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Cyperus pluribracteatus

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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 UUID643ff6546e946179505864
Scientific name Cyperus pluribracteatus
Authority (Kük.) Govaerts
First published in World Checkl. Cyperaceae : 350 (2007)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cyperus psilostachys (C.B.Clarke) Kük. Bot. Not. 1934: 69 (1934)
Cyperus psilostachys f. glabrescens Kük. Pflanzenr. IV, 20(101): 546 1936
Cyperus psilostachys var. pluribracteatus Kük. Pflanzenr. , IV, 20(101): 546 (1936)
Cyperus psilostachys var. subrufus Kük. Pflanzenr. IV, 20(101): 546. 1936
Mariscus psilostachys C.B.Clarke J. Bot. 34: 225 (1896)

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

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-0000380014
Tropicos 100177046
KEW urn:lsid:ipni.org:names:77084787-1
The Plant List kew-238039
Open Tree Of Life 3959518
IPNI 77084787-1
GBIF 2714782
EOL 1121621

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
Five flavans from Mariscus psilostachys Eliane Garo, Marc Maillard, Sándor Antus, Steven Mavi, Kurt Hostettmann Elsevier BV 05-Apr-2003
doi:10.1016/S0031-9422(96)00526-2

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 / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one 12310452 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol 11277283 Click to see COC1=C(C=CC(=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
7,4'-Dihydroxy-3'-methoxyflavan 14157887 Click to see COC1=C(C=CC(=C1)C2CCC3=C(O2)C=C(C=C3)O)O 272.29 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-5-ol 102506203 Click to see COC1=CC(=C2CCC(OC2=C1)C3=CC(=C(C=C3)O)OC)O 302.32 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
(2S)-3',4'-Dihydroxy-5,7-dimethoxyflavan 73356683 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C(=C1)OC 302.32 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
(2S)-4'-Hydroxy-5,7,3'-trimethoxyflavan 10495608 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)OC)C(=C1)OC 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
(2S)-4'-Hydroxy-7,3'-dimethoxyflavan 14017332 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)OC)C=C1 286.32 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3,4-dihydro-2H-chromen-5-ol 10851881 Click to see COC1=CC(=C2CCC(OC2=C1)C3=CC(=C(C=C3)O)OC)O 302.32 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
3',4'-Dihydroxy-5,7-dimethoxyflavan 44257202 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C(=C1)OC 302.32 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
4-(5,7-dimethoxy-3,4-dihydro-2H-chromen-2-yl)-2-methoxyphenol 49801265 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)OC)C(=C1)OC 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
4'-Hydroxy-7,3'-dimethoxyflavan 14017331 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)OC)C=C1 286.32 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 321347 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)OC)O 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00526-2
Eriodictyol 7,3'-dimethyl ether 14235076 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)OC)O 316.30 unknown https://doi.org/10.1016/S0031-9422(96)00526-2

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