Cistanche phelypaea - Unknown
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Internal ID UUID64401175d1b0e987464846
Scientific name Cistanche phelypaea
Authority (L.) Cout.
First published in Fl. Portugal : 571 (1913)

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Synonyms Top

Scientific name Authority First published in
Lathraea phelypaea L. Sp. Pl. : 606 (1753)
Phelypaea senegalensis Reut. Prodr. 11: 13 (1847)
Phelypaea tinctoria Walp. Repert. Bot. Syst. (Walpers) iii. 462.
Phelypaea brunneri Webb Niger Fl. : 167 (1849)
Phelypaea lusitanica Coss. Notes Pl. Crit. : 43 (1949)
Phelypaea hesperugo Webb Niger Fl. : 167 (1849)
Cistanche allochroa Chiov. Res. Sci. Somalia Ital. 1: 131 (1916)
Cistanche brunneri (Webb) Bég. Pflanzenr. (Engler) Orobanchac. 35. 1930 [9 Sep 1930]
Cistanche hesperugo (Webb) Beck Pflanzenr. , IV, 261: 35 (1930)
Cistanche lusitanica J.A.Guim. Brotéria 3: 190 (1904)
Cistanche lutea Wight Ill. Ind. Bot. ii. 180. t. 158. b. f. 4.
Cistanche lutea f. minor Bég. Ann. Mus. Civico Storia Nat. "Giacomo Doria" III, 8: 47 1920
Cistanche senegalensis (Reut.) Beck Pflanzenr. , IV, 261: 33 (1930)
Cistanche tubulosa (Schenk) Wight Icon. Pl. Ind. Orient. [Wight] t. 1420 bis.
Cistanche tubulosa f. albiflora Gilli Publ. Cairo Univ. Herb. 5: 87. 1974 [1972 publ. 1974]
Cistanche tubulosa var. tomentosa Hook.f. Fl. Brit. India [J. D. Hooker] 4(pt. 11): 324. 1884 [Jan 1884]
Phelipaea lutea Desf. Fl. Atlant. 2: 60, pl. 146 1798

Common names Top

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Language Common/alternative name
English yellow broomrape
German gelbe cistanche

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Africa
    • Macaronesia
      • Canary Islands
      • Cape Verde
      • Selvagens
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Benin
      • Mali
      • Mauritania
      • Niger
      • Senegal
  • Europe
    • Southeastern Europe
      • Italy
      • Kriti
    • Southwestern Europe
      • France
      • Portugal
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000607105
Tropicos 23600009
INPN 91622
KEW urn:lsid:ipni.org:names:661964-1
The Plant List kew-2723172
Open Tree Of Life 675210
Observations.org 138478
NCBI Taxonomy 87754
IPNI 661964-1
iNaturalist 342011
GBIF 7332229
EPPO CJTPH
EOL 3013110
Wikipedia Cistanche_phelypaea
CMAUP NPO6964

