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Biebersteinia orphanidis

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 UUID64400d11b3980986113846
Scientific name Biebersteinia orphanidis
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 1: 113 (1854)

Ethnobotanical Use Top

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General Uses 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-0000565172
Tropicos 50147290
KEW urn:lsid:ipni.org:names:371942-1
The Plant List kew-2675798
Open Tree Of Life 24291
Observations.org 136886
NCBI Taxonomy 74351
IPNI 371942-1
iNaturalist 486377
GBIF 3827244
Elurikkus 419951
CMAUP NPO129

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
Plant Diversity of Mts. Oligirtos and Farmakas (NE Peloponnisos, Greece) with Emphasis on Their Endemic Flora Zikos A, Constantinidis T Plants (Basel) 09-Oct-2022
PMCID:PMC9572623
doi:10.3390/plants11192649
PMID:36235515
The Roles of a Flavone-6-Hydroxylase and 7-O-Demethylation in the Flavone Biosynthetic Network of Sweet Basil Berim A, Gang DR J Biol Chem 26-Nov-2012
PMCID:PMC3548489
doi:10.1074/jbc.M112.420448
PMID:23184958
A distinctive flavonoid chemistry for the anomalous genus Biebersteinia. Greenham J, Vassiliades DD, Harborne JB, Williams CA, Eagles J, Grayer RJ, Veitch NC Phytochemistry 01-Jan-2001
doi:10.1016/S0031-9422(00)00355-1
PMID:11198823

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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
> 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 https://doi.org/10.1016/S0031-9422(00)00355-1
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Tricetin 5281701 Click to see C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 302.23 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12315422 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 139031083 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 5377847 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
5-Hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 74977737 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Isorhoifolin 9851181 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Npc85473 5385553 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Scolymoside 10461109 Click to see 594.50 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Tricetin 7-glucoside 53392996 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 177696 Click to see 360.30 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Demethoxysudachitin 3083845 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Hymenoxin 171488 Click to see 374.30 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/S0031-9422(00)00355-1
Sudachitin 12443122 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)00355-1

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