Scientific name	Authority	First published in
Nauclea aculeata	Willd.	Sp. Pl., ed. 4 , 1: 929 (1798)
Nauclea guianensis	Poir.	Bot. Nomencl. : 130 (1794)
Ourouparia guianensis	Aubl.	Hist. Pl. Guiane : 177 (1775)
Uncaria aculeata	Willd.	Delect. Opusc. Bot. 2: 200 (1793)
Uncaria spinosa	Raeusch.	Nomencl. Bot. : 55 (1797)
Uruparia guianensis	(Aubl.) Kuntze	Revis. Gen. Pl. 1: 301. 1891 (1891)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	nauclea guianensis
Spanish	ourouparia guianensis
Spanish	uncaria aculeata
Spanish	uncaria spinosa
Spanish	uruparia versicolor

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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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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil West-central
- Caribbean
  - Trinidad-Tobago
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Paraguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000329248
Tropicos	27903887
INPN	734936
KEW	urn:lsid:ipni.org:names:768250-1
The Plant List	kew-209803
PFAF	Uncaria guianensis
Open Tree Of Life	1089068
NCBI Taxonomy	170183
IPNI	768250-1
iNaturalist	706980
GBIF	5338243
Freebase	/m/0cz92jv
EOL	1108381
USDA GRIN	413468
Wikipedia	Uncaria_guianensis
CMAUP	NPO358

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

Machine learning applications for multi-source data of edible crops: A review of current trends and future prospects

Zhang Y, Wang Y

Food Chem X

03-Sep-2023

PMCID:	PMC10534232
doi:	10.1016/j.fochx.2023.100860
PMID:	37780348

Recent trends of machine learning applied to multi-source data of medicinal plants

Zhang Y, Wang Y

J Pharm Anal

25-Jul-2023

PMCID:	PMC10785154
doi:	10.1016/j.jpha.2023.07.012
PMID:	38223450

Chloroplast genome characterization of Uncaria guianensis and Uncaria tomentosa and evolutive dynamics of the Cinchonoideae subfamily

Castro AA, Nunes R, Carvalho LR, Targueta CP, dos Santos Braga-Ferreira R, de Melo-Ximenes AA, Corvalán LC, Bertoni BW, Pereira AM, de Campos Telles MP

Sci Rep

24-May-2023

PMCID:	PMC10209157
doi:	10.1038/s41598-023-34334-1
PMID:	37225737

Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach

De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K

In Silico Pharmacol

28-Apr-2023

PMCID:	PMC10141836
doi:	10.1007/s40203-023-00143-7
PMID:	37131867

Indoor microbiome, microbial and plant metabolites, chemical compounds, and asthma symptoms in junior high school students: a multicentre association study in Malaysia

Sun Y, Zhang M, Ou Z, Meng Y, Chen Y, Lin R, Hashim JH, Hashim Z, Wieslander G, Chen Q, Norbäck D, Fu X

Eur Respir J

10-Nov-2022

PMCID:	PMC9647074
doi:	10.1183/13993003.00260-2022
PMID:	35618276

Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review

Salazar-Gómez A, Alonso-Castro AJ

Pharmaceuticals (Basel)

31-Aug-2022

PMCID:	PMC9505834
doi:	10.3390/ph15091095
PMID:	36145316

Effects of diet on the outcomes of rheumatic and musculoskeletal diseases (RMDs): systematic review and meta-analyses informing the 2021 EULAR recommendations for lifestyle improvements in people with RMDs

Gwinnutt JM, Wieczorek M, Rodríguez-Carrio J, Balanescu A, Bischoff-Ferrari HA, Boonen A, Cavalli G, de Souza S, de Thurah A, Dorner TE, Moe RH, Putrik P, Silva-Fernández L, Stamm T, Walker-Bone K, Welling J, Zlatković-Švenda M, Guillemin F, Verstappen SM

RMD Open

11-May-2022

PMCID:	PMC9096533
doi:	10.1136/rmdopen-2021-002167
PMID:	35654458

Operational definition of complementary, alternative, and integrative medicine derived from a systematic search

Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D

BMC Complement Med Ther

12-Apr-2022

PMCID:	PMC9006507
doi:	10.1186/s12906-022-03556-7
PMID:	35413882

Potential plants for inflammatory dysfunction in the SARS-CoV-2 infection

Marmitt DJ

Inflammopharmacology

07-Apr-2022

PMCID:	PMC8987270
doi:	10.1007/s10787-022-00981-5
PMID:	35389124

Genetic diversity among genotypes of Uncaria guianensis (Aubl.) J.F. Gmel. maintained in an in vitro germplasm bank

Pinto GH, Lopes AA, de Freitas Morel LJ, Crevelin EJ, Miranda CE, Contini SH, de Castro França S, Bertoni BW, Pereira AM

3 Biotech

07-Dec-2021

PMCID:	PMC8651866
doi:	10.1007/s13205-021-03016-y
PMID:	34956811

Endometriosis and Phytoestrogens: Friends or Foes? A Systematic Review

Bartiromo L, Schimberni M, Villanacci R, Ottolina J, Dolci C, Salmeri N, Viganò P, Candiani M

