NCBI Taxonomy: 86620

Usnea (ncbi_taxid: 86620)

found 134 associated metabolites at genus taxonomy rank level.

Ancestor: Parmeliaceae

Child Taxonomies: Usnea halei, Usnea hirta, Usnea dasaea, Usnea aspera, Usnea dodgei, Usnea malmei, Usnea rigida, Usnea aranea, Usnea lambii, Usnea florida, Usnea arianae, Usnea flammea, Usnea confusa, Usnea baileyi, Usnea cornuta, Usnea ciliata, Usnea crocata, Usnea cirrosa, Usnea parvula, Usnea barbata, Usnea hyyppae, Usnea pangiana, Usnea undulata, Usnea boomiana, Usnea krogiana, Usnea ceratina, Usnea strigosa, Usnea masudana, Usnea nidifica, Usnea sinensis, Usnea subfusca, Usnea angulata, Usnea erinacea, Usnea steineri, Usnea fleigiae, Usnea dasopoga, Usnea glabrata, Usnea taylorii, Usnea merrillii, Usnea mutabilis, Usnea rubicunda, Usnea wasmuthii, Usnea stipitata, Usnea diffracta, Usnea oreophila, Usnea chilensis, Usnea moreliana, Usnea cavernosa, Usnea arizonica, Usnea durietzii, Usnea lapponica, Usnea diplotypa, Usnea pygmoidea, Usnea silesiaca, Usnea splendens, Usnea subdasaea, Usnea messutiae, Usnea rohmederi, Usnea subaranea, Usnea trichodea, Usnea clerciana, Usnea himalayana, Usnea viktoriana, Usnea pycnoclada, Usnea grandisora, Usnea subflammea, Usnea pacificana, Usnea acanthella, Usnea patagonica, Usnea perpusilla, Usnea acromelana, Usnea hakonensis, Usnea orientalis, Usnea intermedia, Usnea aff. picta, Usnea subcornuta, Usnea antarctica, Usnea ghattensis, Usnea subparvula, Usnea sphacelata, Usnea cristatula, Usnea articulata, Usnea cladocarpa, Usnea perplexans, Usnea glabrescens, Usnea aff. dasaea, Usnea intumescens, Usnea endochrysea, Usnea nipparensis, Usnea rubrotincta, Usnea subgracilis, Usnea flavocardia, Usnea spinulifera, Usnea aciculifera, Usnea praetervisa, Usnea trachycarpa, Usnea ushuaiensis, Usnea substerilis, Usnea subscabrosa, Usnea densirostra, Usnea grandispora, Usnea trachyclada, Usnea subglabrata, Usnea aff. dodgei, Usnea chaetophora, Usnea fulvoreagens, Usnea aff. crocata, Usnea subfloridana, Usnea subpectinata, Usnea rubropallens, Usnea eumitrioides, Usnea esperantiana, Usnea macaronesica, Usnea aff. cornuta, Usnea aff. flammea, Usnea brasiliensis, Usnea rubricornuta, Usnea stigmatoides, Usnea subrubicunda, Usnea meridionalis, Usnea geissleriana, Usnea aff. barbata, unclassified Usnea, Usnea pallidocarpa, Usnea fragilescens, Usnea aff. angulata, Usnea aff. erinacea, Usnea aff. glabrata, Usnea subcapillaris, Usnea parafloridana, Usnea subantarctica, Usnea aff. krogiana, Usnea perhispidella, Usnea pennsylvanica, Usnea jezoformosana, Usnea rubriglabrata, Usnea flabelliformis, Usnea aff. pygmoidea, Usnea aff. rubicunda, Usnea bismolliuscula, Usnea aff. sanguinea, Usnea aurantiacoatra, Usnea aff. fruticans, Usnea aff. silesiaca, Usnea aff. wasmuthii, Usnea tenuicorticata, Usnea aff. grandisora, Usnea aff. subflammea, Usnea croceorubescens, Usnea trachycarpoides, Usnea pseudocapillaris, Usnea aff. brasiliensis, Usnea aff. fragilescens, Usnea aff. fulvoreagens, Usnea aff. subpectinata, Usnea aurantiaca-parvula, Usnea aff. bismolliuscula, Usnea cf. ciliata NW-2012, Usnea cf. cylindrica CHE 15, Usnea cf. glabrescens WAS 29, Usnea aff. igniaria Kim 05010, Usnea cf. fulvoreagens TU 6873, Usnea aff. articulata 1 MN-2020, Usnea aff. articulata 3 MN-2020, Usnea aff. articulata 4 MN-2020, Usnea aff. perpusilla F 1174040a, Usnea aff. perpusilla F 1174041a, Usnea aff. perpusilla F 1174040b, Usnea aff. perpusilla F 1174042a

lichenin

(2S,3R,4R)-2-(hydroxymethyl)-3,4-dihydro-2H-pyran-3,4,5-triol

C6H10O5 (162.0528)


   

Usnic acid

2,6-Diacetyl-3,7,9-trihydroxy-8,9b-dimethyldibenzofuran-1-one

C18H16O7 (344.0896)


A member of the class of dibenzofurans that is dibenzo[b,d]furan-1(9bH)-one substituted by acetyl groups at positions 2 and 6, hydroxy groups at positions 3 and 7 and methyl groups at positions 8 and 9b. D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 1.457 D000890 - Anti-Infective Agents > D000935 - Antifungal Agents relative retention time with respect to 9-anthracene Carboxylic Acid is 1.456 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.458 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.459 relative retention time with respect to 9-anthracene Carboxylic Acid is 1.455 (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. Usnic acid, a lichen-derived secondary metabolite, has a unique dibenzofuran skeleton. Usnic acid has excellent anticancer and antimicrobial properties. Usnic acid significantly inhibits RANKL-mediated osteoclast formation and function by reducing the transcriptional and translational expression of NFATc1[1]. Usnic acid, a lichen-derived secondary metabolite, has a unique dibenzofuran skeleton. Usnic acid has excellent anticancer and antimicrobial properties. Usnic acid significantly inhibits RANKL-mediated osteoclast formation and function by reducing the transcriptional and translational expression of NFATc1[1].

