PlantaeDB Logo
Login Sign-up

Quassia undulata

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

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440220b5c5aa585746763
Scientific name Quassia undulata
Authority (Guill. & Perr.) D.Dietr.
First published in Syn. Pl. 2: 1416 (1840)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Zwingera undulata (Guill. & Perr.) Steud. Nomencl. Bot. , ed. 2, 2: 802 (1841)
Simaba undulata Guill. & Perr. Fl. Seneg. Tent. : 136 (1831)
Hannoa chlorantha Engl. & Gilg Kunene-Sambesi Exped. : 270 (1903)
Hannoa undulata (Guill. & Perr.) Planch. London J. Bot. 5: 567 (1846)
Odyendea zimmermannii Engl. Bot. Jahrb. Syst. 46: 280 (1911)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
dag gahaŋ gwolugu
Fulah bummere baaɗi

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000733404
Tropicos 29400241
KEW urn:lsid:ipni.org:names:814052-1
The Plant List kew-2868460
Open Tree Of Life 6128077
NCBI Taxonomy 1899180
IPNI 814052-1
iNaturalist 134151
GBIF 3708691
CMAUP NPO878

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
Tree species composition along environmental and disturbance gradients in tropical sub-montane forests, Tanzania Lolila NJ, Shirima DD, Mauya EW PLoS One 08-Mar-2023
PMCID:PMC9994703
doi:10.1371/journal.pone.0282528
PMID:36888683
Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R Int J Mol Sci 26-Nov-2022
PMCID:PMC9736547
doi:10.3390/ijms232314787
PMID:36499134
Ellagic Acid: A Dietary-Derived Phenolic Compound for Drug Discovery in Mild Cognitive Impairment Wang W, Wang S, Liu Y, Wang X, Nie J, Meng X, Zhang Y Front Aging Neurosci 04-Jul-2022
PMCID:PMC9289475
doi:10.3389/fnagi.2022.925855
PMID:35860668
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Oxidative Stress, Antioxidant Capabilities, and Bioavailability: Ellagic Acid or Urolithins? Alfei S, Marengo B, Zuccari G Antioxidants (Basel) 04-Aug-2020
PMCID:PMC7465258
doi:10.3390/antiox9080707
PMID:32759749
Ecological data in support of an analysis of Guinea-Bissau׳s medicinal flora Catarino L, Havik PJ, Indjai B, Romeiras MM Data Brief 30-Mar-2016
PMCID:PMC5063803
doi:10.1016/j.dib.2016.03.077
PMID:27761498
Antimalarial Activity of Simalikalactone E, a New Quassinoid from Quassia amara L. (Simaroubaceae) Cachet N, Hoakwie F, Bertani S, Bourdy G, Deharo E, Stien D, Houel E, Gornitzka H, Fillaux J, Chevalley S, Valentin A, Jullian V Antimicrob Agents Chemother 10-Aug-2009
PMCID:PMC2764154
doi:10.1128/AAC.00951-09
PMID:19667291
Plants used traditionally to treat malaria in Brazil: the archives of Flora Medicinal Botsaris AS J Ethnobiol Ethnomed 01-May-2007
PMCID:PMC1891273
doi:10.1186/1746-4269-3-18
PMID:17472740
Antimicrobial activity of crenatine, an alkaloid synthesized from indole Edith O. Ajayeoba, Bolanle A. Adeniyi, J. I. Okogun Wiley 18-Oct-2006
doi:10.1002/PTR.2650090117
Indole Alkaloids and Quassin from Quassia africana Luyengi Lumonadio, Maurice Vanhaelen American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50047A037
Canthin-6-one, undulatone and two quassinoids from Hannoa klaineana roots Luyengi Lumonadio, Maurice Vanhaelen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85005-0
Two quassinoids and two coumarinolignoids from Hannoa klaineana roots R. Vanhaelen-Fastré, L. Luyengi, M. Vanhaelen, J.P. Declercq, M. Van Meerssche Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81538-1
Indole alkaloids from Hannoa klaineana roots Luyengi Lumonadio, Maurice Vanhaelen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80351-9
Two quassinoid glycosides and a β-carboline-1-propionic acid from hannoa klaineana Luyengi Lumonadio, Maurice Vanhaelen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83047-2

