Common products:
Clematis terniflora is primarily cultivated as an ornamental plant for horticultural use, with no significant documented commercial products derived from the species.

Industrial and craft applications:
No documented industrial or craft applications are recorded for Clematis terniflora.

Food and beverages (non-medicinal):
No food or beverage applications are documented for this species.

Colorants and tanning:
No documented use for dyes, inks, or tanning is recorded.

Wood and fiber:
No documented timber, fiber, or cordage applications exist.

Fragrance and cosmetics:
No fragrance or cosmetic applications are documented.

Properties relevant to use:
No specific industrial properties have been documented for this species.

Standards and regulation:
No relevant standards or regulatory frameworks are established for this species.

Sustainability and sourcing:
No specific sustainability concerns or sourcing practices are documented for this ornamental species.

Synonyms Top

Scientific name	Authority	First published in
Clematis dioscoreifolia	H.Lév. & Vaniot	Repert. Spec. Nov. Regni Veg. 7: 339 (1909)
Clematis maximowicziana	Franch. & Sav.	Enum. Pl. Jap. 2: 261 (1878)
Clematis paniculata	Thunb.	Trans. Linn. Soc. London 2: 337. 1794 [1 May 1794]
Clematis paniculata var. denticulata	Nakai	Handb. Kor. Manch. For. 110 1939
Clematis recta f. lancifolia	Nakai	J. Coll. Sci. Imp. Univ. Tokyo 26(1): 10 1909
Clematis terniflora f. denticulata	(Nakai) W.Lee	Lin. Fl. Koreae : 327 (1996)
Clematis terniflora var. denticulata	(Nakai) U.C.La	Fl. Coreana 2: 234 (1996)
Clematis terniflora var. lancifolia	(Nakai) U.C.La	Fl. Coreana 2: 234 (1996)
Clematis dioscoreifolia var. robusta	(Carrière) Rehder	J. Arnold Arbor. 26: 70 1945
Clematis flammula var. robusta	Carrière	Rev. Hort. 46: 465 1874
Clematis maximowicziana var. robusta	(Carrière) Nakai	Bull. Natl. Sci. Mus. Tokyo 33: 7 1953
Clematis paniculata var. dioscoreifolia	(H.Lév. & Vaniot) Rehder	J. Arnold Arbor. 1: 195 1920
Clematis terniflora var. robusta	(Carrière) Tamura	Acta Phytotax. Geobot. 15: 18 1953
Clematis terniflora var. koreana	(Nakai) Tamura	Acta Phytotax. Geobot. 15: 18 1953
Clematis recta var. koreana	Nakai	J. Coll. Sci. Imp. Univ. Tokyo 26(1): 9. 1909 [8 Feb 1909]

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	sweet autumn virginsbower
Bulgarian	трицветен повет
Indonesian	kerisih luruh manis
Japanese	キイセンニンソウ
Japanese	クレマティス・テルニフローラ
Japanese	仙人草
Japanese	センニンソウ
Swedish	stor vippklematis
Chinese	黄药子
Chinese	铜脚威灵仙
Chinese	小叶力刚
Chinese	铜威灵
Chinese	圆锥铁线莲
Chinese	蟹珠眼草
Chinese	圓錐鐵線蓮

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Clematis terniflora var. garanbiensis	(Hay.) M.C.Chang	Fl. Reipubl. Popularis Sin. 28: 170 (1980)
Clematis terniflora var. manshurica	(Rupr.) Ohwi	Acta Phytotax. Geobot. 7: 43 1938

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000610758
Florida Plant Atlas	1360
Flora of Alabama	3037
Canadensys	8463
USDA Plants	CLTE4
UConn	113
Tropicos	27100907
KEW	urn:lsid:ipni.org:names:710123-1
The Plant List	kew-2726804
Missouri Botanical Garden	286181
Open Tree Of Life	21289
NCBI Taxonomy	231663
Nature Serve	2.146692
IPNI	710123-1
iNaturalist	62776
GBIF	3033546
Freebase	/m/03d3c_7
EPPO	CLVMX
EOL	594682
Calflora (Californian flora)	8709
USDA GRIN	316251
Wikipedia	Clematis_terniflora

