Scientific name	Authority	First published in
Asplenium curtisorum	Christ	Ann. Jard. Bot. Buitenzorg II. 4. 39. 1904 (1904)
Asplenium ellipticum	Copel.	Leafl. Philipp. Bot. 3. 819 (1910)
Neottopteris elliptica	Fée	Mém. Foug., 5. Gen. Filic. : 203 (1852)
Neottopteris ovata	J.Sm.; Fee	Mém. Foug., 5. Gen. Filic. : 203 (1852)
Neottopteris stenocarpa	Fée	Mém. Foug., 5. Gen. Filic. : 203 (1852)
Neottopteris vulgaris	J.Sm.	J. Bot. (Hooker) 3: 409 (1841)
Thamnopteris nidus	(L.) C.Presl	Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 68 (1851)
Neottopteris nidus	J.Sm.	Gen. Fil. : t. 113 B (1842)
Neottopteris musaefolia	J.Sm.	J. Bot. 3: 409 1861
Asplenium ficifolium	Goldm.	Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 19. Suppl. I. 461. 1843 (1843)

Common names Top

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Filter by language:

Language	Common/alternative name
English	hawai'i birdnest fern
English	bird's nest fern
ace	bayeuek
Arabic	سرخس عش الطير
Persian	سرخس لانه پرنده
Indonesian	paku sarang
Indonesian	paku sarang burung
Malayalam	അസ്പ്ലേനിയം നിഡസ്
Malay	paku sarang burung
Malay	paku langsuir
Malay	daun semun
Malay	pokok daun semun
Malay	pokok paku langsuir
Malay	sakat-sakat
Malay	paku langsuyar
Dutch	vogelnestvaren
Dutch	nestvaren
Polish	zanokcica gniazdowa
Thai	ข้าหลวงหลังลาย
Tonga	hakato
Vietnamese	tổ điểu
Chinese	斩妖剑
Chinese	鸟巢蕨
Chinese	铁蚂蟥
Chinese	臺灣山蘇花
Chinese	巢蕨

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-tropical click to expand
- Indian Subcontinent
  - Bangladesh
- Malesia
  - Borneo
  - Christmas Island
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Queensland

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001108020
UNII	HF6Q4Q39QO
USDA Plants	ASNI
Tropicos	26601011
INPN	446409
KEW	urn:lsid:ipni.org:names:17048040-1
The Plant List	tro-26601011
Missouri Botanical Garden	285707
Open Tree Of Life	239550
NCBI Taxonomy	29642
Nature Serve	2.156841
IPNI	17048040-1
iNaturalist	84356
GBIF	2650676
Freebase	/m/05p755
EPPO	ASLNI
EOL	597615
USDA GRIN	5590
Wikipedia	Asplenium_nidus
CMAUP	NPO11235

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

Dynamic hybridization between two spleenworts, Asplenium incisum and Asplenium ruprechtii in Korea

Kim HT, Park SH, Kim JS

Front Plant Sci

05-Jul-2023

PMCID:	PMC10354290
doi:	10.3389/fpls.2023.1116040
PMID:	37476173

A review on arsenic in the environment: bio-accumulation, remediation, and disposal

Patel KS, Pandey PK, Martín-Ramos P, Corns WT, Varol S, Bhattacharya P, Zhu Y

RSC Adv

16-May-2023

PMCID:	PMC10186335
doi:	10.1039/d3ra02018e
PMID:	37200696

Phenolic compounds as Nrf2 inhibitors: potential applications in cancer therapy

Sharifi-Rad J, Seidel V, Izabela M, Monserrat-Mequida M, Sureda A, Ormazabal V, Zuniga FA, Mangalpady SS, Pezzani R, Ydyrys A, Tussupbekova G, Martorell M, Calina D, Cho WC

Cell Commun Signal

01-May-2023

PMCID:	PMC10152593
doi:	10.1186/s12964-023-01109-0
PMID:	37127651

Rickettsial DNA and a trans-splicing rRNA group I intron in the unorthodox mitogenome of the fern Haplopteris ensiformis

Zumkeller S, Polsakiewicz M, Knoop V

Commun Biol

20-Mar-2023

PMCID:	PMC10027690
doi:	10.1038/s42003-023-04659-8
PMID:	36941328

A systematic review on mitigation of common indoor air pollutants using plant-based methods: a phytoremediation approach

