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Viburnum urceolatum

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 UUID64405af02a323158414136
Scientific name Viburnum urceolatum
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 172 (1846)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Viburnum urceolatum var. brevifolium Makino
Viburnum urceolatum f. brevifolium (Makino) Nakai
Viburnum urceolatum f. procumbens (Nakai) H.Hara Ginkgoana 5: 213. 1983
Viburnum taiwanianum Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 137 (1911)

Common names Top

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Language Common/alternative name
Chinese 壶花荚蒾
Chinese 壺花莢蒾

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
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001291001
Tropicos 6000824
KEW urn:lsid:ipni.org:names:149991-1
The Plant List tro-6000824
Open Tree Of Life 624780
NCBI Taxonomy 237962
IPNI 149991-1
iNaturalist 603441
GBIF 7272689
EPPO VIBUR
EOL 7018942
USDA GRIN 41439
CMAUP NPO8492

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)!
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Title Authors Publication Released IDs
Constituents of the leaves of Macaranga tanarius. Phommart S, Sutthivaiyakit P, Chimnoi N, Ruchirawat S, Sutthivaiyakit S J Nat Prod 01-Jun-2005
doi:10.1021/NP0500272
PMID:15974621
The bitter iridoids from Viburnum urceolatum Tsunao Hase, Hideki Takao, Tetsuo Iwagawa Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80027-2

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E)-tetradec-5-en-1-ol 6431325 Click to see CCCCCCCCC=CCCCCO 212.37 unknown via CMAUP database
6-Tetradecen-1-ol, (E) 6431327 Click to see 212.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Trachelosperogenin A1, >=95% (LC/MS-ELSD) 21637743 Click to see 680.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3R,4R,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,11,14b-hexamethyl-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-tetradecahydropicene-4-carboxylic acid 101673896 Click to see 680.80 unknown via CMAUP database
(5R,8R,9S,10R,13R,14R,17S)-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 12309262 Click to see CC(=CCCC(C)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C 442.70 unknown via CMAUP database
[(3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] hexadecanoate 137705088 Click to see 665.10 unknown https://doi.org/10.1021/NP0500272
[(3R,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-yl] acetate 13688749 Click to see 470.80 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown via CMAUP database
Glutinone 10071029 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(=O)C5(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl] (1R,4aS,6S,7R,7aS)-6-[(1R,4aS,7S,7aR)-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbonyl]oxy-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163008612 Click to see 556.60 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[4,5,6-Trihydroxy-2-(hydroxymethyl)oxan-3-yl] 1-hydroxy-6-(1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbonyl)oxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163008611 Click to see CC1CCC2C1C(OC=C2C(=O)OC3CC4C(C3C)C(OC=C4C(=O)OC5C(OC(C(C5O)O)O)CO)O)O 556.60 unknown https://doi.org/10.1016/0031-9422(83)80027-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Quercitol 441437 Click to see C1C(C(C(C(C1O)O)O)O)O 164.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(1R,4aS,6S,7R,7aS)-1-hydroxy-7-methyl-4-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-6-yl] (1R,4aS,6S,7R,7aS)-1,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162894160 Click to see 678.70 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[1-Hydroxy-7-methyl-4-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-6-yl] 1,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162894158 Click to see 678.70 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl (1R,4aS,6S,7R,7aS)-1,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162858609 Click to see CC1C(CC2C1C(OC=C2C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 482.50 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl (1R,4aS,6S,7R,7aS)-6-[(1R,4aS,7S,7aR)-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbonyl]oxy-1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163092184 Click to see 662.70 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 1-hydroxy-6-(1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbonyl)oxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 102404382 Click to see 662.70 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 1-hydroxy-6-(1-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbonyl)oxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163092182 Click to see 662.70 unknown https://doi.org/10.1016/0031-9422(83)80027-2
[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 1,6-dihydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 162858607 Click to see CC1C(CC2C1C(OC=C2C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 482.50 unknown https://doi.org/10.1016/0031-9422(83)80027-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3R,4R)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 13831071 Click to see 746.60 unknown via CMAUP database
Benzoic acid, 3,4,5-trihydroxy-, (2R,2'R,3R,3'R,4R)-2-(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-5,5',7,7'-tetrahydroxy-2'-(3,4,5-trihydroxyphenyl)(4,8'-bi-2H-1-benzopyran)-3,3'-diyl ester 11622083 Click to see 898.70 unknown via CMAUP database
Epicatechin-(4beta->8)-epigallocatechin 3'-gallate 11513300 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 746.60 unknown via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
Procyanidin B3 3,3'-digallate 12795892 Click to see 882.70 unknown via CMAUP database
Prodelphinidin B3 13831068 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
Gallocatechin 65084 Click to see 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(2R,3R,4S,5R,6S)-4,5-diacetyloxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 10418008 Click to see 824.70 unknown via CMAUP database
3'',4''-Di-O-acetyl-2'',6''-di-O-p-coumaroylastragalin 10328097 Click to see 824.70 unknown via CMAUP database
Kaempferol 3-(2'',6''-di-(E)-p-coumarylglucoside) 10439991 Click to see 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP0500272
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1-Epi-castalagin 12302512 Click to see 934.60 unknown via CMAUP database
Castalagin 12302513 Click to see 934.60 unknown via CMAUP database

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