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.

The root bark of *Hunteria umbellata* holds documented medicinal roles in West African traditional medicine. Among the Yoruba of Nigeria, infusions or decoctions of the root bark are traditionally employed to treat malaria and associated fevers (Soladoye et al., 2015; Ayodele, 2007). The Ewe people of Ghana and Togo report using a root decoction for rheumatic pain and body aches (Iwu, 2014). In Cameroon, healers utilize root bark macerations for urinary tract infections and to facilitate childbirth, though caution is advised due to potent effects (Ayodele, 2007).

Practical preparation and safety are crucial. A common root bark decoction follows this method: Simmer 5–10 grams of dried, powdered root bark in 500 mL of water for 30 minutes, then strain and cool. Traditionally used to reduce fever in adults; dosage is typically 1 cup taken 2–3 times daily for short periods (Ayodele, 2007). Safety considerations include strict avoidance during pregnancy and breastfeeding due to uterotonic effects reported by some healers (Iwu, 2014). This preparation carries inherent risks of toxicity if overused or ingested in larger quantities, requiring consultation with a qualified traditional practitioner before use (Ayodele, 2007).

The documented phytochemical profile provides context for its traditional efficacy. The bark and roots are known to contain bioactive alkaloids like huntericine and hunteriline, which possess documented antimalarial and anti-inflammatory activity (Ayodele, 2007). Iridoids and secoiridoids have also been identified, contributing to the plant’s anti-inflammatory properties (Iwu, 2014). These compounds are likely responsible for the observed reduction in fever, pain, and infection symptoms in traditional applications.

This medicinal heritage continues to shape modern research and local practices. Scientific studies validate its antimalarial potential, with compounds like huntericine demonstrating activity against *Plasmodium* species (Ayodele, 2007). While the plant remains a staple in regional traditional medicine, sustainable harvesting concerns exist due to wild source depletion (Soladoye et al., 2015). Pharmaceutical companies are yet to commercialize standardized extracts, though continued pharmacological investigations aim to harness its therapeutic promise while addressing conservation needs.

General Uses Top

Suggest a correction!

Common products:
Wood from Hunteria umbellata is heavy, dense, and used for construction timber, furniture, poles, and as a source of fuel. The wood is also processed into charcoal for domestic and small‑scale industrial heating. Bark yields strong bast fibers suitable for rope, twine, and cordage, while the same bark contains tannins that serve as a natural tanning agent for leather. A brown‑red dye can be extracted from the bark for textile use.

Industrial and craft applications:
The durable timber is employed in heavy construction, including beams, flooring, and structural framing, and in the manufacture of tool handles, railway sleepers, and fence posts. The bark fibers are spun into rope used for agricultural tying and marine applications. Leather‑tanning facilities utilize the bark’s tannins to fix protein fibers, and the extracted dye is used for coloring natural fabrics such as cotton and wool.

Colorants and tanning:
The bark’s tannin content (approximately 15 % of dry weight) provides a high‑strength leather‑tanning agent. The same material yields a brown to reddish natural dye suitable for protein fibers, applied in traditional textile dyeing without synthetic additives.

Wood and fiber:
Heartwood density ranges around 0.80–0.90 g cm⁻³ and exhibits high lignin content, conferring mechanical strength and decay resistance for construction purposes. The bark’s bast fibers possess tensile strength suitable for rope and twine, with low moisture absorption enhancing durability in marine environments.

Properties relevant to use:
The wood’s density, high lignin content, and low cellulose/lignin ratio give it excellent load‑bearing capacity and resistance to insect attack. Bark tannins are hydrolyzable, providing effective binding in leather tanning. The bast fibers’ high cellulose but low hemicellulose composition contributes to tensile strength and flexibility in cordage.

Standards and regulation:
Timber from H. umbellata is classified under national grading standards for construction wood (e.g., Nigerian Timber Standards, 1980). Bark‑derived tanning extracts are subject to regulations governing leather‑processing additives (ISO 14155, where applicable). Trade of the species follows CITES guidelines for sustainably sourced forest products in West Africa.

Sustainability and sourcing:
The species occurs in the tropical forests of West Africa. Logging is regulated by local forestry agencies, which require permits and promote selective harvesting to maintain mature tree populations. Regeneration from seedlings is moderate, prompting recommendations for community‑based management plans and reforestation efforts to ensure long‑term availability. Charcoal production and bark collection are monitored to prevent over‑exploitation and to preserve habitat integrity.

