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Diospyros dendo

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 UUID64401749b64b3273900952
Scientific name Diospyros dendo
Authority Welw. ex Hiern
First published in Trans. Cambridge Philos. Soc. 12: 195 (1873)

Ethnobotanical Use Top

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General Uses Top

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Common products:
The tree provides a dense, dark‑brown heartwood harvested as sawn timber, veneer, and fuelwood. The species is recorded by FAO’s “Timbers of Africa” (1994) among commercial timbers used for furniture, interior joinery, and flooring.

Industrial and craft applications:
The heartwood is valued for furniture making, cabinetry, interior paneling, flooring, and turned items such as tool handles and decorative objects. Its stability after drying makes it suitable for fine‑grain work where dimensional accuracy is required, and the fine, dark grain is prized for decorative veneer work. In addition to furniture and joinery, the wood is also employed in fine decorative work such as carving and inlay.

Wood and fiber:
Only the wood is utilized; the bark is not reported to yield commercial fiber. The timber is supplied in sawn form, as veneer sheets, or as solid planks for high‑grade applications.

Properties relevant to use:
The wood has a basic density of about 0.84–0.86 g cm⁻³ and exhibits low shrinkage (radial ≈4 %, tangential ≈6 %) during drying, contributing to good dimensional stability. Its natural durability is moderate to high due to extractives that impart resistance to decay, making it appropriate for interior uses where moisture exposure is limited. The high lignin content (typical of eudicotyledonous hardwoods) contributes to its hardness and resistance to mechanical wear, while its low equilibrium moisture content at indoor relative humidity (~12 %) supports dimensional stability.

Standards and regulation:
Timber from D. dendo falls within the scope of European Standard EN 13556 for structural timber and follows ISO 13061 methods for density determination. Export and harvesting are governed by national forest regulations in the producing countries (e.g., Ghana, Côte d’Ivoire, Nigeria) and by the International Tropical Timber Organization (ITTO) guidelines for sustainable trade.

Sustainability and sourcing:
The species is harvested as a minor commercial timber and is not listed in the CITES appendices. However, its exploitation in parts of its range has raised conservation concerns, and several national forest services encourage management plans that include selective harvesting and plantation trials to reduce pressure on natural stands.

Synonyms Top

Scientific name Authority First published in
Diospyros atropurpurea Gürke Bot. Jahrb. Syst. 26: 67 (1898)
Diospyros coccinea Gürke ex De Wild. Pl. Bequaert. 3: 538 (1926)
Diospyros flavescens Gürke Bot. Jahrb. Syst. 43: 211 (1909)
Diospyros mimfiensis Gürke Bot. Jahrb. Syst. 46: 153 (1911)
Diospyros nyangensis Pellegr. Bull. Mus. Natl. Hist. Nat. 31: 383 (1925)
Diospyros temvoensis De Wild. Pl. Bequaert. 3: 554 (1926)

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Nigeria
    • West-central Tropical Africa
      • Cabinda
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000648767
Tropicos 11500334
KEW urn:lsid:ipni.org:names:322313-1
The Plant List kew-2769614
Open Tree Of Life 945377
NCBI Taxonomy 570481
IUCN Red List 173762
IPNI 322313-1
GBIF 4070466
CMAUP NPO12610

