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Pisonia umbellifera

Pisonia umbellifera - 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 UUID644049aab636e771951361
Scientific name Pisonia umbellifera
Authority (J.R.Forst. & G.Forst.) Seem.
First published in Fl. Vit. : 195 (1866)

Description Top

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Synonyms Top

Scientific name Authority First published in
Calpidia subnitens Heimerl mss. in Herb. Mus. Paris

Common names Top

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Language Common/alternative name
English umbrella catchbirdtree
Finnish pisonia
Japanese ウドノキ属
Japanese オオクサボケ
Japanese ウドノキ
Russian Пизония зонтичная
Chinese 胶果木
Chinese 皮孙木
Chinese 皮孫木
Chinese 水冬瓜
Chinese 伞花腺果藤
Chinese 黏鳥樹

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001086710
USDA Plants PIUM2
Tropicos 22500321
INPN 921612
KEW urn:lsid:ipni.org:names:605102-1
The Plant List tro-22500321
Missouri Botanical Garden 282902
Open Tree Of Life 462842
Nature Serve 2.144643
IUCN Red List 49277895
iNaturalist 166917
GBIF 3086266
Freebase /m/043lfh8
EOL 486200
Wikipedia Ceodes_umbellifera

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
Chemical constituents and antitubercular activity of Formosan Pisonia umbellifera. Kuo HT, Peng CF, Huang HY, Lin CH, Chen IS, Tsai IL Planta Med 01-May-2011
doi:10.1055/S-0030-1250534
PMID:21108171
Saponins from Pisonia umbellifera. Lavaud C, Beauvière S, Masşiot G, Le Men-Olivier L, Bourdy G Phytochemistry 01-Sep-1996
doi:10.1016/0031-9422(96)00253-1
PMID:8987513

