Scientific name	Authority	First published in
Dioscorea cliffortiana	Lam.	Encycl. 3: 232 (1789)
Dioscorea glauca	Muhl. ex Beck	Bot. North. Middle States : 355 (1833)
Dioscorea hexaphylla	Raf.	New Fl. 2: 89 (1837)
Dioscorea hirticaulis	Bartlett	Bull. Bur. Pl. Industr. U.S.D.A. 189: 17 (1910)
Dioscorea lloydiana	E.H.L.Krause	Beih. Bot. Centralbl. 32(2): 331 (1914)
Dioscorea longifolia	Raf.	New Fl. 2: 89 (1837)
Dioscorea megaptera	Raf.	New Fl. 2: 88 (1837)
Dioscorea paniculata	Michx.	Fl. Bor.-Amer. 2: 239 (1803)
Dioscorea paniculata var. glabrifolia	Bartlett	Bull. Bur. Pl. Industr. U.S.D.A. 189: 15 (1910)
Dioscorea pruinosa	Kunth	Enum. Pl. 5: 338 (1850)
Dioscorea quaternata	Walter	Fl. Carol. 246. 1788 (1788)
Dioscorea quaternata var. glauca	(Muhl.) Fernald	Rhodora 39: 399 (1937)
Dioscorea quinata	J.F.Gmel.	Syst. Nat., ed. 13[bis]. 2(1): 581. 1791 [late Sep-Nov 1791]
Dioscorea repanda	Raf.	New Fl. 2: 89 (1837)
Dioscorea sativa	L.	Sp. Pl. 2: 1033. 1753 [1 May 1753]
Dioscorea villosa var. glabra	J.Lloyd ex A.Gray	Manual ed. 7: 297. 1908
Dioscorea villosa subsp. glabrifolia	(Bartlett) W.Stone	Pl. S. New Jersey : 358 (1912)
Dioscorea villosa var. glabrifolia	S.F.Blake	Rhodora 20: 49 (1918)
Dioscorea villosa f. glabrifolia	(Bartlett) Fernald	Rhodora 39: 401 (1937)
Dioscorea villosa subsp. glauca	(Muhl. ex L.C.Beck) R.Knuth	Pflanzenr. IV, 43: 173 1924
Dioscorea villosa subsp. hirticaulis	(Bartlett) R.Knuth	Pflanzenr. IV, 43: 173. 1924 (1924)
Dioscorea villosa var. hirticaulis	(Bartlett) H.E.Ahles	J. Elisha Mitchell Sci. Soc. 80: 172 (1964)
Dioscorea villosa var. laeviuscula	Alph.Wood	Class-book Bot. , ed. 2: 544 (1847)
Dioscorea villosa subsp. paniculata	(Michx.) R.Knuth	Pflanzenr. IV, 43: 173. 1924 (1924)
Dioscorea villosa subsp. quaternata	(Walter) R.Knuth	Pflanzenr. IV, 43: 173. 1924 (1924)
Dioscorea waltheri	Desf.	Tabl. École Bot. , ed. 2: 269 (1815)
Merione villosa	Salisb.	Gen. Pl. : 12 (1866)
Dioscorea villosa var. glabrifolia	(Bartlett) W.Stone	Pl. S. New Jersey 358 1912

Common names Top

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Filter by language:

Language	Common/alternative name
English	wild yam
Arabic	ديسقوريا وبرية
German	wilde yams
Persian	یام وحشی
Hungarian	mexikói jamgyökér
Hungarian	ideggyökér
Malay	ubi kuning
Chinese	大西洋薯蓣
Chinese	长柔毛薯蓣

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Northern America click to expand
- Eastern Canada
  - Ontario
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - Oklahoma
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia

Southern America click to expand
- Caribbean
  - Cuba
  - Leeward Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000396542
UNII	Z95519QROX
Florida Plant Atlas	1722
Flora of Alabama	4268
Canadensys	5353
USDA Plants	DIVI4
Tropicos	11000317
KEW	urn:lsid:ipni.org:names:318778-1
The Plant List	kew-241123
Open Tree Of Life	36277
Observations.org	321957
NCBI Taxonomy	330167
Nature Serve	2.153733
IPNI	318778-1
iNaturalist	129324
GBIF	2754553
Freebase	/m/068dgh
WisFlora	3409
EPPO	DIUVI
EOL	1120610
Elurikkus	296138
USDA GRIN	14267
Wikipedia	Dioscorea_villosa
CMAUP	NPO17707
CMAUP	NPO9301

