Scientific name	Authority	First published in
Lunaria japonica	Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 74 (1865)
Wasabia japonica	(Miq.) Matsum.	Index Pl. Jap. 2(2): 161 (1912)
Wasabia okinosimensis	(Takenouchi) Hatus.	J. Nat. Hist. Soc. Fukuoka 2: 33 (1936)
Alliaria wasabi	Prantl	Nat. Pflanzenfam. 3(2): 168 (1893)
Cochlearia wasabi	Siebold	Verh. Batav. Genootsch. Kunst. xii. (1830) 54.
Eutrema japonicum var. sachalinensis	(Miyabe & T.Miyake) Nemoto	Fl. Japan, Suppl. 268 1936
Eutrema japonicum f. terrestris	(Makino) Nemoto	Fl. Japan, Suppl. 268 1936
Eutrema okinosimense	Takenouchi	J. Nat. Hist. Soc. Fukuoka 1: 369 (1935)
Eutrema wasabii	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 18: 283 (1873)
Eutrema wasabi var. sachalinensis	Miyabe & T.Miyake	Fl. Saghalin 50 1915
Eutrema wasabi f. terrestris	Makino	J. Jap. Bot. 8: 35 1932
Wasabia tenue var. okinosimense	(Taken.) Kitam.	Acta Phytotax. Geobot. 20: 201 1962
Wasabia pungens	Matsum.	Bot. Mag. (Tokyo) 13: 71. 1899
Wasabia wasabi	(Siebold) Makino	J. Jap. Bot. 8: 35 (1932)

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese horseradish
English	wasabi
Spanish	wasabi
Afrikaans	wasabi
Arabic	وسابي
Azerbaijani	vasabi
Bulgarian	васаби
Bulgarian	зелено какао
Catalan	rave japonès
Czech	křen wasabi
Czech	euterma japonská
Danish	wasabi
German	wasabi
Greek	Γουασάμπι
Esperanto	vasabio
Estonian	jaapani vasaabi
Basque	wasabi
Persian	واسابی
Finnish	maustekrassi
French	wasabi
Galician	wasabi
Hebrew	ואסאבי
Hindi	वसाबी
Croatian	wasabi
Hungarian	vaszabi
Hungarian	japán zöld torma
Hungarian	japán vízitorma
Indonesian	wasabi
Japanese	和佐比
Japanese	山葵
Japanese	ワサビ
jv	wasabi
Korean	고추냉이
Korean	와사비
ku	wasabi
Lithuanian	japoninis pipirkrienis
Malay	wasabi
nan	wasabi
Norwegian Bokmål	wasabi
Dutch	wasabi
Norwegian Nynorsk	wasabi
oc	wasabi
Polish	wasabi
Polish	wasabia japońska
Polish	chrzan japoński
Portuguese	wasabi
Romanian	wasabi
Russian	Васаби
sco	wasabi
Serbo-Croatian	vasabi
Slovak	wasabi
Slovenian	vasabi
Swedish	wasabi
Thai	วาซาบิ
Turkish	vasabi
Ukrainian	Васабі
Uzbek	vasabi
vec	wasabi
Vietnamese	wasabi
yi	וואסאבי
Chinese	块茎山萮菜
Chinese	山葵

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-temperate click to expand
- Eastern Asia
  - Japan
  - Korea
  - Taiwan
- Russian Far East
  - Sakhalin

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000683668
UNII	WA34673193
Tropicos	4103852
KEW	urn:lsid:ipni.org:names:284345-1
The Plant List	kew-2805492
Open Tree Of Life	185264
Observations.org	129708
NCBI Taxonomy	75806
IPNI	284345-1
iNaturalist	123047
GBIF	5375216
Freebase	/m/084cz
EPPO	ETMWA
EOL	483598
Elurikkus	530224
USDA GRIN	404759
Wikipedia	Wasabi

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_030161315.1	Ej_v1.1.2_hap1	Scaffold	Tokyo Institute of Technology	2023-03-10	114.0x	711.91 Mb

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

Unveiling Glucosinolate Diversity in Brassica Germplasm and In Silico Analysis for Determining Optimal Antioxidant Potential

Iwar K, Desta KT, Ochar K, Kim SH

Antioxidants (Basel)

19-Mar-2024

PMCID:	PMC10968274
doi:	10.3390/antiox13030376
PMID:	38539909

Identification and Characterization of CtUGT3 as the Key Player of Astragalin Biosynthesis in Carthamus tinctorius L.

