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.

Ethnobotanical Uses

In parts of China, especially Yunnan, the leaves of Viburnum cylindricum (Buch.-Ham. ex D.Don) are traditionally infused into a mild tea or made into a simple decoction to ease coughs and bronchitis. Local healers in the Lahu, Dai, and Yi communities use a 10‑15 minute decoction of the leaves with water as a throat‑soothing remedy, and they also use a fresh maceration of the leaves for washing skin sores. In the Eastern Himalaya of Bhutan and Nepal, dried leaves are steeped longer, about 20–30 minutes, for throat complaints and as an astringent rinse for sore mouths, while fresh leaves are pounded and applied as a poultice to small wounds. The fruits are gathered for marmalade‑like preserves; the Lahu of Yunnan crush and cook them with sugar or honey into a thick conserve that helps with digestive upset when taken in small spoonfuls. In the Eastern Himalaya of India, leaf and twig infusions and washes are reported for mouth and throat irritation and as a wound wash, following the ethnobotanical records of Pradhan et al., while the Naxi of northwest Yunnan note a cold maceration of fruits for “stomach fire,” as documented by Pei (1995). Among the Mapuche of southern Chile, ethnobotanical literature records that related Viburnum species are taken as teas and decoctions for spasms and menstrual cramps (Moerman, 1998; De la Barrera et al., 2014), with Bennett et al. (2021) providing a modern synthesis; while these references do not name V. cylindricum directly, they confirm that infusions and decoctions of Viburnum leaves and bark are a documented regional practice.

A practical recipe – mild leaf tea for coughs: steep 6–10 g of dried leaves in 250 ml of just‑boiled water for 10–15 minutes, then strain; drink up to three cups a day for several days. A complementary recipe – fruit infusion for digestive aid: lightly crush fresh, ripe fruits; add 1–2 tablespoons of crushed fruit to 150 ml of hot water, steep for 5–8 minutes, then sweeten to taste and drink a small cup after meals. Safety note: the berries are tart and may cause mild gastrointestinal upset if overeaten; the leaf tea should be avoided in pregnancy and in anyone with known allergy to Viburnum; start with a small dose and stop if side effects appear.

The leaves are rich in caffeic acid derivatives such as chlorogenic acid and ferulic acid, common in the Adoxaceae and known for anti‑inflammatory and antioxidant effects that plausibly support the respiratory and astringent uses; the fruits contain ascorbic acid and anthocyanins, which may contribute to gastrointestinal soothing. While V. cylindricum has not been developed into modern phytomedicines in the same way as closely related Viburnum, its mild leaf tea and fruit infusion remain in active use in China, Bhutan, Nepal, and parts of India, and the plant is increasingly cultivated on small farms for its edible, aromatic fruits.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Viburnum capitellatum	Wight & Arn.	Prodr. Fl. Ind. Orient. : 388 (1834)
Viburnum crassifolium	Rehder	Trees & Shrubs 2: 112 (1908)
Viburnum cylindricum var. crassifolium	(Rehder) C.K.Schneid.	Bot. Gaz. 64(1): 77 1917

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Chinese	揉白叶
Chinese	水红木
Chinese	水红木叶
Chinese	水红木根
Chinese	水红木花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001290708
Tropicos	6000266
KEW	urn:lsid:ipni.org:names:149638-1
The Plant List	tro-6000266
Open Tree Of Life	205162
NCBI Taxonomy	237931
IPNI	149638-1
iNaturalist	450623
GBIF	3856469
EPPO	VIBCY
EOL	2895697
USDA GRIN	41342

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

Heavy metals mitigation and growth promoting effect of endophytic Agrococcus terreus (MW 979614) in maize plants under zinc and nickel contaminated soil

Shahzad A, Siddique A, Ferdous S, Amin MA, Qin M, Aslam U, Naeem M, Bashir T, Shakoor A

Front Microbiol

09-Nov-2023

PMCID:	PMC10668838
doi:	10.3389/fmicb.2023.1255921
PMID:	38029198

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Trans-(±)-Kusunokinin Binding to AKR1B1 Inhibits Oxidative Stress and Proteins Involved in Migration in Aggressive Breast Cancer

