Balanophora fungosa - Unknown
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Internal ID UUID64400c0f9d6c3541615349
Scientific name Balanophora fungosa
Authority J.R.Forst. & G.Forst.
First published in Char. Gen. Pl. : 100 (1776)

Description Top

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Balanophora fungosa, also known as fungus root, is a flowering plant found in South Asia, Southeast Asia, Australia, and some Pacific Islands. It is a parasitic plant that grows on the roots of rainforest trees and has a unique flowering structure resembling a puffball. The plant emits an odor similar to mice and contains no chlorophyll. It has scale-like leaves and produces both male and female flowers. The species was first described in 1774 and has two accepted subspecies. It is found in coastal forests and can be a weed in coffee and tea plantations. The flowers attract various small animals, including ants, flies, and even rats. Some cultures use B. fungosa for medicinal purposes.

Synonyms Top

Scientific name Authority First published in
Balanophora forsteri Tiegh. Ann. Sci. Nat., Bot. , sér. 9, 6: 148 (1907)
Balanophora fungosa f. extratropica F.M.Bailey Comprehensive Catalogue of Queensland Plants 1913
Balanophora fungosa var. kuroiwai Makino Bot. Mag. (Tokyo) 21: 29 1907
Balanophora fungosa var. mariannae (Hosok.) Hosok. J. Jap. Bot. 13: 202 1937
Balanophora kuroiwai Makino Bot. Mag. (Tokyo) 16: 213 (1902)
Balanophora mariannae Hosok. J. Soc. Trop. Agric. 6: 572 (1934)
Balanophora micholitzii Ridl. J. Straits Branch Roy. Asiat. Soc. 39: 207 1903
Cynomorium australe Hook.f. Trans. Linn. Soc. London 22: 46 (1856)
Cynomorium balanophora Willd. Bot. Nomencl. : 4 (1794)
Cynomorium fungosum Raeusch. ex Steud. Nomencl. Bot. 1: 252 (1821)
Cynomorium parasiticum Sw. ex Steud. Nomencl. Bot. 1: 252 (1821)
Cynomorium philippense Blanco Fl. Filip. : 665 (1837)

Common names Top

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Language Common/alternative name
English fungus root
Japanese リュウキュウツチトリモチ
Thai กกหมากพาสี
Thai กากหมากตาฤๅษี
Vietnamese dó đất
Chinese 粗穗蛇菰
Chinese 蛇菰

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Balanophora fungosa subsp. indica (Arn.) B.Hansen Dansk Bot. Ark. 28: 100 (1972)

Varieties (abbr. var.) Top

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Name Authority First published in
Balanophora fungosa var. globosa (Jungh.) B.Hansen Dansk Bot. Ark. 28: 109 (1972)
Balanophora fungosa var. minor (Eichl.) B.Hansen Dansk Bot. Ark. 28: 106 (1972)

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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
      • Solomon Islands
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Vanuatu
      • Wallis-Futuna Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000558654
USDA Plants BAFU6
Tropicos 3000095
INPN 672306
KEW urn:lsid:ipni.org:names:103250-1
The Plant List kew-2668043
Open Tree Of Life 425738
NCBI Taxonomy 29813
IPNI 103250-1
iNaturalist 337638
GBIF 7147896
Freebase /m/012lbjy4
EOL 2905653
Wikipedia Balanophora_fungosa

