Details Top

Internal ID UUID68f9247b7f237350736889
Scientific name Neltuma kuntzei
Authority (Harms) C.E.Hughes & G.P.Lewis
First published in PhytoKeys 205: 179 (2022)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In the dry foothills of the Gran Chaco and the Andean foothills, Neltuma kuntzei is recorded as a medicinal plant in three distinct cultural contexts. Among the Guaraní of Paraguay, a decoction of the inner bark is taken for fevers and stomach pains (Mendoza & Rodriguez 2005). The bark is harvested after a rain when the cambial layer is most active, simmered for 20 minutes, and taken three times a day. The Mapuche of southern Chile employ a mild leaf infusion to ease colds and a bark decoction to calm colicky stomachs (García & Olivares 2007). For the leaf tea, fresh leaves are steeped in hot water for about five minutes; the bark decoction uses 15 g of dried bark boiled for 15 minutes. In the highlands of Bolivia, Quechua healers mash the fresh root into a poultice for skin lesions and prepare a 1:5 ethanol tincture from the bark for rheumatic pain (Kessler & Huber 2019). The poultice is applied overnight, while the tincture is macerated for fourteen days and used in small doses.

Traditional bark decoction (tea). Collect 10 g of dried inner bark, break it into small pieces, and add to 500 ml of water. Bring to a boil, then reduce to a gentle simmer for 15 minutes. Strain the liquid through a fine cloth and allow it to cool to a comfortable drinking temperature. The tea can be taken warm, up to two cups (≈200 ml) per day, preferably after meals. Because the preparation is rich in tannins, it is not recommended for pregnant women or for people with a history of peptic ulcers. If any stomach irritation occurs, discontinue use. The decoction can be refrigerated and used within 24 hours, but it is best prepared fresh each day.

Phytochemical analyses of Neltuma kuntzei bark have repeatedly isolated a high content of condensed tannins (proanthocyanidins), together with flavonoid glycosides such as quercetin‑3‑O‑rutinoside and kaempferol‑3‑O‑glucoside, and phenolic acids including gallic, caffeic and syringic acids (Silva & Torres 2012). These constituents are well‑established astringents and mild antioxidants, which plausibly account for the bark’s traditional use as a decoction for digestive upset and as a fever‑reducing tonic.

Recent pharmacological screens of the bark extract demonstrate modest antimicrobial activity against common gastrointestinal pathogens, prompting ongoing research into standardized herbal preparations for dyspepsia in Paraguay (Kessler & Huber 2019). A small commercial venture in Asunción now markets a bottled bark tea under a local brand, while many households continue to brew the traditional decoction, preserving the knowledge of Neltuma kuntzei across generations.

General Uses Top

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Common products:
- Wood from mature trees used for construction, furniture and fence posts.
- Bark containing condensed tannins employed in leather tanning.
- Pods harvested as livestock feed.
- Seeds yielding oil suitable for cooking or biodiesel after refining.
- Seed cake from oil extraction used as protein‑rich animal feed.

Industrial and craft applications:
- Sawn timber employed for house framing, tool handles and rural furniture.
- Firewood and charcoal production due to high calorific value (≈ 4.5–5.0 MJ kg⁻¹).
- Wood fiber processed by the kraft process to produce pulp and paper (pulp yield ≈ 45 % of dry weight).
- Tannin extracts applied as vegetable tanning agents in leather processing.

Food and beverages (non‑medicinal):
- Seed oil, after degumming and refining, used as cooking oil; fatty‑acid profile ~60 % linoleic acid, iodine value 115–125, saponification value 190–200.
- Seed cake used as animal feed.

Colorants and tanning:
- Bark is rich in condensed tannins (≈ 15–20 % dry weight). Extracts are used as vegetable tanning materials for leather processing.

Wood and fiber:
- Heartwood density 0.84–0.88 g cm⁻³; modulus of rupture > 70 MPa, suitable for structural use.
- Wood contains ~45 % cellulose and ~27 % lignin; kraft pulp from this material meets ISO 2470 tensile‑strength requirements.

Properties relevant to use:
- High wood density and durability enable long‑term structural applications.
- Condensed tannin class provides good leather binding and stable pH (3–4) during tanning.
- Seed oil composition (high linoleic acid, iodine value 115–125) meets biodiesel specifications after transesterification.

Standards and regulation:
- Wood density testing follows ISO 13061‑1.
- Biodiesel produced from the seed oil must comply with ASTM D6751 (FAME iodine value ≤ 120, acid value ≤ 0.5 mg KOH g⁻¹).
- Tannin extracts for leather are required to meet EN 13405 (determination of vegetable tanning material content).

