Exact Mass: 514.35055

Exact Mass Matches: 514.35055

Found 352 metabolites which its exact mass value is equals to given mass value 514.35055, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Flavidulol C

2-{1-hydroxy-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-2-yl}-4-methoxy-7,11-dimethyl-5,8,9,12-tetrahydrobenzo[10]annulen-1-ol

C34H42O4 (514.3082932)

Flavidulol C is found in mushrooms. Flavidulol C is isolated from the edible, but bitter tasting Japanese kihatsudake mushroom (Lactarius flavidulus). Isolated from the edible, but bitter tasting Japanese kihatsudake mushroom (Lactarius flavidulus). Flavidulol C is found in mushrooms.

Oleanderolide 3-acetate

16-Hydroxy-4,5,9,9,13,20,20-heptamethyl-23-oxo-24-oxahexacyclo[15.5.2.0¹,¹⁸.0⁴,¹⁷.0⁵,¹⁴.0⁸,¹³]tetracosan-10-yl acetic acid

C32H50O5 (514.365805)

Oleanderolide 3-acetate is found in fruits. Oleanderolide 3-acetate is a constituent of Rhodomyrtus tomentosa (hill gooseberry) Constituent of Rhodomyrtus tomentosa (hill gooseberry). Oleanderolide 3-acetate is found in fruits.

Tsugaric acid C

2-(3-acetyloxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-5-hydroxy-6-methylhept-6-enoic acid

C32H50O5 (514.365805)

Tsugaric acid C is found in mushrooms. Tsugaric acid C is a constituent of Ganoderma tsugae (red reishi) Constituent of Ganoderma tsugae (red reishi). Tsugaric acid C is found in mushrooms.

16-Acetylpriverogenin A

4a-Formyl-4,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicen-5-yl acetic acid

C32H50O5 (514.365805)

Sapogenin from Primula veris (cowslip). 16-Acetylpriverogenin A is found in tea and herbs and spices. 16-Acetylpriverogenin A is found in herbs and spices. Sapogenin from Primula veris (cowslip

N-Docosahexaenoyl Tryptophan

2-(docosa-4,7,10,13,16,19-hexaenamido)-3-(1H-indol-3-yl)propanoic acid

C33H42N2O3 (514.3195262)

N-docosahexaenoyl tryptophan belongs to the class of compounds known as N-acylamides. These are molecules characterized by a fatty acyl group linked to a primary amine by an amide bond. More specifically, it is a Docosahexaenoyl amide of Tryptophan. It is believed that there are more than 800 types of N-acylamides in the human body. N-acylamides fall into several categories: amino acid conjugates (e.g., those acyl amides conjugated with amino acids), neurotransmitter conjugates (e.g., those acylamides conjugated with neurotransmitters), ethanolamine conjugates (e.g., those acylamides conjugated to ethanolamine), and taurine conjugates (e.g., those acyamides conjugated to taurine). N-Docosahexaenoyl Tryptophan is an amino acid conjugate. N-acylamides can be classified into 9 different categories depending on the size of their acyl-group: 1) short-chain N-acylamides; 2) medium-chain N-acylamides; 3) long-chain N-acylamides; and 4) very long-chain N-acylamides; 5) hydroxy N-acylamides; 6) branched chain N-acylamides; 7) unsaturated N-acylamides; 8) dicarboxylic N-acylamides and 9) miscellaneous N-acylamides. N-Docosahexaenoyl Tryptophan is therefore classified as a very long chain N-acylamide. N-acyl amides have a variety of signaling functions in physiology, including in cardiovascular activity, metabolic homeostasis, memory, cognition, pain, motor control and others (PMID: 15655504). N-acyl amides have also been shown to play a role in cell migration, inflammation and certain pathological conditions such as diabetes, cancer, neurodegenerative disease, and obesity (PMID: 23144998; PMID: 25136293; PMID: 28854168).N-acyl amides can be synthesized both endogenously and by gut microbiota (PMID: 28854168). N-acylamides can be biosynthesized via different routes, depending on the parent amine group. N-acyl ethanolamines (NAEs) are formed via the hydrolysis of an unusual phospholipid precursor, N-acyl-phosphatidylethanolamine (NAPE), by a specific phospholipase D. N-acyl amino acids are synthesized via a circulating peptidase M20 domain containing 1 (PM20D1), which can catalyze the bidirectional the condensation and hydrolysis of a variety of N-acyl amino acids. The degradation of N-acylamides is largely mediated by an enzyme called fatty acid amide hydrolase (FAAH), which catalyzes the hydrolysis of N-acylamides into fatty acids and the biogenic amines. Many N-acylamides are involved in lipid signaling system through interactions with transient receptor potential channels (TRP). TRP channel proteins interact with N-acyl amides such as N-arachidonoyl ethanolamide (Anandamide), N-arachidonoyl dopamine and others in an opportunistic fashion (PMID: 23178153). This signaling system has been shown to play a role in the physiological processes involved in inflammation (PMID: 25136293). Other N-acyl amides, including N-oleoyl-glutamine, have also been characterized as TRP channel antagonists (PMID: 29967167). N-acylamides have also been shown to have G-protein-coupled receptors (GPCRs) binding activity (PMID: 28854168). The study of N-acylamides is an active area of research and it is likely that many novel N-acylamides will be discovered in the coming years. It is also likely that many novel roles in health and disease will be uncovered for these molecules.