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

Functionalized Carbon Nanotubes for Delivery of Ferulic Acid and Diosgenin Anticancer Natural Agents

AbouAitah K, Abdelaziz AM, Higazy IM, Swiderska-Sroda A, Hassan AM, Shaker OG, Szałaj U, Stobinski L, Malolepszy A, Lojkowski W

ACS Appl Bio Mater

22-Jan-2024

PMCID:	PMC10880110
doi:	10.1021/acsabm.3c00700
PMID:	38253026

Medicinal Herbs: Promising Immunomodulators for the Treatment of Infectious Diseases

Alanazi HH, Elasbali AM, Alanazi MK, El Azab EF

Molecules

12-Dec-2023

PMCID:	PMC10745476
doi:	10.3390/molecules28248045
PMID:	38138535

Role of the pharmacist in the management of postmenopausal breast cancer treatment with vasomotor symptoms: A case report

Undeberg MR, Barash A, McKeirnan KC

Explor Res Clin Soc Pharm

24-Aug-2023

PMCID:	PMC10485165
doi:	10.1016/j.rcsop.2023.100324
PMID:	37694166

Analysis of Safety Concerns on Herbal Products with Assumed Phytoestrogenic Activity

Tjeerdsma AM, van Hunsel FP, van de Koppel S, Ekhart C, Vitalone A, Woerdenbag HJ

Pharmaceuticals (Basel)

10-Aug-2023

PMCID:	PMC10459077
doi:	10.3390/ph16081137
PMID:	37631050

Steroidal Saponins: Naturally Occurring Compounds as Inhibitors of the Hallmarks of Cancer

Bouabdallah S, Al-Maktoum A, Amin A

Cancers (Basel)

31-Jul-2023

PMCID:	PMC10417465
doi:	10.3390/cancers15153900
PMID:	37568716

Fortification of orange juice with microencapsulated Kocuria flava Y4 towards a novel functional beverage: Biological and quality aspects

Barik A, Pallavi P, Sen SK, Rajhans G, Bose A, Raut S

Heliyon

26-Jun-2023

PMCID:	PMC10336446
doi:	10.1016/j.heliyon.2023.e17509
PMID:	37449169

Low-coverage whole genome sequencing of eleven species/subspecies in Dioscorea sect. Stenophora (Dioscoreaceae): comparative plastome analyses, molecular markers development and phylogenetic inference

Hu K, Sun XQ, Chen M, Lu RS

Front Plant Sci

06-Jun-2023

PMCID:	PMC10281252
doi:	10.3389/fpls.2023.1196176
PMID:	37346115

Diosgenin Inhibits ROS Generation by Modulating NOX4 and Mitochondrial Respiratory Chain and Suppresses Apoptosis in Diabetic Nephropathy

Zhong Y, Wang L, Jin R, Liu J, Luo R, Zhang Y, Zhu L, Peng X

Nutrients

30-Apr-2023

PMCID:	PMC10181383
doi:	10.3390/nu15092164
PMID:	37432297

The Application of Ethnomedicine in Modulating Megakaryocyte Differentiation and Platelet Counts

Yang F, Lai J, Deng J, Du J, Du X, Zhang X, Wang Y, Huang Q, Xu Q, Yang G, Zhang Y, Zhou X, Zhang X, Yuan Y, Zhang C, Wu J

Int J Mol Sci

05-Feb-2023

PMCID:	PMC9961075
doi:	10.3390/ijms24043168
PMID:	36834579

Targeting the Interplay of Autophagy and ROS for Cancer Therapy: An Updated Overview on Phytochemicals

Dong L, He J, Luo L, Wang K

Pharmaceuticals (Basel)

08-Jan-2023

PMCID:	PMC9865312
doi:	10.3390/ph16010092
PMID:	36678588

Plant vs. Kidney: Evaluating Nephrotoxicity of Botanicals with the Latest Toxicological Tools

Pearson A, Gafner S, Rider CV, Embry M, Ferguson SS, Mitchell CA

Curr Opin Toxicol

31-Aug-2022

PMCID:	PMC9601601
doi:	10.1016/j.cotox.2022.100371
PMID:	36311298

Editorial: Chemosensitizing effect of natural products against cancers: Applications in enhancing chemotherapy and immunotherapy