Ren C, Xi Z, Xian B, Chen C, Huang X, Jiang H, Chen J, Peng C, Pei J

J Agric Food Chem

23-Oct-2023

PMCID:	PMC10623559
doi:	10.1021/acs.jafc.3c05117
PMID:	37870279

Screening for Fungicide Efficacy in Controlling Blackleg Disease in Wasabi (Eutrema japonicum)

Liu Y, Song C, Ren X, Wu G, Ma Z, Zhao M, Xie Y, Li Y, Lai Y

Plants (Basel)

01-Sep-2023

PMCID:	PMC10490250
doi:	10.3390/plants12173149
PMID:	37687395

The allotetraploid horseradish genome provides insights into subgenome diversification and formation of critical traits

Shen F, Xu S, Shen Q, Bi C, Lysak MA

Nat Commun

25-Jul-2023

PMCID:	PMC10368706
doi:	10.1038/s41467-023-39800-y
PMID:	37491530

Haplotype-resolved chromosomal-level assembly of wasabi (Eutrema japonicum) genome

Tanaka H, Hori T, Yamamoto S, Toyoda A, Yano K, Yamane K, Itoh T

Sci Data

11-Jul-2023

PMCID:	PMC10336049
doi:	10.1038/s41597-023-02356-z
PMID:	37433828

Chemical composition of extracts from leaves, stems and roots of wasabi (Eutrema japonicum) and their anti-cancer, anti-inflammatory and anti-microbial activities

Dos Santos Szewczyk K, Skowrońska W, Kruk A, Makuch-Kocka A, Bogucka-Kocka A, Miazga-Karska M, Grzywa-Celińska A, Granica S

Sci Rep

05-Jun-2023

PMCID:	PMC10241793
doi:	10.1038/s41598-023-36402-y
PMID:	37277512

2-Oxindole and related heterocycles: synthetic methodologies for their natural products and related derivatives

Sharma S, Monga Y, Gupta A, Singh S

RSC Adv

11-May-2023

PMCID:	PMC10173257
doi:	10.1039/d3ra02217j
PMID:	37179999

Accelerated germination of aged recalcitrant seeds by K+-rich bulk oxygen nanobubbles

Kim M, Shoji A, Kobayashi T, Shirai Y, Sugawa S, Takahashi M

Sci Rep

27-Feb-2023

PMCID:	PMC9971192
doi:	10.1038/s41598-023-30343-2
PMID:	36849737

Developing multifunctional crops by engineering Brassicaceae glucosinolate pathways

Qin H, King GJ, Borpatragohain P, Zou J

Plant Commun

23-Feb-2023

PMCID:	PMC10363516
doi:	10.1016/j.xplc.2023.100565
PMID:	36823985

Turmeric and Cumin Instead of Stock Cubes: An Internet Survey of Spices and Culinary Herbs Used in Poland Compared with Historical Cookbooks and Herbals

Łuczaj Ł, Dumanowski J, Marszałek C, Parasecoli F

Plants (Basel)

29-Jan-2023

PMCID:	PMC9919365
doi:	10.3390/plants12030591
PMID:	36771675

Volatile Oils Discrepancy between Male and Female Ochradenus arabicus and Their Allelopathic Activity on Dactyloctenium aegyptium

Abd-ElGawad AM, Assaeed AM, El Gendy AE, Dar BA, Elshamy AI

Plants (Basel)

26-Dec-2022

PMCID:	PMC9824887
doi:	10.3390/plants12010110
PMID:	36616238

Enhancement of allyl isothiocyanate-evoked responses of mouse trigeminal ganglion cells by the kokumi substance γ-glutamyl-valyl-glycine (γ-EVG) through activation of the calcium-sensing receptor (CaSR)

Akiyama T, Curtis E, Carstens MI, Carstens E

Physiol Behav

21-Dec-2022

PMCID:	PMC10239685
doi:	10.1016/j.physbeh.2022.114063
PMID:	36563734

Indirect Evidence Based on Mating-Type Ratios for the Role of Sexual Reproduction in European and Chinese Populations of Plenodomus biglobosus (Blackleg of Oilseed Rape)