Kumar R, Verma V, Thakur M, Singh G, Bhargava B

Air Qual Atmos Health

11-Mar-2023

PMCID:	PMC10005924
doi:	10.1007/s11869-023-01326-z
PMID:	37359395

Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health

Sun W, Shahrajabian MH

Molecules

15-Feb-2023

PMCID:	PMC9960276
doi:	10.3390/molecules28041845
PMID:	36838831

Taxonomic Advances from Fungal Flora Associated with Ferns and Fern-like Hosts in Northern Thailand

Seifollahi E, de Farias AR, Jayawardena RS, Hyde KD

Plants (Basel)

03-Feb-2023

PMCID:	PMC9922025
doi:	10.3390/plants12030683
PMID:	36771768

Intercellular Communication during Stomatal Development with a Focus on the Role of Symplastic Connection

Cui Y, He M, Liu D, Liu J, Liu J, Yan D

Int J Mol Sci

30-Jan-2023

PMCID:	PMC9917297
doi:	10.3390/ijms24032593
PMID:	36768915

Response of arboreal Collembola communities to the conversion of lowland rainforest into rubber and oil palm plantations

Mawan A, Hartke TR, Deharveng L, Zhang F, Buchori D, Scheu S, Drescher J

BMC Ecol Evol

14-Dec-2022

PMCID:	PMC9753237
doi:	10.1186/s12862-022-02095-6
PMID:	36517771

A Large Intergenic Spacer Leads to the Increase in Genome Size and Sequential Gene Movement around IR/SC Boundaries in the Chloroplast Genome of Adiantum malesianum (Pteridaceae)

Gu X, Zhu M, Su Y, Wang T

Int J Mol Sci

09-Dec-2022

PMCID:	PMC9778900
doi:	10.3390/ijms232415616
PMID:	36555263

Uncovering Plant Virus Species Forming Novel Provisional Taxonomic Units Related to the Family Benyviridae

Solovyev AG, Morozov SY

Viruses

29-Nov-2022

PMCID:	PMC9781952
doi:	10.3390/v14122680
PMID:	36560684

De novo transcriptome assembly using Illumina sequencing and development of EST-SSR markers in a monoecious herb Sagittaria trifolia Linn

Tang H, Saina JK, Long ZC, Chen J, Dai C

PeerJ

26-Oct-2022

PMCID:	PMC9617548
doi:	10.7717/peerj.14268
PMID:	36317118

Exploring Foods of the Pacific: Cultural Food Identity in the US Affiliated Pacific Region

Dela Cruz R, Wolfe E, Yonemori KM, Fialkowski MK, Wilkens LR, Coleman P, Lameko-Mua S, Johnson E, Gilmatam D, Sigrah C, Shomour M, Remengesau S, Alfred J, Acosta M, Ettienne R, Deenik J, Tanisha A, Salazar KA, Novotny R, Boushey CJ

Hawaii J Health Soc Welf

01-Sep-2022

PMCID:	PMC9460762
PMID:	36118154

Pest categorisation of Pulvinaria psidii

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Maiorano A, Papachristos D, MacLeod A

EFSA J

12-Aug-2022

PMCID:	PMC9372818
doi:	10.2903/j.efsa.2022.7526
PMID:	35978619

Bioinformatic Analysis Predicts a Novel Genetic Module Related to Triple Gene and Binary Movement Blocks of Plant Viruses: Tetra-Cistron Movement Block

