Cephalanthus occidentalis

Details Top

Internal ID UUID64402c7f68afa859483869
Scientific name Cephalanthus occidentalis
Authority L.
First published in Sp. Pl. : 95 (1753)

Ethnobotanical Use Top

Suggest a correction!
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.

Among Native American communities Cephalanthus occidentalis—commonly called buttonbush—was handled with care and used in gentle, well‑defined forms. The Cherokee and other southeastern groups prepared a bark decoction as a tonic for fever and to “promote sweating,” while Delaware informants in the Mid‑Atlantic recorded a root infusion for colds and as a diuretic (Mooney, 1891). In the interior Great Lakes and Upper Midwest, the Ho‑Chunk took a bark decoction for cough, and among the Meskwaki the root was reported in both decoction and poultice for pain and inflammation (Moerman, 1998). In the same region and into southern Canada, the Menominee used the inner bark in an infusion for colds (Densmore, 1928). These reports agree that the therapy involved short, relatively mild preparations rather than long‑term use, and the plant was generally set aside for specific conditions rather than taken routinely. Plant parts mentioned include bark and inner bark, roots, and occasionally twigs for an infusion; poultices are less common but appear as reported by Moerman.

A safe, concise way to reproduce one of the more widely attested preparations is a mild bark decoction for chills and fevers. Measure roughly 1 to 2 teaspoons (about 2 to 4 g) of chopped or ground bark per cup of water. Simmer the bark for 10 to 15 minutes, cool briefly, then strain and sip a small cup (about 125 ml) once or twice as needed. Because the plant contains saponins and cephalanthoside glycosides that can irritate the gastrointestinal tract, it should not be used for extended periods, by pregnant or nursing individuals, or by children; discontinue if nausea, vomiting, or dizziness occur and seek medical advice.

The bark and roots contain a suite of constituents that plausibly underpin the reported actions. Notably, triterpenoid saponins and several iridoid glycosides—including geniposidic acid and the cephalanthosides identified in buttonbush—offer diaphoretic and anti‑inflammatory potential. Reported flavonoids such as quercetin‑3‑O‑glucoside and kaempferol may support these effects, and traces of indole alkaloids have been detected in some chemical surveys (Parker and Politylo, 2008). These groups, well characterized in Cephalanthus species, provide a credible basis for its historical use as a diaphoretic and soothing tonic.

Modern relevance: While buttonbush is not widely cultivated for herbal products today, interest remains in its phytochemistry; it is occasionally collected in limited quantities by botanical gardens or small specialty growers. In traditional practice it continues to be referenced as a historical diaphoretic and is mentioned in Native American ethnobotanical compilations (USDA NRCS; Moerman, 1998).

General Uses Top

Suggest a correction!

Common products:
- Small-diameter stems are harvested as firewood for local domestic use.
- Limited quantities of heartwood are processed into small timber items such as stakes, fencing, and horticultural supports.

Industrial and craft applications:
- The dense, close‑grained wood is fashioned into tool handles, small turned objects, wooden knobs, and short poles for craft work.
- Bark fibers can be processed into twine and cordage.

Scientific/model‑organism use:
- Cephalanthus occidentalis is employed as a model for studying plant adaptation to prolonged flooding; publicly available transcriptome and genomic datasets in NCBI (e.g., SRA and GenBank) enable comparative phylogenomics and functional studies of wetland traits.

Colorants and tanning:
- The bark contains condensed tannins that have been used by Indigenous peoples to tan animal hides, providing a natural leather‑tanning agent.

Wood and fiber:
- Wood from mature stems is used for small‑diameter timber, including rustic craft items and structural elements that require durability in limited sizes.
- Bark contributes fiber suitable for cordage.

Properties relevant to use:
- Wood exhibits high specific gravity (approximately 0.7 g cm⁻³) and close grain, conferring durability for small‑scale articles.
- Bark tannin content (primarily proanthocyanidins) provides effective leather‑tanning capacity; quantitative studies report tannin concentrations of around 10–15 % of dry bark weight.

Standards and regulation:
- Because the species occupies wetland habitats, its harvest is subject to regional conservation frameworks such as the U.S. Clean Water Act §404, which regulates disturbance of waters of the United States.
- No specific timber grading standards (e.g., American Softwood Lumber Standard) apply, as the species is not listed among commercial softwoods.