Butyryl trihexyl citrate

1,2,3-Trihexyl 2-(butanoyloxy)propane-1,2,3-tricarboxylic acid

C28H50O8 (514.35055)

[1-(3,3-Dimethyloxiran-2-yl)-3-[(8S,10S,11S,14R)-11-hydroxy-4,4,8,10,14-pentamethyl-3-oxo-1,2,5,6,7,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-17-yl]butyl] acetate

C32H50O5 (514.365805)

DG(8:0/18:1(12Z)-2OH(9,10)/0:0)

(2S)-1-Hydroxy-3-(octanoyloxy)propan-2-yl (9S,10S,12Z)-9,10-dihydroxyoctadec-12-enoic acid

C29H54O7 (514.3869334)

DG(8:0/18:1(12Z)-2OH(9,10)/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(8:0/18:1(12Z)-2OH(9,10)/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.

DG(18:1(12Z)-2OH(9,10)/8:0/0:0)

(2S)-3-Hydroxy-2-(octanoyloxy)propyl (9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoic acid

C29H54O7 (514.3869334)

DG(18:1(12Z)-2OH(9,10)/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(18:1(12Z)-2OH(9,10)/8:0/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.

DG(8:0/0:0/18:1(12Z)-2OH(9,10))

(2R)-2-Hydroxy-3-(octanoyloxy)propyl (9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoic acid

C29H54O7 (514.3869334)

DG(8:0/0:0/18:1(12Z)-2OH(9,10)) 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(18:1(12Z)-2OH(9,10)/0:0/8:0)

(2S)-2-Hydroxy-3-(octanoyloxy)propyl (9R,10R,12Z)-9,10-dihydroxyoctadec-12-enoic acid

C29H54O7 (514.3869334)

DG(18:1(12Z)-2OH(9,10)/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.

3-O-Acetyl-16α-hydroxytrametenolic acid

(2R)-2-[(3S,10S,13R,14R,16R,17R)-3-acetyloxy-16-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-enoic acid

C32H50O5 (514.365805)

3-O-Acetyl-16α-hydroxytrametenolic acid (Compound 3) is a triterpene found in Poria cocos, with anti-oxidant and anti-cancer activity[1].

23-acetate

(1S,3R)-1-((R)-3,3-dimethyloxiran-2-yl)-3-((5R,8S,9S,10S,11S,14R)-11-hydroxy-4,4,8,10,14-pentamethyl-3-oxo-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl

C32H50O5 (514.365805)

Alisol b acetate is a triterpenoid. Alisol B 23-acetate is a natural product found in Alisma, Alisma plantago-aquatica, and other organisms with data available. See also: Alisma plantago-aquatica subsp. orientale root (part of). Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors. Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors.

Alisol

(1S,3R)-1-((R)-3,3-dimethyloxiran-2-yl)-3-((5R,8S,9S,10S,11S,14R)-11-hydroxy-4,4,8,10,14-pentamethyl-3-oxo-2,3,4,5,6,7,8,9,10,11,12,14,15,16-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)butyl

C32H50O5 (514.365805)

3-O-Acetyl-1α-hydroxytrametenolic

(2R)-2-[(3S,10S,13R,14R,16R,17R)-3-acetyloxy-16-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-enoic acid

C32H50O5 (514.365805)

3-O-Acetyl-16α-hydroxytrametenolic acid (Compound 3) is a triterpene found in Poria cocos, with anti-oxidant and anti-cancer activity[1].