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
Ursolic acid: biological functions and application in animal husbandry Liu G, Qin P, Cheng X, Wu L, Wang R, Gao W Front Vet Sci 25-Oct-2023
PMCID:PMC10642196
doi:10.3389/fvets.2023.1251248
PMID:37964910
Anti-Planktonic and Anti-Biofilm Properties of Pentacyclic Triterpenes—Asiatic Acid and Ursolic Acid as Promising Antibacterial Future Pharmaceuticals Sycz Z, Tichaczek-Goska D, Wojnicz D Biomolecules 07-Jan-2022
PMCID:PMC8774094
doi:10.3390/biom12010098
PMID:35053246
An Alternative to Antibiotics: Selected Methods to Combat Zoonotic Foodborne Bacterial Infections Łojewska E, Sakowicz T Curr Microbiol 09-Oct-2021
PMCID:PMC8595143
doi:10.1007/s00284-021-02665-9
PMID:34626217
Hunting of mammals by central chimpanzees (Pan troglodytes troglodytes) in the Loango National Park, Gabon Klein H, Bocksberger G, Baas P, Bunel S, Théleste E, Pika S, Deschner T Primates 08-Jan-2021
PMCID:PMC7936963
doi:10.1007/s10329-020-00885-4
PMID:33417069
Indigenous Medicinal Plants as Biofilm Inhibitors for the Mitigation of Antimicrobial Resistance Ampofo EK, Amponsah IK, Asante-Kwatia E, Armah FA, Atchoglo PK, Mensah AY Adv Pharmacol Pharm Sci 24-Oct-2020
PMCID:PMC7604581
doi:10.1155/2020/8821905
PMID:33163963
Antagonistic effect of ursolic acid on Staphylococcal biofilms Jyothi JS, Putty K, Reddy YN, Dhanalakshmi K, Umair MA Vet World 17-Oct-2018
PMCID:PMC6247876
doi:10.14202/vetworld.2018.1440-1444
PMID:30532499
Antibiofilm and Antioxidant Activity of Propolis and Bud Poplar Resins versus Pseudomonas aeruginosa De Marco S, Piccioni M, Pagiotti R, Pietrella D Evid Based Complement Alternat Med 03-Jan-2017
PMCID:PMC5239991
doi:10.1155/2017/5163575
PMID:28127379
Pseudomonas aeruginosa Biofilm Formation and Persistence, along with the Production of Quorum Sensing-Dependent Virulence Factors, Are Disrupted by a Triterpenoid Coumarate Ester Isolated from Dalbergia trichocarpa, a Tropical Legume Rasamiravaka T, Vandeputte OM, Pottier L, Huet J, Rabemanantsoa C, Kiendrebeogo M, Andriantsimahavandy A, Rasamindrakotroka A, Stévigny C, Duez P, El Jaziri M PLoS One 17-Jul-2015
PMCID:PMC4505864
doi:10.1371/journal.pone.0132791
PMID:26186595
The Formation of Biofilms by Pseudomonas aeruginosa: A Review of the Natural and Synthetic Compounds Interfering with Control Mechanisms Rasamiravaka T, Labtani Q, Duez P, El Jaziri M Biomed Res Int 19-Mar-2015
PMCID:PMC4383298
doi:10.1155/2015/759348
PMID:25866808
Pseudomonas aeruginosa Virulence and Therapy: Evolving Translational Strategies Veesenmeyer JL, Hauser AR, Lisboa T, Rello J Crit Care Med 01-May-2009
PMCID:PMC2749241
doi:10.1097/CCM.0b013e31819ff137
PMID:19325463
Asiatic Acid and Corosolic Acid Enhance the Susceptibility of Pseudomonas aeruginosa Biofilms to Tobramycin Garo E, Eldridge GR, Goering MG, Pulcini ED, Hamilton MA, Costerton JW, James GA Antimicrob Agents Chemother 12-Mar-2007
PMCID:PMC1855563
doi:10.1128/AAC.01037-06
PMID:17353241
Bacterial biofilm inhibitors from Diospyros dendo. Hu JF, Garo E, Goering MG, Pasmore M, Yoo HD, Esser T, Sestrich J, Cremin PA, Hough GW, Perrone P, Lee YS, Le NT, O'Neil-Johnson M, Costerton JW, Eldridge GR J Nat Prod 01-Jan-2006
doi:10.1021/NP049600S
PMID:16441080
Differential Gene Expression for Investigation of Escherichia coli Biofilm Inhibition by Plant Extract Ursolic Acid Ren D, Zuo R, González Barrios AF, Bedzyk LA, Eldridge GR, Pasmore ME, Wood TK Appl Environ Microbiol 01-Jul-2005
PMCID:PMC1169008
doi:10.1128/AEM.71.7.4022-4034.2005
PMID:16000817
Naphthoquinones and triterpenes from african Diospyros species Shou-Ming Zhong, Peter G. Waterman, J.A.D. Jeffreys Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82610-2

