Exact Mass: 584.2257506

Exact Mass Matches: 584.2257506

Found 500 metabolites which its exact mass value is equals to given mass value 584.2257506, within given mass tolerance error 0.05 dalton. Try search metabolite list with more accurate mass tolerance error 0.01 dalton.

Bilirubin

3-(2-{[3-(2-carboxyethyl)-5-{[(2Z)-4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene]methyl}-4-methyl-1H-pyrrol-2-yl]methyl}-5-{[(2Z)-3-ethenyl-4-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene]methyl}-4-methyl-1H-pyrrol-3-yl)propanoic acid

C33H36N4O6 (584.2634716)

Bilirubin is a yellow bile pigment that is a degradation product of heme. It occurs in the normal catabolic pathway that breaks down heme in vertebrates. This catabolism is a necessary process in the bodys clearance of waste products that arise from the destruction of aged or abnormal red blood cells. Bilirubin has been found in all vertebrates and in certain plants including Strelitzia nicolai (PMID: 28573242). Bilirubin levels in humans are elevated in certain diseases such as jaundice and liver disease and it is responsible for the yellow color of bruises and the yellow discoloration in jaundice. Bilirubin breakdown products, such as stercobilin, cause the brown color of feces. A different breakdown product, urobilin, is the main component of the straw-yellow color in urine. Bilirubin consists of an open chain of four pyrroles (tetrapyrrole). It is formed by oxidative cleavage of a porphyrin in heme, which leads to biliverdin, a green tetrapyrrolic bile pigment that is also a product of heme catabolism. Biliverdin is then reduced to bilirubin via biliverdin reductase. After conjugation with glucuronic acid, bilirubin can be excreted in the urine. Bilirubin is structurally similar to the pigment phycobilin used by certain algae to capture light energy, and to the pigment phytochrome used by plants to sense light. Elevated bilirubin levels in humans are associated with Crigler-Najjar syndrome type I, which is an inborn error of metabolism. Crigler-Najjar syndrome is a rare genetic disorder characterized by an inability to properly convert and clear bilirubin from the body. Affected individuals cannot convert unconjugated bilirubin to the conjugated form because they lack a specific liver enzyme required to break down (metabolize) bilirubin. Since they cannot convert bilirubin, they develop abnormally high levels of unconjugated bilirubin in the blood (hyperbilirubinemia). Crigler-Najjar syndrome is caused by mutations in the UGT1A1 gene. The hallmark finding of Crigler-Najjar syndrome is a persistent yellowing of the skin, mucous membranes and whites of the eyes (jaundice). Elevation of both alanine aminotransferase and bilirubin levels in serum or plasma can be indicative of serious liver injury. High levels of bilirubin are indicative of jaundice, which is easily recognizable due to a yellowing of the skin and eyes. Bilirubin is also an antioxidant. Bilirubins antioxidant activity may be particularly important in the brain, where it prevents excitotoxicity and neuronal death by scavenging superoxide during N-methyl-D-aspartic acid neurotransmission (PMID: 31353321). Bilirubin is a bile pigment that is a degradation product of heme. In particular, bilirubin is a yellow breakdown product of normal heme catabolism. Its levels are elevated in certain diseases and it is responsible for the yellow color of bruises. Bilirubin is an excretion product, and the body does not control levels. Bilirubin levels reflect the balance between production and excretion. Thus, there is no "normal" level of bilirubin. Bilirubin consists of an open chain of four pyrroles (tetrapyrrole); by contrast, the heme molecule is a closed ring of four pyrroles, called porphyrin. -- Wikipedia [HMDB]. Bilirubin is found in many foods, some of which are barley, mustard spinach, other bread, and sesbania flower. Bilirubin (BR) (from the Latin for "red bile") is a red-orange compound that occurs in the normal catabolic pathway that breaks down heme in vertebrates. This catabolism is a necessary process in the body's clearance of waste products that arise from the destruction of aged or abnormal red blood cells.[3] In the first step of bilirubin synthesis, the heme molecule is stripped from the hemoglobin molecule. Heme then passes through various processes of porphyrin catabolism, which varies according to the region of the body in which the breakdown occurs. For example, the molecules excreted in the urine differ from those in the feces.[4] The production of biliverdin from heme is the first major step in the catabolic pathway, after which the enzyme biliverdin reductase performs the second step, producing bilirubin from biliverdin.[5][6] Ultimately, bilirubin is broken down within the body, and its metabolites excreted through bile and urine; elevated levels may indicate certain diseases.[7] It is responsible for the yellow color of healing bruises and the yellow discoloration in jaundice. The bacterial enzyme bilirubin reductase is responsible for the breakdown of bilirubin in the gut.[8] One breakdown product, urobilin, is the main component of the straw-yellow color in urine.[9] Another breakdown product, stercobilin, causes the brown color of feces. Although bilirubin is usually found in animals rather than plants, at least one plant species, Strelitzia nicolai, is known to contain the pigment.[10] Bilirubin is created by the activity of biliverdin reductase on biliverdin, a green tetrapyrrolic bile pigment that is also a product of heme catabolism. Bilirubin, when oxidized, reverts to become biliverdin once again. This cycle, in addition to the demonstration of the potent antioxidant activity of bilirubin,[14] has led to the hypothesis that bilirubin's main physiologic role is as a cellular antioxidant.[15][16] Consistent with this, animal studies suggest that eliminating bilirubin results in endogenous oxidative stress.[17] Bilirubin's antioxidant activity may be particularly important in the brain, where it prevents excitotoxicity and neuronal death by scavenging superoxide during N-methyl-D-aspartic acid neurotransmission.[18] Bilirubin in plasma is mostly produced by the destruction of erythrocytes. Heme is metabolized into biliverdin (via heme oxygenase) and then into bilirubin (via biliverdin reductase) inside the macrophages. [11] Bilirubin is then released into the plasma and transported to the liver bound by albumin, since it is insoluble in water in this state. In this state, bilirubin is called unconjugated (despite being bound by albumin). [11] In the liver, unconjugated bilirubin is up-taken by the hepatocytes and subsequently conjugated with glucuronic acid (via the enzyme uridine diphosphate–glucuronyl transferase). In this state, bilirubin is soluble in water and it is called conjugated bilirubin. [11] Conjugated bilirubin is excreted into the bile ducts and enters the duodenum. During its transport to the colon, it is converted into urobilinogen by the bacterial enzyme bilirubin reductase.[8] Most of the urobilinogen is further reduced into stercobilinogen and is excreted through feces (air oxidizes stercobilinogen to stercobilin, which gives feces their characteristic brown color). [11] A lesser amount of urobilinogen is re-absorbed into portal circulation and transferred to the liver. For the most part, this urobilinogen is recycled to conjugated bilirubin and this process closes the enterohepatic circle. There is also an amount of urobilinogen which is not recycled, but rather enters the systemic circulation and subsequently the kidneys, where it is excreted. Air oxidizes urobilinogen into urobilin, which gives urine its characteristic color.[11][19] In parallel, a small amount of conjugated billirubin can also enter the systemic circulation and get excreted through urine. This is exaggerated in various pathological situations.[19]