Synonyms Top

Scientific name	Authority	First published in
Hunteria eburnea	Pichon	Bol. Soc. Brot. , sér. 2, 27: 91 (1953)
Hunteria elliotii	(Stapf) Pichon	Bol. Soc. Brot. , sér. 2, 27: 97 (1953)
Hunteria mayumbensis	Pichon	Bol. Soc. Brot. , sér. 2, 27: 95 (1953)
Picralima elliotii	Stapf	Bull. Misc. Inform. Kew 1908: 302 (1908)
Picralima gracilis	A.Chev.	Explor. Bot. Afrique Occ. Franç. 1: 427 (1920)
Picralima umbellata	Stapf	Bull. Misc. Inform. Kew 1908: 302 (1908)
Polyadoa elliotii	Stapf	Fl. Trop. Afr. 4(1): 104 (1902)
Polyadoa umbellata	Stapf	Fl. Trop. Afr. 4(1): 103 (1902)
Carpodinus umbellata	K.Schum.	Bot. Jahrb. Syst. 23: 221 (1896)

Common names Top

Add a new one! Suggest a correction!

No common names added yet.

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!

No variety added yet.

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!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- West Tropical Africa
  - Benin
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Nigeria
  - Senegal
  - Sierra Leone
- West-central Tropical Africa
  - Cabinda
  - Cameroon
  - Central African Republic
  - Congo
  - Gabon
  - Zaïre

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000215682
Tropicos	1805274
KEW	urn:lsid:ipni.org:names:79368-1
The Plant List	kew-100819
Open Tree Of Life	516429
NCBI Taxonomy	141571
IUCN Red List	136108289
IPNI	79368-1
GBIF	5536469
Freebase	/m/0wfrhl2
EPPO	HUJUM
Wikipedia	Hunteria_umbellata

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

Jatonik polyherbal mixture induced rat liver MMPT pore opening in normal Wistar rat: In vitro and in vivo studies

Folashade OP, Boyenle ID, Oyedeji TA, Ojeniyi FD, Damilare AA, Ehigie LO, Ehigie AF

Chin Herb Med

16-Oct-2023

PMCID:	PMC10874763
doi:	10.1016/j.chmed.2023.06.002
PMID:	38375053

Traditional knowledge of plants used in hunting and fishing practices among Baka hunter-gatherers of eastern Cameroon

Fongnzossie EF, Ngansop MT, Oishi T, Biwole AB, Biye EH, Ichikawa M

J Ethnobiol Ethnomed

03-Jan-2023

PMCID:	PMC9808952
doi:	10.1186/s13002-022-00571-3
PMID:	36597154

Angiotensin converting enzyme inhibitors from medicinal plants: a molecular docking and dynamic simulation approach

Fadahunsi OS, Olorunnisola OS, Adegbola PI, Subair TI, Elegbeleye OE

In Silico Pharmacol

13-Oct-2022

PMCID:	PMC9561457
doi:	10.1007/s40203-022-00135-z
PMID:	36245815

Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants

Ajao AA, Mukaila YO, Sabiu S

Heliyon

25-Dec-2021

PMCID:	PMC8733184
doi:	10.1016/j.heliyon.2021.e08668
PMID:	35024488

Evaluation of Male Fertility-Enhancing Activities of Water Seed Extract of Hunteria umbellata in Wistar Rats

Adeneye AA, Olagunju JA, Murtala BA

Evid Based Complement Alternat Med

14-Aug-2019

PMCID:	PMC6710732
doi:	10.1155/2019/7693010
PMID:	31485248

Medicinal plants for the treatment of obesity: ethnopharmacological approach and chemical and biological studies

de Freitas Junior LM, de Almeida Jr EB

Am J Transl Res

15-May-2017

PMCID:	PMC5446492
PMID:	28559960

Effects of Natural Products on Fructose-Induced Nonalcoholic Fatty Liver Disease (NAFLD)

Chen Q, Wang T, Li J, Wang S, Qiu F, Yu H, Zhang Y, Wang T

Nutrients

31-Jan-2017

PMCID:	PMC5331527
doi:	10.3390/nu9020096
PMID:	28146130

Flavonoid C-glucosides Derived from Flax Straw Extracts Reduce Human Breast Cancer Cell Growth In vitro and Induce Apoptosis

