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Salazinic acid

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Asshaima Paramita Devi, Thuc-Huy Duong, Solenn Ferron, Mehdi A Beniddir, Minh-Hiep Dinh, Van-Kieu Nguyen, Nguyen-Kim-Tuyen Pham, Dinh-Hung Mac, Joël Boustie, Warinthorn Chavasiri, Pierre Le Pogam (2020). "Salazinic acid-derived depsidones and diphenylethers with α-glucosidase inhibitory activity from
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is higher where the annual mean temperature is higher, and the content of the lichens growing on the dark-coloured rock or on the southern rock face is higher than that of the lichens growing on the light-coloured rock or on the northern rock face.
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species showed higher quantities of salazinic acid correlating with increases in altitude. An earlier study demonstrated other possible effects of environmental conditions on salazinic acid content. It was shown that the salazinic acid content of
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Pham, Nguyen-Kim-Tuyen; Tran, Nguyen-Minh-An; Truong Nguyen, Huy; Pham, Duc-Dung; Nguyen, Thi-Quynh-Trang; Nguyen, Thi-Hong-Anh; Nguyen, Huu-Tri; Do, Thanh-Hung; Nguyen, Ngoc-Hong; Duong, Thuc-Huy (2022).
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Shukla, Vertika; Patel, D.K.; Bajpai, Rajesh; Semwal, Manoj; Upreti, D.K. (2015). "Ecological implication of variation in the secondary metabolites in Parmelioid lichens with respect to altitude".
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Papong, Khwanruan Butsatorn; Mangold, Armin; Lücking, Robert; Lumbsch, H. Thorsten (2014). "New species and new records of thelotremoid Graphidaceae (Ascomycota: Ostropales) from Thailand".
452:. Subsequent studies tried to determine the influence of environmental factors on the production of salazinic acid in culture. For example, two studies in the late 1980s showed that only 4- 93: 1298:
Ingólfsdóttir, Kristı́n; Chung, Gavin A.C.; Skúlason, Vilhjálmur G.; Gissurarson, Stefán R.; Vilhelmsdóttir, Margrét (1998). "Antimycobacterial activity of lichen metabolites in vitro".
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van den Boom, Pieter P.G.; Sipman, Harrie J.M. (2013). "Sixty-two species of lirelliform Graphidaceae (Ascomycota) new to Panama, with four species newly described to science".
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Sutjaritturakan, Jutarat; Saipunkaew, Wanaruk; Boonpragob, Kansri; Kalb, Kalb (2014). "New species of Graphidaceae (Ostropales) Lecanoromycetes) from southern Thailand".
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of that genus. A 2020 revision included 66 salazinic acid-containing species. The presence or absence of the compound is also important in the classification of genus
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Eifler-Lima, V. L.; Sperry, A.; Sinbandhit, S.; Boustie, J.; Tomasi, S.; Schenkel, E. (2000). "NMR spectral data of salazinic acid isolated from some species of
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Papierska, Katarzyna; Krajka-Kuźniak, Violetta; Paluszczak, Jarosław; Kleszcz, Robert; Skalski, Marcin; Studzińska-Sroka, Elżbieta; Baer-Dubowska, Wanda (2021).
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Honda, N.K.; Pavan, F.R.; Coelho, R.G.; de Andrade Leite, S.R.; Micheletti, A.C.; Lopes, T.I.B.; Misutsu, M.Y.; Beatriz, A.; Brum, R.L.; Leite, C.Q.F. (2010).
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Elix, John A.; Wardlaw, Judith H. (1999). "The structure of chalybaeizanic acid and quaesitic acid, two new lichen depsidones related to salazinic acid".
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Manojlovića, Nedeljko; Ranković, Branislav; Kosanić, Marijana; Vasiljević, Perica; Stanojković, Tatjana (2012). "Chemical composition of three
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Hamada, Nobuo; Miyagawa, Hisashi (1995). "Secondary metabolites from isolated lichen mycobionts cultured under different osmotic conditions".
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O'Donovan, Donal G.; Roberts, George; Keogh, Myles F. (1980). "Structure of the β-orcinol depsidones, connorstictic and consalazinic acids".
