Details Top

Internal ID UUID644008a775e05244388509
Scientific name Alvaradoa haitiensis
Authority Urb.
First published in Symb. Antill. 5: 379 (1908)

Ethnobotanical Use Top

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  • 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.
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General Uses Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000529105
Tropicos 100368304
KEW urn:lsid:ipni.org:names:10503-2
The Plant List kew-2631690
Open Tree Of Life 6123674
Observations.org 497269
NCBI Taxonomy 2686335
IPNI 10503-2
iNaturalist 852322
GBIF 7574516
Elurikkus 606534
CMAUP NPO30060

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
The Chemotherapeutic Potentials of Compounds Isolated from the Plant, Marine, Fungus, and Microorganism: Their Mechanism of Action and Prospects Shakya AK, Naik RR J Trop Med 10-Oct-2022
PMCID:PMC9576449
doi:10.1155/2022/5919453
PMID:36263439
Discovery of new anticancer agents from higher plants Pan L, Chai HB, Kinghorn AD Front Biosci (Schol Ed) 01-Jan-2012
PMCID:PMC3314490
doi:10.2741/257
PMID:22202049
Discovery of Natural Product Anticancer Agents from Biodiverse Organisms Kinghorn AD, Chin YW, Swanson SM Curr Opin Drug Discov Devel 01-Mar-2009
PMCID:PMC2877274
PMID:19333864
Discovery of anticancer agents of diverse natural origin Kinghorn AD, Carcache de Blanco EJ, Chai HB, Orjala J, Farnsworth NR, Soejarto DD, Oberlies NH, Wani MC, Kroll DJ, Pearce CJ, Swanson SM, Kramer RA, Rose WC, Fairchild CR, Vite GD, Emanuel S, Jarjoura D, Cope FO Pure Appl Chem 01-Jan-2009
PMCID:PMC2765058
doi:10.1351/PAC-CON-08-10-16
PMID:20046887
Identification of a Cranberry Juice Product that Inhibits Enteric CYP3A-Mediated First-Pass Metabolism in Humans Ngo N, Yan Z, Graf TN, Carrizosa DR, Kashuba AD, Dees EC, Oberlies NH, Paine MF Drug Metab Dispos 29-Dec-2008
PMCID:PMC2650736
doi:10.1124/dmd.108.024968
PMID:19114462
Alvaradoins E-N, Antitumor and Cytotoxic Anthracenone C-glycosides from the Leaves of Alvaradoa haitiensis Phifer SS, Lee D, Seo EK, Kim NC, Graf TN, Kroll DJ, Navarro HA, Izydore RA, Jiménez F, Garcia R, Rose WC, Fairchild CR, Wild R, Soejarto DD, Farnsworth NR, Kinghorn AD, Oberlies NH, Wall ME, Wani MC J Nat Prod 07-Jun-2007
PMCID:PMC2442713
doi:10.1021/np070005a
PMID:17552563
Alvaradoins E-N, antitumor and cytotoxic anthracenone C-glycosides from the leaves of Alvaradoa haitiensis. Phifer SS, Lee D, Seo EK, Kim NC, Graf TN, Kroll DJ, Navarro HA, Izydore RA, Jiménez F, Garcia R, Rose WC, Fairchild CR, Wild R, Soejarto DD, Farnsworth NR, Kinghorn AD, Oberlies NH, Wall ME, Wani MC J Nat Prod 01-Jun-2007
PMCID:PMC2442713
doi:10.1021/NP070005A
PMID:17552563

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 / Anthracenes
[(2R,3R,4R,5R,6R)-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl] acetate 44424597 Click to see 430.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3R,4R,5R,6S)-2-acetyloxy-3,5-dihydroxy-6-[(9R)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-4-yl] 3-methylbut-2-enoate 44424600 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)OC(=O)C)O)OC(=O)C=C(C)C)O)O)C=CC=C3O 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3R,4R,5R,6S)-2-acetyloxy-3,5-dihydroxy-6-[(9S)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-4-yl] 3-methylbut-2-enoate 44424601 Click to see 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-[(9S)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-2-yl] acetate 44424605 Click to see 446.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3R,4R,5S,6R)-2-acetyloxy-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,5-dihydroxyoxan-4-yl] 3-methylbut-2-enoate 44424598 Click to see 512.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3R,4R,5S,6S)-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-2,4,5-trihydroxyoxan-3-yl] 3-methylbut-2-enoate 163026234 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3R,4R,5S,6S)-6-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-2,4,5-trihydroxyoxan-3-yl] 3-methylbut-2-enoate 163026235 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2R,3S,4R,5R,6S)-2-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,5,6-trihydroxyoxan-4-yl] 3-methylbut-2-enoate 44424604 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5R,6R)-2-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,5,6-trihydroxyoxan-4-yl] 3-methylbut-2-enoate 162945117 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-[(9S)-4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl]oxan-2-yl] acetate 16736467 Click to see 446.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5R,6R)-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-2,4,5-trihydroxyoxan-3-yl] 3-methylbut-2-enoate 44424602 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5R,6R)-6-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-2,4,5-trihydroxyoxan-3-yl] 3-methylbut-2-enoate 44424603 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5R,6S)-2-acetyloxy-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,5-dihydroxyoxan-4-yl] 3-methylbut-2-enoate 163074146 Click to see 512.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5R,6S)-2-acetyloxy-6-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,5-dihydroxyoxan-4-yl] 3-methylbut-2-enoate 163074147 Click to see 512.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5S,6S)-6-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl] acetate 162886600 Click to see 430.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[(2S,3R,4R,5S,6S)-6-[(9S)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-3,4,5-trihydroxyoxan-2-yl] acetate 162886598 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)OC(=O)C)O)O)O)C=CC=C3O 430.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[2-(4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl)-3,5,6-trihydroxyoxan-4-yl] 3-methylbut-2-enoate 73316255 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[2-Acetyloxy-3,5-dihydroxy-6-(4,5,9-trihydroxy-2-methyl-10-oxoanthracen-9-yl)oxan-4-yl] 3-methylbut-2-enoate 73316086 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2(C4C(C(C(C(O4)OC(=O)C)O)OC(=O)C=C(C)C)O)O)C=CC=C3O 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[2-acetyloxy-6-(4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl)-3,5-dihydroxyoxan-4-yl] 3-methylbut-2-enoate 56681238 Click to see 512.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[6-(4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl)-2,4,5-trihydroxyoxan-3-yl] 3-methylbut-2-enoate 73316175 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
[6-(4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl)-3,4,5-trihydroxyoxan-2-yl] acetate 56677470 Click to see 430.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin E 16736655 Click to see 430.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin F 16736468 Click to see 430.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin G 16736656 Click to see 512.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin H 16736265 Click to see 512.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin I 16736464 Click to see 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin J 16736024 Click to see 528.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin K 16736465 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)O)OC(=O)C=C(C)C)O)O)C=CC=C3O 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin L 16736243 Click to see 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin M 16736466 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C(C(C(C(O4)O)O)OC(=O)C=C(C)C)O)C=CC=C3O 470.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
Alvaradoin N 70678737 Click to see 448.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/
> Benzenoids / Anthracenes / Anthraquinones
Chrysophanol 10208 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442713/

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