NCBI Taxonomy: 39934
Lecanora (ncbi_taxid: 39934)
found 140 associated metabolites at genus taxonomy rank level.
Ancestor: Lecanoraceae
Child Taxonomies: Lecanora laxa, Lecanora kohu, Lecanora densa, Lecanora varia, Lecanora helva, Lecanora horiza, Lecanora remota, Lecanora layana, Lecanora achroa, Lecanora masana, Lecanora aitema, Lecanora anopta, Lecanora leprosa, Lecanora plumosa, Lecanora confusa, Lecanora ulrikii, Lecanora expersa, Lecanora albella, Lecanora saligna, Lecanora muralis, Lecanora kenyana, Lecanora tropica, Lecanora solaris, Lecanora vainioi, Lecanora sinuosa, Lecanora formosa, Lecanora cenisia, Lecanora pacifica, Lecanora wilsonii, Lecanora saxigena, Lecanora cateilea, Lecanora concolor, Lecanora epibryon, Lecanora orosthea, Lecanora swartzii, Lecanora symmicta, Lecanora kalbiana, Lecanora neohelva, Lecanora cavicola, Lecanora bicincta, Lecanora rupicola, Lecanora glabrata, Lecanora helmutii, Lecanora impudens, Lecanora lendemeri, Lecanora expallens, Lecanora fulvastra, Lecanora kurokawae, Lecanora farinaria, Lecanora farinacea, Lecanora parachroa, Lecanora allophana, Lecanora intricata, Lecanora polytropa, Lecanora albellula, Lecanora mughicola, Lecanora loekoesii, Lecanora sulphurea, Lecanora subravida, Lecanora stanislai, Lecanora excludens, Lecanora parahelva, Lecanora cadubriae, Lecanora norvegica, Lecanora rubicunda, Lecanora straminea, Lecanora subcarnea, Lecanora ecoronata, Lecanora lojkaeana, Lecanora subrugosa, Lecanora rugosella, Lecanora valesiaca, Lecanora burgaziae, Lecanora paramerae, Lecanora pulicaris, Lecanora argentata, Lecanora hybocarpa, Lecanora leptacina, Lecanora imshaugii, Lecanora leproplaca, Lecanora strobilina, Lecanora subimmersa, Lecanora toroyensis, Lecanora quercicola, Lecanora poliophaea, Lecanora caperatica, Lecanora populicola, Lecanora leptyrodes, Lecanora frustulosa, Lecanora physciella, Lecanora garovaglii, Lecanora oreinoides, Lecanora flotowiana, Lecanora menthoides, Lecanora brasiliana, Lecanora subsaligna, Lecanora compallens, Lecanora saepiphila, Lecanora darlingiae, Lecanora campestris, Lecanora agardhiana, Lecanora alaskensis, Lecanora salicicola, Lecanora coronulans, Lecanora cf. aitema, Lecanora fuscescens, Lecanora argopholis, Lecanora fuegiensis, Lecanora chlarotera, Lecanora margarodes, Lecanora phaeocardia, Lecanora ussuriensis, Lecanora coniferarum, Lecanora aff. layana, Lecanora subcavicola, Lecanora hypoptoides, Lecanora barkmaniana, Lecanora macrocyclos, Lecanora substerilis, Lecanora subcarpinea, Lecanora praeferenda, Lecanora alboflavida, Lecanora phryganitis, Lecanora aff. achroa, Lecanora praepostera, Lecanora perpruinosa, Lecanora hypocrocina, Lecanora subcinctula, Lecanora rabdotoides, Lecanora flavocaesia, Lecanora somervellii, Lecanora pseudistera, Lecanora notatictria, Lecanora glaucomodes, Lecanora phaeostigma, Lecanora intumescens, Lecanora bermudensis, Lecanora praesistens, Lecanora