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Bosistoa transversa

Bosistoa transversa - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64400d965a636866658671
Scientific name Bosistoa transversa
Authority J.F.Bailey & C.T.White
First published in Bot. Bull. Dept. Agric. Queensland 19: 6 (1917)

Description Top

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Synonyms Top

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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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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-0000569606
Tropicos 100299628
KEW urn:lsid:ipni.org:names:771729-1
The Plant List kew-2680399
Open Tree Of Life 5747613
Observations.org 367606
NCBI Taxonomy 1619367
IPNI 771729-1
iNaturalist 543968
GBIF 3831358
Freebase /m/0fqqxm1
EOL 5623421
Elurikkus 420706
Wikipedia Bosistoa_transversa

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
Novel Prenylated Acetophenones from<i>Bosistoa selwynii</i> Abdurazag A. Auzi, Thomas G. Hartley, Roger D. Waigh, Peter G. Waterman Informa UK Limited 07-Jul-2007
doi:10.1080/10575639808041210
Acridone alkaloids from Bosistoa transversa Abdurazag A. Auzi, Thomas G. Hartley, Roger D. Waigh, Peter G. Waterman Elsevier BV 01-May-2003
doi:10.1016/0031-9422(95)00843-8
A xanthine alkaloid from the leaves of Bosistoa floydii Abdurazag A. Auzi, Alexander I. Gray, Thomas G. Hartley, Roger D. Waigh, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)97111-5
Heterocycle-Fused Acridines Groundwater PW, Munawar MA Adv Heterocycl Chem 01-Jan-1997
PMCID:PMC7112105
doi:10.1016/S0065-2725(08)60930-7
PMID:32287461

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 / 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 https://doi.org/10.1080/10575639808041210
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/10.1080/10575639808041210
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-[5-Hydroxy-8-(2-hydroxypropan-2-yl)-2,2-dimethyl-8,9-dihydrofuro[2,3-h]chromen-6-yl]ethanone 163192802 Click to see CC(=O)C1=C2C(=C3C(=C1O)C=CC(O3)(C)C)CC(O2)C(C)(C)O 318.40 unknown https://doi.org/10.1080/10575639808041210
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1,3,5-Trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-10-methyl-4-(3-methylbut-2-enyl)acridin-9-one 101696513 Click to see CC(=CCC1=C2C(=C(C(=C1O)CC(C(=C)C)O)O)C(=O)C3=C(N2C)C(=CC=C3)O)C 409.50 unknown https://doi.org/10.1016/S0031-9422(00)97111-5
https://doi.org/10.1016/0031-9422(95)00843-8
1,3,5-Trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-10-methylacridin-9-one 101696512 Click to see CC(=C)C(CC1=C(C=C2C(=C1O)C(=O)C3=C(N2C)C(=CC=C3)O)O)O 341.40 unknown https://doi.org/10.1016/0031-9422(95)00843-8
1,3,5-trihydroxy-2-[(1R)-1-hydroxy-3-methylbut-3-enyl]-10-methyl-4-(3-methylbut-2-enyl)acridin-9-one 163064945 Click to see CC(=CCC1=C2C(=C(C(=C1O)C(CC(=C)C)O)O)C(=O)C3=C(N2C)C(=CC=C3)O)C 409.50 unknown https://doi.org/10.1016/S0031-9422(00)97111-5
1,3,5-trihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-10-methyl-4-(3-methylbut-2-enyl)acridin-9-one 162947150 Click to see CC(=CCC1=C2C(=C(C(=C1O)CC(C(=C)C)O)O)C(=O)C3=C(N2C)C(=CC=C3)O)C 409.50 unknown https://doi.org/10.1016/0031-9422(95)00843-8
https://doi.org/10.1016/S0031-9422(00)97111-5
1,3,5-trihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-10-methylacridin-9-one 163084590 Click to see CC(=C)C(CC1=C(C=C2C(=C1O)C(=O)C3=C(N2C)C(=CC=C3)O)O)O 341.40 unknown https://doi.org/10.1016/0031-9422(95)00843-8
5,10-Dihydroxy-12-(2-hydroxy-3-methylbut-3-enyl)-2,2,11-trimethylpyrano[3,2-b]acridin-6-one 15286418 Click to see CC(=C)C(CC1=C2C(=C(C3=C1N(C4=C(C3=O)C=CC=C4O)C)O)C=CC(O2)(C)C)O 407.50 unknown https://doi.org/10.1016/0031-9422(95)00843-8
5,10-dihydroxy-12-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2,2,11-trimethylpyrano[3,2-b]acridin-6-one 162955149 Click to see CC(=C)C(CC1=C2C(=C(C3=C1N(C4=C(C3=O)C=CC=C4O)C)O)C=CC(O2)(C)C)O 407.50 unknown https://doi.org/10.1016/0031-9422(95)00843-8
7H-Pyrano[2,3-c]acridin-7-one, 3,12-dihydro-6,11-dihydroxy-3,3,12-trimethyl-5-(3-methyl-2-butenyl)- 633176 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(N3C)C(=CC=C4)O)C=CC(O2)(C)C)C 391.50 unknown https://doi.org/10.1016/0031-9422(95)00843-8
Citrusamine 14038956 Click to see CN1C2=C(C(=CC(=C2)OC)O)C(=O)C3=C1C(=CC=C3)O 271.27 unknown https://doi.org/10.1016/0031-9422(95)00843-8
Junosine 15286413 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(N2C)C(=CC=C3)O)O)C 325.40 unknown https://doi.org/10.1016/0031-9422(95)00843-8
N-Methylatalaphylline 15286416 Click to see CC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=C(N2C)C(=CC=C3)O)C 393.50 unknown https://doi.org/10.1016/0031-9422(95)00843-8
Yukocitrine 15286417 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(N3C)C(=CC=C4)O)C 323.30 unknown https://doi.org/10.1016/0031-9422(95)00843-8
> 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/10.1080/10575639808041210
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Braylin 618370 Click to see CC1(C=CC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1080/10575639808041210

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