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 / Harmala alkaloids
1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole 5317256 Click to see CCC1=NC=C(C2=C1NC3=CC=CC=C32)OC 226.27 unknown https://doi.org/10.1002/PTR.2650090117
1-ethyl-9H-pyrido[3,4-b]indole 5324325 Click to see CCC1=NC=CC2=C1NC3=CC=CC=C23 196.25 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)80351-9
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 https://doi.org/10.1016/S0031-9422(00)83047-2
Ethyl beta-carboline-1-propionate 54093642 Click to see CCOC(=O)CCC1=NC=CC2=C1NC3=CC=CC=C23 268.31 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)80351-9
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Methoxycanthinone 483522 Click to see COC1=CN=C2C=CC(=O)N3C2=C1C4=CC=CC=C43 250.25 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Lignans, neolignans and related compounds / Coumarinolignans
(2S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 5315965 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
CID 14282057 14282057 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
CID 335652 335652 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
Cleomiscosin A 442510 Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O 386.40 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sterculic acid 12921 Click to see CCCCCCCCC1=C(C1)CCCCCCCC(=O)O 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
(1S,2R,6R,7R,9R,13R,14R,16R,17S)-6,16-dihydroxy-2,6,14,17-tetramethyl-14-[(3R)-5-oxooxolane-3-carbonyl]-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11-dione 14543556 Click to see CC1(CC(C2C3(C(CC4C2(C1CC(=O)O4)C)C(C=CC3=O)(C)O)C)O)C(=O)C5CC(=O)OC5 460.50 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
(1S,4R,5R,6S,7S,8R,11R,13S,17S,18S,19R)-4,5,17-trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 162984014 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC6C(C(C(C(O6)CO)O)O)O)CO)O)(OC5)O)C)O 572.60 unknown https://doi.org/10.1016/S0031-9422(00)83047-2
https://doi.org/10.1021/NP50047A037
(1S,4R,5R,6S,7S,8R,11R,13S,17S,18S,19R)-8-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,17-trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 163193315 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC6C(C(C(C(O6)COC7C(C(C(O7)CO)O)O)O)O)O)CO)O)(OC5)O)C)O 704.70 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
(4,5,8,16,17-Pentahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl) 2-methylbut-2-enoate 435724 Click to see CC=C(C)C(=O)OC1C2C(=CC(C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)O)C 494.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
(4,5,8,17-Tetrahydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl) 2-methylbut-2-enoate 435310 Click to see CC=C(C)C(=O)OC1C2C(=CC(=O)C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)C 492.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
[(1S,4R,5R,6R,7S,8R,11S,12R,13S,16S,17S,18S,19R)-4,5,8,16,17-pentahydroxy-6,14,18-trimethyl-9-oxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl] (E)-2-methylbut-2-enoate 162856572 Click to see CC=C(C)C(=O)OC1C2C(=CC(C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)O)C 494.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
[(1S,4R,5R,6R,7S,8R,11S,12R,13S,17S,18S,19R)-4,5,8,17-tetrahydroxy-6,14,18-trimethyl-9,16-dioxo-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-en-12-yl] (Z)-2-methylbut-2-enoate 162951138 Click to see CC=C(C)C(=O)OC1C2C(=CC(=O)C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)C 492.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
https://doi.org/10.1021/NP50047A037
4,5,17-Trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 4260530 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC6C(C(C(C(O6)CO)O)O)O)CO)O)(OC5)O)C)O 572.60 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
6-alpha-Tigloyl-oxyglaucarubol 5458897 Click to see CC=C(C)C(=O)OC1C2C(=CC(C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)O)C)O)O)C 494.50 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
6,16-Dihydroxy-2,6,14,17-tetramethyl-14-(5-oxooxolane-3-carbonyl)-10-oxatetracyclo[7.7.1.02,7.013,17]heptadec-4-ene-3,11-dione 14543555 Click to see CC1(CC(C2C3(C(CC4C2(C1CC(=O)O4)C)C(C=CC3=O)(C)O)C)O)C(=O)C5CC(=O)OC5 460.50 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
8-[6-[[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-4,5,17-trihydroxy-6-(hydroxymethyl)-14,18-dimethyl-3,10-dioxapentacyclo[9.8.0.01,7.04,19.013,18]nonadec-14-ene-9,16-dione 163049028 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4C(C(=O)O3)OC6C(C(C(C(O6)COC7C(C(C(O7)CO)O)O)O)O)O)CO)O)(OC5)O)C)O 704.70 unknown https://doi.org/10.1021/NP50047A037
https://doi.org/10.1016/S0031-9422(00)83047-2
Hannoaenone 5476831 Click to see CC=C(C)C(=O)OC1C2C(=CC(=O)C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)OC(=O)C)C)O)C 534.60 unknown via CMAUP database
Undulatone 5281311 Click to see CC=C(C)C(=O)OC1C2C(=CC(=O)C(C2(C3C45C1OC(=O)C(C4C(C(C3(OC5)O)O)C)OC(=O)C)C)O)C 534.60 unknown https://doi.org/10.1016/S0031-9422(00)81538-1
https://doi.org/10.1016/S0031-9422(00)85005-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see C[N+](C)(C)CC(=O)[O-] 117.15 unknown via CMAUP database
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
cyclo[N(Me)Ile-ObAla(2R-Me,3S-pentyl)-Val-N(Me)Phe-OVal-Pro] 162925012 Click to see CCCCCC1C(C(=O)NC(C(=O)N(C(C(=O)OC(C(=O)N2CCCC2C(=O)N(C(C(=O)O1)C(C)CC)C)C(C)C)CC3=CC=CC=C3)C)C(C)C)C 741.00 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
9H-Pyrido[3,4-B]indole 64961 Click to see C1=CC=C2C(=C1)C3=C(N2)C=NC=C3 168.19 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Organoheterocyclic compounds / Indolizidines
Isorhynchophylline 3037048 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown https://doi.org/10.1016/S0031-9422(00)80351-9
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(00)83047-2
https://doi.org/10.1021/NP50047A037
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 https://doi.org/10.1016/S0031-9422(00)83047-2
https://doi.org/10.1021/NP50047A037
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)85005-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.