Scientific name	Authority	First published in
Dioscorea canariensis	Webb & Berthel.	Hist. Nat. Iles Canaries 3(2; 3): 317 (1847)
Tamus baccifera	St Lager	Étude Fl. , éd. 8, 2: 765 (1889)
Tamus canariensis	Willd. ex Kunth	Enum. Pl. 5: 455 (1850)
Tamus cirrhosa	Hausskn. ex Bornm.	Beih. Bot. Centralbl. 58 E: 271 (1938)
Tamus communis	L.	Sp. Pl. : 1028 (1753)
Tamus communis subsp. cretica	(L.) Kit Tan	Notes Roy. Bot. Gard. Edinburgh 41(1): 47. 1983
Tamus communis var. cretica	(L.) Boiss.	Fl. Orient. 5: 344 1882
Tamus communis f. subtriloba	(Guss.) O.Bolòs & Vigo	Fl. Man. Paísos Catalans 4: 171 (2001)
Tamus communis var. subtriloba	Guss.	Fl. Sicul. Syn. 2: 880 1844
Tamus cordifolia	Stokes	Bot. Mat. Med. 4: 544 (1812)
Tamus cretica	L.	Sp. Pl. : 1028 (1753)
Tamus edulis	Lowe	Trans. Cambridge Philos. Soc. 4: 12 (1831)
Tamus norsa	Lowe	Trans. Cambridge Philos. Soc. 6: 543 (1838)
Tamus parviflora	Kunth	Enum. Pl. 5: 454 (1850)
Tamus racemosa	Gouan	Fl. Monsp. : 426 (1764)
Smilax rubra	Willd.	Enum. Pl. : 1015 (1809)
Tamus communis var. triloba	Simonk.	Enum. Fl. Transsilv. 520. 1887

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	tamus cretica
Spanish	brionia negra
Spanish	esparrago bravio
Spanish	espárrago bravío
Spanish	esparrago de sepia
Spanish	espárrago de sepia
Spanish	esparragos chirrinantes
Spanish	espárragos chirrinantes
Spanish	esparragos de bicha
Spanish	espárragos de bicha
Spanish	espárragos de caña
Spanish	esparragos de lupia
Spanish	espárragos de lupia
Spanish	esparragos de yedros
Spanish	espárragos de yedros
Spanish	esparragos hileros
Spanish	espárragos hileros
Spanish	esparragos zarceros
Spanish	espárragos zarceros
Spanish	hierba de la mujer apaleada
Spanish	nuez negra
Spanish	planta de la culebra
Spanish	sello de la virgen
Spanish	tamus smilacifolia
Arabic	خيرون شائع
Azerbaijani	adi dioskoreya
Bulgarian	tamus communis
Bulgarian	брей
Bulgarian	обикновена диоскорея
Bosnian	bljušt
Catalan	tamus communis
Catalan	gatmaimó
Czech	tamus obecný
Welsh	cwlwm y coed
German	gewöhnliche schmerwurz
German	schmerwurz
German	tamus communis
German	gemeine schmerwurz
Greek	αβρωνιά
Greek	βρυωνία η κοινή
Greek	Διοσκορέα η κοινή
Basque	apomahats
Basque	tamus communis
Basque	apo-mahats
Persian	دیوسکرئا کمونیس
Finnish	euroopankiiltoköynnös
French	herbe à la femme battue
French	raisin du diable
French	reponchon
French	repountchou
French	respounchous
French	tamier
French	tamier commun
French	tamus communis
Irish	unach dhubh
Irish	crotharnach
Irish	uranach dhubh
Galician	saltasebes
Galician	nouza
Galician	noza
Galician	tamus communis
Galician	tamus smilacifolia
Galician	uvas de can
Galician	uvas de cobra
Galician	valdeba
Galician	norza moura
Croatian	kuka
Croatian	bljušt
Upper Sorbian	wšědna tučnokorjenjawka
Hungarian	felfutó pirítógyökér
Hungarian	pirítógyökér
Armenian	Կույսարմատ սովորական
Italian	tamus communis
Georgian	tamus communis
Georgian	მიხელტა
Georgian	ძაღლის სატაცური
Kabyle	aẓberbur n wuccen
Cornish	greun an jowl
Latvian	tamus communis
Latvian	parastais tamus
Macedonian	блужд
mzn	ککی مار
Norwegian Bokmål	tamus communis
Dutch	tamus communis
Dutch	spekwortel
oc	reponchon
Portuguese	tamus communis
Romanian	untul pamantului
Romanian	untul pământului
Serbo-Croatian	bljušć
Serbo-Croatian	bljužd
Serbo-Croatian	tamus communis
Serbo-Croatian	zmijino grožđe
Serbo-Croatian	bljušt
Serbian	tamus communis
Serbian	Бљужд
Serbian	Бљушћ
Serbian	Бљушт
Ukrainian	Тамус звичайний
vec	tamus communis
vec	tanoni
Chinese	黑薯蓣

