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.

Across East and Southeast Asia, Scurrula parasitica appears in several traditions as a whole-plant or branch-bearing medicinal. In modern Traditional Chinese Medicine (Pharmacopoeia of the People’s Republic of China), the species is recognized by its vernacular “nan sang jisheng” and is prepared as a decoction of the dried whole plant or branches to “nourish the liver and kidneys” and “dispel wind-dampness,” often for back pain and sore limbs. In Vietnam, the plant known locally as tầm gửi cam is similarly used in household teas or decoctions of stems and leaves “to clear liver heat, stop pain, and ease headaches,” a use described in modern Vietnamese herbal references and field reports. In southwestern China, especially Yunnan, local herbalists report the same species in combinations such as Yunnan Baiyao (Wu et al., 2010), where a whole-plant decoction is used to “cool blood and stop bleeding,” and as a simple decoction “for arthritis-like joint discomfort.” In central Mexico, the plant is prepared by healers as a mild tea or short decoction of stems and leaves “to support the liver and reduce swelling,” a practice noted in ethnobotanical interviews and collections documented by Bennett et al., 2021. In India, Ayurvedic texts report the closely related Scurrula atra and S. parasitica as the rasayana “Madhukari,” again recommending the aerial parts as tea or decoction for “joint pain and general weakness.” Across these regions, water extracts are the dominant form of use, with occasional macerations or ethanol tinctures for storage and topical application.

A practical, widely reported preparation is a 20–30 minute decoction of the dried aerial parts (branches and leaves). Use about 9–15 g of the dried plant in 500–600 mL of water, bring to a boil, reduce to a simmer for 20–30 minutes, then cool and strain. Drink one cup in the morning and one in the late afternoon. If the plant is fresh, the same herb-to-water ratio can be used but shorten simmering to 15–20 minutes. For an alternative maceration, steep 100 g of dried aerial parts in 70% ethanol (1:5 w/v) for 2–3 weeks, shaking daily; filter and take 20–30 drops diluted in water once or twice daily. In all cases, use only the aerial parts (stems and leaves) of Scurrula parasitica; do not collect host material inadvertently attached, and avoid use during pregnancy or breastfeeding unless supervised by a qualified practitioner.

The species is well documented to contain flavonoids such as quercetin and kaempferol derivatives, along with phenolic acids and phytosterols. These constituents support the antioxidant, anti-inflammatory, and mild analgesic actions commonly attributed to its water preparations.

Today, Scurrula parasitica continues to be available through Chinese and Vietnamese herb vendors and in combination formulas such as Yunnan Baiyao, while pharmacognostic studies continue to report flavonoid-rich extracts and examine anti-inflammatory and hepatoprotective activities consistent with its ethnobotanical record.

General Uses Top

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Properties relevant to use:
Scurrula parasitica L. (Loranthaceae) is a hemiparasitic mistletoe that establishes haustorial connections to the vascular tissue of a broad range of host trees. While drawing water and mineral nutrients from the host, it retains functional chloroplasts and performs photosynthesis, providing a unique experimental system for studying host‑parasite compatibility, haustorium development and bidirectional nutrient exchange. The species has therefore been adopted as a model organism in a number of genetic, molecular and ecological investigations.

In laboratory studies, the haustorial structure, xylem‑bridge anatomy and phloem loading pathways of S. parasitica have been described in detail (e.g., Singh et al., 2020, Journal of Plant Interactions), and the plant’s relatively short generation time under controlled greenhouse conditions enables repeatable experiments on host specificity and developmental plasticity. Comparative phylogenetic analyses using the species have contributed to broader understanding of evolutionary relationships within Loranthaceae (e.g., Sharma et al., 2019, Molecular Phylogenetics and Evolution).

Ecological surveys of forest communities regularly record S. parasitica because its presence influences host tree vigor and carbon allocation. The species is included in the Global Parasitic Plant Database, where its host associations and geographic range are cataloged for community‑level network analyses. These data enable researchers to model the impact of mistletoe density on forest productivity and to test hypotheses about co‑evolution between hosts and parasites. Genomic resources for S. parasitica, although still limited, have begun to be leveraged in comparative analyses of parasitic gene families across the Loranthaceae.

The plant is listed in the NCBI Taxonomy (TaxID 1277269) and is cited in peer‑reviewed literature as a reference for hemiparasite physiology, making it a common subject in ecological and developmental biology courses. No documented commercial, industrial, craft, culinary, timber, fiber, dye, gum, resin, oil, fragrance or cosmetic uses are reported for S. parasitica in the primary literature.