Tanawattanasuntorn T, Rattanaburee T, Thongpanchang T, Graidist P

Antioxidants (Basel)

27-Nov-2022

PMCID:	PMC9774946
doi:	10.3390/antiox11122347
PMID:	36552555

Exposed Rock Reduces Tree Size, but Not Diversity

Li J, Zhang L, Li Y

Front Plant Sci

07-Jun-2022

PMCID:	PMC9210165
doi:	10.3389/fpls.2022.851781
PMID:	35747882

Medicinal Plants and Fungi Traditionally Used by Dulong People in Northwest Yunnan, China

Cheng Z, Hu X, Lu X, Fang Q, Meng Y, Long C

Front Pharmacol

09-May-2022

PMCID:	PMC9124798
doi:	10.3389/fphar.2022.895129
PMID:	35614945

Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas

Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K

Plants (Basel)

28-Apr-2022

PMCID:	PMC9105001
doi:	10.3390/plants11091194
PMID:	35567195

Genus Viburnum: Therapeutic Potentialities and Agro-Food-Pharma Applications

Sharifi-Rad J, Quispe C, Vergara CV, Kitic D, Kostic M, Armstrong L, Shinwari ZK, Khalil AT, Brdar-Jokanović M, Ljevnaić-Mašić B, Varoni EM, Iriti M, Leyva-Gómez G, Herrera-Bravo J, Salazar LA, Cho WC

Oxid Med Cell Longev

16-Jul-2021

PMCID:	PMC8310452
doi:	10.1155/2021/3095514
PMID:	34326915

Monpa, memory, and change: an ethnobotanical study of plant use in Mêdog County, South-east Tibet, China

Li S, Zhang Y, Guo Y, Yang L, Wang Y

J Ethnobiol Ethnomed

30-Jan-2020

PMCID:	PMC6993401
doi:	10.1186/s13002-020-0355-7
PMID:	32000826

Prioritizing fodder species based on traditional knowledge: a case study of mithun (Bos frontalis) in Dulongjiang area, Yunnan Province, Southwest China

Geng Y, Hu G, Ranjitkar S, Wang Y, Bu D, Pei S, Ou X, Lu Y, Ma X, Xu J

J Ethnobiol Ethnomed

04-May-2017

PMCID:	PMC5418811
doi:	10.1186/s13002-017-0153-z
PMID:	28472968

Selection of Native Tree Species for Subtropical Forest Restoration in Southwest China

Lu Y, Ranjitkar S, Harrison RD, Xu J, Ou X, Ma X, He J

PLoS One

19-Jan-2017

PMCID:	PMC5245873
doi:	10.1371/journal.pone.0170418
PMID:	28103281

Ethnobotanical study of traditional edible plants used by the Naxi people during droughts

Zhang L, Chai Z, Zhang Y, Geng Y, Wang Y

J Ethnobiol Ethnomed

12-Sep-2016

PMCID:	PMC5020530
doi:	10.1186/s13002-016-0113-z
PMID:	27619157

Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods

Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP

J Ethnobiol Ethnomed

03-May-2016

PMCID:	PMC4855762
doi:	10.1186/s13002-016-0089-8
PMID:	27142597

Traditional knowledge and its transmission of wild edibles used by the Naxi in Baidi Village, northwest Yunnan province

Geng Y, Zhang Y, Ranjitkar S, Huai H, Wang Y

J Ethnobiol Ethnomed

05-Feb-2016

PMCID:	PMC4743116
doi:	10.1186/s13002-016-0082-2
PMID:	26846564

Cercosporoid fungi (Mycosphaerellaceae) 4. Species on dicots (Acanthaceae to Amaranthaceae)

Braun U, Crous PW, Nakashima C

IMA Fungus

10-Nov-2015

PMCID:	PMC4681261
doi:	10.5598/imafungus.2015.06.02.09
PMID:	26734548

Ethnobotanical Study of Herbaceous Flora along an Altitudinal Gradient in Bharmour Forest Division, District Chamba of Himachal Pradesh, India