Mg-protoporphyrin IX

C34H32MgN4O4 (584.2273931999999)

(3Z)-phytochromobilin

C33H36N4O6 (584.2634716)

15,16-Dihydrobiliverdin

15,16-Dihydrobiliverdin; 15,16-Dihydrobiliverdin IXalpha; 15,16-Dihydrobiliverdin ixa

C33H36N4O6 (584.2634716)

12-Ethyl-8-propyl-3-vinylbacteriochlorophyllide d

C35H36MgN4O3 (584.2637766)

A chlorophyllide obtained by hydrolysis of the terpenoid ester moiety of 12-ethyl-8-propyl-3-vinylbacteriochlorophyll d.

(4E,15Z)-Bilirubin

3-(2-{[3-(2-carboxyethyl)-5-{[(2E)-4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene]methyl}-4-methyl-1H-pyrrol-2-yl]methyl}-5-{[(2Z)-3-ethenyl-4-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene]methyl}-4-methyl-1H-pyrrol-3-yl)propanoic acid

C33H36N4O6 (584.2634716)

(4E,15Z)-Bilirubin IXa belongs to the class of organic compounds known as bilirubins. These are organic compounds containing a dicarboxylic acyclic tetrapyrrole derivative. Bilirubin (BR) is a yellow compound that occurs in the normal catabolic pathway that breaks down heme in vertebrates. (4E,15Z)-Bilirubin IXa is a linear tetrapyrrole, and a product of heme degradation. It is a member of the class of compounds known as biladienes. Biladienes consist of two linear tetrapyrroles in which the carbon bridges contain two more double bonds than bilane. (4E,15Z)-Bilirubin IXa is an isomer of bilirubin, which appears to have antioxidant effects. Bilirubins antioxidant activity may be particularly important in the brain, where it prevents excitotoxicity and neuronal death by scavenging superoxide during N-methyl-D-aspartic acid neurotransmission. (4E,15Z)-Bilirubin IXa is formed by oxidative cleavage of a porphyrin in heme, which first produces biliverdin. Biliverdin is then reduced to bilirubin by biliverdin reductase. Some of the double-bonds in bilirubin isomerize when exposed to light. The E,Z-isomers of bilirubin, such s (4E,15Z)-Bilirubin IXa formed upon light exposure are more soluble than the unilluminated Z,Z-isomer. Altered levels of (4E,15Z)-Bilirubin IXa in human serum have been used as a biomarker of acrylamide exposure (PMID: 28163100). 4E,15Z-Bilirubin IXa is an isomer of bilirubin, which has antioxidative effects. When bilirubin reacts with reactive oxygen species, oxidized metabolites of bilirubin are formed, such as biliverdin and propentdyopents. A decrease in serum bilirubin concentration and an increase in serum and urinary oxidized metabolites of bilirubin may indicate the protective action of bilirubin against reactive oxygen species. (PMID 10986860) [HMDB] COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

(4E,15E)-Bilirubin

3-(2-{[3-(2-carboxyethyl)-5-{[(2E)-4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene]methyl}-4-methyl-1H-pyrrol-2-yl]methyl}-5-{[(2E)-3-ethenyl-4-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene]methyl}-4-methyl-1H-pyrrol-3-yl)propanoic acid

C33H36N4O6 (584.2634716)

(4E,15E)-Bilirubin is an isomer of bilirubin and is less lipophilic and more polar than the naturally occurring Z-Z isomer (PMID: 426785). Bilirubin is a bile pigment that is a degradation product of heme. In particular, bilirubin is a yellow breakdown product of normal heme catabolism. Its levels are elevated in certain diseases and it is responsible for the yellow colour of bruises. Bilirubin is an excretion product and the body does not control its levels. Bilirubin levels reflect the balance between production and excretion. Thus, there is no "normal" level of bilirubin. Bilirubin consists of an open chain of four pyrroles (tetrapyrrole). In contrast, the heme molecule is a closed ring of four pyrroles, called porphyrin (Wikipedia).

Benzoylpaeoniflorin

[3-({6-[(benzoyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl}oxy)-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl benzoate

C30H32O12 (584.1893672)

Benzoylpaeoniflorin, a natural product from Chinese paeony root, has the potential for coronary heart disease by decreasing apoptosis. Benzoylpaeoniflorin, a natural product from Chinese paeony root, has the potential for coronary heart disease by decreasing apoptosis.

