PlantaeDB Logo
Login Sign-up

Artemisia pallens

Artemisia pallens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643fcf7e222cd610477376
Scientific name Artemisia pallens
Authority Wall. ex DC.
First published in Prodr. 6: 120 (1838)

Description Top

Suggest a correction or write a new one!
It is also commercially cultivated for its fragrant leaves and flowers. The plant has two distinct morphological types, one with shorter stature and early flowering, and the other with taller plants and later flowering. It is grown from seeds and cuttings and reaches maturity in four months. The plant is woody at the base but has yearly branches. It is mostly grown in the Indian states of Andhra Pradesh, Karnataka, Maharashtra, and Tamil Nadu. The plant is also a preferred food for the larvae of various butterfly species. The dried davana plant is used as an aromatic bouquet and its essential oil is extracted from the leaves and flowers. The major constituents of davana oil include davanone, davan ether, davana furan, and linalool. Other compounds such as methyl cinnamate, ethyl cinnamate, and geranyl acetate are also found in the oil. Davana oil is known for its sweet and fruity fragrance and is used in making perfumes. The leaves and stalks are also used in making bouquets, garlands, and fresh or dry flower arrangements. Additionally, the plant has medicinal properties and has been observed to reduce blood glucose levels in animals.

Synonyms Top

Scientific name Authority First published in
Artemisia absinthii B.Heyne ex Hook.f. Fl. Brit. India 3(8): 329 (1881)
Artemisia paniculata Roxb. Hort. Bengal. 61; Fl. Ind. iii. 418
Artemisia orientalis Herb.Madr. ex DC. Prodr. 6: 120 (1838)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Hindi दवना
Kannada ದವನ
Marathi दवणा
Burmese ဒေါနပန်း
Telugu దవనం
Telugu దవనము

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000090831
UNII 39JKR5IL2G
Tropicos 100398625
KEW urn:lsid:ipni.org:names:179911-1
The Plant List gcc-47113
Open Tree Of Life 7596377
NCBI Taxonomy 2867270
IPNI 179911-1
iNaturalist 785997
GBIF 3121392
Freebase /m/05c1rcj
USDA GRIN 409554
Wikipedia Artemisia_pallens

