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Dahlstedtia pinnata

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd653c68b7460553586
Scientific name Dahlstedtia pinnata
Authority (Benth.) Malme
First published in Ark. Bot.4(9): 4 (1905)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Dahlstedtia pinnata is documented as a source of timber. The wood is commercialized in Brazil under local trade names such as “camboim” and “camboim-rajado.” It is used for heavy construction and general carpentry.

Industrial and craft applications:
The timber is employed in civil construction and carpentry for general framing, structural components, beams, and carpentry work. Its mechanical strength supports structural applications.

Food and beverages (non-medicinal):
No documented non-medicinal food or beverage uses.

Colorants and tanning:
No reliable references report tannin extracts or dye uses.

Wood and fiber:
Timber is sold as sawn wood; specific fiber properties (e.g., bast fibers) are not documented in reliable sources.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses.

Properties relevant to use:
The wood is reported to be durable, with natural resistance to deterioration. Density and mechanical properties are consistent with heavy-duty timber use, supporting structural applications in construction and carpentry.

Standards and regulation:
Timber is commercialized under common Brazilian names; national regulations on timber trade and legal documentation apply but specific standards (ISO/ASTM/EN) are not specified in the referenced literature.

Sustainability and sourcing:
Dahlstedtia pinnata is assessed as Endangered in the IUCN Red List, indicating supply constraints. Its use carries sustainability implications; alternative timber and source verification are recommended where possible.

Synonyms Top

Scientific name Authority First published in
Camptosema pinnatum Benth. C.F.P.von Martius & auct. suc. (eds.), Fl. Bras.15(1): 325 (1862)

Common names Top

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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
World Flora Online wfo-0000168982
Tropicos 13013938
KEW urn:lsid:ipni.org:names:75873-2
The Plant List ild-15316
Open Tree Of Life 869824
NCBI Taxonomy 62116
IPNI 1025744-2
GBIF 2960230
EPPO DALPI
EOL 414789
USDA GRIN 436018
CMAUP NPO26020

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
Antidiabetic and Cytotoxic Activities of Rotenoids and Isoflavonoids Isolated from Millettia pachycarpa Benth Suthiphasilp V, Rujanapun N, Kumboonma P, Chaiyosang B, Tontapha S, Maneerat T, Patrick BO, Andersen RJ, Duangyod T, Charoensup R, Laphookhieo S ACS Omega 06-Jul-2022
PMCID:PMC9301698
doi:10.1021/acsomega.2c02163
PMID:35874225
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
Flower development of Goniorrhachis marginata reveals new insights into the evolution of the florally diverse detarioid legumes Prenner G, Cardoso D Ann Bot 26-Dec-2016
PMCID:PMC5314645
doi:10.1093/aob/mcw223
PMID:28025284
Prenylated flavonoids as evolutionary indicators in the genus Dahlstedtia Fernanda Rodrigues Garcez, Shirlei Scramin, Maria Célia Do Nascimento, Walter B. Mors Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80277-2

Phytochemical Profile Top

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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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one 14465808 Click to see 442.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Neoruscogenin 9910474 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6 428.60 unknown via CMAUP database
Ruscogenin 441893 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol 13754059 Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol 100982641 Click to see 754.90 unknown via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-4,5-dihydroxy-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 44575746 Click to see 708.90 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,3'S,4S,6S,7S,8R,9S,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-16-hydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-3'-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 10581939 Click to see 1047.10 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 21590070 Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O 1139.20 unknown via CMAUP database
[(3S,4S,5R,6S)-5-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxyoxan-3-yl] acetate 101937241 Click to see 911.00 unknown via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown via CMAUP database
Aculeoside B 154169 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O 1205.30 unknown via CMAUP database
CID 10462472 10462472 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8 706.90 unknown via CMAUP database
Ruscin(P) 13935613 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 869.00 unknown via CMAUP database
Ruscoside 91936850 Click to see 1049.20 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
> Organoheterocyclic compounds / Benzofurans
Euparone 104654 Click to see 218.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran 323624 Click to see 254.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
Isoderricin A 12310898 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)OC)C 322.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Furanoflavones
Karanjin 100633 Click to see 292.30 unknown https://doi.org/10.1016/0031-9422(88)80277-2
Lanceolatin B 10978265 Click to see 262.26 unknown https://doi.org/10.1016/0031-9422(88)80277-2
Pongaglabrone 10957726 Click to see 306.30 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-[3-[(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-3-yl]-4-hydroxyphenyl]-5-hydroxy-7-methoxychromen-4-one 163068812 Click to see 554.50 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(-)-Isolonchocarpin 12311091 Click to see 306.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
(2R)-8,8-dimethyl-2-phenyl-2,3-dihydropyrano[2,3-f]chromen-4-one 38364014 Click to see 306.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
8,8-Dimethyl-2-phenyl-4H,8H-benzo(1,2-b:3,4-b')dipyran-4-one 11358607 Click to see 304.30 unknown https://doi.org/10.1016/0031-9422(88)80277-2
Isopongaflavone 10958572 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
Karanjachromene 14033983 Click to see 334.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
Sumatrol 442824 Click to see CC(=C)C1CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O 410.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Pongachalcone I 11056805 Click to see 336.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Ovalichalcone 14033977 Click to see CC(=CCC1=C(C(=C(C=C1OC)OC)C(=O)C=CC2=CC=CC=C2)O)C 352.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
Ovalichalcone A 6274715 Click to see 396.40 unknown https://doi.org/10.1016/0031-9422(88)80277-2
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
Ovalitenone 627910 Click to see 338.30 unknown https://doi.org/10.1016/0031-9422(88)80277-2
Pongamol 689051 Click to see 294.30 unknown https://doi.org/10.1016/0031-9422(88)80277-2

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