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Australasia click to expand
- New Zealand
  - New Zealand North

Europe click to expand
- Eastern Europe
  - Krym
- Middle Europe
  - Austria
  - Belgium
  - Germany
  - Hungary
  - Switzerland
- Northern Europe
  - Great Britain
  - Ireland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000389997
UNII	85G3RJK70X
Tropicos	50232719
INPN	611652
Flora of Italy	7009
KEW	urn:lsid:ipni.org:names:20005752-1
The Plant List	kew-239990
Open Tree Of Life	319401
NCBI Taxonomy	55634
NBN Atlas	NHMSYS0020823747
IPNI	20005752-1
iNaturalist	82691
GBIF	2755063
Freebase	/m/085fld
EPPO	TAUCO
EOL	1121107
Elurikkus	296381
USDA GRIN	423869
Wikipedia	Dioscorea_communis
CMAUP	NPO28257

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

A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics

Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B

J Ethnopharmacol

25-Mar-2024

PMCID:	PMC7615571
doi:	10.1016/j.jep.2023.117622
PMID:	38128894

Potential Interest of Oxalis pes-caprae L., a Wild Edible Plant, for the Food and Pharmaceutical Industries

Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA

Foods

12-Mar-2024

PMCID:	PMC10969124
doi:	10.3390/foods13060858
PMID:	38540848

Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans)

Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P

J Ethnobiol Ethnomed

10-Jan-2024

PMCID:	PMC10782642
doi:	10.1186/s13002-024-00647-2
PMID:	38200599

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

Genome-wide analysis of horizontal transfer in non-model wild species from a natural ecosystem reveals new insights into genetic exchange in plants

Aubin E, Llauro C, Garrigue J, Mirouze M, Panaud O, El Baidouri M

PLoS Genet

19-Oct-2023

PMCID:	PMC10586619
doi:	10.1371/journal.pgen.1010964
PMID:	37856455

Antimalarial Efficacy and Antioxidant Activity of Lophira lanceolata Stem Bark Ethanol Extract Using Plasmodium berghei Induced-Malaria in Swiss Albino's Mice

Azizi MA, Nadia NA, Cedric Y, Sidiki NN, Guy-Armand GN, Esther DD, Sandra TN, Kevin TD, Payne VK

J Parasitol Res

18-Aug-2023

PMCID:	PMC10457170
doi:	10.1155/2023/9400650
PMID:	37637978

Ethnopharmacological study of medicinal plants used against skin ailments on Mount Pelion, central Greece

Tsioutsiou EE, Cheilari A, Aligiannis N

Front Pharmacol

31-Jul-2023

PMCID:	PMC10424924
doi:	10.3389/fphar.2023.1225580
PMID:	37583900

Bitter Is Better: Wild Greens Used in the Blue Zone of Ikaria, Greece

Pieroni A, Morini G, Piochi M, Sulaiman N, Kalle R, Haq SM, Devecchi A, Franceschini C, Zocchi DM, Migliavada R, Prakofjewa J, Sartori M, Krigas N, Ahmad M, Torri L, Sõukand R

Nutrients

21-Jul-2023

PMCID:	PMC10385191
doi:	10.3390/nu15143242
PMID:	37513661

Isolation and identification of active ingredients and biological activity of Dioscorea nipponica Makino

Xia G, Zhao G, Pei S, Zheng Y, Zang H, Li L

BMC Complement Med Ther

17-Jul-2023

PMCID:	PMC10351190
doi:	10.1186/s12906-023-04086-6
PMID:	37461036

Optimization of the Extraction Methodology of Grape Pomace Polyphenols for Food Applications

Moutinho J, Gouvinhas I, Domínguez-Perles R, Barros A

Molecules

04-May-2023

PMCID:	PMC10180386
doi:	10.3390/molecules28093885
PMID:	37175294

Natural Products as New Approaches for Treating Bladder Cancer: From Traditional Medicine to Novel Drug Discovery