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InChI=1S/C18H12O10/c1-5-2-8(21)6(3-19)13-9(5)16(23)27-14-7(4-20)12(22)10-11(15(14)26-13)18(25)28-17(10)24/h2-3,18,20-22,25H,4H2,1H3
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range between 260–268 °C (500–514 °F) that undergo a colour change to brown at about 240 °C (464 °F). Its
2147: 1442: 986: 1039:"Formation of lichen substances by mycobionts of lichens. Isolation of (+) usnic acid and salazinic acid from mycobionts of 568: 1002:
Shibata, Shoji (2000). "Yasuhiko Asahina (1880–1975) and his studies on lichenology and chemistry of lichen metabolites".
1376:"Lichen-derived depsides and depsidones modulate the Nrf2, NF-κB and STAT3 signaling pathways in colorectal cancer cells" 1101:
Hamada, Nobuo (1989). "The effect of various culture conditions on depside production by an isolated lichen mycobiont".
1857: 243: 2183: 470:. When extra sucrose was added to the growth medium, the production of salazinic acid was observed; the increased 340: 1015: 151: 1621:
Hamada, N. (1982). "The effect of temperature on the content of the medullary depsidone salazinic acid in
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Iskandar, I.K.; Syers, J.K. (1971). "Solubility of lichen compounds in water: pedogenetic implications".
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of their published lichen species, thereby acknowledging the presence of this compound as an important
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lichens and antioxidant, antimicrobial and cytotoxic activities of some their major metabolites".
456:-demethylbarbatic acid (a precursor of salazinic acid) was produced by the isolated mycobiont of 449: 2043: 1959: 1874: 396: 1756: 879: 855: 752: 471: 133: 39: 2188: 927: 913: 8: 845: 832: 819: 584: 537: 228: 155: 69: 59: 2089: 1827: 1744: 1696: 1603: 1446: 1402: 1375: 1241: 1188: 1153: 1118: 1019: 776: 723: 689: 593: 458: 1692: 1311: 1206:
Candan, Mehmet; Yılmaz, Meral; Tay, Turgay; Erdem, Murat; Türk, Ayşen Özdemir (2007).
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Hale: the isidiate, sorediate, and pustulate species with medullary salazinic acid"
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Hamada, Nobuo; Ueno, Tamio (1987). "Depside from an isolated lichen mycobiont".
541:. Recent (2021) research indicates that salazinic acid is a potent modulator of 405:
as salazinic acid. Later studies showed that the compound he named was actually
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Hale: the species with medullary salazinic acid lacking vegetative propagules"
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rings. Japanese chemists demonstrated in the late 1960s that the isolated
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in Great Smoky Mountains National Park; southeastern North America:
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10.1002/1097-458X(200006)38:6<472::AID-MRC658>3.0.CO;2-P
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Except where otherwise noted, data are given for materials in their
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1,3-Dihydro-1,4,10-trihydroxy-5-(hydroxymethyl)-8-methyl-3,7-dioxo-7
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named the chemical he originally isolated from the African species
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spectral assignments for salazinic acid were reported in 2000.
510:. In its purified form, it exists as colourless needles with a 364: 104: 2018:(Pertusariales, lichenized Ascomycota) from eastern Australia" 1803: 1457: 550: 384: 82: 771:
Several authors have explicitly named salazinic acid in the
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Spielmann, Adriano Afonso; Marcelli, Marcelo Pinto (2020).
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10.1639/0007-2745(2000)103[0710:yaahso]2.0.co;2
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and J. Asano studied salazinic acid they had isolated from
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CC1=CC(=C(C2=C1C(=O)OC3=C(O2)C4=C(C(=C3CO)O)C(=O)OC4O)C=O)O
2068:; Nash, Thomas H. (1992). "A synopsis of the lichen genus 950:
Zopf, Wilhelm (1897). "Zur Kenntniss der Flechtenstoffe".