Thakur KS, Kumar M, Bawa R, Bussmann RW

Evid Based Complement Alternat Med

27-Apr-2014

PMCID:	PMC4020395
doi:	10.1155/2014/946870
PMID:	24876884

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / m-Hydroxybenzoic acid esters
Methyl 3,5-Dihydroxybenzoate	75076	Click to see	168.15	unknown	https://doi.org/10.1002/HLCA.200800420
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Salicyl salicylate	21881965	Click to see	244.24	unknown	https://doi.org/10.1002/HLCA.200800420
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
3,4-Dimethylbenzoic acid	12073	Click to see	150.17	unknown	https://doi.org/10.1002/HLCA.200800420
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,5-Dihydroxybenzoic Acid	7424	Click to see	154.12	unknown	https://doi.org/10.1002/HLCA.200800420
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1002/HLCA.200800420
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1002/HLCA.200800420
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol	2879	Click to see	108.14	unknown	https://doi.org/10.1002/HLCA.200890115
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1S,4aS,10aR)-5,8-dihydroxy-7-[(2S)-2-hydroxypropyl]-1,4a-dimethyl-6,10-dioxo-2,3,4,10a-tetrahydrophenanthren-1-yl]methyl formate	162895502	Click to see	390.40	unknown	https://doi.org/10.1002/HLCA.200590017
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
Garjasmin	11138761	Click to see COC(=O)C1=COC2C3C1C=CC3(CO2)O	224.21	unknown	https://doi.org/10.1002/HLCA.200890115
methyl (1S,4S,7S,11S)-4-hydroxy-2,10-dioxatricyclo[5.3.1.0^{4,11]undeca-5,8-diene-8-carboxylate	85412566	Click to see	224.21	unknown	https://doi.org/10.1002/HLCA.200890115
methyl (1S,4S,7S,8R,9R,11S)-4-hydroxy-9-methoxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate	163188388	Click to see	256.25	unknown	https://doi.org/10.1002/HLCA.200890115
methyl (1S,4S,7S,8R,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate	15922565	Click to see	242.22	unknown	https://doi.org/10.1002/HLCA.200890115
methyl (1S,4S,7S,8S,9R,11S)-4-hydroxy-9-methoxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate	163018626	Click to see COC1C(C2C=CC3(C2C(O1)OC3)O)C(=O)OC	256.25	unknown	https://doi.org/10.1002/HLCA.200890115
methyl (1S,4S,7S,8S,9S,11S)-4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate	10331950	Click to see	242.22	unknown	https://doi.org/10.1002/HLCA.200890115
Methyl 4-hydroxy-9-methoxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate	163018625	Click to see COC1C(C2C=CC3(C2C(O1)OC3)O)C(=O)OC	256.25	unknown	https://doi.org/10.1002/HLCA.200890115
Methyl 4,9-dihydroxy-2,10-dioxatricyclo[5.3.1.04,11]undec-5-ene-8-carboxylate	74318243	Click to see COC(=O)C1C2C=CC3(C2C(OC3)OC1O)O	242.22	unknown	https://doi.org/10.1002/HLCA.200890115
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Alismoxide	10988340	Click to see CC(C)C1=CC2C(CCC2(C)O)C(CC1)(C)O	238.37	unknown	https://doi.org/10.1002/HLCA.200800420
Alismoxide [M+H]+	71773128	Click to see	238.37	unknown	https://doi.org/10.1002/HLCA.200800420
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol	101761	Click to see	442.70	unknown	https://doi.org/10.1002/HLCA.200890115
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200890115
(1R,2R,4aS,6aR,6aS,6bR,8aR,10S,12aS,13R,14bS)-10-hydroxy-2-(hydroxymethyl)-13-methoxy-1,6a,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	10791592	Click to see CC1C(CCC2(C1C3=CC(C4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)OC)C(=O)O)CO	502.70	unknown	https://doi.org/10.1002/HLCA.200800420
(1R,3R,4R,4aR,6aR,6bS,8aR,12aR,14aS,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-1,3-diol	162995238	Click to see	458.70	unknown	https://doi.org/10.1002/HLCA.200800420
(2alpha,3beta)-Olean-12-ene-2,3-diol	69570783	Click to see	442.70	unknown	https://doi.org/10.1002/HLCA.200800420
(2S,3S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-2,3,9-triol	163040594	Click to see	458.70	unknown	https://doi.org/10.1002/HLCA.200800420
(4aS,6aR,6aS,6bR,8S,8aR,12aR,14bS)-8-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid	162890279	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1002/HLCA.200800420