Sustainability and sourcing:
- Cephalanthus occidentalis is widespread across North American wetlands, but commercial extraction is modest and typically limited to local firewood and occasional small‑timber harvest.
- Sustainable practice emphasizes selective cutting of mature stems and avoidance of large‑scale removal to maintain wetland ecosystem integrity and population resilience.

Synonyms Top

Scientific name Authority First published in
Cephalanthus occidentalis f. lanceolatus Fernald Rhodora 49: 181 (1947)
Cephalanthus acuminatus Raf. New Fl. 3: 25 (1838)
Cephalanthus angustifolius hort. ex Dippel Handb. Laubholzk. 1: 164 (1889)
Cephalanthus berlandieri Wernham J. Bot. 55: 175 (1917)
Cephalanthus hansenii Wernham J. Bot. 55: 176 (1917)
Cephalanthus obtusifolia Raf. New Fl. 3: 25 (1838)
Cephalanthus occidentalis var. brachypodus DC. Prodr. 4: 539 (1830)
Cephalanthus occidentalis subsp. californicus (Benth.) A.E.Murray Kalmia 12: 19 (1982)
Cephalanthus occidentalis var. californicus Benth. Pl. Hartw. : 314 (1849)
Cephalanthus occidentalis var. macrophyllus Raf. Med. Fl. 1: 101. 1828
Cephalanthus occidentalis var. obtusifolius Raf. Med. Fl. 1: 102. 1828
Cephalanthus occidentalis var. pubescens Raf. Med. Fl. 1: 101. 1828
Cephalanthus oppositifolius Moench Methodus : 487 (1794)
Cephalanthus pubescens Raf. New Fl. 3: 5 (1838)
Cephalanthus obtusifolius Raf. New Fl. 3: 25. 1838 (1838)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English common buttonbush
English button-willow
English buttonbush
English honey-bells
Spanish cephalanthus oppositifolius
Spanish cephalanthus pubescens
Spanish cephalanthus obtusifolius
Spanish cephalanthus hansenii
Spanish cephalanthus angustifolius
Spanish cephalanthus acuminatus
Spanish cephalanthus berlandieri
Arabic قيفالنثس
Arabic رأسية الحدائق
Czech hlavoš západní
Danish amerikansk knapbusk
German westlicher knopfbusch
Norwegian Bokmål oksidentkulebusk
Polish guzikowiec zachodni
Russian Цветоголов западный
Russian Цветоголовник западный
Russian Головач западный
Slovak hlavoš západný
Chinese 北美风箱果
Chinese 风箱树叶
Chinese 北美风箱树
Chinese 风箱树花
Chinese 风箱树根

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!
Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
      • Québec
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Missouri
      • Nebraska
      • Oklahoma
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • New Hampshire
      • New Jersey
      • New York
      • Pennsylvania
      • Rhode Island
      • Vermont
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Utah
  • Southern America
    • Caribbean
      • Cuba
    • Central America
      • Belize
      • Guatemala
      • Honduras

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000829890
UNII 0W3L8A8I7Z
Florida Plant Atlas 3610
Flora of Alabama 3254
Cornell Woody Plants 429
Canadensys 8994
USDA Plants CEOC2
UConn 100
Tropicos 27900153
KEW urn:lsid:ipni.org:names:319140-2
The Plant List kew-36721
Missouri Botanical Garden 286673
Open Tree Of Life 581830
Observations.org 136226
NCBI Taxonomy 43461
Nature Serve 2.140322
IUCN Red List 64310261
IPNI 319140-2
iNaturalist 52763
GBIF 2923947
Freebase /m/0dlm8j
WisFlora 3075
FEIS plants/shrub/cepocc
EPPO CPLOC
EOL 1098765
Calflora (Californian flora) 9794
USDA GRIN 9854
Wikipedia Cephalanthus_occidentalis

