NCBI Taxonomy: 279627
Hyrtios (ncbi_taxid: 279627)
found 500 associated metabolites at genus taxonomy rank level.
Ancestor: Thorectinae
Child Taxonomies: Hyrtios altus, Hyrtios erectus, Hyrtios proteus, Hyrtios spinifer, Hyrtios violaceus, Hyrtios reticulatus, unclassified Hyrtios, Hyrtios cf. erectus GW3258, Hyrtios cf. erectus GW3259, Hyrtios cf. erectus GW3266, Hyrtios cf. erectus GW3302, Hyrtios cf. erectus GW3306, Hyrtios cf. erectus GW3313, Hyrtios cf. erectus GW3371, Hyrtios cf. erectus GW3384, Hyrtios cf. erectus GW3546, Hyrtios cf. erectus GW5782, Hyrtios cf. erectus GW5787, Hyrtios cf. erectus GW5858, Hyrtios cf. erectus GW5864, Hyrtios cf. erectus GW5913, Hyrtios cf. erectus GW5916, Hyrtios cf. erectus GW5933, Hyrtios cf. erectus GW5959, Hyrtios cf. erectus GW5996, Hyrtios cf. erectus GW6024, Hyrtios cf. erectus GW6115, Hyrtios cf. erectus GW6170, Hyrtios cf. erectus GW6179, Hyrtios cf. erectus GW6185, Hyrtios cf. erectus GW26957, Hyrtios cf. erectus GW27002, Hyrtios cf. erectus GW33312, Hyrtios cf. erectus GW33313, Hyrtios cf. erectus GW33314, Hyrtios cf. erectus GW33315, Hyrtios cf. erectus GW33550, Hyrtios cf. erectus GW33551, Hyrtios cf. erectus QM G333625, Hyrtios cf. erectus QM G333628, Hyrtios cf. proteus BR2008-065-001
Serotonin
Serotonin or 5-hydroxytryptamine (5-HT) is a molecule that belongs to the class of compounds known as indoleamines. An indoleamine consists of an indole ring that bears an amino group or an alkyl amino group attached to the indole ring. Serotonin has an aminoethyl at position 2 and a hydroxyl group at position 5 of the indole ring. Serotonin exists in all living organisms, ranging from bacteria to plants to humans. In mammals, serotonin functions as a monoamine neurotransmitter, a biochemical messenger and regulator. It is synthesized from the essential amino acid L-Tryptophan. Approximately 90\\\\% of the human bodys total serotonin is located in the enterochromaffin cells in the GI tract, where it regulates intestinal movements. About 8\\\\% is found in platelets and 1–2\\\\% in the CNS. Serotonin in the nervous system acts as a local transmitter at synapses, and as a paracrine or hormonal modulator of circuits upon diffusion, allowing a wide variety of "state-dependent" behavioral responses to different stimuli. Serotonin is widely distributed in the nervous system of vertebrates and invertebrates and some of its behavioral effects have been preserved along evolution. Such is the case of aggressive behavior and rhythmic motor patterns, including those responsible for feeding. In vertebrates, which display a wider and much more sophisticated behavioral repertoire, serotonin also modulates sleep, the arousal state, sexual behavior, and others. Deficiencies of the serotonergic system causes disorders such as depression, obsessive-compulsive disorder, phobias, posttraumatic stress disorder, epilepsy, and generalized anxiety disorder. Serotonin has three different modes of action in the nervous system: as transmitter, acting locally at synaptic boutons; upon diffusion at a distance from its release sites, producing paracrine (also called volume) effects, and by circulating in the blood stream, producing hormonal effects. The three modes can affect a single neuronal circuit. (PMID: 16047543). Serotonin is also a microbial metabolite that can be found in the feces and urine of mammals. Urinary serotonin is produced by Candida, Streptococcus, Escherichia, and Enterococcus (PMID: 24621061). In plants, serotonin was first found and reported in a legume called Mucuna pruriens. The greatest concentration of serotonin in plants has been found in walnuts and hickory. In pineapples, banana, kiwi fruit, plums and tomatoes the concentration of serotonin is around 3 to 30 mg/kg. Isolated from bananas and other fruitsand is also from cotton (Gossypium hirsutum) [DFC]. Serotonin is found in many foods, some of which are common pea, eggplant, swiss chard, and dill. Serotonin. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=50-67-9 (retrieved 2024-07-01) (CAS RN: 50-67-9). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
