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Erythroxylum pervillei

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64401b990abaa002538504
Scientific name Erythroxylum pervillei
Authority Baill.
First published in Bull. Mens. Soc. Linn. Paris 1: 606 (1886)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erythroxylum pervillei f. majusculum H.Perrier Mém. Inst. Sci. Madagascar, Sér. B, Biol. Vég. 2: 250 1949
Erythroxylum pervillei var. suborbiculare H.Perrier Mém. Inst. Sci. Madagascar, Sér. B, Biol. Vég. 2: 250 1949

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000680051
Tropicos 12500306
KEW urn:lsid:ipni.org:names:337026-1
The Plant List kew-2801608
Open Tree Of Life 6100352
Observations.org 441008
NCBI Taxonomy 2589513
IPNI 337026-1
iNaturalist 713699
GBIF 3694234
Elurikkus 396987

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
Genesis and Mechanism of Some Cancer Types and an Overview on the Role of Diet and Nutrition in Cancer Prevention Kamal N, Ilowefah MA, Hilles AR, Anua NA, Awin T, Alshwyeh HA, Aldosary SK, Jambocus NG, Alosaimi AA, Rahman A, Mahmood S, Mediani A Molecules 09-Mar-2022
PMCID:PMC8955916
doi:10.3390/molecules27061794
PMID:35335158
A novel graph mining approach to predict and evaluate food-drug interactions Rahman MM, Vadrev SM, Magana-Mora A, Levman J, Soufan O Sci Rep 20-Jan-2022
PMCID:PMC8776972
doi:10.1038/s41598-022-05132-y
PMID:35058561
Extracts of select endemic plants from the Republic of Mauritius exhibiting anti-cancer and immunomodulatory properties Kauroo S, Govinden-Soulange J, Ranghoo-Sanmukhiya VM, Miranda K, Cotham WE, Walla MD, Nagarkatti M, Nagarkatti P Sci Rep 19-Feb-2021
PMCID:PMC7895923
doi:10.1038/s41598-021-83461-0
PMID:33608608
Erythroxylum in Focus: An Interdisciplinary Review of an Overlooked Genus Restrepo DA, Saenz E, Jara-Muñoz OA, Calixto-Botía IF, Rodríguez-Suárez S, Zuleta P, Chavez BG, Sanchez JA, D’Auria JC Molecules 21-Oct-2019
PMCID:PMC6833119
doi:10.3390/molecules24203788
PMID:31640255
Research progress in the biological activities of 3,4,5-trimethoxycinnamic acid (TMCA) derivatives Zhao Z, Song H, Xie J, Liu T, Zhao X, Chen X, He X, Wu S, Zhang Y, Zheng X Eur J Med Chem 06-Apr-2019
PMCID:PMC7115657
doi:10.1016/j.ejmech.2019.04.009
PMID:31009908
Natural Products Mediated Targeting of Virally Infected Cancer Fatima I, Kanwal S, Mahmood T Dose Response 08-Jan-2019
