Seseli libanotis

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Subtypes (subspecies, varieties, subvarieties, forms)

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Distribution

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Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID643ffc88ddaa0488724790
Scientific name	Seseli libanotis
Authority	W.D.J.Koch
First published in	Nova Acta Phys.-Med. Acad. Caes. Leop.-Carol. Nat. Cur. 12(1): 111 (1824)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Libanotis pumila	Schur	Enum. Pl. Transsilv. : 258 (1866)
Libanotis nitens	Vis.	Fl. Dalmat. 3: 43 (1850)
Libanotis pubescens	Nyman	Consp. Fl. Eur. : 295 (1879)
Libanotis montana	Crantz	Stirp. Austr. Fasc. 3: 117 (1767)
Libanotis major	Hall. ex Gouan	Ill. Observ. Bot. : t. 26 (1773)
Libanotis pubescens	(Retz.) Schloss. & Vuk.	Fl. Croat. : 463 (1869)
Libanotis riviniana	Scop.	Fl. Carniol. , ed. 2, 1: 193 (1771)
Libanotis humilis	Schur	Oesterr. Bot. Wochenbl. 8: 21 (1858)
Libanotis alpina	Schur	Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 29 (1853)
Libanotis athamanthoides	DC.	Prodr. 4: 150 (1830)
Libanotis athamantica	G.Gaertn., B.Mey. & Schreb.	Oekon. Fl. Wetterau 1: 427 (1799)
Libanotis athamantoides	Schur	Enum. Pl. Transsilv. : 258 (1866)
Libanotis gracilis	Rchb.	Fl. Germ. Excurs. 2: 468 (1832)
Libanotis daucoides	Scop.	Fl. Carniol. , ed. 2, 1: 193 (1771)
Libanotis hostiana	Schur	Enum. Pl. Transsilv. : 258 (1866)
Libanotis cretensis	Gaertn.	Fruct. Sem. Pl. 1: 84 (1788)
Libanotis crithmoides	Nyman	Consp. Fl. Eur. : 395 (1879)
Libanotis daucifolia	(Scop.) Rchb.	Fl. Germ. Excurs. 2: 468 (1832)
Libanotis daucifolia var. athamantoides	(Spreng.) Poldini	Inform. Bot. Ital. 36: 149 (2004)
Ligusticum athamantoides	Spreng.	Pl. Umbell. Prodr. : 40 (1813)
Ligusticum sibiricum	Spreng.	Pl. Umbell. Prodr. : 40 (1813)
Ligusticum condensatum	Spreng.	Pl. Umbell. Prodr. : 40 (1813)
Sium ammi	Vest	Man. Bot. : 517 (1805)
Selinum libanotis	E.H.L.Krause	Deutschl. Fl. Abbild. , ed. 2, 12: 102 (1904)
Seseli pubicarpum	Simonk.	Magyar Bot. Lapok 3: 84 (1904)
Seseli reichenbachii	Ces.	Linnaea 11: 318 (1837)
Seseli vulgare	Bubani	Fl. Pyren. 2: 376 (1899)
Seseli pencanum	Phil.	Anales Univ. Chile 85: 719 (1894)
Seseli athamantoides	C.A.Mey. ex Ledeb.	Fl. Altaic. 1: 342 (1829)
Ammi daucifolium	Scop.	Fl. Carniol. , ed. 2, 1: 207 (1771)
Athamanta caucasica	Hort.Par. ex Fisch. & C.A.Mey.	Index Seminum (LE, Petropolitanus) 3: 39 (1837)
Athamanta collina	Salisb.	Prodr. Stirp. Chap. Allerton : 163 (1796)
Athamanta daucoides	J.F.Gmel.	Syst. Nat. ed. 13[bis] : 477 (1791)
Athamanta libanotis	L.	Sp. Pl. : 244 (1753)
Athamanta oreoselinum	Huds.	Fl. Angl. : 115 (1762)
Athamanta pubescens	Retz.	Observ. Bot. 3: 28 (1783)
Athamanta riviniana	Host ex Steud.	Nomencl. Bot. , ed. 2, 1: 166 (1840)
Balinotella libanotis	(L.) Soják	Zprávy Krajsk. Vlastiv. Muz. Olomouci 215: 3 (1982)
Balinotella libanotis subsp. leiocarpa	(Heuff.) Soják	Zprávy Krajsk. Vlastiv. Muz. Olomouci 215: 3 (1982)
Balinotella libanotis subsp. pyrenaica	(L.) Soják	Zprávy Krajsk. Vlastiv. Muz. Olomouci 215: 3 (1982)
Bubon libanotis	Dumort.	Fl. Belg. : 79 (1827)
Bubon pyrenaicus	Dumort.	Fl. Belg. : 79 (1827)
Crithmum pyrenaicum	L.	Sp. Pl. : 246 (1753)
Libanotis leiocarpa	Simonk.
Libanotis montana subsp. bipinnata	Dostál
Libanotis pyrenaica	(L.) O.Schwarz	Mitt. Thüring. Bot. Ges. 1(1): 108. 1949
Libanotis pyrenaica subsp. bipinnata	(Čelak.) Holub	Folia Geobot. Phytotax. 9(3): 273. 1974
Libanotis pyrenaica subsp. montana	Lemke & Rothm.
Seseli intermedium	N.Vodopianova
Seseli libanotis var. bipinnatum	Čelak.
Libanotis vulgaris	DC.	Prodr. 4: 150 (1830)
Libanotis pyrenaica subvar. libanotis	(L.) Reduron	Ombellif. France 3: 1694 (2007)