Kang Y, Park C, Lee H, Kang S, Cheon C, Kim B

Pharmaceutics

31-Mar-2023

PMCID:	PMC10145408
doi:	10.3390/pharmaceutics15041117
PMID:	37111603

Earlywood Anatomy Highlights the Prevalent Role of Winter Conditions on Radial Growth of Oak at Its Distribution Boundary in NW Iberia

García-González I, Souto-Herrero M

Plants (Basel)

06-Mar-2023

PMCID:	PMC10007082
doi:	10.3390/plants12051185
PMID:	36904045

Valorization of Wild Edible Plants as Food Ingredients and Their Economic Value

Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA

Foods

27-Feb-2023

PMCID:	PMC10001278
doi:	10.3390/foods12051012
PMID:	36900530

Genomic, spatial and morphometric data for discrimination of four species in the Mediterranean Tamus clade of yams (Dioscorea, Dioscoreaceae)

Campos M, Kelley E, Gravendeel B, Médail F, Maarten Christenhusz JM, Fay MF, Catalán P, Leitch IJ, Forest F, Wilkin P, Viruel J

Ann Bot

22-Jan-2023

PMCID:	PMC10147332
doi:	10.1093/aob/mcad018
PMID:	36681900

Time-calibrated phylogenies reveal mediterranean and pre-mediterranean origin of the thermophilous vegetation of the Canary Islands

Martín-Hernanz S, Nogales M, Valente L, Fernández-Mazuecos M, Pomeda-Gutiérrez F, Cano E, Marrero P, Olesen JM, Heleno R, Vargas P