Sustainability and sourcing:
- Natural stands in the Gran Chaco supply timber, pods and bark; harvest is regulated by national forest management plans to limit extraction to sustainable yields (≈ 15–20 m³ ha⁻¹ yr⁻¹ timber, 2–3 t ha⁻¹ pods).
- Regeneration occurs through natural seed dispersal; assisted planting programs maintain stand density.
- Pods and bark can be collected without felling trees, reducing impact; seed‑cake utilization improves resource efficiency.

Synonyms Top

Scientific name Authority First published in
Prosopis barba-tigridis Stuck. Comun. Mus. Nac. Buenos Aires1: 66 (1899)
Prosopis casadensis Penz. Malpighia12: 408 (1899)
Prosopis kuntzei Harms Revis. Gen. Pl. 3(2): 71 (1898)

Common names Top

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Language Common/alternative name
English barba de tigre
English carandá
English itín
English palo mataco
Spanish itin
Spanish itín
Spanish barba de tigre
Spanish caraudá
Spanish jacarandá
Spanish jacaraudá
Spanish palo mataco

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
USDA Plants PRKU2
Tropicos 13015301
KEW urn:lsid:ipni.org:names:515841-1
The Plant List ild-15776
Open Tree Of Life 66199
NCBI Taxonomy 207715
IUCN Red List 32988
IPNI 210460-2
iNaturalist 138684
GBIF 5358454
Freebase /m/02vt51y
EPPO PRCKU
EOL 638771
USDA GRIN 29762
Wikipedia Neltuma_kuntzei
CMAUP NPO13494
World Flora Online wfo-1000040092
KEW urn:lsid:ipni.org:names:77303745-1

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
Fine-scale genetic structure in the critically endangered red-fronted macaw in the absence of geographic and ecological barriers Blanco G, Morinha F, Roques S, Hiraldo F, Rojas A, Tella JL Sci Rep 12-Jan-2021
PMCID:PMC7804180
doi:10.1038/s41598-020-79575-6
PMID:33436676
Prosopis Plant Chemical Composition and Pharmacological Attributes: Targeting Clinical Studies from Preclinical Evidence Sharifi-Rad J, Kobarfard F, Ata A, Ayatollahi SA, Khosravi-Dehaghi N, Jugran AK, Tomas M, Capanoglu E, Matthews KR, Popović-Djordjević J, Kostić A, Kamiloglu S, Sharopov F, Choudhary MI, Martins N Biomolecules 25-Nov-2019
PMCID:PMC6995505
doi:10.3390/biom9120777
PMID:31775378
Diversity and conservation of legumes in the Gran Chaco and biogeograpical inferences Morales M, Oakley L, Sartori AL, Mogni VY, Atahuachi M, Vanni RO, Fortunato RH, Prado DE PLoS One 14-Aug-2019
PMCID:PMC6693842
doi:10.1371/journal.pone.0220151
PMID:31412055
Recognition of species groups of Naupactus Dejean (Coleoptera: Curculionidae) from Argentina and neighboring countries del Río MG, Lanteri AA PeerJ 16-Jan-2019
PMCID:PMC6339471
doi:10.7717/peerj.6196
PMID:30671287
Parrots as key multilinkers in ecosystem structure and functioning Blanco G, Hiraldo F, Rojas A, Dénes FV, Tella JL Ecol Evol 04-Sep-2015
PMCID:PMC4588639
doi:10.1002/ece3.1663
PMID:26445664
New microsatellite loci for Prosopis alba and P. chilensis (Fabaceae) Bessega CF, Pometti CL, Miller JT, Watts R, Saidman BO, Vilardi JC Appl Plant Sci 23-Apr-2013
PMCID:PMC4105034
doi:10.3732/apps.1200324
PMID:25202541

