PlantaeDB Logo
Login Sign-up

Artemisia lancea

We don't have an image yet. Upload an 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 UUID643fcce40bd8d966963762
Scientific name Artemisia lancea
Authority Vaniot
First published in Bull. Acad. Int. Géogr. Bot. , sér. 3, 12(167-168): 500 (1903)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Artemisia minutiflora Nakai Bot. Mag. (Tokyo) 25: 56 (1911)
Artemisia feddei subsp. arschantinica (Darijma) Gubanov & Kamelin in I.A. Gubanov, Konsp. Fl. Vneshnei Mongolii (Sosud. Rast.) 97 (1996):.
Artemisia feddei H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 8: 138 (1910)
Artemisia arschantinica Darjima
Artemisia lavandulifolia var. feddei (H.Lév. & Vaniot) Pamp. Nuovo Giorn. Bot. Ital., n.s., 36: 467 (1930)
Artemisia arschantinica Darijma Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. 97(5): 65 (1992).

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 小艾
Chinese 小蓬蒿
Chinese 矮蒿
Chinese 细叶艾
Chinese 野艾
Chinese 野艾蒿
Chinese 鸭脚艾
Chinese 牛尾蒿
Chinese 矮蒿(野艾、野艾蒿）

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Kuril Islands
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000067134
Tropicos 2744666
KEW urn:lsid:ipni.org:names:179713-1
The Plant List gcc-24005
Open Tree Of Life 7050942
NCBI Taxonomy 2291100
IPNI 179713-1
iNaturalist 709035
GBIF 3120857
EOL 6180234
USDA GRIN 464996
PFAF Artemisia lancea

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
Roles of Essential Oils, Polyphenols, and Saponins of Medicinal Plants as Natural Additives and Anthelmintics in Ruminant Diets: A Systematic Review Ramdani D, Yuniarti E, Jayanegara A, Chaudhry AS Animals (Basel) 20-Feb-2023
PMCID:PMC9951870
doi:10.3390/ani13040767
PMID:36830554
Essential Oils as Novel Anthelmintic Drug Candidates Panda SK, Daemen M, Sahoo G, Luyten W Molecules 29-Nov-2022
PMCID:PMC9735941
doi:10.3390/molecules27238327
PMID:36500419
Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L J Ethnobiol Ethnomed 23-May-2022
PMCID:PMC9125852
doi:10.1186/s13002-022-00532-w
PMID:35606860
Wild Egyptian medicinal plants show in vitro and in vivo cytotoxicity and antimalarial activities Abdou AM, Seddek AL, Abdelmageed N, Badry MO, Nishikawa Y BMC Complement Med Ther 12-May-2022
PMCID:PMC9101831
doi:10.1186/s12906-022-03566-5
PMID:35550108
A Systematic Review on Comparative Analysis, Toxicology, and Pharmacology of Medicinal Plants Against Haemonchus contortus Ali R, Rooman M, Mussarat S, Norin S, Ali S, Adnan M, Khan SN Front Pharmacol 10-May-2021
PMCID:PMC8141741
doi:10.3389/fphar.2021.644027
PMID:34040520
Long-term responses of riparian plants’ composition to water level fluctuation in China's Three Gorges Reservoir Jian Z, Ma F, Guo Q, Qin A, Xiao W PLoS One 28-Nov-2018
PMCID:PMC6261589
doi:10.1371/journal.pone.0207689
PMID:30485328
Cellular engineering of Artemisia annua and Artemisia dubia with the rol ABC genes for enhanced production of potent anti-malarial drug artemisinin Kiani BH, Suberu J, Mirza B Malar J 04-May-2016
PMCID:PMC4855502
doi:10.1186/s12936-016-1312-8
PMID:27142388
Survey of artemisinin production by diverse Artemisia species in northern Pakistan Mannan A, Ahmed I, Arshad W, Asim MF, Qureshi RA, Hussain I, Mirza B Malar J 04-Nov-2010
PMCID:PMC2989329
doi:10.1186/1475-2875-9-310
PMID:21047440
STRUCTURE OF YOMOGIARTEMIN, A NOVEL SESQUITERPENE α-METHYLENE-γ-LACTONE FROM <i>Artemisia feddei</i> Masato Koreeda, Sumu Matsueda, Takehiro Satomi, Ken Hirotsu, Jon Clardy Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1979.81
Studies on Peroxides of Artemisia lamcea Luo Shide, Ning Bingmei, Hu Wangyu, Xie Jinlun American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50074A034
Yomogi alcohol a, a new monoterpene alcohol from artemisia feddei lév. et van. Shûichi Hayashi, Katsumi Yano, Tamon Matsuura Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)70841-0
Two sesquiterpene lactones from artemisia species Masahiko Nagaki Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80354-4
Sesquiterpenes and acetylenes from Artemisia feddei R.X. Tan, Jia Z.J., J. Zhao, S.L. Feng Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83460-G
Scopoletin: an inducible nitric oxide synthesis inhibitory active constituent from Artemisia feddei. Kang TH, Pae HO, Jeong SJ, Yoo JC, Choi BM, Jun CD, Chung HT, Miyamoto T, Higuchi R, Kim YC Planta Med 01-Jun-1999
doi:10.1055/S-1999-14014
PMID:10418323
Sesquiterpene Lactones and Other Constituents from Artemisia feddei. Tan RX, Jia ZJ, Zhao Y Planta Med 01-Oct-1992
doi:10.1055/S-2006-961513
PMID:17226503