manoalide
A sesterterpenoid isolated from the marine sponge Luffariella variabilis and which has been shown to exhibit inhibitory activity towards phospholipase A2. D018373 - Peripheral Nervous System Agents > D018689 - Sensory System Agents D004791 - Enzyme Inhibitors > D010726 - Phosphodiesterase Inhibitors D002317 - Cardiovascular Agents > D002121 - Calcium Channel Blockers D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents D002491 - Central Nervous System Agents > D000700 - Analgesics D000077264 - Calcium-Regulating Hormones and Agents D049990 - Membrane Transport Modulators D000893 - Anti-Inflammatory Agents D018501 - Antirheumatic Agents
12-epi-Scalaradial
5-Hydroxytryptophol
5-Hydroxytryptophol is a relatively minor metabolite of serotonin that is excreted primarily as the glucuronide conjugate in human urine. 5-Hydroxytryptophol becomes more important quantitatively during alcohol intoxication, when a shift in the metabolism of serotonin occurs from 5-hydroxyindole acetic acid toward increased (15-fold higher) formation of 5-hydroxytryptophol due to the inhibition of aldehyde dehydrogenase by ethanol-derived acetaldehyde. Urinary excretion of 5-hydroxytryptophol has also been shown to be markedly increased for several hours following intake of foods rich in serotonin, such as bananas. Wide interspecies variation has been reported in the metabolism serotonin to 5-hydroxytryptophol; 5-Hydroxytryptophol makes up 35\\\% of the excreted serotonin metabolites in the rat on average and 10 to 20\\\% in several other species. Human UDP-glucuronosyltransferase 1A6 (UGT1A6) plays a predominant role in the glucuronidation of 5-hydroxytryptophol by human liver microsomes. (PMID 15258112) [HMDB]. 5-Hydroxytryptophol is found in many foods, some of which are climbing bean, macadamia nut (m. tetraphylla), pepper (c. frutescens), and scarlet bean. 5-Hydroxytryptophol is a relatively minor metabolite of serotonin that is excreted primarily as the glucuronide conjugate in human urine. 5-Hydroxytryptophol becomes more important quantitatively during alcohol intoxication, when a shift in the metabolism of serotonin occurs from 5-hydroxyindole acetic acid toward increased (15-fold higher) formation of 5-hydroxytryptophol due to the inhibition of aldehyde dehydrogenase by ethanol-derived acetaldehyde. Urinary excretion of 5-hydroxytryptophol has also been shown to be markedly increased for several hours following intake of foods rich in serotonin, such as bananas. Wide interspecies variation has been reported in the metabolism serotonin to 5-hydroxytryptophol; 5-Hydroxytryptophol makes up 35\\\% of the excreted serotonin metabolites in the rat on average and 10 to 20\\\% in several other species. Human UDP-glucuronosyltransferase 1A6 (UGT1A6) plays a predominant role in the glucuronidation of 5-hydroxytryptophol by human liver microsomes. (PMID 15258112). 5-Hydroxytryptophol is a mammalian serotonin metabolite, acting as a marker of acute alcohol consumption.
manoalide
Serotonin
C10H12N2O (176.09495819999998)
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists
12-epi-Scalarin
The 12-epimer of scalarin, a metabolite of marine sponges of the genus Spongia.