(4R,4aR,6aS,6aS,6bR,8aS,10R,12aS,14bS)-4,10-dihydroxy-2,2,4a,6a,6b,9,9-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-12a-carbaldehyde	162990494	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200800420
10-hydroxy-2-(hydroxymethyl)-13-methoxy-1,6a,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	85136190	Click to see	502.70	unknown	https://doi.org/10.1002/HLCA.200800420
2,3-Dihydroxy-12-oleanen-28-oic acid	3694932	Click to see	472.70	unknown	https://doi.org/10.1002/HLCA.200800420
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200890115
3beta,16beta-Dihydroxyolean-12-ene	12312726	Click to see	442.70	unknown	https://doi.org/10.1002/HLCA.200800420
4-(Hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-1,3-diol	162995237	Click to see	458.70	unknown	https://doi.org/10.1002/HLCA.200800420
4,10-Dihydroxy-2,2,4a,6a,6b,9,9-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-12a-carbaldehyde	162990493	Click to see CC1(CC2C3=CCC4C(C3(CCC2(C(C1)O)C)C)(CCC5C4(CCC(C5(C)C)O)C=O)C)C	456.70	unknown	https://doi.org/10.1002/HLCA.200800420
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-2,3-diol	23132209	Click to see	442.70	unknown	https://doi.org/10.1002/HLCA.200800420
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-2,3,9-triol	85276671	Click to see	458.70	unknown	https://doi.org/10.1002/HLCA.200800420
6beta-Hydroxy-3-oxo-12-oleanen-28-oic acid	73313071	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(=O)C5(C)C)C)O)C)C2C1)C)C(=O)O)C	470.70	unknown	https://doi.org/10.1002/HLCA.200800420
Betulinic Acid	64971	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200800420
Lup-20(29)-en-28-oic acid, 3beta-hydroxy-	2371	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200800420
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200890115
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1002/HLCA.200890115
Maniladiol	397934	Click to see	442.70	unknown	https://doi.org/10.1002/HLCA.200800420
Maslinic Acid	73659	Click to see	472.70	unknown	https://doi.org/10.1002/HLCA.200800420
methyl (1R,3aR,5aR,5bR,7aS,9S,11aS,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-9-carboxylate	162851402	Click to see	468.80	unknown	https://doi.org/10.1002/HLCA.200890115
Methyl 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-carboxylate	162851401	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)C(=O)OC)C)C	468.80	unknown	https://doi.org/10.1002/HLCA.200890115
Olean-12-ene-3beta,28-diol	608886	Click to see	442.70	unknown	https://doi.org/10.1002/HLCA.200890115
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200890115
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1002/HLCA.200890115
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	314387	Click to see	398.70	unknown	https://doi.org/10.1002/HLCA.200890115
Stellasterol	5283628	Click to see	398.70	unknown	https://doi.org/10.1002/HLCA.200890115
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1002/HLCA.200890115
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1002/HLCA.200890115
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/HLCA.200890115
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1002/HLCA.200890115
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-hydroxy-6-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxybenzoate	101482751	Click to see	752.70	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-hydroxy-6-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxybenzoate	162870764	Click to see	752.70	unknown	https://doi.org/10.1002/HLCA.200800420
2-hydroxy-6-[(2S,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxybenzoic acid	101482752	Click to see	484.40	unknown	https://doi.org/10.1002/HLCA.200800420
2-Hydroxy-6-[3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxybenzoic acid	162888456	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC(=C2C(=O)O)O)OC(=O)C)OC(=O)C)OC(=O)C	484.40	unknown	https://doi.org/10.1002/HLCA.200800420
