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Selaginella tamariscina

Selaginella tamariscina - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stachygynandrum tamariscinum P.Beauv. Mag. Encycl. 9(5): 483 (1804)
Lycopodioides tamariscina (Beauv.) H.S.Kung Fl. Sichuanica 6: 62 (1988)
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)

Common names Top

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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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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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Ogasawara-Shoto
      • Taiwan
  • Asia-tropical
    • 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
Name Level Submitter Released Coverage Size
GCA_003024785.1 ASM302478v1 Scaffold Chinese Academy of Medical Sciences & Peking Union Medical College 2018-03-29 50.0x 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
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
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
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
Development of radiation countermeasure agents for acute radiation syndromes Guan B, Li D, Meng A Animal Model Exp Med 29-Aug-2023
PMCID:PMC10486342
doi:10.1002/ame2.12339
PMID:37642199
Companion Plants of Tea: From Ancient to Terrace to Forest Wu H, Long X, Geng Y Plants (Basel) 25-Aug-2023
PMCID:PMC10490072
doi:10.3390/plants12173061
PMID:37687308
Traditional medicine consumption in postpartum for HBV-infected women enrolled in the ANRS 12345 TA PROHM study in Cambodia Moeung S, Chassagne F, Goyet S, Nhoeung S, Sun L, Yang D, Vilhem S, Dim B, Ly S, Sov L, Sreng V, Chorn S, Chhun S, Borand L, Kim S, Segeral O PLoS One 10-Aug-2023
PMCID:PMC10414559
doi:10.1371/journal.pone.0288389
PMID:37561767
Proteome and Interactome Linked to Metabolism, Genetic Information Processing, and Abiotic Stress in Gametophytes of Two Woodferns Ojosnegros S, Alvarez JM, Grossmann J, Gagliardini V, Quintanilla LG, Grossniklaus U, Fernández H Int J Mol Sci 04-Aug-2023
PMCID:PMC10419320
doi:10.3390/ijms241512429
PMID:37569809
A systematic review on antimicrobial activities of green synthesised Selaginella silver nanoparticles Wadhwa K, Kaur H, Kapoor N, Ghorai SM, Gupta R, Sahgal A Expert Rev Mol Med 03-Aug-2023
PMCID:PMC10752228
doi:10.1017/erm.2023.21
PMID:37534437
Phylogeny, character evolution, and classification of Selaginellaceae (lycophytes) Zhou XM, Zhang LB Plant Divers 20-Jul-2023
PMCID:PMC10772194
doi:10.1016/j.pld.2023.07.003
PMID:38197007
Green synthetic natural carbon dots derived from Fuligo Plantae with inhibitory effect against alcoholic gastric ulcer Zhao Y, Cheng G, Gao Y, Cui L, Zhao Y, Zhang Y, Tian Y, Zhao Y, Zhang Y, Qu H, Kong H Front Mol Biosci 07-Jul-2023
PMCID:PMC10360179
doi:10.3389/fmolb.2023.1223621
PMID:37484528
Total biflavonoids extraction from Selaginella chaetoloma utilizing ultrasound-assisted deep eutectic solvent: Optimization of conditions, extraction mechanism, and biological activity in vitro Liu C, Qiao L, Gao Q, Zhang F, Zhang X, Lei J, Ren M, Xiao S, Kuang J, Deng S, Yuan X, Jiang Y, Wang G Ultrason Sonochem 19-Jun-2023
PMCID:PMC10320385
doi:10.1016/j.ultsonch.2023.106491
PMID:37379745
Replitrons: A major group of eukaryotic transposons encoding HUH endonuclease Craig RJ Proc Natl Acad Sci U S A 12-Jun-2023
PMCID:PMC10288648
doi:10.1073/pnas.2301424120
PMID:37307447
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191

Phytochemical Profile Top

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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 / Anthracenes / Anthraquinones
2-Methyl-4-methoxyanthrachinon 13412788 Click to see CC1=CC2=C(C(=C1)OC)C(=O)C3=CC=CC=C3C2=O 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 CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 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 COC1=CC(=CC(=C1O)OC)C(=O)O 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, dihydro-3,4-dipiperonyl-, trans-(-)- 11002708 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 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 CCCCCCCCCCCCCCCCC(=O)O 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
Artemisiifolin 5281424 Click to see CC1=CCCC(=CC(C2C(C1)OC(=O)C2=C)O)CO 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 CC(C)CCCC(C1C(CC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)O)C(=O)O 434.70 unknown https://doi.org/10.1055/S-2007-981562
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
Beta-Sitosterol 222284 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 C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
(2S)-2-ammonio-3-(4-hydroxyphenyl)propanoate 6942100 Click to see C1=CC(=CC=C1CC(C(=O)[O-])[NH3+])O 181.19 unknown via CMAUP database
2-Amino-3-(4-hydroxyphenyl)-propanoic acid 6919035 Click to see C1=CC(=CC=C1CC(C(=O)[O-])[NH3+])O 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 C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 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 C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 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 C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 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 C1=CC(=C(C=C1C=CC(=O)O)O)O 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 COC1=C(C=CC(=C1)C=CC(=O)O)O 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 C1=CC(=CC=C1C#CC2=C(C=CC(=C2C=O)C3=CC=C(C=C3)O)O)O 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-[[2-[2-(3,4-Dihydroxyphenyl)ethynyl]-3-(hydroxymethyl)-6-(4-hydroxyphenyl)phenyl]-(4-hydroxyphenyl)methylidene]cyclohexa-2,5-dien-1-one 123383224 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)O)CO)C5=CC=C(C=C5)O 528.50 unknown https://doi.org/10.1080/10286020.2010.536535
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 F 123373962 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=C(C=C(C=C5)O)O 528.50 unknown https://doi.org/10.1080/10286020.2010.536535
Selaginellin T (1) 90767663 Click to see C1=CC(=C(C(=C1)C2=CC=C(C=C2)O)C(=C3C=CC(=O)C=C3)C4=CC=C(C=C4)O)C#CC5=CC=C(C=C5)O 482.50 unknown https://doi.org/10.1248/CPB.56.982
Selaginellin U (2) 101863274 Click to see CC1=C(C(=C(C=C1)C2=CC=C(C=C2)O)C(=C3C=CC(=O)C=C3)C4=CC=C(C=C4)O)C#CC5=CC=C(C=C5)O 496.50 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
2,3-Dihydrorobustaflavone 102441560 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-oxochromen-2-yl)-2-hydroxyphenyl]-5,6,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one 24936074 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O)O)O)O 554.50 unknown https://doi.org/10.1016/J.BMC.2007.10.036
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/10.1016/S0031-9422(00)97392-8
https://doi.org/10.1248/BPB.32.1427
https://doi.org/10.1248/CPB.58.549
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
Cupressuflavone 5281609 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 538.50 unknown via CMAUP database
Heveaflavone 15559724 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O 580.50 unknown https://doi.org/10.1248/CPB.58.549
https://doi.org/10.1248/CPB.56.982
Robustaflavone 5281694 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O)O 538.50 unknown https://doi.org/10.1016/J.BMC.2007.10.036
Sequoiaflavone 5484010 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O 552.50 unknown https://doi.org/10.1248/CPB.56.982
Sotetsuflavone 5494868 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 552.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2',8'-Biapigenin 11958336 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)O)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 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 C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=CC(=C4)C(=O)O)O)O)O 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 C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 269.23 unknown via CMAUP database
Hinokiflavone 5281627 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 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 COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O 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/10.1016/S0031-9422(00)97392-8
https://doi.org/10.1055/S-2006-957887
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
Acide tannique [French] 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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