Scientific name	Authority	First published in
Nymphona lutea	(L.) Bubani	Fl. Pyren. 3: 260 (1901)
Nymphozanthus vulgaris	Rich.	Ann. Mus. Hist. Nat. 17: 230 (1811)
Nymphozanthus sericeus	Fernald	Rhodora 21: 187 (1919)
Nymphozanthus affinis	Fernald	Rhodora 21: 188 (1919)
Nymphozanthus luteus	Fernald	Rhodora 21: 185 (1919)
Nymphaea umbilicalis	Salisb.	Ann. Bot. (König & Sims) 2: 71 (1806)
Nuphar systyla	Wallr.	Erst. Beitr. Fl. Hercyn. 2: 212 (1840)
Nuphar spathulifera	Rchb.	Iconogr. Bot. Pl. Crit. 2: 10 (1824)
Nuphar sericea	Láng	Syll. Pl. Nov. 1: 180 (1824)
Nuphar rivularis	Dumort.	Bull. Soc. Roy. Bot. Belgique 3: 5 (1864)
Nuphar tenella	Rchb.	Iconogr. Bot. Pl. Crit. 2: 10 (1824)
Nymphaea affinis	Hayek	Fl. Steiermark 1: 437 (1908)
Nymphaea lutea	L.	Sp. Pl. : 510 (1753)
Nenuphar luteum	Link	Enum. Hort. Berol. Alt. 2: 70 (1822)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	yellow pond-lily
English	yellow water-lily
English	yellow cowlily
English	yellow pondlily
Spanish	ambudillo
Spanish	botellera
Spanish	cuencas del guadiana
Spanish	embudillo
Spanish	lampazo del guadaira
Spanish	maravilla de rio
Spanish	maravilla de río
Spanish	maravillas de rio
Spanish	nenufar amarillo
Spanish	nenufar de flor amarilla
Spanish	ninfa amarilla
Arabic	نينوفر أصفر
Arabic	بشنين اصفر
Arabic	نينوفر اصفر
atj	ockitepokw
Azerbaijani	sarı nelufər
ba	Һары томбойоҡ
Belarusian	лялея
Belarusian	булдоўка
Belarusian	гарлачыкі
Belarusian	глечыкі
Belarusian	жбанкі
Belarusian	жоўтая вадзяная лілея
Belarusian	жоўтая лілея
Belarusian	звычайны жоўты гарлачык
Belarusian	кушынкі
Belarusian	лопух
Belarusian	плывунцы жоўтыя
Belarusian	гарлачык жоўты жоўты
Bulgarian	Жълта водна роза
Bulgarian	жълта водна роза
Bulgarian	жълта водна лилия
Bengali	স্বর্ণকুমুদ
Catalan	nenúfar groc
Catalan	nénuphar jaune
Czech	stulík žlutý
cv	Сарă шыв хупаххи
Welsh	lili'r dŵr felen
Danish	gul Åkande
German	gelbe teichrose
German	grosse teichrose
German	große teichrose
German	gelbe teichmummel
German	große mummel
German	nénuphar jaune
German	seekandel
German	teichmummel
Esperanto	flava nufaro
Estonian	kollane vesikupp
Basque	nenufar hori
Persian	نیلوفر آبی زرد
Persian	نیلوفر ابی زرد
Finnish	isoulpukka
Finnish	ulpukka
French	nénuphar jaune
French	nénufar jaune
French	nenuphar jaune
fy	giele plomp
Hebrew	נופר צהוב
Croatian	Žuti lokvanj
Upper Sorbian	Žołta gingawa
Hungarian	sárga vízitök
Armenian	Կոկոռ դեղին
Italian	nannufero
Japanese	ネムロコウホネ
Japanese	セイヨウコウホネ
Georgian	ყვითელი დუმფარა
Kazakh	Кәдімгі сарытұңғиық
Lithuanian	paprastoji lūgnė
Lithuanian	nénuphar jaune
Latvian	dzeltenā lēpe
Macedonian	жолта водна лилија
Macedonian	жолта барска тиква
Norwegian Bokmål	gul nøkkerose
Dutch	gele plomp
Norwegian Nynorsk	gul nykkerose
Polish	grążel żółty
Romanian	nufăr galben
Russian	Кубышка жёлтая
Russian	кубышка желтая
Russian	кувшинка желтая
Russian	кубышка жёлтая
Samogitian	lūgnos
Serbo-Croatian	Žuti lokvanj
Slovak	leknica žltá
Slovenian	rumeni blatnik
Serbian	Жути локвањ
stq	woaterkinkes
stq	jeele poapske
stq	roode poapske
Swedish	gul näckros
Swedish	bäckaros
Swedish	bäckeblomma
Swedish	nénuphar jaune
Ukrainian	Глечики жовті
Ukrainian	Жовта латаття
Ukrainian	Кубишка жовта
Ukrainian	Латаття жовте
vep	häč
Chinese	欧亚萍蓬草
Chinese	歐亞萍蓬草

