Woodfordia fruticosa - Unknown
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Internal ID UUID644047ca68f69859555459
Scientific name Woodfordia fruticosa
Authority Kurz
First published in J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 40: 56 (1871)

Description Top

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Woodfordia fruticosa is a plant species belonging to the family Lythraceae. It is found in various regions including E-Tanzania, Madagascar, Comores, Saudi Arabia, Oman, Myanmar, Bhutan, Indonesia, China, India, Sri Lanka, Nepal, Pakistan, and Vietnam.

Synonyms Top

Scientific name Authority First published in
Lythrum punctatum Span. Linnaea 15: 202 (1841)
Woodfordia floribunda Salisb. Parad. Lond. 1: t. 42 (1806)
Acistoma coccineum Zipp. ex Span. Linnaea 15: 202 (1841)
Grislea punctata Buch.-Ham. ex Sm. Cycl. 17: n.º 2 (1811)
Grislea tomentosa Roxb. Pl. Coromandel 1: 29 (1795)
Lythrum fruticosum L. Syst. Nat. ed. 10 , 2: 1045 (1759)
Woodfordia tomentosa Bedd. Fl. Sylv. Madr. 117.
Lythrum hunteri DC. Prodr. 3: 83 (1828)

Common names Top

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Language Common/alternative name
Arabic ثعابة مخشوشبة
Hindi गुल धावी
Indonesian sidowayah
mad podhi
Malayalam താതിരി
Marathi धायटी
Nepali धाइरो
Chinese 红皮水锦树
Chinese 虾子花
Chinese 虾子花叶
Chinese 吴福花
Chinese 蝦子花

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
  • Africa
    • East Tropical Africa
      • Tanzania
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • China
      • China South-central
      • China Southeast
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Philippines
      • Sulawesi

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001075906
UNII 24E8P75N3J
Tropicos 19200233
INPN 706934
KEW urn:lsid:ipni.org:names:554290-1
The Plant List tro-19200233
PFAF Woodfordia fruticosa
Open Tree Of Life 690828
Observations.org 460836
NCBI Taxonomy 141189
IUCN Red List 39058
IPNI 554290-1
iNaturalist 444872
GBIF 5635525
Freebase /m/02z05ss
EOL 2890103
Elurikkus 560338
USDA GRIN 42056
Wikipedia Woodfordia_fruticosa

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
Correction: Chakraborty et al. Bromelain a Potential Bioactive Compound: A Comprehensive Overview from a Pharmacological Perspective. Life 2021, 11, 317 Chakraborty AJ, Mitra S, Tallei TE, Tareq AM, Nainu F, Cicia D, Dhama K, Emran TB, Simal-Gandara J, Capasso R Life (Basel) 07-Apr-2024
PMCID:PMC11050791
doi:10.3390/life14040483
PMID:38672810
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Spectrophotometric Analysis and Determination of Anti-inflammatory Effect of Punica granatum and Woodfordia fruticosa in Subjects With Chronic Periodontitis – A Randomized Controlled Clinical Trial Bhavana S, Nallamilli SM, Thippani M, Gundapaneni N, Sahitya Y, Keerthi Reddy V, Dey S, Takkella BK, Prabhat MV, Venkata Anusha N Cureus 17-Dec-2023
PMCID:PMC10790239
doi:10.7759/cureus.50654
PMID:38229772
Leaf nitrogen and phosphorus resorption efficiencies are related to drought resistance across woody species in a Chinese savanna Zhang SB, Song Y, Wen HD, Chen YJ Tree Physiol 15-Dec-2023
PMCID:PMC10849754
doi:10.1093/treephys/tpad149
PMID:38102768
Ethnomedicinal plants in Champadevi rural municipality, Okhaldhunga district, Nepal Karki D, Khadka D, Kunwar RM, Aryal PC, Paudel HR, Bhatta S, Shi S J Ethnobiol Ethnomed 11-Dec-2023
PMCID:PMC10712033
doi:10.1186/s13002-023-00627-y
PMID:38072922
Phenolic Compounds from By-Products for Functional Textiles Afonso TB, Bonifácio-Lopes T, Costa EM, Pintado ME Materials (Basel) 20-Nov-2023
PMCID:PMC10672813
doi:10.3390/ma16227248
PMID:38005176
Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ Foods 08-Nov-2023
PMCID:PMC10671036
doi:10.3390/foods12224066
PMID:38002124
Ayurvedic and herbal plaque control agents in gingivitis: A systematic review and meta-analysis of randomized controlled trials Javed D, Dixit AK, Anwar S, Rai A, Krishan K J Educ Health Promot 31-Oct-2023
PMCID:PMC10744006
doi:10.4103/jehp.jehp_204_23
PMID:38144032
Exploring therapeutic potential of Woodfordia fruticosa (L.) Kurz leaf and bark focusing on antioxidant, antithrombotic, antimicrobial, anti‐inflammatory, analgesic, and antidiarrheal properties Rahman MM, Soma MA, Sultana N, Hossain MJ, Sufian MA, Rahman MO, Rashid MA Health Sci Rep 25-Oct-2023
PMCID:PMC10599101
doi:10.1002/hsr2.1654
PMID:37885464
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
Unravelling the gut-lung axis: insights into microbiome interactions and Traditional Indian Medicine's perspective on optimal health Haldar S, Jadhav SR, Gulati V, Beale DJ, Balkrishna A, Varshney A, Palombo EA, Karpe AV, Shah RM FEMS Microbiol Ecol 01-Sep-2023
PMCID:PMC10508358
doi:10.1093/femsec/fiad103
PMID:37656879
Erythema Multiforme: Unveiling the Unusual Effect of an Ayurvedic Medication ‘Jambavasa’ Used in the Treatment of Type 2 Diabetes Mellitus Gemnani R, Mahajan S, Saboo K, Pradeep U, Gupta A Cureus 10-Aug-2023
PMCID:PMC10492666
doi:10.7759/cureus.43306
PMID:37701014
Effect of Dietary Supplementation with a Mixture of Natural Antioxidants on Milk Yield, Composition, Oxidation Stability and Udder Health in Dairy Ewes Karageorgou A, Tsafou M, Goliomytis M, Hager-Theodorides A, Politi K, Simitzis P Antioxidants (Basel) 06-Aug-2023
PMCID:PMC10451849
doi:10.3390/antiox12081571
PMID:37627566
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
A comprehensive genus-level phylogeny and biogeographical history of the Lythraceae based on whole plastome sequences Inglis PW, Cavalcanti TB, Facco MG, Bakker FT, Graham SA Ann Bot 13-Jul-2023
PMCID:PMC10583215
doi:10.1093/aob/mcad091
PMID:37439499

