Scientific name	Authority	First published in
Mastacanthus barbula	Steud.	Nomencl. Bot. , ed. 2, 2: 105 (1841)
Nepeta incana	Thunb. ex Houtt.	Nat. Hist. 2(9): 307 (1778)
Caryopteris incana var. candida	C.K.Schneid.	Ill. Handb. Laubholzk. 2: 596. 1911
Caryopteris incana f. candida	(C.K.Schneid.) H.Hara	Enum. Sperm. Jap. 1: 187 1948
Caryopteris mastacanthus var. nana	Borsch	Hardy Alp. Pl. 8. 1927
Caryopteris mastacanthus var. superba	Dreer	Gard. Book 21, 117. 1935

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	أبو ذقن زرقاء
Arabic	ابو ذقن زرقه
Arabic	أبو ذقن زرقة
Czech	ořechokřídlec šedivý
Danish	viol-blåskæg
Korean	층꽃나무
Slovak	bradavec sivý
Chinese	兰香草
Chinese	灰葉蕕
Chinese	莸

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Caryopteris incana var. angustifolia	S.L.Chen & R.L.Guo	Fl. Reipubl. Popularis Sin. 65(1): 213 (1982)
Caryopteris incana var. incana		Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Taiwan

Europe click to expand
- Southeastern Europe
  - Bulgaria

Northern America click to expand
- North-central U.S.A.
  - Illinois

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000808950
UNII	9Y284K559O
Tropicos	33702327
KEW	urn:lsid:ipni.org:names:861591-1
The Plant List	kew-34719
Open Tree Of Life	215075
NCBI Taxonomy	41386
IPNI	861591-1
iNaturalist	627199
GBIF	7308640
EPPO	CRBIN
EOL	2893518
USDA GRIN	9274

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

Evaluation of Anticancer and Anti-Inflammatory Activities of Some Synthetic Rearranged Abietanes

Ait El Had M, Zentar H, Ruiz-Muñoz B, Sainz J, Guardia JJ, Fernández A, Justicia J, Alvarez-Manzaneda E, Reyes-Zurita FJ, Chahboun R

Int J Mol Sci

01-Sep-2023

PMCID:	PMC10487843
doi:	10.3390/ijms241713583
PMID:	37686389

Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities

Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S

Biomolecules

02-Dec-2022

PMCID:	PMC9775335
doi:	10.3390/biom12121807
PMID:	36551235

Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach

Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP

Plants (Basel)

13-Nov-2022

PMCID:	PMC9696113
doi:	10.3390/plants11223070
PMID:	36432799

Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments

Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W

BMC Complement Med Ther

19-Sep-2022

PMCID:	PMC9484230
doi:	10.1186/s12906-022-03712-z
PMID:	36123737

Efficacy of a Horticultural Therapy Program Designed for Emotional Stability and Career Exploration among Adolescents in Juvenile Detention Centers

Park KH, Kim SY, Park SA

Int J Environ Res Public Health

20-Jul-2022

PMCID:	PMC9319874
doi:	10.3390/ijerph19148812
PMID:	35886667

Complete chloroplast genome sequence and phylogenetic analysis of Clerodendrum japonicum (Thunb.) Sweet (Ajugoideae, Lamiaceae)

Chen G, Wang LG, Wang YH

Mitochondrial DNA B Resour

05-Jul-2021

PMCID:	PMC8259852
doi:	10.1080/23802359.2021.1944367
PMID:	34263052

An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines

Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T

Cancers (Basel)

13-Oct-2020

PMCID:	PMC7601952
doi:	10.3390/cancers12102957
PMID:	33066157

A Narrow Endemic or a Species Showing Disjunct Distribution? Studies on Meehania montis-koyae Ohwi (Lamiaceae)

Takano A, Sakaguchi S, Li P, Matsuo A, Suyama Y, Xia GH, Liu X, Isagi Y

Plants (Basel)

