Scientific name	Authority	First published in
Dioscorea opposita	Thunb.	Fl. Jap. : 151 (1784)
Dioscorea oppositifolia var. dukhunensis	Prain & Burkill	J. Proc. Asiat. Soc. Bengal 10: 30. 1914
Dioscorea oppositifolia var. linnaei	Prain & Burkill	J. Proc. Asiat. Soc. Bengal 10: 30. 1914
Dioscorea oppositifolia var. thwaitesii	Prain & Burkill	J. Proc. Asiat. Soc. Bengal 10: 30. 1914

Common names Top

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Filter by language:

Language	Common/alternative name
English	chinese yam
Arabic	ديسقوريا متقابلة الأوراق
Czech	jam obecný
Indonesian	kelunak
Italian	nagaimo
Japanese	ツクネイモ
Japanese	仏掌薯
Japanese	つくね芋
Japanese	ながいも
Japanese	ヤマトイモ
Japanese	大和芋
Japanese	山薬
Japanese	薯預
Japanese	長いも
Japanese	長イモ
Japanese	長芋
Japanese	ナガイモ
Japanese	ショヨ
Japanese	サンヤク
Japanese	イチョウイモ
Japanese	薯蕷
Japanese	チャイニーズヤム
Korean	마
lo	ເຜືອກຍາວ
Lithuanian	batatinė dioskorėja
Malayalam	നൂറൻ കിഴങ്ങ്
Malay	ubi kelonak
Malay	ubi kelona
Malay	akar kelana
nan	hoâi-san
Polish	chiński ziemniak
Polish	pochrzyn chiński
Polish	jams chiński
pwn	qaqilj
Swedish	jams
Tamil	மலையன்கிழங்கு
Thai	ฮ่วยซัว
Chinese	面山药
Chinese	薯蕷
Chinese	山药
Chinese	野脚板薯
Chinese	對葉薯蕷
Chinese	山藥
Chinese	對葉薯蕷、薯蕷
Chinese	薯蓣
Chinese	薯药

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

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Sri Lanka
- Indo-China
  - Myanmar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000393046
UNII	KZY1A7K8MD
USDA Plants	DIOP
Tropicos	11000029
KEW	urn:lsid:ipni.org:names:318348-1
The Plant List	kew-240599
Open Tree Of Life	981893
NCBI Taxonomy	569628
IPNI	318348-1
iNaturalist	161932
GBIF	2754965
Freebase	/m/0bf6y0
EOL	1120830
USDA GRIN	402570
Wikipedia	Dioscorea_oppositifolia
CMAUP	NPO7863

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

Identification of WRKY gene family in Dioscorea opposita Thunb. reveals that DoWRKY71 enhanced the tolerance to cold and ABA stress

Xing L, Zhang Y, Ge M, Zhao L, Huo X

PeerJ

28-Mar-2024

PMCID:	PMC10981886
doi:	10.7717/peerj.17016
PMID:	38560473

Jian-Pi-Gu-Shen-Hua-Yu Decoction Alleviated Diabetic Nephropathy in Mice through Reducing Ferroptosis

Lv S, Fan L, Chen X, Su X, Dong L, Wang Q, Wang Y, Zhang H, Cui H, Zhang S, Wang L

J Diabetes Res

16-Mar-2024

PMCID:	PMC10960652
doi:	10.1155/2024/9990304
PMID:	38523631

Jianpi Gushen Huayu decoction ameliorated diabetic nephropathy through modulating metabolites in kidney, and inhibiting TLR4/NF-κB/NLRP3 and JNK/P38 pathways

Ma ZA, Wang LX, Zhang H, Li HZ, Dong L, Wang QH, Wang YS, Pan BC, Zhang SF, Cui HT, Lv SQ

World J Diabetes

15-Mar-2024

PMCID:	PMC10999033
doi:	10.4239/wjd.v15.i3.502
PMID:	38591083

Zhuang-Gu-Fang intervenes vasculogenic and osteogenic coupling in GK rats through Notch1/Noggin/VEGF pathway

Jin X, Sun Y, Bai R, Shi J, Zhai L, Jiang Y, Jiang M, He J, Li J, Wang T, Li S, Chen W