2-O-Acetylmaslinic acid

(+)-2-O-Acetylmaslinic acid

C32H50O5 (514.365805)

Nanjiol A

C31H46O6 (514.3294215999999)

(+)-Methyl ganolucidate A

C31H46O6 (514.3294215999999)

3alpha-Acetoxy-27-hydroxylup-20(29)-en-24-oic acid

(+)-3alpha-Acetoxy-27-hydroxylup-20(29)-en-24-oic acid

C32H50O5 (514.365805)

Alisol B acetate

alisol B 23-acetate

C32H50O5 (514.365805)

Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors. Alisol B 23-acetate (23-Acetylalismol B) is a triterpenoid that promotes regeneration of damaged liver through activation of farnesoid receptors.

Cathafuran A

C34H42O4 (514.3082932)

Pomolic acid acetate

3-O-Acetylpomolic acid

C32H50O5 (514.365805)

A tricyclic triterpenoid of the isomalabaricane group.

Phyllofolactone J

(+)-Phyllofolactone J

C32H50O5 (514.365805)

3beta-Acetoxy-18alpha-hydroperoxy-12-oleanen-11-one

(+)-3beta-Acetoxy-18alpha-hydroperoxy-12-oleanen-11-one

C32H50O5 (514.365805)

11-Epifusidic acid

C31H46O6 (514.3294215999999)

Camaldulic acid

(+)-Camaldulic acid

C32H50O5 (514.365805)

Peroxydehydrotumulosic acid

(+)-5alpha,8alpha-Peroxydehydrotumulosic acid

C31H46O6 (514.3294215999999)

11-Ketofusidic acid

11-monoketofusidic acid

C31H46O6 (514.3294215999999)

Poricoic acid HM

(-)-Poricoic acid HM

C32H50O5 (514.365805)

Tomoeone H

C31H46O6 (514.3294215999999)

3beta-Acetoxy-16beta-hydroxybetulinic acid

C32H50O5 (514.365805)

3-O-Acetylmaslinic acid

C32H50O5 (514.365805)

Rubiarbonone C

C32H50O5 (514.365805)

A pentacyclic triterpenoid of the class of arborinane-type terpenoids isolated from the roots of Rubia yunnanensis.

Globostellatic acid G

C31H46O6 (514.3294215999999)

Phyllofolactone K

(+)-Phyllofolactone K

C32H50O5 (514.365805)

Butyryl trihexyl citrate

n-Butyryl tri-n-hexyl citrate

C28H50O8 (514.35055)

MGMG 18:3

1-(9Z,12Z,15Z-octadecatrienoy)l-3-O-beta-D-galactosyl)-sn-glycerol

C27H46O9 (514.3141666)

Annotation level-3

Radermasinin

C32H50O5 (514.365805)

3-O-Acetyl-16|A-hydroxytrametenolic acid

C32H50O5 (514.365805)

Lanost-9(11)-en-18-oic acid, 23-(acetyloxy)-3,20-dihydroxy-, .gamma.-lactone, (3.beta.,20.xi.)-

C32H50O5 (514.365805)

3alpha-hydroxy-lup-20(29)-ene-23,28-dioic acid dimethyl ester|3alpha-hydroxylup-20(29)-ene-23,28-dioic acid dimethyl ester

C32H50O5 (514.365805)

3-acetylmaslinic acid (TARB-2)|3-O-acetylmaslinic acid

C32H50O5 (514.365805)

Karachic acid

C32H50O5 (514.365805)

Methyl-Pseudomonat A|Pseudomonic acid methylester

C27H46O9 (514.3141666)

(2I<<,3EC)- 2-(Acetyloxy)-3-hydroxy- olean-12-en-28-oic acid

C32H50O5 (514.365805)

C27H46O9

C27H46O9 (514.3141666)

striatic acid

C32H50O5 (514.365805)

acutaxyline B

C31H46O6 (514.3294215999999)

1,3,7-Trihydroxy-3,7-dimethyl-2-(3-methylbutanoyl)-6,6-diprenyl-2,3,3a,4,7,7a-hexahydrospiro[1-cyclohexene-4,5(6H)-[1H]indene]-3,5-dione

C31H46O6 (514.3294215999999)

(22S,24S)-16,24;22,25-dianhydro-16,22,22,24,25-pentahydroxy-2beta-methoxy-3,11-dioxocucurbit-5-ene

C31H46O6 (514.3294215999999)

3alpha-hydroxyolean-12,28-dioic dimethyl ester

C32H50O5 (514.365805)

Frangulanine

C29H46N4O4 (514.3518875999999)

C32H50O5

C32H50O5 (514.365805)

Methyl serjanate

C32H50O5 (514.365805)

microsporin B

C28H42N4O5 (514.3155042)

Onekotanogenin

C32H50O5 (514.365805)

Spergulagenic acid

C32H50O5 (514.365805)

3??-Acetoxy-25-hydroxyolean-12-en-28-oic acid

C32H50O5 (514.365805)

methyl jessate

C32H50O5 (514.365805)