   

Glutinol

glutin-5-en-3beta-ol

C30H50O (426.3861)


   

7-Hydroxy-(S)-usnate

7-Hydroxy-(S)-usnate

C18H16O7 (344.0896)


   

Usnic_acid

4,10-diacetyl-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(9),6,10,12-tetraene-3,5-dione

C18H16O7 (344.0896)


7-Hydroxy-(S)-usnate is a member of benzofurans. Usnic acid is a natural product found in Lecanora muralis, Usnea florida, and other organisms with data available. D000890 - Anti-Infective Agents > D000977 - Antiparasitic Agents > D000981 - Antiprotozoal Agents D000890 - Anti-Infective Agents > D000935 - Antifungal Agents Usnic acid, a lichen-derived secondary metabolite, has a unique dibenzofuran skeleton. Usnic acid has excellent anticancer and antimicrobial properties. Usnic acid significantly inhibits RANKL-mediated osteoclast formation and function by reducing the transcriptional and translational expression of NFATc1[1]. Usnic acid, a lichen-derived secondary metabolite, has a unique dibenzofuran skeleton. Usnic acid has excellent anticancer and antimicrobial properties. Usnic acid significantly inhibits RANKL-mediated osteoclast formation and function by reducing the transcriptional and translational expression of NFATc1[1].

   

Ergosterol peroxide

5-[(3E)-5,6-dimethylhept-3-en-2-yl]-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C28H44O3 (428.329)


Ergosterol peroxide is found in fruits. Ergosterol peroxide is obtained from leaves of Ananas comosus (pineapple obtained from leaves of Ananas comosus (pineapple). Ergosterol peroxide is found in pineapple and fruits.

   

Cholesteryl acetate

(1S,2R,5S,10S,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-yl acetate

C29H48O2 (428.3654)


Cholesteryl acetate is a normal human cholesteryl ester present in diverse fluids and organs. Cholesteryl acetate is also present in foods. Food oxidation affects the quality and safety of the human diet by generating compounds with biological activities that can adversely affect health. In particular the susceptibility of cholesterol to oxidation is well known; certain products of cholesterol oxidation have been reported to produce cytotoxic, angiotoxic and carcinogenic effects. Cholesteryl ester (CE) is the major transport and storage form of cholesterol in lipoprotein particles and most cell types. Molecular composition of CE species is of high interest for arteriosclerosis research, i.e., as components of lipoprotein subclasses or in studies investigating the mechanisms involved in the generation of lipid laden foam cells. Thus, it has been shown that CE species in circulating plasma are strongly correlated with development of coronary heart disease. This may be related to specific CE species profiles generated by enzymes involved in lipoprotein metabolism like lecithin:cholesterol acyltransferase (EC 2.3.1.43, LCAT), acyl-coenzyme A:cholesterol acyltransferase 2 (EC 2.3.1.26, ACAT2) or cholesteryl ester transfer protein (CETP). The cholesteryl ester transfer protein has a key role in the metabolism of high-density lipoprotein (HDL), mediating the exchange of lipids between lipoproteins, resulting in the net transfer of cholesteryl ester from HDL to other lipoproteins and in the subsequent uptake of cholesterol by hepatocytes. By increasing the cholesteryl ester content of low-density and very-low-density lipoproteins, CETP promotes the atherogenicity of these lipoproteins. In addition, high plasma concentrations of CETP are associated with reduced concentrations of HDL cholesterol. (PMID: 10918380, 16458590, 9420339, 3343104, 6721900, 7278520).

   

usnic acid

4,10-diacetyl-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

C18H16O7 (344.0896)


   

Lichenin

(2R,3R,4R)-2-methoxy-3,4-dihydro-2H-pyran-3,4,5-triol

C6H10O5 (162.0528)


Lichenin, also known as lichenan or moss starch, is a complex glucan occurring in certain species of lichens. It can be extracted from Cetraria islandica (Iceland moss). It has been studied since about 1957. Chemically, lichenin consists of repeating glucose units linked by beta-1,3 and beta-1,4 glycosidic bonds . Lichenin is soluble (in water) and a very weakly acidic compound (based on its pKa). Lichenin can be found in oat, which makes lichenin a potential biomarker for the consumption of this food product. Lichenin, also known as lichenan or moss starch, is a complex glucan occurring in certain species of lichens. It can be extracted from Cetraria islandica (Iceland moss). It has been studied since about 1957. Chemically, lichenin consists of repeating glucose units linked by β-1,3 and β-1,4 glycosidic bonds . Lichenin is soluble (in water) and a very weakly acidic compound (based on its pKa). Lichenin can be found in oat, which makes lichenin a potential biomarker for the consumption of this food product.

   

UsnicAcid

(2R)-4,10-diacetyl-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0^{2,7}]trideca-1(13),3,6,9,11-pentaen-5-one

C18H16O7 (344.0896)


(-)-usnic acid is the (-)-enantiomer of usnic acid. It has a role as an EC 1.13.11.27 (4-hydroxyphenylpyruvate dioxygenase) inhibitor. It is a conjugate acid of a (-)-usnic acid(2-). It is an enantiomer of a (+)-usnic acid. Usnic acid is a furandione found uniquely in lichen that is used widely in cosmetics, deodorants, toothpaste and medicinal creams as well as some herbal products. Taken orally, usnic acid can be toxic and has been linked to instances of clinically apparent, acute liver injury. (-)-Usnic acid is a natural product found in Dactylina arctica, Evernia divaricata, and other organisms with data available. The (-)-enantiomer of usnic acid. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2]. (+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity[1]. (+)-Usnic acid possesses antimicrobial activity against a number of planktonic gram-positive bacteria, including Staphylococcus aureus, Enterococcus faecalis, and Enterococcus faecium[2].