2-hydroxy-3-(5-hydroxy-1H-indol-3-yl)propanoic acid
Hyrtial
A scalarane sesterterpenoid with formula C26H40O3, originally isolated from the marine sponge Hyrtios erecta.
Serotonin
C10H12N2O (176.09495819999998)
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists A primary amino compound that is the 5-hydroxy derivative of tryptamine. MS2 deconvoluted using MS2Dec from all ion fragmentation data, MetaboLights identifier MTBLS1040; QZAYGJVTTNCVMB_STSL_0135_Serotonin_8000fmol_180506_S2_LC02_MS02_147; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. MS2 deconvoluted using CorrDec from all ion fragmentation data, MetaboLights identifier MTBLS1040; Spectrum acquired as described in Naz et al 2017 PMID 28641411. Preparation and submission to MassBank of North America by Chaleckis R. and Tada I. relative retention time with respect to 9-anthracene Carboxylic Acid is 0.054 relative retention time with respect to 9-anthracene Carboxylic Acid is 0.053
Scalarin
A scalarane sesterterpenoid lactone, a metabolite of marine sponges of the family Thorectidae (order dictyoceratida).
5-Hydroxytryptophol
5-Hydroxytryptophol is a mammalian serotonin metabolite, acting as a marker of acute alcohol consumption.
12-O-acetyl-16-O-deacetyl-16-epi-scalarobutenolide
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus that exhibits antineoplastic activity.
Hyrtios sesterterpene 1
Scalaradial
A scalarane sesterterpenoid with formula C27H40O4. It is a natural product found in the marine sponges Spongia officinalis and Cacospongia mollior, and exhibits anti-inflammatory activity.
5-HTA
C10H12N2O (176.09495819999998)
D018377 - Neurotransmitter Agents > D018490 - Serotonin Agents > D017366 - Serotonin Receptor Agonists
Sesterstatin 2
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus and has been shown to exhibit antineoplastic activity.
Sesterstatin 3
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus and has been shown to exhibit antineoplastic activity.
Sesterstatin 1
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus and has been shown to exhibit antineoplastic activity.
16-O-deacetyl-16-epi-scalarolbutenolide
A scalarane sesterterpenoid isolated from the marine sponge Hyrtios erectus that exhibits antineoplastic activity.
12-hydroxy-4b,7,7,10a,12a-pentamethyl-3,4,4a,5,6,6a,8,9,10,10b,11,12-dodecahydrochrysene-2-carbaldehyde
(4s,5as,5br,7as,11as,11br,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1-oxo-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4-yl acetate
(1s,2s,3r,4s,6s,10s,13r,14s,16s,17r,18s)-3,13,17-trihydroxy-18-[(1e)-3-hydroxy-3-methylbut-1-en-1-yl]-11,11-dimethyl-5,12,15-trioxahexacyclo[8.7.1.0²,⁸.0⁴,⁶.0¹³,¹⁸.0¹⁴,¹⁶]octadec-8-en-7-one
13-hydroxy-5b,8,8,11a,13a-pentamethyl-5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4-one
[(1r,5as,5bs,7ar,8r,11ar,11br,13s,13as,13bs)-13-(acetyloxy)-1-hydroxy-5b,8,11a,13a-tetramethyl-1h,3h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate
