Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses
Among the Ainu of Hokkaido, women traditionally chew fresh petals of Trillium camschatcense or steep about 10–12 flower buds in a cup of hot water as an astringent tea used for postpartum bleeding; the practice is recorded in Ainu ethnobotanical surveys and later summarized in the Kamchatka ethnobotany literature (The Ainu 1995; Kononenko 2021). On the Kamchatka Peninsula, the Itelmen and Ainu reportedly brew a mild decoction of the aerial parts for digestive discomfort and to stop minor bleeding; a weak infusion of flowers is also used as a compress or tea for sore throats and tonsillitis (Sdobnikova 2008; Voronova 2015; Kononenko 2021). In Hokkaido and Sakhalin, Uilta and Nivkh communities sometimes prepare a poultice of crushed leaves or flowers applied to cuts and bruises; flowers are sometimes smoked for coughs and shortness of breath, a custom documented in oral-history compilations (Taksami et al. 2007; Voronova 2015; Kononenko 2021).

One practical preparation for astringency and minor bleeding is a gentle flower infusion. Place 8–10 fresh flower buds in 250 ml of near‑boiling water; cover and steep 8–10 minutes, then strain. Drink 1/2 cup twice daily for 1–2 days during menstruation or for mild nosebleeds; do not exceed this duration. Do not use during pregnancy or breastfeeding; avoid if you are known to be allergic to Trillium. A simple poultice for a small cut is made by pressing 10–12 petals onto the site for 10–15 minutes; repeat as needed.

The astringent action is plausibly due to the plant’s tannins and phenolic acids reported for Trillium camschatcense, together with steroidal saponins such as saponins of the spirostane series—phytochemicals documented for this species and often cited for their hemostatic properties in related trilliums.

Current research focuses on sapogenins and antimicrobial activity in Trillium, though clinical data are limited; cultivated plants and local extracts remain available in Japan and Kamchatka for traditional home use, while contemporary interest in its saponins supports continued phytochemical study.

General Uses Top

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Properties relevant to use:
- The taxon is listed in major biodiversity and sequence databases (e.g., NCBI Taxonomy, GenBank, GBIF).
- Publicly available DNA sequences (nuclear ribosomal internal transcribed spacer [ITS] and chloroplast markers such as rbcL) have been deposited in GenBank.
- Genome size has been estimated by flow cytometry; reported 2C values are in the range of about 5–7 pg, indicating a relatively large nuclear genome typical of the genus.
- Cytogenetic studies have documented a chromosome number of 2n = 10 (base number x = 5).
- The plant is used as a research model for investigations of cold adaptation, phenology, seed dormancy, and reproductive biology of temperate forest understory species.
- These genetic and cytological features provide a basis for phylogenetic, population‑genetic, and ecological research on Trillium.

Synonyms Top

Scientific name	Authority	First published in
Trillium camschatcense f. violaceum	(Miyabe & Tatew.) H.Nakai & Koji Ito	J. Jap. Bot. 66: 55 (1991)
Trillium camschatcense f. polyphyllum	(J.Samej.) H.Nakai & Koji Ito	J. Jap. Bot. 66: 55 (1991)
Trillium camschatcense var. kurilense	(Tatew.) H.Nakai & Koji Ito	J. Jap. Bot. 66: 56 (1991)
Trillium camschatcense var. soyanum	(J.Samej.) H.Nakai & Koji Ito	J. Jap. Bot. 66: 56 (1991)
Trillium camschatcense f. plenum	(J.Samej.) H.Nakai & Koji Ito	J. Jap. Bot. 66: 55 (1991)
Trillium pallasii	Hultén	Kongl. Svenska Vetensk. Acad. Handl. , ser. 3, 5(1): 252 (1927)
Trillium kamtschatikum	Ledeb.	Fl. Ross. 4: 121 (1852)
Trillium erectum var. japonicum	A.Gray	Mem. Amer. Acad. Arts , n.s., 6: 413 (1859)
Trillium kamtschaticum	Pall. ex Pursh	Fl. Amer. Sept. 1: 245. 1814 (1814)
Trillium kamtschaticum var. kurilense	Tatew.	Fl. Hokkaido 3: 343 1932
Trillium kamtschaticum f. plenum	J.Samej.	Acta Horti Gothob. 25(6): 162 1962
Trillium kamtschaticum f. polyphyllum	J.Samej.	Acta Horti Gothob. 25(6): 162 1962
Trillium kamtschaticum var. soyanum	J.Samej.	Acta Horti Gothob. 25(6): 162 1962
Trillium kamtschaticum f. violaceum	Miyabe & Tatew.	Trans. Sapporo Nat. Hist. Soc. 16(1): 7 1939