Common names Top

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Language	Common/alternative name
English	moon carrot
English	mooncarrot
Czech	žebřice pyrenejská
Welsh	lloerforonen
Danish	hjorterod
German	berg-heilwurz
German	heilwurz
Estonian	pildigalerii
Finnish	hirvenputki
Finnish	niittyhirvenputki
French	libanotis
Hungarian	hegyi gurgolya
Hungarian	tömjénillat
Armenian	անճիտան
Armenian	կապնդեղ Լիբանանի
Georgian	libanotis
Georgian	სასუქა
Norwegian Bokmål	hjorterot
Norwegian Nynorsk	hjorterot
Russian	Жабрица порезниковая
Swedish	säfferot
Chinese	欧洲岩风
Chinese	歐洲岩風

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Seseli libanotis subsp. intermedium	(Rupr.) P.W.Ball	Feddes Repert. 79: 64. 1968 (1968)

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northern Africa
  - Morocco

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Kazakhstan
- Siberia
  - Altay
  - Irkutsk
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Southeastern U.S.A.
  - District Of Columbia
  - Maryland

Southern America click to expand
- Southern South America
  - Chile Central

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000434770
USDA Plants	SELI2
Tropicos	1700232
INPN	610580
Flora of Italy	3490
KEW	urn:lsid:ipni.org:names:848608-1
The Plant List	kew-2479607
Open Tree Of Life	164503
Observations.org	81659
NCBI Taxonomy	63037
NBN Atlas	NHMSYS0000463473
Nature Serve	2.128804
IPNI	848608-1
iNaturalist	168867
GBIF	3034133
EPPO	SSELI
EOL	581460
Elurikkus	7249
USDA GRIN	406726
Wikipedia	Seseli_libanotis
CMAUP	NPO18424

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

The complete plastomes of thirteen Libanotis (Apiaceae, Apioideae) plants: comparative and phylogenetic analyses provide insights into the plastome evolution and taxonomy of Libanotis

Liu LJ, Liu CK, Cai J, Deng JJ, He X, Zhou S

BMC Plant Biol

12-Feb-2024

PMCID:	PMC10860227
doi:	10.1186/s12870-024-04784-4
PMID:	38342898

Edge Effects in the Distribution of Coleoptera in the Forests of the Center of the European Part of Russia

Ruchin AB, Egorov LV, Khapugin AA

Insects

10-Apr-2023

PMCID:	PMC10144564
doi:	10.3390/insects14040371
PMID:	37103186

The phylogeny of Seseli (Apiaceae, Apioideae): insights from molecular and morphological data