1879:(Graphidaceae) in Australia: new reports and new species" 1775: 1678: 1672: 1291: 1129: 970: 2014:"Seven new species and a new record in the lichen genus 1164: 1030: 1645: 1577: 1418: 2005: 1252: 674:, helping the lichen to survive in conditions of both 379:, where its presence or absence is often used to help 1367: 1067: 726:
similar to salazinic acid. In consalazinic acid, the
2058: 1205: 643:). The compound is common in the large lichen genus 1978: 1809: 1571: 1208:"Antimicrobial activity of extracts of the lichen 1466: 1335:"Antimycobacterial activity of lichen substances" 1326: 1199: 2160: 1951: 1927:Tønsberg, T. (2007). "Notes on the lichen genus 1769: 1707: 531:properties, but it did not have any substantive 430:components. The fundamental structure was named 194: 1844: 1473:(Parmeliaceae, Ascomycota) with salazinic acid" 68: 2127: 1845:Brodo, Irwin M.; Hawksworth, David L. (1977). 1135: 976: 1920: 1534: 1170: 1036: 1957: 1761:: CS1 maint: multiple names: authors list ( 1580:Environmental Science and Pollution Research 1497: 47:-isobenzofurobenzodioxepin-11-carboxaldehyde 2035: 1958:Wang, S.L.; Chen, J.B.; Elix, J.A. (2001). 1866: 1651: 1614: 1300:European Journal of Pharmaceutical Sciences 995: 730:group of salazinic acid is replaced with a 518:in water is about 27 milligrams per litre. 448:could produce salazinic acid when grown in 2011: 1094: 1073: 977:Asahina, Yasuhiko; Shibata, Shoji (1954). 478:-demethylbarbatic acid to salazinic acid. 227: 154: 132: 2133: 1893: 1794: 1562: 1525: 1488: 1401: 1391: 1350: 1227: 1058: 2064: 1926: 943: 741:-Methylsalazinic acid was isolated from 466:medium supplemented with low amounts of 1540: 1503: 1037:Komiya, Takeya; Shibata, Shoji (1969). 1001: 666:In nature, salazinic acid serves as an 223: 16:Chemical compound found in some lichens 2161: 2041: 1964:(Parmeliaceae, Ascomycota) from China" 1872: 1620: 1100: 145: 1960:"Two new species of the lichen genus 1076:Agricultural and Biological Chemistry 649:, and plays an important role in the 255:Key: QQTKVXCQLZIJPP-UHFFFAOYSA-N 112: 1899: 1047:Chemical and Pharmaceutical Bulletin 949: 874:Papong, Mangold & Lücking (2014) 697: 2179:Heterocyclic compounds with 4 rings 1212:and its salazinic acid constituent" 783:are listed here, followed by their 185: 13: 1850:and allied genera in North America 623:Salazinic acid is derived via the 426:with seven members containing two 14: 2205: 2012:Archer, A.W.; Elix, J.A. (2017). 1902:"A monograph of the lichen genus 952:Justus Liebigs Annalen der Chemie 367:, and is especially prevalent in 2140:(Alectoriaceae) in the New World 1216:Zeitschrift für Naturforschung C 797:van den Boom & Sipman (2013) 592: 583: 303: 25: 2134:Esslinger, Theodore L. (1989). 2072:(Ascomycotina, Parmeliaceae)". 1654:Australian Journal of Chemistry 1431:Magnetic Resonance in Chemistry 521:The compound has been shown in 337:(at 25 °C , 100 kPa). 