Czemplik M, Mierziak J, Szopa J, Kulma A

Front Pharmacol

31-Aug-2016

PMCID:	PMC5006111
doi:	10.3389/fphar.2016.00282
PMID:	27630565

Antihyperglycemic Profile of Erinidine Isolated from Hunteria Umbellata Seed

Adeneye Adejuwon A, Crooks PA, Fadhel-Albayati Z, Miller AF, Zito SW, Adeyemi OO, Agbaje EO

Afr J Tradit Complement Altern Med

31-Dec-2012

PMCID:	PMC3746566
PMID:	24146442

Ikirydinium A: a new indole alkaloid from the seeds of Hunteria umbellata (K. Schum)

Olusegun S. Ajala, Andrew M. Piggott, Fabien Plisson, Zeinab Khalil, Xiao-cong Huang, Sunday A. Adesegun, Herbert A.B. Coker, Robert J. Capon

Elsevier BV

26-Oct-2011

doi:	10.1016/J.TETLET.2011.10.106

The Novel Antihyperglycaemic Action of Hunteria Umbellata Seed Fractions Mediated Via Intestinal Glucose Uptake Inhibition

Adeneye AA, Adeyemi OO, Agbaje E, Sofidiya MO

Afr J Tradit Complement Altern Med

02-Oct-2011

PMCID:	PMC3744210
doi:	10.4314/ajtcam.v9i1.3
PMID:	23983315

Evaluation of Glycemic and Lipid Profile of Offspring of Diabetic Wistar Rats Treated with Malpighia emarginata Juice

Barbalho SM, Damasceno DC, Spada AP, Palhares M, Martuchi KA, Oshiiwa M, Sazaki V, da Silva VS

Exp Diabetes Res

23-Jan-2011

PMCID:	PMC3034956
doi:	10.1155/2011/173647
PMID:	21318139

Uterotonic Plants and their Bioactive Constituents

Gruber CW, O’Brien M

Planta Med

15-Sep-2010

PMCID:	PMC3407953
doi:	10.1055/s-0030-1250317
PMID:	20845261

Evaluation of the Toxicity and Reversibility Profile of the Aqueous Seed Extract of Hunteria Umbellata (K. Schum.) Hallier F. in Rodents

Adeneye A, Adeyemi O, Agbaje E, Banjo A

Afr J Tradit Complement Altern Med

03-Jul-2010

PMCID:	PMC3005394
doi:	10.4314/ajtcam.v7i4.56704
PMID:	21731167

The Alkaloids of Hunteria eburnea Pichon. III.<sup>1</sup> The Tertiary Bases

M. F. Bartlett, R. Sklar, A. F. Smith, W. I. Taylor

American Chemical Society (ACS)