Lumirubin

3-(5-{[3-(2-carboxyethyl)-5-[(4-ethenyl-3-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-2-yl]methyl}-7,11-dimethyl-12-oxo-4,13-diazatricyclo[8.3.0.0³,⁷]trideca-1,3,5,9-tetraen-6-yl)propanoic acid

C33H36N4O6 (584.2634716)

Sampatrilat

3-[(6-Amino-1-hydroxy-2-methanesulphonamidohexylidene)amino]-2-[(1-{[1-carboxy-2-(4-hydroxyphenyl)ethyl]-C-hydroxycarbonimidoyl}cyclopentyl)methyl]propanoic acid

C26H40N4O9S (584.2515870000001)

hemsleyanoside

1-(4-hydroxy-3-methoxyphenyl)-2-{4-[4-(4-hydroxy-3-methoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenoxy}propane-1,3-diol

C31H36O11 (584.2257506)

bilirubin

C33H36N4O6 (584.2634716)

D020011 - Protective Agents > D000975 - Antioxidants COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

6-O-Apiosyl-5-O-Methylvisammioside

(2S)-2-[2-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxypropan-2-yl]-4-methoxy-7-methyl-2,3-dihydrofuro[3,2-g]chromen-5-one

C27H36O14 (584.2104956000001)

6”-O-Apiosyl-5-O-Methylvisammioside is one of the components of the traditional Chinese medicine Kang-Jing.

Benzoylpaeoniflorin

4-O-benzoylpaeoniflorin

C30H32O12 (584.1893672)

Benzoylpaeoniflorin is a terpene glycoside. It has a role as a metabolite. Benzoylpaeoniflorin is a natural product found in Paeonia suffruticosa and Paeonia rockii with data available. A natural product found in Paeonia rockii subspeciesrockii. Benzoylpaeoniflorin, a natural product from Chinese paeony root, has the potential for coronary heart disease by decreasing apoptosis. Benzoylpaeoniflorin, a natural product from Chinese paeony root, has the potential for coronary heart disease by decreasing apoptosis.

buddlenol E

C31H36O11 (584.2257506)

A lignan isolated from the seeds of Euryale ferox.

Sachaliside 2

(2R,3S) -2- (3,4-Dihydroxyphenyl) -3,4-dihydro-3,5-dihydroxy-6- [ (2E) -3- (4-hydroxyphenyl) -2-propenyl ] -2H-1-benzopyran-7-yl beta-D-glucopyranoside

C30H32O12 (584.1893672)

A guaiacyl lignin that is medioresinol in which one of the phenolic hydrogens is replaced by a guaiacylglycerol group. It is found in Arabidopsis thaliana.

6-Demethoxyneocalycopterone

C34H32O9 (584.2046222)

Ficusesquilignan B

C31H36O11 (584.2257506)

Junceellonoid A

C28H37ClO11 (584.2024282)

Lucidumoside C

An isoquinoline alkaloid that is a dimer of 8-methoxydehydroanonaine. Isolated from the roots of Polyalthia debilis, it exhibits moderate antimalarial activity by inhibiting the growth of the malarial parasite Plasmodium falciparum.

C28H40O13

C28H40O13 (584.246879)

citrafungin A

C28H40O13 (584.246879)

A carboxylic ester obtained by the formal condensation of 4-carboxy group of (2R)-2-hydroxy-2-{(3R,5R)-2-oxo-5-[(1E,5Z)-tetradeca-1,5-dien-1-yl]tetrahydrofuran-3-yl}butanedioic acid with the hydroxy group of 3-carboxy-2,3-dideoxy-L-threo-pentaric acid. It is a fungal metabolite that acts as an inhibitor of geranylgeranyltransferase type I(GGTase I) of pathogenic fungal species.

2-[4-(beta-D-glucopyranosyloxy)-2-hydroxy-6-methylbenzyl]-5-hydroxy-3-methylphenyl beta-D-glucopyranoside|orcinoside C

C27H36O14 (584.2104956000001)

3,3,5,5-tetramethoxy-8,4-oxyneolignan-4,9,9-triol 4-beta-D-glucopyranoside|4-{3-hydroxy-2-[4-(3-hydroxypropyl)-2,6-dimethoxyphenoxy]propyl}-2,6-dimethoxyphenyl beta-D-glucopyranoside

C28H40O13 (584.246879)

Syvestroside III

C27H36O14 (584.2104956000001)

3,3-(2,7,13,17-tetramethyl-1,19-dioxo-3,18-divinyl-1,10,19,22,23,24-hexahydro-21H-biline-8,12-diyl)-bis-propionic acid|Bilirubin

C33H36N4O6 (584.2634716)

Bonafousioside

C28H40O13 (584.246879)

BIDEBILINE D

C36H28N2O6 (584.1947268)

An isoquinoline alkaloid that is a dimer of 10-methoxydehydroanonaine. Isolated from the roots of Polyalthia debilis, it exhibits moderate antimalarial activity by inhibiting the growth of the malarial parasite Plasmodium falciparum.

2-[2-(beta-D-glucopyranosyloxy)-6-hydroxy-4-methylbenzyl]-3-hydroxy-5-methylphenyl beta-D-glucopyranoside|orcinoside A

C27H36O14 (584.2104956000001)

Gly Phe Asn Thr Phe

C28H36N6O8 (584.2594496)

FORBESOSIDE

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[(2R)-7-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yloxy]oxan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C30H32O12 (584.1893672)

6-Feruloylnodakenin is a natural product found in Hansenia forbesii with data available.