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Nuphar lutea subsp. advena	(Aiton) Kartesz & Gandhi	Phytologia 67: 463. 1989

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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
  - Algeria

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Uzbekistan
- Russian Far East
  - Primorye
- Siberia
  - Altay
  - Irkutsk
  - Krasnoyarsk
  - West Siberia
- Western Asia
  - Iran
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

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
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000382140
UNII	Z5W3730NWW
USDA Plants	NULU
Tropicos	22600080
INPN	109732
Flora of Italy	983
KEW	urn:lsid:ipni.org:names:30385379-2
The Plant List	kew-2384511
Plantarium	25190
Missouri Botanical Garden	282915
PFAF	Nuphar lutea
Open Tree Of Life	440936
NCBI Taxonomy	77113
NBN Atlas	NHMSYS0000461107
Nature Serve	2.149432
IUCN Red List	164316
IPNI	30385379-2
iNaturalist	57850
iNaturalist	244443
GBIF	7551339
Freebase	/m/0d_3k3
EPPO	NUPLU
EOL	486680
Elurikkus	5902
USDA GRIN	416165
Wikipedia	Nuphar_lutea
CMAUP	NPO21679

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

A Nuphar lutea plant active ingredient, 6,6′-dihydroxythiobinupharidine, ameliorates kidney damage and inflammation in a mouse model of chronic kidney disease

Landau D, Khalilia J, Arazi E, Tobar AF, Benharroch D, Golan-Goldhirsh A, Gopas J, Segev Y

Sci Rep

30-Mar-2024

PMCID:	PMC10981724
doi:	10.1038/s41598-024-58055-1
PMID:	38555397

Odonata Assemblages in Urban Semi-Natural Wetlands

Vilenica M, Brigić A, Štih Koren A, Koren T, Sertić Perić M, Schmidt B, Bužan T, Gottstein S

Insects

20-Mar-2024

PMCID:	PMC10971236
doi:	10.3390/insects15030207
PMID:	38535402

Ecological and phylogenetic aspects of the spring diet of three palaearctic species of swans

Kouzov SA, Kravchuk AV, Koptseva EM, Gubelit YI, Zaynagutdinova EM, Abakumov EV

BMC Ecol Evol

02-Feb-2024

PMCID:	PMC10835875
doi:	10.1186/s12862-024-02204-7
PMID:	38302909

Initial decomposition of floating leaf blades of Nymphoides peltata (S.G. Gmel.) O. Kuntze (Menyanthaceae): causes, impact and succession

Klok PF, van der Velde G

PeerJ

21-Dec-2023

PMCID:	PMC10749093
doi:	10.7717/peerj.16689
PMID:	38144198

First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand

Norphanphoun C, Hyde KD

Pathogens

10-Dec-2023

PMCID:	PMC10747506
doi:	10.3390/pathogens12121436
PMID:	38133319

Community structure, environmental conditions and anthropogenic pressure on the habitat of the European endemic aquatic plant Luronium natans (L.) Raf.

Banaś K, Ronowski R, Chmara R, Szmeja J

BMC Plant Biol

28-Nov-2023

PMCID:	PMC10683176
doi:	10.1186/s12870-023-04518-y
PMID:	38017375

Caddisflies (Trichoptera) of Protected Calcareous Fen Habitats: Assemblages, Environmental Drivers, Indicator Species, and Conservation Issues

Buczyńska E, Tarkowski A, Sugier P, Płaska W, Zawal A, Janicka A, Buczyński P

Insects

31-Oct-2023

PMCID:	PMC10671576
doi:	10.3390/insects14110850
PMID:	37999048

Characterization of Colletotrichum Species Infecting Litchi in Hainan, China

Cao X, Li F, Xu H, Li H, Wang S, Wang G, West JS, Wang J

J Fungi (Basel)