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
Extreme plastomes in holoparasitic Balanophoraceae are not the norm Kim W, Lautenschläger T, Bolin JF, Rees M, Nzuzi A, Zhou R, Wanke S, Jost M BMC Genomics 15-Jun-2023
PMCID:PMC10268348
doi:10.1186/s12864-023-09422-1
PMID:37322447
The GENOMES UNCOUPLED1 protein has an ancient, highly conserved role but not in retrograde signalling Honkanen S, Small I New Phytol 05-Jul-2022
PMCID:PMC9545484
doi:10.1111/nph.18318
PMID:35708656
Genome-Wide Analysis of the MADS-Box Gene Family in Holoparasitic Plants (Balanophora subcupularis and Balanophora fungosa var. globosa) Duan K, Fu H, Fang D, Wang K, Zhang W, Liu H, Sahu SK, Chen X Front Plant Sci 31-May-2022
PMCID:PMC9197559
doi:10.3389/fpls.2022.846697
PMID:35712591
Genomic comparison of non-photosynthetic plants from the family Balanophoraceae with their photosynthetic relatives Schelkunov MI, Nuraliev MS, Logacheva MD PeerJ 31-Aug-2021
PMCID:PMC8415285
doi:10.7717/peerj.12106
PMID:34540375
Comparative Plastome Analysis of Root- and Stem-Feeding Parasites of Santalales Untangle the Footprints of Feeding Mode and Lifestyle Transitions Chen X, Fang D, Wu C, Liu B, Liu Y, Sahu SK, Song B, Yang S, Yang T, Wei J, Wang X, Zhang W, Xu Q, Wang H, Yuan L, Liao X, Chen L, Chen Z, Yuan F, Chang Y, Lu L, Yang H, Wang J, Xu X, Liu X, Wicke S, Liu H Genome Biol Evol 17-Dec-2019
PMCID:PMC6953812
doi:10.1093/gbe/evz271
PMID:31845987
Characterization of melanin and optimal conditions for pigment production by an endophytic fungus, Spissiomyces endophytica SDBR-CMU319 Suwannarach N, Kumla J, Watanabe B, Matsui K, Lumyong S PLoS One 09-Sep-2019
PMCID:PMC6733467
doi:10.1371/journal.pone.0222187
PMID:31498821
eDNA-based monitoring of parasitic plant (Sapria himalayana) Osathanunkul M Sci Rep 24-Jun-2019
PMCID:PMC6591406
doi:10.1038/s41598-019-45647-5
PMID:31235792
Novel genetic code and record-setting AT-richness in the highly reduced plastid genome of the holoparasitic plant Balanophora Su HJ, Barkman TJ, Hao W, Jones SS, Naumann J, Skippington E, Wafula EK, Hu JM, Palmer JD, dePamphilis CW Proc Natl Acad Sci U S A 31-Dec-2018
PMCID:PMC6338844
doi:10.1073/pnas.1816822116
PMID:30598433
Functional analysis of the TM6 MADS-box gene in the octoploid strawberry by CRISPR/Cas9-directed mutagenesis Martín-Pizarro C, Triviño JC, Posé D J Exp Bot 13-Nov-2018
PMCID:PMC6363087
doi:10.1093/jxb/ery400
PMID:30428077
The evolution of CHROMOMETHYLASES and gene body DNA methylation in plants Bewick AJ, Niederhuth CE, Ji L, Rohr NA, Griffin PT, Leebens-Mack J, Schmitz RJ Genome Biol 01-May-2017
PMCID:PMC5410703
doi:10.1186/s13059-017-1195-1
PMID:28457232
Rate heterogeneity in six protein-coding genes from the holoparasite Balanophora (Balanophoraceae) and other taxa of Santalales Su HJ, Hu JM Ann Bot 21-Sep-2012
PMCID:PMC3478055
doi:10.1093/aob/mcs197
PMID:23041381
Pharmacognostical Studies on Balanophora fungosa - a Negative Listed Plant Kannan R, Babu UV Anc Sci Life 01-Jul-2011
PMCID:PMC3377038
PMID:22736886
Melanin synthesis inhibitors from Balanophora fungosa. Ogi T, Higa M, Maruyama S J Agric Food Chem 23-Feb-2011
doi:10.1021/JF1035542
PMID:21265535
Galloyl and hexahydroxydiphenoyl esters of phenylpropanoid glucosides, phenylpropanoids and phenylpropanoid glucosides from rhizome of Balanophora fungosa. Panthama N, Kanokmedhakul S, Kanokmedhakul K Chem Pharm Bull (Tokyo) 01-Dec-2009
doi:10.1248/CPB.57.1352
PMID:19952443
Ethnobotanical investigations among tribes in Madurai District of Tamil Nadu (India) Ignacimuthu S, Ayyanar M, Sivaraman K S J Ethnobiol Ethnomed 11-May-2006
PMCID:PMC1475842
doi:10.1186/1746-4269-2-25
PMID:16689985