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
Therapeutic potential of Thai herbal formula for cognitive impairment: A metabolomics approach for Comprehensive Insights Akarasereenont P, Pattanapholkornsakul S, Limsuvan S, Mamaethong D, Booranasubkajorn S, Pakaprot N, Tripatara P, Pilakasiri K Heliyon 16-Mar-2024
PMCID:PMC10981045
doi:10.1016/j.heliyon.2024.e28027
PMID:38560220
Investigation of Corrosion Inhibition of Mild Steel in 0.5 M H2SO4 with Lachancea fermentati Inhibitor Extracted from Rotten Grapefruits (Vitis vinifera): Adsorption, Thermodynamic, Electrochemical, and Quantum Chemical Studies Tamilselvi B, Bhuvaneshwari DS, Karuppasamy P, Padmavathy S, Nikhil S, Siddegowda SB, Ananda Murthy HC ACS Phys Chem Au 08-Dec-2023
PMCID:PMC10811774
doi:10.1021/acsphyschemau.3c00055
PMID:38283783
Assessing lead and cadmium tolerance of Chenopodium ambrosioides during micropropagation: an in-depth qualitative and quantitative analysis Jan T, Khan N, Wahab M, Okla MK, Abdel-Maksoud MA, Saleh IA, Abu-Harirah HA, AlRamadneh TN, AbdElgawad H PeerJ 29-Nov-2023
PMCID:PMC10693238
doi:10.7717/peerj.16369
PMID:38047032
Enhanced Production of Nitrogenated Metabolites with Anticancer Potential in Aristolochia manshuriensis Hairy Root Cultures Shkryl YN, Tchernoded GK, Yugay YA, Grigorchuk VP, Sorokina MR, Gorpenchenko TY, Kudinova OD, Degtyarenko AI, Onishchenko MS, Shved NA, Kumeiko VV, Bulgakov VP Int J Mol Sci 08-Jul-2023
PMCID:PMC10379662
doi:10.3390/ijms241411240
PMID:37511000
Mapping of traditional healthcare providers and their healing approaches in a tribal community of district Sirohi, Rajasthan Dwivedi R, Goyal P, Yadav SS, Dwivedi P, Singh P, Singh K J Family Med Prim Care 30-Jun-2023
PMCID:PMC10451593
doi:10.4103/jfmpc.jfmpc_1610_22
PMID:37636156
Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK Antibiotics (Basel) 08-Mar-2023
PMCID:PMC10044610
doi:10.3390/antibiotics12030543
PMID:36978410
Effects of Vegetal Extracts and Metabolites against Oxidative Stress and Associated Diseases: Studies in Caenorhabditis elegans Hernández-Cruz EY, Eugenio-Pérez D, Ramírez-Magaña KJ, Pedraza-Chaverri J ACS Omega 27-Feb-2023
PMCID:PMC10018526
doi:10.1021/acsomega.2c07025
PMID:36936291
Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent Nahar L, Al-Groshi A, Kumar A, Sarker SD Molecules 11-Dec-2022
PMCID:PMC9787540
doi:10.3390/molecules27248786
PMID:36557918
Enantioselective total synthesis of putative dihydrorosefuran, a monoterpene with an unique 2,5-dihydrofuran structure Torres-García I, López-Martínez JL, López-Domene R, Muñoz-Dorado M, Rodríguez-García I, Álvarez-Corral M Beilstein J Org Chem 19-Sep-2022
PMCID:PMC9520846
doi:10.3762/bjoc.18.132
PMID:36225730
In Silico Evaluation of Bioactive Compounds of Artemisia pallens Targeting the Efflux Protein of Multidrug-Resistant Acinetobacter baumannii (LAC-4 Strain) Suvaithenamudhan S, Ananth S, Mariappan V, Dhayabaran VV, Parthasarathy S, Ganesh PS, Shankar EM Molecules 15-Aug-2022
PMCID:PMC9414700
doi:10.3390/molecules27165188
PMID:36014428
Agrobacterium-mediated genetic transformation and cloning of candidate reference genes in suspension cells of Artemisia pallens Wall. ex DC Jogam P, Sandhya D, Alok A, Shekhawat MS, Peddaboina V, Singh K, Allini VR 3 Biotech 28-Jul-2022
PMCID:PMC9334505
doi:10.1007/s13205-022-03251-x
PMID:35910289
Synergistic Effects of Natural Product Combinations in Protecting the Endothelium Against Cardiovascular Risk Factors Yousaf M, Razmovski-Naumovski V, Zubair M, Chang D, Zhou X J Evid Based Integr Med 18-Jul-2022
PMCID:PMC9297466
doi:10.1177/2515690X221113327
PMID:35849068
Production and Functionalities of Specialized Metabolites from Different Organic Sources Oladipo A, Enwemiwe V, Ejeromedoghene O, Adebayo A, Ogunyemi O, Fu F Metabolites 10-Jun-2022
PMCID:PMC9228302
doi:10.3390/metabo12060534
PMID:35736468
Bacillus cereus Enhanced Medicinal Ingredient Biosynthesis in Glycyrrhiza uralensis Fisch. Under Different Conditions Based on the Transcriptome and Polymerase Chain Reaction Analysis Zhang Y, Lang D, Zhang W, Zhang X Front Plant Sci 02-Jun-2022
PMCID:PMC9201524
doi:10.3389/fpls.2022.858000
PMID:35720602
Ayurvedic formulations: Potential COVID-19 therapeutics? Mahaboob Ali AA, Bugarcic A, Naumovski N, Ghildyal R Phytomed Plus 20-Apr-2022
PMCID:PMC9020642
doi:10.1016/j.phyplu.2022.100286
PMID:35474908