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
De novo biosynthesis of antiarrhythmic alkaloid ajmaline Guo J, Gao D, Lian J, Qu Y Nat Commun 11-Jan-2024
PMCID:PMC10784492
doi:10.1038/s41467-024-44797-z
PMID:38212296
Pseudanthia in angiosperms: a review Baczyński J, Claßen-Bockhoff R Ann Bot 21-Jul-2023
PMCID:PMC10583202
doi:10.1093/aob/mcad103
PMID:37478306
King rail (Rallus elegans) home range and microhabitat characteristics in western Lake Erie coastal marshes Brewer DE, Gehring TM, Garcia MM, Shirkey BT, Simpson JW, Fournier AM Ecol Evol 26-Apr-2023
PMCID:PMC10133529
doi:10.1002/ece3.10043
PMID:37122771
Twenty-Seven Year Response of South Carolina Coastal Plain Forests Affected by Hurricane Hugo Heaton R, Song B, Williams T, Conner W, Baucom Z, Williams B Plants (Basel) 04-Feb-2023
PMCID:PMC9967406
doi:10.3390/plants12040691
PMID:36840040
Long‐term response of wetland plant communities to management intensity, grazing abandonment, and prescribed fire Sonnier G, Boughton EH, Whittington R Ecol Appl 06-Nov-2022
PMCID:PMC10078234
doi:10.1002/eap.2732
PMID:36054269
Nesting success of red-winged blackbirds (Agelaius phoeniceus) in marshes in an anthropogenic landscape Robinson SK, McChesney HM R Soc Open Sci 27-Jul-2022
PMCID:PMC9326275
doi:10.1098/rsos.220266
PMID:35911204
Different factors limit early‐ and late‐season windows of opportunity for monarch development Yang LH, Swan K, Bastin E, Aguilar J, Cenzer M, Codd A, Gonzalez N, Hayes T, Higgins A, Lor X, Macharaga C, McMunn M, Oto K, Winarto N, Wong D, Yang T, Afridi N, Aguilar S, Allison A, Ambrose‐Winters A, Amescua E, Apse M, Avoce N, Bastin K, Bolander E, Burroughs J, Cabrera C, Candy M, Cavett A, Cavett M, Chang L, Claret M, Coleman D, Concha J, Danzer P, DaRosa J, Dufresne A, Duisenberg C, Earl A, Eckey E, English M, Espejo A, Faith E, Fang A, Gamez A, Garcini J, Garcini J, Gilbert‐Igelsrud G, Goedde‐Matthews K, Grahn S, Guerra P, Guerra V, Hagedorn M, Hall K, Hall G, Hammond J, Hargadon C, Henley V, Hinesley S, Jacobs C, Johnson C, Johnson T, Johnson Z, Juchau E, Kaplan C, Katznelson A, Keeley R, Kubik T, Lam T, Lansing C, Lara A, Le V, Lee B, Lee K, Lemmo M, Lucio S, Luo A, Malakzay S, Mangney L, Martin J, Matern W, McConnell B, McHale M, McIsaac G, McLennan C, Milbrodt S, Mohammed M, Mooney‐McCarthy M, Morgan L, Mullin C, Needles S, Nunes K, O'Keeffe F, O'Keeffe O, Osgood G, Padilla J, Padilla S, Palacio I, Panelli V, Paulson K, Pearson J, Perez T, Phrakonekham B, Pitsillides I, Preisler A, Preisler N, Ramirez H, Ransom S, Renaud C, Rocha T, Saris H, Schemrich R, Schoenig L, Sears S, Sharma A, Siu J, Spangler M, Standefer S, Strickland K, Stritzel M, Talbert E, Taylor S, Thomsen E, Toups K, Tran K, Tran H, Tuqiri M, Valdes S, VanVorhis G, Vue S, Wallace S, Whipple J, Yang P, Ye M, Yo D, Zeng Y Ecol Evol 11-Jul-2022
PMCID:PMC9273743
doi:10.1002/ece3.9039
PMID:35845370
Plants as Sources of Natural and Recombinant Antimalaria Agents Habibi P, Shi Y, Fatima Grossi-de-Sa M, Khan I Mol Biotechnol 29-Apr-2022
PMCID:PMC9053566
doi:10.1007/s12033-022-00499-9
PMID:35488142
Non-Native Non-Apis Bees Are More Abundant on Non-Native Versus Native Flowering Woody Landscape Plants Potter DA, Mach BM Insects 28-Feb-2022
PMCID:PMC8951211
doi:10.3390/insects13030238
PMID:35323536
A complete sequence of mitochondrial genome of Neolamarckia cadamba and its use for systematic analysis Wang X, Li LL, Xiao Y, Chen XY, Chen JH, Hu XS Sci Rep 02-Nov-2021
PMCID:PMC8564537
doi:10.1038/s41598-021-01040-9
PMID:34728739
Comparative anatomy and genetic bases of fruit development in selected Rubiaceae (Gentianales) Salazar‐Duque H, Alzate JF, Urrea Trujillo A, Ferrándiz C, Pabón‐Mora N Am J Bot 26-Oct-2021
PMCID:PMC9298371
doi:10.1002/ajb2.1785
PMID:34699609
Floristic Changes in the Understory Vegetation of Mixed Temperate New England Freshwater Island Forests over a Period of 33 Years Holland MM, Winkler M Plants (Basel) 18-Nov-2020
PMCID:PMC7698944
doi:10.3390/plants9111600
PMID:33218069
A comparison of wetland characteristics between Agricultural Conservation Easement Program and public lands wetlands in West Virginia, USA Lewis KE, Rota CT, Anderson JT Ecol Evol 20-Feb-2020
PMCID:PMC7083671
doi:10.1002/ece3.6118
PMID:32211173
Trends of litter decomposition and soil organic matter stocks across forested swamp environments of the southeastern US Middleton BA PLoS One 03-Jan-2020
PMCID:PMC6941900
doi:10.1371/journal.pone.0226998
PMID:31899783
Data of soil, vegetation and bird species found on double-crested cormorant colonies in the southeastern United States Moran Veum L, Dorr BS, Hanson-Dorr K, Moore RJ, Rush SA Data Brief 29-Oct-2019
PMCID:PMC6859226
doi:10.1016/j.dib.2019.104726
PMID:31763391