(5z)-5-[(5,6-dibromo-1h-indol-3-yl)methylidene]-2-imino-3-methylimidazolidin-4-one
(1s,3s)-6-hydroxy-1-methyl-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid
[(1r,5as,5br,7ar,8r,11ar,11bs,13as,13br)-1-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate
(1r,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid
C16H16N4O3 (312.12223459999996)
(5as,5br,7as,11as,11br,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-1-one
(2s,3s,3ar,5as,9as,9br)-3-[(2s)-2-(furan-3-yl)-2-hydroxyethyl]-2,3a,6,6,9a-pentamethyl-octahydro-1h-cyclopenta[a]naphthalene-2-carbaldehyde
5b,8,8,11a,13a-pentamethyl-1h,3h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1,13-diol
(4r,5as,5br,7as,11as,11br,13r,13as)-1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one
(1s,4s,5ar,5br,7ar,11as,11bs,13r,13as,13br)-4-(acetyloxy)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
methyl 3-{[(1r,2s,4as,8as)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]methyl}-4-hydroxybenzoate
(5as,5br,7ar,9s,11ar,11br,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1-oxo-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-9-yl acetate
(1r,5as,5br,7as,11as,11br,13r,13as,13bs)-5b,8,8,11a,13a-pentamethyl-1h,3h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1,13-diol
(1s,2r,9r,10r)-10-hydroxy-2-methoxy-9,10-dimethyl-11-methylidene-3-oxatricyclo[7.3.1.0²,⁶]tridec-5-en-4-one
(5as,5br,7as,11as,11br,13r,13as,13br)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-3-one
4-hydroxy-1,11,14,18,18-pentamethyl-8-oxapentacyclo[11.8.0.0²,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-5(9),6-dien-10-yl acetate
(4s,5as,5br,7as,11as,11br,13r,13as)-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4,13-diol
(4s,5as,5br,7as,11as,11br,13s,13ar)-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-b]furan-4,13-diol
(4as,4br,6r,6ar,10as,10br,12as)-8-formyl-1,1,4a,6a,10b-pentamethyl-2,3,4,4b,5,6,7,10,10a,11,12,12a-dodecahydrochrysen-6-yl acetate
5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4,13-diol
(4s,5as,5br,7as,11as,11br,13r,13ar,13bs)-4,13-dihydroxy-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-b]furan-2-one
(1s,4s,5ar,5br,7as,11as,11bs,13s,13as,13br)-4-(acetyloxy)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
(5as,5br,7as,11as,11br,13r,13as,13br)-5b,8,8,11a,13a-pentamethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-13-yl acetate
(5s)-5-hydroxy-4-[(2r,6r)-6-hydroxy-5-[(3e)-4-methyl-6-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-3-en-1-yl]-3,6-dihydro-2h-pyran-2-yl]-5h-furan-2-one
5-[(5,6-dibromo-1h-indol-3-yl)methylidene]-2-imino-3-methylimidazolidin-4-one
[6-hydroxy-3-(6-hydroxy-1h-indol-3-yl)-9h-pyrido[3,4-b]indol-4-yl](oxo)acetic acid
C21H13N3O5 (387.08551680000005)
(5r,8s,11s)-6,13-dihydroxy-8-isopropyl-5-methyl-11-[(1e)-4-(octanoylsulfanyl)but-1-en-1-yl]-10-oxa-3,17-dithia-7,14,19,20-tetraazatricyclo[14.2.1.1²,⁵]icosa-1(18),2(20),6,13,16(19)-pentaen-9-one
C29H42N4O5S3 (622.2317201999999)