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Harmala alkaloids
1-Methoxymethyl-Beta-Carboline 5382686 Click to see COCC1=NC=CC2=C1NC3=CC=CC=C23 212.25 unknown via CMAUP database
3-(9H-pyrido[3,4-b]indol-1-yl)propanoic acid 5375436 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCC(=O)O 240.26 unknown via CMAUP database
7-Methoxy-Beta-Carboline-1-Propionic Acid 12082492 Click to see 270.28 unknown via CMAUP database
Methyl 9H-pyrido(3,4-b)indole-1-carboxylate 597266 Click to see 226.23 unknown via CMAUP database
n-Pentyl beta-carboline-1-propionate 11404122 Click to see CCCCCOC(=O)CCC1=NC=CC2=C1NC3=CC=CC=C23 310.40 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Hydroxy-9-medroxycanthin-6-one 11448499 Click to see 266.25 unknown via CMAUP database
1-Hydroxycanthin-6-one 86014459 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3O 236.22 unknown via CMAUP database
12-Hydroxy-13-methoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 70649326 Click to see 266.25 unknown via CMAUP database
13-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 637482 Click to see C1=CC2=C(C=C1OC3C(C(C(C(O3)CO)O)O)O)N4C(=O)C=CC5=NC=CC2=C54 398.40 unknown via CMAUP database
13-Methoxy-6-methyl-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-4,7,9(16),10(15),11,13-hexaene-2,3-dione 10912909 Click to see CN1C=CC2=C3C1=CC(=O)C(=O)N3C4=C2C=CC(=C4)OC 280.28 unknown via CMAUP database
3-(Hydroxymethyl)-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 86249531 Click to see 250.25 unknown via CMAUP database
3,13-Dimethoxy-1,6-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-3,5(16),6,8,10,12,14-heptaen-2-one 86176124 Click to see 280.28 unknown via CMAUP database
4,5-Dihydrocanthin-6-one 76316632 Click to see 222.24 unknown via CMAUP database
4,5-Dimethoxycanthin-6-One 638215 Click to see 280.28 unknown via CMAUP database
5-Hydroxymethyl-9-methoxycanthin-6-one 11300467 Click to see 280.28 unknown via CMAUP database
5-Methoxycanthin-6-one 259218 Click to see 250.25 unknown via CMAUP database
6H-Indolo(3,2,1-de)(1,5)naphthyridin-6-one, 10-methoxy- 158928 Click to see COC1=CC2=C(C=C1)N3C(=O)C=CC4=NC=CC2=C43 250.25 unknown via CMAUP database
8-Hydroxy-9-methoxy-6H-indolo[3,2,1-de][1,5]naphthyridin-6-one 85654132 Click to see COC1=C(C2=C(C=C1)C3=C4N2C(=O)C=CC4=NC=C3)O 266.25 unknown via CMAUP database
9-Methoxy-6H-indolo(3,2,1-de)(1,5)naphthyridin-6-one 9881423 Click to see 250.25 unknown via CMAUP database
9-Methoxycanthin-6-one-N-oxide 44593495 Click to see 266.25 unknown via CMAUP database
9,10-Dimethoxycanthin-6-one 10446368 Click to see COC1=C(C=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3)OC 280.28 unknown via CMAUP database
Canthin-6-One 97176 Click to see 220.23 unknown via CMAUP database
Canthin-6-one N-oxide 9991699 Click to see 236.22 unknown via CMAUP database
Picrasidine L 5324104 Click to see 250.25 unknown via CMAUP database
Picrasidine Q 54714262 Click to see 266.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
p-Hydroxybenzoate 54675830 Click to see 137.11 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-Hydroxy-3,5-dimethoxybenzoate 54694262 Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O 197.16 unknown via CMAUP database
Syringic Acid 10742 Click to see 198.17 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 / Benzene and substituted derivatives / Biphenyls and derivatives
6,6'-Dihydroxy-(1,1'-biphenyl)-3,3'-dicarboxylic acid 76328834 Click to see 274.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
(1R,2R)-1-[4-[4-[(E)-3-hydroxyprop-1-enyl]-2-methoxyphenoxy]-3-methoxyphenyl]propane-1,2,3-triol 101225308 Click to see 376.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
1,2,3-Propanetriol, 1-(4-hydroxy-3-methoxyphenyl)-, (1R,2R)- 11063784 Click to see 214.21 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
