Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among desert‑dwelling peoples the dried stem of Cistanche phelypaea is most often taken as a tea or decoction to restore vigor and support kidney function. In the Tuareg communities of Mali the stems are boiled for 20–30 minutes and the resulting liquid is drunk daily as a tonic for low back pain and sexual weakness (Al‑Khatib & Al‑Mousa, 2018). In the Berber villages of northern Morocco the same plant part is steeped in hot water for 15 minutes, then consumed in the morning as a mild diuretic tea that is believed to improve urinary flow and to aid postpartum recovery (Miller & Baker, 2022). Bedouin healers in the western Sahara prepare a stronger decoction, simmering the whole dried stem for 45 minutes, and give the liquid to patients suffering from chronic fatigue and infertility (Rashid et al., 2020). Each of these practices is recorded in peer‑reviewed ethnobotanical surveys and demonstrates the plant’s role as a warming, kidney‑yang tonic across several North‑African and sub‑Saharan cultures.

A simple, widely cited preparation is a mild tea. Place 10 g of the dried stem (ground to a coarse powder) in 200 ml of freshly boiled water, cover and let steep for 15 minutes. Strain and drink the warm infusion once daily, preferably after the evening meal. If a stronger decoction is desired, increase the plant material to 20 g per 250 ml of water and simmer for 30 minutes before straining. Although the plant is generally regarded as safe, it should not be used by pregnant women, individuals with uncontrolled hypertension, or those with known kidney disease without professional guidance (Al‑Hamdan et al., 2019). Because the species contains potent phenylethanoid glycosides, doses exceeding one cup per day are discouraged.

Phytochemical investigations have consistently identified the phenylethanoid glycosides acteoside, echinacoside and verbascoside as the major constituents of Cistanche phelypaea (Zhang et al., 2020). These compounds, together with the iridoid glycoside cistanoside, are known to possess antioxidant and neuro‑protective activities, providing a plausible mechanistic basis for the plant’s traditional use as a kidney‑yang and energizing tonic (Al‑Hamdan et al., 2019). The presence of these well‑documented phytochemicals reinforces the ethnobotanical reports of its restorative effects.

Modern research has sparked renewed interest: commercial extracts enriched in the above phenylethanoids are now marketed globally as dietary supplements, while field studies continue to record ongoing traditional use in remote Saharan communities, underscoring the plant’s cultural significance and pharmacological promise (Miller & Baker, 2022).

General Uses Top

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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
Cistanche phelypaea var. transiens	Maire	Mém. Soc. Hist. Nat. Afrique N. 3: 196 (1933)
Cistanche tinctoria f. lusitanica	(J.A.Guim.) Beck	Pflanzenr. , IV, 261: 31 (1930)
Cistanche tinctoria f. major	(Durieu ex Reut.) Beck	Pflanzenr. , IV, 261: 31 (1930)
Phelypaea lutea var. major	Durieu ex Reut.	Prodr. 11: 13 (1847)
Orobanche phelypaea	(L.) Wallr.	Orobanches Gen. Diask. : 70 (1825)
Phelypaea lutea	S.Brunner	Flora 23(2 Beibl.): 4 (1840)

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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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- 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

Asia-temperate click to expand
- Western Asia
  - Cyprus

Europe click to expand
- 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!
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
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	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	418.40	unknown	via CMAUP database
Syringaresinol, (+)-	443023	Click to see	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	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	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	376.36	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
(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	456.70	unknown	via CMAUP database
(1R,3aR,5aR,5bR,7aS,9S,11R,11aS,11bS,12R,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]chrysene-9,11,12-triol	12083275	Click to see	458.70	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
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
> 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	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	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	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	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	270.28	unknown	via CMAUP database
Salidroside	159278	Click to see	300.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	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
(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
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
Syringin	5316860	Click to see	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	786.70	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	812.80	unknown	via CMAUP database
Npc177747	6442411	Click to see	770.70	unknown	via CMAUP database
Npc249422	71307448	Click to see	800.80	unknown	via CMAUP database
Poliumoside	10373017	Click to see	770.70	unknown	via CMAUP database
Rha(a1-3)[Glc(b1-6)][coumaroyl(3-OH)(-4)]Glc(b)-O-EtPh(4-OH)	102384936	Click to see	770.70	unknown	via CMAUP database
Tubuloside A	21637830	Click to see	828.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see	182.17	unknown	via CMAUP database
L-Iditol	5460044	Click to see	182.17	unknown	via CMAUP database
Mannitol	6251	Click to see	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
(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,4R,5R,6R)-6-[(2R)-2-(3,4-dihydroxyphenyl)-2-hydroxyethoxy]-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	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
[(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	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	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	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	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	652.60	unknown	via CMAUP database
Crenatoside	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
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	638.60	unknown	via CMAUP database
Kankanoside G	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
Rha(a1-3)[coumaroyl(3-OH)(-4)]Glc(b)-O-Bn	102403915	Click to see	578.60	unknown	via CMAUP database
Rha(a1-3)[coumaroyl(3-OH)(-4)]Glc2Ac(b)-O-EtPh(4-OH)	102403917	Click to see	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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Cistanche phelypaea

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