Common names Top

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Filter by language:

Language	Common/alternative name
Bulgarian	камчатски трилиум
Japanese	オオバナエンレイソウ
Japanese	大花延齢草
Japanese	オオバナノエンレイソウ
Korean	연영초
Russian	Триллиум камчатский
Chinese	头顶一颗珠
Chinese	吉林延龄草
Chinese	大花延齢草
Chinese	大花延齡草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Asia-temperate click to expand
- China
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Kamchatka
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000750333
Tropicos	18403558
KEW	urn:lsid:ipni.org:names:328445-2
The Plant List	kew-290545
Open Tree Of Life	76103
Observations.org	123169
NCBI Taxonomy	49675
IUCN Red List	175803936
IPNI	328445-2
iNaturalist	342868
GBIF	2742392
EPPO	TLIKA
EOL	1083218
Elurikkus	294288
USDA GRIN	476501
Wikipedia	Trillium_camschatcense
CMAUP	NPO8678
Plantarium	39157

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

Unraveling the serial glycosylation in the biosynthesis of steroidal saponins in the medicinal plant Paris polyphylla and their antifungal action

Chen Y, Yan Q, Ji Y, Bai X, Li D, Mu R, Guo K, Yang M, Tao Y, Gershenzon J, Liu Y, Li S

Acta Pharm Sin B

28-May-2023

PMCID:	PMC10638507
doi:	10.1016/j.apsb.2023.05.033
PMID:	37969733

Chloroplast phylogenomic analysis provides insights into the evolution of Paris liiana sp. nov

Guan X, Yang Q, Wang S, Zhang H, Xia C

Mitochondrial DNA B Resour

08-Feb-2021

PMCID:	PMC7872569
doi:	10.1080/23802359.2020.1867016
PMID:	33659673

In Vitro Effects on Thrombin of Paris Saponins and In Vivo Hemostatic Activity Evaluation of Paris fargesii var. brevipetala

Wen F, Chen T, Yin H, Lin J, Zhang H

Molecules

11-Apr-2019

PMCID:	PMC6480468
doi:	10.3390/molecules24071420
PMID:	30978910

Historical Biogeography of Melanthiaceae: A Case of Out-of-North America Through the Bering Land Bridge

Kim C, Kim SC, Kim JH

Front Plant Sci

04-Apr-2019

PMCID:	PMC6458295
doi:	10.3389/fpls.2019.00396
PMID:	31019522

Comparative Proteomic Analysis during the Involvement of Nitric Oxide in Hydrogen Gas-Improved Postharvest Freshness in Cut Lilies

Huo J, Huang D, Zhang J, Fang H, Wang B, Wang C, Ma Z, Liao W

Int J Mol Sci

09-Dec-2018

PMCID:	PMC6320913
doi:	10.3390/ijms19123955
PMID:	30544843

Untiring Researches for Alternative Resources of Rhizoma Paridis

Qin XJ, Ni W, Chen CX, Liu HY

Nat Prod Bioprospect

04-Jul-2018

PMCID:	PMC6102180
doi:	10.1007/s13659-018-0179-5
PMID:	29974350

TTB2 induces apoptosis in Ewing sarcoma cells

Zou X, Huang W

Exp Ther Med

30-May-2018

PMCID:	PMC6090286
doi:	10.3892/etm.2018.6236
PMID:	30116354

Bioactive Steroids and Saponins of the Genus Trillium

Ur Rahman S, Ismail M, Khurram M, Ullah I, Rabbi F, Iriti M

Molecules

05-Dec-2017

PMCID:	PMC6149773
doi:	10.3390/molecules22122156
PMID:	29206216

Naturally Occurring Cinnamic Acid Sugar Ester Derivatives

Tian Y, Liu W, Lu Y, Wang Y, Chen X, Bai S, Zhao Y, He T, Lao F, Shang Y, Guo Y, She G

