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Leucas volkensii

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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 UUID643fe13f3742a076863207
Scientific name Leucas volkensii
Authority Gürke
First published in Pflanzenw. Ost-Afrikas , C: 342 (1895)

Description 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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Name Authority First published in
Leucas volkensii var. parviflora Sebald Stuttgarter Beitr. Naturk., A 341: 119 (1980)

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

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Database ID/link to page
World Flora Online wfo-0000227213
Tropicos 50089339
KEW urn:lsid:ipni.org:names:449526-1
The Plant List kew-111928
Open Tree Of Life 582405
NCBI Taxonomy 483847
IPNI 449526-1
GBIF 7306936
CMAUP NPO26674

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
Potential Anti-Mycobacterium tuberculosis Activity of Plant Secondary Metabolites: Insight with Molecular Docking Interactions Kumar M, Singh SK, Singh PP, Singh VK, Rai AC, Srivastava AK, Shukla L, Kesawat MS, Kumar Jaiswal A, Chung SM, Kumar A Antioxidants (Basel) 14-Dec-2021
PMCID:PMC8750514
doi:10.3390/antiox10121990
PMID:34943093
Morphology, Anatomy and Secondary Metabolites Investigations of Premna odorata Blanco and Evaluation of Its Anti-Tuberculosis Activity Using In Vitro and In Silico Studies Youssef FS, Ovidi E, Musayeib NM, Ashour ML Plants (Basel) 18-Sep-2021
PMCID:PMC8467642
doi:10.3390/plants10091953
PMID:34579484
Antimycobacterial activity of (E)-phytol and derivatives: a preliminary structure-activity study. Rajab MS, Cantrell CL, Franzblau SG, Fischer NH Planta Med 01-Feb-1998
doi:10.1055/S-2006-957354
PMID:9491760

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2006-957354
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
3b-Acetoxycholest-5,24-diene 10916916 Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 101614311 Click to see CC=C(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5C)O)C)C)C(C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
Funtumine 101702 Click to see CC(=O)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N)C)C 317.50 unknown via CMAUP database
Irehdiamine A 92198 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)C)N 316.50 unknown via CMAUP database
Irehdiamine B 15560372 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
[(1R,2S,5S,6S,9S,10R,12S,13R,16S)-6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-10-yl] 4-methylpent-3-enoate 11178537 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)NC)C)OC(=O)CC=C(C)C 454.70 unknown via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)- 11225162 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown via CMAUP database
Conessine 441082 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Isoconessimine 11772257 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1C 342.60 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine 76330309 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)C=N1 312.50 unknown via CMAUP database

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