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate 70164 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC 212.20 unknown https://doi.org/10.1055/S-0030-1250534
> Benzenoids / Phenols / Methoxyphenols
(1S,2S)-1-(4-hydroxy-3,5-dimethoxyphenyl)propane-1,2-diol 162867204 Click to see CC(C(C1=CC(=C(C(=C1)OC)O)OC)O)O 228.24 unknown https://doi.org/10.1055/S-0030-1250534
4-[(1S,2S)-2-hydroxy-1-methoxypropyl]-2,6-dimethoxyphenol 122207108 Click to see CC(C(C1=CC(=C(C(=C1)OC)O)OC)OC)O 242.27 unknown https://doi.org/10.1055/S-0030-1250534
Berfussinol 54586911 Click to see COC1=CC(=CC(=C1O)OC)C(CO)C(=O)OC 256.25 unknown https://doi.org/10.1055/S-0030-1250534
Goldfussinol 71460595 Click to see COC1=CC(=CC(=C1O)OC)C(CO)C(=O)OC 256.25 unknown https://doi.org/10.1055/S-0030-1250534
methyl (2R)-3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propanoate 162867207 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)OC)O 226.23 unknown https://doi.org/10.1055/S-0030-1250534
methyl (3R)-3-hydroxy-3-(4-hydroxy-3-methoxyphenyl)propanoate 162865626 Click to see COC1=C(C=CC(=C1)C(CC(=O)OC)O)O 226.23 unknown https://doi.org/10.1055/S-0030-1250534
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1055/S-0030-1250534
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1055/S-0030-1250534
> Lignans, neolignans and related compounds / Lignan lactones
Zhepeiresinol 192547 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(=O)C3CO2 280.27 unknown https://doi.org/10.1055/S-0030-1250534
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 101688371 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1089.20 unknown https://doi.org/10.1016/0031-9422(96)00253-1
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 101999461 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C2C1)C)C(=O)OC1C(C(C(C(O1)CO)O)O)O)C 1251.40 unknown https://doi.org/10.1016/0031-9422(96)00253-1
(S)-(3beta)-28-(beta-D-Glucopyranosyloxy)-28-oxoolean-12-en-3-yl 3-O-[carboxy(carboxymethoxy)methyl]-beta-D-glucopyranosiduronic acid 100929764 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC(C(=O)O)OCC(=O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 927.00 unknown https://doi.org/10.1016/0031-9422(96)00253-1
6-[(8a-Carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]-4-[carboxy(carboxymethoxy)methoxy]-3,5-dihydroxyoxane-2-carboxylic acid 131751632 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC(C(=O)O)OCC(=O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown https://doi.org/10.1016/0031-9422(96)00253-1
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxane-2-carboxylic acid 14608075 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1089.20 unknown https://doi.org/10.1016/0031-9422(96)00253-1
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 13909679 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown https://doi.org/10.1016/0031-9422(96)00253-1
6-[[4,4,6a,6b,11,11,14b-Heptamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163061984 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C2C1)C)C(=O)OC1C(C(C(C(O1)CO)O)O)O)C 1251.40 unknown https://doi.org/10.1016/0031-9422(96)00253-1
Calendulaglycoside F 5104673 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown https://doi.org/10.1016/0031-9422(96)00253-1
Calenduloside E 176079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown https://doi.org/10.1016/0031-9422(96)00253-1
Calenduloside F 13909684 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown https://doi.org/10.1016/0031-9422(96)00253-1
Spinacoside C 85118552 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC(C(=O)O)OCC(=O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 927.00 unknown https://doi.org/10.1016/0031-9422(96)00253-1
Spinacoside D 15834378 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC(C(=O)O)OCC(=O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown https://doi.org/10.1016/0031-9422(96)00253-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-[(1S,4R,5R,8S,9S,12S,13R)-4,8-dimethyl-5-[(2R)-6-methyl-5-methylideneheptan-2-yl]-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 13943213 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 454.70 unknown https://doi.org/10.1055/S-0030-1250534
3-[4,8-Dimethyl-5-(6-methyl-5-methylideneheptan-2-yl)-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 13943212 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 454.70 unknown https://doi.org/10.1055/S-0030-1250534
3-[5-(6-Hydroxy-6-methylhept-4-en-2-yl)-4,8-dimethyl-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 75604385 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 456.70 unknown https://doi.org/10.1055/S-0030-1250534
Gardenoin H 51040600 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 456.70 unknown https://doi.org/10.1055/S-0030-1250534
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1055/S-0030-1250534
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxyphenyl)propan-1-one 162958208 Click to see C1=CC(=CC=C1C(=O)C(CO)O)O 182.17 unknown https://doi.org/10.1055/S-0030-1250534
(2S)-2-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 162935570 Click to see CC(C(=O)C1=CC(=C(C(=C1)OC)O)OC)O 226.23 unknown https://doi.org/10.1055/S-0030-1250534
(S)-alpha,4'-Dihydroxy-3'-methoxypropiophenone 12181418 Click to see CC(C(=O)C1=CC(=C(C=C1)O)OC)O 196.20 unknown https://doi.org/10.1055/S-0030-1250534
2-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one 200415 Click to see CC(C(=O)C1=CC(=C(C=C1)O)OC)O 196.20 unknown https://doi.org/10.1055/S-0030-1250534
2-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 14123045 Click to see CC(C(=O)C1=CC(=C(C(=C1)OC)O)OC)O 226.23 unknown https://doi.org/10.1055/S-0030-1250534
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 54353627 Click to see COC1=CC(=CC(=C1O)OC)C(=O)CCO 226.23 unknown https://doi.org/10.1055/S-0030-1250534
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
3,4,4,5-Tetramethoxycyclohexa-2,5-dien-1-one 13815814 Click to see COC1=CC(=O)C=C(C1(OC)OC)OC 214.21 unknown https://doi.org/10.1055/S-0030-1250534
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6-Hydroxy-7-methoxy-3,4-dihydro-2H-isoquinolin-1-one 38358169 Click to see COC1=C(C=C2CCNC(=O)C2=C1)O 193.20 unknown https://doi.org/10.1055/S-0030-1250534
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(4-hydroxy-3-methoxyphenyl)-N-[2-(3-hydroxy-4-methoxyphenyl)ethyl]prop-2-enamide 67111365 Click to see COC1=C(C=C(C=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1055/S-0030-1250534
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1055/S-0030-1250534
N-trans-feruloyl-4'-O-methyldopamine 14412557 Click to see COC1=C(C=C(C=C1)CCNC(=O)C=CC2=CC(=C(C=C2)O)OC)O 343.40 unknown https://doi.org/10.1055/S-0030-1250534
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 4-hydroxy-3-methoxy-cinnamate 16830 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1055/S-0030-1250534
Methyl ferulate 5357283 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1055/S-0030-1250534
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6,8-Dimethylisogenistein 70697886 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=CO2)C3=CC=CC=C3O)C)O 298.29 unknown https://doi.org/10.1055/S-0030-1250534

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