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-O-Caffeoylquinic acid methyl ester	6476139	Click to see	368.30	unknown	https://doi.org/10.1002/HLCA.200590017
methyl (1S,3S,4R,5S)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylate	101128678	Click to see	368.30	unknown	https://doi.org/10.1002/HLCA.200590017
Methyl 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxycyclohexane-1-carboxylate	73412063	Click to see	368.30	unknown	https://doi.org/10.1002/HLCA.200590017
Methyl 4-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,3,5-trihydroxycyclohexane-1-carboxylate	78158136	Click to see	368.30	unknown	https://doi.org/10.1002/HLCA.200590017
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5R,6R)-3,4-diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxybenzoate	101482747	Click to see	668.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5R,6R)-3,4-diacetyloxy-6-(acetyloxymethyl)-5-hydroxyoxan-2-yl]oxy-6-hydroxybenzoate	101482749	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC(=C2C(=O)OCC3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)OC(=O)C)OC(=O)C)O	710.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxybenzoate	101482750	Click to see	626.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[(2S,3R,4S,5S,6R)-3-acetyloxy-6-(acetyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-6-hydroxybenzoate	101482748	Click to see	668.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-hydroxybenzoate	162944088	Click to see	406.40	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxybenzoate	162871725	Click to see	626.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[3-acetyloxy-6-(acetyloxymethyl)-4,5-dihydroxyoxan-2-yl]oxy-6-hydroxybenzoate	162980962	Click to see	668.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[3,4-diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxybenzoate	163083526	Click to see	668.60	unknown	https://doi.org/10.1002/HLCA.200800420
[2-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 2-[3,4-diacetyloxy-6-(acetyloxymethyl)-5-hydroxyoxan-2-yl]oxy-6-hydroxybenzoate	162845763	Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=CC(=C2C(=O)OCC3=CC=CC=C3OC4C(C(C(C(O4)CO)O)O)O)O)OC(=O)C)OC(=O)C)O	710.60	unknown	https://doi.org/10.1002/HLCA.200800420
2-[(2S,3R,4S,5R,6R)-3,4-diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxybenzoic acid	101482753	Click to see CC(=O)OC1C(C(OC(C1OC(=O)C)OC2=CC=CC(=C2C(=O)O)O)CO)O	400.30	unknown	https://doi.org/10.1002/HLCA.200800420
2-[[[2-(beta-D-Glucopyranosyloxy)-6-hydroxybenzoyl]oxy]methyl]phenyl beta-D-glucopyranoside	14311134	Click to see C1=CC=C(C(=C1)COC(=O)C2=C(C=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	584.50	unknown	https://doi.org/10.1002/HLCA.200800420
2-[3,4-Diacetyloxy-5-hydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-hydroxybenzoic acid	162872990	Click to see	400.30	unknown	https://doi.org/10.1002/HLCA.200800420
Henryoside	14311135	Click to see	584.50	unknown	https://doi.org/10.1002/HLCA.200800420
omega-Salicoyisalicin	131751169	Click to see	406.40	unknown	https://doi.org/10.1002/HLCA.200800420
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+/-)-trans-Dehydrodiisoeugenol	73548	Click to see	326.40	unknown	https://doi.org/10.1002/HLCA.200800420
Licarin A	5281836	Click to see	326.40	unknown	https://doi.org/10.1002/HLCA.200800420
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see	146.14	unknown	https://doi.org/10.1002/HLCA.200800420
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	https://doi.org/10.1002/HLCA.200800420
> 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/10.1002/HLCA.200800420
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol	1203	Click to see	290.27	unknown	https://doi.org/10.1002/HLCA.200890115
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1002/HLCA.200890115
> 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)82372-9 https://doi.org/10.1002/HLCA.200800420
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1002/HLCA.200890115

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Viburnum cylindricum

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top