Cai J, Qin HH, Lei JQ, Liu CK, He XJ, Zhou SD

BMC Plant Biol

16-Nov-2022

PMCID:	PMC9667662
doi:	10.1186/s12870-022-03919-9
PMID:	36380268

Chemical Composition and Evaluation of Insecticidal Activity of Seseli bocconei Essential Oils against Stored Products Pests

Vaglica A, Peri E, Badalamenti N, Ilardi V, Bruno M, Guarino S

Plants (Basel)

10-Nov-2022

PMCID:	PMC9697863
doi:	10.3390/plants11223047
PMID:	36432776

Phytochemical Classification of Medicinal Plants Used in the Treatment of Kidney Disease Based on Traditional Persian Medicine

Rabizadeh F, Mirian MS, Doosti R, Kiani-Anbouhi R, Eftekhari E

Evid Based Complement Alternat Med

31-Jul-2022

PMCID:	PMC9357710
doi:	10.1155/2022/8022599
PMID:	35958915

Interspecific and intraspecific analysis of Selinum spp. collected from Indian Himalayas using DNA barcoding

Srivastava RP, Saxena G, Singh L, Singh A, Verma PC, Kaur G

J Genet Eng Biotechnol

22-Apr-2022

PMCID:	PMC9033919
doi:	10.1186/s43141-022-00345-0
PMID:	35451659

Synopsis of Leptosphaeriaceae and Introduction of Three New Taxa and One New Record from China

Xu R, Su W, Tian S, Bhunjun CS, Tibpromma S, Hyde KD, Li Y, Phukhamsakda C

J Fungi (Basel)

19-Apr-2022

PMCID:	PMC9146790
doi:	10.3390/jof8050416
PMID:	35628672

Environmental variables drive plant species composition and distribution in the moist temperate forests of Northwestern Himalaya, Pakistan

Rahman IU, Hart RE, Ijaz F, Afzal A, Iqbal Z, Calixto ES, Abd_Allah EF, Alqarawi AA, Hashem A, Al-Arjani AB, Kausar R, Haq SM

PLoS One

24-Feb-2022

PMCID:	PMC8870539
doi:	10.1371/journal.pone.0260687
PMID:	35202409

Classification and Characterization of the Manoor Valley’s (Lesser Himalaya) Vegetation from the Subtropical-Temperate Ecotonal Forests to the Alpine Pastures along Ecological Variables

Rahman IU, Afzal A, Iqbal Z, Alzain MN, Al-Arjani AB, Alqarawi AA, Abd_Allah EF, Ali N, Sakhi S, Khan MA, Khan U, Ijaz F, Mumtaz S, Calixto ES

Plants (Basel)

28-Dec-2021

PMCID:	PMC8747448
doi:	10.3390/plants11010087
PMID:	35009089

Comparison of Volatile Organic Compounds of Sideritis romana L. and Sideritis montana L. from Croatia

Marić T, Friščić M, Marijanović Z, Maleš Ž, Jerković I

Molecules

01-Oct-2021

PMCID:	PMC8512722
doi:	10.3390/molecules26195968
PMID:	34641513

Fungi of quarantine concern for China I: Dothideomycetes

Zhao P, Crous PW, Hou LW, Duan WJ, Cai L, Ma ZY, Liu F

Persoonia

25-Aug-2021

PMCID:	PMC10784663
doi:	10.3767/persoonia.2023.47.02
PMID:	38352971

Fungi of quarantine concern for China I: Dothideomycetes

Zhao P, Crous PW, Hou LW, Duan WJ, Cai L, Ma ZY, Liu F

Persoonia

25-Aug-2021

PMCID:	PMC10486631
doi:	10.3767/persoonia.2021.47.02
PMID:	37693796

Restoration of species‐rich grasslands by transfer of local plant material and its impact on species diversity and genetic variation—Findings of a practical restoration project in southeastern Germany

