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Lippia integrifolia

Lippia integrifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fe18da9ecd937423222
Scientific name Lippia integrifolia
Authority Hieron.
First published in Bol. Acad. Nac. Ci. Republ. Argent. 4: 406 (1881)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lippia boliviana Rusby Mem. Torrey Bot. Club 4: 243 (1895)
Lippia boliviana var. angusta Moldenke Phytologia 14: 325 (1967)
Lippia boliviana var. integrifolia Moldenke Phytologia 42: 199 (1979)
Lippia integrifolia var. beckii Moldenke Phytologia 52: 19 (1982)
Lippia turbinata var. integrifolia Griseb. Abh. Königl. Ges. Wiss. Göttingen 19: 243. 1874

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
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Chile North
    • Western South America
      • Bolivia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000228913
Tropicos 33700258
KEW urn:lsid:ipni.org:names:863673-1
The Plant List kew-113540
Open Tree Of Life 812012
NCBI Taxonomy 925356
IPNI 863673-1
iNaturalist 1187578
GBIF 7297704

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
Synthetic polyploid induction influences morphological, physiological, and photosynthetic characteristics in Melissa officinalis L. Bharati R, Gupta A, Novy P, Severová L, Šrédl K, Žiarovská J, Fernández-Cusimamani E Front Plant Sci 14-Dec-2023
PMCID:PMC10752996
doi:10.3389/fpls.2023.1332428
PMID:38155852
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
Genomic and epigenomic variation in Psidium species and their outcome under the yield and composition of essential oils Silva MA, Soares FA, Clarindo WR, Mendes LA, Alves LB, Ferreira A, da Silva Ferreira MF Sci Rep 25-Jan-2023
PMCID:PMC9876884
doi:10.1038/s41598-023-27912-w
PMID:36697447
Flavonoids-Rich Plant Extracts Against Helicobacter pylori Infection as Prevention to Gastric Cancer Ivyna de Araújo Rêgo R, Guedes Silvestre GF, Ferreira de Melo D, Albino SL, Pimentel MM, Silva Costa Cruz SB, Silva Wurzba SD, Rodrigues WF, Goulart de Lima Damasceno BP, Cançado Castellano LR Front Pharmacol 31-Aug-2022
PMCID:PMC9470917
doi:10.3389/fphar.2022.951125
PMID:36120379
Whole-Genome Doubling Affects Pre-miRNA Expression in Plants Esposito S, Aversano R, Tripodi P, Carputo D Plants (Basel) 18-May-2021
PMCID:PMC8157229
doi:10.3390/plants10051004
PMID:34069771
Induced autopolyploidy—a promising approach for enhanced biosynthesis of plant secondary metabolites: an insight Gantait S, Mukherjee E J Genet Eng Biotechnol 08-Jan-2021
PMCID:PMC7794262
doi:10.1186/s43141-020-00109-8
PMID:33417015
Bicyclo [6.3.0] Undecane Sesquiterpenoids: Structures, Biological Activities, and Syntheses Qin GF, Liang HB, Liu WX, Zhu F, Li PL, Li GQ, Yao JC Molecules 30-Oct-2019
PMCID:PMC6864671
doi:10.3390/molecules24213912
PMID:31671644
Antimicrobial Activity and Chemical Composition of Essential Oils from Verbenaceae Species Growing in South America Pérez Zamora CM, Torres CA, Nuñez MB Molecules 01-Mar-2018
PMCID:PMC6017629
doi:10.3390/molecules23030544
PMID:29494478
Rapid plant regeneration, validation of genetic integrity by ISSR markers and conservation of Reseda pentagyna an endemic plant growing in Saudi Arabia Al-Qurainy F, Nadeem M, Khan S, Alansi S, Tarroum M, Al-Ameri AA, Gaafar AR, Alshameri A Saudi J Biol Sci 18-Jul-2017
PMCID:PMC5775100
doi:10.1016/j.sjbs.2017.07.003
PMID:29379366
Biomedical properties and potentiality of Lippia microphylla Cham. and its essential oils Simões ER, Santos EA, de Abreu MC, Silva JD, Nunes NM, da Costa MP, Pessoa OD, Pessoa C, Ferreira PM J Intercult Ethnopharmacol 26-Jun-2015
PMCID:PMC4579491
doi:10.5455/jice.20150610104841
PMID:26401417
Anti dermatophytic therapy - Prospects for the discovery of new drugs from natural products Soares LA, de Cássia Orlandi Sardi J, Gullo FP, de Souza Pitangui N, Scorzoni L, Leite FS, Giannini MJ, Almeida AM Braz J Microbiol 10-Mar-2014
PMCID:PMC3958166
doi:10.1590/S1517-83822014005000011
PMID:24688490
Synthesis of the Reported Structure of trans-Africanan-1α-ol Taber DF, Bai S, Tian W J Org Chem 10-Nov-2011
PMCID:PMC3248816
doi:10.1021/jo2018558
PMID:22053815
Vibrational circular dichroism of Africanane and lippifoliane sesquiterpenes from Lippia integrifolia. Cerda-García-Rojas CM, Catalán CA, Muro AC, Joseph-Nathan P J Nat Prod 01-Jun-2008
doi:10.1021/NP8000927
PMID:18500843
Trace Constituents of Lippia integrifolia César A. N. Catalán, Marina E. P. de Lampasona, Carlos M. Cerda-García-Rojas, Pedro Joseph-Nathan American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50125A010
Structure and Conformation of a Humulenedione from Lippia integrifolia César A. N. Catalán, Marina E. P. de Lampasona, Inés J. S. de Fenik, Carlos M. Cerda-García-Rojas, Pedro Joseph-Nathan American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50093A010