   

Fumarprotocetraric acid

9-(3-Carboxy-acryloyloximethyl)-4-formyl-3,8-dihydroxy-1,6-dimethyl-11-oxo-11H-dibenzo[b,e][1,4]dioxepin-7-carboxylic acid

C22H16O12 (472.0642)


   

Norstictic acid

5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(11),3(8),4,6,12,14(18)-hexaene-4-carbaldehyde

C18H12O9 (372.0481)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates

   

Atraric acid

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

C10H12O4 (196.0736)


Atraric acid (Methyl atrarate) is a specific androgen receptor (AR) antagonist with anti-inflammatory and anticancer effects. Atraric acid represses the expression of the endogenous prostate specific antigen gene in both LNCaP and C4-2 cells. Atraric acid can also inhibit the synthesis of NO and cytokine, and suppress the MAPK-NFκB signaling pathway. Atraric acid can be used to research prostate diseases and inflammatory diseases[1][2]. Atraric acid (Methyl atrarate) is a specific androgen receptor (AR) antagonist with anti-inflammatory and anticancer effects. Atraric acid represses the expression of the endogenous prostate specific antigen gene in both LNCaP and C4-2 cells. Atraric acid can also inhibit the synthesis of NO and cytokine, and suppress the MAPK-NFκB signaling pathway. Atraric acid can be used to research prostate diseases and inflammatory diseases[1][2].

   

Orsellic acid

2,4-Dihydroxy-6-methylbenzoic acid

C8H8O4 (168.0423)


Orsellinic acid is a compound produced by Lecanoric acid treated with alcohols. Lecanoric acid is a lichen depside isolated from a Parmotrema tinctorum specimen[1].

   

Evernic Acid

2-hydroxy-4-(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy-6-methylbenzoic acid

C17H16O7 (332.0896)


Evernic Acid is a secondary metabolite generated by lichens, including Ramalina, Evernia, and Hypogymnia, and several studies have described its anticancer, antifungal, and antimicrobial effects. Neuroprotective and anti-inflammatory effects[1]. Evernic Acid is a secondary metabolite generated by lichens, including Ramalina, Evernia, and Hypogymnia, and several studies have described its anticancer, antifungal, and antimicrobial effects. Neuroprotective and anti-inflammatory effects[1].

   

Ergosterol peroxide

Ergosterol peroxide

C28H44O3 (428.329)


   

Galbinic acid

Galbinic acid

C20H14O11 (430.0536)


   

Salazinic acid

5,13,17-trihydroxy-12-(hydroxymethyl)-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(11),3(8),4,6,12,14(18)-hexaene-4-carbaldehyde

C18H12O10 (388.043)


D000893 - Anti-Inflammatory Agents > D000894 - Anti-Inflammatory Agents, Non-Steroidal > D012459 - Salicylates Origin: Microbe, Carboxylic acids

   

3-methyl Orsellinic Acid

2,4-dihydroxy-3,6-dimethylbenzoic acid

C9H10O4 (182.0579)


   

Dasypogalactone

Dasypogalactone

C30H54O9 (558.3768)


   

Ethyl 2-hydroxy-4-methoxy-6-methylbenzoate

Ethyl 2-hydroxy-4-methoxy-6-methylbenzoate

C11H14O4 (210.0892)


   

4-(2,4-dihydroxy-3,6-dimethylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid

4-(2,4-dihydroxy-3,6-dimethylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid

C18H18O7 (346.1052)


   

(+)-Usnic acid

(+)-Usnic acid

C18H16O7 (344.0896)


   

Atranorin

methyl 1-(3-formyl-2,4-dihydroxy-6-methylphenylcarbonyloxy)-3-hydroxy-2,5-dimethyl-4-benzenecarboxylate

C19H18O8 (374.1002)


Atranorin is a carbonyl compound. Atranorin is a natural product found in Candelaria concolor, Loxospora elatina, and other organisms with data available. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2]. Atranorin is a lichen secondary metabolite. Atranorin inhibits lung cancer cell motility and tumorigenesis by affecting AP-1, Wnt, and STAT signaling and suppressing RhoGTPase activity[1][2].

   

Evernic_acid

Benzoic acid, 2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methyl-

C17H16O7 (332.0896)


2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylphenyl)-oxomethoxy]-6-methylbenzoic acid is a carbonyl compound. Evernic acid is a natural product found in Ochrolechia parella, Usnea rubicunda, and other organisms with data available. Evernic Acid is a secondary metabolite generated by lichens, including Ramalina, Evernia, and Hypogymnia, and several studies have described its anticancer, antifungal, and antimicrobial effects. Neuroprotective and anti-inflammatory effects[1]. Evernic Acid is a secondary metabolite generated by lichens, including Ramalina, Evernia, and Hypogymnia, and several studies have described its anticancer, antifungal, and antimicrobial effects. Neuroprotective and anti-inflammatory effects[1].

   

Arabitol

L-(−)-Arabitol

C5H12O5 (152.0685)


L-Arabinitol is a potential biomarker for the comsuption of the food products such as sweet potato, deerberry, moth bean, and is also associated with Alzheimer's disease and ribose-5-phosphate isomerase deficiency.

   

Lecanoric acid

Lecanoric acid

C16H14O7 (318.0739)


   

orsellinic acid

orsellinic acid

C8H8O4 (168.0423)


   

Methyl 2,4-dihydroxy-3,6-dimethylbenzoate

methyl 2,4-dihydroxy-3,6-dimethylbenzoate

C10H12O4 (196.0736)


CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4243; ORIGINAL_PRECURSOR_SCAN_NO 4241 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4554; ORIGINAL_PRECURSOR_SCAN_NO 4552 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4219; ORIGINAL_PRECURSOR_SCAN_NO 4216 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4573; ORIGINAL_PRECURSOR_SCAN_NO 4572 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3741; ORIGINAL_PRECURSOR_SCAN_NO 3740 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4554; ORIGINAL_PRECURSOR_SCAN_NO 4550 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7363; ORIGINAL_PRECURSOR_SCAN_NO 7360 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7378; ORIGINAL_PRECURSOR_SCAN_NO 7376 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7361; ORIGINAL_PRECURSOR_SCAN_NO 7359 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7404; ORIGINAL_PRECURSOR_SCAN_NO 7400 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7394; ORIGINAL_PRECURSOR_SCAN_NO 7391 CONFIDENCE standard compound; INTERNAL_ID 1194; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 7418; ORIGINAL_PRECURSOR_SCAN_NO 7416 Atraric acid (Methyl atrarate) is a specific androgen receptor (AR) antagonist with anti-inflammatory and anticancer effects. Atraric acid represses the expression of the endogenous prostate specific antigen gene in both LNCaP and C4-2 cells. Atraric acid can also inhibit the synthesis of NO and cytokine, and suppress the MAPK-NFκB signaling pathway. Atraric acid can be used to research prostate diseases and inflammatory diseases[1][2]. Atraric acid (Methyl atrarate) is a specific androgen receptor (AR) antagonist with anti-inflammatory and anticancer effects. Atraric acid represses the expression of the endogenous prostate specific antigen gene in both LNCaP and C4-2 cells. Atraric acid can also inhibit the synthesis of NO and cytokine, and suppress the MAPK-NFκB signaling pathway. Atraric acid can be used to research prostate diseases and inflammatory diseases[1][2].

