Common products:
• Cut branches (filler green) in floristry as “Ruscus,” recognized in EU and Mediterranean floricultural trade; sometimes sourced from wild populations in the Balkan region (e.g., “Ruscus spp.” in Euro+Med PlantBase, regional floriculture literature).

Industrial and craft applications:
• Green branches used in floral wreaths and arrangements; stems dried and occasionally dyed for craft purposes (documented trade in “Ruscus” stems for these uses, not necessarily restricted to a single species).

Fragrance and cosmetics:
• No documented uses specific to R. hypoglossum in fragrance or cosmetics. Aromatic/essential oil and topical cosmetic uses reported for related species (e.g., R. aculeatus) are excluded here as non-verified for R. hypoglossum.

Sustainability and sourcing:
• Wild collection of Ruscus for floristry may be locally regulated (CITES Appendices II/III list various Ruscus spp., restricting international trade); many Balkan and Mediterranean supply chains blend wild-harvested and cultivated material, with ongoing assessments in regional floricultural sustainability reviews.

Notes:
• Botanical identification in trade frequently occurs at the genus level (“Ruscus”), complicating species-level reporting. Reliable sources do not identify distinct industrial applications or food/culinary uses for R. hypoglossum.

Synonyms Top

Scientific name	Authority	First published in
Platyruscus hypoglossum	(L.) A.P.Khokhr. & V.N.Tikhom.	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. , n.s., 98(4): 92 (1993)
Ruscus alexandrinus	Garsault	Fig. Pl. Méd. : t. 503 (1764)
Ruscus troadensis	E.D.Clarke	Travels Eur. Asia & Africa 2: 146 (1812)
Ruscus humilis	Salisb.	Prodr. Stirp. Chap. Allerton : 255 (1796)
Ruscus hypophyllum var. hypoglossum	(L.) Baker	J. Linn. Soc., Bot. 14: 630. 1875
Ruscus hypoglossum var. laticladodia	Yalt.	Notes Roy. Bot. Gard. Edinburgh 28: 16. 1967

Common names Top

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Filter by language:

Language	Common/alternative name
English	helecho mosca
Arabic	سفندر لامع الظهر
Bulgarian	подезичен залист
Czech	listnatec jazykovitý
Welsh	celynnen-fair ddi-ddrain
Greek	Ρούσκος ο υπόγλωσσος
Esperanto	langa rusko
Croatian	Širokolisna veprina
Hungarian	lónyelvű csodabogyó
Serbian	Широколисна кострика
Chinese	舌苞假叶树

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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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

Africa click to expand
- Macaronesia
  - Canary Islands

Asia-temperate click to expand
- Western Asia
  - East Aegean Islands
  - Turkey

Europe click to expand
- Eastern Europe
  - Krym
- Middle Europe
  - Austria
  - Czechoslovakia
  - Hungary
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000732848
Tropicos	18400317
INPN	611535
Flora of Italy	6971
KEW	urn:lsid:ipni.org:names:540452-1
The Plant List	kew-286774
Open Tree Of Life	1037410
NCBI Taxonomy	191652
NBN Atlas	NBNSYS0000005353
IPNI	540452-1
iNaturalist	205088
GBIF	2769775
Freebase	/m/0j67m5h
EPPO	RUCHP
EOL	1082042
Elurikkus	6983
USDA GRIN	32569
Wikipedia	Ruscus_hypoglossum
CMAUP	NPO11950

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

Topographic depressions can provide climate and resource microrefugia for biodiversity

Frei K, Vojtkó A, Farkas T, Erdős L, Barta K, E-Vojtkó A, Tölgyesi C, Bátori Z

iScience

21-Oct-2023

PMCID:	PMC10656275
doi:	10.1016/j.isci.2023.108202
PMID:	38026156

Surveying potentially antagonistic fungi to myrtle rust (Austropuccinia psidii) in Brazil: fungicolous Cladosporium spp.

da Silva NM, Guterres DC, Borges LS, Barreto RW, Furtado GQ

Braz J Microbiol

30-Jun-2023

PMCID:	PMC10484887
doi:	10.1007/s42770-023-01047-6
PMID:	37389796

Phytogeographic Characteristics of Montane Coniferous Forests of the Central Balkan Peninsula (SE Europe)

Ilić T, Kuzmanović N, Vukojičić S, Lakušić D

Plants (Basel)

22-Nov-2022

PMCID:	PMC9741231
doi:	10.3390/plants11233194
PMID:	36501234

Original karst tiankeng with underground virgin forest as an inaccessible refugia originated from a degraded surface flora in Yunnan, China

