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Smilax corbularia

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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 UUID644022635d767934164603
Scientific name Smilax corbularia
Authority Kunth
First published in Enum. Pl. 5: 262 (1850)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 光叶菝葜
Chinese 筐条菝葜
Chinese 筐條菝葜
Chinese 粉叶菝葜
Chinese 裡白菝葜

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Smilax corbularia var. corbularia Unknown
Smilax corbularia var. woodii (Merr.) T.Koyama Quart. J. Taiwan Mus. 13: 15 (1960)

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 South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000740672
Tropicos 18407404
KEW urn:lsid:ipni.org:names:541374-1
The Plant List kew-288491
Open Tree Of Life 628572
NCBI Taxonomy 1045139
IPNI 541374-1
iNaturalist 569588
GBIF 5295395
EPPO SMICB
EOL 1082541
USDA GRIN 428210

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: Zhang et al. Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br. Genes 2023, 14, 1299 Zhang R, Zeng B, Chen T, Hu B Genes (Basel) 09-Feb-2024
PMCID:PMC10887675
doi:10.3390/genes15020221
PMID:38397249
Understory vegetation diversity patterns of Platycladus orientalis and Pinus elliottii communities in Central and Southern China Deng N, Caixia L, Ma F, Song Q, Tian Y Open Life Sci 22-Dec-2023
PMCID:PMC10752000
doi:10.1515/biol-2022-0791
PMID:38152580
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
The Inhibitory Effect of KerraTM, KSTM, and MinozaTM on Human Papillomavirus Infection and Cervical Cancer Choowongkomon K, Choengpanya K, Pientong C, Ekalaksananan T, Talawat S, Srathong P, Chuerduangphui J Medicina (Kaunas) 14-Dec-2023
PMCID:PMC10745032
doi:10.3390/medicina59122169
PMID:38138272
In vitro antioxidant and anticancer activities of Smilax corbularia extract combined with Phellinus linteus extract against breast cancer cell lines Syukriya AJ, Bankeeree W, Prasongsuk S, Yanatatsaneejit P Biomed Rep 07-Aug-2023
PMCID:PMC10442767
doi:10.3892/br.2023.1645
PMID:37614981
Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br Zhang R, Zeng B, Chen T, Hu B Genes (Basel) 20-Jun-2023
PMCID:PMC10298161
doi:10.3390/genes14061299
PMID:37372479
Effect of Smilax spp. and Phellinus linteus combination on cytotoxicity and cell proliferation of breast cancer cells Chalertpet K, Sangkheereeput T, Somjit P, Bankeeree W, Yanatatsaneejit P BMC Complement Med Ther 01-Jun-2023
PMCID:PMC10233913
doi:10.1186/s12906-023-04003-x
PMID:37264344
The Complete Chloroplast Genomes of Nine Smilacaceae Species from Hong Kong: Inferring Infra- and Inter-Familial Phylogeny Wong KH, Siu TY, Tsang SS, Kong BL, Wu HY, But GW, Hui JH, Shaw PC, Lau DT Int J Mol Sci 18-Apr-2023
PMCID:PMC10138973
doi:10.3390/ijms24087460
PMID:37108622
Tentative Identification of Phytochemicals from Smilax glabra and Smilax corbularia Extracts by LC-QTOF/MS and Their Bioactive Potential Jeeno P, Tongban S, Yana P, Wongta A, Sutan K, Yadoung S, Hongsibsong S Plants (Basel) 11-Aug-2022
PMCID:PMC9415527
doi:10.3390/plants11162089
PMID:36015393
Multigene Phylogeny, Beauvericin Production and Bioactive Potential of Fusarium Strains Isolated in India Rana S, Singh SK, Dufossé L J Fungi (Basel) 24-Jun-2022
PMCID:PMC9320867
doi:10.3390/jof8070662
PMID:35887419
Local Wisdom and Diversity of Medicinal Plants in Cha Miang Forest in Mae Kampong Village, Chiang Mai, Thailand, and Their Potential for Use as Osteoprotective Products Sukkho T, Khanongnuch C, Lumyong S, Ruangsuriya J, Pattananandecha T, Apichai S, Ogata F, Kawasaki N, Saenjum C Plants (Basel) 01-Jun-2022
PMCID:PMC9182823
doi:10.3390/plants11111492
PMID:35684265
A Medicinal Halophyte Ipomoea pes-caprae (Linn.) R. Br.: A Review of Its Botany, Traditional Uses, Phytochemistry, and Bioactivity Akinniyi G, Lee J, Kim H, Lee JG, Yang I Mar Drugs 17-May-2022
PMCID:PMC9144928
doi:10.3390/md20050329
PMID:35621980
Ethnomedicinal Plants in Herbal Remedies Used for Treatment of Skin Diseases by Traditional Healers in Songkhla Province, Thailand Saising J, Maneenoon K, Sakulkeo O, Limsuwan S, Götz F, Voravuthikunchai SP Plants (Basel) 25-Mar-2022
PMCID:PMC9003147
doi:10.3390/plants11070880
PMID:35406860
Astilbin prevents osteoarthritis development through the TLR4/MD‐2 pathway Sun S, Yan Z, Shui X, Qi W, Chen Y, Xu X, Hu Y, Guo W, Shang P J Cell Mol Med 16-Oct-2020
PMCID:PMC7701562
doi:10.1111/jcmm.15915
PMID:33063931
Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Plants (Basel) 28-Jun-2020
PMCID:PMC7412036
doi:10.3390/plants9070811
PMID:32605228