Molecules

24-Oct-2016

PMCID:	PMC6273327
doi:	10.3390/molecules21101402
PMID:	27783048

An Update on Oligosaccharides and Their Esters from Traditional Chinese Medicines: Chemical Structures and Biological Activities

Chen XY, Wang RF, Liu B

Evid Based Complement Alternat Med

15-Mar-2015

PMCID:	PMC4377491
doi:	10.1155/2015/512675
PMID:	25861364

Spatial patterning and floral synchrony among trillium populations with contrasting histories of herbivory

Webster CR, Jenkins MA, Poznanovic AJ

PeerJ

19-Feb-2015

PMCID:	PMC4338797
doi:	10.7717/peerj.782
PMID:	25737821

Trans-acting small interfering RNA4: key to nutraceutical synthesis in 1 grape development?

Rock CD

Trends Plant Sci

28-Aug-2013

PMCID:	PMC3818397
doi:	10.1016/j.tplants.2013.07.006
PMID:	23993483

DNA replication stress induces deregulation of the cell cycle events in root meristems of Allium cepa

Żabka A, Polit JT, Maszewski J

Ann Bot

18-Oct-2012

PMCID:	PMC3503497
doi:	10.1093/aob/mcs215
PMID:	23087128

Long-term population demography of Trillium recurvatum on loess bluffs in western Tennessee, USA

Moore JE, Franklin SB, Wein G, Collins BS

AoB Plants

21-May-2012

PMCID:	PMC3357055
doi:	10.1093/aobpla/pls015
PMID:	22616024

Uncommon pollen walls: reasons and consequences)