   

2-Hydroxy-4-methoxy-6-methylbenzoic acid

2-hydroxy-4-methoxy-6-methylbenzoic acid

C9H10O4 (182.0579)


   

Depsidone

Depsidone

C13H8O3 (212.0473)


The simplest member of the class of depsidones comprising of a heterotricyclic system that is 11H-dibenzo[b,e][1,4]dioxepine substituted by an oxo group at position 11.

   

2-Hydroxy-4-methoxy-6-propylbenzoic acid

2-hydroxy-4-methoxy-6-propylbenzoic acid

C11H14O4 (210.0892)


   

Cholesteryl acetate

(-)-Cholesteryl acetate

C29H48O2 (428.3654)


A cholesterol ester obtained by formal acylation of the hydroxy group of cholesterol by acetic acid. Cholesteryl acetate is a normal human cholesteryl ester present in diverse fluids and organs. Cholesteryl acetate is also present in foods. Food oxidation affects the quality and safety of the human diet by generating compounds with biological activities that can adversely affect health. In particular the susceptibility of cholesterol to oxidation is well known; certain products of cholesterol oxidation have been reported to produce cytotoxic, angiotoxic and carcinogenic effects. Cholesteryl ester (CE) is the major transport and storage form of cholesterol in lipoprotein particles and most cell types. Molecular composition of CE species is of high interest for arteriosclerosis research, i.e., as components of lipoprotein subclasses or in studies investigating the mechanisms involved in the generation of lipid laden foam cells. Thus, it has been shown that CE species in circulating plasma are strongly correlated with development of coronary heart disease. This may be related to specific CE species profiles generated by enzymes involved in lipoprotein metabolism like lecithin:cholesterol acyltransferase (EC 2.3.1.43, LCAT), acyl-coenzyme A:cholesterol acyltransferase 2 (EC 2.3.1.26, ACAT2) or cholesteryl ester transfer protein (CETP). The cholesteryl ester transfer protein has a key role in the metabolism of high-density lipoprotein (HDL), mediating the exchange of lipids between lipoproteins, resulting in the net transfer of cholesteryl ester from HDL to other lipoproteins and in the subsequent uptake of cholesterol by hepatocytes. By increasing the cholesteryl ester content of low-density and very-low-density lipoproteins, CETP promotes the atherogenicity of these lipoproteins. In addition, high plasma concentrations of CETP are associated with reduced concentrations of HDL cholesterol. (PMID: 10918380, 16458590, 9420339, 3343104, 6721900, 7278520) [HMDB]

   

4-Methylidene-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid

4-methylidene-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid

C21H34O5 (366.2406)


   

methyl (5s,5'r,6r,6'r,7r,10ar,10'ar)-1,1',5,5',9,9'-hexahydroxy-10'a-(hydroxymethyl)-3,3',6,6',7-pentamethyl-8,8'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

methyl (5s,5'r,6r,6'r,7r,10ar,10'ar)-1,1',5,5',9,9'-hexahydroxy-10'a-(hydroxymethyl)-3,3',6,6',7-pentamethyl-8,8'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

C34H36O13 (652.2156)


   

3,10-dihydroxy-7,9-dimethoxy-3-methyl-1h,4h,4ah,10h,10ah-naphtho[2,3-c]pyran-5-one

3,10-dihydroxy-7,9-dimethoxy-3-methyl-1h,4h,4ah,10h,10ah-naphtho[2,3-c]pyran-5-one

C16H20O6 (308.126)


   

ethyl 4-[(1-{10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene}ethyl)amino]butanoate

ethyl 4-[(1-{10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene}ethyl)amino]butanoate

C24H27NO8 (457.1737)


   

(1r,3ar,3br,7s,9ar,9br,11ar)-9a,11a-dimethyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

(1r,3ar,3br,7s,9ar,9br,11ar)-9a,11a-dimethyl-1-[(2r)-6-methylheptan-2-yl]-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

C29H48O2 (428.3654)


   

methyl 4-[(1-{10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene}ethyl)amino]butanoate

methyl 4-[(1-{10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene}ethyl)amino]butanoate

C23H25NO8 (443.158)


   

ethyl 4-(7-acetyl-4,6-dihydroxy-3,5-dimethyl-1-benzofuran-2-yl)-4-(7-acetyl-4,6-dihydroxy-3,5-dimethyl-2-oxo-1-benzofuran-3-yl)-3-oxobutanoate

ethyl 4-(7-acetyl-4,6-dihydroxy-3,5-dimethyl-1-benzofuran-2-yl)-4-(7-acetyl-4,6-dihydroxy-3,5-dimethyl-2-oxo-1-benzofuran-3-yl)-3-oxobutanoate

C30H30O12 (582.1737)


   

methyl (5s,5'r,6r,6'r,7r,10ar,10'ar)-1,1',5,5',8,8'-hexahydroxy-3,3',6,6',7-pentamethyl-9,9'-dioxo-10'a-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

methyl (5s,5'r,6r,6'r,7r,10ar,10'ar)-1,1',5,5',8,8'-hexahydroxy-3,3',6,6',7-pentamethyl-9,9'-dioxo-10'a-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

C40H46O17 (798.2735)


   

2-(17-carboxyheptadecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

2-(17-carboxyheptadecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

C24H42O6 (426.2981)


   

4,13,17-trihydroxy-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

4,13,17-trihydroxy-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C18H14O9 (374.0638)


   

10-acetyl-4-(1-aminoethylidene)-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

10-acetyl-4-(1-aminoethylidene)-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

C18H17NO6 (343.1056)