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1248/CPB.38.2687
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1055/S-0028-1097262
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-0028-1097262
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1055/S-0028-1097262
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-0028-1097262
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-0028-1097262
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-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 122411793 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097262
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/10.1055/S-0028-1097262
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1016/0378-8741(93)90056-B
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 44259215 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1248/CPB.38.2687
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1248/CPB.38.2687
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose 374874 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1248/CPB.38.1211
1,2,3,6-Tetragalloyl-beta-D-glucopyranose 5153644 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown https://doi.org/10.1248/CPB.38.1211
1,2,4,6-Tetragalloyl-beta-D-glucopyranose 14464350 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown https://doi.org/10.1248/CPB.38.1211
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown https://doi.org/10.1248/CPB.38.1211
NP-003686 73178 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 788.60 unknown https://doi.org/10.1248/CPB.38.1211
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1248/CPB.38.1211
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,12,13,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl) 3,4,5-trihydroxybenzoate 13932611 Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1248/CPB.38.1211
[(10R,11R,12R,13R,15R)-3,4,5,12,21,22,23-heptahydroxy-8,18-dioxo-13-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 14481558 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.38.1211
[(10R,11R,12R,13S,15R)-3,4,5,12,13,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 10461723 Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1248/CPB.38.1211
[(11R,12R,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,20,21,22,25,26,30,31,32,38,46,47,48,51,52-heptadecahydroxy-9,17,35,43,55,61-hexaoxo-12,64-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate 16137984 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1721.20 unknown https://doi.org/10.1248/CPB.38.1211
https://doi.org/10.1248/CPB.38.2687
[(11R,12S,14R,15R,37R,38R,40R,57R,58S,64S)-4,5,6,20,21,22,25,26,30,31,32,38,46,47,48,51,52-heptadecahydroxy-9,17,35,43,55,61-hexaoxo-12,64-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,13,16,28,36,39,42,56,62-decaoxaundecacyclo[35.15.6.514,27.111,15.03,8.018,23.029,34.040,57.044,49.050,54.024,60]tetrahexaconta-1(52),3,5,7,18,20,22,24,26,29,31,33,44,46,48,50,53,59-octadecaen-58-yl] 3,4,5-trihydroxybenzoate 118856192 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1721.20 unknown https://doi.org/10.1248/CPB.38.2687
[11-Formyl-4,5,6,14,21,22,25,26,30,31,32,46,47,48,51,52-hexadecahydroxy-9,17,35,43,55,61-hexaoxo-38,58-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,16,28,36,39,42,56,62-nonaoxadecacyclo[38.12.5.413,27.137,41.03,8.018,23.029,34.044,49.050,54.024,60]dohexaconta-1(52),3,5,7,18(23),19,21,24,26,29,31,33,44,46,48,50,53,59-octadecaen-12-yl] 3,4,5-trihydroxybenzoate 16197486 Click to see C1C(C2C(C(OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O2)C2=C(C=CC(=C2O)O)C(=O)O1)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O 1705.20 unknown https://doi.org/10.1248/CPB.40.2023
https://doi.org/10.1055/S-2006-961195
https://doi.org/10.3987/COM-89-5199
https://doi.org/10.1248/CPB.38.2687
https://doi.org/10.1248/CPB.38.1211