King KM, Canning G, Zhou K, Liu Z, Wu M, West JS

Pathogens

20-Dec-2022

PMCID:	PMC9864567
doi:	10.3390/pathogens12010003
PMID:	36678351

Clinical effects of wasabi extract containing 6-MSITC on myalgic encephalomyelitis/chronic fatigue syndrome: an open-label trial

Oka T, Yamada Y, Lkhagvasuren B, Nakao M, Nakajima R, Kanou M, Hiramatsu R, Nabeshima YI

Biopsychosoc Med

12-Dec-2022

PMCID:	PMC9742665
doi:	10.1186/s13030-022-00255-0
PMID:	36510244

A New Approach Using the SYBR Green-Based Real-Time PCR Method for Detection of Soft Rot Pectobacterium odoriferum Associated with Kimchi Cabbage

Jin YJ, Jo D, Kwon SW, Jee S, Kim JS, Raman J, Kim SJ

Plant Pathol J

01-Dec-2022

PMCID:	PMC9742793
doi:	10.5423/PPJ.OA.09.2022.0138
PMID:	36503194

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
Phenethyl isothiocyanate	16741	Click to see C1=CC=C(C=C1)CCN=C=S	163.24	unknown	https://doi.org/10.3136/NSKKK1962.37.4_256
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1271/BBB.58.2131
> Organic acids and derivatives / Organic sulfonic acids and derivatives / Organosulfonic acids and derivatives / Organosulfonamides
6-cyano-N-methylhexane-1-sulfonamide	163192506	Click to see CNS(=O)(=O)CCCCCCC#N	204.29	unknown	https://doi.org/10.1016/S0031-9422(98)00424-5
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
1-Penten-3-OL	12020	Click to see CCC(C=C)O	86.13	unknown	https://doi.org/10.1271/BBB.58.2131
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses / Desulfoglucosinolates
1-S-(N-hydroxybut-3-enimidoyl)-1-thio-beta-D-glucopyranose	134160268	Click to see C=CCC(=NO)SC1C(C(C(C(O1)CO)O)O)O	279.31	unknown	https://doi.org/10.1207/S15327914NC4802_11
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(3,5-Dihydroxyphenyl)nonan-1-one	49778007	Click to see CCCCCCCCC(=O)C1=CC(=CC(=C1)O)O	250.33	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
> Organoheterocyclic compounds / Indoles and derivatives
Wasalexin A	44333108	Click to see CON1C2=CC=CC=C2C(=CN=C(SC)SC)C1=O	294.40	unknown	https://doi.org/10.1016/S0960-894X(99)00523-5
Wasalexin B	11380859	Click to see CON1C2=CC=CC=C2C(=CN=C(SC)SC)C1=O	294.40	unknown	https://doi.org/10.1016/S0960-894X(99)00523-5
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
1-Methoxyindole-3-carboxylic acid	124476	Click to see CON1C=C(C2=CC=CC=C21)C(=O)O	191.18	unknown	https://doi.org/10.1016/S0031-9422(98)00424-5
1-Methylindole-3-carboxylic acid	854040	Click to see CN1C=C(C2=CC=CC=C21)C(=O)O	175.18	unknown	https://doi.org/10.1016/S0960-894X(99)00523-5
> Organosulfur compounds / Allyl sulfur compounds
Allyl thiocyanate	69816	Click to see C=CCSC#N	99.16	unknown	https://doi.org/10.1007/BF02290237
> Organosulfur compounds / Isothiocyanates
3-Butenyl isothiocyanate	76922	Click to see C=CCCN=C=S	113.18	unknown	https://doi.org/10.3136/NSKKK1962.37.4_256 https://doi.org/10.1271/BBB.58.2131
4-Pentenyl isothiocyanate	87436	Click to see C=CCCCN=C=S	127.21	unknown	https://doi.org/10.1271/BBB.58.2131
5-Hexenyl isothiocyanate	184852	Click to see C=CCCCCN=C=S	141.24	unknown	https://doi.org/10.3136/NSKKK1962.37.4_256 https://doi.org/10.1271/BBB.58.2131
7-Isothiocyanato-1-heptene	11571834	Click to see C=CCCCCCN=C=S	155.26	unknown	https://doi.org/10.1271/BBB.58.2131
Allyl isothiocyanate	5971	Click to see C=CCN=C=S	99.16	unknown	https://doi.org/10.3136/NSKKK1962.37.4_256 https://doi.org/10.1271/BBB.58.2131 https://doi.org/10.1007/BF02290237
Butyl isothiocyanate	11613	Click to see CCCCN=C=S	115.20	unknown	https://doi.org/10.3136/NSKKK1962.37.4_256
sec-Butyl isothiocyanate	78151	Click to see CCC(C)N=C=S	115.20	unknown	https://doi.org/10.1271/BBB.58.2131
> Organosulfur compounds / Sulfoxides
1-Isothiocyanato-7-(methylsulfinyl)heptane	9837367	Click to see CS(=O)CCCCCCCN=C=S	219.40	unknown	https://doi.org/10.1080/00021369.1990.10870168