Heliyon

13-Mar-2024

PMCID:	PMC10958413
doi:	10.1016/j.heliyon.2024.e28014
PMID:	38524608

A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics

Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL

Chin Med

07-Mar-2024

PMCID:	PMC10918936
doi:	10.1186/s13020-024-00915-z
PMID:	38454483

Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy

Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J

Heliyon

06-Mar-2024

PMCID:	PMC10945194
doi:	10.1016/j.heliyon.2024.e27530
PMID:	38501018

JianPiYiShen formula prevents cisplatin-induced acute kidney injury in mice by improving necroptosis through MAPK pathway

Li Z, He R, Liu J, Jin X, Jiang B, Lao Y, Yang S

BMC Complement Med Ther

24-Feb-2024

PMCID:	PMC10893720
doi:	10.1186/s12906-024-04366-9
PMID:	38402163

Identification and Characterization of Nigrospora Species and a Novel Species, Nigrospora anhuiensis, Causing Black Leaf Spot on Rice and Wild Rice in the Anhui Province of China

Liu Y, An J, Safdar A, Shen Y, Sun Y, Shu W, Tan X, Zhu B, Xiao J, Schirawski J, He F, Zhu G

J Fungi (Basel)

16-Feb-2024

PMCID:	PMC10890061
doi:	10.3390/jof10020156
PMID:	38392829

Advances in Traditional Chinese Medicine research in diabetic kidney disease treatment

Shen S, Zhong H, Zhou X, Li G, Zhang C, Zhu Y, Yang Y

Pharm Biol

15-Feb-2024

PMCID:	PMC10877659
doi:	10.1080/13880209.2024.2314705
PMID:	38357845

Traditional Chinese Medicine is Associated with the Reduction in Endpoint Events in Patients with Gouty Arthritis: Cohort Study and Association Rule Analysis

Chen Y, Liu J, Cong C, Li Y, Hu Y

Int J Gen Med

13-Feb-2024

PMCID:	PMC10874188
doi:	10.2147/IJGM.S451097
PMID:	38371521

Effect of Konjac Glucomannan on Structure, Physicochemical Properties, and In Vitro Digestibility of Yam Starch during Extrusion

Hao M, Zhu X, Ji X, Shi M, Yan Y

Foods

01-Feb-2024

PMCID:	PMC10855837
doi:	10.3390/foods13030463
PMID:	38338597

Comprehensive widely targeted metabolomics to decipher the molecular mechanisms of Dioscorea opposita thunb. cv. Tiegun quality formation during harvest

An L, Yuan Y, Chen H, Li M, Ma J, Zhou J, Zheng L, Ma H, Chen Z, Hao C, Wu X

Food Chem X

01-Feb-2024

PMCID:	PMC10847880
doi:	10.1016/j.fochx.2024.101159
PMID:	38328697

Molecular Characterization and Pathogenicity of an Infectious cDNA Clone of Youcai Mosaic Virus on Solanum nigrum

Gu T, Feng C, Hua Y, Liu D, Chen H, He Z, Xu K, Zhang K

Int J Mol Sci

28-Jan-2024

PMCID:	PMC10855738
doi:	10.3390/ijms25031620
PMID:	38338897

Mechanisms of Bushen Tiaoxue Granules against controlled ovarian hyperstimulation-induced abnormal morphology of endometrium based on network pharmacology

Zhang JC, Zhang HL, Xin XY, Zhu YT, Mao X, Hu HQ, Jin YX, Fan RW, Zhang XH, Ye Y, Li D

J Ovarian Res

26-Jan-2024

PMCID:	PMC10811918
doi:	10.1186/s13048-023-01339-3
PMID:	38279186

The reporting quality of randomized controlled trials in Chinese herbal medicine (CHM) formulas for diabetes based on the consort statement and its extension for CHM formulas

Liu Y, Hu C, Zhou K, Zhang Y, Kang J, Wen Y, Yuan R, Li J, Zhao Q, Zhang L, Yang X

