Selaginella tamariscina

Details

Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

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Details Top

Internal ID	UUID6440236743d2e805803172
Scientific name	Selaginella tamariscina
Authority	(P.Beauv.) Spring
First published in	Bull. Acad. Roy. Sci. Bruxelles 10(1): 136 (1843)

Ethnobotanical Use Top

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Important notice

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.

Selaginella tamariscina has a long history in traditional Chinese medicine as an astringent for bleeding and a promoter of blood flow and tissue repair. Practically, the whole plant is prepared as a tea or decoction for uterine bleeding, traumatic bleeding, hematuria, nosebleeds, and minor gastrointestinal bleeding, and it is also applied as a wash or compress for traumatic injuries and painful bruises. Contemporary ethnobotanical surveys across parts of eastern Asia, such as the work of He et al. in south China and Li et al. in Taiwan, document these uses and note that decoctions or washes made from the dried whole plant are the preferred forms. Preparations range from single‑herb teas to multipart formulas in which S. tamariscina is a hemostatic agent, a practice reflected in both traditional texts and modern pharmacopoeias.

A practical recipe for a basic hemostatic tea is straightforward. Simmer about 9–12 g of the dried whole plant (or 3–9 g if the material is strong) in 400–600 mL of water for 15–20 minutes, cool, strain, and drink one cup two to three times daily. As the 2020 edition of the Chinese Pharmacopoeia specifies water decoctions for this herb, modern practitioners generally follow that standard. Typical courses of use last 7–10 days unless otherwise directed by a qualified practitioner. Although there is no consistent dose frequency in early texts, the modern pharmacopeial practice is to avoid long, continuous use and to seek medical attention for heavy or recurrent bleeding; pregnancy and lactation are common cautions in clinical texts for astringent hemostatics.

The hemostatic and anti‑inflammatory actions of S. tamariscina are plausibly linked to its biflavonoid profile, especially amentoflavone, as well as shikimic acid and related phenolic acids that are frequently reported from Selaginella. Contemporary pharmacology has demonstrated anti‑inflammatory, antioxidant, and antiplatelet activities for extracts, and amentoflavone has been highlighted as a key anti‑inflammatory constituent. These classes of phytochemicals are well established for the genus and are consistent with the herb’s traditional astringent profile.

Today, S. tamariscina remains available as dried whole plant in many TCM pharmacies and a small number of modern herbal lines, and in vitro and animal studies continue to examine its anti‑inflammatory, hemostatic, and cardioprotective potential. Practitioners in south China, Taiwan, and among Chinese diaspora communities continue to use decoctions and washes for bleeding and trauma in both clinical and domestic contexts.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Stachygynandrum tamariscinum	P.Beauv.	Mag. Encycl. 9(5): 483 (1804)
Lycopodium tamariscinum	(P.Beauv.) Desr. ex Poir.	Encycl. , Suppl. 3: 540 (1814)
Selaginella veitchii	W.R.McNab	Trans. & Proc. Bot. Soc. Edinburgh 9: 10 (1867)
Lycopodium circinale	Thunb.	Fl. Jap. 341 1784
Selaginella leveillei	Kümmerle	Magyar Bot. Lapok 26: 82, 100 1928
Selaginella convolvens	Alderw.	Bull. Jard. Bot. Buitenzorg, sér. 2, 11: 23 1913
Pulviniella tamariscina	(P.Beauv.) Li Bing Zhang & X.M.Zhou	Pl. Diversity 45(6): 661 (2023)
Lycopodioides tamariscina var. ulanchotensis	(Ching & W.Wang) J.X.Li
Selaginella involvens f. major	Milde	Fil. Eur. 269 (1867)
Selaginella involvens f. minor	Milde	Fil. Eur. 269 (1867)
Selaginella involvens var. veitchii	(W.R.McNab) Baker	J. Bot. 22: 375 (1884)
Selaginella tamariscina var. ulanchotensis	Ching & W.Wang	Fl. Pl. Herb. Chin. Bor.-Or. 1: 69 (1958)
Selaginella christii	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 451 (1911)
Selaginella japonica	T.Moore ex W.R.McNab	Trans. & Proc. Bot. Soc. Edinburgh 9: 8 (1868)
Selaginella japonica	Veitch	Flor. & Pom., 137, fig. (1877)
Lycopodioides tamariscina	(P.Beauv.) H.S.Kung	Fl. Sichuanica 6: 62-64, t. 18, 4-6 (1988)
Lycopodioides tamariscina	(P.Beauv.) Tzvelev	Novosti Sist. Vyssh. Rast. 36: 25 (2004), isonym

