Arisaema amurense

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID643fe70b46119282197886
Scientific name	Arisaema amurense
Authority	Maxim.
First published in	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 264 (1859)

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Synonyms Top

Scientific name	Authority	First published in
Arisaema amurense f. denticulatum	Makino	Bot. Mag. (Tokyo) 15: 132 1901
Arisaema amurense var. denticulatum	Engl.	Pflanzenr. IV, 23F: 204. 1920
Arisaema amurense var. magnidens	N.E.Br.	J. Linn. Soc., Bot. 36: 176. 1903
Arisaema amurense f. purpureum	(Nakai) Kitag.	Neolin. Fl. Manshur. : 157 (1979)
Arisaema amurense var. purpureum	Nakai	Bot. Mag. (Tokyo) 43: 530 1929
Arisaema amurense var. robustum	Engl.	Monogr. Phan. 2: 550 1879
Arisaema amurense subsp. robustum	(Engl.) H.Ohashi & J.Murata	J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 12(6): 292 (1980)
Arisaema amurense var. serratum	Nakai	Bot. Mag. (Tokyo) 43: 530. 1929
Arisaema amurense f. violaceum	(Engl.) Y.S.Kim & S.C.Ko	Korean J. Pl. Taxon. 15(2): 76 (1985)
Arisaema amurense var. violaceum	Engl.	Pflanzenr. IV, 23F: 204 1920
Arisaema robustum	Nakai	Bot. Mag. (Tokyo) 43: 531 (1929)
Arisaema robustum f. abense	Sugim.	Shizuoka-ken Shokubutsu-shi 486. 1967
Arisaema robustum var. furusei	Sugim.	Keys Herb. Pl. Jap. Monoc. 564. 1973
Arisaema robustum var. purpureum	Nakai	J. Jap. Bot. 16: 3. 1940
Arisaema komarovii	Tzvelev	Bot. Zhurn. (Moscow & Leningrad) 70: 997. 1985 (1985)
Arisaema amurense f. serratum	(Nakai) Kitag.	Lin. Fl. Manshur. 124 1939
Arisaema robustum f. variegatum	Y.N.Lee	Bull. Korea Pl. Res. 5: 36 (2005)
Arisaema robustum var. sachalinense	Miyabe & Kudô	J. Fac. Agric. Hokkaido Imp. Univ. 26: 282. 1932

Common names Top

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Filter by language:

Language	Common/alternative name
Azerbaijani	arisaema amurense var. serratum
Azerbaijani	amur arizeması
Bulgarian	амурска аризема
Japanese	アムールテンナンショウ
Korean	둥근잎천남성
Russian	Аризема амурская
Chinese	东北南星
Chinese	东北南星（东北天南星）
Chinese	天南星
Chinese	胆星
Chinese	雪里见
Chinese	大参
Chinese	山苞米
Chinese	长虫苞米
Chinese	東北南星

Subspecies (abbr. subsp./ssp.) Top

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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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.

sow thinly, keep dry when dormant, leave in pot for 2 years

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Korea
- Russian Far East
  - Khabarovsk
  - Primorye
  - Sakhalin

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000269464
UNII	8MR1W1W43M
USDA Plants	ARAM7
Tropicos	2101460
KEW	urn:lsid:ipni.org:names:85565-1
The Plant List	kew-15239
Plantarium	3680
Open Tree Of Life	727020
Observations.org	114764
NCBI Taxonomy	227494
IPNI	85565-1
iNaturalist	335575
GBIF	2866903
EOL	1135097
Elurikkus	320311
USDA GRIN	3990
CMAUP	NPO28204

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

Syringa reticulata potently inhibits the activity of SARS-CoV-2 3CL protease

Hao Z, Liu Y, Guan W, Pan J, Li M, Wu J, Liu Y, Kuang H, Yang B

Biochem Biophys Rep

26-Dec-2023

PMCID:	PMC10873874
doi:	10.1016/j.bbrep.2023.101626
PMID:	38371528

Insight into Nephrotoxicity and Processing Mechanism of Arisaema erubescens (Wall.) Schott by Metabolomics and Network Analysis

Wang M, Yang N, Wu X, Zou T, Zheng J, Zhu H, Zhao C, Wang J

Drug Des Devel Ther

19-Jun-2023

PMCID:	PMC10289099
doi:	10.2147/DDDT.S406551
PMID:	37360574

Ecological and Geographical Structure of the Plant Cover of the East Asian Boreal–Nemoral Ecotone (the Lower Amur Region, Far East Russia)

Kryukova MV

Plants (Basel)

30-Jan-2023

PMCID:	PMC9919551
doi:	10.3390/plants12030615
PMID:	36771699

The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research

Song Y, Chen W, Fu K, Wang Z

Front Pharmacol

23-Aug-2022

PMCID:	PMC9445187
doi:	10.3389/fphar.2022.893229
PMID:	36081944

Biosynthesis of Iron Oxide Nanoparticles: Physico-Chemical Characterization and Their In Vitro Cytotoxicity on Healthy and Tumorigenic Cell Lines