Roy NK, Tewari D, Esposito MT

Front Pharmacol

30-Aug-2022

PMCID:	PMC9469189
doi:	10.3389/fphar.2022.988226
PMID:	36110549

A Novel Diosgenin-Based Liposome Delivery System Combined with Doxorubicin for Liver Cancer Therapy

Chen L, Lan J, Li Z, Zeng R, Wang Y, Zhen L, Jin H, Ding Y, Zhang T

Pharmaceutics

12-Aug-2022

PMCID:	PMC9416271
doi:	10.3390/pharmaceutics14081685
PMID:	36015311

Diosgenin and Its Analogs: Potential Protective Agents Against Atherosclerosis

Wang D, Wang X

Drug Des Devel Ther

17-Jul-2022

PMCID:	PMC9304635
doi:	10.2147/DDDT.S368836
PMID:	35875677

Design, synthesis and biological evaluation of novel diosgenin–benzoic acid mustard hybrids with potential anti-proliferative activities in human hepatoma HepG2 cells

Zhang J, Wang W, Tian Y, Ma L, Zhou L, Sun H, Ma Y, Hou H, Wang X, Ye J, Wang X

J Enzyme Inhib Med Chem

02-Jun-2022

PMCID:	PMC9176691
doi:	10.1080/14756366.2022.2070161
PMID:	35652316

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
> Alkaloids and derivatives / Aristolactams
2-Hydroxy-1,5-dimethoxydibenzo[cd,f]indol-4(5H)-one	622222	Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3N(C2=O)OC)O	295.29	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,5-Trimethoxybenzaldehyde	20525	Click to see COC1=CC(=C(C=C1C=O)OC)OC	196.20	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(1S,5R,6R,7R,8S)-7-(3,4-dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one	44470608	Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C=C3)OC)OC	358.40	unknown	via CMAUP database
Kadsurenin L	3083437	Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)OC(=O)C)C3=CC(=C(C=C3)OC)OC	400.50	unknown	via CMAUP database
Piperenone	36406703	Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC(=C(C=C3)OC)OC	388.50	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Aminophenyl ethers
2,4,6-Trimethoxyaniline	84271	Click to see COC1=CC(=C(C(=C1)OC)N)OC	183.20	unknown	via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see COC1=CC(=CC(=C1OC)OC)CC=C	208.25	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin	11175182	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	via CMAUP database
(2S)-2alpha-(3,4-Dimethoxyphenyl)-3beta,4alpha-dimethyl-5alpha-(1,3-benzodioxole-5-yl)tetrahydrofuran	26113495	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
4-[(2R,3S,4R,5R)-5-(1,3-Benzodioxol-5-yl)tetrahydro-3,4-dimethyl-2-furanyl]-2-methoxyphenol	11078392	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	via CMAUP database
4-[(2S,3R,4R,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol	93061877	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
5-((2R,3R,4S,5R)-5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl)-1,3-benzodioxole	188429	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
Futokadsurin A	9548904	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
futokadsurin B	9548905	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
futokadsurin C	9548906	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C	356.40	unknown	via CMAUP database
Galbelgin	11975378	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Galgravin	101749	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Machillin F	10450045	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C	342.40	unknown	via CMAUP database
nectandrin A	156516	Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C	358.40	unknown	via CMAUP database
Veraguensin	443026	Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C	372.50	unknown	via CMAUP database
Zuihonin A	338287	Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C	340.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Pellitorine	5318516	Click to see CCCCCC=CC=CC(=O)NCC(C)C	223.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol	6474938	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one	101833872	Click to see CC(=CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC	354.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Plumieride	72319	Click to see CC(C1=CC2(C=CC3C2C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)O	470.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,4S,8R,10S,11S,14S)-11-ethyl-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylic acid	38348951	Click to see CCC1C2C3(C=CC4C3C(O2)OC=C4C(=O)O)OC1=O	278.26	unknown	via CMAUP database
Allamandin	5281540	Click to see CC=C1C2C3(C=CC4C3C(O2)OC(C4C(=O)OC)O)OC1=O	308.28	unknown	via CMAUP database
Isoplumericin	5281543	Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O	290.27	unknown	via CMAUP database
methyl (1S,4S,8R,10S,11S,14S)-11-ethyl-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate	95790359	Click to see CCC1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O	292.28	unknown	via CMAUP database
Plumericin	5281545	Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O	290.27	unknown	via CMAUP database
Plumeridoid C	123964288	Click to see CC(C1=CC2(C=CC3C2COC(C3C(=O)OC)O)OC1=O)O	310.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
beta-Amyrin acetate	92156	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Lupeol	259846	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
Lupeol acetate	92157	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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(24R)-Cycloarta-25-ene-3beta,24-diol	14313591	Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-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]icos-18-en-16-yl]oxy]-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	163102837	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)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	1079.20	unknown	https://doi.org/10.1002/MRC.2071