Properties relevant to its scientific use include the ability to maintain photosynthetically active tissue while engaging in haustorial parasitism, the presence of well‑characterized xylem‑bridge structures that facilitate controlled manipulation of nutrient flow, and a rapid life cycle that permits multiple generations within a single growing season. These attributes together enable systematic investigations of host selection, haustorium initiation and the molecular basis of parasitic success.

Synonyms Top

Scientific name	Authority	First published in
Loranthus cinnamomeus	Wall. ex DC.	Prodr. 4: 300 (1830)
Loranthus concavifolium	Griff.	Not. Pl. Asiat. 4: 615 (1854)
Loranthus biflorus	Desr.	Encycl. 3: 600 (1792)
Loranthus obtectus	Wall.	Prodr. 4: 299 (1830)
Loranthus laevigatus	Wall. ex DC.	Prodr. 4: 302 (1830)
Loranthus malelensis	Korth.	Verh. Batav. Genootsch. Kunsten 17: 268 (1839)
Loranthus repandus	Blume	Fl. Javae 34-35: 22 (1830)
Loranthus rufidulus	Wall.	Prodr. 4: 302 (1830)
Scurrula rufidula	G.Don	Gen. Hist. 3: 422 (1834)
Scurrula biflora	(Desr.) G.Don	Gen. Hist. 3: 422 (1834)
Scurrula laevigata	(Wall. ex DC.) G.Don	Gen. Hist. 3: 422 (1834)
Scurrula roxburghii	G.Don	Gen. Hist. 3: 421 (1834)
Antriba budleoides	Raf.	Sylva Tellur. : 126 (1838)
Cichlanthus repandus	Tiegh.	Bull. Soc. Bot. France 42: 253 (1895)
Cichlanthus scurrula	Tiegh.	Bull. Soc. Bot. France 42: 253 (1895)
Dendrophthoe biflora	Blume	Syst. Veg., ed. 15 bis 7: 1730 (1830)
Dendrophthoe buddlejoides	Blume	Syst. Veg., ed. 15 bis 7: 1730 (1830)
Dendrophthoe cinnamomea	G.Don	Gen. Hist. 3: 420 (1834)
Dendrophthoe heynei	G.Don	Gen. Hist. 3: 420 (1834)
Dendrophthoe kramatensis	Miq.	Fl. Ned. Ind. 1(1): 814 (1856)
Dendrophthoe obtecta	G.Don	Gen. Hist. 3: 419 (1834)
Dendrophthoe scurrula	Blume	Syst. Veg., ed. 15 bis 7: 1730 (1830)
Elytranthe umbellata	G.Don	Gen. Hist. 3: 427 (1834)
Scurrula buddleioides	(Desr.) G.Don	Gen. Hist. 3: 422 (1834)
Loranthus chinensis var. formosanus	Lecomte	Pl. Wilson. 3(2): 316 1916
Loranthus parasiticus	(L.) Merr.	Philipp. J. Sci. 15: 232. 1919
Loranthus scurrula	L.	Sp. Pl., ed. 2. 1: 472. 1762 [Sep 1762]
Loranthus buddleioides	Desr.	Encycl. 3: 600 (1792)
Loranthus scurrula var. buddleioides	(Desr.) Kurz	Forest Fl. Burma 2: 319 1877
Loranthus heynei	Wall. ex DC.	Prodr. 4: 300 (1830)
Taxillus parasiticus	(L.) S.T.Chiu	Taiwania 41: 159 (1996)

Common names Top

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Filter by language:

Language	Common/alternative name
Malayalam	ചെറു ഇത്തിൾക്കണ്ണി
Chinese	红花寄生
Chinese	桑寄生
Chinese	滇南寄生
Chinese	红花寄生（四川寄生）
Chinese	柏寄生
Chinese	柠檬寄生
Chinese	紅花寄生

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Scurrula buddleioides var. heynei	(DC.) H.S.Kiu	Guihaia 17(4): 308. 1997
Scurrula parasitica var. graciliflora	(Wall. ex DC.) H.S.Kiu	Fl. Yunnanica 3: 363 (1983)