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
Effects of genus Epimedium in the treatment of osteoarthritis and relevant signaling pathways Tong X, Wang Y, Dong B, Li Y, Lang S, Ma J, Ma X Chin Med 31-Jul-2023
PMCID:PMC10388486
doi:10.1186/s13020-023-00788-8
PMID:37525296
Diversity and potential plant growth promoting capacity of seed endophytic bacteria of the holoparasite Cistanche phelypaea (Orobanchaceae) Petrosyan K, Thijs S, Piwowarczyk R, Ruraż K, Kaca W, Vangronsveld J Sci Rep 22-Jul-2023
PMCID:PMC10363106
doi:10.1038/s41598-023-38899-9
PMID:37481658
Controlled Drug Release from Nanoengineered Polysaccharides Bayer IS Pharmaceutics 28-Apr-2023
PMCID:PMC10221078
doi:10.3390/pharmaceutics15051364
PMID:37242606
Iridoid Derivatives as Anticancer Agents: An Updated Review from 1970–2022 Ndongwe T, Witika BA, Mncwangi NP, Poka MS, Skosana PP, Demana PH, Summers B, Siwe-Noundou X Cancers (Basel) 26-Jan-2023
PMCID:PMC9913650
doi:10.3390/cancers15030770
PMID:36765728
Vascular Plants from the Journey through Portugal (1797–1801) by Hoffmannsegg and Link at the Herbarium of the Real Jardín Botánico of Madrid Medina L, Aedo C Plants (Basel) 19-Sep-2022
PMCID:PMC9501163
doi:10.3390/plants11182438
PMID:36145838
Structural mutations of small single copy (SSC) region in the plastid genomes of five Cistanche species and inter-species identification Miao Y, Chen H, Xu W, Yang Q, Liu C, Huang L BMC Plant Biol 25-Aug-2022
PMCID:PMC9404617
doi:10.1186/s12870-022-03682-x
PMID:36008757
In vitro characterization of iridoid and phenylethanoid glycosides from Cistanche phelypaea for nutraceutical and pharmacological applications Delicato A, Masi M, de Lara F, Rubiales D, Paolillo I, Lucci V, Falco G, Calabrò V, Evidente A Phytother Res 03-Jul-2022
PMCID:PMC9796874
doi:10.1002/ptr.7548
PMID:35781895
Endophytes and Halophytes to Remediate Industrial Wastewater and Saline Soils: Perspectives from Qatar Yasseen BT, Al-Thani RF Plants (Basel) 02-Jun-2022
PMCID:PMC9182595
doi:10.3390/plants11111497
PMID:35684269
Plant Parasites under Pressure: Effects of Abiotic Stress on the Interactions between Parasitic Plants and Their Hosts Zagorchev L, Stöggl W, Teofanova D, Li J, Kranner I Int J Mol Sci 10-Jul-2021
PMCID:PMC8304456
doi:10.3390/ijms22147418
PMID:34299036
Targeted enrichment of novel chloroplast-based probes reveals a large-scale phylogeny of 412 bamboos Wang J, Mu W, Yang T, Song Y, Hou YG, Wang Y, Gao Z, Liu X, Liu H, Zhao H BMC Plant Biol 05-Feb-2021
PMCID:PMC7863319
doi:10.1186/s12870-020-02779-5
PMID:33546593
Comparative Studies of Fraxinus Species from Korea Using Microscopic Characterization, Phytochemical Analysis, and Anti-Lipase Enzyme Activity Akter KM, Park WS, Kim HJ, Khalil AA, Ahn MJ Plants (Basel) 20-Apr-2020
PMCID:PMC7238101
doi:10.3390/plants9040534
PMID:32326102
Interspecific variations in the habitats of Reichardia tingitana (L.) Roth leading to changes in its bioactive constituents and allelopathic activity Abd-ElGawad AM, El-Amier YA, Assaeed AM, Al-Rowaily SL Saudi J Biol Sci 25-Nov-2019
PMCID:PMC6933205
doi:10.1016/j.sjbs.2019.11.015
PMID:31889875
Extensive plastome reduction and loss of photosynthesis genes in Diphelypaea coccinea, a holoparasitic plant of the family Orobanchaceae Gruzdev EV, Kadnikov VV, Beletsky AV, Mardanov AV, Ravin NV PeerJ 02-Oct-2019
PMCID:PMC6778433
doi:10.7717/peerj.7830
PMID:31592357
Phylogenetic Relationships in Orobanchaceae Inferred From Low-Copy Nuclear Genes: Consolidation of Major Clades and Identification of a Novel Position of the Non-photosynthetic Orobanche Clade Sister to All Other Parasitic Orobanchaceae Li X, Feng T, Randle C, Schneeweiss GM Front Plant Sci 16-Jul-2019
PMCID:PMC6646720
doi:10.3389/fpls.2019.00902
PMID:31379896
The complete chloroplast genome of the endangered species Triaenophora shennongjiaensis (Orobanchaceae s.l.) Xia Z, Wen J Mitochondrial DNA B Resour 26-Apr-2018
PMCID:PMC7799507
doi:10.1080/23802359.2018.1467242
PMID:33474222