(2r,3r,3as,5as,6s,9as,9bs)-3-[(2r)-2-(furan-3-yl)-2-hydroxyethyl]-2,3a,6,9a-tetramethyl-octahydro-1h-cyclopenta[a]naphthalene-2,6-dicarbaldehyde
(5as,5br,7as,11as,11br,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4-one
(1s,3r,11r,12r,13s,14s,19s)-12-hydroxy-1,11,14,18,18-pentamethyl-7-oxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicos-5(9)-en-8-one
(1s,3r,11r,12r,13s,14s,17s,19r)-12-hydroxy-1,11,14,18,18-pentamethyl-8-oxo-7-oxapentacyclo[11.8.0.0³,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicos-5(9)-en-17-yl acetate
5b,8,8,11a,13a-pentamethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-13-yl acetate
(1r,3r)-6-hydroxy-1-methyl-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid
1-hydroxy-5b,8,8,11a,13a-pentamethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-13-yl acetate
(1s,5as,5br,7as,11as,11br,13r,13as,13bs)-1-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,3h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-13-yl acetate
(1r,4s,5as,5br,7as,11as,11br,13r,13as)-1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one
13-hydroxy-8-(hydroxymethyl)-5b,8,11a,13a-tetramethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-1-one
(1s,4s,5as,5br,7as,11as,11br,13r,13as,13br)-4-(acetyloxy)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
(23e)-3-(acetyloxy)-11-[(5e)-7-chloro-4-hydroxy-2-methylideneocta-5,7-dien-1-yl]-10,14,15,17,27,43-hexahydroxy-31-methoxy-18,36,38,43,49-pentamethyl-39-methylidene-7,35-dioxo-8,12,45,46,47,48,50-heptaoxaheptacyclo[39.3.1.1¹,⁵.1⁹,¹³.1¹⁵,¹⁹.1²⁵,²⁹.1²⁹,³³]pentacont-23-en-37-yl acetate
3-[2-(furan-3-yl)-2-hydroxyethyl]-2,3a,6,9a-tetramethyl-octahydro-1h-cyclopenta[a]naphthalene-2,6-dicarbaldehyde
(1s,3s)-6-hydroxy-1-(3h-imidazol-4-ylmethyl)-1h,2h,3h,4h,9h-pyrido[3,4-b]indole-3-carboxylic acid
C16H16N4O3 (312.12223459999996)
(1s,2r,9r,11r)-11-hydroxy-2-methoxy-9,11-dimethyl-10-methylidene-3-oxatricyclo[7.3.1.0²,⁶]tridec-5-en-4-one
[(5as,5br,7ar,8s,11ar,11br,13r,13as,13br)-13-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate
(1r)-1-methyl-1h,2h,3h,4h,9h-pyrido[3,4-b]indol-6-ol
1-{20-hydroxy-3,13-diazapentacyclo[11.7.0.0²,¹⁰.0⁴,⁹.0¹⁴,¹⁹]icosa-1,3,5,7,9,11,14,16,18-nonaen-20-yl}propan-2-one
C21H16N2O2 (328.12117159999997)
(5as,7as,11as,11br)-2,3-dihydroxy-5a,8,8,11a-tetramethyl-7,7a,9,10,11,11b-hexahydro-6h-5-oxatetraphen-12-one
4,8,8,12,21,25,25,29-octamethyl-13,30-dioxanonacyclo[17.15.1.1²,¹⁴.0³,¹².0⁴,⁹.0²⁰,²⁹.0²¹,²⁶.0³¹,³⁵.0¹⁸,³⁶]hexatriaconta-1,14,18(36),19(35),31-pentaene-16,17,33,34-tetrone
1,13-dihydroxy-5b,8,8,11a,13a-pentamethyl-1h,3h,5h,5ah,6h,7h,7ah,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-9-one
(2s)-2-hydroxy-3-(5-hydroxy-1h-indol-3-yl)propanoic acid
6,10,10,14,23,27,27,31-octamethyl-15,20,32-trioxanonacyclo[19.15.1.0²,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁶,¹¹.0²²,³¹.0²³,²⁸.0³³,³⁷]heptatriaconta-1(36),2(19),3(16),4,17,33(37),34-heptaene-18,35,36-triol