Benzoylalbiflorin

[6-[[9-(Benzoyloxymethyl)-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.03,9]nonan-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

C30H32O12 (584.1893672)

C30H32O12_{(1R,2S,3R,5R,6R,8S)-3-[(6-O-Benzoyl-beta-D-glucopyranosyl)oxy]-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.0~2,5~.0~3,8~]dec-2-yl}methyl benzoate

NCGC00380749-01_C30H32O12_{(1R,2S,3R,5R,6R,8S)-3-[(6-O-Benzoyl-beta-D-glucopyranosyl)oxy]-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.0~2,5~.0~3,8~]dec-2-yl}methyl benzoate

C30H32O12 (584.1893672)

C27H36O14_1,3-Cyclohexanedione, 5-hydroxy-6-(2-hydroxy-2-methylpropylidene)-2,2,4,4-tetramethyl-5-[[6-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranosyl]oxy]-, (6Z)

NCGC00380468-01_C27H36O14_1,3-Cyclohexanedione, 5-hydroxy-6-(2-hydroxy-2-methylpropylidene)-2,2,4,4-tetramethyl-5-[[6-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranosyl]oxy]-, (6Z)-

(2R)-2-[(2S)-2-[(2S)-2-[(2S)-2-amino-3-(4-hydroxyphenyl)propanamido]-3-(4-hydroxyphenyl)propanamido]-3-(1H-imidazol-4-yl)propanamido]-3-sulfanylpropanoic acid

C27H32N6O7S (584.2053082)

GFNTF

Gly-Phe-Asn-Thr-Phe

C28H36N6O8 (584.2594496)

Pubescenol

C32H40O10 (584.2621340000001)

4Z,15E-Bilirubin IXa

C33H36N4O6 (584.2634716)

4E,15Z-Bilirubin IXa

C33H36N4O6 (584.2634716)

A linear tetrapyrrole, product of heme degradation. An isomer of bilirubin. COVID info from COVID-19 Disease Map Corona-virus Coronavirus SARS-CoV-2 COVID-19 SARS-CoV COVID19 SARS2 SARS

Sampatrilat

C26H40N4O9S (584.2515870000001)

Naphthol AS-BR

C36H28N2O6 (584.1947268)

For-Met-Leu-Phe-Phe-OH

C30H40N4O6S (584.266842)

L-755,507

C30H40N4O6S (584.266842)

L755507 is a potent, selective agonist of β3-AR with an IC50 of 35 nM. L755507 enhances the homology-directed repair (HDR)-mediated genome editing in CRISPR/Cas9 nickase system[1][2][3].

5-o-(dimethoxytrityl)-2-o-methylinosine

C32H32N4O7 (584.2270882)

3,17-Divinyl-1,10,19,22,23,24-hexahydro-2,7,13,18-tetramethyl-1,19-dioxo-21H-biline-8,12-dipropionic acid

C33H36N4O6 (584.2634716)

SPERMIDINE PHOSPHATE

C14H47N6O12P3 (584.2464692000001)

TOP-53 dihydrochloride

C28H38Cl2N2O7 (584.2055938)

D-Valyl-L-phenylalanyl-N-(4-nitrophenyl)-L-lysinamide dihydrochloride

C26H38Cl2N6O5 (584.2280598)

2,9-Bis(naphthalen-2-yl)-4,7-diphenyl-1,10-phenanthroline

C44H28N2 (584.2252368000001)

Cyclopropaneacetamide, 1-[[[(1R)-1-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]

C35H37ClN2O2S (584.2264132)

S-4-oxide-4-hydroxy-2,6-bis(2,4,6-triMethylphenyl)-Dinaphtho[2,1-d:1,2-f][1,3,2]dioxaphosphepin

C38H33O4P (584.2116348)

1-S-Ethyl 2,3,4,6-tetra-O-benzyl-b-D-thiogalactopyranoside

C36H40O5S (584.259631)

Ajugamarin chlorohydrin

C29H41ClO10 (584.2388116000001)

butane-1,4-diol,1,3-diisocyanato-2-methylbenzene,2,4-diisocyanato-1-methylbenzene,hexanedioic acid

C28H32N4O10 (584.2118332)

Buddlenol B

C31H36O11 (584.2257506)

A guaiacyl lignin that is found in Arabidopsis thaliana.

Lumirubin

C33H36N4O6 (584.2634716)

Withalongolide G

C28H40O11S (584.2291210000001)

A withanolide that is 2,3-dihydrowithaferin A substituted by a hydroxy group at position 19 and a sulfoxy group at position 3. Isolated from Physalis longifolia, it exhibits antineoplastic activity.

3-[2-[[3-(2-carboxyethyl)-4-methyl-5-[(E)-(4-methyl-5-oxo-3-vinyl-2-pyrrolylidene)methyl]-1H-pyrrol-2-yl]methyl]-4-methyl-5-[(E)-(3-methyl-5-oxo-4-vinyl-2-pyrrolylidene)methyl]-1H-pyrrol-3-yl]propanoic acid

3-[2-[[3-(2-carboxyethyl)-5-[(E)-(5-keto-4-methyl-3-vinyl-3-pyrrolin-2-ylidene)methyl]-4-methyl-1H-pyrrol-2-yl]methyl]-5-[(E)-(5-keto-3-methyl-4-vinyl-3-pyrrolin-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propionic acid

C33H36N4O6 (584.2634716)

hemsleyanoside

1-(4-hydroxy-3-methoxyphenyl)-2-{4-[4-(4-hydroxy-3-methoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenoxy}propane-1,3-diol

Bilirubin IIIalpha

C33H36N4O6 (584.2634716)

3-(2-[(Z)-{3-(2-carboxyethyl)-5-[(Z)-(4-ethenyl-3-methyl-5-oxo-1,5-dihydro-2H-pyrrol-2-ylidene)methyl]-4-methyl-2H-pyrrol-2-ylidene}methyl]-5-{(Z)-[(3E,4R)-3-ethylidene-4-methyl-5-oxopyrrolidin-2-ylidene]methyl}-4-methyl-1H-pyrrol-3-yl)propanoic acid

3-(2-[(Z)-{3-(2-carboxyethyl)-5-[(Z)-(4-ethenyl-3-methyl-5-oxo-1,5-dihydro-2H-pyrrol-2-ylidene)methyl]-4-methyl-2H-pyrrol-2-ylidene}methyl]-5-{(Z)-[(3E,4R)-3-ethylidene-4-methyl-5-oxopyrrolidin-2-ylidene]methyl}-4-methyl-1H-pyrrol-3-yl)propanoic acid

C35H35ClNO3S- (584.2026050000001)

(-)-(7R,7R,7R,8S,8S,8S)-4,4-dihydroxy-3,3,3,5-tetramethoxy-7,9:7,9-diepoxy-4,8-oxy-8,8-sesquineolignan-7,9-diol

C31H36O11 (584.2257506)

A neolignan isolated from the stems of Sinocalamus affinis.