24-Oct-2023

PMCID:	PMC10672147
doi:	10.3390/jof9111042
PMID:	37998848

The response of zooplankton network indicators to winter water warming using shallow artificial reservoirs as model case study

Goździejewska AM, Kruk M

Sci Rep

21-Oct-2023

PMCID:	PMC10590368
doi:	10.1038/s41598-023-45430-7
PMID:	37865664

Human consumption of seaweed and freshwater aquatic plants in ancient Europe

Buckley S, Hardy K, Hallgren F, Kubiak-Martens L, Miliauskienė Ž, Sheridan A, Sobkowiak-Tabaka I, Subirà ME

Nat Commun

17-Oct-2023

PMCID:	PMC10582258
doi:	10.1038/s41467-023-41671-2
PMID:	37848451

Beyond taxonomic diversity patterns – investigating how α and β components of macrophyte functional diversity respond to environmental gradients in lotic ecosystems of Greece

Stefanidis K, Oikonomou A, Dimitrellos G, Tsoukalas D, Papastergiadou E

Front Plant Sci

08-Sep-2023

PMCID:	PMC10514920
doi:	10.3389/fpls.2023.1204383
PMID:	37746009

The first comprehensive population size estimations for the highly endangered largest diving beetle Dytiscus latissimus in Europe

Balalaikins M, Schmidt G, Aksjuta K, Hendrich L, Kairišs K, Sokolovskis K, Valainis U, Zolovs M, Nitcis M

Sci Rep

15-Jun-2023

PMCID:	PMC10272167
doi:	10.1038/s41598-023-36242-w
PMID:	37322014

Macrophyte communities as bioindicator of stormwater pollution in rivers: a quantitative analysis

Babko R, Diachenko T, Zaburko J, Danko Y, Kuzmina T, Szulżyk-Cieplak J, Czarnota J, Łagód G

PeerJ

01-Jun-2023

PMCID:	PMC10239615
doi:	10.7717/peerj.15248
PMID:	37283889

In Vitro and In Vivo Therapeutic Potential of 6,6′-Dihydroxythiobinupharidine (DTBN) from Nuphar lutea on Cells and K18-hACE2 Mice Infected with SARS-CoV-2

Weiss S, Waidha K, Rajendran S, Benharroch D, Khalilia J, Levy H, Bar-David E, Golan-Goldhirsh A, Gopas J, Ben-Shmuel A

Int J Mol Sci

05-May-2023

PMCID:	PMC10179516
doi:	10.3390/ijms24098327
PMID:	37176034

Genetic Diversity and Population Structure Assessed Using Microsatellite (SSR) Markers from Relict Populations of Nuphar pumila (Nymphaeaceae)

González-Toral C, Cuesta C, Cires E

Plants (Basel)