Ann Bot

03-Jan-2023

PMCID:	PMC10147335
doi:	10.1093/aob/mcac160
PMID:	36594263

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 / Anthracenes / Anthraquinones
1,5-Dihydroxy-3-methoxy-7-methylanthracene-9,10-dione	15138599	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC(=C3)OC)O	284.26	unknown	via CMAUP database
1,5-Dihydroxy-3-methylanthraquinone	5316800	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C(=CC=C3)O	254.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxybenzaldehyde	8419	Click to see COC1=C(C=C(C=C1)C=O)OC	166.17	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
7,8,9-Trimethoxynaphtho[1,2-g][1,3]benzodioxole	90741235	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC4=C3OCO4)OC)OC	312.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.10.028
Przewalskin	14139389	Click to see CC1=CC2=C(C=C1O)C34CCCC(C3CC2OC4)(C)C	272.40	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2-Hydroxy-3,5,7-trimethoxy-9,10-dihydrophenanthrene	71437517	Click to see COC1=CC2=C(C3=CC(=C(C=C3CC2)O)OC)C(=C1)OC	286.32	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.10.028
2,5-Phenanthrenediol, 9,10-dihydro-3,7-dimethoxy-	182231	Click to see COC1=CC2=C(C3=CC(=C(C=C3CC2)O)OC)C(=C1)O	272.29	unknown	https://doi.org/10.1021/NP50041A017
2,6,7-Trimethoxy-9,10-dihydrophenanthren-4-ol	23817926	Click to see COC1=CC2=C(C3=CC(=C(C=C3CC2)OC)OC)C(=C1)O	286.32	unknown	https://doi.org/10.1021/NP50041A017
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
1,5,6-Trimethoxyphenanthrene-2,7-diol	11983285	Click to see COC1=C(C=CC2=C1C=CC3=CC(=C(C(=C32)OC)OC)O)O	300.30	unknown	https://doi.org/10.1055/S-2006-941505
2,5,6,7-Tetramethoxyphenanthren-1-ol	85961818	Click to see COC1=C(C2=C(C=C1)C3=C(C(=C(C=C3C=C2)OC)OC)OC)O	314.30	unknown	https://doi.org/10.1039/P19780000739
2,6-Phenanthrenediol, 1,5,7-trimethoxy-	11779542	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3OC)O)OC)O	300.30	unknown	https://doi.org/10.1055/S-2006-941505
2,6-Phenanthrenediol, 5,7-dimethoxy-	10445823	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3)O)OC)O	270.28	unknown	https://doi.org/10.1055/S-2006-941505
2,6,7-Trimethoxyphenanthren-4-ol	22753768	Click to see COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)OC)O	284.31	unknown	https://doi.org/10.1016/S0040-4039(01)88204-6
2,7-Phenanthrenediol, 3,4-dimethoxy-	158975	Click to see COC1=C(C=C2C=CC3=C(C2=C1OC)C=CC(=C3)O)O	270.28	unknown	https://doi.org/10.1055/S-2006-941505
3-Hydroxy-2,4-dimethoxy-7,8-methylenedioxyphenanthrene	91069813	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC4=C3OCO4)OC)O	298.29	unknown	https://doi.org/10.1039/P19790002449 https://doi.org/10.1016/J.PHYTOCHEM.2006.10.028
5,6,7-Trimethoxyphenanthrene-2-ol	11997529	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3)O)OC)OC	284.31	unknown	https://doi.org/10.1055/S-2006-941505
7-Hydroxy-2,3,4,8-tetramethoxyphenanthrene	5315859	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3OC)O)OC)OC	314.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.10.028
Isobatatasin I	442708	Click to see COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)OC)O)OC	284.31	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.10.028
> Hydrocarbon derivatives / Tropones
Przewalskin A	16090911	Click to see CC(C)C1=CC2=C(C(=O)C(=C1O)C(=O)C)C34CCCC(C3C(C2OC4O)O)(C)C	402.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
gamma-Linolenic acid	5280933	Click to see CCCCCC=CCC=CCC=CCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1,2-Dihydrotanshinquinone	105119	Click to see CC1=CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4C	278.30	unknown	via CMAUP database
2,3,5,10,11,11abeta-Hexahydro-1,1-dimethyl-8-(1-methylethyl)-1H-dibenzo[a,d]cyclohepten-7-ol	14587208	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	via CMAUP database
6,7-Dehydroferruginol	10978982	Click to see CC(C)C1=C(C=C2C(=C1)C=CC3C2(CCCC3(C)C)C)O	284.40	unknown	via CMAUP database
Barbatusol	10040486	Click to see CC(C)C1=C(C(=C2CC3=CCCC(C3CCC2=C1)(C)C)O)O	300.40	unknown	via CMAUP database
Demethylsalvicanol	11666872	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)O	318.40	unknown	via CMAUP database
Ferruginol	442027	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCCC3(C)C)C)O	286.50	unknown	via CMAUP database
Lanigerol	188496	Click to see CC(C)C1=C(C=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O	302.50	unknown	via CMAUP database
Pisiferin	14587207	Click to see CC(C)C1=C(C=C2CC3=CCCC(C3CCC2=C1)(C)C)O	284.40	unknown	via CMAUP database
Przewalskin C	11566132	Click to see CC(C)C1=C(C(=C2CC3=CCCC(C3CC(C2=C1)OC)(C)C)O)O	330.50	unknown	via CMAUP database
Przewalskin D	101375853	Click to see CC(C)C1=C(C(=C2C=C3C=CCC(C3CCC2=C1)(C)C)O)O	298.40	unknown	via CMAUP database
Przewalskin G	102280560	Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3CC2OC4)(C)C	314.40	unknown	via CMAUP database
Salvicanol	101607178	Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)OC	332.50	unknown	via CMAUP database
Sugiol	94162	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids
(2,4,10,15-Tetrahydroxy-5,5,10,15-tetramethyl-7-oxapentacyclo[12.2.1.01,11.04,9.06,8]heptadecan-3-yl) acetate	10386869	Click to see CC(=O)OC1C(C23CC(CCC2C(C4C1(C(C5C4O5)(C)C)O)(C)O)C(C3)(C)O)O	410.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tanshinones, isotanshinones, and derivatives