PMCID:PMC6328957
doi:10.1177/1559325818813227
PMID:30670935
Herbal Bioenhancers in Veterinary Phytomedicine Yurdakok-Dikmen B, Turgut Y, Filazi A Front Vet Sci 10-Oct-2018
PMCID:PMC6191517
doi:10.3389/fvets.2018.00249
PMID:30364115
Natural Products as Alternative Choices for P-Glycoprotein (P-gp) Inhibition Dewanjee S, K. Dua T, Bhattacharjee N, Das A, Gangopadhyay M, Khanra R, Joardar S, Riaz M, De Feo V, Zia-Ul-Haq M Molecules 25-May-2017
PMCID:PMC6152721
doi:10.3390/molecules22060871
PMID:28587082
The most used medicinal plants by communities in Mahaboboka, Amboronabo, Mikoboka, Southwestern Madagascar Randrianarivony TN, Ramarosandratana AV, Andriamihajarivo TH, Rakotoarivony F, Jeannoda VH, Randrianasolo A, Bussmann RW J Ethnobiol Ethnomed 09-Mar-2017
PMCID:PMC5345199
doi:10.1186/s13002-017-0147-x
PMID:28279184
P-glycoprotein inhibitors of natural origin as potential tumor chemo-sensitizers: A review Abdallah HM, Al-Abd AM, El-Dine RS, El-Halawany AM J Adv Res 01-Dec-2014
PMCID:PMC4293676
doi:10.1016/j.jare.2014.11.008
PMID:25685543
Potentiating Effect of the Flavonolignan (-)-Hydnocarpin in Combination with Vincristine in a Sensitive and P-gp-Expressing Acute Lymphoblastic Leukemia Cell Line Pérez LB, Pan L, Sass E, Gupta SV, Lehman A, Kinghorn AD, Lucas DM Phytother Res 28-Dec-2012
PMCID:PMC3639301
doi:10.1002/ptr.4903
PMID:23280566
The Relevance of Higher Plants in Lead Compound Discovery Programs Kinghorn AD, Pan L, Fletcher JN, Chai H J Nat Prod 08-Jun-2011
PMCID:PMC3158731
doi:10.1021/np200391c
PMID:21650152
Evaluation of the Cholinergic and Adrenergic Effects of Two Tropane Alkaloids from Erythroxylum pervillei Chin YW, Kinghorn AD, Patil PN Phytother Res 01-Oct-2007
PMCID:PMC2798816
doi:10.1002/ptr.2155
PMID:17602438
Tropane aromatic ester alkaloids from a large-scale re-collection of Erythroxylum pervillei stem bark obtained in Madagascar. Chin YW, Jones WP, Waybright TJ, McCloud TG, Rasoanaivo P, Cragg GM, Cassady JM, Kinghorn AD J Nat Prod 01-Mar-2006
PMCID:PMC2614919
doi:10.1021/NP050366V
PMID:16562848
Tropane Aromatic Ester Alkaloids Obtained from a Large-Scale Recollection of Erythroxylum pervillei Stem Bark Collected in Madagascar Chin YW, Jones WP, Waybright TJ, McCloud TG, Rasoanaivo P, Cragg GM, Cassady JM, Kinghorn AD J Nat Prod 01-Mar-2006
PMCID:PMC2614919
doi:10.1021/np050366v
PMID:16562848