26-Apr-2023

PMCID:	PMC10181053
doi:	10.3390/plants12091771
PMID:	37176829

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see C1=CC(=C(C=C1O)C(=O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Resorcinol	5054	Click to see C1=CC(=CC(=C1)O)O	110.11	unknown	https://doi.org/10.1007/BF02029542
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Himeic Acid A	11774903	Click to see CC(CC(=O)NC(=O)C1=COC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	435.50	unknown	via CMAUP database
Himeic acid B	21579676	Click to see C1=C(OC=C(C1=O)C(=O)N)C=CCCCCCCCCC(=O)O	321.40	unknown	via CMAUP database
himeic acid C	21777983	Click to see CC(CC(=O)NC(=O)C1=CNC(=CC1=O)C=CCCCCCCCCC(=O)O)C(=O)O	434.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E)-tetradec-5-en-1-ol	6431325	Click to see CCCCCCCCC=CCCCCO	212.37	unknown	via CMAUP database
6-Tetradecen-1-ol, (E)	6431327	Click to see CCCCCCCC=CCCCCCO	212.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Hexadecanoic acid propylamide	10379895	Click to see CCCCCCCCCCCCCCCC(=O)NCCC	297.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alloxanthin	6443740	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(CC(CC2(C)C)O)C)C)C	564.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol	92097	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Trachelosperoside A-1	21637743	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	680.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	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
(2R,3R,4R,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	101673896	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	680.80	unknown	via CMAUP database
(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 CC1CC(=O)CC(C1(CC(=O)C(=CC=CC(=CC=CC=C(C)C=CC=C(C)C#CC2=C(CC(CC2(C)C)O)C)C)C)O)(C)C	598.90	unknown	via CMAUP database
(5R,8R,9S,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	12309262	Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C	442.70	unknown	via CMAUP database
19'-Hexanoyloxyisomytiloxanthin	16061209	Click to see CCCCCC(=O)OCC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(=O)CC1(C)C)C)O)C)C#CC2=C(CC(CC2(C)C)O)C	713.00	unknown	via CMAUP database
3alpha-Acetoxyfriedelane	13688749	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)OC(=O)C	470.80	unknown	via CMAUP database
Amarouciaxanthin B/Sidnyaxanthin	16061221	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC2(C(=CC(=O)CC2(C)C)C)O)C)C	596.80	unknown	via CMAUP database
CID 23428237	23428237	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)C=C2C(=CC(=O)CC2(C)C)C)C)C	578.80	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Glutinol	9932254	Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C	426.70	unknown	via CMAUP database
Glutinone	10071029	Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C	424.70	unknown	via CMAUP database
Halocynthiaxanthin	11966451	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC23C(CC(CC2(O3)C)O)(C)C)C)C	598.90	unknown	via CMAUP database
Mytiloxanthin	11365423	Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C2(CC(CC2(C)C)O)C)O)C)C	598.90	unknown	via CMAUP database
NV766Twa77	102146782	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(CC(CC2(C)O)O)(C)C)O)C)C	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 CC(C)CCCC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	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 / 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
> 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 C[N+](C)(C)CC(=O)[O-]	117.15	unknown	via CMAUP database
N,N,N-trimethylglycinium	248	Click to see C[N+](C)(C)CC(=O)O	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
Arginine	6322	Click to see C(CC(C(=O)O)N)CN=C(N)N	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 C1=CC(=C(C=C1CC(C(=O)O)N)CC2=C(C=CC(=C2)CC(C(=O)O)N)O)O	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 CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O	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 C(CS(=O)(=O)O)N	125.15	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Alkanolamines / 1,2-aminoalcohols / N-acylethanolamines
Anandamide	5281969	Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)NCCO	347.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Quercitol	441437	Click to see C1C(C(C(C(C1O)O)O)O)O	164.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Aspermytin A	9993091	Click to see CC1CCC2C(C1)C=CC(C2(C)C(=O)CCO)(C)O	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 CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5C(=O)N4)C(C)(C)C=C)C	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 CC1(C=CC2=C(O1)C=CC3=C2NC4(C3=O)C(C5CC67CCCN6C(=O)C5(C(O4)O)NC7=O)(C)C)C	479.50	unknown	via CMAUP database