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

Anti-Inflammatory Effects of Clematis terniflora Leaf on Lipopolysaccharide-Induced Acute Lung Injury

Park JY, Kim MJ, Choi YA, Kim YY, Lee S, Chung JM, Kim SY, Jeong GS, Kim SH

Evid Based Complement Alternat Med

09-Jan-2024

PMCID:	PMC10791263
doi:	10.1155/2024/6653893
PMID:	38230250

In Vitro Cytotoxic Potential of Selected Jordanian Flora and Their Associated Phytochemical Analysis

Alruwad MI, Sabry MM, Gendy AM, El-Dine RS, El Hefnawy HM

Plants (Basel)

12-Apr-2023

PMCID:	PMC10142466
doi:	10.3390/plants12081626
PMID:	37111849

Comparative metabolomic profiling of Arabidopsis thaliana roots and leaves reveals complex response mechanisms induced by a seaweed extract

Tran TL, Callahan DL, Islam MT, Wang Y, Arioli T, Cahill D

Front Plant Sci

09-Mar-2023

PMCID:	PMC10035662
doi:	10.3389/fpls.2023.1114172
PMID:	36968386

Recent Advances of Polyphenol Oxidases in Plants

Zhang S

Molecules

25-Feb-2023

PMCID:	PMC10004730
doi:	10.3390/molecules28052158
PMID:	36903403

Pest categorisation of Icerya aegyptiaca

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, MacLeod A

EFSA J

09-Jan-2023

PMCID:	PMC9827230
doi:	10.2903/j.efsa.2023.7739
PMID:	36628331

Integrative Proteomic and Phosphoproteomic Analyses Revealed the Regulatory Mechanism of the Response to Ultraviolet B Stress in Clematis ternifloraDC

Tao M, Liu S, Liu A, Li Y, Tian J, Yang B, Zhu W

ACS Omega

29-Dec-2022

PMCID:	PMC9835548
doi:	10.1021/acsomega.2c07258
PMID:	36643485

Rapid Identification of Paeoniae Radix and Moutan Radicis Cortex Using a SCAR Marker-Based Conventional PCR Assay

Kim WJ, Noh S, Choi G, Moon BC

Plants (Basel)

27-Oct-2022

PMCID:	PMC9653921
doi:	10.3390/plants11212870
PMID:	36365322

Exogenous gibberellin can effectively and rapidly break intermediate physiological dormancy of Amsonia elliptica seeds

Lee SY, Park K, Jang BK, Ji B, Lee H, Baskin CC, Cho JS

Front Plant Sci

26-Oct-2022

PMCID:	PMC9643720
doi:	10.3389/fpls.2022.1043897
PMID:	36388572

Stem cambial variants of Taiwan lianas

Yang SZ, Chen PH, Chen JJ

Bot Stud

24-Sep-2022

PMCID:	PMC9509506
doi:	10.1186/s40529-022-00358-5
PMID:	36153445

Characterization of the complete chloroplast genome of the Helleborus atrorubens Waldst. & Kit. (Ranunculaceae)

Shi X, Mao L, Jin L, Ma G

Mitochondrial DNA B Resour

07-Sep-2022

PMCID:	PMC9467529
doi:	10.1080/23802359.2022.2119105
PMID:	36106185

Aurantiamide Acetate Ameliorates Lung Inflammation in Lipopolysaccharide-Induced Acute Lung Injury in Mice

Fang Z, Fang J, Gao C, Wu Y, Yu W

Biomed Res Int

22-Aug-2022

PMCID:	PMC9424011
doi:	10.1155/2022/3510423
PMID:	36046440

Solanum nigrum Linn.: An Insight into Current Research on Traditional Uses, Phytochemistry, and Pharmacology

