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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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

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

Potential Effects of Traditional Chinese Medicine in Anti-Aging and Aging-Related Diseases: Current Evidence and Perspectives

Ding X, Ma X, Meng P, Yue J, Li L, Xu L

Clin Interv Aging

01-May-2024

PMCID:	PMC11070163
doi:	10.2147/CIA.S447514
PMID:	38706635

Codonopsis radix: a review of resource utilisation, postharvest processing, quality assessment, and its polysaccharide composition

Liang W, Sun J, Bai G, Qiu D, Li Q, Dong P, Chen Y, Guo F

Front Pharmacol

30-Apr-2024

PMCID:	PMC11091420
doi:	10.3389/fphar.2024.1366556
PMID:	38746010

Liver fat as a dietary target by Chinese Medical Nutrition Therapy (CMNT) diet for treating type 2 diabetes with non-alcoholic fatty liver disease: study protocol for a randomised controlled trial

Luo W, Xiao Z, Yang X, Wu R, Li J, Yu Z, Guo S, Nie B, Liu D

BMJ Open

29-Apr-2024

PMCID:	PMC11086286
doi:	10.1136/bmjopen-2023-081263
PMID:	38684277

Investigation of the hypoglycemic mechanism of the ShenQi compound formula through metabonomics and 16S rRNA sequencing

Gao J, Zhou X, Gao H, Xu G, Xie C, Xie H

Front Pharmacol

19-Apr-2024

PMCID:	PMC11066276
doi:	10.3389/fphar.2024.1349244
PMID:	38708085

Zhibai dihuang pill (ZBDH) exhibits therapeutic effects on idiopathic central sexual precocity in rats by modulating the gut microflora

Yi C, Zou H, Lin X, Liu S, Wang J, Tian Y, Deng X, Luo J, Li C, Long Y

Heliyon

16-Apr-2024

PMCID:	PMC11066310
doi:	10.1016/j.heliyon.2024.e29723
PMID:	38707434

Bulbil initiation: a comprehensive review on resources, development, and utilisation, with emphasis on molecular mechanisms, advanced technologies, and future prospects

Shu F, Wang D, Sarsaiya S, Jin L, Liu K, Zhao M, Wang X, Yao Z, Chen G, Chen J

Front Plant Sci

08-Apr-2024

PMCID:	PMC11033377
doi:	10.3389/fpls.2024.1343222
PMID:	38650701

Traditional Chinese medicine in osteoporosis: from pathogenesis to potential activity

Cao G, Hu S, Ning Y, Dou X, Ding C, Wang L, Wang Z, Sang X, Yang Q, Shi J, Hao M, Han X

Front Pharmacol

02-Apr-2024

PMCID:	PMC11019011
doi:	10.3389/fphar.2024.1370900
PMID:	38628648

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

Medicinal plants and natural products for treating overactive bladder

Chen H, Hoi MP, Lee SM

Chin Med

27-Mar-2024

PMCID:	PMC10967063
doi:	10.1186/s13020-024-00884-3
PMID:	38532487

The Role and Mechanism of Paeoniae Radix Alba in Tumor Therapy

Yang Y, Yuan L, Wang K, Lu D, Meng F, Xu D, Li W, Nan Y

Molecules

22-Mar-2024

PMCID:	PMC11012976
doi:	10.3390/molecules29071424
PMID:	38611704

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

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
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
Oleic acid-d2	13011408	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	284.50	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
CID 443457	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/
Gibbane-1,10-dicarboxylic acid, 2,4a-dihydroxy-1-methyl-8-methylene-, 1,4a-lactone, (1alpha,2beta,4aalpha,4bbeta,10beta)-	622971	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)C(=C)C5)C(=O)O)OC2=O)O	332.40	unknown	via CMAUP database
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
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-ol, acetate, (3beta)-	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
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
1,7-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
Tsaokoarylone	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
> 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-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	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
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
> 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
3,2'-Dihydroxy-4,5-dimethoxybibenzyl	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
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-(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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