Notoamide Q	46919487	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C3(CC4C(=O)N5CCCC5(C(=O)N4)OC)C(C)(C)C=C)C	479.60	unknown	via CMAUP database
Sclerotiamide	10647785	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC(=O)C34C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	463.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Furopelargone A	6451194	Click to see CC1CCC(C1C2=C(C=CO2)C(C)C)C(=O)C	234.33	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 CC1(C=CC2=C(O1)C=CC3=C2NC4(C3(CC5(N4C(=O)C6CCCN6C5=O)O)O)C(C)(C)C=C)C	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 CC1(C=CC2=C(O1)C=CC3=C2NC4=C3CC56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	431.50	unknown	via CMAUP database
Notoamide F	25180710	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)C	461.60	unknown	via CMAUP database
Notoamide G	25180707	Click to see CC1(C=CC2=C(O1)C=CC3=C2N(C4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)OC)O)C	477.60	unknown	via CMAUP database
Notoamide I	25180708	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(=O)C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)C	445.50	unknown	via CMAUP database
notoamide R	46919488	Click to see CC1(C=CC2=C(O1)C=CC3=C2NC4=C3C(C56C(C4(C)C)CC7(CCCN7C5=O)C(=O)N6)O)C	447.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolizidines
(1R,3S,5R,8R,9R,12R,14R,16R,19R,20R)-5,16-bis(furan-3-yl)-1,8,12,19-tetramethyl-2,13-dioxa-4,15-diazapentacyclo[12.8.0.03,12.04,9.015,20]docosane	163098804	Click to see CC1CCC(N2C1CCC3(C2OC4(CCC5C(CCC(N5C4O3)C6=COC=C6)C)C)C)C7=COC=C7	494.70	unknown	https://doi.org/10.1021/JA00779A038
(1S,2S,5S,8R,9S,11S,13R,15R,16S,19S)-5,19-bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosane	162940529	Click to see CC1CCC(N2C1CC3C(C2)(C4(CN5C(CCC(C5CC4S3)C)C6=COC=C6)C)C)C7=COC=C7	494.70	unknown	https://doi.org/10.1007/BF00567988
5,16-Bis(furan-3-yl)-1,8,12,19-tetramethyl-2,13-dioxa-4,15-diazapentacyclo[12.8.0.03,12.04,9.015,20]docosane	73833904	Click to see CC1CCC(N2C1CCC3(C2OC4(CCC5C(CCC(N5C4O3)C6=COC=C6)C)C)C)C7=COC=C7	494.70	unknown	https://doi.org/10.1021/JA00779A038
5,19-Bis(furan-3-yl)-1,2,8,16-tetramethyl-12-thia-4,20-diazapentacyclo[11.8.0.02,11.04,9.015,20]henicosane	162940528	Click to see CC1CCC(N2C1CC3C(C2)(C4(CN5C(CCC(C5CC4S3)C)C6=COC=C6)C)C)C7=COC=C7	494.70	unknown	https://doi.org/10.1007/BF00567988
> Organoheterocyclic compounds / Quinolizines
(3R,4R,6S,9R,9aS)-6-(furan-3-yl)-3,9-dimethyl-1,2,4,6,7,8,9,9a-octahydroquinolizine-3,4-diol	163193393	Click to see CC1CCC(N2C1CCC(C2O)(C)O)C3=COC=C3	265.35	unknown	https://doi.org/10.1021/JA00779A038
(6R,9S,9aR)-6-(furan-3-yl)-9-(hydroxymethyl)-2,6,7,8,9,9a-hexahydro-1H-quinolizine-3-carbaldehyde	163024755	Click to see C1CC(N2C=C(CCC2C1CO)C=O)C3=COC=C3	261.32	unknown	https://doi.org/10.1016/0031-9422(88)80065-7
2H-Quinolizin-3-ol, 6-(3-furanyl)octahydro-3,9-dimethyl-, (3R,6S,9R,9aS)-	575171	Click to see CC1CCC(N2C1CCC(C2)(C)O)C3=COC=C3	249.35	unknown	https://doi.org/10.1007/BF02029541
6-(Furan-3-yl)-3,9-dimethyl-1,2,4,6,7,8,9,9a-octahydroquinolizine-3,4-diol	162991249	Click to see CC1CCC(N2C1CCC(C2O)(C)O)C3=COC=C3	265.35	unknown	https://doi.org/10.1021/JA00779A038
CID 162856136	162856136	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)SC3)C7=COC=C7	510.70	unknown	https://doi.org/10.1021/JA00800A030
CID 162856137	162856137	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)SC3)C7=COC=C7	510.70	unknown	https://doi.org/10.1021/JO00864A022
CID 162887206	162887206	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CCN5C(CCC(C5C4)C)C6=COC=C6)S(=O)C3)C7=COC=C7	526.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 162887207	162887207	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CCN5C(CCC(C5C4)C)C6=COC=C6)S(=O)C3)C7=COC=C7	526.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 162935810	162935810	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCN5C(CCC(C5C4)C)C6=COC=C6)CS3)C7=COC=C7	494.70	unknown	https://doi.org/10.1007/BF00567988
CID 162935811	162935811	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCN5C(CCC(C5C4)C)C6=COC=C6)CS3)C7=COC=C7	494.70	unknown	https://doi.org/10.1007/BF00567988
CID 162965489	162965489	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4)C6=COC=C6)C)SC3)C7=COC=C7	494.70	unknown	https://doi.org/10.1016/S0031-9422(00)86394-3
CID 163000453	163000453	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)CS3)C7=COC=C7	510.70	unknown	https://doi.org/10.1021/JO00864A022
CID 163017651	163017651	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CC5C(CCC(N5C(C4)O)C6=COC=C6)C)CS3)C7=COC=C7	526.70	unknown	https://doi.org/10.1007/BF02029541
CID 163017652	163017652	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CC5C(CCC(N5C(C4)O)C6=COC=C6)C)CS3)C7=COC=C7	526.70	unknown	https://doi.org/10.1007/BF02029541