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 / Terpene lactones
(1R,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one 137704955 Click to see CC1CCC2C(C(=O)OC3C24C1CCC(O3)(OO4)C)C 282.33 unknown https://doi.org/10.1021/NP50074A034
Artemisinin 68827 Click to see CC1CCC2C(C(=O)OC3C24C1CCC(O3)(OO4)C)C 282.33 unknown https://doi.org/10.1021/NP50074A034
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1R,3R,7R,9R,10R,12R,14R)-9,14-dimethyl-4-methylidene-6,11-dioxatetracyclo[7.5.0.03,7.010,12]tetradecane-5,13-dione 162885327 Click to see CC1C2CC3C(CC2(C4C(C1=O)O4)C)OC(=O)C3=C 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80354-4
(3S,3aR,4aR,8aR,9aR)-4a-hydroxy-3,8a-dimethyl-5-methylidene-3,3a,4,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 13992469 Click to see CC1C2CC3(C(=C)CCCC3(CC2OC1=O)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(92)83460-G
3,8a-Dimethyl-5-methylidene-dodecahydronaphtho[2,3-b]furan-2-one 5104810 Click to see CC1C2CC3C(=C)CCCC3(CC2OC1=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(92)83460-G
4a-Hydroxy-3,8a-dimethyl-5-methylidene-3,3a,4,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 13992468 Click to see CC1C2CC3(C(=C)CCCC3(CC2OC1=O)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(92)83460-G
4a-hydroxy-8a-methyl-3,5-dimethylidene-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 331387 Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(92)83460-G
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one 98958 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1055/S-2006-961513
8a-Methyl-3,5-dimethylidene-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 605266 Click to see CC12CCCC(=C)C1CC3C(C2)OC(=O)C3=C 232.32 unknown https://doi.org/10.1016/0031-9422(92)83460-G
9,14-Dimethyl-4-methylidene-6,11-dioxatetracyclo[7.5.0.03,7.010,12]tetradecane-5,13-dione 14021291 Click to see CC1C2CC3C(CC2(C4C(C1=O)O4)C)OC(=O)C3=C 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80354-4
Dihydroisoalantolactone 6451323 Click to see CC1C2CC3C(=C)CCCC3(CC2OC1=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(92)83460-G
Himeyoshin 101320208 Click to see CC1C2CC3C(CC2(C4C(C1=O)O4)C)OC(=O)C3=C 262.30 unknown https://doi.org/10.1016/S0031-9422(00)80354-4
Isoalantolactone 73285 Click to see CC12CCCC(=C)C1CC3C(C2)OC(=O)C3=C 232.32 unknown https://doi.org/10.1016/0031-9422(92)83460-G
Reynosin 482788 Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C 248.32 unknown https://doi.org/10.1055/S-2006-961513
Telekin 12443309 Click to see CC12CCCC(=C)C1(CC3C(C2)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1016/0031-9422(92)83460-G
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(8-acetyloxy-10-hydroperoxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-5-yl) acetate 162849433 Click to see CC1=CC(CC(CC2C(CC1OC(=O)C)C(=C)C(=O)O2)(C)OO)OC(=O)C 382.40 unknown https://doi.org/10.1016/0031-9422(92)83460-G
[(3aR,5S,6Z,8R,10R,11aS)-8-acetyloxy-10-hydroperoxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-5-yl] acetate 162849434 Click to see CC1=CC(CC(CC2C(CC1OC(=O)C)C(=C)C(=O)O2)(C)OO)OC(=O)C 382.40 unknown https://doi.org/10.1016/0031-9422(92)83460-G