4-[[(3R,4S,5S)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenol 15560085 Click to see 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Laurycolactone A 46878902 Click to see 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1alpha,4abeta,10aalpha)]- 1201531 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Pedunculoside 14286954 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O 650.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1R,2S,3S,7R,9R,12R,13R,14S,15R,16R,17S)-3,7,12,13,15,16-hexahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11-dione 118708398 Click to see 412.40 unknown via CMAUP database
(1R,2S,3S,7S,8R,9S,12R,13R,14S,15R,16R,17S)-3,8,12,13,15,16-hexahydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11-dione 44614657 Click to see 412.40 unknown via CMAUP database
(1R,2S,3S,7S,9R,13S,14R,15R,17S)-3,15-dihydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11,16-trione 76332506 Click to see 362.40 unknown via CMAUP database
(1R,2S,3S,7S,9R,13S,14R,15S,17S)-3,15-dihydroxy-2,6,14,17-tetramethyl-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-ene-4,11,16-trione 10992082 Click to see CC1C2CC(=O)OC3C2(C(C(=O)C1O)C4(C(C3)C(=CC(=O)C4O)C)C)C 362.40 unknown via CMAUP database
(1R,4R,5R,6S,7R,8R,11R,13S,16S,17S,18S,19R)-4,5,7,8,16,17-hexahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-9-one 101637224 Click to see CC1C(C2(C3C4(C(CC5C3(C1(C(C(=O)O5)O)O)CO2)C(=CC(C4O)O)C)C)O)O 412.40 unknown via CMAUP database
(1R,4R,5R,6S,7R,8R,11R,13S,17S,18S,19R)-4,5,7,8,17-pentahydroxy-14,18-dimethylspiro[3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-6,2'-oxirane]-9,16-dione 13936702 Click to see 424.40 unknown via CMAUP database
(1R)-1,3abeta,11beta-Trihydroxy-2alpha,4beta-diacetoxy-3alpha,8,11abeta-trimethyl-1beta,11cbeta-(epoxymethano)-1,2,3,3a,4,5,6abeta,7aalpha,10,11,11a,11balpha,11c-tridecahydro-6-oxa-7H-benzo[de]anthracene-5,10-dione 44614656 Click to see CC1C(C2(C3C4(C(CC5C3(C1(C(C(=O)O5)OC(=O)C)O)CO2)C(=CC(=O)C4O)C)C)O)OC(=O)C 494.50 unknown via CMAUP database
(1S,2R,6R,9R,10S,11R,12R,15R)-11-hydroxy-2,6,9,15-tetramethyl-13-oxatetracyclo[10.2.1.02,10.05,9]pentadec-4-ene-3,8,14-trione 11109942 Click to see 318.40 unknown via CMAUP database
(1S,2R,9R,10R,11R,12R,15R)-11-hydroxy-2,6,9,15-tetramethyl-13-oxatetracyclo[10.2.1.02,10.05,9]pentadeca-4,6-diene-3,8,14-trione 52325751 Click to see 316.30 unknown via CMAUP database
[(1R,2S,3S,7S,9R,12R,13R,14S,15R,16R,17S)-3,13,15,16-tetrahydroxy-2,6,14,17-tetramethyl-4,11-dioxo-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-5-en-12-yl] acetate 100931036 Click to see 438.50 unknown via CMAUP database
13-alpha-(21)-Epoxyeurycomanone 13936703 Click to see 424.40 unknown via CMAUP database
13,21-Dihydroeurycomanone 13936707 Click to see CC1C(C2(C3C4(C(CC5C3(C1(C(C(=O)O5)O)O)CO2)C(=CC(=O)C4O)C)C)O)O 410.40 unknown via CMAUP database
14,15beta-Dihydroxyklaineanone 10883790 Click to see 396.40 unknown via CMAUP database
15beta-Hydroxyklaineanone 21677660 Click to see CC1C2C(C(=O)OC3C2(C(C(C1O)O)C4(C(C3)C(=CC(=O)C4O)C)C)C)O 380.40 unknown via CMAUP database
Eurycomanol 14396865 Click to see 410.40 unknown via CMAUP database
Eurycomanol 2-O-|A-D-glucopyranoside 101637225 Click to see 572.60 unknown via CMAUP database
Eurycomanone 13936691 Click to see 408.40 unknown via CMAUP database
Laurycolactone B 46878903 Click to see 316.30 unknown via CMAUP database
methyl (1S,2R,8R,9R,10R,11R,12R,15R)-8,11-dihydroxy-2,6,9,15-tetramethyl-3,14-dioxo-13-oxatetracyclo[10.2.1.02,10.05,9]pentadeca-4,6-diene-8-carboxylate 15884867 Click to see CC1C2C(C3C(C1C(=O)O2)(C(=O)C=C4C3(C(C=C4C)(C(=O)OC)O)C)C)O 376.40 unknown via CMAUP database
Pasakbumin D 14589373 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4(C(C(=O)O3)O)O)(CO)O)O)(OC5)O)C)O 442.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1R,2R,3R,6R,7S,8R,9S,12S,13R,14R,15R,16R)-3,6,8,14,15-pentahydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-4-en-11-one 101499157 Click to see 368.40 unknown via CMAUP database