schofieldii, Lecanora californica, Lecanora elatinoides, Lecanora cinereofusca, Lecanora pseudomellea, Lecanora subimmergens, Lecanora flavoleprosa, Lecanora subintricata, Lecanora pulverulenta, Lecanora parasymmicta, Lecanora variolascens, Lecanora thysanophora, unclassified Lecanora, Lecanora conizaeoides, Lecanora aff. leprosa, Lecanora sulfurescens, Lecanora aff. plumosa, Lecanora flavopallida, Lecanora pallidachroa, Lecanora chondroderma, Lecanora sublivescens, Lecanora fuscobrunnea, Lecanora flavoviridis, Lecanora gangaleoides, Lecanora lividocinerea, Lecanora queenslandica, Lecanora atromarginata, Lecanora chloroleprosa, Lecanora caesiorubella, Lecanora xanthoplumosa, Lecanora sarcopidoides, Lecanora parmelinoides, Lecanora nigrilobulata, Lecanora mugosphagneti, Lecanora hyperboreorum, Lecanora cf. intricata, Lecanora cf. polytropa, Lecanora austrotropica, Lecanora atrosulphurea, Lecanora anakeestiicola, Lecanora nothocaesiella, Lecanora aff. argentata, Lecanora aff. farinacea, Lecanora chlorophaeodes, Lecanora markjohnstonii, Lecanora aff. ecoronata, Lecanora aff. polytropa, Lecanora aff. sulphurea, Lecanora fluorosaxicola, Lecanora pseudargentata, Lecanora circumborealis, Lecanora viridipruinosa, Lecanora strobilinoides, Lecanora immersocalcarea, Lecanora cf. subcavicola, Lecanora aff. frustulosa, Lecanora orientoafricana, Lecanora xanthoverrucosa, Lecanora sorediomarginata, Lecanora aff. fimbriatula, Lecanora aff. thallophila, Lecanora dispersoareolata, Lecanora irregularicrocea, Lecanora flavidomarginata, Lecanora aff. gangaleoides, Lecanora cf. dispersa Hill, Lecanora austrocalifornica, Lecanora baekdudaeganensis, Lecanora cf. fulvastra SPO8, Lecanora pseudogangaleoides, Lecanora cf. stramineoalbida, Lecanora aff. expallens SPO15, Lecanora cf. achroa HTL19841a, Lecanora aff. xanthoverrucosa, Lecanora aff. pangerangoensis, Lecanora cf. mons-nivis MDV h01, Lecanora cf. ecoronata 1 IM-2021, Lecanora cf. ecoronata 2 IM-2021, Lecanora cf. ecoronata 3 IM-2021, Lecanora aff. allophana Ekman 3434, Lecanora cf. caesiorubella 1 IM-2021, Lecanora cf. caesiorubella 2 IM-2021, Lecanora cf. dispersa Leavitt 12_002
Usnic acid
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].
Usnic_acid
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].
usnic acid
Atranorin
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].
(2s,3r,4r)-2-[(14s)-14-hydroxypentadecyl]-4-methyl-5-oxooxolane-3-carboxylic acid
2,4,5-trichloro-1,3,6-trihydroxy-8-methylxanthen-9-one
C14H7Cl3O5 (359.93590620000003)
4-(2,4-dimethoxy-6-pentylbenzoyloxy)-2-heptyl-6-methoxybenzoic acid
4-chloro-3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-5,11-diol
2,4-dichloro-1,3,6-trihydroxy-8-methylxanthen-9-one
2,4-dichloro-3,8-dihydroxy-6-methoxy-1-methylxanthen-9-one
C15H10Cl2O5 (339.99052700000004)
(2s,3s,4r)-2-[(14r)-14-hydroxypentadecyl]-4-methyl-5-oxooxolane-3-carboxylic acid
