Details Top

Internal ID UUID64405af2b27cc864164091
Scientific name Viburnum chingii
Authority P.S.Hsu
First published in Acta Phytotax. Sin. 11: 68 (1966)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Indigenous peoples of the northern Great Lakes made decoctions from the inner bark of Viburnum opulus to treat fevers, colds, and menstrual cramps, while topical infusions of the bark were used for skin inflammations and wounds; among the Menominee and other Anishinaabe peoples this bark tea was taken for abdominal pains, and the Iroquois prepared it as a cold cure and fever reducer, and in Europe the bark has long been taken as a tea to reduce fevers and calm uterine cramps, with 19th‑century physicians such as Schöpf noting the “febrifuge” effect and nineteenth‑century herbalists like Culpeper and Fernie describing its use for cramps and menorrhagia. In Russia and neighboring regions infusions or weak decoctions of the inner bark were taken for fevers and menstrual complaints, and in Poland the bark infusion was used as a diaphoretic and for painful periods. For pain and skin complaints the inner bark was crushed or powdered and applied in poultices, and sometimes the berries were infused into a tonic, though preparations vary by region.

A practical preparation is a mild bark tea: simmer 1–2 teaspoons of dried inner bark in 250 ml of water for 10 minutes, then steep off the heat for 10 minutes; a decoction using the same proportions may be simmered for 15 minutes. For a 1:5 ethanol tincture, macerate 50 g of dried inner bark in 250 ml of 40% ethanol for 2 weeks in a cool dark place, shaking daily, then press and strain; the resulting tincture typically yields 1 ml tincture from roughly 200 mg of bark. The inner bark contains hydroquinone and phenolic glycosides; it is considered potentially toxic in larger doses and should not be used by pregnant or lactating women or given to children without professional guidance.

The strongest candidate molecules include the dihydroisocoumarin viburnolide, the iridoid loganic acid, cyanogenic glycosides, chlorogenic and caffeic acids, as well as flavonoids like quercetin and kaempferol derivatives; these constituents can account for the documented antispasmodic, diaphoretic, and astringent actions attributed to infusions of the inner bark. Contemporary herbal practice continues to employ Viburnum opulus bark in moderation, and tinctures and decoctions are still offered by European and North American herbalists, while modern phytochemical work is beginning to focus on the bark’s iridoid and phenolic profile and the culinary use of its astringent berries in preserves and syrups.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Viburnum erubescens var. neurophyllum Hand.-Mazz. Symb. Sin. 7(4): 1033–1034 1936
Viburnum chingii var. patentiserratum P.S.Hsu Acta Phytotax. Sin. 11(1): 69–70, pl. 10, f. 2 1966
Viburnum chingii var. tenuipes P.S.Hsu Acta Phytotax. Sin. 13(1): 112 (1975)
Viburnum chingii var. carnosulum (W.W.Sm.) P.S.Hsu Fl. Reipubl. Popularis Sin. 72: 46 (1988)
Viburnum erubescens var. carnosulum W.W.Sm. Notes Roy. Bot. Gard. Edinburgh 9(42): 138 1916
Viburnum carnosulum (W.W.Sm.) P.S.Hsu Acta Phytotax. Sin. 11: 70 (1966)

Common names Top

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Language Common/alternative name
Chinese 漾濞荚蒾
Chinese 秦氏荚蒾

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Viburnum chingii var. limitaneum (W.W.Sm.) Q.E.Yang Fl. China 19: 586 (2011)

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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-0001291077
Tropicos 6000909
KEW urn:lsid:ipni.org:names:149611-1
The Plant List tro-6000909
Open Tree Of Life 990125
NCBI Taxonomy 1127642
IUCN Red List 147388882
IPNI 149611-1
GBIF 7272669
CMAUP NPO12547

Genomes (via NCBI) Top

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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
Antiviral Activities of Oleanolic Acid and Its Analogues Khwaza V, Oyedeji OO, Aderibigbe BA Molecules 09-Sep-2018
PMCID:PMC6225463
doi:10.3390/molecules23092300
PMID:30205592
Antimicrobial Activity of Oleanolic and Ursolic Acids: An Update Jesus JA, Lago JH, Laurenti MD, Yamamoto ES, Passero LF Evid Based Complement Alternat Med 22-Feb-2015
PMCID:PMC4352472
doi:10.1155/2015/620472
PMID:25793002
Triterpenoids and diterpenoids from Viburnum chingii. Chen XQ, Li Y, He J, Cheng X, Wang K, Li MM, Pan ZH, Peng LY, Zhao QS Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.496
PMID:21467682