1088:10.1080/00021369.1987.10868233 979:Chemistry of Lichen Substances 713:Xanthoparmelia amphixanthoides 309: 297: 1: 1693:10.1016/s0031-9422(00)91070-7 1312:10.1016/s0928-0987(97)00078-x 1150:10.1016/s0024-2829(95)80018-2 937: 860:Sheng L.Wang, J.B.Chen & 574: 481: 474:enhances the reaction from 4- 1796:10.1016/j.arabjc.2021.103535 1783:Arabian Journal of Chemistry 1477:Plant and Fungal Systematics 1352:10.1016/j.phymed.2009.07.018 1277:10.1016/j.phymed.2012.07.012 884:A.W.Archer & Elix (2017) 710:, isolated from the lichens 617:that contain salazinic acid. 535:effects when tested against 7: 2121:10.11646/PHYTOTAXA.189.1.22 1999:10.11646/phytotaxa.189.1.16 10: 2210: 1627:Canadian Journal of Botany 766: 625:acetyl polymalonyl pathway 390: 363:ring. It is found in some 1824:10.13158/heia.26.1.2013.9 1592:10.1007/s11356-015-5311-z 1490:10.35535/pfsyst-2020-0028 1393:10.3390/molecules26164787 1185:10.1017/s0024282971000082 787:and year of publication: 757:Friedel-Crafts alkylation 331: 284: 264: 239: 52: 38: 33: 24: 2025:Australasian Lichenology 1541:Benatti, Michel (2012). 1527:10.5943/mycosphere/4/1/1 964:10.1002/jlac.18972950209 900:Psiloparmelia salazinica 890:Phaeographina salazinica 793:Acanthothecis salazinica 2184:Hydroxymethyl compounds 1564:10.3897/mycokeys.5.3342 1543:"A review of the genus 1506:"A review of the genus 610:Parmotrema subisidiosum 1941:Opuscula Philolichenum 1504:Benatti, M.N. (2012). 1229:10.1515/znc-2007-7-827 870:Ocellularia salazinica 779:characteristic. These 402:Stereocaulon salazinum 397:Friedrich Wilhelm Zopf 2042:Archer, A.W. (2003). 1873:Archer, A.W. (2001). 880:Pertusaria salazinica 856:Myelochroa salazinica 753:nucleophilic addition 719:Hypotrachyna quaesita 486:Salazinic acid has a 422:, and found a unique 1717:Parmotrema dilatatum 928:Oropogon salazinicus 914:Diorygma salazinicum 744:Parmotrema dilatatum 722:, respectively, are 1900:Hale, M.E. (1989). 1733:10.1055/a-1203-0623 1060:10.1248/cpb.17.1305 846:Lepraria salazinica 833:Karoowia salazinica 820:Graphina salazinica 785:taxonomic authority 704:chalybaeizanic acid 682:. A study of three 604:Parmotrema stuppeum 538:Mycobacterium aurum 462:when grown in malt 327: g·mol 21: 1875:"The lichen genus 1623:Ramalina siliquosa 803:Bryoria salazinica 734:functional group. 690:Ramalina siliquosa 459:Ramalina siliquosa 450:laboratory culture 341:Infobox references 19: 2149:978-0-912861-28-9 1727:(16): 1216–1224. 1687:(11): 2497–2499. 1469:"Type studies on 1271:(13): 1166–1172. 1173:The Lichenologist 1138:The Lichenologist 988:978-0-598-82060-0 894:A.W.Archer (2003) 773:specific epithets 698:Related compounds 629:metabolic pathway 558:colorectal cancer 533:antimycobacterial 488:molecular formula 383:species in those 349:Chemical compound 347: 346: 208:CompTox Dashboard 94:Interactive image 2201: 2154: 2153: 2131: 2125: 2124: 2104: 2098: 2097: 2062: 2056: 2055: 2039: 2033: 2032: 2022: 2009: 2003: 2002: 1982: 1976: 1975: 1955: 1949: 1948: 1924: 1918: 1917: 1897: 1891: 1890: 1870: 1864: 1863: 1842: 1836: 1835: 1807: 1801: 1800: 1798: 1773: 1767: 1766: 1760: 1752: 1711: 1705: 1704: 1676: 1670: 1669: 1649: 1643: 1642: 1618: 1612: 1611: 1586:(2): 1391–1397. 