1,4-dimethyl 2-(hex-1-en-1-yl)-3-methylbut-2-enedioate
4,5-dichloro-1,3,6-trihydroxy-8-methylxanthen-9-one
1,2-diethyl-5,7,8,11,13,16,17,19-octahydroxy-6,18-dimethyl-12-oxapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosa-4,6,8,15,17,19-hexaene-3,10,14,21-tetrone
3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-5,11-diol
2,4,7-trichloro-3,6,8-trihydroxy-1-methylxanthen-9-one
C14H7Cl3O5 (359.93590620000003)
4-(2-heptyl-4,6-dimethoxybenzoyloxy)-2-methoxy-6-pentylbenzoic acid
(2s,3s)-3-(methoxycarbonyl)-2-tetradecylpentanedioic acid
2,4,5-trichloro-1,3-dihydroxy-6-methoxy-8-methylxanthen-9-one
(2r,3s,4e)-3-(methoxycarbonyl)-2-methylnon-4-enoic acid
11-methoxy-3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-5-ol
(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
2,4,5,7-tetrachloro-1,3,6-trihydroxy-8-methylxanthen-9-one
C14H6Cl4O5 (393.89693460000007)
2,4,5-trichloro-3,6,8-trihydroxy-1-methylxanthen-9-one
C14H7Cl3O5 (359.93590620000003)
4-(2,4-dimethoxy-6-pentylbenzoyloxy)-2-methoxy-6-pentylbenzoic acid
4-(3,5-dichloro-2,4-dihydroxy-6-propylbenzoyloxy)-2-methoxy-6-pentylbenzoic acid
7-[(acetyloxy)methyl]-15-formyl-6,14-dihydroxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3(8),4,6,11,13-hexaene-5-carboxylic acid
4-(3,5-dichloro-2,4-dihydroxy-6-pentylbenzoyloxy)-2-methoxy-6-pentylbenzoic acid
6,14-dihydroxy-4,7,12,15-tetramethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid
methyl 13,15-dichloro-6,14-dihydroxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-5-carboxylate
2,4,7-trichloro-3,8-dihydroxy-6-methoxy-1-methylxanthen-9-one
4-(3-chloro-4,6-dihydroxy-2-pentylbenzoyloxy)-2-methoxy-6-pentylbenzoic acid
3-methoxy-2,5,6-trimethylphenyl 2-hydroxy-4-methoxy-3,5,6-trimethylbenzoate
4-chloro-1,3,6-trihydroxy-8-methylxanthen-9-one
C14H9ClO5 (292.01384939999997)
(2r)-2-[(2s)-1-methoxy-1-oxohexadecan-2-yl]butanedioic acid
(1s,2s,11s,13s)-1,2-diethyl-5,7,8,11,13,16,17,19-octahydroxy-6,18-dimethyl-12-oxapentacyclo[11.8.0.0²,¹¹.0⁴,⁹.0¹⁵,²⁰]henicosa-4,6,8,15,17,19-hexaene-3,10,14,21-tetrone
1,4-dimethyl (2z)-2-[(1e)-hex-1-en-1-yl]-3-methylbut-2-enedioate
4-(3,5-dichloro-2,4-dihydroxy-6-pentylbenzoyloxy)-2-heptyl-6-methoxybenzoic acid
6,14-dihydroxy-7-(hydroxymethyl)-4,12,15-trimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(11),3,5,7,12,14-hexaene-5-carboxylic acid
(2s,3r)-2-[(14s)-14-hydroxypentadecyl]-4-methylidene-5-oxooxolane-3-carboxylic acid
2-heptyl-4-(2-heptyl-4,6-dimethoxybenzoyloxy)-6-methoxybenzoic acid
3-methoxy-2,5,6-trimethylphenyl 2,4-dimethoxy-3,5,6-trimethylbenzoate
methyl 13,15-dichloro-14-hydroxy-6-methoxy-4,12-dimethyl-10-oxo-2,9-dioxatricyclo[9.4.0.0³,⁸]pentadeca-1(15),3,5,7,11,13-hexaene-5-carboxylate
12-chloro-11-methoxy-3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaen-5-ol
4,12-dichloro-3,13-dimethyl-8-oxatricyclo[7.4.0.0²,⁷]trideca-1(9),2(7),3,5,10,12-hexaene-5,11-diol
C14H10Cl2O3 (296.00069700000006)