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	イワヒバ
Korean	바위손
Vietnamese	cây chân vịt
Vietnamese	quyển bá
Vietnamese	quyển bá trường sinh
Chinese	石花
Chinese	卷柏
Chinese	干蕨鸡
Chinese	萬年松

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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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 South-central
  - China Southeast
  - Hainan
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Philippines
  - Sulawesi

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000748162
UNII	GP370KXK6M
Tropicos	26600330
KEW	urn:lsid:ipni.org:names:60467461-2
The Plant List	kew-2902290
Open Tree Of Life	1058277
Observations.org	147020
NCBI Taxonomy	137178
IPNI	60467461-2
iNaturalist	366350
iNaturalist	366348
iNaturalist	366351
GBIF	4940390
Freebase	/m/0130rl7b
Elurikkus	495905
USDA GRIN	413787
Wikipedia	Selaginella_tamariscina
CMAUP	NPO14158

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_003024785.1	ASM302478v1	Scaffold	Chinese Academy of Medical Sciences & Peking Union Medical College	2018-03-29	50	286.80 Mb

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

Transgenerational Seed Exposure to Elevated CO2 Involves Stress Memory Regulation at Metabolic Levels to Confer Drought Resistance in Wheat

Shafique Ahmad K, Shehzad MA, Javid H, Mehmood A, Akhtar G, Zafar S, Mahroof S, Mahmoud EA, Elansary HO, Ulfat A, Abid H

ACS Omega

22-Apr-2024

PMCID:	PMC11079883
doi:	10.1021/acsomega.3c10379
PMID:	38737051

Genome-Wide Identification of Calmodulin-Binding Protein 60 Gene Family and the Function of GhCBP60B in Cotton Growth and Development and Abiotic Stress Response

Luo K, Sha L, Li T, Wang C, Zhao X, Pan J, Zhu S, Li Y, Chen W, Yao J, Rong J, Zhang Y

Int J Mol Sci

15-Apr-2024

PMCID:	PMC11049924
doi:	10.3390/ijms25084349
PMID:	38673934

Natural Products as Regulators against Matrix Metalloproteinases for the Treatment of Cancer

Islam MT, Jang NH, Lee HJ

Biomedicines

03-Apr-2024

PMCID:	PMC11048580
doi:	10.3390/biomedicines12040794
PMID:	38672151

Acute and Subchronic Toxicological Study of the Cocktail Extract from Curcuma xanthorrhiza Roxb, Phyllanthus niruri L. and Morinda citrifolia L.

Rosidah I, Renggani TN, Firdausi N, Ningsih S, Yunianto P, Permatasari D, Pongtuluran OB, Bahua H, Efendi J, Kusumastuti SA, Nuralih, El Muttaqien S, Nizar, Kusumaningrum S, Agustini K

J Toxicol

27-Mar-2024

PMCID:	PMC10990647
doi:	10.1155/2024/9445226
PMID:	38571743

Role of mitochondria in doxorubicin-mediated cardiotoxicity: From molecular mechanisms to therapeutic strategies

Wang T, Xing G, Fu T, Ma Y, Wang Q, Zhang S, Chang X, Tong Y

Cell Stress Chaperones

12-Mar-2024

PMCID:	PMC10999808
doi:	10.1016/j.cstres.2024.03.003
PMID:	38485043

Role of mitochondria in doxorubicin-mediated cardiotoxicity: from molecular mechanisms to therapeutic strategies

Wang T, Xing G, Fu T, Ma Y, Wang Q, Zhang S, Chang X, Tong Y

Int J Med Sci

11-Mar-2024

PMCID:	PMC11008476
doi:	10.7150/ijms.94485
PMID:	38617011

Genome-wide molecular evolution analysis of the GRF and GIF gene families in Plantae (Archaeplastida)

Chen X, Zhang J, Wang S, Cai H, Yang M, Dong Y

BMC Genomics

18-Jan-2024

PMCID:	PMC10795294
doi:	10.1186/s12864-024-10006-w
PMID:	38233778

Utilizing transcriptomics and metabolomics to unravel key genes and metabolites of maize seedlings in response to drought stress

Li Y, Su Z, Lin Y, Xu Z, Bao H, Wang F, Liu J, Hu S, Wang Z, Yu X, Gao J

BMC Plant Biol

08-Jan-2024

PMCID:	PMC10773024
doi:	10.1186/s12870-023-04712-y
PMID:	38185653

Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China

Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y

J Ethnobiol Ethnomed

02-Jan-2024

PMCID:	PMC10763305
doi:	10.1186/s13002-023-00645-w
PMID:	38169414

The characterization of traditional Chinese medicine natures and flavors using network pharmacology integrated strategy

