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Internal ID UUID64401cc388f90911977391
Scientific name Flindersia laevicarpa
Authority C.T.White
First published in Bull. Dept. Agric. Queensland 22: 8 (1920)

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Language Common/alternative name
Persian فلیندرسیا لاویکارپا

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Name Authority First published in
Flindersia laevicarpa var. heterophylla (Merr. & L.M.Perry) T.G.Hartley J. Arnold Arbor. 50: 492. 1969 (1969)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000691387
Tropicos 100339293
KEW urn:lsid:ipni.org:names:773628-1
The Plant List kew-2813500
Open Tree Of Life 499511
NCBI Taxonomy 67931
IUCN Red List 38148
IPNI 773628-1
iNaturalist 192449
GBIF 7269298
Freebase /m/02x95l1
Wikipedia Flindersia_laevicarpa

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
Recent Advances in the Synthesis of β-Carboline Alkaloids Szabó T, Volk B, Milen M Molecules 27-Jan-2021
PMCID:PMC7866041
doi:10.3390/molecules26030663
PMID:33513936
Monitoring the Chemical Profile in Agarwood Formation within One Year and Speculating on the Biosynthesis of 2-(2-Phenylethyl)Chromones Liao G, Dong WH, Yang JL, Li W, Wang J, Mei WL, Dai HF Molecules 25-May-2018
PMCID:PMC6100365
doi:10.3390/molecules23061261
PMID:29799457
Leveraging biodiversity knowledge for potential phyto-therapeutic applications Sharma V, Sarkar IN J Am Med Inform Assoc 21-Mar-2013
PMCID:PMC3721164
doi:10.1136/amiajnl-2012-001445
PMID:23518859
The Chemical Constituents of Australian Flindersia Species. XVI. The Constituents of the Wood of Flindersia laevicarpa C. T. White & Francis GJW Breen, E Ritchie, WC Taylor CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9620819
Chemical constituents of the Flindersia. XXIII. Determination of the structure of flindercarpin-2 as methyl (S)-(Acetoxy){[3'S-(3α,3aα,4α,5β,6α,6aα,7α,10aα,11aα)]-5',6'-diacetoxy-7'-(furan-3'-yl)-2',2',3a',6a', 11a'-pentamethyl-12'-methylene-9'-oxo-2',3',3a',4',5',6',6a',9', 10', 11a'-decahydro-7'H-4', 10a'-methano-10a'H-furo[2,3-b]pyrano[3,4-g]oxocin-3'-yl)acetate GW Breen, K Picker, CL Raston, BW Skelton, WC Taylor, AH White CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9841461
The chemical constituents of Australian Flindersia species. XXI. An examination of the bark and the leaves of F. laevicarpa K Picker, E Ritchie, WC Taylor CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9762023
Frequency of Cyanogenesis in Tropical Rainforests of Far North Queensland, Australia MILLER RE, JENSEN R, WOODROW IE Ann Bot 01-Jun-2006
PMCID:PMC2803397
doi:10.1093/aob/mcl048
PMID:16520340

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
> Benzenoids / Benzene and substituted derivatives
1,5-Diphenylpentan-3-ol 12838510 Click to see C1=CC=C(C=C1)CCC(CCC2=CC=CC=C2)O 240.34 unknown https://doi.org/10.1071/CH9620819
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1071/CH9762023
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1071/CH9762023
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1071/CH9762023
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/10.1071/CH9762023
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Flindercarpin 2 102156440 Click to see CC(=O)OC1C2C(=C)C3(CC(=O)OC(C3(C1OC(=O)C)C)C4=COC=C4)OC5(C2(C(C(O5)(C)C)C(C(=O)OC)OC(=O)C)C)C 632.70 unknown https://doi.org/10.1071/CH9841461
Methyl 2-acetyloxy-2-[7,8-diacetyloxy-5-(furan-3-yl)-6,10,12,12,14-pentamethyl-16-methylidene-3-oxo-4,13,15-trioxatetracyclo[7.6.1.01,6.010,14]hexadecan-11-yl]acetate 162954847 Click to see CC(=O)OC1C2C(=C)C3(CC(=O)OC(C3(C1OC(=O)C)C)C4=COC=C4)OC5(C2(C(C(O5)(C)C)C(C(=O)OC)OC(=O)C)C)C 632.70 unknown https://doi.org/10.1071/CH9841461
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(R)-Flindersiachromanone 71713832 Click to see C1C(OC2=CC=CC=C2C1=O)CCC3=CC=CC=C3 252.31 unknown https://doi.org/10.1071/CH9762023
2-(2-Phenylethyl)-2,3-dihydrochromen-4-one 14814968 Click to see C1C(OC2=CC=CC=C2C1=O)CCC3=CC=CC=C3 252.31 unknown https://doi.org/10.1071/CH9762023
8-Methoxy-2-(2-phenylethyl)-4H-1-benzopyran-4-one 71391868 Click to see COC1=CC=CC2=C1OC(=CC2=O)CCC3=CC=CC=C3 280.30 unknown https://doi.org/10.1071/CH9762023
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1071/CH9620819
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (S)- 3594 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1071/CH9620819
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown https://doi.org/10.1071/CH9620819
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1071/CH9762023

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