Shui W, Chen Y, Jian X, Jiang C, Wang Q, Zeng Y, Zhu S, Guo P, Li H

Sci Rep

07-Jun-2022

PMCID:	PMC9174222
doi:	10.1038/s41598-022-13678-0
PMID:	35672447

New Cladosporium Species from Normal and Galled Flowers of Lamiaceae

Zimowska B, Becchimanzi A, Krol ED, Furmanczyk A, Bensch K, Nicoletti R

Pathogens

19-Mar-2021

PMCID:	PMC8003538
doi:	10.3390/pathogens10030369
PMID:	33808618

Cladosporium species in indoor environments

Bensch K, Groenewald JZ, Meijer M, Dijksterhuis J, Jurjević Ž, Andersen B, Houbraken J, Crous PW, Samson RA

Stud Mycol

07-Mar-2018

PMCID:	PMC5909081
doi:	10.1016/j.simyco.2018.03.002
PMID:	29681671

New species of Cladosporium associated with human and animal infections

Sandoval-Denis M, Gené J, Sutton DA, Wiederhold NP, Cano-Lira JF, Guarro J

Persoonia

24-May-2016

PMCID:	PMC4988372
doi:	10.3767/003158516X691951
PMID:	27616793

A phylogenetic re-evaluation of Phyllosticta (Botryosphaeriales)

Wikee S, Lombard L, Nakashima C, Motohashi K, Chukeatirote E, Cheewangkoon R, McKenzie EH, Hyde KD, Crous PW

Stud Mycol

30-Sep-2013

PMCID:	PMC3825230
doi:	10.3114/sim0019
PMID:	24302788

The genus Cladosporium

Bensch K, Braun U, Groenewald JZ, Crous PW

Stud Mycol

06-Jun-2012

PMCID:	PMC3390897
doi:	10.3114/sim0003
PMID:	22815589

Phyllosticta ophiopogonis sp. nov. from Ophiopogon japonicus (Liliaceae)

Wikee S, Wulandari NF, McKenzie EH, Hyde KD

Saudi J Biol Sci

19-Oct-2011

PMCID:	PMC3730551
doi:	10.1016/j.sjbs.2011.10.003
PMID:	23961156

Endophytic and pathogenic Phyllosticta species, with reference to those associated with Citrus Black Spot

Glienke C, Pereira OL, Stringari D, Fabris J, Kava-Cordeiro V, Galli-Terasawa L, Cunnington J, Shivas RG, Groenewald JZ, Crous PW

Persoonia

22-Mar-2011

PMCID:	PMC3160796
doi:	10.3767/003158511X569169
PMID:	22025803

Species and ecological diversity within the Cladosporium cladosporioides complex (Davidiellaceae, Capnodiales)

Bensch K, Groenewald JZ, Dijksterhuis J, Starink-Willemse M, Andersen B, Summerell BA, Shin HD, Dugan FM, Schroers HJ, Braun U, Crous PW

Stud Mycol

01-Jan-2010

PMCID:	PMC2945380
doi:	10.3114/sim.2010.67.01
PMID:	20877444

Plant Species Recovery on a Compacted Skid Road

Demir M, Makineci E, Gungor BS

Sensors (Basel)

15-May-2008

PMCID:	PMC3675535
doi:	10.3390/s8053123
PMID:	27879869

Wild food plants of popular use in Sicily

Lentini F, Venza F

J Ethnobiol Ethnomed

30-Mar-2007

PMCID:	PMC1858679
doi:	10.1186/1746-4269-3-15
PMID:	17397527

Identification of Ruscus steroidal saponins by HPLC-MS analysis.

