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Internal ID UUID64400d709fa5e932022805
Scientific name Bonnetia paniculata
Authority Spruce ex Benth.
First published in J. Proc. Linn. Soc., Bot. 5: 63 (1860)

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Synonyms Top

Scientific name Authority First published in
Bonnetia dinizii Huber Bol. Mus. Goeldi Hist. Nat. Ethnogr. 7: 302 (1913)
Bonnetia paniculata var. parviflora (Spruce ex Benth.) Wawra Fl. Bras. 12(1): 325 (1886)
Bonnetia parviflora Spruce ex Benth. J. Proc. Linn. Soc., Bot. 5: 63 (1860)

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Northern South America
      • Guyana
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000568785
Tropicos 31600051
KEW urn:lsid:ipni.org:names:828487-1
The Plant List kew-2679514
Open Tree Of Life 646458
Observations.org 517792
NCBI Taxonomy 999555
IUCN Red List 180071469
IPNI 828487-1
iNaturalist 542677
GBIF 7330003
Elurikkus 589419
USDA GRIN 450854
CMAUP NPO14730

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)!
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Title Authors Publication Released IDs
The complete chloroplast genome of Calophyllum soulattri Burm. f. (Calophyllaceae) Pahayo DG, Cadorna CA, Quimado MO, Rey JD Mitochondrial DNA B Resour 25-May-2023
PMCID:PMC10215020
doi:10.1080/23802359.2023.2215350
PMID:37250208
Characterization of the plastid genome of Cratoxylum species (Hypericaceae) and new insights into phylogenetic relationships Sudmoon R, Kaewdaungdee S, Tanee T, Siripiyasing P, Ameamsri U, Syazwan SA, Lee SY, Chaveerach A Sci Rep 05-Nov-2022
PMCID:PMC9637187
doi:10.1038/s41598-022-23639-2
PMID:36335203
Calophyllaceae plastomes, their structure and insights in relationships within the clusioids Trad RJ, Cabral FN, Bittrich V, Silva SR, Amaral MD Sci Rep 20-Oct-2021
PMCID:PMC8528878
doi:10.1038/s41598-021-99178-z
PMID:34671062
Plastome Structural Conservation and Evolution in the Clusioid Clade of Malpighiales Jin DM, Jin JJ, Yi TS Sci Rep 04-Jun-2020
PMCID:PMC7272398
doi:10.1038/s41598-020-66024-7
PMID:32499506
Xanthones from Bonnetia dinizii☆ Wanderley G. de Oliveira, Antonio A.L. Mesquita, Klaus Kubitzki, Otto R. Gottlieb Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85035-E

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(E)-8-Decene-4,6-diynyl 6-O-D-apio-beta-D-furanosyl beta-D-glucopyranoside 46830373 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O 442.50 unknown via CMAUP database
[(3S,8E)-3-Hydroxy-8-decene-4,6-diynyl]beta-D-glucopyranoside 10268235 Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 326.34 unknown via CMAUP database
Bidenoside C 70695725 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)O 310.34 unknown via CMAUP database
Bidensyneoside A1 10903496 Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 326.34 unknown via CMAUP database
Gymnasterkoreaside B 11091753 Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O)O 458.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Gymnasterkoreayne C 11779567 Click to see CC(=O)OC(C=C)C#CC#CC(C=CCCCCCC=C)O 300.40 unknown via CMAUP database
Gymnasterkoreayne D 9972025 Click to see CC(=O)OCC=CC#CC#CC(C=CCCCCCC=C)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,8S,9Z)-2,9,16-Heptadecatriene-4,6-diyne-8-ol 101745966 Click to see CC=CC#CC#CC(C=CCCCCCC=C)O 242.36 unknown via CMAUP database
(8S,9Z)-1,9,16-Heptadecatriene-4,6-diyne-8-ol 10399497 Click to see C=CCCCCCC=CC(C#CC#CCC=C)O 242.36 unknown via CMAUP database
Gymnasterkoreayne A 636738 Click to see CC=CC#CC#CC(CCO)O 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(2E,9Z)-2,9,16-heptadecatrien-4,6-diyn-1,8-diol 24205422 Click to see C=CCCCCCC=CC(C#CC#CC=CCO)O 258.35 unknown via CMAUP database
(2R,3S,8R,9Z)-heptadeca-9,16-dien-4,6-diyne-2,3,8-triol 60144702 Click to see CC(C(C#CC#CC(C=CCCCCCC=C)O)O)O 276.40 unknown via CMAUP database
(8Z,10S,15R,16S)-1,8-Heptadecadiene-11,13-diyne-10,15,16-triol 11514622 Click to see CC(C(C#CC#CC(C=CCCCCCC=C)O)O)O 276.40 unknown via CMAUP database
1,9,16-Heptadecatriene-4,6-diyne-3,8-diol 5469786 Click to see C=CCCCCCC=CC(C#CC#CC(C=C)O)O 258.35 unknown via CMAUP database
Gymnasterkoreayne F 10355169 Click to see C=CCCCCCC=CC(C#CC#CC=CCO)O 258.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(1R)-4alpha-Hydroxy-4,8aalpha-dimethyl-6-isopropyl-1,2,3,4,4abeta,5,8,8a-octahydronaphthalene-1alpha-yl]beta-D-glucopyranoside 102523032 Click to see CC(C)C1=CCC2(C(CCC(C2C1)(C)O)OC3C(C(C(C(O3)CO)O)O)O)C 400.50 unknown via CMAUP database
[(1R)-4alpha-Hydroxy-4,8aalpha-dimethyl-6-isopropyl-1,2,3,4,4abeta,7,8,8a-octahydronaphthalene-1alpha-yl]beta-D-glucopyranoside 102523031 Click to see CC(C)C1=CC2C(CC1)(C(CCC2(C)O)OC3C(C(C(C(O3)CO)O)O)O)C 400.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(90)85035-E
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85035-E
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)85035-E
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)85035-E
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)85035-E
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(90)85035-E
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eugenyl glucoside 3084296 Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,3-Dihydroxy-2,5-dimethoxyxanthone 5480344 Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=C(C(=C3)O)OC)O 288.25 unknown https://doi.org/10.1016/0031-9422(90)85035-E
1,3,5-Trihydroxy-2-methoxyxanthen-9-one 5480342 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O 274.22 unknown https://doi.org/10.1016/0031-9422(90)85035-E
1,6-Dihydroxy-7,8-dimethoxyxanthone 14630572 Click to see COC1=C(C2=C(C=C1O)OC3=CC=CC(=C3C2=O)O)OC 288.25 unknown https://doi.org/10.1016/0031-9422(90)85035-E
2,8-Dihydroxy-1-methoxyxanthone 5464640 Click to see COC1=C(C=CC2=C1C(=O)C3=C(C=CC=C3O2)O)O 258.23 unknown https://doi.org/10.1016/0031-9422(90)85035-E
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/0031-9422(90)85035-E
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(90)85035-E
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(90)85035-E

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