Common products:
- Ornamental vine: sold by specialty nurseries under cultivar names or as “Hinds’ bittersweet” (Celastrus hindsii). Employed for vertical garden elements such as trellises, arbors, fences and walls, as well as groundcover for erosion control.
- Fruit clusters: bright orange‑red berries that persist on the vine through winter; harvested for use in cut‑flower designs and dried‑flower arrangements, adding colour in late‑season decorations.

Properties relevant to use:
- Fast‑growing, woody, twining climber capable of reaching 5–10 m in length under favourable conditions. Tolerates pruning, enabling shaping and maintenance of the desired form. Performs well in full sun to light shade and in a range of well‑drained soils; reported hardy in USDA zones 6–9. Fruit retention: berries remain on the plant from late autumn through winter, providing long‑lasting ornamental value and facilitating late‑season harvesting.

Sustainability and sourcing:
- Propagated primarily by semi‑hardwood cuttings or layering, with seed propagation less common due to stratification requirements. Nursery production is labour‑intensive but low‑input, requiring minimal chemical inputs. Plants are typically grown in containers (2–5 L) and sold as rooted cuttings, allowing controlled release of planting stock and reducing wild‑collection pressure. Because the species is vigorous and can self‑layer, it is often managed in production fields to prevent spread, aligning with sustainable horticultural practices.

Synonyms Top

Scientific name	Authority	First published in
Celastrus approximatus	Craib	Bull. Misc. Inform. Kew 1926: 349 (1926)
Celastrus axillaris	Ridl.	J. Malayan Branch Roy. Asiat. Soc. 1: 56 (1923)
Celastrus cantonensis	Hance	J. Bot. 23: 323 (1885)
Celastrus merrillii	Tardieu	Bull. Soc. Bot. France 95: 180 (1948)
Celastrus oblongifolius	Hayata	Icon. Pl. Formosan. 3: 58 (1913)
Celastrus racemulosus	Hassk.	Hort. Bogor. Descr. 1: 155 (1858)
Celastrus venulosus	Wall.	Numer. List [Wallich] n. 4321. 1831
Celastrus xizangensis	Y.R.Li	Acta Bot. Yunnan. 3: 356 (1981)
Celastrus hindsii var. henryi	Loes.	Bot. Jahrb. Syst. 29: 444 1900
Flueggea serrata	Miq.	Fl. Ned. Ind. 1(2): 356 (1859)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Vietnamese	cây xạ đen
Chinese	南華南蛇藤
Chinese	青江藤
Chinese	夜茶藤
Chinese	黄果藤
Chinese	一种维管植物

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 South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
- Indo-China
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Maluku
  - Sulawesi
  - Sumatera

Pacific click to expand
- Northwestern Pacific
  - Marianas

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000592744
Tropicos	6600830
KEW	urn:lsid:ipni.org:names:160316-1
The Plant List	kew-2707528
Open Tree Of Life	709258
Observations.org	430689
NCBI Taxonomy	489979
IPNI	160316-1
GBIF	3793742
EOL	2888819
Elurikkus	415421
USDA GRIN	9715

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

Enrichment and Evaluation of Antitumor Properties of Total Flavonoids from Juglans mandshurica Maxim

Yang S, Chu G, Wu J, Zhang G, Du L, Lin R

Molecules

25-Apr-2024

PMCID:	PMC11085465
doi:	10.3390/molecules29091976
PMID:	38731467

Antioxidant polysaccharide-enriched fractions obtained from olive leaves by ultrasound-assisted extraction with α-amylase inhibition, and antiproliferative activities

Elayeb R, Bermúdez-Oria A, Lazreg Aref H, Majdoub H, Ritzoulis C, Mannu A, Le Cerf D, Carraro M, Achour S, Fernández-Bolaños J, Trigui M

3 Biotech

27-Feb-2024

PMCID:	PMC10899153
doi:	10.1007/s13205-024-03939-2
PMID:	38425411

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

Optimization Conditions of Ultrasound-Assisted Extraction for Phenolic Compounds and Antioxidant Activity from Rubus alceifolius Poir Leaves