(2S,3R,4R,5R,6S)-2-[(2S,3S,4S,5R,6S)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-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-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	154496365	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/10.1007/S11418-006-0126-3
(2S,3R,4S,5R,6S)-2-[(2R,3S,4S,5R,6S)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3S,4R,5S,6S)-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,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	162997664	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)O	1049.20	unknown	https://doi.org/10.1007/S11418-006-0126-3
2-[4-Hydroxy-2-(hydroxymethyl)-6-(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-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	271916	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/10.1016/J.BBAMEM.2012.12.010 https://doi.org/10.1002/MRC.2071
2-[4-Hydroxy-6-(hydroxymethyl)-2-[[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-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	14080167	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)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	1079.20	unknown	https://doi.org/10.1002/MRC.2071
CID 75049187	75049187	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)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1047.20	unknown	https://doi.org/10.1002/MRC.2071
Deltonin	441884	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)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	885.00	unknown	https://doi.org/10.1002/MRC.2071
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/10.1002/MRC.2071
Furostane base-2H + O-Hex, O-Hex-dHex-dHex	500375	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)O	1049.20	unknown	https://doi.org/10.1055/S-0030-1249960
Methylprotodioscin	11263254	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/10.1002/MRC.2071 https://doi.org/10.1007/S11418-006-0126-3
NSC-698790;Smilax saponin B	500376	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/10.1002/MRC.2071
Ophiopogonin C'	4483248	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	https://doi.org/10.1002/MRC.2071
Progenin II	44429638	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)O)C)C)C)OC1	722.90	unknown	https://doi.org/10.1007/S11418-006-0126-3
Prosapogenin A	11061578	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1	722.90	unknown	https://doi.org/10.1007/S11418-006-0126-3 https://doi.org/10.1002/MRC.2071
Protodioscin	441891	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)O	1049.20	unknown	https://doi.org/10.1055/S-0030-1249960
Trilloside A	4483040	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)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	885.00	unknown	https://doi.org/10.1002/MRC.2071
Zingiberen newsaponin	102475150	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)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1047.20	unknown	https://doi.org/10.1002/MRC.2071
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paroxypropione	6271	Click to see CCC(=O)C1=CC=C(C=C1)O	150.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(2beta,4beta,5alpha,5abeta)-4-(1,3-Benzodioxol-5-yl)-2,3,4,5-tetrahydro-7-methoxy-5-methyl-8H-2,5a-methano-1-benzoxepin-8-one	101820916	Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5	340.40	unknown	via CMAUP database
(E,E)-Futoamide	15596445	Click to see CC(C)CNC(=O)C=CCCC=CC1=CC2=C(C=C1)OCO2	301.40	unknown	via CMAUP database
Kadsurin A	442885	Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	372.40	unknown	via CMAUP database
Kadsurin B	10022290	Click to see CC1C(OC2(C1(C=C(C(C2)O)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4	374.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-azaniumyl-3-(1H-indol-3-yl)propanoate	6923516	Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+]	204.22	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Fulvoplumierin	5281541	Click to see CC=CC=C1C=CC2=C1C(=O)OC=C2C(=O)OC	244.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives
Plumericidine	45101897	Click to see CC(C1=CC2(CCC3=C2C=NC=C3)OC1=O)O	231.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolizines
Plumerinine	14583329	Click to see CC1CCC(N2C1CC(CC2C(C)C)O)C	225.37	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2beta-(3,4-Dimethoxyphenyl)-3alpha-methyl-3aalpha-methoxy-5-allyl-2,3,3a,6-tetrahydrobenzofuran-6-one	10915273	Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC	356.40	unknown	via CMAUP database
Kadsurenin M	208856	Click to see CC1C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C=C3)OC)OC	328.40	unknown	via CMAUP database
Kadsurenone	122159	Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC	356.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[[(2R,3S)-3-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	14757896	Click to see COC1=CC2=C(CC(C(O2)C3=CC(=C(C(=C3)OC)O)OC)O)C(=C1)OC4C(C(C(C(O4)CO)O)O)O	510.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin	5280682	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O	344.30	unknown	via CMAUP database
Pilloin	5320496	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database

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Dioscorea villosa

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