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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
4-Hydroxybenzene ethanol 17785442 Click to see CCO.C1=CC=C(C=C1)O 140.18 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-) Syringaresinol 332426 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
8-Hydroxy geraniol 6430784 Click to see CC(=CCO)CCCC(=C)CO 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Panaxytriol 93484 Click to see CCCCCCCC(C(CC#CC#CC(C=C)O)O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
2,6-Dimethyl-2,6-octadiene-1,8-diol, (2E,6E)- 5363397 Click to see CC(=CCO)CCC=C(C)CO 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganic acid 158144 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
Adoxosidic acid 13892717 Click to see C1CC2C(C1CO)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown via CMAUP database
Geniposidic acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11R,11aS,11bS,12R,13aR,13bR)-11,12-dihydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 13969547 Click to see CC(=C)C1CCC2(C1C3CC(C4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)O)C 456.70 unknown via CMAUP database
20(29)-Lupene-1beta,3beta-diol 488250 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Nepetidin 12083275 Click to see CC(=C)C1CCC2(C1C3CC(C4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)O)C 458.70 unknown via CMAUP database
Sumaresinol 12443148 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)C)O)C)O)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 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
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
1-((2r,5r)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1h-pyrimidine-2,4-dione 45356795 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see C[N+](C)(C)CC(=O)[O-] 117.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown via CMAUP database
6-Deoxycatalpol 14729927 Click to see C1C2C=COC(C2C3(C1O3)CO)OC4C(C(C(C(O4)CO)O)O)O 346.33 unknown via CMAUP database
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown via CMAUP database
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Coniferin 91895380 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
(Z)-Syringin 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
Androsin 164648 Click to see CC(=O)C1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 328.31 unknown via CMAUP database
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44429857 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 786.70 unknown via CMAUP database
[6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 6442411 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)C)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 770.70 unknown via CMAUP database
Cistanbuloside A 102384936 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC=C(C=C5)O)O)O)O)O 770.70 unknown via CMAUP database
Cistanoside 71307448 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCC3C(C(C(C(O3)OCCC4=CC(=C(C=C4)O)OC)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)CO)O)O)O)O 800.80 unknown via CMAUP database
Echinacoside 5281771 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 786.70 unknown via CMAUP database
Kankanoside H1 46228746 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O)O 812.80 unknown via CMAUP database
Poliumoside 10373017 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)C)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 770.70 unknown via CMAUP database
Tubuloside A 21637830 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 828.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
L-Iditol 5460044 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
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide 936 Click to see C1=CC(=CN=C1)C(=O)N 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(R)-Campneoside II 102000758 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCC(C4=CC(=C(C=C4)O)O)O)O)O)O)O 640.60 unknown via CMAUP database
(S)-Campneoside II 102000759 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCC(C4=CC(=C(C=C4)O)O)O)O)O)O)O 640.60 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]-4-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]methoxy]oxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44205526 Click to see CC1C(C(C(C(O1)COC2C(C(OC(C2O)OCCC3=CC=C(C=C3)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 622.60 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-(hydroxymethyl)-4-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]methoxy]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 46228750 Click to see CC1C(C(C(C(O1)COC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 680.60 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]methoxy]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 46228751 Click to see CC1C(C(C(C(O1)COC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 842.80 unknown via CMAUP database
[(2R,3R,4S,5R,6R)-5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3-hydroxy-4-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]methoxy]oxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 46228758 Click to see CC1C(C(C(C(O1)COC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 680.60 unknown via CMAUP database
[(2R,3R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 45358104 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
[5-acetyloxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)methoxy]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 56667837 Click to see CC1C(C(C(C(O1)COC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 842.80 unknown via CMAUP database
[6-[2-(3,4-Dihydroxyphenyl)-2-hydroxyethoxy]-5-hydroxy-2-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 85091108 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCC(C4=CC(=C(C=C4)O)O)O)O)O)O)O 640.60 unknown via CMAUP database
2-Acetylacteoside 21629996 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC(=C(C=C3)O)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 666.60 unknown via CMAUP database
beta-Hydroxyacteoside 10009317 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCC(C4=CC(=C(C=C4)O)O)O)O)O)O)O 640.60 unknown via CMAUP database
Cistanoside D 5315930 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)OC)O)O)O)O 652.60 unknown via CMAUP database
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
Isocistanoside C 72707180 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 638.60 unknown via CMAUP database
Orobanchoside 44593361 Click to see CC1C(C(C(C(O1)OC2C3C(OCC(O3)C4=CC(=C(C=C4)O)O)OC(C2OC(=O)C=CC5=CC(=C(C=C5)O)O)CO)O)O)O 622.60 unknown via CMAUP database
Salsaside B 102403915 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCC4=CC=CC=C4)O)O)O)O 578.60 unknown via CMAUP database
Salsaside D 102403917 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCCC3=CC=C(C=C3)O)CO)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O 650.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
osmanthuside B 10438425 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC=C(C=C3)O)CO)OCCC4=CC=C(C=C4)O)O)O)O)O 592.60 unknown via CMAUP database

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