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Lepechinia floribunda

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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
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Details Top

Internal ID UUID643fe110206b5063789706
Scientific name Lepechinia floribunda
Authority (Benth.) Epling
First published in Repert. Spec. Nov. Regni Veg. Beih. 85: 22. 1935

Description Top

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Synonyms Top

Scientific name Authority First published in
Lepechinia sagittata Epling Bull. Torrey Bot. Club 71: 487 (1944)
Sphacele floribunda Benth. Prodr. [A. P. de Candolle] 12: 254. 1848 [5 Nov 1848]
Sphacele grisebachii Kurtz in Revista Mus. La Plata [Sert. Cordob.] 14 v. (1893) 292.
Sphacele hastata Griseb. Abh. Königl. Ges. Wiss. Göttingen 19: 238. 1874
Sphacele hieronymi Briq. Bull. Herb. Boissier 4: 804 (1896)
Sphacele pampeana Speg. Contr. Fl. Sierra Vent. : 49 (1896)
Alguelaguen hieronymi Briq. Bull. Herb. Boissier 4: 804 (1896)
Alguelagum floribundum Kuntze Revis. Gen. Pl. 2: 512 (1891)
Alguelagum grisebachii Kuntze Revis. Gen. Pl. 2: 512 (1891)

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000226031
Tropicos 17602037
KEW urn:lsid:ipni.org:names:137871-2
The Plant List kew-110772
Open Tree Of Life 5265177
NCBI Taxonomy 1405036
IPNI 449262-1
iNaturalist 564994
GBIF 3888808
USDA GRIN 21761

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
Ecological interactions affect the bioactivity of medicinal plants Camina JL, Usseglio V, Marquez V, Merlo C, Dambolena JS, Zygadlo JA, Ashworth L Sci Rep 27-Jul-2023
PMCID:PMC10374891
doi:10.1038/s41598-023-39358-1
PMID:37500739
Phytochemical profile and rosmarinic acid purification from two Peruvian Lepechinia Willd. species (Salviinae, Mentheae, Lamiaceae) Serrano CA, Villena GK, Rodríguez EF Sci Rep 31-Mar-2021
PMCID:PMC8012630
doi:10.1038/s41598-021-86692-3
PMID:33790349
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Content Snapshots N/A Ann Bot 09-Mar-2020
PMCID:PMC7061166
doi:10.1093/aob/mcaa017
Daily fluctuations in pollination effectiveness explain higher efficiency of native over exotic bees in Lepechinia floribunda (Lamiaceae) Baranzelli MC, Benitez-Vieyra S, Glinos E, Trenchi A, Córdoba S, Camina J, Ashworth L, Sérsic AN, Cocucci AA, Fornoni J Ann Bot 20-Nov-2019
PMCID:PMC7061175
doi:10.1093/aob/mcz187
PMID:31745546
A comprehensive review on tyrosinase inhibitors Zolghadri S, Bahrami A, Hassan Khan MT, Munoz-Munoz J, Garcia-Molina F, Garcia-Canovas F, Saboury AA J Enzyme Inhib Med Chem 03-Jan-2019
PMCID:PMC6327992
doi:10.1080/14756366.2018.1545767
PMID:30734608
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776
Antimicrobial potentials of medicinal plant’s extract and their derived silver nanoparticles: A focus on honey bee pathogen Khan SU, Anjum SI, Ansari MJ, Khan MH, Kamal S, Rahman K, Shoaib M, Man S, Khan AJ, Khan SU, Khan D Saudi J Biol Sci 21-Feb-2018
PMCID:PMC6864162
doi:10.1016/j.sjbs.2018.02.010
PMID:31762664
ANTI-VIRAL EFFECTS OF MEDICINAL PLANTS IN THE MANAGEMENT OF DENGUE: A SYSTEMATIC REVIEW Frederico ÉH, Cardoso AL, Moreira-Marconi E, de Sá-Caputo DD, Guimarães CA, Dionello CD, Morel DS, Paineiras-Domingos LL, de Souza PL, Brandão-Sobrinho-Neto S, Carvalho-Lima RP, Guedes-Aguiar ED, Costa-Cavalcanti RG, Kutter CR, Bernardo-Filho M Afr J Tradit Complement Altern Med 07-Jul-2017
PMCID:PMC5514443
doi:10.21010/ajtcam.v14i4S.5
PMID:28740942
Essential Oil of<i>Lepechinia floribunda</i>(Benth.) Epl. Arturo Velasco-Negueruela, María José Pérez-Alonso, Joaquín L. Esteban, Carlos A. Guzmán, Julio A. Zygadlo, Luis Ariza-Espinar Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1994.9698446

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1994.9698446
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1080/10412905.1994.9698446
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698446
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1994.9698446
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
(+)-gamma-Cadinene 6432404 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-Guaiene 5317844 Click to see CC1CCC(CC2=C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
trans-Nerolidol 5284507 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698446
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
alpha-Gurjunene 15560276 Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Viridiflorene 10910653 Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene 288227 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Valencene 9855795 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1994.9698446

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