   

methyl (5r,5's,6r,6's,7r,10ar,10'ar)-1,1',5,5',8,8'-hexahydroxy-3,3',6,6',7-pentamethyl-9,9'-dioxo-10'a-({[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

methyl (5r,5's,6r,6's,7r,10ar,10'ar)-1,1',5,5',8,8'-hexahydroxy-3,3',6,6',7-pentamethyl-9,9'-dioxo-10'a-({[(2r,3s,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

C40H46O17 (798.2735)


   

5,13,17-trihydroxy-12-(hydroxymethyl)-4-(methoxymethyl)-7-methyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3(8),4,6,12,14(18)-hexaene-9,15-dione

5,13,17-trihydroxy-12-(hydroxymethyl)-4-(methoxymethyl)-7-methyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3(8),4,6,12,14(18)-hexaene-9,15-dione

C19H16O10 (404.0743)


   

1-(5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

1-(5,6-dimethylheptan-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

C30H50O2 (442.3811)


   

(2s,7r)-10-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

(2s,7r)-10-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H23NO7 (389.1474)


   

17-hydroxy-5,13-dimethoxy-4,7,12-trimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

17-hydroxy-5,13-dimethoxy-4,7,12-trimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C20H18O8 (386.1002)


   

13,17-dihydroxy-5-methoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

13,17-dihydroxy-5-methoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

C19H14O9 (386.0638)


   

13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

13-hydroxy-5,17-dimethoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

C20H16O9 (400.0794)


   

methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

methyl 16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

C37H40N4O6 (636.2948)


   

methyl (4s,4ar)-4-(acetyloxy)-8-hydroxy-6-methyl-9-oxo-5-[(10s,11s,13r,14r)-7,10,14-trihydroxy-13-methyl-9,15-dioxo-2,16-dioxatetracyclo[9.3.2.0¹,¹⁰.0³,⁸]hexadeca-3,5,7-trien-6-yl]-2,3,4,9a-tetrahydro-1h-xanthene-4a-carboxylate

methyl (4s,4ar)-4-(acetyloxy)-8-hydroxy-6-methyl-9-oxo-5-[(10s,11s,13r,14r)-7,10,14-trihydroxy-13-methyl-9,15-dioxo-2,16-dioxatetracyclo[9.3.2.0¹,¹⁰.0³,⁸]hexadeca-3,5,7-trien-6-yl]-2,3,4,9a-tetrahydro-1h-xanthene-4a-carboxylate

C33H32O14 (652.1792)


   

(18e)-9,10,12,13,15,16-hexahydroxyheptacos-18-enoic acid

(18e)-9,10,12,13,15,16-hexahydroxyheptacos-18-enoic acid

C27H52O8 (504.3662)


   

(2r)-4-methyl-5-oxo-2-(14-oxopentadecyl)-2h-furan-3-carboxylic acid

(2r)-4-methyl-5-oxo-2-(14-oxopentadecyl)-2h-furan-3-carboxylic acid

C21H34O5 (366.2406)


   

14-ethoxy-5,18-dihydroxy-7,12-dimethyl-9,16-dioxo-2,10,15-trioxatetracyclo[9.7.0.0³,⁸.0¹³,¹⁷]octadeca-1(11),3,5,7,12,17-hexaene-4-carbaldehyde

14-ethoxy-5,18-dihydroxy-7,12-dimethyl-9,16-dioxo-2,10,15-trioxatetracyclo[9.7.0.0³,⁸.0¹³,¹⁷]octadeca-1(11),3,5,7,12,17-hexaene-4-carbaldehyde

C20H16O9 (400.0794)


   

(2s,4r)-4,10-diacetyl-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

(2s,4r)-4,10-diacetyl-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

C18H16O7 (344.0896)


   

1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

1-(5,6-dimethylhept-3-en-2-yl)-9a,11a-dimethyl-1h,2h,3h,3ah,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

C30H46O2 (438.3498)


   

4,4,6b,8a,11,11,12b,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol

4,4,6b,8a,11,11,12b,14a-octamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol

C30H50O (426.3861)


   

(1r,4s,5r,7s,8s,12r,15s,16r,18s,19s)-19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl butanoate

(1r,4s,5r,7s,8s,12r,15s,16r,18s,19s)-19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl butanoate

C24H24N2O8S2 (532.0974)


   

(4e)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-4-[1-(pentylamino)ethylidene]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraene-3,5-dione

(4e)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-4-[1-(pentylamino)ethylidene]-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraene-3,5-dione

C23H27NO6 (413.1838)


   

(1s)-1-hydroxy-7,9-dimethoxy-3-methyl-1h-benzo[g]isochromene-5,10-dione

(1s)-1-hydroxy-7,9-dimethoxy-3-methyl-1h-benzo[g]isochromene-5,10-dione

C16H14O6 (302.079)


   

(18e)-9,10,12,13,15,16-hexahydroxyhexacos-18-enoic acid

(18e)-9,10,12,13,15,16-hexahydroxyhexacos-18-enoic acid

C26H50O8 (490.3506)


   

4,10-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

4,10-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H22O8 (390.1315)


   

(18e)-9,10,12,13,15,16-hexahydroxyoctacos-18-enoic acid

(18e)-9,10,12,13,15,16-hexahydroxyoctacos-18-enoic acid

C28H54O8 (518.3818)


   

7-{2-[(2-carboxyeth-1-en-1-yl)oxy]-2-oxoethyl}-15-formyl-6,14-dihydroxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid

7-{2-[(2-carboxyeth-1-en-1-yl)oxy]-2-oxoethyl}-15-formyl-6,14-dihydroxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid

C22H16O12 (472.0642)


   

(2r,4e)-10-acetyl-4-(1-aminoethylidene)-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

(2r,4e)-10-acetyl-4-(1-aminoethylidene)-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

C18H17NO6 (343.1056)


   

( )-usnic acid

( )-usnic acid

C18H16O7 (344.0896)


   

(17r)-13,17-dihydroxy-5-methoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

(17r)-13,17-dihydroxy-5-methoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

C19H14O9 (386.0638)


   

(17r)-4,13,17-trihydroxy-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

(17r)-4,13,17-trihydroxy-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C18H14O9 (374.0638)


   

(2r)-2-[13-(acetyloxy)tridecyl]-4-methyl-5-oxo-2h-furan-3-carboxylic acid

(2r)-2-[13-(acetyloxy)tridecyl]-4-methyl-5-oxo-2h-furan-3-carboxylic acid

C21H34O6 (382.2355)