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
4H-1-Benzopyran-4-one, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-5,7-dihydroxy- 5488575 Click to see CC1C(C(C(C(O1)OC2=COC3=CC(=CC(=C3C2=O)O)O)O)O)O 340.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
5,7-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 14214024 Click to see CC1C(C(C(C(O1)OC2=COC3=CC(=CC(=C3C2=O)O)O)O)O)O 340.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
5-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-3,4-dihydroxycyclohexene-1-carboxylic acid 4484226 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
5-Caffeoylshikimic acid 5281762 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechin 73160 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-pyrano[2,3-f]chromen-10-one 162866699 Click to see C1C(C(OC2=C1C(=CC3=C2C(=O)C=CO3)O)C4=CC(=C(C=C4)O)O)O 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4R,8R,9S)-4,8-bis(3,4-dihydroxyphenyl)-5,9-dihydroxy-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-2-one 100978387 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4S,8R,9S)-4,8-Bis(3,4-dihydroxyphenyl)-3,4,9,10-tetrahydro-5,9-dihydroxy-2H,8H-benzo[1,2-b:3,4-b']dipyran-2-one 71661208 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4-dihydro-2H-pyrano[2,3-f]chromen-8-one 50908817 Click to see C1C(C(OC2=C1C(=CC3=C2C=CC(=O)O3)O)C4=CC(=C(C=C4)O)O)O 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
2,10-bis(3,4-dihydroxyphenyl)-3,5-dihydroxy-3,4,9,10-tetrahydro-2H-pyrano[2,3-h]chromen-8-one 496377 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
4,8-bis(3,4-dihydroxyphenyl)-5,9-dihydroxy-4,8,9,10-tetrahydro-3H-pyrano[2,3-h]chromen-2-one 73822599 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
9,10-Dihydro-10-(3,4-dihydroxyphenyl)-pyrano[2,3-h]catechin-8-one 10343836 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Cinchonain Ia 442675 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Cinchonain Ib 10456516 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
cinchonain Ic 21676383 Click to see C1C(C(OC2=C1C3=C(C(CC(=O)O3)C4=CC(=C(C=C4)O)O)C(=C2)O)C5=CC(=C(C=C5)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Phyllocoumarin 44257095 Click to see C1C(C(OC2=C1C(=CC3=C2C=CC(=O)O3)O)C4=CC(=C(C=C4)O)O)O 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Astilbin 119258 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
CID 9981176 9981176 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Engeletin 6453452 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Isoastilbin 316844 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Isoengeletin 101937309 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Isoengelitin 12309470 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Neoisoastilbin 10114809 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(2R,3R,10R)-10-(3,4-dihydroxyphenyl)-3,5-dihydroxy-2-(4-hydroxyphenyl)-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-8-one 52937584 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC=C(C=C5)O)O 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(2R,3R,10S)-10-(3,4-dihydroxyphenyl)-3,5-dihydroxy-2-(4-hydroxyphenyl)-3,4,9,10-tetrahydro-2H-pyrano[2,3-f]chromen-8-one 52937585 Click to see C1C(C(OC2=C1C(=CC3=C2C(CC(=O)O3)C4=CC(=C(C=C4)O)O)O)C5=CC=C(C=C5)O)O 436.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Isoflavonoids / Hydroxyisoflavonoids
3-(3,4-Dihydroxyphenyl)-5,7-dihydroxychromen-2-one 52937587 Click to see C1=CC(=C(C=C1C2=CC3=C(C=C(C=C3OC2=O)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavans
(4R)-4-(3,4-dihydroxyphenyl)-5-[(E)-2-(3,4-dihydroxyphenyl)ethenyl]-7-hydroxy-3,4-dihydrochromen-2-one 162866692 Click to see C1C(C2=C(C=C(C=C2OC1=O)O)C=CC3=CC(=C(C=C3)O)O)C4=CC(=C(C=C4)O)O 406.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4R)-4-(3,4-dihydroxyphenyl)-5-[2-(3,4-dihydroxyphenyl)ethenyl]-7-hydroxy-3,4-dihydrochromen-2-one 162866693 Click to see C1C(C2=C(C=C(C=C2OC1=O)O)C=CC3=CC(=C(C=C3)O)O)C4=CC(=C(C=C4)O)O 406.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4R)-4-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(E)-2-(4-hydroxyphenyl)ethenyl]-3,4-dihydrochromen-2-one 163189276 Click to see C1C(C2=C(C=C(C=C2OC1=O)O)C=CC3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)O 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4R)-4-(3,4-dihydroxyphenyl)-7-hydroxy-5-[2-(4-hydroxyphenyl)ethenyl]-3,4-dihydrochromen-2-one 162866697 Click to see C1C(C2=C(C=C(C=C2OC1=O)O)C=CC3=CC=C(C=C3)O)C4=CC(=C(C=C4)O)O 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4R)-7-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-5-[(E)-2-(4-hydroxyphenyl)ethenyl]-3,4-dihydrochromen-2-one 163189566 Click to see COC1=C(C=CC(=C1)C2CC(=O)OC3=CC(=CC(=C23)C=CC4=CC=C(C=C4)O)O)O 404.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
(4R)-7-hydroxy-4-(4-hydroxy-3-methoxyphenyl)-5-[2-(4-hydroxyphenyl)ethenyl]-3,4-dihydrochromen-2-one 162933191 Click to see COC1=C(C=CC(=C1)C2CC(=O)OC3=CC(=CC(=C23)C=CC4=CC=C(C=C4)O)O)O 404.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
3,4',5-Trihydroxy-3'-methoxystilbene 53395093 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Isorhapontigenin 5318650 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.12.018

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