Tran CH, Nghiem MT, Dinh AM, Dang TT, Van Do TT, Chu TN, Mai TH, Phan VM

Int J Food Sci

10-Oct-2023

PMCID:	PMC10581860
doi:	10.1155/2023/7576179
PMID:	37854461

Cytotoxic Activity of Wild Plant and Callus Extracts of Ageratina pichinchensis and 2,3-Dihydrobenzofuran Isolated from a Callus Culture

Sánchez-Ramos M, Encarnación-García JG, Marquina-Bahena S, Sánchez-Carranza JN, Bernabé-Antonio A, Domínguez-Villegas V, Cabañas-García E, Cruz-Sosa F

Pharmaceuticals (Basel)

03-Oct-2023

PMCID:	PMC10609924
doi:	10.3390/ph16101400
PMID:	37895871

Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review

Tung XY, Yip JQ, Gew LT

ACS Omega

06-Sep-2023

PMCID:	PMC10515176
doi:	10.1021/acsomega.3c02994
PMID:	37744793

Optimization of ultrasound-assisted extraction of bioactive chemicals from Hemidesmus indicus (L.) R.Br. using response surface methodology and adaptive neuro-fuzzy inference system

Vellur S, Pavadai P, Pandian SR, Palanichamy C, Kabilan SJ, Sundar K, Kannan S, Kunjiappan S

Food Sci Biotechnol

17-Jun-2023

PMCID:	PMC10786805
doi:	10.1007/s10068-023-01351-9
PMID:	38222910

Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens

Kernou ON, Azzouz Z, Madani K, Rijo P

Molecules

22-May-2023

PMCID:	PMC10220798
doi:	10.3390/molecules28104243
PMID:	37241981

Quinones as Promising Compounds against Respiratory Viruses: A Review

Chan-Zapata I, Borges-Argáez R, Ayora-Talavera G

Molecules

20-Feb-2023

PMCID:	PMC9967002
doi:	10.3390/molecules28041981
PMID:	36838969

Metabolite Profiling and Bioassay-Guided Fractionation of Zataria multiflora Boiss. Hydroethanolic Leaf Extracts for Identification of Broad-Spectrum Pre and Postharvest Antifungal Agents

Karimi A, Meiners T, Böttcher C

Molecules

14-Dec-2022

PMCID:	PMC9785509
doi:	10.3390/molecules27248903
PMID:	36558036

Stem cambial variants of Taiwan lianas

Yang SZ, Chen PH, Chen JJ

Bot Stud

24-Sep-2022

PMCID:	PMC9509506
doi:	10.1186/s40529-022-00358-5
PMID:	36153445

A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight

Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M

Molecules

20-May-2022

PMCID:	PMC9143754
doi:	10.3390/molecules27103292
PMID:	35630768

α-Amyrin and β-Amyrin Isolated from Celastrus hindsii Leaves and Their Antioxidant, Anti-Xanthine Oxidase, and Anti-Tyrosinase Potentials

Viet TD, Xuan TD, Anh LH

Molecules

29-Nov-2021

PMCID:	PMC8658892
doi:	10.3390/molecules26237248
PMID:	34885832

Ultrasound-Assisted “Green” Extraction (UAE) of Antioxidant Compounds (Betalains and Phenolics) from Opuntia stricta var. Dilenii’s Fruits: Optimization and Biological Activities

Gómez-López I, Lobo-Rodrigo G, Portillo MP, Cano MP

Antioxidants (Basel)

08-Nov-2021

PMCID:	PMC8614683
doi:	10.3390/antiox10111786
PMID:	34829657

Green Metallic Nanoparticles for Cancer Therapy: Evaluation Models and Cancer Applications

Tinajero-Díaz E, Salado-Leza D, Gonzalez C, Martínez Velázquez M, López Z, Bravo-Madrigal J, Knauth P, Flores-Hernández FY, Herrera-Rodríguez SE, Navarro RE, Cabrera-Wrooman A, Krötzsch E, Carvajal ZY, Hernández-Gutiérrez R