Moacă EA, Watz CG, (Ionescu) DF, Păcurariu C, Tudoran LB, Ianoș R, Socoliuc V, Drăghici GA, Iftode A, Liga S, Dragoș D, Dehelean CA

Nanomaterials (Basel)

10-Jun-2022

PMCID:	PMC9230869
doi:	10.3390/nano12122012
PMID:	35745350

Effect of mineral excipients on processing traditional Chinese medicines: an insight into the components, pharmacodynamics and mechanism

Liu Y, Li X, Chen C, Leng A, Qu J

Chin Med

24-Dec-2021

PMCID:	PMC8709976
doi:	10.1186/s13020-021-00554-8
PMID:	34952619

Botanical, Traditional Use, Phytochemical, and Toxicological of Arisaematis rhizoma

Qi CY, Wang J, Wu X, He SR, Zhang Q, Wu JH, Zhao CB

Evid Based Complement Alternat Med

30-Nov-2021

PMCID:	PMC8651355
doi:	10.1155/2021/9055574
PMID:	34887934

Temporal Variation Dominates in Local Carabid Beetle Communities in Korean Mountains

Park Y, Jang T, Kim J, Kim SK, Kim IK, Kim CJ, Takami Y

Insects

12-Nov-2021

PMCID:	PMC8624729
doi:	10.3390/insects12111019
PMID:	34821819

Integrative Medicine (Herbal Medicine Combined with Drug Therapy) for Behcet’s Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

Jun JH, Ang L, Choi TY, Lee HW, Lee MS

Pharmaceutics

01-Apr-2021

PMCID:	PMC8065893
doi:	10.3390/pharmaceutics13040476
PMID:	33915947

Fuyuan Xingnao Decoction Promotes Angiogenesis Through the Rab1/AT1R Pathway in Diabetes Mellitus Complicated With Cerebral Infarction

Deng D, Qu Y, Sun L, Jia L, Bu J, Ye M, Chen Z, Geng Y, Zhou S, Fang B

Front Pharmacol

17-Feb-2021

PMCID:	PMC7925884
doi:	10.3389/fphar.2021.616165
PMID:	33679398

The Species Identification in Traditional Herbal Patent Medicine, Wuhu San, Based on Shotgun Metabarcoding

Liu J, Mu W, Shi M, Zhao Q, Kong W, Xie H, Shi L

Front Pharmacol

16-Feb-2021

PMCID:	PMC7921783
doi:	10.3389/fphar.2021.607200
PMID:	33664667

A review of green methods for phyto-fabrication of hematite (α-Fe2O3) nanoparticles and their characterization, properties, and applications

Al-Hakkani MF, Gouda GA, Hassan SH

Heliyon

06-Jan-2021

PMCID:	PMC7809383
doi:	10.1016/j.heliyon.2020.e05806
PMID:	33490660

Identification of candidate medicinal herbs for skincare via data mining of the classic Donguibogam text on Korean medicine

Cho G, Park HM, Jung WM, Cha WS, Lee D, Chae Y

Integr Med Res

03-Jun-2020

PMCID:	PMC7388188
doi:	10.1016/j.imr.2020.100436
PMID:	32742921

Potential Synergy between Spores of Metarhizium anisopliae and Plant Secondary Metabolite, 1-Chlorooctadecane for Effective Natural Acaricide Development

Hussain A, AlJabr AM

Molecules

20-Apr-2020

PMCID:	PMC7221990
doi:	10.3390/molecules25081900
PMID:	32326009

Bazhu Decoction, a Traditional Chinese Medical Formula, Ameliorates Cognitive Deficits in the 5xFAD Mouse Model of Alzheimer’s Disease

Peng A, Gao Y, Zhuang X, Lin Y, He W, Wang Y, Chen W, Chen T, Huang X, Yang R, Huang Y, Xi S, Zhang X