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
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol 12309636 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1248/CPB.57.1352
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1248/CPB.57.1352
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1248/CPB.57.1352
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1248/CPB.57.1352
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
[11-Ethyl-4,8,17-trihydroxy-16-methoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-6-yl] 4-methoxybenzoate 162922262 Click to see CCN1CC2(CCC(C34C1C(CC23O)C5(CC(C6CC4C5C6O)OC(=O)C7=CC=C(C=C7)OC)O)OC)COC 557.70 unknown https://doi.org/10.1248/CPB.57.1352
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) hexadecanoate 13915598 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1248/CPB.57.1352
[(3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] hexadecanoate 137705088 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1248/CPB.57.1352
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.57.1352
beta-Amyrin palmitate 13915599 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1248/CPB.57.1352
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1248/CPB.57.1352
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.57.1352
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/10.1248/CPB.57.1352
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1248/CPB.57.1352
Lupeol palmitate 161739 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1248/CPB.57.1352
Sambuculin a 14486636 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1248/CPB.57.1352
> 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.57.1352
24-Ethylcholest-5-en-3beta-ol 22012 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.57.1352
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.57.1352
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(e)-caffeyl alcohol 4-O-beta-d-glucopyranoside 101273492 Click to see C1=CC(=C(C=C1C=CCO)O)OC2C(C(C(C(O2)CO)O)O)O 328.31 unknown https://doi.org/10.1248/CPB.57.1352
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 3496897 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1021/JF1035542
2-[2-Hydroxy-4-(3-hydroxyprop-1-enyl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162883796 Click to see C1=CC(=C(C=C1C=CCO)O)OC2C(C(C(C(O2)CO)O)O)O 328.31 unknown https://doi.org/10.1248/CPB.57.1352
3-[4-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]prop-2-enoic acid 69029049 Click to see C1=CC(=CC=C1C=CC(=O)O)C2C(C(C(C(O2)CO)O)O)O 310.30 unknown https://doi.org/10.1248/CPB.57.1352
3-[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 73208527 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1248/CPB.57.1352
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1248/CPB.57.1352
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1248/CPB.57.1352
https://doi.org/10.1021/JF1035542
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(3S)-6-methoxy-3-[(3S)-6-methoxy-3,4-dihydro-2H-chromen-3-yl]-3,4-dihydro-2H-chromene 162990341 Click to see COC1=CC2=C(C=C1)OCC(C2)C3CC4=C(C=CC(=C4)OC)OC3 326.40 unknown https://doi.org/10.1248/CPB.57.1352
6-methoxy-3-(6-methoxy-3,4-dihydro-2H-chromen-3-yl)-3,4-dihydro-2H-chromene 78384604 Click to see COC1=CC2=C(C=C1)OCC(C2)C3CC4=C(C=CC(=C4)OC)OC3 326.40 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
3-Phenyl-2-propenoic acid methyl ester 7644 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1248/CPB.57.1352
Methyl cinnamate 637520 Click to see COC(=O)C=CC1=CC=CC=C1 162.18 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters / O-cinnamoyl glycosides
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-phenylprop-2-enoate 3340171 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O 310.30 unknown https://doi.org/10.1248/CPB.57.1352
1-O-trans-Cinnamoyl-beta-D-glucopyranose 5280653 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O 310.30 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1248/CPB.57.1352
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 4484225 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O)O 342.30 unknown https://doi.org/10.1248/CPB.57.1352
https://doi.org/10.1021/JF1035542
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 72983454 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown https://doi.org/10.1248/CPB.57.1352
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate 72727649 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 326.30 unknown https://doi.org/10.1248/CPB.57.1352
[5-Hydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-3,4-bis[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 75079316 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)COC(=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)O 782.60 unknown https://doi.org/10.1248/CPB.57.1352
[6-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-5-hydroxy-3,4-bis[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 75079317 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)COC(=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)O)O 798.60 unknown https://doi.org/10.1021/JF1035542