Pharmaceutics

18-Oct-2021

PMCID:	PMC8537602
doi:	10.3390/pharmaceutics13101719
PMID:	34684012

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
> Alkaloids and derivatives
[(1R,3R,13R,14R,17S,18R,19R,20R,21R,22R,23S,24S,25S)-22,24-diacetyloxy-20-(acetyloxymethyl)-19,21,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-18-yl] 1-methyl-6-oxopyridine-3-carboxylate	162935876	Click to see	814.80	unknown	https://doi.org/10.1248/CPB.48.1079
[(1S,3R,13S,14S,17S,18R,19R,20R,21S,22S,23R,24S,25S)-22,24-diacetyloxy-20-(acetyloxymethyl)-19,21,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-18-yl] 1-methyl-6-oxopyridine-3-carboxylate	101032512	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)O)COC(=O)C)O)OC(=O)C6=CN(C(=O)C=C6)C)C	814.80	unknown	https://doi.org/10.1248/CPB.48.1079
[(1S,3R,13S,14S,17S,18S,19R,20R,21R,22R,23R,24R,25S)-18,22-diacetyloxy-20-(acetyloxymethyl)-19,21-dibenzoyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl] benzoate	162821386	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C7=CC=CC=C7)COC(=O)C)OC(=O)C8=CC=CC=C8)OC(=O)C)C	992.00	unknown	https://doi.org/10.1021/NP50125A015
Celahinine A	101688190	Click to see	992.00	unknown	https://doi.org/10.1021/NP50125A015
Emarginatine A	44567101	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C6=CN(C(=O)C=C6)C)C	898.90	unknown	https://doi.org/10.1021/NP50125A015
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[4,12-Diacetyloxy-6-(acetyloxymethyl)-5-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate	85090205	Click to see	532.60	unknown	https://doi.org/10.1016/0031-9422(95)00588-9
Celahin C	10007243	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)O)OC(=O)C	532.60	unknown	https://doi.org/10.1016/0031-9422(95)00588-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
5,8a,9',13'-Tetramethyl-4'-methylidenespiro[3a,4,9,9a-tetrahydrobenzo[f][1]benzofuran-3,15'-6-oxatetracyclo[9.2.2.01,9.03,7]pentadec-12-ene]-2,5',6,10'-tetrone	14021299	Click to see	488.60	unknown	https://doi.org/10.1248/CPB.48.1079
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,6S,7aR,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-6,9-diol	21672679	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CC(C4(C3(CC2)C)C)O)(C)C)O)C)C	442.70	unknown	https://doi.org/10.1248/CPB.48.1079
(1R,3aR,5aR,5bR,6S,7aR,9S,11aS,11bR,13aR,13bS)-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-6,9-diol	163047036	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CC(C4(C3(CC2)C)C)O)(C)C)O)C)C	442.70	unknown	https://doi.org/10.1248/CPB.48.1079
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one	7092730	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	https://doi.org/10.1248/CPB.48.1079
(4R,4aS,6aR,6aS,6bR,8aS,12aS,14aS,14bR)-8a-(hydroxymethyl)-4,4a,6a,6b,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	7330580	Click to see	442.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
(4R,4aS,6aS,6aS,6bR,8aR,12aR,13S,14aS,14bR)-13-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,6-dione	10623700	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
(4R,4aS,6aS,6aS,6bR,8R,8aS,11S,12aS,14aS,14bS)-8-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	10647574	Click to see	458.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
13-Hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,6-dione	77512992	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
2-Hydroxy-4,8,9,14,17,20-hexamethyl-22-oxahexacyclo[18.3.2.01,18.04,17.05,14.08,13]pentacosane-10,21-dione	73106255	Click to see	470.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
8-hydroxy-11-(hydroxymethyl)-4,4a,6a,6b,8a,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	85218341	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)CO)C)O)C)C)C)C	458.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
8-hydroxy-8a-(hydroxymethyl)-4,4a,6a,6b,11,11,14a-heptamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	85135682	Click to see	458.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
Celasdin B	10575883	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)CO)O)C)C)C)C	458.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
D:A-Friedooleanan-3-one, 28-hydroxy-	623591	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
Friedelanol	348029	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1021/JF1022115 https://doi.org/10.1248/CPB.48.1079
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
Friedelinol	101341	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1248/CPB.48.1079
Lupenone	92158	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	https://doi.org/10.1248/CPB.48.1079