Front Pharmacol

22-Jan-2024

PMCID:	PMC10839105
doi:	10.3389/fphar.2024.1288479
PMID:	38318135

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 / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
7-Methoxy-9,10-dihydrophenanthrene-2,5-diol	442702	Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O	242.27	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
Hircinol	442705	Click to see COC1=CC(=CC2=C1C3=C(CC2)C=CC=C3O)O	242.27	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
3,5-Dimethoxy-2,7-phenanthrenediol	44572330	Click to see COC1=C2C(=CC(=C1)O)C=CC3=CC(=C(C=C32)OC)O	270.28	unknown	https://doi.org/10.1016/J.BMC.2009.02.057 https://doi.org/10.1016/S0031-9422(00)81417-X
6,7-Dihydroxy-2-methoxy-1,4-phenanthrenedione	135520438	Click to see COC1=CC(=O)C2=C(C1=O)C=CC3=CC(=C(C=C32)O)O	270.24	unknown	https://doi.org/10.1021/NP050021C
Batatasin I	442694	Click to see COC1=CC(=C2C(=C1)C=CC3=CC(=C(C=C32)O)OC)OC	284.31	unknown	https://doi.org/10.1055/S-0028-1097298
Moscatin	194774	Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C(=CC=C3)O	240.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-9,10-dideuteriooctadec-9-enoic acid	13011408	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
Elaidic Acid	637517	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	https://doi.org/10.1248/CPB.52.1235
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid	2266	Click to see C(CCCC(=O)O)CCCC(=O)O	188.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphocholines / Phosphatidylcholines
(2s)-3-(Hexadecanoyloxy)-2-[(9z)-Octadec-9-Enoyloxy]propyl 2-(Trimethylammonio)ethyl Phosphate	10908846	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC	760.10	unknown	https://doi.org/10.1248/CPB.52.1235
1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine	5497103	Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC	760.10	unknown	https://doi.org/10.1248/CPB.52.1235
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
(1R,2R,5S,8R,9S,10R,11S,12S)-12-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	3034393	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	via CMAUP database
(1R,2R,8S,9S,10R,11R)-5-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	45109787	Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O	332.40	unknown	via CMAUP database
(1S,2S,5S,8S,9R,10S,11R,12S)-12-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	49868293	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	via CMAUP database
(2R,5R,9S,10R,11S,12S)-12-hydroxy-11-methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	71306853	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	via CMAUP database
1-Methyl-8-methylidene-13-oxododecahydro-4a,1-(epoxymethano)-7,9a-methanobenzo[a]azulene-10-carboxylic acid	443456	Click to see CC12CCCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O	316.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075870/
11-Methyl-6-methylidene-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	623366	Click to see CC12CCCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O	316.40	unknown	via CMAUP database
4aalpha,4bbeta-Gibbane-1alpha,10beta-dicarboxylic acid, 2beta,4a-dihydroxy-1-methyl-8-methylene-, 1,4a-lactone	622971	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	via CMAUP database
Gibbane-1,10-dicarboxylic acid, 2,4a-dihydroxy-1-methyl-8-methylene-, 1,4a-lactone, (1alpha,2beta,4aalpha,4bbeta,10beta)-	443457	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075870/
Gibberellin 20	439635	Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O	332.40	unknown	via CMAUP database
Gibberellin A20	5280481	Click to see CC12CCCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O	332.40	unknown	via CMAUP database
Gibberellin A4	92109	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	via CMAUP database
Gibberellin A9	5281984	Click to see CC12CCCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O	316.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
Gibberellin A12	443450	Click to see CC12CCCC(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)(C)C(=O)O	332.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075870/
gibberellin A12(2-)	25244528	Click to see CC12CCCC(C1C(C34C2CCC(C3)C(=C)C4)C(=O)[O-])(C)C(=O)[O-]	330.40	unknown	via CMAUP database
Gibberellin A19	5460209	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C=O)C(=O)O	362.40	unknown	via CMAUP database
gibberellin A19(2-)	25200921	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)[O-])C=O)C(=O)[O-]	360.40	unknown	via CMAUP database
Gibberellin A24	443454	Click to see CC1(CCCC2(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)C=O)C(=O)O	346.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075870/
Gibberellin A36	443455	Click to see CC1(C(CCC2(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)C=O)O)C(=O)O	362.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075870/
Gibberellin A53	440914	Click to see CC12CCCC(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)(C)C(=O)O	348.40	unknown	via CMAUP database