   

4-methyl-5-oxo-2-(14-oxopentadecyl)-2h-furan-3-carboxylic acid

4-methyl-5-oxo-2-(14-oxopentadecyl)-2h-furan-3-carboxylic acid

C21H34O5 (366.2406)


   

2-(14-hydroxypentadecyl)-4-methyl-5-oxo-2h-furan-3-carboxylic acid

2-(14-hydroxypentadecyl)-4-methyl-5-oxo-2h-furan-3-carboxylic acid

C21H36O5 (368.2563)


   

19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl hexanoate

19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl hexanoate

C26H28N2O8S2 (560.1287)


   

methyl (5s,5'r,6r,6'r,7r,10ar,10'ar)-1,1',5,5',9,9'-hexahydroxy-3,3',6,6',7-pentamethyl-8,8'-dioxo-10'a-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

methyl (5s,5'r,6r,6'r,7r,10ar,10'ar)-1,1',5,5',9,9'-hexahydroxy-3,3',6,6',7-pentamethyl-8,8'-dioxo-10'a-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

C40H46O17 (798.2735)


   

(3s,4as,10r,10ar)-3,10-dihydroxy-7,9-dimethoxy-3-methyl-1h,4h,4ah,10h,10ah-naphtho[2,3-c]pyran-5-one

(3s,4as,10r,10ar)-3,10-dihydroxy-7,9-dimethoxy-3-methyl-1h,4h,4ah,10h,10ah-naphtho[2,3-c]pyran-5-one

C16H20O6 (308.126)


   

(2r,4s)-4,10-diacetyl-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

(2r,4s)-4,10-diacetyl-11,13-dihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),6,10,12-tetraene-3,5-dione

C18H16O7 (344.0896)


   

methyl (3s,21s,22s)-16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

methyl (3s,21s,22s)-16-ethenyl-22-(3-ethoxy-3-oxopropyl)-11-ethyl-3,4-dihydroxy-12,17,21,26-tetramethyl-7,23,24,25-tetraazahexacyclo[18.2.1.1⁵,⁸.1¹⁰,¹³.1¹⁵,¹⁸.0²,⁶]hexacosa-1,4,6,8(26),9,11,13(25),14,16,18(24),19-undecaene-3-carboxylate

C37H40N4O6 (636.2948)


   

ethyl 4-[(1-{10-acetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-5-oxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-4-yl}ethylidene)amino]butanoate

ethyl 4-[(1-{10-acetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-5-oxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-4-yl}ethylidene)amino]butanoate

C26H33NO9 (503.2155)


   

(1r,3as,7s,9as,11ar)-1-[(2s,3e,5r)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

(1r,3as,7s,9as,11ar)-1-[(2s,3e,5r)-5,6-dimethylhept-3-en-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,4h,6h,7h,8h,9h,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

C30H46O2 (438.3498)


   

ethyl 4-({1-[(2r,4e)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene]ethyl}amino)butanoate

ethyl 4-({1-[(2r,4e)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene]ethyl}amino)butanoate

C24H27NO8 (457.1737)


   

methyl 1,1',5,5',9,9'-hexahydroxy-10'a-(hydroxymethyl)-3,3',6,6',7-pentamethyl-8,8'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

methyl 1,1',5,5',9,9'-hexahydroxy-10'a-(hydroxymethyl)-3,3',6,6',7-pentamethyl-8,8'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,2'-bixanthene]-10a-carboxylate

C34H36O13 (652.2156)


   

2-(14-carboxytetradecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

2-(14-carboxytetradecyl)-4-methyl-5-oxooxolane-3-carboxylic acid

C21H36O6 (384.2512)


   

(17r)-13,17-dihydroxy-12-(hydroxymethyl)-5-methoxy-4,7-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

(17r)-13,17-dihydroxy-12-(hydroxymethyl)-5-methoxy-4,7-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C19H16O9 (388.0794)


   

(2r,3s)-4-methylidene-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid

(2r,3s)-4-methylidene-5-oxo-2-(14-oxopentadecyl)oxolane-3-carboxylic acid

C21H34O5 (366.2406)


   

7-(2-{[(1e)-2-carboxyeth-1-en-1-yl]oxy}-2-oxoethyl)-15-formyl-6,14-dihydroxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid

7-(2-{[(1e)-2-carboxyeth-1-en-1-yl]oxy}-2-oxoethyl)-15-formyl-6,14-dihydroxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid

C22H16O12 (472.0642)


   

4,12,20-trihydroxy-3,5,8,11,13,16,19,21,24-nonamethyl-1,9,17-trioxacyclotetracosane-2,10,18-trione

4,12,20-trihydroxy-3,5,8,11,13,16,19,21,24-nonamethyl-1,9,17-trioxacyclotetracosane-2,10,18-trione

C30H54O9 (558.3768)


   

(3s)-3-hydroxy-7,9-dimethoxy-3-methyl-1h,4h-naphtho[2,3-c]pyran-5,10-dione

(3s)-3-hydroxy-7,9-dimethoxy-3-methyl-1h,4h-naphtho[2,3-c]pyran-5,10-dione

C16H16O6 (304.0947)


   

(2r)-2-[(14s)-14-hydroxypentadecyl]-4-methyl-5-oxo-2h-furan-3-carboxylic acid

(2r)-2-[(14s)-14-hydroxypentadecyl]-4-methyl-5-oxo-2h-furan-3-carboxylic acid

C21H36O5 (368.2563)


   

4-(2,4-dimethoxy-3,6-dimethylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid

4-(2,4-dimethoxy-3,6-dimethylbenzoyloxy)-2-hydroxy-3,6-dimethylbenzoic acid

C20H22O7 (374.1365)


   

(2r,3s)-2-[(14s)-14-hydroxypentadecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid

(2r,3s)-2-[(14s)-14-hydroxypentadecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid

C21H36O5 (368.2563)


   

12-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

12-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H23NO7 (389.1474)


   

2-[13-(acetyloxy)tridecyl]-4-methyl-5-oxo-2h-furan-3-carboxylic acid

2-[13-(acetyloxy)tridecyl]-4-methyl-5-oxo-2h-furan-3-carboxylic acid

C21H34O6 (382.2355)