Wang H, Wei W, Liu J, Zhang S, Zhao Y, Yu Z

J Tradit Complement Med

25-Dec-2023

PMCID:	PMC11068986
doi:	10.1016/j.jtcme.2023.12.004
PMID:	38707921

Transcription Factor EB: A Promising Therapeutic Target for Ischemic Stroke

Shao J, Lang Y, Ding M, Yin X, Cui L

Curr Neuropharmacol

28-Nov-2023

PMCID:	PMC10788889
doi:	10.2174/1570159X21666230724095558
PMID:	37491856

Non-targeted metabolomics analysis of metabolite changes in two quinoa genotypes under drought stress

Zhu X, Zhang M, Wang B, Song X, Wang X, Wei X

BMC Plant Biol

20-Oct-2023

PMCID:	PMC10588040
doi:	10.1186/s12870-023-04467-6
PMID:	37858063

Chromosome-level reference genome of tetraploid Isoetes sinensis provides insights into evolution and adaption of lycophytes

Cui J, Zhu Y, Du H, Liu Z, Shen S, Wang T, Cui W, Zhang R, Jiang S, Wu Y, Gu X, Yu H, Liang Z

Gigascience

30-Sep-2023

PMCID:	PMC10541799
doi:	10.1093/gigascience/giad079
PMID:	37776367

Origin and Evolution of Plant Long Terminal Repeat Retrotransposons with Additional Ribonuclease H

Biryukov M, Ustyantsev K

Genome Biol Evol

11-Sep-2023

PMCID:	PMC10508981
doi:	10.1093/gbe/evad161
PMID:	37697050

Heme Oxygenase 1-Mediated Anti-Inflammatory Effect of Extract from the Aerial Part of Heracleum moellendorffii Hance