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 / Polycyclic hydrocarbons
1-Africanene 10750737 Click to see CC1CCC2C1=CC(CC3C2(C3)C)(C)C 204.35 unknown https://doi.org/10.1021/NP980424V
3,3,5,7b-tetramethyl-1a,2,5,6,7,7a-hexahydro-1H-cyclopropa[e]azulene 85255689 Click to see CC1CCC2C1=CC(CC3C2(C3)C)(C)C 204.35 unknown https://doi.org/10.1021/NP980424V
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,5R,7bR)-3,3,5,7b-tetramethyl-1a,2,5,6-tetrahydro-1H-cyclopropa[h]azulene-4,7-dione 10537549 Click to see CC1CC(=O)C2=C1C(=O)C(CC3C2(C3)C)(C)C 232.32 unknown https://doi.org/10.1021/NP8000927
(1aS,4aS,5R,7bR)-3,3,5,7b-tetramethyl-1a,2,4,4a,5,6-hexahydro-1H-cyclopropa[e]azulene 101939196 Click to see CC1CC=C2C1CC(CC3C2(C3)C)(C)C 204.35 unknown https://doi.org/10.1021/NP980424V
(1aS,5R,7bS)-3,3,5,7b-tetramethyl-1,1a,2,5,6,7-hexahydrocyclopropa[e]azulen-4-one 162938834 Click to see CC1CCC2=C1C(=O)C(CC3C2(C3)C)(C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)80411-2
(3aR)-2,2,8-Trimethyl-4-methylene-2,3,3aalpha,4,5,6,9,9aalpha-octahydro-1H-cyclopentacyclooctene 15519994 Click to see CC1=CCCC(=C)C2CC(CC2C1)(C)C 204.35 unknown https://doi.org/10.1021/NP980424V
2,2,5-trimethyl-9-methylidene-3,3a,4,7,8,9a-hexahydro-1H-cyclopenta[8]annulene 72833140 Click to see CC1=CCCC(=C)C2CC(CC2C1)(C)C 204.35 unknown https://doi.org/10.1021/NP980424V
3,3,5,7b-tetramethyl-1a,2,5,6-tetrahydro-1H-cyclopropa[h]azulene-4,7-dione 85177045 Click to see CC1CC(=O)C2=C1C(=O)C(CC3C2(C3)C)(C)C 232.32 unknown https://doi.org/10.1021/NP8000927
Africanone 583980 Click to see CC1CCC2=C1C(=O)C(CC3C2(C3)C)(C)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)80411-2
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80411-2
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80411-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1021/NP50093A010
https://doi.org/10.1016/S0031-9422(00)80411-2
https://doi.org/10.1016/S0031-9422(00)97577-0
(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/10.1016/S0031-9422(00)97577-0
https://doi.org/10.1016/S0031-9422(00)80411-2
https://doi.org/10.1021/NP50093A010
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
(-)-alpha-Himachalene 11830551 Click to see CC1=CC2C(CC1)C(=C)CCCC2(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)80411-2
1,6-trans-Lippifolian-1 alpha-ol-5-one 91750058 Click to see CC1CCC2(C(C1=O)C(CC3C2(C3)C)(C)C)O 236.35 unknown https://doi.org/10.1021/NP50125A010
3,3,5,7b-Tetramethyl-1,1a,2,5,6,7-hexahydrocyclopropa[a]naphthalen-4-one 14830859 Click to see CC1CCC2=C(C1=O)C(CC3C2(C3)C)(C)C 218.33 unknown https://doi.org/10.1021/NP50125A010
