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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No subspecies added yet.

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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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 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

Suggest others/fix!

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

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

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

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

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

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

The Complete Plastomes of Five Hemiparasitic Plants (Osyris wightiana, Pyrularia edulis, Santalum album, Viscum liquidambaricolum, and V. ovalifolium): Comparative and Evolutionary Analyses Within Santalales

Guo X, Liu C, Zhang G, Su W, Landis JB, Zhang X, Wang H, Ji Y

Front Genet

16-Jun-2020

PMCID:	PMC7308561
doi:	10.3389/fgene.2020.00597
PMID:	32612639

Phytochemical Profile Top

Add a new one!

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 CC(=CCCC(=CC=O)C)C	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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	618.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(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 CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	via CMAUP database
beta-Amyrine	15942855	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
Monogynol B (6CI)	44586882	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Oleanolic Acid (Caryophyllin)	49867939	Click to see CC1(CC2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(C1)C(=O)O)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
(2S,3R,4E,8E)-1-(beta-D-Glucopyranosyloxy)-2-[[(2R)-2-hydroxymyristoyl]amino]-4,8-octadecadiene-3-ol	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
(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
1-O-beta-D-Glucopyranosyl-N-[(2R)-2-hydroxypalmitoyl]sphingosine	101948670	Click to see CCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C=CCCCCCCCCCCCCC)O)O	716.00	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 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
> 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 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,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 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)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	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 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)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O	1439.50	unknown	via CMAUP database
(25R)-3beta-[[4-O-[2-O,3-O-Bis(beta-D-glucopyranosyl)-beta-D-glucopyranosyl]-beta-D-galactopyranosyl]oxy]-5alpha-spirostan-2alpha-ol	101932450	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(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)O)C)C)C)OC1	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 CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)C)C)OC1	1197.30	unknown	via CMAUP database
Eruboside B	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
> 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 CS(=O)CC(C(=O)[O-])[NH3+]	151.19	unknown	via CMAUP database
L-selenomethionine	105024	Click to see C[Se]CCC(C(=O)O)N	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 C=CCSCC(C(=O)[O-])[NH3+]	161.22	unknown	via CMAUP database
(2R)-2-azaniumyl-3-propylsulfanylpropanoate	40565896	Click to see CCCSCC(C(=O)[O-])[NH3+]	163.24	unknown	via CMAUP database
s-Allylmercaptocysteine	9794159	Click to see C=CCSSCC(C(=O)O)N	193.30	unknown	via CMAUP database
S-Methylthiocysteine	3080775	Click to see CSSCC(C(=O)O)N	167.30	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-ALLYLCYSTEINE	11346811	Click to see C=CCSCC(C(=O)O)NC(=O)CCC(C(=O)O)N	290.34	unknown	via CMAUP database
gamma-glutamyl-S-allylmercaptocysteine	101630431	Click to see C=CCSSCC(C(=O)O)NC(=O)CCC(C(=O)O)N	322.40	unknown	via CMAUP database
gamma-glutamyl-S-propyl cysteine	54090099	Click to see CCCSCC(C(=O)O)NC(=O)CCC(C(=O)O)N	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
N-gamma-Glutamyl-S-trans-(1-propenyl)cysteine	87289205	Click to see CC=CSCC(C(=O)O)NC(=O)CCC(C(=O)O)N	290.34	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 C=CCOS(=O)(=O)OCC=CSCC=C	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 C=CCSS(=O)(=O)[O-]	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 C=CCSS(=O)CC=C	162.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Allyl alcohol	7858	Click to see C=CCO	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 COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O	488.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Valeraldehyde	8063	Click to see CCCCC=O	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
Propen-2-ol	141483	Click to see CC(=C)O	58.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Aminopyrimidines and derivatives
N-[(4-amino-2-methylpyrimidin-5-yl)methyl]-N-[(Z)-5-hydroxy-3-(prop-2-enyldisulfanyl)pent-2-en-2-yl]formamide	3037212	Click to see CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SSCC=C)C	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 CC1=CSSC1	118.20	unknown	via CMAUP database
5-Methyl-3H-1,2-dithiol	5319596	Click to see CC1=CCSS1	118.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
CID 169700	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
Corianin	10880921	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 CC(=C)C1C2C(C3(C4(CO4)C5C(C3(C1C(=O)O2)O)O5)C)O	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
(E)-1-Propenyl 2-propenyl disulfide	5352907	Click to see CC=CSSCC=C	146.30	unknown	via CMAUP database
Allyl methyl disulfide	62434	Click to see CSSCC=C	120.20	unknown	via CMAUP database
Allyl methyl sulfide	66282	Click to see CSCC=C	88.17	unknown	via CMAUP database
Allyl methyl tetrasulfide	525329	Click to see CSSSSCC=C	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 C=CCSCC=C	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
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Dimethyl Disulfide	12232	Click to see CSSC	94.20	unknown	via CMAUP database
Dipropyl disulfide	12377	Click to see CCCSSCCC	150.30	unknown	via CMAUP database
Methyl propyl disulfide	16592	Click to see CCCSSC	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
Allyl methyl trisulfide	61926	Click to see CSSSCC=C	152.30	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 CCCSSSC	154.30	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 C=CCSSCC=CS(=O)(=O)CC=C	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 C=CCSSC=CCS(=O)CC=C	234.40	unknown	via CMAUP database
(Z)-1-(prop-2-enyldisulfanyl)-3-[(R)-prop-2-enylsulfinyl]prop-1-ene	76960957	Click to see C=CCSSC=CCS(=O)CC=C	234.40	unknown	via CMAUP database
> Organosulfur compounds / Thioacetals / Dithioacetals
1,3-Dithiole	5316944	Click to see C1SC=CS1	104.20	unknown	via CMAUP database
> Organosulfur compounds / Thioethers / Dialkylthioethers
Dimethyl sulfide	1068	Click to see CSC	62.14	unknown	via CMAUP database
> Organosulfur compounds / Thioethers / Thioenol ethers
Divinyl sulfide	12321	Click to see C=CSC=C	86.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate	46906036	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O	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 COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(O3)CO)O)O)C4=CC(=C(C=C4)O)O)O	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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