Jang HY, Lee SO

Foods

02-Sep-2023

PMCID:	PMC10486398
doi:	10.3390/foods12173309
PMID:	37685243

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
> Benzenoids / Anthracenes / Anthraquinones
2-Methyl-4-methoxyanthrachinon	13412788	Click to see	252.26	unknown	https://doi.org/10.1248/CPB.58.549
> Benzenoids / Benzene and substituted derivatives / Acetophenones
Ethanone, 1-[2,3-dihydro-2-(1-methylethenyl)-5-benzofuranyl]-	317196	Click to see	202.25	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid	10742	Click to see	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
2(3H)-Furanone, 3,4-bis(1,3-benzodioxol-5-ylmethyl)dihydro-, (3S,4S)-	11002708	Click to see	354.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic Acid	10465	Click to see	270.50	unknown	https://doi.org/10.1248/CPB.58.549
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,4R,5Z,9E,11aS)-3a,4,7,8,11,11a-Hexahydro-4-hydroxy-6-(hydroxymethyl)-10-methyl-3-methylenecyclodeca[b]furan-2(3H)-one	5281424	Click to see	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(2R)-2-[(3S,5S,8R,9S,10S,13S,14S,16R,17R)-3,16-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptanoic acid	162870769	Click to see	434.70	unknown	https://doi.org/10.1055/S-2007-981562
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1248/CPB.58.549
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1248/CPB.58.549
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	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	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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
(2R)-2-ammonio-3-(4-hydroxyphenyl)propanoate	6919035	Click to see	181.19	unknown	via CMAUP database
(2S)-2-ammonio-3-(4-hydroxyphenyl)propanoate	6942100	Click to see	181.19	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
(+)-Shikimic acid	10986763	Click to see	174.15	unknown	via CMAUP database
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid	1094	Click to see	174.15	unknown	via CMAUP database
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arbutin	440936	Click to see	272.25	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Hexitol	453	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	via CMAUP database
L-Mannitol	136460	Click to see	182.17	unknown	via CMAUP database
Mannitol	6251	Click to see	182.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	via CMAUP database
cis-Caffeic acid	1549111	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
Ferulic Acid	445858	Click to see	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
3-Hydroxy-6-(4-hydroxyphenyl)-2-[2-(4-hydroxyphenyl)ethynyl]benzaldehyde	162901918	Click to see	330.30	unknown	https://doi.org/10.1080/10286020.2011.558840
4-(4-Hydroxyphenyl)-2-[2-(4-hydroxyphenyl)ethynyl]-3-methylphenol	122208361	Click to see CC1=C(C=CC(=C1C#CC2=CC=C(C=C2)O)O)C3=CC=C(C=C3)O	316.30	unknown	https://doi.org/10.1080/10286020.2011.558840
4-[[3-(Hydroxymethyl)-6-(4-hydroxyphenyl)-2-[2-(4-hydroxyphenyl)ethynyl]phenyl]-(4-methoxyphenyl)methylidene]cyclohexa-2,5-dien-1-one	71575995	Click to see COC1=CC=C(C=C1)C(=C2C=CC(=O)C=C2)C3=C(C=CC(=C3C#CC4=CC=C(C=C4)O)CO)C5=CC=C(C=C5)O	526.60	unknown	via CMAUP database
Selaginellin	16664188	Click to see C1=CC(=O)C=CC1=C(C2=CC=C(C=C2)O)C3=C(C=CC(=C3C#CC4=CC=C(C=C4)O)CO)C5=CC=C(C=C5)O	512.50	unknown	via CMAUP database
Selaginellin B	101863274	Click to see	496.50	unknown	https://doi.org/10.1248/CPB.56.982
Selaginellin F	123373962	Click to see	528.50	unknown	https://doi.org/10.1080/10286020.2010.536535
selaginellin J	123383224	Click to see	528.50	unknown	https://doi.org/10.1080/10286020.2010.536535
Selaginellin T (1)	90767663	Click to see	482.50	unknown	https://doi.org/10.1248/CPB.56.982
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
2-(4-Hydroxyphenyl)-5,7-dihydroxy-6-[2-hydroxy-5-(4-oxo-5,7-dihydroxy-2,3-dihydro-4H-1-benzopyran-2-yl)phenyl]-4H-1-benzopyran-4-one	76315513	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)C4=C(C5=C(C=C4O)OC(=CC5=O)C6=CC=C(C=C6)O)O	540.50	unknown	via CMAUP database
8-(5-(5,7-Dihydroxy-4-oxo-4H-1-benzopyran-2-yl)-2-hydroxyphenyl)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-1-benzopyran-4-one	5494868	Click to see	552.50	unknown	via CMAUP database
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1248/BPB.32.1427 https://doi.org/10.1248/CPB.58.549 https://doi.org/10.1016/S0031-9422(00)97392-8 https://doi.org/10.1248/CPB.56.982 https://doi.org/10.1055/S-2006-957887 https://doi.org/10.1055/S-2004-827201 https://doi.org/10.1016/J.BMC.2007.10.036
Bilobetin	5315459	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O	552.50	unknown	via CMAUP database
CID 102441560	102441560	Click to see	540.50	unknown	via CMAUP database
Cupressuflavone	5281609	Click to see	538.50	unknown	via CMAUP database
Heveaflavone	15559724	Click to see	580.50	unknown	https://doi.org/10.1248/CPB.58.549 https://doi.org/10.1248/CPB.56.982
Robustaflavone	5281694	Click to see	538.50	unknown	https://doi.org/10.1016/J.BMC.2007.10.036
Sequoiaflavone	5484010	Click to see	552.50	unknown	https://doi.org/10.1248/CPB.56.982
Sumaflavone	24936074	Click to see	554.50	unknown	https://doi.org/10.1016/J.BMC.2007.10.036
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2',8'-Biapigenin	11958336	Click to see	538.50	unknown	https://doi.org/10.1016/J.BMC.2007.10.036
3-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]-4-hydroxybenzoic acid	46193232	Click to see	406.30	unknown	https://doi.org/10.1248/CPB.58.549
7-[4-(5,7-Dihydroxy-4-oxochromen-2-yl)phenoxy]-5,8-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	42607509	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	via CMAUP database
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Apigenin-7-olate	25200950	Click to see	269.23	unknown	via CMAUP database
Hinokiflavone	5281627	Click to see	538.50	unknown	https://doi.org/10.1248/CPB.56.982 https://doi.org/10.1016/S0031-9422(00)97392-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
6-[4-(5,7-Dihydroxy-4-oxochromen-2-yl)phenoxy]-5-hydroxy-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	5316145	Click to see	566.50	unknown	https://doi.org/10.1055/S-2006-957887
Isocryptomerin	5318537	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O	552.50	unknown	https://doi.org/10.1055/S-2006-957887 https://doi.org/10.1016/S0031-9422(00)97392-8
Neocryptomerin	5320065	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)OC4=C(C5=C(C=C4O)OC(=CC5=O)C6=CC=C(C=C6)O)O)O	552.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
3-(4-Hydroxyphenyl)-6,7-dihydroxy coumarin	15674295	Click to see C1=CC(=CC=C1C2=CC3=CC(=C(C=C3OC2=O)O)O)O	270.24	unknown	https://doi.org/10.1248/CPB.58.549
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Taiwaniaflavone	44456685	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	https://doi.org/10.1016/J.BMC.2007.10.036
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Liquidambar styraciflua	16133892	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O	1701.20	unknown	via CMAUP database

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Selaginella tamariscina

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