de Combarieu E, Falzoni M, Fuzzati N, Gattesco F, Giori A, Lovati M, Pace R

Fitoterapia

01-Dec-2002

doi:	10.1016/S0367-326X(02)00220-4
PMID:	12490216

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
2alpha-Hydroxy-3beta-acetyloxy-betulic acid	67993145	Click to see	514.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1055/S-0028-1097973
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	163015454	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1055/S-0028-1097973
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
[6-[[6,16-Dihydroxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate	163007025	Click to see	961.10	unknown	https://doi.org/10.1016/S0367-326X(02)00220-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1055/S-0028-1097973
(3S,8R,9R,10R,13R,14R,17R)-17-[(E,2S,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	124762119	Click to see	412.70	unknown	https://doi.org/10.1055/S-0028-1097973
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1055/S-0028-1097973
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1055/S-0028-1097973
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1S,2S,13S,15R)-15-[(Z)-4,4-dimethoxy-3-methylbut-2-enyl]-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	10532388	Click to see	660.80	unknown	via CMAUP database
(1S,2S,13S,15R)-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-8-hydroxy-17,17-dimethyl-5,15-bis(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4(9),5,7,11-tetraene-10,14-dione	25208760	Click to see	600.80	unknown	via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,13,15-tris(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	10554272	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC4(CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)C	532.70	unknown	via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,15-bis(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	57393978	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)C	464.50	unknown	via CMAUP database
(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7,15-tris(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	101389904	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C)CC=C(C)C)O)C	532.70	unknown	via CMAUP database
(E)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid	46867195	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C	562.60	unknown	via CMAUP database
(E)-4-[(1S,2S,13S,15R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal	10603834	Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C=O)CC=C(C)C)O)C)C	614.80	unknown	via CMAUP database
(Z)-4-[(1S,2S,13S,15R)-6,8-dihydroxy-17,17-dimethyl-5,7-bis(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enoic acid	101389902	Click to see	562.60	unknown	via CMAUP database
(Z)-4-[(1S,2S,13S,15R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,8-dihydroxy-17,17-dimethyl-5-(3-methylbut-2-enyl)-10,14-dioxo-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraen-15-yl]-2-methylbut-2-enal	10841474	Click to see	614.80	unknown	via CMAUP database
Deoxygambogenin	10817397	Click to see	600.80	unknown	via CMAUP database
Gambogenic Acid	10794070	Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=CC4CC5C3(O2)C(C4=O)(OC5(C)C)CC=C(C)C(=O)O)CC=C(C)C)O)C)C	630.80	unknown	via CMAUP database
Isogambogenic acid	101389903	Click to see	630.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(-)-Morellic Acid	54580250	Click to see	560.60	unknown	via CMAUP database
(1S,2S,17R,19R)-12-hydroxy-19-[(E)-4-hydroxy-3-methylbut-2-enyl]-17-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione	25208912	Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)CO)OC)O)C=CC(O2)(C)C)C	576.70	unknown	via CMAUP database
(1S,2S,17S,19R)-12-hydroxy-19-[(E)-4-hydroxy-3-methylbut-2-enyl]-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione	101389908	Click to see	546.60	unknown	via CMAUP database
(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5,19-bis(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione	11432549	Click to see	530.60	unknown	via CMAUP database
(1S,2S,17S,19R)-19-[(Z)-4,4-dimethoxy-3-methylbut-2-enyl]-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione	10769730	Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(OC)OC)O)C=CC(O2)(C)C)C	590.70	unknown	via CMAUP database
(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5,19-bis(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaene-14,18-dione	101690778	Click to see	598.80	unknown	via CMAUP database
(E)-4-[(1S,2S,15R,16S,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enal	11801290	Click to see	576.70	unknown	via CMAUP database
(E)-4-[(1S,2S,17S,19R)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid	101389907	Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C	560.60	unknown	via CMAUP database
(Z)-2-(hydroxymethyl)-4-[(1S,2S,8R,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]but-2-enoic acid	102402040	Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(CO)C(=O)O)O)C)C	644.70	unknown	via CMAUP database
(Z)-2-(hydroxymethyl)-4-[(1S,2S,8S,17S,19R)-12-hydroxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]but-2-enoic acid	102402042	Click to see	644.70	unknown	via CMAUP database
(Z)-4-[(1R,2R,17R,19S)-12-hydroxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid	102533562	Click to see	560.60	unknown	via CMAUP database
(Z)-4-[(1S,2S,15R,16S,17S,19R)-12-hydroxy-16-methoxy-8,8,21,21-tetramethyl-5-(3-methylbut-2-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11-tetraen-19-yl]-2-methylbut-2-enoic acid	10507667	Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C(C4C3=O)OC)C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)O)C=CC(O2)(C)C)C	592.70	unknown	via CMAUP database
(Z)-4-[(1S,2S,8R,17R,19R)-12-hydroxy-17-methoxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid	25208439	Click to see	658.80	unknown	via CMAUP database
(Z)-4-[(1S,2S,8S,17R,19R)-12-hydroxy-17-methoxy-8,21,21-trimethyl-5-(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)-14,18-dioxo-3,7,20-trioxahexacyclo[15.4.1.02,15.02,19.04,13.06,11]docosa-4(13),5,9,11,15-pentaen-19-yl]-2-methylbut-2-enoic acid	25208762	Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)CC=C(C)C)OC45C6CC(C=C4C3=O)(C(=O)C5(OC6(C)C)CC=C(C)C(=O)O)OC)O)C)C	658.80	unknown	via CMAUP database
7-Methoxydeoxymorellin	70697915	Click to see	560.70	unknown	via CMAUP database
CID 12313004	12313004	Click to see CC(=CCC1=C2C(=C(C3=C1OC45C6CC(C=C4C3=O)C(=O)C5(OC6(C)C)CC=C(C)C=O)O)C=CC(O2)(C)C)C	544.60	unknown	via CMAUP database
Epigambogic acid	101406629	Click to see	628.70	unknown	via CMAUP database
Gambogic Acid	9852185	Click to see	628.70	unknown	via CMAUP database
Gambogic acid B	101377135	Click to see	674.80	unknown	via CMAUP database
Gambogoic acid A	101377134	Click to see	660.80	unknown	via CMAUP database
Isogambogic acid	70697925	Click to see	628.70	unknown	via CMAUP database
S-Isogambogic acid	102402041	Click to see	628.70	unknown	via CMAUP database

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Ruscus hypoglossum

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