(-)-(7R,7R,7S,8S,8S,8S)-4,4-dihydroxy-3,3,3,5-tetramethoxy-7,9:7,9-diepoxy-4,8-oxy-8,8-sesquineolignan-7,9-diol

C31H36O11 (584.2257506)

A neolignan isolated from the stems of Sinocalamus affinis.

[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(6Z)-1-hydroxy-6-(2-hydroxy-2-methylpropylidene)-2,2,4,4-tetramethyl-3,5-dioxocyclohexyl]oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate

C27H36O14 (584.2104956000001)

1-Hexyl-3-[4-[[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethyl]phenyl]sulfamoyl]phenyl]urea

C30H40N4O6S (584.266842)

kirkinine D

C33H36N4O6 (584.2634716)

paeonin A

C30H32O12 (584.1893672)

A natural product found in Paeonia emodi.

Bilirubin ixalpha

ST 28:5;O8;S

C28H40O11S (584.2291210000001)

ST 29:4;O7;S

C29H44O10S (584.2655044)

(1s,2r,4r,6r,7r,11r,12r,14r,15r,16r,18s)-7-(furan-3-yl)-18-(2-methoxy-2-oxoethyl)-1,6,17,17-tetramethyl-9,19-dioxo-3,8,13-trioxahexacyclo[13.3.1.0²,⁴.0²,¹².0⁶,¹¹.0¹²,¹⁴]nonadecan-16-yl (2r)-2-methylbutanoate

13-o-acetylwallifoliol

C31H36O11 (584.2257506)

{"Ingredient_id": "HBIN001271","Ingredient_name": "13-o-acetylwallifoliol","Alias": "NA","Ingredient_formula": "C31H36O11","Ingredient_Smile": "CC1=C2C3(CC1OC(=O)C)C(C4C(C2(C(=O)OC3(C)C)O)(C(CC5C4(CO5)OC(=O)C)O)C)OC(=O)C6=CC=CC=C6","Ingredient_weight": "584.6 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "531","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "101221618","DrugBank_id": "NA"}

2-hydroxy-3-o-tigloylswietenolide

C32H40O10 (584.2621340000001)

{"Ingredient_id": "HBIN005751","Ingredient_name": "2-hydroxy-3-o-tigloylswietenolide","Alias": "NA","Ingredient_formula": "C32H40O10","Ingredient_Smile": "CC=C(C)C(=O)OC1C(C(C2(C3CCC4(C(OC(=O)CC4=C3CC1(C2=O)O)C5=COC=C5)C)C)C(C(=O)OC)O)(C)C","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "10767","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

(+)-5,5'-dimethoxy-9-o-β-d-glucopyranosylsecoisolariciresinol

C28H40O13 (584.246879)

{"Ingredient_id": "HBIN011074","Ingredient_name": "(+)-5,5'-dimethoxy-9-o-\u03b2-d-glucopyranosylsecoisolariciresinol","Alias": "NA","Ingredient_formula": "C28H40O13","Ingredient_Smile": "COC1=CC(=CC(=C1O)OC)CC(CO)C(CC2=CC(=C(C(=C2)OC)O)OC)COC3C(C(C(C(O3)CO)O)O)O","Ingredient_weight": "NA","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "6230","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "NA","DrugBank_id": "NA"}

6''-demethoxyneocalycopterone

C34H32O9 (584.2046222)

{"Ingredient_id": "HBIN012307","Ingredient_name": "6''-demethoxyneocalycopterone","Alias": "NA","Ingredient_formula": "C34H32O9","Ingredient_Smile": "COC1=CC(=O)C2C=CC(OC23C1(C4=C(C(=C5C(=C4O3)C(CC(O5)C6=CC=CC=C6)O)OC)OC)OC)C7=CC=CC=C7","Ingredient_weight": "584.6 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "5050","TCMSP_id": "NA","TCM_ID_id": "NA","PubChem_id": "101727393","DrugBank_id": "NA"}

6'-O-trans-feruloylnodakenin

6'-o-trans-feruloylnodakenin

C30H32O12 (584.1893672)

{"Ingredient_id": "HBIN012719","Ingredient_name": "6'-O-trans-feruloylnodakenin","Alias": "6'-o-trans-feruloylnodakenin","Ingredient_formula": "C30H32O12","Ingredient_Smile": "CC(C)(C1CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)OC4C(C(C(C(O4)COC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O)O","Ingredient_weight": "584.6 g/mol","OB_score": "NA","CAS_id": "NA","SymMap_id": "NA","TCMID_id": "38137","TCMSP_id": "NA","TCM_ID_id": "21432","PubChem_id": "102060651","DrugBank_id": "NA"}

6-methoxy-8-(3-methylbut-2-en-1-yl)-7-{[3,4,5-trihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-2-one

C27H36O14 (584.2104956000001)

11,12,14-tris(acetyloxy)-3,4,16-trihydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadec-8-en-2-yl acetate

C28H40O13 (584.246879)

(1r,2s,5r,6r,10s,13s,14r,16s)-6-[(5s)-5-hydroxy-2-oxo-5h-furan-3-yl]-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

(1r,2s,5r,6r,10s,13s,14r,16s)-6-[(5s)-5-hydroxy-2-oxo-5h-furan-3-yl]-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

(1r,2s,5r,6r,13r,14s,16s)-6-(furan-3-yl)-13-hydroxy-16-[(1r)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate

(1r,2s,5r,6r,13r,14s,16s)-6-(furan-3-yl)-13-hydroxy-16-[(1r)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-10-en-14-yl (2e)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