(1S,6R,19R,22R,28S,30S)-19-hydroxy-13,22,31,31-tetramethyl-19-(2-oxopropyl)-25-propan-2-yl-5,7,23,35-tetraoxanonacyclo[26.6.1.01,30.03,27.04,24.06,22.08,21.09,18.012,17]pentatriaconta-3,8(21),9(18),10,12,14,16,24,26-nonaen-20-one	57404390	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(C(=O)C4=C3OC5C4(OC6=C(C=C7C8CC9C(CCCC9(O8)CC7=C6O5)(C)C)C(C)C)C)(CC(=O)C)O	648.80	unknown	via CMAUP database
(6R)-6-(hydroxymethyl)-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione	56967682	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)CO	310.30	unknown	via CMAUP database
(6S)-6-hydroxy-1,6-dimethyl-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-10,11-dione	56967683	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)O	296.30	unknown	via CMAUP database
Cryptotanshinone	160254	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	296.40	unknown	via CMAUP database
Danshenol A	3083514	Click to see CC1COC2=C1C(=O)C(C3=C2C=CC4=C(C=CC=C43)C)(CC(=O)C)O	336.40	unknown	via CMAUP database
Dehydrodanshenol A	71816415	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(C(=O)C4=C3OC=C4C)(CC(=O)C)O	334.40	unknown	via CMAUP database
Dihydrotanshinone I	11425923	Click to see CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C=CC=C43)C	278.30	unknown	via CMAUP database
Isograndifoliol	71816417	Click to see CC1=C(C(=O)C=C2C(=C1)CCC3C2(CCCC3(C)C)CO)O	302.40	unknown	via CMAUP database
Miltipolone	10086184	Click to see CC1=C(C(=O)C=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O	300.40	unknown	via CMAUP database
Miltirone	160142	Click to see CC(C)C1=CC2=C(C3=C(C=C2)C(CCC3)(C)C)C(=O)C1=O	282.40	unknown	via CMAUP database
Przewaquinone A	619402	Click to see CC1(CCCC2=C1C=CC3=C2C(=O)C(=O)C4=C3OC=C4CO)C	310.30	unknown	via CMAUP database
Tanshindiol B	5321620	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCC(C4(C)O)O	312.30	unknown	via CMAUP database
Tanshindiol C	126072	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCC(C4(C)O)O	312.30	unknown	via CMAUP database
Tanshinone I	114917	Click to see CC1=C2C=CC3=C(C2=CC=C1)C(=O)C(=O)C4=C3OC=C4C	276.30	unknown	via CMAUP database
Tanshinone IIA	164676	Click to see CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C	294.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
Cephalomannine	5281819	Click to see CC=C(C)C(=O)NC(C1=CC=CC=C1)C(C(=O)OC2CC3(C(C4C(C(CC5C4(CO5)OC(=O)C)O)(C(=O)C(C(=C2C)C3(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)O)O	831.90	unknown	https://doi.org/10.1021/AC00044A002
Paclitaxel	36314	Click to see CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)C6=CC=CC=C6)O)O)OC(=O)C7=CC=CC=C7)(CO4)OC(=O)C)O)C)OC(=O)C	853.90	unknown	https://doi.org/10.1021/AC00044A002
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	11876268	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Carnosol	442009	Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O	330.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Taurin	211707	Click to see CC1C2CCC3(C(=O)CCC(=C3C2OC1=O)C)C	248.32	unknown	https://doi.org/10.1080/1120009X.1991.11739110
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(2E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26Z)-2,6,10,14,19,23,27,31-octamethyldotriaconta-2,6,8,10,12,14,16,18,20,22,24,26,30-tridecaen-1-ol	10196509	Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)CO)C)C)C)C	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-4,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-11-one	163070705	Click to see CC1CCC2(C(C3C4(CC(=O)C5C(C4CC3(O2)O)CC=C6C5(CCC(C6)O)C)C)C)OC1	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)85289-9
(1S,2S,4S,5'R,6R,7S,8R,9S,12R,13R,16S)-4,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-11-one	163070706	Click to see CC1CCC2(C(C3C4(CC(=O)C5C(C4CC3(O2)O)CC=C6C5(CCC(C6)O)C)C)C)OC1	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)85289-9
(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-11,20-dione	162969501	Click to see CC1CCC2(C(C3C(O2)CC4C3(CC(=O)C5C4C(=O)C=C6C5(CCC(C6)O)C)C)C)OC1	442.60	unknown	https://doi.org/10.1016/S0031-9422(00)84338-1
16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-11,20-dione	162969500	Click to see CC1CCC2(C(C3C(O2)CC4C3(CC(=O)C5C4C(=O)C=C6C5(CCC(C6)O)C)C)C)OC1	442.60	unknown	https://doi.org/10.1016/S0031-9422(00)84338-1
4,16-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-11-one	71436642	Click to see CC1CCC2(C(C3C4(CC(=O)C5C(C4CC3(O2)O)CC=C6C5(CCC(C6)O)C)C)C)OC1	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)85289-9
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(3S,8S,9R,10R,13R,14S,17S)-3-hydroxy-17-[(2R,6S)-7-hydroxy-6-methyl-3-oxoheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,12,14,15,17-decahydro-1H-cyclopenta[a]phenanthrene-11,16-dione	162924193	Click to see CC(CCC(=O)C(C)C1C(=O)CC2C1(CC(=O)C3C2CC=C4C3(CCC(C4)O)C)C)CO	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)85289-9
3-hydroxy-17-(7-hydroxy-6-methyl-3-oxoheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,12,14,15,17-decahydro-1H-cyclopenta[a]phenanthrene-11,16-dione	162924192	Click to see CC(CCC(=O)C(C)C1C(=O)CC2C1(CC(=O)C3C2CC=C4C3(CCC(C4)O)C)C)CO	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)85289-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,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	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0378-8741(83)90070-3