1-isothiocyanato-7-[(S)-methylsulfinyl]heptane	163100623	Click to see CS(=O)CCCCCCCN=C=S	219.40	unknown	https://doi.org/10.1080/00021369.1990.10870168
Alyssin	206035	Click to see CS(=O)CCCCCN=C=S	191.30	unknown	https://doi.org/10.1080/00021369.1990.10870168
Alyssin, (S)-	51548324	Click to see CS(=O)CCCCCN=C=S	191.30	unknown	https://doi.org/10.1080/00021369.1990.10870168
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 4-hydroxy-3,5-dimethoxycinnamate; Sinapic acid methyl ester	159894	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC	238.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Methyl ferulate	5357283	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O	208.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Methyl sinapate	5321318	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC	238.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
(E)-3,4-Dihydroxy-5-methoxycinnamoyl 6-O-(beta-D-glucopyranosyl)-beta-D-glucopyranoside	24827938	Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O	534.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoate	74327080	Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O	534.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[6-[[4,5-Dihydroxy-3-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoate	74326966	Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC(=C(C(=C4)OC)O)OC)O)O)O	740.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[6-[[4,5-Dihydroxy-3-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	74327018	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)CO)O)O	724.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Sinapinic acid	637775	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O	224.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[[3,4,5-trihydroxy-6-[5-hydroxy-7-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-2-(4-hydroxyphenyl)-4-oxochromen-6-yl]oxan-2-yl]methoxy]oxan-3-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	72765144	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC(=O)C=CC7=CC(=C(C(=C7)OC)O)OC)O)O)O)CO)O)O	1006.90	unknown	https://doi.org/10.1016/J.TET.2005.04.061
2-(4-Hydroxyphenyl)-5-hydroxy-6-[6-O-[2-O-(3,5-dimethoxy-4-hydroxycinnamoyl)-beta-D-glucopyranosyl]-beta-D-glucopyranosyl]-7-(3,5-dimethoxy-4-hydroxycinnamoyloxy)-4H-1-benzopyran-4-one	11787982	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC(=O)C=CC7=CC(=C(C(=C7)OC)O)OC)O)O)O)CO)O)O	1006.90	unknown	https://doi.org/10.1016/J.TET.2005.04.061
Isovitexin	162350	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/J.TET.2005.04.061
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[[3,4,5-trihydroxy-6-[5-hydroxy-7-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-4-oxo-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-6-yl]oxan-2-yl]methoxy]oxan-3-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	72760382	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)OC7C(C(C(C(O7)CO)O)O)O)OC(=O)C=CC8=CC(=C(C(=C8)OC)O)OC)O)O)O)CO)O)O	1169.00	unknown	https://doi.org/10.1016/J.TET.2005.04.061
[5-Hydroxy-4-oxo-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-7-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	73091401	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)C6C(C(C(C(O6)CO)O)O)O	800.70	unknown	https://doi.org/10.1016/J.TET.2005.04.061
2-[4-[6-O-(3,5-Dimethoxy-4-hydroxycinnamoyl)-beta-D-glucopyranosyloxy]phenyl]-5-hydroxy-6-(beta-D-glucopyranosyl)-7-(3,5-dimethoxy-4-hydroxycinnamoyloxy)-4H-1-benzopyran-4-one	102352342	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(C(=C(C=C5O4)OC(=O)C=CC6=CC(=C(C(=C6)OC)O)OC)C7C(C(C(C(O7)CO)O)O)O)O)O)O)O	1006.90	unknown	https://doi.org/10.1016/J.TET.2005.04.061

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Eutrema japonicum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top