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Bituminaria morisiana

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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 UUID6440461264992131763620
Scientific name Bituminaria morisiana
Authority (Pignatti & Metlesics) Greuter
First published in Willdenowia16: 108 (1986)

Description Top

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Synonyms Top

Scientific name Authority First published in
Psoralea morisiana Pignatti & Metlesics Boll. Soc. Sarda Sci. Nat.15: 53 (1975 publ. 1976)

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

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-0001062205
Tropicos 13075543
Flora of Italy 2399
KEW urn:lsid:ipni.org:names:942911-1
The Plant List tro-13075543
IPNI 942911-1
iNaturalist 505239
GBIF 3974149
Freebase /m/0gg7x7_
EOL 6318915
Wikipedia Bituminaria_morisiana

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)!
Title Authors Publication Released IDs
A pterocarpan from the seeds of Bituminaria morisiana. Leonti M, Casu L, Gertsch J, Bonsignore L, Floris C, Casu M, Cottiglia F J Nat Med 01-Jul-2010
doi:10.1007/S11418-010-0408-7
PMID:20238177
New cytotoxic prenylated isoflavonoids from Bituminaria morisiana. Cottiglia F, Casu L, Bonsignore L, Casu M, Floris C, Leonti M, Gertsch J, Heilmann J Planta Med 01-Mar-2005
doi:10.1055/S-2005-837841
PMID:15770547

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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
8H-Furo(3,2-h)(1)benzopyran-8-one 3083917 Click to see C1=CC2=C(C3=C1C=CC(=O)O3)OC=C2 186.16 unknown https://doi.org/10.1055/S-2005-837841
Angelicin 10658 Click to see C1=CC2=C(C=CO2)C3=C1C=CC(=O)O3 186.16 unknown https://doi.org/10.1007/S11418-010-0408-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1007/S11418-010-0408-7
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Coumestrol 5281707 Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)OC4=C3C=CC(=C4)O 268.22 unknown https://doi.org/10.1055/S-2005-837841
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(1R,12R)-17-(3-methylbut-2-enyl)-7,11,19-trioxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2(10),3,5,8,13(18),14,16-heptaen-16-ol 163003489 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C5C=COC5=C4)O)C 348.40 unknown https://doi.org/10.1007/S11418-010-0408-7
(1S,13S)-7,7-dimethyl-18-(3-methylbut-2-enyl)-8,12,20-trioxapentacyclo[11.8.0.02,11.04,9.014,19]henicosa-2(11),3,5,9,14(19),15,17-heptaen-17-ol 163019840 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C5C=CC(OC5=C4)(C)C)O)C 390.50 unknown https://doi.org/10.1055/S-2005-837841
(6aR,11aR)-3,9-Dihydroxy-4,8-diprenylpterocarpan 11581938 Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1055/S-2005-837841
https://doi.org/10.1007/S11418-010-0408-7
(6aS,11aS)-3,9-dimethoxy-4,8-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 163020714 Click to see CC(=CCC1=CC2=C(C=C1OC)OC3C2COC4=C3C=CC(=C4CC=C(C)C)OC)C 420.50 unknown https://doi.org/10.1055/S-2005-837841
17-(3-Methylbut-2-enyl)-7,11,19-trioxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2(10),3,5,8,13(18),14,16-heptaen-16-ol 163003488 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C5C=COC5=C4)O)C 348.40 unknown https://doi.org/10.1007/S11418-010-0408-7
3,9-Dihydroxy-4-prenyl-[6aR,11aR]pterocarpan 46880035 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC(=C4)O)O)C 324.40 unknown https://doi.org/10.1055/S-2005-837841
3,9-dimethoxy-4,8-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene 163020713 Click to see CC(=CCC1=CC2=C(C=C1OC)OC3C2COC4=C3C=CC(=C4CC=C(C)C)OC)C 420.50 unknown https://doi.org/10.1055/S-2005-837841
4-(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 75223805 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=CC(=C4)O)O)C 324.40 unknown https://doi.org/10.1055/S-2005-837841
Erybraedin D 471689 Click to see CC(=CCC1=C(C=CC2=C1OCC3C2OC4=C3C=C5C=CC(OC5=C4)(C)C)O)C 390.50 unknown https://doi.org/10.1055/S-2005-837841
Erybreadin C 21147013 Click to see CC(=CCC1=CC2=C(C=C1O)OC3C2COC4=C3C=CC(=C4CC=C(C)C)O)C 392.50 unknown https://doi.org/10.1055/S-2005-837841
https://doi.org/10.1007/S11418-010-0408-7
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
8-Prenyldaidzein 14841119 Click to see CC(=CCC1=C(C=CC2=C1OC=C(C2=O)C3=CC=C(C=C3)O)O)C 322.40 unknown https://doi.org/10.1055/S-2005-837841
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1055/S-2005-837841
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(8R,9S)-9-hydroxy-3-(4-hydroxyphenyl)-8-methoxy-10,10-dimethyl-8,9-dihydropyrano[2,3-f]chromen-4-one 163020973 Click to see CC1(C(C(OC2=C1C3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)O)OC)O)C 368.40 unknown https://doi.org/10.1055/S-2005-837841
3-(4-Hydroxyphenyl)-8,8-dimethylpyrano[2,3-f]chromen-4-one 9996115 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC=C(C3=O)C4=CC=C(C=C4)O)C 320.30 unknown https://doi.org/10.1055/S-2005-837841
9-Hydroxy-3-(4-hydroxyphenyl)-8-methoxy-10,10-dimethyl-8,9-dihydropyrano[2,3-f]chromen-4-one 163020972 Click to see CC1(C(C(OC2=C1C3=C(C=C2)C(=O)C(=CO3)C4=CC=C(C=C4)O)OC)O)C 368.40 unknown https://doi.org/10.1055/S-2005-837841

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