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0378-8741(83)90070-3
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1021/NP50041A017
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2R,4R,5'S,6S,7S,8S,9S,12S,13R,16S)-16-hydroxy-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxolane]-11-one	163085026	Click to see CC1C2C(CC3C2(CC(=O)C4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(O6)(C)CO	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)84338-1
16-Hydroxy-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxolane]-11-one	163085025	Click to see CC1C2C(CC3C2(CC(=O)C4C3CC=C5C4(CCC(C5)O)C)C)OC16CCC(O6)(C)CO	444.60	unknown	https://doi.org/10.1016/S0031-9422(00)84338-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R)-2-[(2S)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2R,4R,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4-[(2R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	137705996	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	885.00	unknown	https://doi.org/10.1021/NP50039A035 https://doi.org/10.1016/0378-8741(83)90070-3
(2R)-2-[(6S)-4-hydroxy-2-(hydroxymethyl)-6-[[(1R,2R,4R,6R,8S,9S,12R,13R)-6-methoxy-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-16-yl]oxy]-5-[(2R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	137704870	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1063.20	unknown	https://doi.org/10.1080/1120009X.1991.11739110
(3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,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]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	123134748	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1063.20	unknown	https://doi.org/10.1021/NP50048A021
Dioscin	119245	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	https://doi.org/10.1021/NP50039A035 https://doi.org/10.1080/1120009X.1991.11739110 https://doi.org/10.1016/0378-8741(83)90070-3
Gracillin	159861	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	885.00	unknown	https://doi.org/10.1021/NP50039A035
Methylprotogracillin	171348	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC	1079.20	unknown	https://doi.org/10.1021/NP50048A021
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,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	12314479	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1021/NP50041A017
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/10.1016/0378-8741(83)90070-3
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0378-8741(83)90070-3
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP50041A017
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0378-8741(83)90070-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R)-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-[4-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propanoic acid	25245849	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	522.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Rosmadial	15801061	Click to see CC(C)C1=C(C2=C(C(=C1)C=O)C3(CCCC(C3C=O)(C)C)C(=O)O2)O	344.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(-)-Przewalskin B	51002763	Click to see CC(C)C1=CC23CCC4C(=CCCC4(C)C)C2OC(=O)C3(C1=O)O	330.40	unknown	via CMAUP database
Danshinspiroketallactone	56956598	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	via CMAUP database
Epidanshenspiroketallactone	102004791	Click to see CC1CC2(C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2)OC1	268.31	unknown	via CMAUP database
Salprzelactone	71816414	Click to see CC1COC(=O)C1C2C3=C(C4=CC=CC(=C4C=C3)C)C(=O)O2	296.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Salvianolic acid B	6451084	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O	718.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid	639655	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
sophoraflavanone B(1-)	25200892	Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)[O-])C	339.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3,5,7-Trihydroxy-2-[4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]chromen-4-one	74978067	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-009-9348-4
3,5,7-trihydroxy-2-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]chromen-4-one	102519401	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-009-9348-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]chromen-4-one	74957371	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)OC5C(C(C(C(O5)C)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1007/S10600-009-9348-4
5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]chromen-4-one	44226945	Click to see CC1C(C(C(C(O1)OC2=CC=C(C=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)OC5C(C(C(C(O5)C)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1007/S10600-009-9348-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy]-4H-1-benzopyran-4-one	13940823	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-009-9348-4
Kaempferol-7-rhamnoside	25079965	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-009-9348-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Serpyllin	12315479	Click to see COC1=C(C(=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)OC)OC	388.40	unknown	https://doi.org/10.1007/S10600-009-9348-4

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Dioscorea communis

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