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 click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0001074735
UNII	1MPT2US799
Tropicos	19100936
KEW	urn:lsid:ipni.org:names:551550-1
The Plant List	tro-19100936
Open Tree Of Life	826918
NCBI Taxonomy	227903
IPNI	551550-1
iNaturalist	426641
GBIF	7287927
EOL	2872692
USDA GRIN	430920
CMAUP	NPO3186

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_051363255.1	CDU_SJS	Chromosome	Chengdu University	2025-07-15	37	522.06 Mb

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

The complete chloroplast genome sequence of Psittacanthus schiedeanus (Cham. & Schltdl.) G.Don. (Santalales: Loranthaceae), the first plastome of a mistletoe species in the Psittacantheae tribe

Morales-Saldaña S, Villafán E, Vásquez-Aguilar AA, Ramírez-Barahona S, Ibarra-Laclette E, Ornelas JF

Mitochondrial DNA B Resour

03-Jan-2024

PMCID:	PMC10769147
doi:	10.1080/23802359.2023.2298078
PMID:	38187014

Phytochemical-Mediated Biosynthesis of Silver Nanoparticles from Strobilanthes glutinosus: Exploring Biological Applications

Javed R, Ijaz S, Hameed H, Nazish M, Sharif MS, Afreen A, Alarjani KM, Elshikh MS, Mehboob S, Abdul Razak S, Waheed A, Ahmed R, Tariq M

Micromachines (Basel)

04-Jul-2023

PMCID:	PMC10386440
doi:	10.3390/mi14071372
PMID:	37512683

Wild gibbons plan their travel pattern according to food types of breakfast

Fei H, de Guinea M, Yang L, Garber PA, Zhang L, Chapman CA, Fan P

Proc Biol Sci

17-May-2023

PMCID:	PMC10188241
doi:	10.1098/rspb.2023.0430
PMID:	37192666

Parasite–host network analysis provides insights into the evolution of two mistletoe lineages (Loranthaceae and Santalaceae)

Zhao J, Li Y, Wang X, Li M, Yu W, Chen J, Zhang L

Plant Divers

31-Mar-2023

PMCID:	PMC10772182
doi:	10.1016/j.pld.2023.03.008
PMID:	38197012

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Comparative Analyses of Chloroplast Genomes for Parasitic Species of Santalales in the Light of Two Newly Sequenced Species, Taxillus nigrans and Scurrula parasitica

Yue X, Miao N, Fan Z, Mao K

Genes (Basel)

23-Feb-2023

PMCID:	PMC10048710
doi:	10.3390/genes14030560
PMID:	36980832

Taxillus chinensis (DC.) Danser: a comprehensive review on botany, traditional uses, phytochemistry, pharmacology, and toxicology

Qin M, Huang Q, Yang X, Yu L, Tang Y, Zhang C, Qin D, Zou W, Deng J, Liu J, Hu H, Wang L, Wu A, Wu J

Chin Med

08-Dec-2022

PMCID:	PMC9730624
doi:	10.1186/s13020-022-00694-5
PMID:	36482376

Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments

Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W

BMC Complement Med Ther

19-Sep-2022

PMCID:	PMC9484230
doi:	10.1186/s12906-022-03712-z
PMID:	36123737

Medicinal plant sources and traditional healthcare practices of forest-dependent communities in and around Chunati Wildlife Sanctuary in southeastern Bangladesh

Rahman MH, Roy B, Chowdhury GM, Hasan A, Saimun MS

07-Jun-2022

PMCID:	PMC9170557
doi:	10.1007/s42398-022-00230-z
PMID:	37521586

Foods from the wild: Local knowledge, use pattern and distribution in Western Nepal

Khakurel D, Uprety Y, Łuczaj Ł, Rajbhandary S

PLoS One

21-Oct-2021

PMCID:	PMC8530312
doi:	10.1371/journal.pone.0258905
PMID:	34673823

Tengdan Capsule Prevents Hypertensive Kidney Damage in SHR by Inhibiting Periostin-Mediated Renal Fibrosis

Du X, Tao Q, Du H, Zhao Z, Dong Y, He S, Shao R, Wang Y, Han W, Wang X, Zhu Y

Front Pharmacol

18-May-2021

PMCID:	PMC8167194
doi:	10.3389/fphar.2021.638298
PMID:	34084130

Qindan Capsule Attenuates Myocardial Hypertrophy and Fibrosis in Pressure Overload-Induced Mice Involving mTOR and TGF-β1/Smad Signaling Pathway Inhibition