Nutrients

24-Jul-2021

PMCID:	PMC8398277
doi:	10.3390/nu13082532
PMID:	34444692

The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis

Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E

Front Pharmacol

08-Jun-2021

PMCID:	PMC8248671
doi:	10.3389/fphar.2021.690432
PMID:	34220515

Dietary Interventions with Polyphenols in Osteoarthritis: A Systematic Review Directed from the Preclinical Data to Randomized Clinical Studies

Valsamidou E, Gioxari A, Amerikanou C, Zoumpoulakis P, Skarpas G, Kaliora AC

Nutrients

23-Apr-2021

PMCID:	PMC8145539
doi:	10.3390/nu13051420
PMID:	33922527

Nutraceutical supplements in management of pain and disability in osteoarthritis: a systematic review and meta-analysis of randomized clinical trials

Aghamohammadi D, Dolatkhah N, Bakhtiari F, Eslamian F, Hashemian M

Sci Rep

01-Dec-2020

PMCID:	PMC7708648
doi:	10.1038/s41598-020-78075-x
PMID:	33262447

Antimycobacterial and PknB Inhibitory Activities of Venezuelan Medicinal Plants

Aranaga CA, Fraile S, Torres A, Falco A, Michelangeli F, Takiff H

Int J Microbiol

01-Aug-2020

PMCID:	PMC7416274
doi:	10.1155/2020/8823764
PMID:	32802074

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
Hirsutine	3037884	Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34	368.50	unknown	via CMAUP database
Isocorynantheidine	10948612	Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34	368.50	unknown	via CMAUP database
methyl (Z)-2-[(2S,3R,12bR)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate	5318054	Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3)C(=O)OC	366.50	unknown	via CMAUP database
> Alkaloids and derivatives / Yohimbine alkaloids
3-Isoajmalicine	11416867	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1590/S0100-40422004000600007
Lamuran	251561	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1590/S0100-40422004000600007 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446702/
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate	13250	Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O	198.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid	101602332	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O	632.80	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-6a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	14060280	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C(=O)O	957.10	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
3beta-(beta-D-Fucopyranosyloxy)urs-12-ene-27,28-dioic acid 27-(beta-D-glucopyranosyl) ester	44567012	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C(=O)O	795.00	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
Quinovic acid 3-O-alpha-L-rhamnopyranoside	3508071	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O	632.80	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
Quinovic acid glycoside 1	44593498	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C(=O)O	957.10	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
Quinovin	11411086	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O	632.80	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(2-O,3-O-diacetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid	53483549	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)OC(=O)C)OC(=O)C)O)O)O	967.10	unknown	via CMAUP database
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(3-O-acetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid	53483550	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)OC(=O)C)O)O)O)O	925.10	unknown	via CMAUP database
3beta-[2-O-(3-O-alpha-L-Arabinopyranosyl-alpha-L-rhamnopyranosyl)-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid	21637697	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	via CMAUP database
3beta-[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyloxy]-23-hydroxyolean-12-en-28-oic acid	101682282	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)O)O)O)O)O	883.10	unknown	via CMAUP database
Hederagenin	73299	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Rarasaponin III	24866792	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O	925.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(1R,2S,5S,6S,9R,12S,13S,16S,18R)-16-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-2-hydroxy-13-methylspiro[7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icosane-6,4'-oxolane]-2'-one	162981104	Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC56C4(CCC5C7(CC(=O)OC7)OC6)O)C)O)OC)O	550.70	unknown	https://doi.org/10.1016/0031-9422(91)84223-F
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
2(5H)-Furanone, 4-(hydroxymethyl)-	157706	Click to see C1C(=CC(=O)O1)CO	114.10	unknown	via CMAUP database
> Organoheterocyclic compounds / Furofurans
lappaceolide B	11572139	Click to see C1C(=O)OCC12COC3(C2OC(=O)C3)CO	228.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Indolizidines
(1S,4aS,5aS,6S,10aR)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylic acid	101176445	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)O)C5=CC=CC=C5NC4=O	354.40	unknown	https://doi.org/10.1590/S0100-40422004000600007
(3R,20S)-19alpha-Methyl-2-oxoformosanan-16-carboxylic acid methyl ester	98363	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1055/S-2006-960860
Isomitraphylline	11726520	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1590/S0100-40422004000600007 https://doi.org/10.1078/0944-7113-00117
Isopteropodine	9885603	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1055/S-2006-960860
Isorhynchophylline	3037048	Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O	384.50	unknown	via CMAUP database
methyl (1R,4aS,5aR,6R,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate	11943653	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	via CMAUP database
methyl (1S,5aS,6S,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate	134823823	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1055/S-2006-960860 https://doi.org/10.1078/0944-7113-00117
methyl (Z)-2-[(6'R,7'S)-6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate	5318653	Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O	384.50	unknown	via CMAUP database
Mitraphylline	94160	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1078/0944-7113-00117
Pteropodine	10429112	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	https://doi.org/10.1055/S-2006-960860
Speciophylline	168985	Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O	368.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1078/0944-7113-00117
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1078/0944-7113-00117
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside	5320686	Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside	21606527	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database

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Uncaria guianensis

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