[21-[2-[[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl]oxycarbonyl]-3,4,5-trihydroxyphenoxy]-3,4,5,13,22,23-hexahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 163195972 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=C(C=C(C(=C3O)O)O)OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)O)OC(=O)C7=CC(=C(C(=C7OC8=C(C9=C2C(=C8)C(=O)OC3=C2C(=CC(=C3O)O)C(=O)O9)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.40.2023
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[3,4,5,13,22,23-hexahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-12-[3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoyl]oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoate 162906631 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)O)OC(=O)C7=CC(=C(C(=C7OC8=C(C9=C2C(=C8)C(=O)OC3=C2C(=CC(=C3O)O)C(=O)O9)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1871.30 unknown https://doi.org/10.1248/CPB.40.2023
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 5153915 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.38.1211
CID 16170051 16170051 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1O)CO)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1569.10 unknown https://doi.org/10.1248/CPB.40.2023
CID 16170952 16170952 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9OC2=C(C(=C(C(=C2)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1721.20 unknown https://doi.org/10.1055/S-2006-961195
https://doi.org/10.1248/CPB.40.2023
https://doi.org/10.1248/CPB.38.1211
https://doi.org/10.1248/CPB.38.2687
https://doi.org/10.3987/COM-89-5199
CID 16182043 16182043 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1723.20 unknown https://doi.org/10.1248/CPB.38.1211
CID 442690 442690 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.38.1211
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1248/CPB.38.2687
Gemin D 471119 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C=O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 634.50 unknown https://doi.org/10.1248/CPB.38.1211
Heterophylliin A 471120 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.38.1211
Isoschimawalin A 16130370 Click to see C1C(C(C(=O)OC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)OC4=C(C(=C(C=C4C(=O)O)O)O)O)C(C(C=O)OC(=O)C5=CC(=C(C(=C5OC6=C(C7=C8C(=C6)C(=O)OC9=C8C(=CC(=C9O)O)C(=O)O7)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O 1254.80 unknown https://doi.org/10.1248/CPB.40.2023
Oenothein B 16129800 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O3)C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1569.10 unknown https://doi.org/10.1248/CPB.38.1211
Woodfordin A 16130308 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)OC9C(C(C(OC9OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O 1725.20 unknown https://doi.org/10.1248/CPB.40.2023
https://doi.org/10.1248/CPB.38.1211
https://doi.org/10.3987/COM-89-5199
Woodfordin B 16130309 Click to see C1C(C(OC(=O)C2=C(C(=C(C(=C2)C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C(C(C=O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OCC7C(C(C(C(O7)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C16)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O 1723.20 unknown https://doi.org/10.1248/CPB.40.2023
https://doi.org/10.1248/CPB.38.1211
https://doi.org/10.3987/COM-89-5199
Woodfordin D 16131182 Click to see C1C(C2C(C(OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O2)C2=C(C(=C(C=C2C(=O)O1)OC1=C(C(=C(C=C1C(=O)OC(C=O)C(C1C(COC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)OC(=O)C1=CC(=C(C(=C15)O)O)O)O)O)O)O)O)C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O 2505.70 unknown https://doi.org/10.1248/CPB.40.2023
Woodfordin I 16130412 Click to see C1C(C2C(C(OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OC(C(COC(=O)C6=CC(=C(C(=C65)O)O)OC7=C(C(=C(C=C7C(=O)O)O)O)O)O)C(C(OC(=O)C8=CC(=C(C(=C8OC9=C(C(=C(C(=C9)C(=O)O1)C1=C(C(=C(C=C1C(=O)O2)O)O)O)O)O)O)O)O)C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)C=O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O 1737.20 unknown https://doi.org/10.1248/CPB.40.2023

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