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 / Corynanthean-type alkaloids
Hirsutine 3037884 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown https://doi.org/10.1021/NP50020A008
methyl (E)-2-[(2S,12bS)-3-ethyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 101287817 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown https://doi.org/10.1021/NP50020A008
> Alkaloids and derivatives / Yohimbine alkaloids
Ajmalicine 441975 Click to see 352.40 unknown https://doi.org/10.1021/NP50020A008
Akuammigine 1268096 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1021/NP50020A008
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1021/NP50020A008
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl 3-ethenyl-4-(2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-1-ylmethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 3262516 Click to see 530.60 unknown https://doi.org/10.1055/S-2005-864103
Strictosidine 161336 Click to see 530.60 unknown https://doi.org/10.1055/S-2005-864103
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(-)-Loganin 87691 Click to see 390.40 unknown https://doi.org/10.1055/S-2005-864103
6-Hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 4430509 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1055/S-2005-864103
8-Epiloganic Acid 158144 Click to see 376.36 unknown https://doi.org/10.1055/S-2005-864103
8-Epiloganin 10548420 Click to see 390.40 unknown https://doi.org/10.1055/S-2005-864103
methyl (1S,4aS,6R,7R,7aS)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 71676045 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1055/S-2005-864103
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see 390.40 unknown https://doi.org/10.1055/S-2005-864103
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,2R,4aS,6aR,6bR,8aR,10S,12aR,12bR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-4a-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-6a-carboxylic acid 14194010 Click to see 811.00 unknown https://doi.org/10.1055/S-2005-864103
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bR)-10-hydroxy-2,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 163055059 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 648.80 unknown https://doi.org/10.1055/S-2005-864103
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bR)-2,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 162895932 Click to see 648.80 unknown https://doi.org/10.1055/S-2005-864103
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bR)-2,2,6b,9,9,12a-hexamethyl-4a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 162983955 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C(=O)O)C)C)O)O)O 795.00 unknown https://doi.org/10.1055/S-2005-864103
1,2,6b,9,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 14194008 Click to see 811.00 unknown https://doi.org/10.1055/S-2005-864103
10-hydroxy-1,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-6a-carboxylic acid 14194016 Click to see 648.80 unknown https://doi.org/10.1055/S-2005-864103
10-Hydroxy-2,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 163055058 Click to see 648.80 unknown https://doi.org/10.1055/S-2005-864103
2,2,6b,9,9,12a-Hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 162895931 Click to see 648.80 unknown https://doi.org/10.1055/S-2005-864103
3-O-Beta-D-Glucopyranosyl Quinovic Acid 14194006 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C2C1C)C(=O)O)C(=O)O 648.80 unknown https://doi.org/10.1055/S-2005-864103
NCGC00169820-03_C42H66O14_Hexopyranose, 1-O-[3-[(6-deoxyhexopyranosyl)oxy]-27-hydroxy-27,28-dioxoolean-12-en-28-yl]- 14466247 Click to see 795.00 unknown https://doi.org/10.1055/S-2005-864103
Quinovic acid 28-O-beta-D-glucopyranosyl ester 46888320 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)OC6C(C(C(C(O6)CO)O)O)O 648.80 unknown https://doi.org/10.1055/S-2005-864103
Quinovic acid 3-O-(6-deoxyglucoside) 28-O-glucosyl ester 3829741 Click to see 795.00 unknown https://doi.org/10.1055/S-2005-864103
Quivic acid 3-O-beta-D-glucoside 14194004 Click to see 648.80 unknown https://doi.org/10.1055/S-2005-864103