1575: 1569: 1568: 1566: 1538: 1532: 1531: 1529: 1501: 1495: 1494: 1492: 1464: 1455: 1454: 1422: 1416: 1415: 1405: 1395: 1371: 1365: 1364: 1354: 1330: 1324: 1323: 1295: 1289: 1288: 1256: 1250: 1249: 1231: 1222:(7–8): 619–621. 1210:Parmelia sulcata 1203: 1197: 1196: 1168: 1162: 1161: 1133: 1127: 1126: 1098: 1092: 1091: 1082:(6): 1705–1706. 1071: 1065: 1064: 1062: 1053:(6): 1305–1306. 1034: 1028: 1027: 999: 993: 992: 974: 968: 967: 947: 933: 923: 909: 895: 885: 875: 865: 851: 841: 828: 815: 798: 639:(derivatives of 613:(right) are two 596: 587: 527:studies to have 419:Parmelia cetrata 414:Yasuhiko Asahina 326: 311: 305: 299: 292:Chemical formula 232: 231: 216: 214: 198: 187: 166: 158: 147: 136: 116: 96: 72: 29: 22: 18: 2209: 2208: 2204: 2203: 2202: 2200: 2199: 2198: 2194:Benzodioxepines 2174:Lichen products 2159: 2158: 2157: 2150: 2136:Systematics of 2132: 2128: 2105: 2101: 2086:10.2307/3243562 2063: 2059: 2040: 2036: 2020: 2010: 2006: 1983: 1979: 1956: 1952: 1933:Lepraria lanata 1925: 1921: 1898: 1894: 1871: 1867: 1860: 1843: 1839: 1808: 1804: 1774: 1770: 1754: 1753: 1712: 1708: 1677: 1673: 1666:10.1071/CH99056 1650: 1646: 1639:10.1139/b82-053 1619: 1615: 1576: 1572: 1539: 1535: 1502: 1498: 1465: 1458: 1423: 1419: 1372: 1368: 1331: 1327: 1296: 1292: 1257: 1253: 1204: 1200: 1169: 1165: 1134: 1130: 1115:10.2307/3243399 1099: 1095: 1072: 1068: 1035: 1031: 1000: 996: 989: 975: 971: 948: 944: 940: 931: 917: 903: 893: 883: 873: 859: 850:Tønsberg (2007) 849: 836: 823: 806: 796: 769: 702:The depsidones 700: 672:photoprotectant 621: 620: 619: 618: 615:foliose lichens 599: 598: 597: 589: 588: 577: 506:of 388.3 grams/ 501: 497: 493: 484: 445:Ramalina crassa 407:norstictic acid 393: 350: 343: 338: 324: 314: 308: 302: 294: 280: 277: 272: 271: 260: 257: 256: 253: 247: 246: 235: 225:DTXSID001317270 217: 210: 201: 188: 176: 139: 119: 99: 86: 75: 62: 48: 20:Salazinic acid 17: 12: 11: 5: 2207: 2197: 2196: 2191: 2186: 2181: 2176: 2171: 2156: 2155: 2148: 2126: 2115:(1): 312–324. 2099: 2074:The Bryologist 2057: 2034: 2004: 1977: 1950: 1919: 1892: 1865: 1859:978-9154602117 1858: 1837: 1802: 1768: 1706: 1681:Phytochemistry 1671: 1660:(7): 713–716. 1644: 1633:(4): 383–385. 1613: 1570: 1533: 1496: 1483:(2): 403–508. 1456: 1437:(6): 472–474. 1417: 1366: 1345:(5): 328–332. 1325: 1306:(2): 141–144. 1290: 1251: 1198: 1179:(1–2): 45–50. 1163: 1144:(3): 201–205. 1128: 1109:(3): 310–313. 1103:The Bryologist 1093: 1066: 1029: 1010:(4): 710–719. 1004:The Bryologist 994: 987: 969: 958:(2): 222–256. 