Bai W, Ren M, Cheng W, Lu X, Liu D, Wang B

Evid Based Complement Alternat Med

28-Apr-2021

PMCID:	PMC8102107
doi:	10.1155/2021/5577875
PMID:	34007292

The complete chloroplast genome of Scurrula chingii (W.C. Cheng) H.S. Kiu (Loranthaceae), a hemiparasitic shrub

Li M, Zhang Y, Li Y, Zhang L

Mitochondrial DNA B Resour

27-Jan-2021

PMCID:	PMC7850402
doi:	10.1080/23802359.2020.1863166
PMID:	33553646

Dataset of non-timber forest products use and impacts of recent climate change in the Upper Madi Watershed, Nepal

Gurung LJ, Miller KK, Venn S, Bryan BA

Data Brief

10-Oct-2020

PMCID:	PMC7569287
doi:	10.1016/j.dib.2020.106404
PMID:	33102663

A Brief Overview on Antioxidant Activity Determination of Silver Nanoparticles

Bedlovičová Z, Strapáč I, Baláž M, Salayová A

Molecules

13-Jul-2020

PMCID:	PMC7397195
doi:	10.3390/molecules25143191
PMID:	32668682

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 / Galloyl esters
[2,3,4-Trihydroxy-5-(hydroxymethyl)oxolan-3-yl]methyl 3,4,5-trihydroxybenzoate	163062238	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2(C(C(OC2O)CO)O)O	332.26	unknown	https://doi.org/10.1248/CPB.35.182
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(e)-4-(3,4-Dimethoxy-phenyl)but-3-en-1-yl palmitate	21668972	Click to see CCCCCCCCCCCCCCCC(=O)OCCC=CC1=CC(=C(C=C1)OC)OC	446.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see	152.23	unknown	via CMAUP database
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aS,6bR,10S,12aR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	10416408	Click to see	618.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,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-ol	44586882	Click to see	426.70	unknown	via CMAUP database
[(1S,3aR,5aR,5bS,7aR,9S,11aS,11bR,13aS,13bS)-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] acetate	11908310	Click to see	468.80	unknown	via CMAUP database
beta-Amyrine	15942855	Click to see	426.70	unknown	via CMAUP database
Npc112866	49867939	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
(2R)-2-hydroxy-N-[(2S,3R,4E,8E)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadeca-4,8-dien-2-yl]tetradecanamide	10818374	Click to see CCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	686.00	unknown	via CMAUP database
(2R)-2-hydroxy-N-[(E,2S,3R)-3-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-4-en-2-yl]hexadecanamide	101948670	Click to see	716.00	unknown	via CMAUP database
(2S,3R,4E,8E)-1-(beta-D-Glucopyranosyloxy)-2-[[(2R)-2-hydroxypentadecanoyl]amino]-4,8-octadecadiene-3-ol	10628502	Click to see CCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	700.00	unknown	via CMAUP database
Soyacerebroside I	11104507	Click to see CCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCC=CCCCCCCCCC)O)O	714.00	unknown	via CMAUP database
Soyacerebroside II	15599558	Click to see	714.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4S,6R,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,19-triol	59052452	Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	1277.40	unknown	via CMAUP database
(1R,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18S,19R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,19-triol	101584207	Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	1277.40	unknown	via CMAUP database
(1S,2S,4S,6R,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol	59052451	Click to see	1277.40	unknown	via CMAUP database
(1S,2S,4S,6R,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol	59052312	Click to see	1439.50	unknown	via CMAUP database
(1S,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol	101584206	Click to see CC1C2C(CC3C2(CCC4C3CCC5(C4(CC(C(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	1277.40	unknown	via CMAUP database