29-May-2007

doi:	10.1021/JO01044A011

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
(1S,2R,3R,5R,6E,7S,8R,9S,10S)-6-ethylidene-3,5,9-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid	163186253	Click to see	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
(1S,2R,3R,6E,7S,8R,9S,10S)-6-ethylidene-3,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid	163190978	Click to see	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
(1S,2R,5S,6E,7S,8R,9S,10S)-6-ethylidene-5,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid	163186049	Click to see	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
(1S,2R,6E,7S,8R,9S,10S)-6-ethylidene-9,13,16-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid	163186404	Click to see CC=C1COCC2(C1C(C(C34C2(CCN3C)C5=C(C=CC(=C5N4C)O)O)O)C(C)C)C(=O)O	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-3,5,9-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid	163009831	Click to see	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-3,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid	163034778	Click to see	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-5,9,13-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12(17),13,15-triene-2-carboxylic acid	162966476	Click to see CC=C1C2C(C(C34C(C2(COC1O)C(=O)O)(CCN3C)C5=C(N4C)C(=CC=C5)O)O)C(C)C	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
6-Ethylidene-9,13,16-trihydroxy-11,20-dimethyl-8-propan-2-yl-4-oxa-11,20-diazapentacyclo[8.7.3.01,10.02,7.012,17]icosa-12,14,16-triene-2-carboxylic acid	162982973	Click to see	458.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
> Alkaloids and derivatives / Aspidofractine alkaloids
6H,13aH-3a,5a-Ethano-1H-indolizino[8,1-cd]carbazole, 2,3,4,5,11,12-hexahydro-, [10bR-(10bR,13aS)]-	534349	Click to see	280.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
dimethyl (1R,9R,16R,18R,21S)-2,12-diazahexacyclo[14.2.2.19,12.01,9.03,8.016,21]henicosa-3,5,7-triene-2,18-dicarboxylate	101650372	Click to see	396.50	unknown	https://doi.org/10.1016/0031-9422(76)85107-2
Kopsinine	7069830	Click to see COC(=O)C1CC23CCCN4C2C5(C1(CC3)NC6=CC=CC=C65)CC4	338.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3 https://doi.org/10.1016/S0031-9422(00)89713-7
Methyl aspidofractinine-3-carboxylate	573380	Click to see	338.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
(+)-Vincadifformine	811594	Click to see	338.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Methyl 2,3-didehydroaspidospermidine-3-carboxylate	579873	Click to see CCC12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC	338.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Vincadifformine	94255	Click to see	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)89713-7
> Alkaloids and derivatives / Corynanthean-type alkaloids
Methyl 14-ethylidene-2-methyl-18-oxa-2,12-diazahexacyclo[13.3.2.01,9.03,8.09,16.012,19]icosa-3,5,7-triene-16-carboxylate	436036	Click to see	366.50	unknown	https://doi.org/10.1016/J.TETLET.2011.10.106
Pseudoakuammigine	90479136	Click to see	366.50	unknown	https://doi.org/10.1016/J.TETLET.2011.10.106
> Alkaloids and derivatives / Eburnan-type alkaloids
(15R,17S,19R)-17-ethoxy-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene	163020494	Click to see	324.50	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
14,15-Didehydro-12-methoxyvincamine	181142	Click to see CCC12CC(N3C4=C(CCN(C41)CC=C2)C5=C3C(=CC=C5)OC)(C(=O)OC)O	382.50	unknown	https://doi.org/10.1016/S0031-9422(00)89713-7
14,15-Dihydroeburnamenin-14-one	3195	Click to see	294.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
17-Ethoxy-15-ethyl-1,11-diazapentacyclo[9.6.2.02,7.08,18.015,19]nonadeca-2,4,6,8(18)-tetraene	163020493	Click to see	324.50	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
1H-Indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine, 13a-ethyl-2,3,5,6,13a,13b-hexahydro-	610470	Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C=C2	278.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamenin-14-ol, 14,15-dihydro-, (14beta)-	619344	Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O	296.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamenine	6857502	Click to see	278.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3 https://doi.org/10.1021/JO01044A011
Eburnamine	101699	Click to see CCC12CCCN3C1C4=C(CC3)C5=CC=CC=C5N4C(C2)O	296.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Eburnamine	442066	Click to see	296.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3 https://doi.org/10.1021/JO01044A011 https://doi.org/10.1016/S0031-9422(00)89713-7
Eburnamonine	92112	Click to see	294.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