941: 939: 936: 935: 934: 924: 918:Sutjar. & 910: 896: 886: 876: 866: 852: 842: 829: 816: 799: 768: 765: 761:esterification 732:benzyl alcohol 708:quaesitic acid 699: 696: 684:foliose lichen 601: 600: 591: 590: 582: 581: 580: 579: 578: 576: 573: 504:molecular mass 499: 495: 491: 483: 480: 442:of the lichen 392: 389: 353:Salazinic acid 348: 345: 344: 339: 335:standard state 332: 329: 328: 322: 316: 315: 312: 306: 300: 295: 290: 287: 286: 282: 281: 279: 278: 275: 267: 266: 265: 262: 261: 259: 258: 254: 251: 250: 242: 241: 240: 237: 236: 234: 233: 220: 218: 206: 203: 202: 200: 199: 191: 189: 181: 178: 177: 175: 174: 170: 168: 160: 159: 149: 141: 140: 138: 137: 129: 127: 121: 120: 118: 117: 109: 107: 101: 100: 98: 97: 89: 87: 80: 77: 76: 74: 73: 65: 63: 58: 55: 54: 50: 49: 42: 36: 35: 31: 30: 15: 9: 6: 4: 3: 2: 2206: 2195: 2192: 2190: 2187: 2185: 2182: 2180: 2177: 2175: 2172: 2170: 2167: 2166: 2164: 2151: 2145: 2141: 2137: 2130: 2122: 2118: 2114: 2110: 2103: 2095: 2091: 2087: 2083: 2079: 2075: 2071: 2070:Psiloparmelia 2067: 2066:Elix, John A. 2061: 2053: 2049: 2045: 2038: 2030: 2026: 2019: 2017: 2008: 2000: 1996: 1992: 1988: 1981: 1973: 1969: 1965: 1963: 1954: 1946: 1942: 1938: 1937:L. salazinica 1934: 1930: 1923: 1915: 1911: 1907: 1905: 1896: 1888: 1884: 1880: 1878: 1869: 1861: 1855: 1851: 1847: 1841: 1833: 1829: 1825: 1821: 1817: 1813: 1806: 1797: 1792: 1789:(1): 103535. 1788: 1784: 1780: 1772: 1764: 1758: 1750: 1746: 1742: 1738: 1734: 1730: 1726: 1722: 1721:Planta Medica 1718: 1710: 1702: 1698: 1694: 1690: 1686: 1682: 1675: 1667: 1663: 1659: 1655: 1648: 1640: 1636: 1632: 1628: 1624: 1617: 1609: 1605: 1601: 1597: 1593: 1589: 1585: 1581: 1574: 1565: 1560: 1556: 1552: 1548: 1546: 1537: 1528: 1523: 1519: 1515: 1511: 1509: 1500: 1491: 1486: 1482: 1478: 1474: 1472: 1463: 1461: 1452: 1448: 1444: 1440: 1436: 1432: 1428: 1421: 1413: 1409: 1404: 1399: 1394: 1389: 1385: 1381: 1377: 1370: 1362: 1358: 1353: 1348: 1344: 1340: 1339:Phytomedicine 1336: 1329: 1321: 1317: 1313: 1309: 1305: 1301: 1294: 1286: 1282: 1278: 1274: 1270: 1266: 1265:Phytomedicine 1262: 1255: 1247: 1243: 1239: 1235: 1230: 1225: 1221: 1217: 1213: 1211: 1202: 1194: 1190: 1186: 1182: 1178: 1174: 1167: 1159: 1155: 1151: 1147: 1143: 1139: 1132: 1124: 1120: 1116: 1112: 1108: 1104: 1097: 1089: 1085: 1081: 1077: 1070: 1061: 1056: 1052: 1048: 1044: 1042: 1033: 1025: 1021: 1017: 1013: 1009: 1005: 998: 990: 984: 980: 973: 965: 961: 957: 954:(in German). 953: 946: 942: 930: 929: 925: 921: 916: 915: 911: 907: 902: 901: 897: 892: 891: 887: 882: 881: 877: 872: 871: 867: 863: 858: 857: 853: 848: 847: 843: 839: 835: 834: 830: 826: 822: 821: 817: 813: 809: 805: 804: 800: 795: 794: 790: 789: 788: 786: 782: 778: 774: 764: 762: 758: 754: 750: 746: 745: 740: 735: 733: 729: 725: 721: 720: 715: 714: 709: 705: 695: 692: 691: 685: 681: 680:biotic stress 677: 673: 670:as well as a 669: 664: 662: 661: 656: 652: 651:chemotaxonomy 648: 647: 642: 638: 634: 630: 626: 616: 612: 611: 606: 605: 595: 586: 572: 570: 566: 563:The complete 561: 559: 555: 552: 548: 544: 540: 539: 534: 530: 529:antimicrobial 526: 525: 519: 517: 513: 512:melting point 509: 505: 489: 479: 477: 473: 469: 465: 464:yeast extract 461: 460: 455: 451: 447: 446: 441: 437: 433: 429: 425: 