(1r,3ar,3br,5as,6s,7r,8s,9as,9bs,10s,11ar)-6,9a,11a-trimethyl-1-[(2s,3e)-6-methyl-5-methylidenehept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthrene-3b,7,8,10-tetrol
(4e)-5-chloro-3-hydroxy-4-[(2-hydroxy-2,5,5,8a-tetramethyl-hexahydro-1h-naphthalen-1-yl)methylidene]cyclopent-2-en-1-one
(1s,3e,5r,7e,11e)-1-(furan-3-yl)-4,8,12,16-tetramethylheptadeca-3,7,11,15-tetraene-1,5-diol
(2e,5e)-2-[(3r)-3-hydroxy-3-[(2r)-2-hydroxy-5-oxo-2h-furan-3-yl]propylidene]-6-methyl-8-(2,6,6-trimethylcyclohex-1-en-1-yl)oct-5-enal
(1r,4r,5as,5br,7as,11as,11br,13r,13as)-1,4,13-trihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-3-one
(1r,2r,9r,11r)-11-hydroxy-2-methoxy-9,11-dimethyl-10-methylidene-3-oxatricyclo[7.3.1.0²,⁶]tridec-5-en-4-one
1-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,3h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-13-yl acetate
(10e)-11-[5-({[(3s)-3-carboxy-1-hydroxy-3-methylpropylidene]amino}carbonyl)-4-oxopyran-2-yl]undec-10-enoic acid
(4as,4br,6as,10as,10br,12r,12ar)-12-hydroxy-4b,7,7,10a,12a-pentamethyl-3,4,4a,5,6,6a,8,9,10,10b,11,12-dodecahydrochrysene-2-carbaldehyde
13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-3-one
bis(5-hydroxy-1h-indol-3-yl)ethane-1,2-dione
C18H12N2O4 (320.07970320000004)
(1s,4s,5as,5br,7as,11as,11br,13as,13br)-4-(acetyloxy)-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
7-hydroxy-9-(5-hydroxy-1h-indol-3-yl)-3,10-diazatricyclo[6.4.1.0⁴,¹³]trideca-1,4,6,8(13),9-pentaene-11-carboxylic acid
C20H15N3O4 (361.10625100000004)
(4s,5as,5br,7as,11as,11br,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4-yl acetate
(1r,2s,7s,10s,15s)-15-hydroxy-2,6,6,10-tetramethyl-11-oxatetracyclo[8.7.0.0²,⁷.0¹²,¹⁶]heptadeca-12,16-dien-14-one
(2s,3s,3as,5as,9bs)-3-[(2s)-2-(furan-3-yl)-2-hydroxyethyl]-2,3a,6,6,9a-pentamethyl-octahydro-1h-cyclopenta[a]naphthalene-2-carbaldehyde
1-(furan-3-yl)-4,8,12,16-tetramethylheptadeca-3,7,11,15-tetraene-1,5-diol
4-(acetyloxy)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
5-hydroxy-4-{6-hydroxy-5-[(3z,7e)-4,8,12-trimethyltrideca-3,7,11-trien-1-yl]-3,6-dihydro-2h-pyran-2-yl}-5h-furan-2-one
(4s,5as,5br,7as,11as,11br,13r,13ar,13bs)-4-hydroxy-5b,8,8,11a,13a-pentamethyl-2-oxo-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-b]furan-13-yl acetate
13-hydroxy-5b,8,8,11a,13a-pentamethyl-1-oxo-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-9-yl acetate
(5as,5br,7ar,9s,11ar,11bs,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1-oxo-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-9-yl acetate
(5as,5br,7as,11as,11br,13s,13as)-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-13-yl acetate
(5as,7as,11as,11br)-5a,8,8,11a-tetramethyl-6,7,7a,9,10,11,11b,12-octahydro-5-oxatetraphene-1-carboxylic acid
4-hydroxy-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-13-yl acetate
(2z,5e)-2-[3-hydroxy-3-(2-hydroxy-5-oxo-2h-furan-3-yl)propylidene]-6-methyl-8-(2,6,6-trimethylcyclohex-1-en-1-yl)oct-5-enal
(4s,5as,5br,7as,11as,11br,13r,13as)-4,13-dihydroxy-5b,8,8,11a,13a-pentamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-1-one