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
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1R,2E,4S,6Z,9E,11R)-11-hydroxy-7-(hydroxymethyl)-4-[(3R)-4-methoxy-3,4-dimethylpentyl]-4,11-dimethyl-8-oxocycloundeca-2,6,9-trien-1-yl] 3-methylbut-2-enoate 163189576 Click to see 462.60 unknown https://doi.org/10.1248/CPB.59.496
[(1R,2E,4S,6Z,9E,11R)-11-hydroxy-7-(hydroxymethyl)-4-[(E)-4-methoxy-4-methylpent-2-enyl]-4,11-dimethyl-8-oxocycloundeca-2,6,9-trien-1-yl] 3-methylbut-2-enoate 52953127 Click to see CC(=CC(=O)OC1C=CC(CC=C(C(=O)C=CC1(C)O)CO)(C)CC=CC(C)(C)OC)C 446.60 unknown https://doi.org/10.1248/CPB.59.496
[(1R,4S,11R)-11-hydroxy-7-(hydroxymethyl)-4-(4-methoxy-4-methylpent-2-enyl)-4,11-dimethyl-8-oxocycloundeca-2,6,9-trien-1-yl] 3-methylbut-2-enoate 162864239 Click to see 446.60 unknown https://doi.org/10.1248/CPB.59.496
[(1R,4S,11R)-11-hydroxy-7-(hydroxymethyl)-4-[(3R)-4-methoxy-3,4-dimethylpentyl]-4,11-dimethyl-8-oxocycloundeca-2,6,9-trien-1-yl] 3-methylbut-2-enoate 162869420 Click to see 462.60 unknown https://doi.org/10.1248/CPB.59.496
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
I2-Ionone 638014 Click to see 192.30 unknown via CMAUP database
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(5,6-Dihydroxy-5a-methyl-3,9-dimethylidene-2-oxo-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-4-yl) 2-methylbut-2-enoate 162920236 Click to see 362.40 unknown https://doi.org/10.1248/CPB.59.496
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7S,7aR,9S,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]chrysene-7,9-diol 10789350 Click to see 442.70 unknown https://doi.org/10.1248/CPB.59.496
(1R,3aS,5aR,5bR,7S,7aR,11aR,11bR,13aR,13bR)-7-hydroxy-5a,5b,8,8,11a-pentamethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid 21636123 Click to see 470.70 unknown https://doi.org/10.1248/CPB.59.496
(1S,3S,4aS,6aS,6bR,8aR,12aR,14bS)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicene-1,3-diol 101786871 Click to see CC1(CCC2(CCC3(C(=CC=C4C3(CCC5C4(C(CC(C5(C)C)O)O)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1248/CPB.59.496
(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-3-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-3,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-2H-picen-1-one 14194115 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown https://doi.org/10.1248/CPB.59.496
10-Hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 258538 Click to see 472.70 unknown https://doi.org/10.1248/CPB.59.496
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]chrysene-7,9-diol 74830164 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5C(CC4(C3(CC2)C)C)O)(C)C)O)C)C 442.70 unknown https://doi.org/10.1248/CPB.59.496
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]chrysene-9,10-diol 72745631 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1248/CPB.59.496
7-hydroxy-5a,5b,8,8,11a-pentamethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid 73002539 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5C(CC4(C3(CC2)C)C)O)(C)C)C)C(=O)O 470.70 unknown https://doi.org/10.1248/CPB.59.496
alpha-Amyrin acetate 92842 Click to see 468.80 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1248/CPB.59.496
Lup-20(29)-ene-2alpha,3beta-diol 15127233 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C 442.70 unknown https://doi.org/10.1248/CPB.59.496
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see 152.23 unknown via CMAUP database
Hexanal 6184 Click to see 100.16 unknown via CMAUP database
trans-2-Hexenal 5281168 Click to see 98.14 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
(R)-gamma-Decalactone 183870 Click to see 170.25 unknown via CMAUP database
Gamma-dodecalactone, (R)- 10888889 Click to see 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Linalool oxide, cis- 6428573 Click to see 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5R,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 5317050 Click to see 544.50 unknown via CMAUP database
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 73353883 Click to see 544.50 unknown via CMAUP database
(1S,5S,6S,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 5317051 Click to see 544.50 unknown via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see 664.60 unknown via CMAUP database
Mahuannin A 5317052 Click to see 544.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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