Tetra-Ac-(2R,3S,4R)-1,2,3,4-Eicosanetetrol|Tetra-Ac-(2S,3R,4R)-1,2,3,4-Eicosanetetrol|Tetra-Ac------(2S,3S,4R)-1,2,3,4-Eicosanetetrol

C28H50O8 (514.35055)

Nuatigenin diacetate

C31H46O6 (514.3294215999999)

8,9,13-triacetoxydocosanoic acid

C28H50O8 (514.35055)

3beta-acetoxy-16alpha-hydroxyoleanane-13beta,28-olide

C32H50O5 (514.365805)

MS000086487

C32H50O5 (514.365805)

3-O-Acetylcorosolic acid

C32H50O5 (514.365805)

Di-Me ester-3-Hydroxy-3,4-seco-4(24),12-oleanadiene-23,28-dioic acid

C32H50O5 (514.365805)

2-O-acetylcorosolic acid|2alpha,3alpha-diacetoxyurs-12-en-28-oic acid

C32H50O5 (514.365805)

poricoic acid DM

C31H46O6 (514.3294215999999)

9,11-Anhydro-12-hydroxyfusidic acid

C31H46O6 (514.3294215999999)

kotalagenin 16-acetate

C32H50O5 (514.365805)

methyl quadrangularate N

C31H46O6 (514.3294215999999)

Rubiprasin C

C32H50O5 (514.365805)

3beta-(acetyloxy)-12beta,13-dihydroxyursan-28-oic acid gamma-lactone|3beta-acetoxy-12beta-hydroxyurs-28,13-olide

C32H50O5 (514.365805)

poricoic acid D

C31H46O6 (514.3294215999999)

poricoic acid F

C31H46O6 (514.3294215999999)

Kryptogenin-3,26-diacetate

C31H46O6 (514.3294215999999)

Delta25,27-gitogenin diacetate

C31H46O6 (514.3294215999999)

dysoxylic acid A

C32H50O5 (514.365805)

3??-Methoxy-16??-hydroxyursa-12,19(29)-dien-27,28-dioic acid

C31H46O6 (514.3294215999999)

25-anhydroalisol A 24-acetate

C32H50O5 (514.365805)

Glaucone A

C31H46O6 (514.3294215999999)

Ganoderic acid B

C31H46O6 (514.3294215999999)

(3beta,15alpha)-3-(acetyloxy)-15-hydroxylanosta-8,24-dien-21-oic acid

C32H50O5 (514.365805)

2alpha,3beta-dihydroxy-urs-12,19(29)-dien-28-oic acid|euscaphic acid J

C31H46O6 (514.3294215999999)

GANODERIC ACID A

C31H46O6 (514.3294215999999)

23-O-Acetylalisol B

C32H50O5 (514.365805)

gypensapogenin G

C32H50O5 (514.365805)

schiglausin J

C32H50O5 (514.365805)

kadpolysperin C

C32H50O5 (514.365805)

(3beta,7beta)-ergost-5,24(28)-diene-3beta,7beta,19-triol 7,19-diacetate

C32H50O5 (514.365805)

alisol B 11-monoacetate

C32H50O5 (514.365805)

(24E,3alpha,22alpha)-3-hydroxy-22-acetoxylanosta-8,24-dien-26-oic acid|astraodoric acid D

C32H50O5 (514.365805)

kadpolysperin N

C32H50O5 (514.365805)

ganoderic acid Df

C31H46O6 (514.3294215999999)

C31H46O6

C31H46O6 (514.3294215999999)

(20R)-5alpha-pregnane-2alpha,3alpha,16beta,20-tetrol 2-O-beta-D-glucopyranoside

C27H46O9 (514.3141666)

RubiarbononeC

C32H50O5 (514.365805)

Methyl (24E)-9??,23??-dihydroxy-3,15-dioxo-17,15-friedo-lanostan-8(14),24-dien-26-oate

C31H46O6 (514.3294215999999)

SpinosinsaeureB-dimethylester

C32H50O5 (514.365805)

3-O-Acetyl-11-hydroxy-beta-boswellic acid

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

C32H50O5 (514.365805)

3-O-acetyl-11-hydroxy-beta-boswellic acid is a natural product found in Boswellia sacra with data available. 3-O-Acetyl-11-hydroxy-beta-boswellic acid is a potent 5-lipoxygenase (5-LO) inhibitor[1]. 3-O-Acetyl-11-hydroxy-beta-boswellic acid is a potent 5-lipoxygenase (5-LO) inhibitor[1].