https://doi.org/10.1016/S0031-9422(00)80411-2
https://doi.org/10.1021/NP8000927
5-hydroxy-3,3,5,7b-tetramethyl-1a,2,6,7-tetrahydro-1H-cyclopropa[a]naphthalen-4-one 162984224 Click to see CC1(CC2CC2(C3=C1C(=O)C(CC3)(C)O)C)C 234.33 unknown https://doi.org/10.1021/NP50125A010
7a-hydroxy-3,3,5,7b-tetramethyl-1a,2,3a,5,6,7-hexahydro-1H-cyclopropa[a]naphthalen-4-one 162959553 Click to see CC1CCC2(C(C1=O)C(CC3C2(C3)C)(C)C)O 236.35 unknown https://doi.org/10.1021/NP50125A010
Lippifoli-1(6)-en-4 beta-ol-5-one 91750064 Click to see CC1(CC2CC2(C3=C1C(=O)C(CC3)(C)O)C)C 234.33 unknown https://doi.org/10.1021/NP50125A010
Lippifoli-1(6)-en-5-one 91750065 Click to see CC1CCC2=C(C1=O)C(CC3C2(C3)C)(C)C 218.33 unknown https://doi.org/10.1021/NP50125A010
https://doi.org/10.1016/S0031-9422(00)80411-2
https://doi.org/10.1021/NP8000927
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1aS,5R,7aR,7bR)-3,3,5,7b-tetramethyl-1,1a,2,5,6,7-hexahydrocyclopropa[e]azulen-7a-ol 100964032 Click to see CC1CCC2(C1=CC(CC3C2(C3)C)(C)C)O 220.35 unknown https://doi.org/10.1021/NP980424V
3,3,5,7b-Tetramethyl-1,1a,2,5,6,7-hexahydrocyclopropa[e]azulen-7a-ol 85195461 Click to see CC1CCC2(C1=CC(CC3C2(C3)C)(C)C)O 220.35 unknown https://doi.org/10.1021/NP980424V
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(2R,3S,4S,5R,6R)-6-[[(3aR,4S,9aR,9bR)-4-hydroxy-6-methyl-3-methylidene-2-oxo-3a,4,5,7,9a,9b-hexahydroazuleno[8,7-b]furan-9-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 2-(4-hydroxyphenyl)acetate 101176807 Click to see CC1=C2CC=C(C2C3C(C(C1)O)C(=C)C(=O)O3)COC4C(C(C(C(O4)COC(=O)CC5=CC=C(C=C5)O)O)O)O 558.60 unknown https://doi.org/10.1021/NP980424V
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(1R,2S,7S)-1,5,5-trimethyl-2-(3-oxobutyl)bicyclo[5.1.0]octan-3-one 21775422 Click to see CC(=O)CCC1C(=O)CC(CC2C1(C2)C)(C)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)97577-0
(1R,5R,10S)-1,5,8,8-tetramethylbicyclo[8.1.0]undecane-2,6-dione 14830857 Click to see CC1CCC(=O)C2(CC2CC(CC1=O)(C)C)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84049-2
(1S,5R,10S)-1,5,8,8-Tetramethylbicyclo[8.1.0]undecane-2,6-dione 572978 Click to see CC1CCC(=O)C2(CC2CC(CC1=O)(C)C)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84049-2
1,5,5-Trimethyl-2-(3-oxobutyl)bicyclo[5.1.0]octan-3-one 73836757 Click to see CC(=O)CCC1C(=O)CC(CC2C1(C2)C)(C)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)97577-0
CID 22215840 22215840 Click to see CC1CCC(=O)C2(CC2CC(CC1=O)(C)C)C 236.35 unknown https://doi.org/10.1016/S0031-9422(00)84049-2

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