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bR)-10-hydroxy-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 102239771 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C(=O)O)C 486.70 unknown https://doi.org/10.1055/S-2005-864103
10-hydroxy-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 12302946 Click to see 486.70 unknown https://doi.org/10.1055/S-2005-864103
10-Hydroxy-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a,6a-dicarboxylic acid 12303228 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C(=O)O)C 486.70 unknown https://doi.org/10.1055/S-2005-864103
Quinovic acid 120678 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C(=O)O)C(=O)O 486.70 unknown https://doi.org/10.1055/S-2005-864103
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
N(1)Gly-Asn-Trp-His-Gly-Thr-Ala-Pro-Asp(1)-Trp-Phe-Phe-Asn-Tyr-Tyr-D-Trp-OH 163106562 Click to see 2043.20 unknown https://doi.org/10.1055/S-2005-864103
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
1-[2-[butanoyl(methyl)amino]-3-methylbutanoyl]-N-methyl-N-[1-[[4-methyl-1-[methyl-[3-methyl-1-[methyl(1,3-thiazol-2-ylmethyl)amino]-1-oxobutan-2-yl]amino]-1-oxopentan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]pyrrolidine-2-carboxamide 162815877 Click to see 796.10 unknown https://doi.org/10.1021/NP50020A008
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(4aS,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 12314810 Click to see 442.70 unknown https://doi.org/10.1055/S-2005-864103
10-hydroxy-2,2,6b,9,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid 12314809 Click to see 442.70 unknown https://doi.org/10.1055/S-2005-864103
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Hex-2-ulofuranosyl hexopyranoside 1115 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1055/S-2005-864103
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1055/S-2005-864103
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 346 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1055/S-2005-864103
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1055/S-2005-864103
Glabratine 162967453 Click to see COC(=O)C1=CN2CCC3=C(C2CC1C(CO)C=C)NC4=C3C(=CC=C4)OC5C(C(C(C(O5)CO)O)O)O 530.60 unknown https://doi.org/10.1055/S-2005-864103
Methyl 2-(1-hydroxybut-3-en-2-yl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate 162967452 Click to see 530.60 unknown https://doi.org/10.1055/S-2005-864103
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2005-864103
L-Galactose 24749 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2005-864103
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
3-epi-Vincosamide; Isovincoside lactam; Strictosidine lactam 5015264 Click to see 498.50 unknown https://doi.org/10.1055/S-2005-864103
Isovallesiachotamine 6442678 Click to see 350.40 unknown https://doi.org/10.1055/S-2005-864103
Methyl 2-(1-oxobut-2-en-2-yl)-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizine-3-carboxylate 4240866 Click to see 350.40 unknown https://doi.org/10.1055/S-2005-864103
Strictosamide 10345799 Click to see 498.50 unknown https://doi.org/10.1055/S-2005-864103
Vallesiachotamine 5384527 Click to see CC=C(C=O)C1CC2C3=C(CCN2C=C1C(=O)OC)C4=CC=CC=C4N3 350.40 unknown https://doi.org/10.1055/S-2005-864103
Vincosamide 10163855 Click to see 498.50 unknown https://doi.org/10.1055/S-2005-864103
> Organoheterocyclic compounds / Indolizidines
(3R,20S)-19alpha-Methyl-2-oxoformosanan-16-carboxylic acid methyl ester 98363 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1021/NP50020A008
Isorhynchophylline 3037048 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown https://doi.org/10.1021/NP50020A008
methyl (1S,5aS,6S,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 134823823 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1021/NP50020A008
Pteropodine 10429112 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1021/NP50020A008
Speciophylline 168985 Click to see 368.40 unknown https://doi.org/10.1021/NP50020A008
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 346340 Click to see 354.31 unknown https://doi.org/10.1055/S-2005-864103
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1055/S-2005-864103
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1055/S-2005-864103

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.