421: 420: 415: 410: 408: 404: 403: 398: 388: 386: 382: 378: 377: 372: 371: 366: 362: 358: 354: 342: 336: 330: 323: 321: 318: 317: 296: 293: 289: 288: 283: 274: 273: 270: 263: 249: 248: 245: 238: 230: 226: 222: 221: 219: 209: 205: 204: 197: 193: 192: 190: 184: 180: 179: 172: 171: 169: 167: 162: 161: 157: 153: 150: 148: 146:ECHA InfoCard 143: 142: 135: 131: 130: 128: 126: 123: 122: 115: 111: 110: 108: 106: 103: 102: 95: 91: 90: 88: 84: 79: 78: 71: 67: 66: 64: 61: 57: 56: 51: 46: 41: 37: 32: 28: 23: 2139: 2135: 2129: 2112: 2108: 2102: 2077: 2073: 2069: 2060: 2051: 2047: 2037: 2028: 2024: 2015: 2007: 1990: 1986: 1980: 1971: 1967: 1961: 1953: 1944: 1940: 1936: 1932: 1928: 1922: 1913: 1909: 1903: 1895: 1886: 1882: 1876: 1868: 1849: 1846: 1840: 1815: 1811: 1805: 1786: 1782: 1771: 1757:cite journal 1724: 1720: 1716: 1709: 1684: 1680: 1674: 1657: 1653: 1647: 1630: 1626: 1625:(lichens)". 1622: 1616: 1583: 1579: 1573: 1554: 1550: 1544: 1536: 1517: 1513: 1507: 1499: 1480: 1476: 1470: 1434: 1430: 1426: 1420: 1386:(16): 4787. 1383: 1379: 1369: 1342: 1338: 1328: 1303: 1299: 1293: 1268: 1264: 1260: 1254: 1219: 1215: 1209: 1201: 1176: 1172: 1166: 1141: 1137: 1131: 1106: 1102: 1096: 1079: 1075: 1069: 1050: 1046: 1040: 1032: 1007: 1003: 997: 978: 972: 955: 951: 945: 932:Essl. (1989) 926: 912: 898: 888: 878: 868: 854: 844: 831: 818: 801: 791: 770: 742: 738: 736: 724:structurally 717: 711: 701: 688: 665: 658: 644: 622: 608: 602: 562: 556:pathways in 536: 522: 520: 485: 475: 457: 453: 443: 417: 411: 400: 394: 374: 368: 352: 351: 114:ChEMBL172439 53:Identifiers 44: 2189:Polyphenols 1939:spp. nov". 1715:the lichen 1520:(1): 1–30. 904:Elix & 749:bromination 668:antioxidant 655:systematics 637:malonyl-CoA 607:(left) and 424:ring system 285:Properties 152:100.007.558 2163:Categories 2080:(4): 388. 2054:: 143–147. 2016:Pertusaria 1993:(1): 238. 1962:Myelochroa 1545:Bulbothrix 1514:Mycosphere 1508:Bulbothrix 1471:Parmotrema 1427:Parmotrema 938:References 825:A.W.Archer 660:Bulbothrix 646:Parmotrema 641:coenzyme A 633:acetyl-CoA 631:that uses 575:Occurrence 516:solubility 482:Properties 472:osmolality 376:Bulbothrix 370:Parmotrema 320:Molar mass 125:ChemSpider 81:3D model ( 60:CAS Number 40:IUPAC name 2109:Phytotaxa 2048:Mycotaxon 1987:Phytotaxa 1968:Mycotaxon 1916:(1): 189. 1910:Mycotaxon 1883:Mycotaxon 1848:Alectoria 1749:221221650 1608:207276246 1380:Molecules 812:D.Hawksw. 777:taxonomic 554:signaling 440:mycobiont 432:depsidone 412:In 1933, 395:In 1897, 357:depsidone 173:208-312-0 165:EC Number 2169:Lactones 2138:Oropogon 1974:: 25–30. 1947:: 51–54. 1929:Lepraria 1904:Karoowia 1877:Graphina 1832:84432921 1818:: 9–20. 1812:Herzogia 1741:32819010 1701:85350700 1600:26370809 1557:: 1–30. 1551:MycoKeys 1451:96531766 1412:34443375 1361:19683421 1285:22921748 1261:Parmelia 1246:20709081 1238:17913083 1193:86701324 1158:84545779 1041:Ramalina 1024:86351217 906:T.H.Nash 728:aldehyde 524:in vitro 502:, and a 436:aromatic 428:phenolic 381:classify 70:521-39-1 2094:3243562 1403:8400444 1320:9795033 1123:3243399 781:eponyms 767:Eponyms 676:abiotic 560:cells. 