5-chloro-2-[3-(dichloromethylidene)hexyl]benzene-1,3-diol
[13-(acetyloxy)-1-hydroxy-8,8,11a,13a-tetramethyl-1h,3h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-5b-yl]methyl acetate
(4s,5as,5br,7as,11as,11br,13r,13ar,13bs)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-2-oxo-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-b]furan-4-yl acetate
(1r,3ar,3br,5as,6s,7s,8r,9as,9br,10s,11ar)-6,9a,11a-trimethyl-1-[(2r,3e)-6-methyl-5-methylidenehept-3-en-2-yl]-tetradecahydrocyclopenta[a]phenanthrene-3b,7,8,10-tetrol
(1r,5as,5br,7ar,11ar,11bs,13r,13as)-1,13-dihydroxy-5b,8,8,11a,13a-pentamethyl-1h,3h,5h,5ah,6h,7h,7ah,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-9-one
3-{6-hydroxy-9h-pyrido[3,4-b]indole-1-carbonyl}-1h-indol-5-ol
C20H13N3O3 (343.09568680000007)
(5as,5br,7as,11as,11br,13r,13as)-13-hydroxy-5b,8,8,11a,13a-pentamethyl-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-3-one
5-{6-hydroxy-2h-pyrido[3,4-b]indole-1-carbonyl}-1,3-dimethyl-4-(methylsulfanyl)imidazol-1-ium
[C18H17N4O2S]+ (353.10721620000004)
9,13-dihydroxy-5b,8,8,11a,13a-pentamethyl-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-1-one
methyl 3-{[(1r,2s,4ar,8as)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]methyl}-4,5-dihydroxybenzoate
{13-hydroxy-5b,8,11a,13a-tetramethyl-1-oxo-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-8-yl}methyl acetate
4-(acetyloxy)-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
1,4-dihydroxy-5b,8,8,11a,13a-pentamethyl-3-oxo-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-13-yl acetate
(1r,2s,4s,10s,11s,13r,14s,19s)-4-hydroxy-1,11,14,18,18-pentamethyl-8-oxapentacyclo[11.8.0.0²,¹¹.0⁵,⁹.0¹⁴,¹⁹]henicosa-5(9),6-dien-10-yl acetate
13-hydroxy-5b,8,8,11a,13a-pentamethyl-1-oxo-3h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4-yl acetate
[13-(acetyloxy)-5b,8,11a,13a-tetramethyl-3-oxo-1h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-8-yl]methyl acetate
(4s,5s,6s,11s,14s,21s,22s,23s,28s,31s)-6,10,10,14,23,27,27,31-octamethyl-15,20,32,38-tetraoxadecacyclo[19.15.1.1⁴,³⁶.0²,¹⁹.0³,¹⁶.0⁵,¹⁴.0⁶,¹¹.0²²,³¹.0²³,²⁸.0³³,³⁷]octatriaconta-1(37),2,16,18,33,35-hexaene-18,35-diol
4-hydroxy-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-b]furan-13-yl acetate
13-hydroxy-5b,8,8,11a,13a-pentamethyl-4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h-chryseno[1,2-c]furan-4-yl acetate
2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraene-7,18-dione
(5as,7as,11as)-1-chloro-5a,8,8,11a-tetramethyl-6,7,7a,9,10,11-hexahydro-5-oxatetraphene-2,3-diol
5-{4-hydroxy-3-[4-methyl-6-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-3-en-1-yl]but-2-en-1-yl}-4-(hydroxymethyl)-5h-furan-2-one
4,13-dihydroxy-5b,8,8,11a,13a-pentamethyl-1h,4h,5h,5ah,6h,7h,7ah,9h,10h,11h,11bh,12h,13h,13bh-chryseno[1,2-c]furan-1-yl acetate
(11r)-7-hydroxy-9-(5-hydroxy-1h-indol-3-yl)-3,10-diazatricyclo[6.4.1.0⁴,¹³]trideca-1,4,6,8(13),9-pentaene-11-carboxylic acid
C20H15N3O4 (361.10625100000004)