Scientific name	Authority	First published in
Gymnogramma caudiformis	Hook.	Sp. Fil. 5. 158. 1864 (1864)
Grammitis caudiformis	Hook.	Bot. Mag. 88: t. 5328 (1862)
Gymnogramma feei	Hook.	Sp. Fil. 5. 158. 1864 (1864)
Dryostachyum caudatum	J.Sm.	J. Bot. (Hooker) 4: 62 (1841)
Asplenium linguiforme	Roxb.	Calcutta J. Nat. Hist. 4: 497 (1844)
Polypodium feei	(Bory) Mett.	Pol. 110: n. 212. 1857 ; & NPfl. 316
Polypodium pedunculatioides	Ching	Sinensia 1: 48 (1930)
Pleopeltis feei	Alderw.	Bull. Dép. Agric. Indes Néerl. 27: 12 (1909)
Grammitis vulcanica	Blume	Enum. Pl. Javae 2: 118 (1828)

Common names Top

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Filter by language:

Language	Common/alternative name
Indonesian	pakis tangkur
Japanese	セリグエア・フェーイ
Chinese	修蕨

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  - China Southeast

Asia-tropical click to expand
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001115939
Tropicos	26610507
KEW	urn:lsid:ipni.org:names:17222060-1
The Plant List	tro-26610507
Open Tree Of Life	214069
NCBI Taxonomy	194882
IPNI	17222060-1
iNaturalist	487698
GBIF	4024959
Freebase	/m/080pd9k
EOL	6119037
Wikipedia	Selliguea_feei
CMAUP	NPO20671

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

Oligomeric Proanthocyanidins: An Updated Review of Their Natural Sources, Synthesis, and Potentials

Nie F, Liu L, Cui J, Zhao Y, Zhang D, Zhou D, Wu J, Li B, Wang T, Li M, Yan M

Antioxidants (Basel)

26-Apr-2023

PMCID:	PMC10215713
doi:	10.3390/antiox12051004
PMID:	37237870

Biotechnology of the Tree Fern Cyathea smithii (J.D. Hooker; Soft Tree Fern, Katote) II Cell Suspension Culture: Focusing on Structure and Physiology in the Presence of 2,4-D and BAP

Rybczyński JJ, Kaźmierczak A, Dos Santos Szewczyk K, Tomaszewicz W, Miazga-Karska M, Mikuła A

Cells

20-Apr-2022

PMCID:	PMC9100639
doi:	10.3390/cells11091396
PMID:	35563701

Screening of plant-based natural compounds as a potential COVID-19 main protease inhibitor: an in silico docking and molecular dynamics simulation approach

Majumder R, Mandal M

J Biomol Struct Dyn

08-Sep-2020

PMCID:	PMC7544942
doi:	10.1080/07391102.2020.1817787
PMID:	32897138

Structure-Dependent Activity of Plant-Derived Sweeteners

Ҫiçek SS

Molecules

22-Apr-2020

PMCID:	PMC7221985
doi:	10.3390/molecules25081946
PMID:	32331403

Allelopathy of Bracken Fern (Pteridium arachnoideum): New Evidence from Green Fronds, Litter, and Soil

de Jesus Jatoba L, Varela RM, Molinillo JM, Ud Din Z, Juliano Gualtieri SC, Rodrigues-Filho E, Macías FA

PLoS One

23-Aug-2016

PMCID:	PMC4995010
doi:	10.1371/journal.pone.0161670
PMID:	27552161

Antioxidant Activity and Proanthocyanidin Profile of Selliguea feei Rhizomes

Fu C, Wang H, Ng WL, Song L, Huang D

Molecules

11-Apr-2013

PMCID:	PMC6270089
doi:	10.3390/molecules18044282
PMID:	23579995

Flavonoids and a proanthocyanidin from rhizomes of Selliguea feei

Nam-In Baek, Edward J. Kennelly, Leonardus B.S. Kardono, Soefjan Tsauri, Kosasih Padmawinata, D. Doel Soejarto, A. Douglas Kinghorn

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)97105-X

Selligueain A, a novel highly sweet proanthocyanidin from the rhizomes of Selliguea feei.

Baek NI, Chung MS, Shamon L, Kardono LB, Tsauri S, Padmawinata K, Pezzuto JM, Soejarto DD, Kinghorn AD

J Nat Prod

01-Sep-1993

doi:	10.1021/NP50099A011
PMID:	8254348

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
> 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 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 / 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,2R,4S)-1-[(1E,3E,5E,7E,9E,11E,13E,15E)-18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15-octaen-17-ynyl]-2,6,6-trimethylcyclohexane-1,2,4-triol	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
(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
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
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
Anhydroamarouciaxanthin B	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
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
Isomytiloxanthin	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
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
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
> 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
(6'S)-Isodomoic acid G	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 / 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 / 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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Epiafzelechin-(4beta-8,2beta-0-7)-epiafzelechin-(4beta-8)-afzelechin	132944	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC=C(C=C8)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC=C(C=C1)O)O	816.80	unknown	https://doi.org/10.1021/NP50099A011
methyl 2-[(2R,3R,4S)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(1R,5R,6R,7S,13S,21R)-6,9,17,19,21-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-7-yl]-3,4-dihydro-2H-chromen-4-yl]acetate	10056530	Click to see COC(=O)CC1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC=C(C=C8)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC=C(C=C1)O)O	888.80	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
methyl 2-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[6,9,17,19,21-pentahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-7-yl]-3,4-dihydro-2H-chromen-4-yl]acetate	85106070	Click to see COC(=O)CC1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC=C(C=C8)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC=C(C=C1)O)O	888.80	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
Selligueain A	10463123	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC=C(C=C8)O)O)O)C9=CC=C(C=C9)O)O)O)O)C1=CC=C(C=C1)O)O	816.80	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Dryopteric acid	11393902	Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)CC(=O)O)O)O)O	348.30	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
2-[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]acetic acid	162945769	Click to see C1=CC(=CC=C1C2C(C(C3=C(C=C(C=C3O2)O)O)CC(=O)O)O)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
3'-Deoxydryopteric acid	10088118	Click to see C1=CC(=CC=C1C2C(C(C3=C(C=C(C=C3O2)O)O)CC(=O)O)O)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R,3S)-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,4-dihydro-2H-chromene-3,5,7-triol	10094553	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,4-dihydro-2H-chromene-3,5,7-triol	74977161	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	436.40	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside	21606527	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
Kaempferol-3-O-glucoside-7-O-rhamnoside	14035324	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)97105-X
> 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

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