08-Sep-2020

PMCID:	PMC7570357
doi:	10.3390/plants9091159
PMID:	32911695

The tropical-subtropical evergreen forest transition in East Asia: An exploration

Ashton P, Zhu H

Plant Divers

25-May-2020

PMCID:	PMC7567766
doi:	10.1016/j.pld.2020.04.001
PMID:	33094198

Antiprotozoal activity of diterpenoids isolated from Zhumeria majdae- absolute configuration by circular dichroism

Zadali R, Nejad Ebrahimi S, Tofighi Z, Es-haghi A, Hamburger M, Kaiser M, D’ Ambola M, De Tommasi N, Hadjiakhoondi A

Daru

11-May-2020

PMCID:	PMC7704868
doi:	10.1007/s40199-020-00345-w
PMID:	32394309

Pollen record of climate change during the last deglaciation from the eastern Tibetan Plateau

Shi W, Jiang H, Mao X, Xu H

PLoS One

06-May-2020

PMCID:	PMC7202599
doi:	10.1371/journal.pone.0232803
PMID:	32374789

GC-MS Analysis of the Composition of the Extracts and Essential Oil from Myristica fragrans Seeds Using Magnesium Aluminometasilicate as Excipient

Matulyte I, Marksa M, Ivanauskas L, Kalvėnienė Z, Lazauskas R, Bernatoniene J

Molecules

18-Mar-2019

PMCID:	PMC6471610
doi:	10.3390/molecules24061062
PMID:	30889896

Molecular phylogenetics and biogeography of the mint tribe Elsholtzieae (Nepetoideae, Lamiaceae), with an emphasis on its diversification in East Asia

Li P, Qi ZC, Liu LX, Ohi-Toma T, Lee J, Hsieh TH, Fu CX, Cameron KM, Qiu YX

Sci Rep

17-May-2017

PMCID:	PMC5435694
doi:	10.1038/s41598-017-02157-6
PMID:	28515478

New Iridoid Glucosides from Caryopteris incana (Thunb.) Miq. and Their α-Glucosidase Inhibitory Activities

Mao XD, Chou GX, Zhao SM, Zhang CG

Molecules

21-Dec-2016

PMCID:	PMC6273012
doi:	10.3390/molecules21121749
PMID:	28009847

ChemInform Abstract: Abietane Diterpenoids from Caryopteris incana (Thunb.) Miq.