Kaulfuß F, Reisch C

Ecol Evol

22-Aug-2021

PMCID:	PMC8462159
doi:	10.1002/ece3.8029
PMID:	34594541

On genetic diversity in caraway: Genotyping of a large germplasm collection

von Maydell D, Lehnert H, Berner T, Klocke E, Junghanns W, Keilwagen J, Marthe F

PLoS One

29-Dec-2020

PMCID:	PMC7771672
doi:	10.1371/journal.pone.0244666
PMID:	33373410

7-Isopentenyloxycoumarin: What Is New across the Last Decade

Preziuso F, Genovese S, Marchetti L, Sharifi-Rad M, Palumbo L, Epifano F, Fiorito S

Molecules

14-Dec-2020

PMCID:	PMC7765079
doi:	10.3390/molecules25245923
PMID:	33327602

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Aporphines
Anolobine	164710	Click to see C1CNC2CC3=C(C=CC(=C3)O)C4=C2C1=CC5=C4OCO5	281.30	unknown	via CMAUP database
Anonaine	160597	Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5	265.31	unknown	via CMAUP database
Asimilobine	160875	Click to see COC1=C(C=C2CCNC3C2=C1C4=CC=CC=C4C3)O	267.32	unknown	via CMAUP database
Atherospermidine	77514	Click to see COC1=C2C(=C3C4=CC=CC=C4C(=O)C5=NC=CC1=C35)OCO2	305.30	unknown	via CMAUP database
Boldine 2-methyl ether	16573	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC	341.40	unknown	via CMAUP database
Dicentrinone	177744	Click to see COC1=C(C=C2C(=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O)OC	335.30	unknown	via CMAUP database
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	via CMAUP database
Lanuginosine	97622	Click to see COC1=CC2=C(C=C1)C3=C4C(=CC5=C3OCO5)C=CN=C4C2=O	305.30	unknown	via CMAUP database
Laurotetanine	31415	Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC	327.40	unknown	via CMAUP database
Liriodenine	10144	Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53	275.26	unknown	via CMAUP database
Lysicamine	122691	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC	291.30	unknown	via CMAUP database
Norisocorydine	12313549	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	via CMAUP database
Norstephalagine	133381	Click to see COC1=C2C(=C3C4=CC=CC=C4CC5C3=C1CCN5)OCO2	295.30	unknown	via CMAUP database
O-Nornuciferine	197017	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=CC=C43)OC)O	281.30	unknown	via CMAUP database
Oxoglaucine	97662	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC(=C(C=C42)OC)OC)OC	351.40	unknown	via CMAUP database
Romucosine	10734687	Click to see COC(=O)N1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3	323.30	unknown	via CMAUP database
Romucosine H	5320994	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3C(=O)OC)OC)OC)C=C1)O	385.40	unknown	via CMAUP database
Xylopine	160503	Click to see COC1=CC2=C(C=C1)C3=C4C(C2)NCCC4=CC5=C3OCO5	295.30	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines / Hydroxy-7-aporphines
Michelalbine	10378981	Click to see C1CNC2C(C3=CC=CC=C3C4=C2C1=CC5=C4OCO5)O	281.30	unknown	via CMAUP database
Ushinsunine	197018	Click to see CN1CCC2=CC3=C(C4=C2C1C(C5=CC=CC=C54)O)OCO3	295.30	unknown	via CMAUP database
> Alkaloids and derivatives / Proaporphines
(4S)-10,11-dimethoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one	830726	Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)OC	297.30	unknown	via CMAUP database
Pronuciferine, (-)-	793841	Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC	311.40	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Corydalmine	161665	Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)OC	341.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Halobenzoic acids and derivatives / Halobenzoic acids
3-Chlorobenzoic acid	447	Click to see C1=CC(=CC(=C1)Cl)C(=O)O	156.56	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic acid	8357	Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O	212.20	unknown	via CMAUP database
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate	19844	Click to see COC1=C(C=CC(=C1)C(=O)OC)O	182.17	unknown	via CMAUP database
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid	12575	Click to see COC1=C(C=C(C=C1)C(=O)O)O	168.15	unknown	via CMAUP database