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadien-1-ol 4458 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0040-4039(01)91378-4
https://doi.org/10.1016/0031-9422(91)83725-Z
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1002/PCA.564
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
https://doi.org/10.1016/S0040-4039(01)91378-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1002/HLCA.19740570717
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1002/HLCA.19740570717
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3E,6E,10S)-2,10-dihydroxy-2,6,10-trimethyldodeca-3,6,11-trien-5-one 163015498 Click to see CC(=CCCC(C)(C=C)O)C(=O)C=CC(C)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
2,10-Dihydroxy-2,6,10-trimethyldodeca-3,6,11-trien-5-one 85612428 Click to see CC(=CCCC(C)(C=C)O)C(=O)C=CC(C)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
Cedrelanol 160799 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1002/PCA.564
cis-beta-Guaiene 15560253 Click to see CC1CCC(=C(C)C)CC2=C1CCC2C 204.35 unknown https://doi.org/10.1002/PCA.564
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(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/10.1002/PCA.564
Alloaromadendren 91746537 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/PCA.564
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1002/PCA.564
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1002/PCA.564
> 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/10.1002/PCA.564
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1002/PCA.564
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2R,4R,6E,8R,11S,12R)-8-hydroxy-4,8,12-trimethyl-3,14-dioxatricyclo[9.3.0.02,4]tetradec-6-ene-5,13-dione 162907939 Click to see CC1C2CCC(C=CC(=O)C3(C(C2OC1=O)O3)C)(C)O 280.32 unknown https://doi.org/10.1016/0031-9422(95)00772-5
8-Hydroxy-4,8,12-trimethyl-3,14-dioxatricyclo[9.3.0.02,4]tetradec-6-ene-5,13-dione 162907937 Click to see CC1C2CCC(C=CC(=O)C3(C(C2OC1=O)O3)C)(C)O 280.32 unknown https://doi.org/10.1016/0031-9422(95)00772-5
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3S,3aS,5aR,9S,9aR,9bS)-9-hydroxy-3,5a,9-trimethyl-3,3a,4,5,9a,9b-hexahydrobenzo[g][1]benzofuran-2,6-dione 102484747 Click to see CC1C2CCC3(C(C2OC1=O)C(C=CC3=O)(C)O)C 264.32 unknown https://doi.org/10.1002/HLCA.201000125
3,5a,9-Trimethyl-3a,5,5a,9b-tetrahydronaphtho[1,2-b]furan-2,8(3H,4H)-dione 5156 Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C 246.30 unknown https://doi.org/10.1055/S-0031-1296236
https://doi.org/10.1002/HLCA.201000125
Barrelin 619337 Click to see CC1C2CCC3(C(C2OC1=O)C(C=CC3=O)(C)O)C 264.32 unknown https://doi.org/10.1002/HLCA.201000125
Santonin 221071 Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C 246.30 unknown https://doi.org/10.1002/HLCA.201000125
https://doi.org/10.1055/S-0031-1296236
> Organoheterocyclic compounds / Dihydrofurans
(2S)-3-methyl-2-(3-methylbut-2-enyl)-2,5-dihydrofuran 101600447 Click to see CC1=CCOC1CC=C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
(5R)-4-methyl-5-(3-methylbut-2-enyl)-2H-furan-5-ol 163022955 Click to see CC1=CCOC1(CC=C(C)C)O 168.23 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