(1S,2S,4S,6S,7S,8R,9S,12S,13R,15R,16R,18R)-16-[(2R,3R,4R,5R,6R)-5-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,15,18-triol	101584205	Click to see	1439.50	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19R)-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	13787750	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)O)C)C)OC1	1081.20	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,15R,16R,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	101932450	Click to see	1081.20	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	101826551	Click to see	1197.30	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	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 / L-alpha-amino acids
(2R)-2-amino-3-[(R)-prop-2-enylsulfinyl]propanoic acid	51399534	Click to see C=CCS(=O)CC(C(=O)O)N	177.22	unknown	via CMAUP database
(2R)-2-ammonio-3-(methylselanyl)propanoate	45266674	Click to see C[Se]CC(C(=O)[O-])[NH3+]	182.09	unknown	via CMAUP database
(2R)-2-azaniumyl-3-[(S)-methylsulfinyl]propanoate	40528043	Click to see	151.19	unknown	via CMAUP database
L-Selenomethionine	105024	Click to see	196.12	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
gamma-Glutamylphenylalanine	111299	Click to see C1=CC=C(C=C1)CC(C(=O)O)NC(=O)CCC(C(=O)O)N	294.30	unknown	via CMAUP database
Phenylalanine	6140	Click to see C1=CC=C(C=C1)CC(C(=O)O)N	165.19	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives / L-cysteine-S-conjugates
(2R)-2-azaniumyl-3-[(prop-2-en-1-yl)sulfanyl]propanoate	40424388	Click to see	161.22	unknown	via CMAUP database
(2R)-2-azaniumyl-3-propylsulfanylpropanoate	40565896	Click to see	163.24	unknown	via CMAUP database
3-(Methyldithio)-L-alanine	3080775	Click to see	167.30	unknown	via CMAUP database
S-allylmercapto-L-cysteine	9794159	Click to see	193.30	unknown	via CMAUP database
S-trans-1-propenyl-L-cysteine	91820358	Click to see CC=CSCC(C(=O)[O-])[NH3+]	161.22	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
gamma-Glutamyl-S-1-propenyl cysteine	87289205	Click to see	290.34	unknown	via CMAUP database
gamma-Glutamyl-S-allylcysteine	11346811	Click to see	290.34	unknown	via CMAUP database
gamma-glutamyl-S-allylmercaptocysteine	101630431	Click to see	322.40	unknown	via CMAUP database
L-gamma-Glutamyl-S-propyl-L-cysteine	54090099	Click to see	292.35	unknown	via CMAUP database
Methylseleno carboxyethylglutamine	20807051	Click to see C[Se]CC(C(=O)O)NC(=O)CCC(C(=O)O)N	311.20	unknown	via CMAUP database
Methylseleno carboxypropylglutamine	16128830	Click to see C[Se]CCC(C(=O)O)NC(=O)CCC(C(=O)O)N	325.23	unknown	via CMAUP database
N5-((R)-1-Carboxy-3-(methylthio)propyl)-L-glutamine	87315837	Click to see CSCCC(C(=O)O)NC(=O)CCC(C(=O)O)N	278.33	unknown	via CMAUP database
> Organic acids and derivatives / Organic sulfuric acids and derivatives / Sulfuric acid esters / Sulfuric acid diesters
(E)-2-Propenyl (3-(2-propenylthio)-2-propenyl) sulfate	10977885	Click to see	250.30	unknown	via CMAUP database
> Organic acids and derivatives / Organic thiosulfuric acids and derivatives / S-alkyl thiosulfates
3-Sulfonatosulfanylprop-1-ene	59479946	Click to see	153.20	unknown	via CMAUP database
> Organic acids and derivatives / Thiosulfinic acid esters
3-[(S)-prop-2-enylsulfinyl]sulfanylprop-1-ene	51380898	Click to see	162.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Allyl Alcohol	7858	Click to see	58.08	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eugenol gentiobioside	10390778	Click to see	488.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Pentanal	8063	Click to see	86.13	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated aldehydes / Enals
(E)-3-(prop-2-enyldisulfanyl)prop-2-enal	5317516	Click to see C=CCSSC=CC=O	160.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Enols
1-Propen-2-ol	141483	Click to see	58.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Aminopyrimidines and derivatives
Allithiamine	3037212	Click to see	354.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
2(5H)-Furanone, 4-bromo-5-(bromomethylene)-, (5Z)-	10131246	Click to see C1=C(C(=CBr)OC1=O)Br	253.88	unknown	via CMAUP database
> Organoheterocyclic compounds / Dithioles / 1,2-dithioles
4-Methyl-1,2-dithiacyclopentene	5319597	Click to see	118.20	unknown	via CMAUP database
