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Erythroxylum monogynum

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 UUID64401b959f4e7241493253
Scientific name Erythroxylum monogynum
Authority Roxb.
First published in Pl. Coromandel 1: 61 (1798)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Sethia indica DC. Prodr. 1: 576 (1824)
Erythroxylum indicum (DC.) Elliot Fl. Andhirica : 46 (1859)
Erythroxylum sideroxyloides Roxb. Fl. Ind. ii. 449.

Common names Top

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Language Common/alternative name
Malayalam വെള്ളദേവതാരം
Tamil செம்புளிச்சான்
Telugu అడవిదేవదారు
Telugu అడివిపగడపు చెట్టు
Telugu అడవిగోరింట

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000679989
Tropicos 12500377
KEW urn:lsid:ipni.org:names:544103-1
The Plant List kew-2801546
Open Tree Of Life 324562
NCBI Taxonomy 591145
IPNI 544103-1
iNaturalist 464612
GBIF 3694251
USDA GRIN 414291
Wikipedia Erythroxylum_monogynum

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
Current Naturopathy to Combat Alzheimer’s Disease Chakrovorty A, Bhattacharjee B, Saxena A, Samadder A, Nandi S Curr Neuropharmacol 30-Mar-2023
PMCID:PMC10227918
doi:10.2174/1570159X20666220927121022
PMID:36173068
Advancements and future prospective of DNA barcodes in the herbal drug industry Mahima K, Sunil Kumar KN, Rakhesh KV, Rajeswaran PS, Sharma A, Sathishkumar R Front Pharmacol 21-Oct-2022
PMCID:PMC9635000
doi:10.3389/fphar.2022.947512
PMID:36339543
Harnessing the Potential of Roots of Traditional Power Plant: Ocimum Pandey V, Swami RK, Narula A Front Plant Sci 01-Nov-2021
PMCID:PMC8591311
doi:10.3389/fpls.2021.765024
PMID:34790216
Fire alters diversity, composition, and structure of dry tropical forests in the Eastern Ghats Neeraja UV, Rajendrakumar S, Saneesh CS, Dyda V, Knight TM Ecol Evol 01-May-2021
PMCID:PMC8207398
doi:10.1002/ece3.7514
PMID:34141243
Pitfalls and promises of raw drug identification techniques in the ayurvedic industry: an overview Unnikrishnan R, Dev SA, Jayaraj R 3 Biotech 30-Oct-2020
PMCID:PMC7599280
doi:10.1007/s13205-020-02482-0
PMID:33150123
Auto-oxidation of Ent-beyer-15-en-19-al isolated from the essential oil of the heartwood of Erythroxylum monogynum Roxb.: formation of 15,16-epoxy-ent-beyeran-19-oic acid and other products Tennakoon TM, Gunaherath GM, De Silva KT, Padumadasa C, Wijesundara DS, Abeysekera AM BMC Chem 13-Mar-2020
PMCID:PMC7071572
doi:10.1186/s13065-020-00671-9
PMID:32190844
Medicinal Plants for the Treatment of Local Tissue Damage Induced by Snake Venoms: An Overview from Traditional Use to Pharmacological Evidence Félix-Silva J, Silva-Junior AA, Zucolotto SM, Fernandes-Pedrosa MD Evid Based Complement Alternat Med 21-Aug-2017
PMCID:PMC5585606
doi:10.1155/2017/5748256
PMID:28904556
Hepatoprotective effect of leaves of Erythroxylum monogynum Roxb. on paracetamol induced toxicity Syed SH, Namdeo AG Asian Pac J Trop Biomed 01-Nov-2013
PMCID:PMC3793160
doi:10.1016/S2221-1691(13)60172-0
Alkaloids of erythroxylum monogynum root-bark Philippe Christen, Margaret F. Roberts, J.David Phillipson, William C. Evans Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(94)00777-Q

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
> Alkaloids and derivatives
1-(1-Methylpyrrolidin-2-yl)acetone 94157 Click to see CC(=O)CC1CCCN1C 141.21 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Cuscohygrine 1201543 Click to see 224.34 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Cuskhygrine 441070 Click to see 224.34 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Hygrine 440933 Click to see 141.21 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
> Alkaloids and derivatives / Tropane alkaloids
3-(2-Methylbutyryloxy)-tropane 91750070 Click to see 225.33 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
3beta-Phenylacetoxytropane 11086474 Click to see 259.34 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
8-Methyl-8-azabicyclo[3.2.1]octan-3-ol 8424 Click to see CN1C2CCC1CC(C2)O 141.21 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Isoporoidine 12311200 Click to see CCC(C)C(=O)OC1CC2CCC(C1)N2 211.30 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Tropine isobutyrate 3083598 Click to see 211.30 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Tropinone 79038 Click to see CN1C2CCC1CC(=O)C2 139.19 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Valeroidine 443012 Click to see CC(C)CC(=O)OC1CC2CC(C(C1)N2C)O 241.33 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
8-Azabicyclo(3.2.1)octan-3-ol, 8-methyl-, benzoate (ester), endo- 637578 Click to see 245.32 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
Benzoyltropein 10834 Click to see 245.32 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Convolamine 420422 Click to see CN1C2CCC1CC(C2)OC(=O)C3=CC(=C(C=C3)OC)OC 305.40 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[[3-Hydroxy-5-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxolan-3-yl]methoxy]-6-methyloxane-3,4,5-triol 75034135 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(CO7)(COC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1 855.00 unknown https://doi.org/10.1016/0031-9422(94)00777-Q
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
Dihydrocuscohygrine 11075129 Click to see CN1CCCC1CC(CC2CCCN2C)O 226.36 unknown https://doi.org/10.1016/0031-9422(94)00777-Q

Gallery Top

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Collections Top

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