.2.1.0¹,¹⁰.0⁴,⁹.0¹³,²².0¹⁴,¹⁹]pentacosan-6-one
(1s,2s,4as,6as,6br,8as,10s,12as,12br,14br)-10-hydroxy-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
(1s,3as,5as,5br,7ar,9s,11ar,11br,13br)-9-hydroxy-1-isopropyl-5a,5b,8,8,11a-pentamethyl-1h,2h,3h,4h,5h,6h,7h,7ah,9h,10h,11h,11bh,12h,13bh-cyclopenta[a]chrysene-3a-carboxylic acid
(4as,6as,6br,10r,12ar)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,7,8,8a,10,11,12,12b,13,14b-tetradecahydropicene-4a-carboxylic acid
(3s,5s)-5-[(1s)-1-[(1r,3ar,7s,9as,11ar)-7-hydroxy-3a,6,6,9a,11a-pentamethyl-1h,2h,3h,5h,5ah,7h,8h,9h,11h-cyclopenta[a]phenanthren-1-yl]ethyl]-2,2-dimethyloxolan-3-ol
13,28-epoxy-11-oleanene-3,16-diol; (3β,13β,16α)-form
{"Ingredient_id": "HBIN001007","Ingredient_name": "13,28-epoxy-11-oleanene-3,16-diol; (3\u03b2,13\u03b2,16\u03b1)-form","Alias": "NA","Ingredient_formula": "C30H48O3","Ingredient_Smile": "NA","Ingredient_weight": "456.7","OB_score": "NA","CAS_id": "79786-12-2","SymMap_id": "NA","TCMID_id": "NA","TCMSP_id": "NA","TCM_ID_id": "9339","PubChem_id": "NA","DrugBank_id": "NA"}
14β,15β-epoxy-21β-hydroxyserratan-3-one
{"Ingredient_id": "HBIN001371","Ingredient_name": "14\u03b2,15\u03b2-epoxy-21\u03b2-hydroxyserratan-3-one","Alias": "NA","Ingredient_formula": "C30H48O3","Ingredient_Smile": "CC1(C2CCC3(CC45C(CCC3C2(CCC1=O)C)C6(CCC(C(C6CC4O5)(C)C)O)C)C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "7144","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
16-oxo-3α-hydroxyserrat-14-en-21β-ol
{"Ingredient_id": "HBIN001940","Ingredient_name": "16-oxo-3\u03b1-hydroxyserrat-14-en-21\u03b2-ol","Alias": "NA","Ingredient_formula": "C30H48O3","Ingredient_Smile": "CC1(C2CCC3(CC4=CC(=O)C5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "16343","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}
1-[(1s,3as,3bs,5ar,6r,7r,9ar,9bs,11as)-1-[(1s)-1-(dimethylamino)ethyl]-6-hydroxy-9a,11a-dimethyl-tetradecahydro-1h-cyclopenta[a]phenanthren-7-yl]-3-(propan-2-ylidene)azetidin-2-one
C29H48N2O2 (456.37155879999995)
(3r)-1-[(1s,3as,3bs,5ar,7r,9ar,9bs,11as)-1-[(1s)-1-(dimethylamino)ethyl]-9a,11a-dimethyl-6-oxo-tetradecahydrocyclopenta[a]phenanthren-7-yl]-3-isopropylazetidin-2-one
C29H48N2O2 (456.37155879999995)
1-{1-[1-(dimethylamino)ethyl]-9a,11a-dimethyl-6-oxo-tetradecahydrocyclopenta[a]phenanthren-7-yl}-3-isopropylazetidin-2-one
C29H48N2O2 (456.37155879999995)
(3r)-1-[(1r,3as,3bs,5ar,7s,9ar,9bs,11as)-1-[1-(dimethylamino)ethyl]-9a,11a-dimethyl-6-oxo-tetradecahydrocyclopenta[a]phenanthren-7-yl]-3-isopropylazetidin-2-one
C29H48N2O2 (456.37155879999995)
n-{18-hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²²]tetracosan-7-yl}ethanimidic acid
C29H48N2O2 (456.37155879999995)
n-[(1s,2r,5s,7s,10s,11s,14s,15r,16s,17r,18s,20s,23s)-18-hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.0²,¹¹.0⁵,¹⁰.0¹⁵,²³.0¹⁷,²²]tetracosan-7-yl]ethanimidic acid
C29H48N2O2 (456.37155879999995)
(3r)-1-[(1s,3as,3bs,5ar,7s,9ar,9bs,11as)-1-[(1s)-1-(dimethylamino)ethyl]-9a,11a-dimethyl-6-oxo-tetradecahydrocyclopenta[a]phenanthren-7-yl]-3-isopropylazetidin-2-one
C29H48N2O2 (456.37155879999995)
1-[(1s,3as,3bs,5ar,7r,9ar,9bs,11as)-1-[1-(dimethylamino)ethyl]-9a,11a-dimethyl-6-oxo-tetradecahydrocyclopenta[a]phenanthren-7-yl]-3-isopropylazetidin-2-one
C29H48N2O2 (456.37155879999995)