Front Pharmacol

27-Nov-2019

PMCID:	PMC6890723
doi:	10.3389/fphar.2019.01391
PMID:	31827437

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
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / 3-O-beta-D-digalactosyl-sn-glycerols
Digalactosyldiacylglycerol	10724471	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	917.20	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (9Z,12Z)-octadeca-9,12-dienoate	101986482	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	755.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] (Z)-octadec-9-enoate	10628915	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCC	757.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] (9Z,12Z,15Z)-octadeca-9,12,15-trienoate	10843454	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	915.20	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[(2S)-1-hexadecanoyloxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] (Z)-octadec-9-enoate	10557725	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCC	919.20	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[(2S)-2-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadecanoate	10795318	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	781.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadecanoate	10701056	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	945.30	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] octadec-9-enoate	72973450	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCC	757.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl] octadeca-9,12-dienoate	74381412	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	755.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] octadec-9-enoate	25201279	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCC	919.20	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[2-Octadeca-9,12-dienoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadec-9-enoate	25201946	Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	781.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[2-Octadeca-9,12-dienoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadeca-9,12-dienoate	75955278	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	779.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[2-Octadeca-9,12-dienoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropyl] octadecanoate	25202928	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	945.30	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
[2-Octadeca-9,12,15-trienoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadecanoate	391318	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCC=CCC	781.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
1-18:2-2-18:2-Monogalactosyldiacylglycerol	90657255	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	779.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols / 1,2-diacyl-3-O-beta-D-galactosyl-sn-glycerols
[(2S)-2-[(9Z,12Z)-octadeca-9,12-dienoyl]oxy-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] (Z)-octadec-9-enoate	10509461	Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCCCCC=CCC=CCCCCC	781.10	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5-Methoxy-3,3,7b-trimethyl-1,1a,2,4,4a,6,7,7a-octahydrocyclopropa[e]azulen-5-yl)methanol	73819953	Click to see CC1(CC2CC2(C3CCC(C3C1)(CO)OC)C)C	252.39	unknown	https://doi.org/10.1016/0031-9422(95)00929-9
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
(2S,3R,4E,8Z)-1-beta-D-Glucopyranosyloxy-2-(2-hydroxypalmitoylamino)octadecane-4,8-dien-3-ol	44593489	Click to see CCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	714.00	unknown	https://doi.org/10.1021/NP960201+
2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]octadecanamide	10169278	Click to see CCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	742.10	unknown	https://doi.org/10.1021/NP960201+
2-hydroxy-N-[(2S,3R,4E,8Z)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]octadecanamide	44584190	Click to see CCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	742.10	unknown	https://doi.org/10.1021/NP960201+
2-hydroxy-N-[(2S,3R,4E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]hexadecanamide	162973747	Click to see CCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	714.00	unknown	https://doi.org/10.1021/NP960201+
2-hydroxy-N-[(2S,3R,4E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]octadecanamide	163049862	Click to see CCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	742.10	unknown	https://doi.org/10.1021/NP960201+
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
(2R)-2-hydroxy-N-[(2S,3R,4E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]icosanamide	162939946	Click to see CCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	770.10	unknown	https://doi.org/10.1021/NP960201+
(R)-N-[(1S,2R,3E,7Z)-1-[(beta-D-Glucopyranosyloxy)methyl]-2-hydroxy-3,7-heptadecadienyl]-2-hydroxyoctadecanamide	10771309	Click to see CCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	742.10	unknown	via CMAUP database
1-O-beta-D-Glucopyranosyl-N-[(R)-2-hydroxy-1-oxoicosyl]-4,8-sphingenine	10771481	Click to see CCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	770.10	unknown	via CMAUP database
1-O-beta-GLUCOPYRANOSYL-(2S,3R,4E,8Z)-2-N-((2'R)-HYDROXYICOSANOYL)-4,8-SPHINGADIENINE	10652772	Click to see CCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	770.10	unknown	https://doi.org/10.1021/NP960201+
2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]icosanamide	6915884	Click to see CCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	770.10	unknown	https://doi.org/10.1021/NP960201+
beta-D-glucosyl-N-(dodecanoyl)sphingosine	20057354	Click to see CCCCCCCCCCCCCC=CC(C(COC1C(C(C(C(O1)CO)O)O)O)NC(=O)CCCCCCCCCCC)O	643.90	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N	283.24	unknown	via CMAUP database
Adenosine	60961	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 / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide	10026486	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	via CMAUP database
Aurantiamide acetate	124319	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	via CMAUP database
Tifentai	9832120	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.4268/CJCMM20111611
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine	190	Click to see C1=NC2=NC=NC(=C2N1)N	135.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790	790	Click to see C1=NC2=C(N1)C(=O)N=CN2	136.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Xanthine	1188	Click to see C1=NC2=C(N1)C(=O)NC(=O)N2	152.11	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Eriostemin	633062	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)O)O	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Apigenin 6-C-alpha-L-arabinopyranoside-8-C-beta-D-glucopyranoside	44257699	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Isoschaftoside	3084995	Click to see C1C(C(C(C(O1)C2=C(C(=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C5C(C(C(C(O5)CO)O)O)O)O)O)O)O	564.50	unknown	via CMAUP database
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-[(2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	163188021	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=C(C=C3)C4=CC(=O)C5=C(C=C(C=C5O4)OC6C(C(C(C(O6)CO)OC(=O)C=CC7=CC=C(C=C7)O)O)O)O)CO)O	772.70	unknown	https://doi.org/10.1016/0031-9422(95)00929-9

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Arisaema amurense

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