CID 163019433	163019433	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCN5C(CCC(C5C4)C)F)S(=O)C3)C6=COC=C6	462.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 163019689	163019689	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CC5C(CCC(N5C(C4)O)C6=COC=C6)C)S(=O)C3)C7=COC=C7	542.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 163019690	163019690	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CC5C(CCC(N5C(C4)O)C6=COC=C6)C)S(=O)C3)C7=COC=C7	542.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 163045738	163045738	Click to see CC1CCC(N2C1CCC3(C2)CC4(CC5C(CCC(N5C(C4)O)C6=COC=C6)C)S(=O)C3)C7=COC=C7	526.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 163185734	163185734	Click to see CC1CCC(N2C1CCC3(C2)CC4(CC5C(CCC(N5C(C4)O)C6=COC=C6)C)S(=O)C3)C7=COC=C7	526.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 163188987	163188987	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCN5C(CCC(C5C4)C)F)S(=O)C3)C6=COC=C6	462.70	unknown	https://doi.org/10.1016/0031-9422(86)80097-8
CID 21769981	21769981	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)SC3)C7=COC=C7	526.70	unknown	https://doi.org/10.1002/JPS.2600620530
CID 5320242	5320242	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)SC3)C7=COC=C7	526.70	unknown	https://doi.org/10.1007/BF00568473
CID 73833905	73833905	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)CS3)C7=COC=C7	510.70	unknown	https://doi.org/10.1021/JO00864A022
CID 73833906	73833906	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)SC3)C7=COC=C7	510.70	unknown	https://doi.org/10.1021/JA00800A030 https://doi.org/10.1021/JO00864A022
CID 73834258	73834258	Click to see CC1CCC(N2C1CCC3(C2O)CC4(CCC5C(CCC(N5C4O)C6=COC=C6)C)SC3)C7=COC=C7	526.70	unknown	https://doi.org/10.1002/JPS.2600620530
Nuphacristine	362093	Click to see C1CC(N2C=C(CCC2C1CO)C=O)C3=COC=C3	261.32	unknown	https://doi.org/10.1016/0031-9422(88)80065-7
Nupharolutine	10777028	Click to see CC1CCC(N2C1CCC(C2)(C)O)C3=COC=C3	249.35	unknown	https://doi.org/10.1007/BF02029541
Thiobinupharidine	442554	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4)C6=COC=C6)C)SC3)C7=COC=C7	494.70	unknown	via CMAUP database
Thionuphlutine A	601443	Click to see CC1CCC(N2C1CCC3(C2)CC4(CCC5C(CCC(N5C4)C6=COC=C6)C)SC3)C7=COC=C7	494.70	unknown	https://doi.org/10.1016/S0031-9422(00)86394-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3S,3'S,4S)-2,2'-Bis(3,4-dihydroxyphenyl)-5,5',7,7'-tetrahydroxy-[4,8'-bichroman]-3,3'-diyl bis(3,4,5-trihydroxybenzoate)	12795892	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	882.70	unknown	via CMAUP database
(2R,2'R)-2alpha-(3,4,5-Trihydroxyphenyl)-2'alpha-(3,4-dihydroxyphenyl)-3alpha-(galloyloxy)-4beta,8'-bichroman-3'beta,5,5',7,7'-pentol	13831071	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O	746.60	unknown	via CMAUP database
Epicatechin 3-O-gallate(4b->8)epigallocatechin-3-O-gallate	11622083	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	898.70	unknown	via CMAUP database
Epicatechin-(4beta->8)-epigallocatechin 3'-gallate	11513300	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	746.60	unknown	via CMAUP database
Procyanidin B3	146798	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Prodelphinidin B3	13831068	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate	107905	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	via CMAUP database
(+)-Catechin gallate	5276454	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	via CMAUP database
Epigallocatechin Gallate	65064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	458.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
Gallocatechin	65084	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate	10418008	Click to see CC(=O)OC1C(C(OC(C1OC(=O)C)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O	824.70	unknown	via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin	10328097	Click to see CC(=O)OC1C(OC(C(C1OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC(=O)C=CC6=CC=C(C=C6)O	824.70	unknown	via CMAUP database
Kaempferol-3-O-(2',6'-di-O-trans-p-coumaroyl)-beta-D-glucopyranoside	10439991	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O)O)O	740.70	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 C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)(O)O	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 C1C(C(C23N1C(=NC(C2NC(=N3)N)COC(=O)NS(=O)(=O)O)N)(O)O)O	395.35	unknown	via CMAUP database
11,11-Dihydroxysaxitoxin	102411284	Click to see C1C(C(C23N1C(=NC(C2N=C(N3)N)COC(=O)N)N)(O)O)(O)O	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
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-Epi-castalagin	12302512	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	via CMAUP database
CID 12302513	12302513	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Nuphar lutea

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top