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1S,2S,10S,12R,14S)-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one 15559180 Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4 246.30 unknown https://doi.org/10.1055/S-2006-961513
[(1S,2R,5R,11R,13S,14R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,15-trioxapentacyclo[8.5.0.01,14.05,9.011,13]pentadecan-4-yl] acetate 11969590 Click to see CC(=O)OC1CC(C23C(C4C1C(=C)C(=O)O4)C5(C(C2O3)O5)C)(C)O 336.30 unknown https://doi.org/10.1246/CL.1979.81
Estafiatin 566474 Click to see CC12C(O1)CC3C2C4C(CCC3=C)C(=C)C(=O)O4 246.30 unknown https://doi.org/10.1055/S-2006-961513
Yomogiartemin 155327 Click to see CC(=O)OC1CC(C23C(C4C1C(=C)C(=O)O4)C5(C(C2O3)O5)C)(C)O 336.30 unknown https://doi.org/10.1246/CL.1979.81
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1055/S-2006-961513
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1055/S-2006-961513
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2006-961513
https://doi.org/10.1016/0031-9422(92)83460-G
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(92)83460-G
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)80354-4
https://doi.org/10.1055/S-2006-961513
https://doi.org/10.1016/0031-9422(92)83460-G
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(92)83460-G
https://doi.org/10.1055/S-2006-961513
https://doi.org/10.1016/S0031-9422(00)80354-4
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1055/S-2006-961513
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1055/S-2006-961513
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(92)83460-G
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
2,4,4-Trimethyl-3-methylidenehex-5-en-2-ol 162932178 Click to see CC(C)(C=C)C(=C)C(C)(C)O 154.25 unknown https://doi.org/10.1016/S0040-4039(00)70841-0
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
1-(1,10-Dioxaspiro[4.5]dec-3-en-2-yl)hexa-2,4-diyn-1-one 162901557 Click to see CC#CC#CC(=O)C1C=CC2(O1)CCCCO2 230.26 unknown https://doi.org/10.1016/0031-9422(92)83460-G
1-[(2R,5R)-1,10-dioxaspiro[4.5]dec-3-en-2-yl]hexa-2,4-diyn-1-one 101631676 Click to see CC#CC#CC(=O)C1C=CC2(O1)CCCCO2 230.26 unknown https://doi.org/10.1016/0031-9422(92)83460-G
1-[(2S,5R)-1,10-dioxaspiro[4.5]dec-3-en-2-yl]hexa-2,4-diyn-1-one 101631675 Click to see CC#CC#CC(=O)C1C=CC2(O1)CCCCO2 230.26 unknown https://doi.org/10.1016/0031-9422(92)83460-G
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aS,9aR,9bS)-6,9-dimethyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2,7-dione 15558827 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1055/S-1999-14014
(3R,3aS,9aS,9bS)-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione 442139 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1055/S-1999-14014
Achillin 291264 Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C 246.30 unknown https://doi.org/10.1055/S-1999-14014
Dehydroachillin 301781 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1055/S-1999-14014
Dehydroleucodine 73440 Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)C 244.28 unknown https://doi.org/10.1016/0031-9422(92)83460-G
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown https://doi.org/10.1016/S0031-9422(00)80354-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1055/S-1999-14014

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.