(1s,2s)-2-{4-[(1r,3as,4r,6as)-4-(4-hydroxy-3,5-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2-methoxyphenoxy}-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol

C31H36O11 (584.2257506)

[(2r,3s,4s,5r,6s)-6-{[(1s,3s,4r,6s,9s)-9-[(benzoyloxy)methyl]-4-hydroxy-6-methyl-8-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

C30H32O12 (584.1893672)

(1s,2r,3r,4r,7r,8s,10z,12r,13s,16s,17s)-2-(acetyloxy)-8-chloro-3,17-dihydroxy-4,13,17-trimethyl-9-methylidene-5-oxo-12-(propanoyloxy)-6-oxatricyclo[11.4.0.0³,⁷]heptadec-10-en-16-yl 2-methylpropanoate

(8s,9s,10s,11r)-3,9,19-trihydroxy-4,5-dimethoxy-9,10-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2,4,6,13,18-hexaen-11-yl (2z)-2-methylbut-2-enoate

(8s,9s,10s,11r)-3,9,19-trihydroxy-4,5-dimethoxy-9,10-dimethyl-8-{[(2z)-2-methylbut-2-enoyl]oxy}-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2,4,6,13,18-hexaen-11-yl (2z)-2-methylbut-2-enoate

C31H36O11 (584.2257506)

(8r,9s,10r,11r)-11-(butanoyloxy)-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.0²,⁷.0¹⁴,¹⁸]nonadeca-1(12),2,4,6,13,18-hexaen-8-yl (2z)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

[(1s,3s,5s,6r,8s)-3-{[(2s,3r,5s,6r)-6-[(benzoyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy}-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl benzoate

C30H32O12 (584.1893672)

[(2r,3s,4s,5r,6s)-6-{[(1s,3s,6r,8r,9r)-9-[(benzoyloxy)methyl]-8-hydroxy-6-methyl-4-oxo-7-oxatricyclo[4.3.0.0³,⁹]nonan-1-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methyl benzoate

C30H32O12 (584.1893672)

7-methoxy-13-{7-methoxy-3,5-dioxa-11-azapentacyclo[10.7.1.0²,⁶.0⁸,²⁰.0¹⁴,¹⁹]icosa-1(20),2(6),7,12,14(19),15,17-heptaen-13-yl}-3,5-dioxa-11-azapentacyclo[10.7.1.0²,⁶.0⁸,²⁰.0¹⁴,¹⁹]icosa-1(20),2(6),7,12,14(19),15,17-heptaene

C32H40O10 (584.2621340000001)

(4r,4ar,6s,7r,7ar)-4-(methoxycarbonyl)-7-methyl-3-oxo-hexahydro-1h-cyclopenta[c]pyran-6-yl (4r,5s,6s)-5-ethenyl-4-(2-oxoethyl)-6-{[(2s,3s,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

(4r,4ar,6s,7r,7ar)-4-(methoxycarbonyl)-7-methyl-3-oxo-hexahydro-1h-cyclopenta[c]pyran-6-yl (4r,5s,6s)-5-ethenyl-4-(2-oxoethyl)-6-{[(2s,3s,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-[(2-{7-oxo-2h,3h-furo[3,2-g]chromen-2-yl}propan-2-yl)oxy]oxan-2-yl]methyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C30H32O12 (584.1893672)

(4s,4as,6s,7r,7as)-4-(methoxycarbonyl)-7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl (4s,5r,6s)-5-ethenyl-4-(2-oxoethyl)-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

(4s,4as,6s,7r,7as)-4-(methoxycarbonyl)-7-methyl-1-oxo-hexahydro-3h-cyclopenta[c]pyran-6-yl (4s,5r,6s)-5-ethenyl-4-(2-oxoethyl)-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

C27H36O14 (584.2104956000001)

C27H36O14 (584.2104956000001)

(1r,2s)-2-{4-[(1r,3ar,4r,6as)-4-(4-hydroxy-3-methoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenoxy}-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol

C31H36O11 (584.2257506)

2,12,14-tris(acetyloxy)-8-chloro-3-hydroxy-4,13-dimethyl-9,17-dimethylidene-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadecan-10-yl acetate

C28H37ClO11 (584.2024282)

6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-(nona-1,3,5-trien-1-yl)-5-oxo-16-(prop-1-en-2-yl)-9,13,15,19-tetraoxahexacyclo[12.4.1.0¹,¹¹.0²,⁶.0⁸,¹⁰.0¹²,¹⁶]nonadec-3-en-17-yl acetate

6,7-dihydroxy-8-(hydroxymethyl)-4,18-dimethyl-14-(nona-1,3,5-trien-1-yl)-5-oxo-16-(prop-1-en-2-yl)-9,13,15,19-tetraoxahexacyclo[12.4.1.0¹,¹¹.0²,⁶.0⁸,¹⁰.0¹²,¹⁶]nonadec-3-en-17-yl acetate

C32H40O10 (584.2621340000001)

1,3,6,8-tetrahydroxy-2-{1-[2-hydroxy-4-(3-hydroxy-5-methylphenoxy)-6-methylphenyl]hexyl}anthracene-9,10-dione

C34H32O9 (584.2046222)

(2s,3r,4s,5s,6s)-2-{[(2r,3r)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-6-[(2e)-3-(4-hydroxyphenyl)prop-2-en-1-yl]-3,4-dihydro-2h-1-benzopyran-7-yl]oxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C30H32O12 (584.1893672)

(1s,2s,5r,6r,10s,13r,14r,16s)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

(1s,2s,5r,6r,10s,13r,14r,16s)-6-(5-hydroxy-2-oxo-5h-furan-3-yl)-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

(1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-9-(furan-3-yl)-15-[(1s)-1-hydroxy-2-methoxy-2-oxoethyl]-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl (2e)-2-methylbut-2-enoate

(1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-9-(furan-3-yl)-15-[(1s)-1-hydroxy-2-methoxy-2-oxoethyl]-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl (2e)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