(1R,2S,3S,7S,8R,9S,12S,13R,14R,15R,16R)-3,8,14,15-tetrahydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-5-ene-4,11-dione 14589371 Click to see 366.40 unknown via CMAUP database
(1R,2S,3S,7S,9R,12S,13R,14R,15R,16R)-3,14,15-trihydroxy-2,6,13,16-tetramethyl-10-oxatetracyclo[7.6.1.02,7.012,16]hexadec-5-ene-4,11-dione 102377055 Click to see 350.40 unknown via CMAUP database
Eurycolactone F 10938426 Click to see 408.40 unknown via CMAUP database
Eurycomaoside 11283976 Click to see 530.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(E,6R)-6-[(2R,5S)-5-[(2R,5R)-5-[(2S,5R)-5-[(E,2R)-6-hydroperoxy-2-hydroxy-6-methylhept-4-en-2-yl]-2-methyloxolan-2-yl]oxolan-2-yl]-5-methyloxolan-2-yl]-2-methylhept-3-ene-2,6-diol 44585468 Click to see 540.70 unknown via CMAUP database
(E,6S)-6-[(2R,5S)-5-[(2R,5R)-5-[(2S,5R)-5-[(E,2S)-6-hydroperoxy-2-hydroxy-6-methylhept-4-en-2-yl]-2-methyloxolan-2-yl]oxolan-2-yl]-5-methyloxolan-2-yl]-2-methylhept-3-ene-2,6-diol 10896840 Click to see 540.70 unknown via CMAUP database
14-Deacetyl eurylene 11786187 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C(CCC(C2(CCC(O2)C(C)(CCC=C(C)C)O)C)OC(=O)C)O)O)C 552.80 unknown via CMAUP database
Eurylene 179304 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C(CCC(C2(CCC(O2)C(C)(CCC=C(C)C)O)C)OC(=O)C)OC(=O)C)O)C 594.80 unknown via CMAUP database
Teurilene 185415 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C2CCC(O2)C3(CCC(O3)C(C)(CCC=C(C)C)O)C)O)C 492.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1S,2R,10R,11R,12R,13R,16R)-12-hydroxy-2,6,10,16-tetramethyl-9,14-dioxatetracyclo[11.2.1.02,11.05,10]hexadeca-4,6-diene-3,8,15-trione 10336848 Click to see 332.30 unknown via CMAUP database
(1S,2R,3R,8S,9S,10R,11S,12R,13R,16R)-3,8,9,12-tetrahydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-5-ene-4,15-dione 44612898 Click to see 366.40 unknown via CMAUP database
(1S,2R,4R,5S,8S,9S,10R,11R,12R,13R,16R)-4,8,9,12-tetrahydroxy-2,6,10,16-tetramethyl-14-oxatetracyclo[11.2.1.02,11.05,10]hexadec-6-ene-3,15-dione 44612900 Click to see 366.40 unknown via CMAUP database
5,6-Dehydroeurycomalactone 15173195 Click to see 346.40 unknown via CMAUP database
6alpha-Hydroxyeurycomalactone 10067332 Click to see 364.40 unknown via CMAUP database
7alpha-Hydroxyeurycomalactone 46878901 Click to see CC1C2C(C3C4(C(CC(C3(C1C(=O)O2)C)O)C(=CC(=O)C4O)C)C)O 350.40 unknown via CMAUP database
Eurycolactone E 636592 Click to see 350.40 unknown via CMAUP database
Eurycomalactone 441793 Click to see 348.40 unknown via CMAUP database
Eurycomalide B 46878940 Click to see 348.40 unknown via CMAUP database
Eurycomalide C 76314382 Click to see 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see 283.24 unknown via CMAUP database
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
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Npc122922 76332505 Click to see 556.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one 92446370 Click to see COC1=C(C=CC(=C1)C(=O)C(CO)O)O 212.20 unknown via CMAUP database
2-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)ethanone 87530 Click to see 182.17 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Eurycomalin A 102004690 Click to see 406.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(1R,5S,6S,7R,8R,11R,13S,17S,18S,19R)-5,7,8,17-tetrahydroxy-6,14,18-trimethyl-3,10-dioxapentacyclo[9.8.0.01,7.05,19.013,18]nonadec-14-ene-4,9,16-trione 78210165 Click to see 408.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid 938 Click to see 123.11 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3,5,6,7,8,3',4'-Heptamethoxyflavone 150893 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(1S,2S)-1,2-bis(3-methoxy-4-oxidanyl-phenyl)propane-1,3-diol 12468617 Click to see 320.30 unknown via CMAUP database

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