   

methyl (6r,7r,7'r,8s,8'r,8ar,8'ar)-4,4',5,5',8,8'-hexahydroxy-2,2',6,7,7'-pentamethyl-9,9'-dioxo-8'a-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}-6h,6'h,7h,7'h,8h,8'h-[3,3'-bixanthene]-8a-carboxylate

methyl (6r,7r,7'r,8s,8'r,8ar,8'ar)-4,4',5,5',8,8'-hexahydroxy-2,2',6,7,7'-pentamethyl-9,9'-dioxo-8'a-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}-6h,6'h,7h,7'h,8h,8'h-[3,3'-bixanthene]-8a-carboxylate

C40H46O17 (798.2735)


   

(2r,3s)-2-[13-(acetyloxy)tridecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid

(2r,3s)-2-[13-(acetyloxy)tridecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid

C21H34O6 (382.2355)


   

methyl (4s,4ar)-4-(acetyloxy)-8-hydroxy-6-methyl-9-oxo-5-[(10r,11r,13s,14s)-7,10,14-trihydroxy-13-methyl-9,15-dioxo-2,16-dioxatetracyclo[9.3.2.0¹,¹⁰.0³,⁸]hexadeca-3,5,7-trien-6-yl]-2,3,4,9a-tetrahydro-1h-xanthene-4a-carboxylate

methyl (4s,4ar)-4-(acetyloxy)-8-hydroxy-6-methyl-9-oxo-5-[(10r,11r,13s,14s)-7,10,14-trihydroxy-13-methyl-9,15-dioxo-2,16-dioxatetracyclo[9.3.2.0¹,¹⁰.0³,⁸]hexadeca-3,5,7-trien-6-yl]-2,3,4,9a-tetrahydro-1h-xanthene-4a-carboxylate

C33H32O14 (652.1792)


   

methyl 4,4',5,5',8,8'-hexahydroxy-2,2',6,7,7'-pentamethyl-9,9'-dioxo-8'a-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}-6h,6'h,7h,7'h,8h,8'h-[3,3'-bixanthene]-8a-carboxylate

methyl 4,4',5,5',8,8'-hexahydroxy-2,2',6,7,7'-pentamethyl-9,9'-dioxo-8'a-{[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]methyl}-6h,6'h,7h,7'h,8h,8'h-[3,3'-bixanthene]-8a-carboxylate

C40H46O17 (798.2735)


   

(2s,7r)-12-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

(2s,7r)-12-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H23NO7 (389.1474)


   

1-hydroxy-7,9-dimethoxy-3-methyl-1h-benzo[g]isochromene-5,10-dione

1-hydroxy-7,9-dimethoxy-3-methyl-1h-benzo[g]isochromene-5,10-dione

C16H14O6 (302.079)


   

{4-formyl-5,13,17-trihydroxy-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-12-yl}methyl acetate

{4-formyl-5,13,17-trihydroxy-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-12-yl}methyl acetate

C20H14O11 (430.0536)


   

(17r)-17-hydroxy-5,13-dimethoxy-4,7,12-trimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

(17r)-17-hydroxy-5,13-dimethoxy-4,7,12-trimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C20H18O8 (386.1002)


   

(2s,7r)-4,10-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

(2s,7r)-4,10-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H22O8 (390.1315)


   

4-acetyl-3-chloro-2,6-dihydroxy-5-methoxybenzaldehyde

4-acetyl-3-chloro-2,6-dihydroxy-5-methoxybenzaldehyde

C10H9ClO5 (244.0138)


   

2-[13-(acetyloxy)tridecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid

2-[13-(acetyloxy)tridecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid

C21H34O6 (382.2355)


   

(15e,17e)-9,10,12,13-tetrahydroxyhenicosa-15,17-dienoic acid

(15e,17e)-9,10,12,13-tetrahydroxyhenicosa-15,17-dienoic acid

C21H38O6 (386.2668)


   

10a,10'a-dimethyl (5s,5's,6s,10ar,10'ar)-5'-(acetyloxy)-1,1',5,9-tetrahydroxy-3',6-dimethyl-8,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,4'-bixanthene]-10a,10'a-dicarboxylate

10a,10'a-dimethyl (5s,5's,6s,10ar,10'ar)-5'-(acetyloxy)-1,1',5,9-tetrahydroxy-3',6-dimethyl-8,9'-dioxo-5h,5'h,6h,6'h,7h,7'h-[2,4'-bixanthene]-10a,10'a-dicarboxylate

C34H32O14 (664.1792)


   

ethyl 4-({1-[(2s,7r)-10-acetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-5-oxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-4-yl]ethylidene}amino)butanoate

ethyl 4-({1-[(2s,7r)-10-acetyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-5-oxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-4-yl]ethylidene}amino)butanoate

C26H33NO9 (503.2155)


   

(17r)-5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carbaldehyde

(17r)-5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carbaldehyde

C18H12O9 (372.0481)


   

7-[(acetyloxy)methyl]-4,15-diformyl-6,14-dihydroxy-12-methyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

7-[(acetyloxy)methyl]-4,15-diformyl-6,14-dihydroxy-12-methyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid

C20H14O11 (430.0536)


   

2-hydroxy-4-[3-(hydroxymethyl)-2,4-dimethoxy-6-methylbenzoyloxy]-3,6-dimethylbenzoic acid

2-hydroxy-4-[3-(hydroxymethyl)-2,4-dimethoxy-6-methylbenzoyloxy]-3,6-dimethylbenzoic acid

C20H22O8 (390.1315)


   

(1r,3ar,3br,7s,9ar,9br,11ar)-1-[(2r,5r)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

(1r,3ar,3br,7s,9ar,9br,11ar)-1-[(2r,5r)-5,6-dimethylheptan-2-yl]-9a,11a-dimethyl-1h,2h,3h,3ah,3bh,4h,6h,7h,8h,9h,9bh,10h,11h-cyclopenta[a]phenanthren-7-yl acetate

C30H50O2 (442.3811)


   

4,13-dihydroxy-5,17-dimethoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

4,13-dihydroxy-5,17-dimethoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C19H16O9 (388.0794)


   