(1r,2s,5r,6r,10s,13r,14s,16s)-6-(furan-3-yl)-13-hydroxy-16-[(1s)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

(1r,2s,5r,6r,10s,13r,14s,16s)-6-(furan-3-yl)-13-hydroxy-16-[(1s)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

(2s,3r,4s,5s,6r)-2-{4-[(2r,3s)-4-hydroxy-3-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-2-(hydroxymethyl)butyl]-2,6-dimethoxyphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C28H40O13 (584.246879)

(2e)-but-2-en-2-yl (1r,2s,5r,6r,10s,13r,14s,16s)-6-(furan-3-yl)-13-hydroxy-16-[(1r)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-ene-14-carboxylate

(2e)-but-2-en-2-yl (1r,2s,5r,6r,10s,13r,14s,16s)-6-(furan-3-yl)-13-hydroxy-16-[(1r)-1-hydroxy-2-methoxy-2-oxoethyl]-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-ene-14-carboxylate

C32H40O10 (584.2621340000001)

(1r,4as,6s,7r,7ar)-1-hydroxy-4-(methoxycarbonyl)-7-methyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-6-yl (4s,5s,6s)-5-ethenyl-4-(2-oxoethyl)-6-{[(2s,3s,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

(1r,4as,6s,7r,7ar)-1-hydroxy-4-(methoxycarbonyl)-7-methyl-1h,4ah,5h,6h,7h,7ah-cyclopenta[c]pyran-6-yl (4s,5s,6s)-5-ethenyl-4-(2-oxoethyl)-6-{[(2s,3s,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-5,6-dihydro-4h-pyran-3-carboxylate

C27H36O14 (584.2104956000001)

C38H32O6 (584.2198771999999)

2-({4-[4-(4-hydroxy-3,5-dimethoxycyclohexa-1,5-dien-1-yl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxycyclohexa-2,4-dien-1-yl}oxy)-6-(hydroxymethyl)oxane-3,4,5-triol

C28H40O13 (584.246879)

(2r,3r,4s,5s,6r)-2-{[(2r,3s,4s)-6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydro-2h-1-benzopyran-3-yl]methoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C27H36O14 (584.2104956000001)

3-(4-methoxyphenyl)-1-[(9s)-1,6,7-trihydroxy-9-[(2r,3r)-4-(4-hydroxyphenyl)-3-methylbutan-2-yl]-3-methoxy-9h-xanthen-2-yl]propan-1-one

C35H36O8 (584.2410056)

3-(2-{[3-(2-carboxyethyl)-5-{[(2z)-3-ethenyl-5-hydroxy-4-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-2-yl]methyl}-5-{[(2z)-4-ethenyl-5-hydroxy-3-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-3-yl)propanoic acid

3-(2-{[3-(2-carboxyethyl)-5-{[(2z)-3-ethenyl-5-hydroxy-4-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-2-yl]methyl}-5-{[(2z)-4-ethenyl-5-hydroxy-3-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-3-yl)propanoic acid

C33H36N4O6 (584.2634716)

[(1r,2s,3s,5s,6r,8s)-3-{[(2s,3r,4s,5s,6r)-6-[(benzoyloxy)methyl]-3,4,5-trihydroxyoxan-2-yl]oxy}-6-hydroxy-8-methyl-9,10-dioxatetracyclo[4.3.1.0²,⁵.0³,⁸]decan-2-yl]methyl benzoate

C30H32O12 (584.1893672)

(4ar,5s,7r,8s,8ar)-5-(acetyloxy)-4a-[(acetyloxy)methyl]-4-(chloromethyl)-4-hydroxy-8-[(2r)-2-hydroxy-2-(5-oxo-2h-furan-3-yl)ethyl]-7,8-dimethyl-hexahydro-1h-naphthalen-1-yl (2e)-2-methylbut-2-enoate

C29H41ClO10 (584.2388116000001)

(3s)-n-{6-benzyl-1-[(1s)-1-(4-methoxy-6-oxopyran-2-yl)-2-phenylethyl]-4-oxopyridine-3-carbonyl}-4-methoxy-3-methyl-4-oxobutanimidic acid

C33H32N2O8 (584.2158552)

(1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-9-(furan-3-yl)-15-[(1r)-1-hydroxy-2-methoxy-2-oxoethyl]-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl (2z)-2-methylbut-2-enoate

(1s,2r,4s,5r,9r,10r,13r,14s,15s,17r)-9-(furan-3-yl)-15-[(1r)-1-hydroxy-2-methoxy-2-oxoethyl]-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl (2z)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

[(2r,3s,4s,5r,6s)-3,4,5-trihydroxy-6-({2-[(2r)-7-oxo-2h,3h-furo[3,2-g]chromen-2-yl]propan-2-yl}oxy)oxan-2-yl]methyl (2e)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C30H32O12 (584.1893672)

1,3,6,8-tetrahydroxy-2-[(1s)-1-[2-hydroxy-4-(3-hydroxy-5-methylphenoxy)-6-methylphenyl]hexyl]anthracene-9,10-dione

C34H32O9 (584.2046222)

(1r,2r,5r,6r,10s,13s,14r,16s)-6-[(2r)-2-hydroxy-5-oxo-2h-furan-3-yl]-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

(1r,2r,5r,6r,10s,13s,14r,16s)-6-[(2r)-2-hydroxy-5-oxo-2h-furan-3-yl]-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.0²,¹¹.0⁵,¹⁰]heptadec-11-en-14-yl (2e)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

2-{3-hydroxy-4-[(4-hydroxy-2-methyl-6-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-5-methylphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C27H36O14 (584.2104956000001)

(2s)-2-({[(2s,10bs)-7,8,10-trihydroxy-2-(1h-indol-3-ylmethyl)-9-methoxy-3-oxo-1h,2h,5h,6h,10bh-imidazo[2,1-a]isoquinolin-5-yl](hydroxy)methylidene}amino)-5-hydroxy-4-(hydroxymethyl)pentanoic acid