Sen‐Miao Zhao, Gui‐Xin Chou, Qing‐Shan Yang, Wei Wang, Jian‐Li Zhou

Wiley

14-Jul-2016

doi:	10.1002/CHIN.201631217

Phytochemical Profile Top

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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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,10aS)-5,6,8-trihydroxy-7-[(2S)-2-hydroxypropyl]-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	162853116	Click to see CC(CC1=C(C2=C(C(=C1O)O)C3(CCCC(C3CC2=O)(C)C)C)O)O	348.40	unknown	https://doi.org/10.1016/S0031-9422(96)00609-7
5,6,8-trihydroxy-7-(2-hydroxypropyl)-1,1,4a-trimethyl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one	3283921	Click to see CC(CC1=C(C2=C(C(=C1O)O)C3(CCCC(C3CC2=O)(C)C)C)O)O	348.40	unknown	https://doi.org/10.1016/S0031-9422(96)00609-7
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one	275529	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(96)00609-7
Incanone	102066392	Click to see CC(CC1=C(C2=C(C(=C1O)O)C3(CCCC(C3CC2=O)(C)C)C)O)O	348.40	unknown	https://doi.org/10.1016/S0031-9422(96)00609-7 https://doi.org/10.1002/CHIN.201631217
Sugiol	94162	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	https://doi.org/10.1016/S0031-9422(96)00609-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5S,7S,7aR)-1,4a,5,6,7,7a-Hexahydro-4a,5,7-trihydroxy-7-methylcyclopenta[c]pyran-1-yl beta-D-glucopyranoside	145706031	Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O	364.34	unknown	https://doi.org/10.1016/S0031-9422(99)00086-2
(2S,3S,5R,6R)-2-[[(1S,4aS,5R,7S,7aR)-4a,5,7-trihydroxy-7-methyl-1,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-one	15489522	Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(=O)C(C(O3)CO)O)O)O)O)O	362.33	unknown	https://doi.org/10.1016/S0031-9422(99)00086-2
[(1S,4aS,5R,7S,7aS)-1-[(2S,3S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-oxooxan-2-yl]oxy-4a,5-dihydroxy-7-methyl-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate	100982868	Click to see CC(=O)OC1(CC(C2(C1C(OC=C2)OC3C(C(=O)C(C(O3)CO)O)O)O)O)C	404.40	unknown	https://doi.org/10.1016/S0031-9422(99)00086-2
[(4aS,7S,7aR)-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] acetate	137703299	Click to see CC(=O)OC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)C	406.40	unknown	https://doi.org/10.1016/S0031-9422(99)00086-2
Harpagide	93045	Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O	364.34	unknown	https://doi.org/10.1016/S0031-9422(99)00086-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,6R,7R,8S,11R,12S,15S,16R,19S,20R,21R)-7,20-diethyl-19-hydroxy-3,7,11,16,20-pentamethyl-8-pentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-enyl] acetate	163191247	Click to see CCC1(C2CCC3(CC4=CCC5C(C4CCC3C2(CCC1OC(=O)C)C)(CCC(C5(C)CC)O)C)C)C	512.80	unknown	https://doi.org/10.1271/BBB.63.983
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	10327934	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	786.70	unknown	https://doi.org/10.1271/BBB.63.983
[(2S,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-3-hydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(3,4-dihydroxyphenyl)propanoate	163195113	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OC(=O)CCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.70	unknown	https://doi.org/10.1271/BBB.63.983
[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-3,5-dihydroxyoxan-2-yl] 3-(3,4-dihydroxyphenyl)propanoate	163188289	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC(=O)CCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.70	unknown	https://doi.org/10.1271/BBB.63.983
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-3-hydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(3,4-dihydroxyphenyl)propanoate	163021017	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OC(=O)CCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.70	unknown	https://doi.org/10.1271/BBB.63.983
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	85098811	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.80	unknown	https://doi.org/10.1248/CPB.48.1075
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethoxy]-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	73092457	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)OC)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.80	unknown	https://doi.org/10.1248/CPB.48.1075
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	162909204	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	800.80	unknown	https://doi.org/10.1248/CPB.48.1075
[4-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxymethyl]-3,5-dihydroxyoxan-2-yl] 3-(3,4-dihydroxyphenyl)propanoate	162965711	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC(=O)CCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.70	unknown	https://doi.org/10.1271/BBB.63.983
Incanoside C	10010564	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	800.80	unknown	https://doi.org/10.1248/CPB.48.1075
Incanoside D	10033344	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.80	unknown	https://doi.org/10.1248/CPB.48.1075
Incanoside E	11765908	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)OC)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	814.80	unknown	https://doi.org/10.1248/CPB.48.1075
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	85140196	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O	342.30	unknown	https://doi.org/10.1271/BBB.63.983
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	73323377	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1271/BBB.63.983
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside	132274946	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1271/BBB.63.983
6-O-caffeoyl-beta-glucose	101419460	Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O	342.30	unknown	https://doi.org/10.1271/BBB.63.983
Acteoside;Kusaginin;TJC160	354009	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1271/BBB.63.983
CID 73157790	73157790	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O	548.50	unknown	https://doi.org/10.1248/CPB.48.1075
Isoacteoside	6476333	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1271/BBB.63.983
Sibiricose A1	6326016	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O	548.50	unknown	https://doi.org/10.1248/CPB.48.1075
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1271/BBB.63.983

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Caryopteris incana

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