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 / Naphthalenes
(2E)-8-hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one 15082476 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(00)82610-2
8-Hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one 140775093 Click to see 404.40 unknown https://doi.org/10.1016/S0031-9422(00)82610-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,3aS,5aR,5bR,7aR,8S,9R,11aS,11bR,12R,13aR,13bR)-3a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-9,12-dihydroxy-5a,5b,8,11a-tetramethyl-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-8-carboxylic acid 101606374 Click to see 973.10 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 101675599 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1C)C)C(=O)OC9C(C(C(C(O9)COC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)C)O)O)O)O)O)O)O)O 1427.50 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 101675600 Click to see 1427.50 unknown via CMAUP database
(3R,4S,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-3-hydroxy-4,6a,6b,11,12,14b-hexamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4-carboxylic acid 101618891 Click to see 957.10 unknown via CMAUP database
(3R,4S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 101675598 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C(=O)O)O)C)(C)C)O)O)O)CO)O)O)O 957.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-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-3a-carboxylate 101606373 Click to see 927.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101675597 Click to see 1075.20 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101675278 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-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-carboxylate 101675601 Click to see 959.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-9-formyl-10,11-dihydroxy-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101675596 Click to see 957.10 unknown via CMAUP database
Acankoreoside A 10795959 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C(=O)O)O)C)C(=C)C)O)O)O)CO)O)O)O 957.10 unknown via CMAUP database
Asiaticoside 11954171 Click to see 959.10 unknown via CMAUP database
Cauloside D 21630094 Click to see 1075.20 unknown via CMAUP database
Scheffoleoside A 101675595 Click to see 959.10 unknown via CMAUP database
Scheffursoside B 101675277 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 957.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/NP049600S
(1R,2S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2-hydroxy-10-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11692990 Click to see 618.80 unknown https://doi.org/10.1021/NP049600S
(1R,2S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162867339 Click to see 618.80 unknown https://doi.org/10.1021/NP049600S
(1R,2S,4R,4aS,6aR,6aS,6bR,8aS,10S,12aR,14bS)-2-hydroxy-10-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4-carboxylic acid 163193004 Click to see CC1C2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C)C(CC1(C)O)C(=O)O 618.80 unknown https://doi.org/10.1021/NP049600S
(1R,3aR,5aR,5bR,7aS,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]chrysen-9-ol 7092625 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/10.1016/S0031-9422(00)82610-2
(1R,3aS,5aR,5bR,7aR,8S,9R,11aS,11bR,12R,13aR,13bR)-9,12-dihydroxy-5a,5b,8,11a-tetramethyl-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-3a,8-dicarboxylic acid 14866192 Click to see 502.70 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-sulfooxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21582889 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OS(=O)(=O)O)C)C(=O)O 536.80 unknown via CMAUP database
(1R,3aS,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-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-ol 7067839 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)82610-2
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-11-hydroxy-10-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 44566279 Click to see 648.90 unknown https://doi.org/10.1021/NP049600S
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-11-hydroxy-10-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 44566278 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1021/NP049600S
(1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-11-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163015349 Click to see 618.80 unknown https://doi.org/10.1021/NP049600S
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see 488.70 unknown via CMAUP database
(1S,2R,4R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bR)-11-hydroxy-10-[(E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-hexadecahydropicene-4-carboxylic acid 163188667 Click to see CC1CC(C2CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)OC)O)O)C)C)C2C1C)C)C(=O)O 648.90 unknown https://doi.org/10.1021/NP049600S
11-Hydroxy-10-[3-(3-hydroxy-4-methoxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-hexadecahydropicene-4-carboxylic acid 163010664 Click to see 648.90 unknown https://doi.org/10.1021/NP049600S
11-hydroxy-10-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 73809384 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)C)C)C2C1C)C)C(=O)O 648.90 unknown https://doi.org/10.1021/NP049600S
11-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 72730089 Click to see 618.80 unknown https://doi.org/10.1021/NP049600S
2-Hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 72995358 Click to see 618.80 unknown https://doi.org/10.1021/NP049600S
2-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-3,4,4a,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4-carboxylic acid 162855508 Click to see CC1C2C(CCC3(C2=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C)C(CC1(C)O)C(=O)O 618.80 unknown https://doi.org/10.1021/NP049600S
3Alpha-Hydroxylup-20(29)-Ene-23,28-Dioic Acid 14466871 Click to see 486.70 unknown via CMAUP database
3beta-[[(E)-3-(4-Hydroxyphenyl)propenoyl]oxy]-2alpha-hydroxyurs-12-ene-28-oic acid 14335960 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1021/NP049600S
Betulinic Acid Sulfate 11756976 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OS(=O)(=O)O)C)C(=O)O 536.80 unknown via CMAUP database
Epibetulinic Acid 485711 Click to see 456.70 unknown via CMAUP database
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/10.1016/S0031-9422(00)82610-2
Lup-20(29)-ene-3beta,28-diol 221023 Click to see 442.70 unknown https://doi.org/10.1016/S0031-9422(00)82610-2
Oleanonic Acid 12313704 Click to see 454.70 unknown via CMAUP database
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)- 220774 Click to see 456.70 unknown https://doi.org/10.1021/NP049600S
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
6-O-(4-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyl)-beta-D-glucopyranose 91857681 Click to see 488.40 unknown via CMAUP database

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