468:sucrose 391:History 365:lichens 361:lactone 359:with a 325:388.284 196:5320418 183:PubChem 134:4478508 2146:  2092:  1889:: 176. 1856:  1830:  1747:  1739:  1699:  1606:  1598:  1449:  1410:  1400:  1359:  1318:  1283:  1244:  1236:  1191:  1156:  1121:  1022:  985:  922:(2014) 908:(1992) 864:(2001) 840:(1989) 827:(2001) 814:(1977) 810:& 759:, and 385:genera 269:SMILES 105:ChEMBL 34:Names 2090:JSTOR 2021:(PDF) 1906:Hale" 1828:S2CID 1745:S2CID 1697:S2CID 1604:S2CID 1447:S2CID 1242:S2CID 1189:S2CID 1154:S2CID 1119:JSTOR 1020:S2CID 808:Brodo 569:C NMR 551:STAT3 547:NF-κB 355:is a 244:InChI 83:JSmol 2144:ISBN 2031:: 6. 1935:and 1854:ISBN 1763:link 1737:PMID 1596:PMID 1408:PMID 1357:PMID 1316:PMID 1281:PMID 1234:PMID 1043:spp" 983:ISBN 920:Kalb 862:Elix 838:Hale 716:and 706:and 678:and 653:and 635:and 627:, a 567:and 549:and 543:Nrf2 508:mole 490:of C 373:and 2117:doi 2113:189 2082:doi 1995:doi 1991:189 1820:doi 1791:doi 1729:doi 1719:". 1689:doi 1662:doi 1635:doi 1588:doi 1559:doi 1522:doi 1485:doi 1439:doi 1429:". 1398:PMC 1388:doi 1347:doi 1308:doi 1273:doi 1224:doi 1181:doi 1146:doi 1111:doi 1084:doi 1055:doi 1012:doi 1008:103 960:doi 956:297 737:8'- 213:EPA 186:CID 2165:: 2111:. 2088:. 2078:95 2076:. 2052:88 2050:. 2046:. 2029:80 2027:. 2023:. 1989:. 1972:77 1970:. 1966:. 1943:. 1914:35 1912:. 1908:. 1887:77 1885:. 1881:. 1826:. 1816:26 1814:. 1787:15 1785:. 1781:. 1759:}} 1755:{{ 1743:. 1735:. 1725:86 1723:. 1695:. 1685:19 1683:. 1658:52 1656:. 1631:60 1629:. 1602:. 1594:. 1584:23 1582:. 1553:. 1549:. 1516:. 1512:. 1481:65 1479:. 1475:. 1459:^ 1445:. 1435:38 1433:. 1406:. 1396:. 1384:26 1382:. 1378:. 1355:. 1343:17 1341:. 1337:. 1314:. 1302:. 1279:. 1269:19 1267:. 1240:. 1232:. 1220:62 1218:. 1214:. 1187:. 1175:. 1152:. 1142:27 1140:. 1117:. 1107:92 1105:. 1080:51 1078:. 1051:17 1049:. 1045:. 1018:. 1006:. 763:. 755:, 751:, 663:. 545:, 500:10 496:12 492:18 409:. 387:. 313:10 307:12 301:18 2152:. 2123:. 2119:: 2096:. 2084:: 2001:. 1997:: 1945:4 1862:. 1834:. 1822:: 1799:. 1793:: 1765:) 1751:. 1731:: 1703:. 1691:: 1668:. 1664:: 1641:. 1637:: 1610:. 1590:: 1567:. 1561:: 1555:5 1530:. 1524:: 1518:4 1493:. 1487:: 1453:. 1441:: 1414:. 1390:: 1363:. 1349:: 1322:. 1310:: 1304:6 1287:. 1275:: 1248:. 1226:: 1195:. 1183:: 1177:5 1160:. 1148:: 1125:. 1113:: 1090:. 1086:: 1063:. 1057:: 1026:. 1014:: 991:. 966:. 962:: 739:O 565:H 498:O 494:H 476:O 454:O 310:O 304:H 298:C 215:) 211:( 85:) 45:H

Index


IUPAC name
CAS Number
521-39-1
JSmol
Interactive image
ChEMBL
ChEMBL172439
ChemSpider
4478508
ECHA InfoCard
100.007.558
Edit this at Wikidata
EC Number
PubChem
5320418
CompTox Dashboard
DTXSID001317270
Edit this at Wikidata
InChI
SMILES
Chemical formula
Molar mass
standard state
Infobox references
depsidone
lactone
lichens
Parmotrema
Bulbothrix

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