3-Methyl-2-(3-methylbut-2-en-1-yl)-2,5-dihydrofuran-2-ol 71341099 Click to see CC1=CCOC1(CC=C(C)C)O 168.23 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
3-Methyl-2-(3-methylbut-2-enyl)-2,5-dihydrofuran 11019056 Click to see CC1=CCOC1CC=C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
beta-Dihydrorosefuran 101600448 Click to see CC1=CCOC1CC=C(C)C 152.23 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
> Organoheterocyclic compounds / Heteroaromatic compounds
1-(5-Methyl-fur-2-yl)-1-(5-methyl-5-vinyl-tetra-hydrofur-2-yl-)-ethane 21569002 Click to see CC1=CC=C(O1)C(C)C2CCC(O2)(C)C=C 220.31 unknown https://doi.org/10.1002/HLCA.19740570718
2-[(1R)-1-[(2R,5R)-5-ethenyl-5-methyloxolan-2-yl]ethyl]-5-methylfuran 162954044 Click to see CC1=CC=C(O1)C(C)C2CCC(O2)(C)C=C 220.31 unknown https://doi.org/10.1002/HLCA.19740570718
2-[(1R)-1-[(2S,5R)-5-ethenyl-5-methyloxolan-2-yl]ethyl]-5-methylfuran 162954043 Click to see CC1=CC=C(O1)C(C)C2CCC(O2)(C)C=C 220.31 unknown https://doi.org/10.1002/HLCA.19740570718
2-[(1S)-1-[(2R,5R)-5-ethenyl-5-methyloxolan-2-yl]ethyl]-5-methylfuran 163193586 Click to see CC1=CC=C(O1)C(C)C2CCC(O2)(C)C=C 220.31 unknown https://doi.org/10.1002/HLCA.19740570718
cis-Davanafuran 91746854 Click to see CC(C1CCC(O1)(C)C=C)C2=CC=CO2 206.28 unknown https://doi.org/10.1002/PCA.564
cis-threo-Davanafuran 91746618 Click to see CC1=CC=C(O1)C(C)C2CCC(O2)(C)C=C 220.31 unknown https://doi.org/10.1002/HLCA.19740570718
Davanafuran 6427516 Click to see CC(C1CCC(O1)(C)C=C)C2=CC=CO2 206.28 unknown https://doi.org/10.1002/PCA.564
> Organoheterocyclic compounds / Oxolanes
2-(5-Ethenyl-5-methyloxolan-2-yl)-6-hydroxy-6-methylhept-4-en-3-one 435004 Click to see CC(C1CCC(O1)(C)C=C)C(=O)C=CC(C)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
CID 12308610 12308610 Click to see CC(C1CCC(O1)(C)C=C)C(=O)C(C)(C)C=C 236.35 unknown https://doi.org/10.1016/S0040-4039(00)85355-1
https://doi.org/10.1002/PCA.564
Nordavanone 6431481 Click to see CC(C1CCC(O1)(C)C=C)C(=O)C 182.26 unknown https://doi.org/10.1002/HLCA.19740570717
Nordavanone 45112410 Click to see CC(C1CCC(O1)(C)C=C)C(=O)C 182.26 unknown https://doi.org/10.1002/HLCA.19740570717
> Organoheterocyclic compounds / Tetrahydrofurans
Davanone 519782 Click to see CC(C1CCC(O1)(C)C=C)C(=O)CC=C(C)C 236.35 unknown https://doi.org/10.1016/S0040-4039(00)85355-1
https://doi.org/10.1002/PCA.564
Hydroxydavanone 5477854 Click to see CC(C1CCC(O1)(C)C=C)C(=O)C=CC(C)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(90)85220-A
https://doi.org/10.1016/S0040-4039(01)91378-4
trans-Hydroxydavanone 102441806 Click to see CC(C1CCC(O1)(C)C=C)C(=O)C=CC(C)(C)O 252.35 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
2-Propenoic acid, 3-phenyl-, 3-phenyl-2-propenyl ester 31224 Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2 264.30 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
Cinnamyl cinnamate 1550890 Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2 264.30 unknown https://doi.org/10.1016/0031-9422(91)83725-Z
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1002/PCA.564
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1002/PCA.564
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/0031-9422(90)85220-A

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.