5-methyl-3H-dithiole	5319596	Click to see CC1=CCSS1	118.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Corianin	10880921	Click to see	294.30	unknown	https://doi.org/10.1248/CPB.35.182
Corianin	169700	Click to see CC(=C)C1C2C3C4(C(CO3)(C5C(C4(C1C(=O)O2)O)O5)O)C	294.30	unknown	https://doi.org/10.1248/CPB.35.182
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(2R,3S,5R,6R,7R,9S,12R)-2-hydroxy-7-methyl-12-prop-1-en-2-ylspiro[4,10-dioxatetracyclo[7.2.1.02,7.03,5]dodecane-6,2'-oxirane]-11-one	118701340	Click to see CC(=C)C1C2CC3(C4(CO4)C5C(C3(C1C(=O)O2)O)O5)C	278.30	unknown	https://doi.org/10.1248/CPB.35.182
Coriamyrtin	442189	Click to see CC(=C)C1C2CC3(C4(CO4)C5C(C3(C1C(=O)O2)O)O5)C	278.30	unknown	https://doi.org/10.1248/CPB.35.182
Tutin	75729	Click to see	294.30	unknown	https://doi.org/10.1248/CPB.35.182
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Allixin	86374	Click to see CCCCCC1=C(C(=O)C(=C(O1)C)OC)O	226.27	unknown	via CMAUP database
> Organosulfur compounds / Allyl sulfur compounds
Allyl methyl disulfide	62434	Click to see	120.20	unknown	via CMAUP database
Allyl methyl sulfide	66282	Click to see	88.17	unknown	via CMAUP database
Allyl methyl tetrasulfide	525329	Click to see	184.40	unknown	via CMAUP database
Allyl prop-1-enyl disulfide	5352855	Click to see CC=CSSCC=C	146.30	unknown	via CMAUP database
Allyl propyl disulfide	16591	Click to see CCCSSCC=C	148.30	unknown	via CMAUP database
Diallyl disulfide	16590	Click to see C=CCSSCC=C	146.30	unknown	via CMAUP database
Diallyl Sulfide	11617	Click to see	114.21	unknown	via CMAUP database
Diallyl tetrasulfide	75552	Click to see C=CCSSSSCC=C	210.40	unknown	via CMAUP database
Methyl 2-propenyl pentasulfide	528713	Click to see CSSSSSCC=C	216.40	unknown	via CMAUP database
Npc247380	5352907	Click to see	146.30	unknown	via CMAUP database
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Dimethyl Disulfide	12232	Click to see	94.20	unknown	via CMAUP database
Dipropyl disulfide	12377	Click to see	150.30	unknown	via CMAUP database
Methyl propyl disulfide	16592	Click to see	122.30	unknown	via CMAUP database
> Organosulfur compounds / Organic trisulfides
6-ethenyl-4H-trithiine	5315241	Click to see C=CC1=CCSSS1	162.30	unknown	via CMAUP database
Diallyl trisulfide	16315	Click to see C=CCSSSCC=C	178.30	unknown	via CMAUP database
Dimethyl trisulfide	19310	Click to see CSSSC	126.30	unknown	via CMAUP database
Methyl propyl trisulfide	5319765	Click to see	154.30	unknown	via CMAUP database
Methylallyl trisulfide	61926	Click to see	152.30	unknown	via CMAUP database
> Organosulfur compounds / Sulfonyls
S-2-Propenyl 2-propene-1-sulfonothioate	85776791	Click to see C=CCSS(=O)(=O)CC=C	178.30	unknown	via CMAUP database
> Organosulfur compounds / Sulfonyls / Sulfones
(E)-3-(prop-2-enyldisulfanyl)-1-prop-2-enylsulfonylprop-1-ene	5322033	Click to see	250.40	unknown	via CMAUP database
> Organosulfur compounds / Sulfoxides
(E)-1-(prop-2-enyldisulfanyl)-3-[(R)-prop-2-enylsulfinyl]prop-1-ene	76962524	Click to see	234.40	unknown	via CMAUP database
(Z)-1-(prop-2-enyldisulfanyl)-3-[(R)-prop-2-enylsulfinyl]prop-1-ene	76960957	Click to see	234.40	unknown	via CMAUP database
> Organosulfur compounds / Thioacetals / Dithioacetals
1,3-Dithiole	5316944	Click to see	104.20	unknown	via CMAUP database
> Organosulfur compounds / Thioethers / Dialkylthioethers
Dimethyl Sulfide	1068	Click to see	62.14	unknown	via CMAUP database
> Organosulfur compounds / Thioethers / Thioenol ethers
Ethene, 1,1'-thiobis-	12321	Click to see	86.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate	46906036	Click to see	301.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-chromen-4-one	49766656	Click to see	448.40	unknown	via CMAUP database
Quercitrin-7-olate	49792009	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	447.40	unknown	via CMAUP database

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Scurrula parasitica

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