C28H32N4O10 (584.2118332)

(2s,3r,4s,5s,6r)-2-{3-hydroxy-4-[(4-hydroxy-2-methyl-6-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)methyl]-5-methylphenoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C27H36O14 (584.2104956000001)

3-(2-{[3-(2-carboxyethyl)-5-{[(2z)-3-ethenyl-5-hydroxy-4-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-2-yl]methyl}-5-{[(2e)-4-ethenyl-5-hydroxy-3-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-3-yl)propanoic acid

3-(2-{[3-(2-carboxyethyl)-5-{[(2z)-3-ethenyl-5-hydroxy-4-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-2-yl]methyl}-5-{[(2e)-4-ethenyl-5-hydroxy-3-methylpyrrol-2-ylidene]methyl}-4-methyl-1h-pyrrol-3-yl)propanoic acid

C33H36N4O6 (584.2634716)

9-(furan-3-yl)-1-hydroxy-15-(2-methoxy-2-oxoethyl)-10,14,16,16-tetramethyl-7,18-dioxo-3,8-dioxapentacyclo[12.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰]octadecan-17-yl 2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

6-methoxy-8-(3-methylbut-2-en-1-yl)-7-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-2-yl]oxy}chromen-2-one

C27H36O14 (584.2104956000001)

(1r,2s,4s,7r,9s,10r,11r)-4-(acetyloxy)-10-[(acetyloxy)methyl]-9,11-dihydroxy-13,16,16-trimethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

C31H36O11 (584.2257506)

(1s,2s,3r,4s,7r,9s,10s,11s,14s)-4,14-bis(acetyloxy)-9,11-dihydroxy-10,13,16,16-tetramethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

C31H36O11 (584.2257506)

(1r,2s)-1-(4-hydroxy-3-methoxyphenyl)-2-{4-[(2s,3r)-3-(hydroxymethyl)-5-[(1e)-3-hydroxyprop-1-en-1-yl]-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2,6-dimethoxyphenoxy}propane-1,3-diol

C31H36O11 (584.2257506)

2-[1-(2,4-dihydroxy-6-methylphenyl)hexyl]-1,3,8-trihydroxy-6-(3-hydroxy-5-methylphenoxy)anthracene-9,10-dione

C34H32O9 (584.2046222)

(1s,2r,4r,6r,7r,11s,12r,14r,15r,16r,18s)-7-(furan-3-yl)-18-(2-methoxy-2-oxoethyl)-1,6,17,17-tetramethyl-9,19-dioxo-3,8,13-trioxahexacyclo[13.3.1.0²,⁴.0²,¹².0⁶,¹¹.0¹²,¹⁴]nonadecan-16-yl (2r)-2-methylbutanoate

(1s,2r,4r,6r,7r,11s,12r,14r,15r,16r,18s)-7-(furan-3-yl)-18-(2-methoxy-2-oxoethyl)-1,6,17,17-tetramethyl-9,19-dioxo-3,8,13-trioxahexacyclo[13.3.1.0²,⁴.0²,¹².0⁶,¹¹.0¹²,¹⁴]nonadecan-16-yl (2r)-2-methylbutanoate

C32H40O10 (584.2621340000001)

9-(furan-3-yl)-19-hydroxy-15-(2-methoxy-2-oxoethyl)-10,14,16-trimethyl-7-oxo-3,8,18-trioxahexacyclo[14.3.1.0²,⁴.0⁴,¹³.0⁵,¹⁰.0¹⁴,¹⁹]icosan-20-yl (2e)-2-methylbut-2-enoate

C32H40O10 (584.2621340000001)

(1s,2s,3r,4s,7r,9s,10r,11s)-4-(acetyloxy)-10-[(acetyloxy)methyl]-9,11-dihydroxy-13,16,16-trimethyl-18-oxo-6,17-dioxapentacyclo[9.4.3.0¹,¹².0³,¹⁰.0⁴,⁷]octadec-12-en-2-yl benzoate

C31H36O11 (584.2257506)

2-{[6-hydroxy-4-(4-hydroxy-3,5-dimethoxyphenyl)-2-(hydroxymethyl)-5,7-dimethoxy-3,4-dihydro-2h-1-benzopyran-3-yl]methoxy}-6-(hydroxymethyl)oxane-3,4,5-triol

C27H36O14 (584.2104956000001)

4,5-dihydroxy-6-(hydroxymethyl)-2-[7-methoxy-5-methyl-4-oxo-2-(2-oxopropyl)chromen-8-yl]oxan-3-yl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate

C30H32O12 (584.1893672)

(3s,7z,8s,8as)-2-acetyl-8-(7-methoxy-2h-1,3-benzodioxol-5-yl)-3-[(7-methoxy-2h-1,3-benzodioxol-5-yl)methyl]-7-(phenylmethylidene)-tetrahydro-1h-pyrrolo[1,2-a]pyrazin-6-one

C33H32N2O8 (584.2158552)

n-{6-benzyl-1-[1-(4-methoxy-6-oxopyran-2-yl)-2-phenylethyl]-4-oxopyridine-3-carbonyl}-4-methoxy-3-methyl-4-oxobutanimidic acid

C33H32N2O8 (584.2158552)

methyl (4s,5e,6s)-4-{2-[(2s)-2-(3,4-dihydroxyphenyl)-2-ethoxyethoxy]-2-oxoethyl}-5-ethylidene-6-{[(2s,3r,4s,5s,6s)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4,6-dihydropyran-3-carboxylate

C27H36O14 (584.2104956000001)

(1r,2s)-2-{4-[(1s,3ar,4s,6ar)-4-(4-hydroxy-3-methoxyphenyl)-hexahydrofuro[3,4-c]furan-1-yl]-2,6-dimethoxyphenoxy}-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol

C31H36O11 (584.2257506)