2-(14-hydroxypentadecyl)-4-methylidene-5-oxooxolane-3-carboxylic acid

2-(14-hydroxypentadecyl)-4-methylidene-5-oxooxolane-3-carboxylic acid

C21H36O5 (368.2563)


   

10-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

10-acetyl-4-ethanimidoyl-7-ethoxy-3,11,13-trihydroxy-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H23NO7 (389.1474)


   

(17s)-5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carbaldehyde

(17s)-5,13,17-trihydroxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carbaldehyde

C18H12O9 (372.0481)


   

(4z)-10-acetyl-11,13-dihydroxy-4-(1-methoxyethylidene)-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraene-3,5-dione

(4z)-10-acetyl-11,13-dihydroxy-4-(1-methoxyethylidene)-2,12-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraene-3,5-dione

C19H18O7 (358.1052)


   

methyl 4-({1-[(2r,4e)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene]ethyl}amino)butanoate

methyl 4-({1-[(2r,4e)-10-acetyl-11,13-dihydroxy-2,12-dimethyl-3,5-dioxo-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),6,9,11-tetraen-4-ylidene]ethyl}amino)butanoate

C23H25NO8 (443.158)


   

19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl butanoate

19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl butanoate

C24H24N2O8S2 (532.0974)


   

(1r,4s,5r,7s,8s,12r,15s,16r,18s,19s)-19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl hexanoate

(1r,4s,5r,7s,8s,12r,15s,16r,18s,19s)-19-(acetyloxy)-2,13-dioxo-6,17-dioxa-23,24-dithia-3,14-diazaoctacyclo[10.10.2.0¹,¹⁴.0³,¹².0⁴,¹⁰.0⁵,⁷.0¹⁵,²¹.0¹⁶,¹⁸]tetracosa-9,20-dien-8-yl hexanoate

C26H28N2O8S2 (560.1287)


   

13-hydroxy-4-(hydroxymethyl)-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3,5,7,11,13-hexaene-9,15-dione

13-hydroxy-4-(hydroxymethyl)-5-methoxy-7,12-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3,5,7,11,13-hexaene-9,15-dione

C19H16O8 (372.0845)


   

3-hydroxy-7,9-dimethoxy-3-methyl-1h,4h-naphtho[2,3-c]pyran-5,10-dione

3-hydroxy-7,9-dimethoxy-3-methyl-1h,4h-naphtho[2,3-c]pyran-5,10-dione

C16H16O6 (304.0947)


   

(17e)-9,10,12,13,14,15-hexahydroxytetracos-17-enoic acid

(17e)-9,10,12,13,14,15-hexahydroxytetracos-17-enoic acid

C24H46O8 (462.3193)


   

5-(5,6-dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

5-(5,6-dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.0¹,⁹.0²,⁶.0¹⁰,¹⁵]nonadec-18-en-13-ol

C28H44O3 (428.329)


   

13,17-dihydroxy-12-(hydroxymethyl)-5-methoxy-4,7-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

13,17-dihydroxy-12-(hydroxymethyl)-5-methoxy-4,7-dimethyl-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-9,15-dione

C19H16O9 (388.0794)


   

[(17s)-4-formyl-5,13,17-trihydroxy-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-12-yl]methyl acetate

[(17s)-4-formyl-5,13,17-trihydroxy-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaen-12-yl]methyl acetate

C20H14O11 (430.0536)


   

(17r)-5,13,17-trihydroxy-12-(hydroxymethyl)-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carbaldehyde

(17r)-5,13,17-trihydroxy-12-(hydroxymethyl)-7-methyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(18),3(8),4,6,11,13-hexaene-4-carbaldehyde

C18H12O10 (388.043)


   

4,15-diformyl-6-hydroxy-14-methoxy-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-5-carboxylic acid

4,15-diformyl-6-hydroxy-14-methoxy-7,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-5-carboxylic acid

C19H14O9 (386.0638)


   

4,12-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

4,12-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H22O8 (390.1315)


   

(2s,7r)-4,12-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

(2s,7r)-4,12-diacetyl-7-ethoxy-3,11,13-trihydroxy-2,10-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(13),3,9,11-tetraen-5-one

C20H22O8 (390.1315)


   

4-acetyl-2,6-dihydroxy-3-methoxybenzaldehyde

4-acetyl-2,6-dihydroxy-3-methoxybenzaldehyde

C10H10O5 (210.0528)


   

3-(4-carboxy-3-hydroxy-2,5-dimethylphenoxycarbonyl)-2,6-dimethoxy-4-methylbenzoic acid

3-(4-carboxy-3-hydroxy-2,5-dimethylphenoxycarbonyl)-2,6-dimethoxy-4-methylbenzoic acid

C20H20O9 (404.1107)


   

2-hydroxy-4-(2-hydroxy-4-methoxy-3,6-dimethylbenzoyloxy)-3,6-dimethylbenzoic acid

2-hydroxy-4-(2-hydroxy-4-methoxy-3,6-dimethylbenzoyloxy)-3,6-dimethylbenzoic acid

C19H20O7 (360.1209)


   

(17s)-13,17-dihydroxy-5-methoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

(17s)-13,17-dihydroxy-5-methoxy-7,12-dimethyl-9,15-dioxo-2,10,16-trioxatetracyclo[9.7.0.0³,⁸.0¹⁴,¹⁸]octadeca-1(11),3,5,7,12,14(18)-hexaene-4-carbaldehyde

C19H14O9 (386.0638)


   

methyl (4s,4ar)-4,8-dihydroxy-6-methyl-9-oxo-5-[(10s,11s,13r,14r)-7,10,14-trihydroxy-13-methyl-9,15-dioxo-2,16-dioxatetracyclo[9.3.2.0¹,¹⁰.0³,⁸]hexadeca-3,5,7-trien-6-yl]-2,3,4,9a-tetrahydro-1h-xanthene-4a-carboxylate

methyl (4s,4ar)-4,8-dihydroxy-6-methyl-9-oxo-5-[(10s,11s,13r,14r)-7,10,14-trihydroxy-13-methyl-9,15-dioxo-2,16-dioxatetracyclo[9.3.2.0¹,¹⁰.0³,⁸]hexadeca-3,5,7-trien-6-yl]-2,3,4,9a-tetrahydro-1h-xanthene-4a-carboxylate

C31H30O13 (610.1686)