https://doi.org/10.1248/CPB.57.1352
1-Caffeoyl-beta-D-glucose 5281761 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O)O 342.30 unknown https://doi.org/10.1248/CPB.57.1352
https://doi.org/10.1021/JF1035542
1-O-(4-Coumaroyl)-beta-D-glucose 14158117 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 326.30 unknown https://doi.org/10.1248/CPB.57.1352
1-O-feruloyl-beta-D-glucose 13962928 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown https://doi.org/10.1248/CPB.57.1352
galloyl(-3)[galloyl(-4)][galloyl(-6)]Glc(b)-O-coumaroyl 44604060 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)COC(=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)O 782.60 unknown https://doi.org/10.1248/CPB.57.1352
galloyl(-3)[galloyl(-4)][galloyl(-6)]Glc(b)-O-coumaroyl(3-OH) 44604061 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)COC(=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)O)O 798.60 unknown https://doi.org/10.1248/CPB.57.1352
https://doi.org/10.1021/JF1035542
galloyl(-3)Glc(b)-O-coumaroyl(3-OH) 11730725 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 494.40 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1248/CPB.57.1352
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Tannins
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(E)-3-phenylprop-2-enoyl]oxyoxan-3-yl] 3,4,5-trihydroxybenzoate 44604129 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.57.1352
[4,5-Dihydroxy-2-(hydroxymethyl)-6-(3-phenylprop-2-enoyloxy)oxan-3-yl] 3,4,5-trihydroxybenzoate 75079345 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 462.40 unknown https://doi.org/10.1248/CPB.57.1352
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,11,12,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl) 3-(3,4-dihydroxyphenyl)prop-2-enoate 85311492 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 644.50 unknown https://doi.org/10.1248/CPB.57.1352
(3,4,5,11,12,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl) 3-(4-hydroxyphenyl)prop-2-enoate 85307165 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=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 628.50 unknown https://doi.org/10.1248/CPB.57.1352
[(10S,11R,12R,13S,15R)-13-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3,4,5,12,21,22,23-heptahydroxy-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 163185211 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=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 796.60 unknown https://doi.org/10.1248/CPB.57.1352
[(10S,11S,12R,13S,15R)-3,4,5,11,12,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 163195023 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 644.50 unknown https://doi.org/10.1248/CPB.57.1352
[(10S,11S,12R,13S,15R)-3,4,5,11,12,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163191241 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=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 628.50 unknown https://doi.org/10.1248/CPB.57.1352
[(10S,11S,12R,13S,15R)-3,4,5,12,21,22,23-heptahydroxy-13-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-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 163193770 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=CC=C(C=C3)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 780.60 unknown https://doi.org/10.1248/CPB.57.1352
[(10S,11S,12R,13S,15R)-3,4,5,12,21,22,23-heptahydroxy-8,18-dioxo-13-[(E)-3-phenylprop-2-enoyl]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 163187872 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=CC=CC=C3)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 764.60 unknown https://doi.org/10.1248/CPB.57.1352
[13-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-3,4,5,12,21,22,23-heptahydroxy-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 85389056 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=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 796.60 unknown https://doi.org/10.1021/JF1035542
https://doi.org/10.1248/CPB.57.1352
[3,4,5,12,21,22,23-Heptahydroxy-13-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-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 75079315 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=CC=C(C=C3)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 780.60 unknown https://doi.org/10.1248/CPB.57.1352
[3,4,5,12,21,22,23-Heptahydroxy-8,18-dioxo-13-(3-phenylprop-2-enoyloxy)-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 75079344 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=CC=CC=C3)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 764.60 unknown https://doi.org/10.1248/CPB.57.1352
1-O-Caffeoyl-3-O-galloyl-4,6-(S)-hexahydroxydiphen 11072809 Click to see C1C2C(C(C(C(O2)OC(=O)C=CC3=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 796.60 unknown https://doi.org/10.1021/JF1035542

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