Methyl 3-hydroxy-4-methoxybenzoate	4056967	Click to see COC1=C(C=C(C=C1)C(=O)OC)O	182.17	unknown	via CMAUP database
Methyl 4-methoxybenzoate	8499	Click to see COC1=CC=C(C=C1)C(=O)OC	166.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see COC(=O)C1=CC=C(C=C1)O	152.15	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
(2S)-3-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,2-diol	86330909	Click to see COC1=CC(=CC(=C1O)OC)CC(CO)O	228.24	unknown	via CMAUP database
Isovanillin	12127	Click to see COC1=C(C=C(C=C1)C=O)O	152.15	unknown	via CMAUP database
n-Dihydroferuloyltyramine	16119667	Click to see COC1=C(C=CC(=C1)CCC(=O)NCCC2=CC=C(C=C2)O)O	315.40	unknown	via CMAUP database
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C	11796268	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Episyringaresinol	12309694	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Acanthoside D	21603207	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC	742.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16R)-17-Hydroxykaura-18-oic acid	44575990	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O	320.50	unknown	via CMAUP database
(1S,4R,9R,10R,13R,14S)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol	12112093	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C	306.50	unknown	via CMAUP database
(1S,4S,5R,9S,10R,13R,14R)-14-(dimethoxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	46210308	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)C(OC)OC)(C)C(=O)O	364.50	unknown	via CMAUP database
(4R)-17-Acetoxykauran-18-oic acid	102425890	Click to see CC(=O)OCC1CC23CCC4C(C2CCC1C3)(CCCC4(C)C(=O)O)C	362.50	unknown	via CMAUP database
[(1S,4S,5R,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol	46210166	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO	306.50	unknown	via CMAUP database
16alphaH-17,19-ent-kauranediol	102594837	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO	306.50	unknown	via CMAUP database
16beta,17-Dihydroxy-ent-kaurane-19-oic acid	469209	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O	336.50	unknown	via CMAUP database
17-Hydroxykaura-18-oic acid	46210307	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)CO)(C)C(=O)O	320.50	unknown	via CMAUP database
Diterpenoid SP-II	442023	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)O	336.50	unknown	via CMAUP database
ent-Kauran-16-beta-ol	21593607	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C	290.50	unknown	via CMAUP database
Kaurane-16alpha,17-diol	13816761	Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C	306.50	unknown	via CMAUP database
Kaurenoic acid	73062	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O	302.50	unknown	via CMAUP database
Methyl 16alpha,17-dihydroxy-ent-kauran-19-oate	46233487	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(C4)(CO)O)(C)C(=O)OC	350.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(5beta,8alpha,9beta,10alpha,12alpha,16R)-16,17-Dihydroxyatisane-18-oic acid methyl ester	25006930	Click to see CC12CCCC(C1CCC34C2CC(CC3)C(C4)(CO)O)(C)C(=O)OC	350.50	unknown	via CMAUP database
methyl (1S,4S,5R,9S,10R,12S,13R)-13-(acetyloxymethyl)-13-hydroxy-5,9-dimethyltetracyclo[10.2.2.01,10.04,9]hexadecane-5-carboxylate	25006927	Click to see CC(=O)OCC1(CC23CCC1CC2C4(CCCC(C4CC3)(C)C(=O)OC)C)O	392.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Sitoindoside I	9832350	Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O	815.30	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasterol glucoside	6602508	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-beta-d-Arabinofuranosylade-nine	12358320	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Cherimolacyclopeptide A	11205172	Click to see CCC(C)C1C(=O)N2CCCC2C(=O)NC(C(=O)NC(C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)CC(C)C)CCSC)C(C)O)CCC(=O)N	838.00	unknown	via CMAUP database
Cherimolacyclopeptide C	11216146	Click to see CCC(C)C1C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NC(C(=O)NC(C(=O)N1)CC4=CNC5=CC=CC=C54)C)C	692.80	unknown	via CMAUP database