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
[(1R,3S,5S,6R,7S)-6-hydroxy-8-methyl-7-[(E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] 3,4,5-trimethoxybenzoate 162953468 Click to see CN1C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC 587.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1S,3S,5R,6S)-8-methyl-6-[(E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] 3,4,5-trimethoxybenzoate 11114492 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC 571.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1S,3S,5R,6S)-8-methyl-6-[(Z)-3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] 3,4,5-trimethoxybenzoate 11713917 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC 571.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[6-Hydroxy-8-methyl-7-[3-(3,4,5-trimethoxyphenyl)prop-2-enoyloxy]-8-azabicyclo[3.2.1]octan-3-yl] 3,4,5-trimethoxybenzoate 390506 Click to see CN1C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC 587.60 unknown https://doi.org/10.1021/NP010295+
[8-Methyl-6-[3-(3,4,5-trimethoxyphenyl)prop-2-enoyloxy]-8-azabicyclo[3.2.1]octan-3-yl] 3,4,5-trimethoxybenzoate 73070670 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC 571.60 unknown https://doi.org/10.1021/NP010295+
Pervilleine A N-oxide 44576219 Click to see C[N+]1(C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC)[O-] 603.60 unknown https://doi.org/10.1021/NP010295+
Tropane-3alpha,6beta,7beta-triol 3-(3,4,5-trimethoxybenzoate)6-(3,4,5-trimethoxycinnamate) 44576218 Click to see CN1C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C4=CC(=C(C(=C4)OC)OC)OC 587.60 unknown https://doi.org/10.1021/NP010295+
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Lissoclibadin 7 16116098 Click to see CN(C)CCC1=CC(=C(C2=C1SSC3=C(C(=CC(=C3O)OC)CCN(C)C)SS2)O)OC 514.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5S,6S)-5-hydroxy-3,4-bis[[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxy]-6-methyloxan-2-yl]oxymethyl]oxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 10725268 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(CO9)O)O)OC1C(C(C(CO1)O)O)O)O)O)O)C)(C)C)OC1C(C(C(C(O1)C)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)OC(=O)C(=CCCC(C)(C=C)O)C)OC(=O)C(=CCCC(C)(C=C)O)C)O 1950.20 unknown https://doi.org/10.1021/NP010295+
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(1R,3S,5S,6R,7S)-6-hydroxy-8-methyl-7-[(E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate 162959685 Click to see CN1C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C=CC4=CC(=C(C(=C4)OC)OC)OC 613.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1R,3S,5S,6S)-8-methyl-3-(2-phenylacetyl)oxy-8-azabicyclo[3.2.1]octan-6-yl] (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate 10300336 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC=CC=C4 495.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1R,3S,5S,6S)-8-methyl-3-(2-phenylacetyl)oxy-8-azabicyclo[3.2.1]octan-6-yl] (Z)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate 163003437 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC=CC=C4 495.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1S,3S,5R,6R)-8-methyl-3-(2-phenylacetyl)oxy-8-azabicyclo[3.2.1]octan-6-yl] (Z)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate 163003436 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC=CC=C4 495.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1S,3S,5R,6S)-3-[2-(3-hydroxyphenyl)acetyl]oxy-8-methyl-8-azabicyclo[3.2.1]octan-6-yl] (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate 11038529 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC(=CC=C4)O 511.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[(1S,3S,5R,6S)-8-methyl-6-[(E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoyl]oxy-8-azabicyclo[3.2.1]octan-3-yl] (E)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate 11814007 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C=CC4=CC(=C(C(=C4)OC)OC)OC 597.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/
[3-[2-(3-Hydroxyphenyl)acetyl]oxy-8-methyl-8-azabicyclo[3.2.1]octan-6-yl] 3-(3,4,5-trimethoxyphenyl)prop-2-enoate 73878006 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC(=CC=C4)O 511.60 unknown https://doi.org/10.1021/NP010295+
[6-Hydroxy-8-methyl-7-[3-(3,4,5-trimethoxyphenyl)prop-2-enoyloxy]-8-azabicyclo[3.2.1]octan-3-yl] 3-(3,4,5-trimethoxyphenyl)prop-2-enoate 73878007 Click to see CN1C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C=CC4=CC(=C(C(=C4)OC)OC)OC 613.70 unknown https://doi.org/10.1021/NP010295+
[8-Methyl-6-[3-(3,4,5-trimethoxyphenyl)prop-2-enoyloxy]-8-azabicyclo[3.2.1]octan-3-yl] 3-(3,4,5-trimethoxyphenyl)prop-2-enoate 73114073 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C=CC4=CC(=C(C(=C4)OC)OC)OC 597.70 unknown https://doi.org/10.1021/NP010295+
Pervilleine C 44576221 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C=CC4=CC(=C(C(=C4)OC)OC)OC 597.70 unknown https://doi.org/10.1021/NP010295+
Pervilleine D 44576222 Click to see CN1C2CC(CC1C(C2O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)C=CC4=CC(=C(C(=C4)OC)OC)OC 613.70 unknown https://doi.org/10.1021/NP010295+
Pervilleine E 44576223 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC(=CC=C4)O 511.60 unknown https://doi.org/10.1021/NP010295+
Pervilleine F 44576224 Click to see CN1C2CC(CC1C(C2)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC)OC(=O)CC4=CC=CC=C4 495.60 unknown https://doi.org/10.1021/NP010295+
Pervilleine G 11494583 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C=CC3=CC(=C(C(=C3)OC)OC)OC 377.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2614919/

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