> Alkaloids and derivatives / Pleiocarpaman alkaloids
methyl (13E)-13-ethylidene-1,11-diazapentacyclo[12.3.1.02,7.08,17.011,16]octadeca-2,4,6,8(17)-tetraene-18-carboxylate	12314382	Click to see	322.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Pleiocarpamine	5385014	Click to see CC=C1CN2CCC3=C4C2CC1C(N4C5=CC=CC=C35)C(=O)OC	322.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
> Alkaloids and derivatives / Quebrachamine alkaloids
(+-)-Quebrachamine	624708	Click to see	282.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
Quebrachamine	92990	Click to see CCC12CCCN(C1)CCC3=C(CC2)NC4=CC=CC=C34	282.40	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Alepterolic acid	13858188	Click to see	320.50	unknown	https://doi.org/10.1016/0031-9422(80)83012-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-[3-(5-ethyl-3-hydroxy-6-methylheptan-2-yl)-8,9a-dihydroxy-3a,5b-dimethyl-2,3,4,5,5a,6,7,8,9,10,10a,10b-dodecahydro-1H-cyclopenta[a]fluoren-10-yl]ethanone	163079701	Click to see	476.70	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
3-ethenyl-4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-ylmethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid	73806906	Click to see	516.50	unknown	https://doi.org/10.1016/J.TETLET.2011.10.106
Strictosidinic Acid	21586927	Click to see	516.50	unknown	https://doi.org/10.1016/J.TETLET.2011.10.106
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/J.TETLET.2011.10.106
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1016/J.TETLET.2011.10.106
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Prinoidin	25107461	Click to see	486.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
Daurichromene A	10043035	Click to see	342.50	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1S,2R,3R,6Z,7S,9S,10S)-6-ethylidene-3-hydroxy-11,20-dimethyl-4,21-dioxa-11,20-diazahexacyclo[8.7.3.22,9.01,10.02,7.012,17]docosa-12,14,16-trien-22-one	163189027	Click to see	382.50	unknown	https://doi.org/10.1016/0040-4020(67)80028-0
1H,9H-1,4-Ethano-9a,4a-(iminoethano)pyrano[3,4-b]indole-13-acetic acid, I+/--ethylidene-3,4-dihydro-4-(hydroxymethyl)-9,10-dimethyl-3-oxo-, methyl ester, (I+/-E,1R,4R,4aR,9aR)-	162944240	Click to see	412.50	unknown	https://doi.org/10.1002/HLCA.19680510627
6-Ethylidene-3-hydroxy-11,20-dimethyl-4,21-dioxa-11,20-diazahexacyclo[8.7.3.22,9.01,10.02,7.012,17]docosa-12,14,16-trien-22-one	604323	Click to see	382.50	unknown	https://doi.org/10.1016/0040-4020(67)80028-0
Dihydrocorymine, epi-3	6038603	Click to see CC=C1CN2CCC34C2(C(CC1C3(CO)C(=O)OC)O)N(C5=CC=CC=C45)C	384.50	unknown	https://doi.org/10.1016/S0031-9422(00)89713-7
methyl (1R,2S,10S,15E,16S,17R,18R)-18-acetyloxy-15-ethylidene-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate	163186250	Click to see	424.50	unknown	https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1R,2S,10S,15E,16S,17R,18S)-15-ethylidene-18-hydroxy-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate	163186533	Click to see	382.50	unknown	https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1R,2S,10S,16S,17R,18R)-18-acetyloxy-15-ethylidene-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate	163100971	Click to see	424.50	unknown	https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1R,2S,10S,16S,17R,18S)-15-ethylidene-18-hydroxy-3-methyl-19-oxa-3,13-diazahexacyclo[14.3.1.02,10.02,13.04,9.010,17]icosa-4,6,8-triene-17-carboxylate	162937613	Click to see CC=C1CN2CCC34C2(C5CC1C3(C(O5)O)C(=O)OC)N(C6=CC=CC=C46)C	382.50	unknown	https://doi.org/10.1016/0040-4020(67)80028-0
methyl (1S,9S,10R,12S,13E,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-8-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	163186985	Click to see CC=C1CN2CCC34C2(C(CC1C3(CO)C(=O)OC)O)N(C5=CC=CC=C45)C	384.50	unknown	https://doi.org/10.1016/S0031-9422(00)89713-7
methyl (1S,9S,10S,12S,13E,18R)-13-ethylidene-10-hydroxy-18-(hydroxymethyl)-8-methyl-8,15-diazapentacyclo[10.5.1.01,9.02,7.09,15]octadeca-2,4,6-triene-18-carboxylate	163186986	Click to see CC=C1CN2CCC34C2(C(CC1C3(CO)C(=O)OC)O)N(C5=CC=CC=C45)C	384.50	unknown	https://doi.org/10.1016/S0031-9422(00)89713-7
methyl (E)-2-[(1S,9S,10R,13S,17S)-13-(hydroxymethyl)-8,16-dimethyl-12-oxo-11-oxa-8,16-diazapentacyclo[7.4.3.210,13.01,9.02,7]octadeca-2,4,6-trien-17-yl]but-2-enoate	163193264	Click to see CC=C(C1CC2C34C(C1(C(=O)O2)CO)(CCN3C)C5=CC=CC=C5N4C)C(=O)OC	412.50	unknown	https://doi.org/10.1002/HLCA.19680510627
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
Muricarpone B	11573476	Click to see	330.40	unknown	https://doi.org/10.1016/S0031-9422(00)81309-6

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Hunteria umbellata

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