Cherimolacyclopeptide D	11599937	Click to see CC1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N1)CC(=O)N)CC(C)C)C(C)O)C(C)C	652.70	unknown	via CMAUP database
Cherimolacyclopeptide F	101773878	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)N3CCCC3C(=O)NCC(=O)NC(C(=O)NCC(=O)N1)CCSC)CCSC)CC(C)C)CC4=CC=C(C=C4)O	960.20	unknown	via CMAUP database
cyclo[Ala-Pro-Gly-Ala-Val-Pro-Ile-Tyr]	11585828	Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)NC(C(=O)NC(C(=O)N3CCCC3C(=O)N1)C(C)C)C)C)CC4=CC=C(C=C4)O	768.90	unknown	via CMAUP database
cyclo[Gly-Leu-Gly-Phe-Tyr-Pro]	71608845	Click to see CC(C)CC1C(=O)NCC(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NCC(=O)N1)CC3=CC=C(C=C3)O)CC4=CC=CC=C4	634.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Koaburaside monomethyl ether	636454	Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)CO)O)O)O	346.33	unknown	via CMAUP database
Thalictoside	21629843	Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O	329.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
Cheritamine	101428698	Click to see CCCCC=CCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCC1=CNC2=CC=CC=C21	593.00	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-1-[(4-Hydroxyphenyl)methyl]-5,6-dimethoxy-1,2,3,4-tetrahydroisoquinolin-7-ol	101687011	Click to see COC1=C2CCNC(C2=CC(=C1OC)O)CC3=CC=C(C=C3)O	315.40	unknown	via CMAUP database
1-[Hydroxy(4-hydroxyphenyl)methyl]-6-methoxyisoquinolin-7-ol	637078	Click to see COC1=C(C=C2C(=C1)C=CN=C2C(C3=CC=C(C=C3)O)O)O	297.30	unknown	via CMAUP database
1alpha-(3-Methoxy-4-hydroxybenzyl)-2-methyl-1,2,3,4-tetrahydro-6-methoxyisoquinoline-7-ol	14357385	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)O)OC)O)OC	329.40	unknown	via CMAUP database
Annocherine B	5319094	Click to see COC1=C(C=C2C(=C1)C=CN=C2C(C3=CC=C(C=C3)O)OC)O	311.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
7-Hydroxy-6-methoxy-2-methylisoquinolin-1-one	59620302	Click to see CN1C=CC2=CC(=C(C=C2C1=O)O)OC	205.21	unknown	via CMAUP database
Cherianoine	5315819	Click to see CN1C=CC2=CC(=C(C(=C2C1=O)OC)O)OC	235.24	unknown	via CMAUP database
Thalifoline	89048	Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC	207.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic acid	938	Click to see C1=CC(=CN=C1)C(=O)O	123.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidine carboxylic acids and derivatives / Pyrrolidinecarboxamides
2-Oxopyrrolidine-1-carboxamide	326996	Click to see C1CC(=O)N(C1)C(=O)N	128.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
4H-pyrano[3,4-c]quinolin-4-one	638628	Click to see C1=CC=C2C(=C1)C3=C(C=N2)C(=O)OC=C3	197.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(3,4-Dihydroxyphenyl)-N-phenethylpropenamide, (E)-	11391937	Click to see C1=CC=C(C=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)O	283.32	unknown	via CMAUP database
cis-Caffeoyltyramine	16119508	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O	299.32	unknown	via CMAUP database
FERULOYL-beta-PHENETHYLAMINE	11162295	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=CC=C2)O	297.30	unknown	via CMAUP database
n-cis-Feruloyltyramine	6440659	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
N-Feruloyl-3-methoxytyramine, (Z)-	5322166	Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O	343.40	unknown	via CMAUP database
N-trans-feruloylmethoxytyramine	5352115	Click to see COC1=C(C=CC(=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O	343.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Paprazine	5372945	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
methyl (2Z)-3-(4-hydroxyphenyl)acrylate	12343877	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	via CMAUP database
Methyl 4-hydroxycinnamate	5319562	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(4-Hydroxyphenyl)propionic acid	10394	Click to see C1=CC(=CC=C1CCC(=O)O)O	166.17	unknown	via CMAUP database

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Seseli libanotis

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