Maytenfolone A	11798592	Click to see	470.70	unknown	https://doi.org/10.1016/S0031-9422(96)00719-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1R,2S,4S,5S,6S,7R,8R,9S,12S)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-7-benzoyloxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] benzoate	154496327	Click to see	694.70	unknown	https://doi.org/10.1248/CPB.48.1079
[(1S,2R,4S,5R,6S,7R,8R,9R,12S)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-7-benzoyloxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-8-yl] benzoate	101032511	Click to see	694.70	unknown	https://doi.org/10.1248/CPB.48.1079
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,2S,4R,5S,6S,7R,9S,12S)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate	163038991	Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C	574.60	unknown	https://doi.org/10.1016/0031-9422(95)00588-9
[(1S,2R,4S,5R,6R,7S,9R,12S)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate	101688443	Click to see	574.60	unknown	https://doi.org/10.1016/0031-9422(95)00588-9
[4,5,12-Triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate	14414923	Click to see	574.60	unknown	https://doi.org/10.1016/0031-9422(95)00588-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1R,2S,3S,4R,5S,6S,8S,10R,11R,12R,15S)-3,4,11-triacetyloxy-2,8-dihydroxy-1,5,15-trimethyl-9-methylidene-14-oxo-16-oxatetracyclo[10.5.0.02,15.05,10]heptadecan-6-yl] acetate	162918963	Click to see	566.60	unknown	https://doi.org/10.1021/NP50125A015
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R)-4-[(E)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid	95224953	Click to see	538.50	unknown	https://doi.org/10.1021/JF052743F
(2S)-2-[(2R,3R)-4-[(2R)-2-carboxy-2-[(2R,3R)-4-[(2R)-2-carboxy-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxyethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxyethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	163191240	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C2C(OC3=C(C=CC(=C23)CC(C(=O)O)OC(=O)C4C(OC5=C(C=CC(=C45)CC(C(=O)O)OC(=O)C=CC6=CC(=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O	1076.90	unknown	https://doi.org/10.1021/JF052743F
(2S)-2-[(2R,3R)-4-[(2R)-2-carboxy-2-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxyethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	163186354	Click to see	718.60	unknown	https://doi.org/10.1021/JF052743F
(2S)-2-[(2R,3R)-4-[(2R)-2-carboxy-2-[(E)-3-[(2R,3R)-3-[(1S)-1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl]oxyethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	163186931	Click to see	1076.90	unknown	https://doi.org/10.1021/JF052743F
2-[4-[2-Carboxy-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]ethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	73068710	Click to see	718.60	unknown	https://doi.org/10.1021/JF052743F
2-[4-[2-Carboxy-2-[3-[3-[1-carboxy-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyloxy]ethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	162997158	Click to see	1076.90	unknown	https://doi.org/10.1021/JF052743F
2-[4-[2-Carboxy-2-[4-[2-carboxy-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]ethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxyethyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carbonyl]oxy-3-(3,4-dihydroxyphenyl)propanoic acid	162974986	Click to see	1076.90	unknown	https://doi.org/10.1021/JF052743F
4-[3-[1-Carboxy-2-(3,4-dihydroxyphenyl)ethoxy]-3-oxoprop-1-enyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-3-carboxylic acid	4482010	Click to see	538.50	unknown	https://doi.org/10.1021/JF052743F
Salvianic acid B	119177	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=C3C(C(OC3=C(C=C2)O)C4=CC(=C(C=C4)O)O)C(=O)OC(CC5=CC(=C(C=C5)O)O)C(=O)O)O)O	718.60	unknown	https://doi.org/10.1021/JF052743F
Salvianolic Acid B	6451084	Click to see	718.60	unknown	https://doi.org/10.1021/JF052743F
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	https://doi.org/10.1021/JF052743F
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1021/JF052743F
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One	12313332	Click to see	594.50	unknown	https://doi.org/10.1021/JF052743F
Kaempferol-3-O-Rutinoside	5318767	Click to see	594.50	unknown	https://doi.org/10.1021/JF052743F
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1021/JF052743F
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1021/JF052743F

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.

Celastrus hindsii

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