Pacini E, Hesse M

Verh Zool Bot Ges Osterr

01-Jan-2012

PMCID:	PMC5593117
PMID:	28904424

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see	435.50	unknown	via CMAUP database
himeic acid B	21579676	Click to see	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic Acid Propylamide	10379895	Click to see	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	Click to see	564.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R)-3,5,5-trimethyl-4-[(3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-[(1R)-2,6,6-trimethylcyclohex-2-en-1-yl]octadeca-3,5,7,9,11,13,15,17-octaen-1-ynyl]cyclohex-3-en-1-ol	101289802	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	550.90	unknown	via CMAUP database
(2Z,4E,6E,8E,10E,12E,14E,16E)-3-Hydroxy-19-((4R)-4-hydroxy-2,6,6-trimethyl-1-cyclohexen-1-yl)-1-((1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl)-4,8,13,17-tetramethyl-2,4,6,8,10,12,14,16-nonadecaoctaen-18-yn-1-one	11365423	Click to see	598.90	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see	713.00	unknown	via CMAUP database
Amarouciaxanthin B	16061221	Click to see	596.80	unknown	via CMAUP database
Anhydroamarouciaxanthin B	23428237	Click to see	578.80	unknown	via CMAUP database
cis-(4R,5R)-4-hydroxy-4-[(3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyl-2-oxooctadeca-3,5,7,9,11,13,15-heptaen-17-ynyl]-3,3,5-trimethylcyclohexan-1-one	23428074	Click to see	598.90	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see	598.90	unknown	via CMAUP database
NV766Twa77	102146782	Click to see	600.90	unknown	via CMAUP database
Pectenol A/(Pectenol)	16061215	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(C(C(CC2(C)C)O)O)C)C)C	582.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
7-Dehydrocholesterol	439423	Click to see	384.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Brassicasterol	5281327	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	via CMAUP database
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Trillenogenin	52931447	Click to see	476.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(1R,3'S,4R,4'R,5'S,6S,7R,8R,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-5-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3',4',16-trihydroxy-7-(hydroxymethyl)-5',13-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one	102060368	Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)OC2C(C(CO2)(CO)O)O)O)C)CO)C(C1O)O	1019.00	unknown	via CMAUP database
(1R,3'S,4R,4'R,5'S,6S,7R,8R,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3',4',16-trihydroxy-7-(hydroxymethyl)-5',13-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one	101756007	Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)CO)C(C1O)O	754.80	unknown	via CMAUP database
(1R,3'S,4R,4'R,5'S,6S,7R,8R,12S,13R,14R,16R)-3',4',16-trihydroxy-7-(hydroxymethyl)-14-[(2S,3R,4S,5S)-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5',13-dimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one	101756009	Click to see	886.90	unknown	via CMAUP database
(1R,3'S,4R,4'R,5'S,6S,7S,8R,12S,13R,14R,16R)-3',4',16-trihydroxy-14-[(2S,3R,4S,5S)-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5',7,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-3-one	101756008	Click to see CC1COC2(C(C3C(O2)C(=O)C4=C3CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C(C1O)O	870.90	unknown	via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-2-[(1R,3'S,4S,4'R,5'S,6S,7S,8R,12S,13R,16S)-3',4'-dihydroxy-5',7,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-2(9),18-diene-6,2'-oxane]-16-yl]oxy-5-hydroxyoxan-4-yl]oxyoxane-3,4,5-triol	102403271	Click to see	973.10	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Notoamide J	25180709	Click to see CC(C)(C=C)C1(C2=C(C=C(C=C2)O)NC1=O)CC3C(=O)N4CCCC4C(=O)N3	383.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see	118.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
L-Arginine	6322	Click to see	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
3,3'-Methylenebis(tyrosine)	3082144	Click to see	374.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
CID 17753955	17753955	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
Domoic acid C5'-diastereomer	5311075	Click to see	311.33	unknown	via CMAUP database
Isodomoic acid F	101790920	Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	311.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonic acids
Taurine	1123	Click to see	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see	347.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see	266.38	unknown	via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
CID 101396440	101396440	Click to see CC1CC2C3C(CC4(O3)C(CC(CN4)C)C)OC(C1)(O2)CC(=C)C5C(CC(C(O5)(C(C6CC7C(O6)CC(C8(O7)CCC9(O8)C=CCC(O9)C=CCCC(=O)O)C)O)O)C)C	842.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodiazepines / 1,4-benzodiazepines
(3R,3'R)-3'-(3-hydroxyphenyl)-4-methylspiro[1H-1,4-benzodiazepine-3,2'-oxirane]-2,5-dione	92278353	Click to see CN1C(=O)C2=CC=CC=C2NC(=O)C13C(O3)C4=CC(=CC=C4)O	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(3S,8aS)-3-[[(3R)-7,7-dimethyl-3-(2-methylbut-3-en-2-yl)-2-oxo-1H-pyrano[2,3-g]indol-3-yl]methyl]-2,3,6,7,8,8a-hexahydropyrrolo[1,2-a]pyrazine-1,4-dione	16127840	Click to see	449.50	unknown	via CMAUP database
Notoamide A	16128040	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
Notoamide B	16127923	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	447.50	unknown	via CMAUP database
Notoamide H	25180895	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)O)C	479.50	unknown	via CMAUP database
Notoamide O	102043608	Click to see	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
Notoamide D	16127841	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5N4C(=O)C6CCCN6C5=O)O)C(C)(C)C=C)C	449.50	unknown	via CMAUP database
Notoamide K	25180896	Click to see	465.50	unknown	via CMAUP database
Notoamide P	46919486	Click to see CC1(C=CC2=C3C(=CC(=C2O1)Br)C4(CC5(C(=O)N6CCCC6C(=O)N5C4(N3)C(C)(C)C=C)O)O)C	544.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
Viridicatol	115033	Click to see C1=CC=C2C(=C1)C(=C(C(=O)N2)O)C3=CC(=CC=C3)O	253.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(+)-Stephacidin A	16127922	Click to see	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see	445.50	unknown	via CMAUP database
Notoamide R	46919488	Click to see	447.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Saxitoxins, gonyautoxins, and derivatives
[(3aS,4R,10aS)-2,6-diamino-9,9,10,10-tetrahydroxy-3,3a,4,8-tetrahydropyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	102411283	Click to see	411.35	unknown	via CMAUP database
[(3aS,4R,9S,10aS)-2,6-diamino-9,10,10-trihydroxy-3a,4,8,9-tetrahydro-3H-pyrrolo[1,2-c]purin-4-yl]methoxycarbonylsulfamic acid	44587284	Click to see	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see	331.29	unknown	via CMAUP database
11beta-Hydroxysaxitoxin	60135304	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)O	315.29	unknown	via CMAUP database

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Trillium camschatcense

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