Gibberellin-A-12	3081953	Click to see CC12CCCC(C1C(C34C2CCC(C3)C(=C)C4)C(=O)O)(C)C(=O)O	332.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S)-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-yl] acetate	6432446	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	via CMAUP database
beta-Sitosterol acetate	5354503	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	via CMAUP database
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Stigmast-5-en-3-yl acetate	521199	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids / Simple glycosylceramides / Glycosyl-N-acylsphingosines
(+)-Soyacerebroside I	131751281	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	https://doi.org/10.1248/CPB.52.1235
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	https://doi.org/10.1248/CPB.52.1235
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,5S,9S,10S,13R,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162852488	Click to see CC(C)C(C)CCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)O	400.70	unknown	https://doi.org/10.1016/0031-9422(91)83651-Z
(3S,5S,9S,10S,13R,17R)-17-[(2R,5S)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162852489	Click to see CC(C)C(C)CCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)O	400.70	unknown	https://doi.org/10.1016/0031-9422(91)83651-Z
alpha-Ergostenol	312796	Click to see CC(C)C(C)CCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)O	400.70	unknown	https://doi.org/10.1016/0031-9422(91)83651-Z
Ergostanol	5283641	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C	402.70	unknown	https://doi.org/10.1016/0031-9422(91)83651-Z
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
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	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	6432744	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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/10.1248/CPB.52.1235
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/10.1248/CPB.52.1235
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/10.1248/CPB.52.1235
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1021/NP050021C
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	https://doi.org/10.1021/NP050021C
> Nucleosides, nucleotides, and analogues / Purine nucleosides
9-alpha-Ribofuranosyladenine	448378	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	https://doi.org/10.1248/CPB.52.1235
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
cyclo(L-tyrosyl-L-phenylalanyl)	11438306	Click to see C1=CC=C(C=C1)CC2C(=O)NC(C(=O)N2)CC3=CC=C(C=C3)O	310.30	unknown	via CMAUP database
Cyclo(tyrosyl-tyrosyl)	192816	Click to see C1=CC(=CC=C1CC2C(=O)NC(C(=O)N2)CC3=CC=C(C=C3)O)O	326.30	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Trimethyl citrate	74112	Click to see COC(=O)CC(CC(=O)OC)(C(=O)OC)O	234.20	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Inositol phosphates
Phytic acid	890	Click to see C1(C(C(C(C(C1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O	660.04	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(4,6-dihydroxyphenanthren-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol	10407945	Click to see C1=CC2=C(C3=C1C=CC(=C3)O)C(=C(C=C2)OC4C(C(C(C(O4)CO)O)O)O)O	388.40	unknown	https://doi.org/10.1248/CPB.52.1235
2-(4,6-Dihydroxyphenanthren-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol	85134650	Click to see C1=CC2=C(C3=C1C=CC(=C3)O)C(=C(C=C2)OC4C(C(C(C(O4)CO)O)O)O)O	388.40	unknown	https://doi.org/10.1248/CPB.52.1235
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Glycoprotein	439212	Click to see CC(=O)NC1C(C(C(OC1NC(=O)CC(C(=O)N)NC(=O)C)CO)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)NC(=O)C)O	741.70	unknown	https://doi.org/10.3136/NSKKK.48.578
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin	204	Click to see C1(C(=O)NC(=O)N1)NC(=O)N	158.12	unknown	https://doi.org/10.1055/S-2006-961841 https://doi.org/10.2503/JJSHS.72.321
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Allantoins
(S)-(+)-allantoin	439714	Click to see C1(C(=O)NC(=O)N1)NC(=O)N	158.12	unknown	via CMAUP database
Allantoin, (-)-	439713	Click to see C1(C(=O)NC(=O)N1)NC(=O)N	158.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
10,11-Dihydro-4-methoxy-dibenz[b,f]oxepin-2-ol	44572329	Click to see COC1=CC(=CC2=C1OC3=CC=CC=C3CC2)O	242.27	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
10,11-Dihydro-dibenz[b,f]oxepin-2,4-diol	44572328	Click to see C1CC2=C(C(=CC(=C2)O)O)OC3=CC=CC=C31	228.24	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,4E,6E)-1,7-bis(4-hydroxyphenyl)hepta-1,4,6-trien-3-one	10447050	Click to see C1=CC(=CC=C1C=CC=CC(=O)C=CC2=CC=C(C=C2)O)O	292.30	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
(4E,6E)-1,7-bis(4-hydroxyphenyl)-4,6-heptadien-3-one	71447176	Click to see C1=CC(=CC=C1CCC(=O)C=CC=CC2=CC=C(C=C2)O)O	294.30	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