Morozov SY, Solovyev AG

Biomolecules

21-Jun-2022

PMCID:	PMC9313169
doi:	10.3390/biom12070861
PMID:	35883420

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 / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid	15548729	Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O	525.60	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10032594	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
Neoorthosiphol A	10055454	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	692.70	unknown	via CMAUP database
Staminol B	11802781	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C	692.70	unknown	via CMAUP database
staminol C	11490943	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)O)OC(=O)C5=CC=CC=C5)(C)C	692.70	unknown	via CMAUP database
staminol D	11455867	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C	568.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13R)-1alpha-(Benzoyloxy)-2alpha-acetoxy-3alpha,7alpha,8-trihydroxypimara-15-ene-11,14-dione	101228589	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)O	528.60	unknown	via CMAUP database
(13R)-1alpha-(Benzoyloxy)-2alpha,8-dihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-11,14-dione	101228590	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C	570.60	unknown	via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,7alpha,8-trihydroxy-3alpha-acetoxypimara-15-ene-14-one	10919284	Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O	634.70	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10327179	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C	676.70	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	9987409	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	718.80	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate	10258500	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C	632.70	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,7R,8aR,9R,10aS)-2,3-diacetyloxy-7-ethenyl-5,8a,9-trihydroxy-1,1,4a,7-tetramethyl-8-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-yl] benzoate	10076785	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C	572.60	unknown	via CMAUP database
[(2S,3S,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	44583688	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
orthosiphol A	15385858	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	676.70	unknown	via CMAUP database
orthosiphol B	15385859	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	676.70	unknown	via CMAUP database
orthosiphol D	44583689	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C)(C)C	552.60	unknown	via CMAUP database
orthosiphol J	10438744	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)(C)C	612.70	unknown	via CMAUP database
Orthosiphol K	10054824	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C	634.70	unknown	via CMAUP database
Orthosiphol L	10101176	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	692.70	unknown	via CMAUP database
Orthosiphol M	10030927	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C	570.60	unknown	via CMAUP database
Orthosiphol N	10258499	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5	632.70	unknown	via CMAUP database
orthosiphol O	10032464	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C	676.70	unknown	via CMAUP database
orthosiphol T	11082749	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)O	634.70	unknown	via CMAUP database
Orthosiphol U	637182	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C)(C)C	614.70	unknown	via CMAUP database
Orthosiphol V	10951947	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C	572.60	unknown	via CMAUP database
Orthosiphol W	11071897	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C	572.60	unknown	via CMAUP database
Orthosiphol X	10054823	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C5=CC=CC=C5	634.70	unknown	via CMAUP database
Orthosiphol Y	11144807	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C)(C)C	448.50	unknown	via CMAUP database
Orthosiphol Z	11090752	Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C	404.50	unknown	via CMAUP database
orthosiphonone A	10439492	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C	674.70	unknown	via CMAUP database
Orthosiphonone B	10055285	Click to see CC(=O)OC1CC2C(C(=O)C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)(C)C	674.70	unknown	via CMAUP database
orthosiphonone C	11226314	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C	528.60	unknown	via CMAUP database
Siphonol A	10952715	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E	10963687	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=O)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	736.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
14-deoxo-14-O-acetylorthosiphol Y	21578028	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C	492.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Staminol A	10628761	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
secoorthosiphol B	15548728	Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)OC	558.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(8-Methoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethan-1-one	10466473	Click to see CC(=O)C1=CC2=C(C(=C1)OC)OC(C=C2)(C)C	232.27	unknown	via CMAUP database
2,2-Dimethyl-6-[(R)-1-hydroxyethyl]-7,8-dimethoxy-2H-1-benzopyran	100945948	Click to see CC(C1=C(C(=C2C(=C1)C=CC(O2)(C)C)OC)OC)O	264.32	unknown	via CMAUP database
Methylripariochromene A	177148	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)C)OC)OC	262.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid	639655	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	via CMAUP database
3,4-Dihydroxycinnamoyl-(Z)-2-(3,4-dihydroxyphenyl)ethenol	14353342	Click to see C1=CC(=C(C=C1C=CC(=O)OC=CC2=CC(=C(C=C2)O)O)O)O	314.29	unknown	via CMAUP database
Caftaric acid	6440397	Click to see C1=CC(=C(C=C1C=CC(=O)OC(C(C(=O)O)O)C(=O)O)O)O	312.23	unknown	via CMAUP database
p-Hydroxyphenethyl trans-ferulate	637308	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O	314.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	14334890	Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	580.50	unknown	https://doi.org/10.1177/1934578X0800301026
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',6,7-tetramethoxyflavone	152430	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC	358.30	unknown	via CMAUP database
Eupatorin	97214	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	via CMAUP database
Ladanein	3084066	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database
Tetramethylscutellarein	96118	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC	342.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one	44584772	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database

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Asplenium nidus

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