Chen X, Dai X, Liu Y, Yang Y, Yuan L, He X, Gong G

Front Pharmacol

16-Aug-2022

PMCID:	PMC9424827
doi:	10.3389/fphar.2022.918071
PMID:	36052142

Plantago asiatica mosaic virus: An emerging plant virus causing necrosis in lilies and a new model RNA virus for molecular research

Komatsu K, Hammond J

Mol Plant Pathol

20-Jul-2022

PMCID:	PMC9452766
doi:	10.1111/mpp.13243
PMID:	35856603

Foliar and Root Comparative Metabolomics and Phenolic Profiling of Micro-Tom Tomato (Solanum lycopersicum L.) Plants Associated with a Gene Expression Analysis in Response to Short Daily UV Treatments

Mannucci A, Santin M, Vanhaelewyn L, Sciampagna MC, Miras-Moreno MB, Zhang L, Lucini L, Quartacci MF, Van Der Straeten D, Castagna A, Ranieri A

Plants (Basel)

12-Jul-2022

PMCID:	PMC9319050
doi:	10.3390/plants11141829
PMID:	35890464

UVB Irradiation-Induced Transcriptional Changes in Lignin- and Flavonoid Biosynthesis and Indole/Tryptophan-Auxin-Responsive Genes in Rice Seedlings

Kim GE, Kim MS, Sung J

Plants (Basel)

20-Jun-2022

PMCID:	PMC9229965
doi:	10.3390/plants11121618
PMID:	35736769

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-3-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	100928195	Click to see	2308.40	unknown	https://doi.org/10.1248/CPB.46.1891
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-3-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	100928198	Click to see	2470.50	unknown	https://doi.org/10.1248/CPB.46.1891
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5R)-5-[(2R,3R,4R,5S,6R)-5-[(2S,3R,4S,5R,6R)-4-[(2S,3R,4R,5S,6R)-6-[[(2R,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]oxymethyl]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-3-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	100928197	Click to see	2470.50	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside H	100928196	Click to see	2292.40	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside K	49799267	Click to see	2308.40	unknown	https://doi.org/10.1248/CPB.46.1891
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162998966	Click to see	1337.50	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside B	49799230	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)OC(=O)C=CC1=CC(=C(C=C1)OC)O)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1837.90	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside C	49799231	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)OC1C(C(C(CO1)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)O)OC(=O)C=CC1=CC(=C(C=C1)OC)O)O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1837.90	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside D	49799265	Click to see	2162.20	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside E	49799266	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)OC)O)OC5C(OC(C(C5O)O)OC6COC(C(C6O)O)OC7C(C(OC(C7O)OC8C(C(COC8OC9CCC1(C(C9(C)C)CCC2(C1CC=C1C2(CCC2(C1CC(CC2)(C)C)C(=O)OC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O)C)C)C)O)O)C)O)CO)CO)O)O)O)O)O)O)O	2146.20	unknown	https://doi.org/10.1248/CPB.46.1891
Clematernoside F	100928193	Click to see	1852.00	unknown	https://doi.org/10.1248/CPB.46.1891
Clematichinenoside C	49799271	Click to see	1499.60	unknown	https://doi.org/10.1248/CPB.46.1891
Huzhangoside B	49799269	Click to see	1337.50	unknown	https://doi.org/10.1248/CPB.46.1891
HuzhangosideB	13880086	Click to see	1337.50	unknown	https://doi.org/10.1248/CPB.46.1891
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One	12313332	Click to see	594.50	unknown	https://doi.org/10.1007/S10600-007-0061-X
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/S10600-007-0061-X
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/S10600-007-0061-X
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1007/S10600-007-0061-X
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1007/S10600-007-0061-X
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1007/S10600-007-0061-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2R,3S,4R,5S,6R)-2-[3,5-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	163189399	Click to see	756.70	unknown	https://doi.org/10.1007/S10600-007-0061-X
[6-[2-[3,5-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	163087003	Click to see	756.70	unknown	https://doi.org/10.1007/S10600-007-0061-X

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Clematis terniflora

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top