1-(4-Hydroxyphenyl)-7-(3-methoxy-4-hydroxyphenyl)-4,6-heptadiene-3-one	24901215	Click to see COC1=C(C=CC(=C1)C=CC=CC(=O)CCC2=CC=C(C=C2)O)O	324.40	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
1,7-Bis (4-hydroxyphenyl)-1,4,6-heptatrien-3-one	71346280	Click to see C1=CC(=CC=C1C=CC=CC(=O)C=CC2=CC=C(C=C2)O)O	292.30	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one	10613719	Click to see C1=CC(=CC=C1CCC(=O)C=CC=CC2=CC=C(C=C2)O)O	294.30	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
7-(4-Hydroxy-3-methoxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one	74349582	Click to see COC1=C(C=CC(=C1)C=CC=CC(=O)CCC2=CC=C(C=C2)O)O	324.40	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(3R,5R)-1,7-bis(4-hydroxy-3-methoxyphenyl)-3,5-heptanediol	10883331	Click to see COC1=C(C=CC(=C1)CCC(CC(CCC2=CC(=C(C=C2)O)OC)O)O)O	376.40	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
(3R,5R)-1,7-Bis(4-hydroxyphenyl)-3,5-heptanediol	11034432	Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC=C(C=C2)O)O)O)O	316.40	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
Hannokinol	14427394	Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC=C(C=C2)O)O)O)O	316.40	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
meso-Hannokinol	25763835	Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC=C(C=C2)O)O)O)O	316.40	unknown	via CMAUP database
Octahydrocurcumin	11068834	Click to see COC1=C(C=CC(=C1)CCC(CC(CCC2=CC(=C(C=C2)O)OC)O)O)O	376.40	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
6-[(2R,4R,5S,6R)-4,5-dihydroxy-6-methyloxan-2-yl]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	162964986	Click to see CC1C(C(CC(O1)C2=C(C3=C(C=C2O)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O	430.40	unknown	https://doi.org/10.1021/NP050021C
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-Dihydroxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	14406833	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1021/NP050021C
Chrysoeriol 4'-O-beta-D-glucopyranoside	14406834	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1021/NP050021C
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496342	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP050021C
7-(4,5-Dihydroxyoxan-2-yl)oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	163036861	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4CC(C(CO4)O)O)O)O	416.40	unknown	https://doi.org/10.1021/NP050021C
7-[(2R,4S,5S)-4,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one	163036862	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4CC(C(CO4)O)O)O)O	416.40	unknown	https://doi.org/10.1021/NP050021C
Chrysoeriol-7-O-beta-D-glucoside	13871877	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP050021C
Thermopsoside	11294177	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	462.40	unknown	https://doi.org/10.1021/NP050021C
> Phenylpropanoids and polyketides / Stilbenes
2-(3,5-Dimethoxyphenethyl)phenol	19423974	Click to see COC1=CC(=CC(=C1)CCC2=CC=CC=C2O)OC	258.31	unknown	https://doi.org/10.1016/S0031-9422(00)81417-X
2-[2-(3,4,5-Trimethoxyphenyl)ethyl]phenol	12888722	Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC=CC=C2O	288.34	unknown	https://doi.org/10.1016/S0031-9422(00)98532-7
2,4'-Dihydroxy-3',5'-dimethoxybibenzyl	14731336	Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC=CC=C2O	274.31	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
3,3',5-Trihydroxy-2'-methoxybibenzyl	44156958	Click to see COC1=C(C=CC=C1O)CCC2=CC(=CC(=C2)O)O	260.28	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
3,5-Dihydroxy-4-methoxybibenzyl	44572212	Click to see COC1=C(C=C(C=C1O)CCC2=CC=CC=C2)O	244.28	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
5-[2-(2-Hydroxyphenyl)ethyl]-2,3-dimethoxy-phenol	10754781	Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC=CC=C2O	274.31	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
5-[2-(3-Methoxyphenyl)ethyl]benzene-1,3-diol	163079590	Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)O)O	244.28	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
Batatasin II	85806015	Click to see COC1=C(C(=C(C(=C1)CCC2=CC=CC=C2)O)O)OC	274.31	unknown	https://doi.org/10.1016/S0031-9422(00)98532-7
batatasin III	10466989	Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O	244.28	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
Batatasin IV	181271	Click to see COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2O	244.28	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
Demethylbatatasin IV	442699	Click to see C1=CC=C(C(=C1)CCC2=CC(=CC(=C2)O)O)O	230.26	unknown	https://doi.org/10.1016/J.BMC.2009.02.057
Dihydropinosylvin	442700	Click to see C1=CC=C(C=C1)CCC2=CC(=CC(=C2)O)O	214.26	unknown	https://doi.org/10.1016/S0031-9422(00)81417-X
Tristin	15736297	Click to see COC1=C(C=CC(=C1)CCC2=CC(=CC(=C2)O)O)O	260.28	unknown	via CMAUP database

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Dioscorea oppositifolia

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