Scientific name	Authority	First published in
Artemisia rupestris subsp. woodii	Neilson	Canad. Field-Naturalist 82: 119 (1968)
Absinthium viridiflorum var. rupestre	(L.) Besser
Absinthium viridifolium var. rupestre	(L.) Besser

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
German	felsen-beifuß
Estonian	kaljupuju
Finnish	kivikkomaruna
Swedish	stenmalört
Chinese	岩蒿（一枝蒿、一支蒿）
Chinese	新疆一支蒿
Chinese	一枝蒿
Chinese	岩蒿
Chinese	鹿角蒿

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Artemisia rupestris subsp. viridis	(Willd.) V.P.Ameljczenko	Sist. Zametki Mater. Gerb. Krylova Tomsk. Gosud. Univ. Kuybysheva 86: 4 (1979), without basiony (1979)

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 click to expand
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Afghanistan

Europe click to expand
- Eastern Europe
  - Baltic States
  - East European Russia
  - North European Russia
- Middle Europe
  - Germany
- Northern Europe
  - Sweden

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000010864
Canadensys	2909
USDA Plants	ARRU14
Tropicos	2717161
KEW	urn:lsid:ipni.org:names:180051-1
The Plant List	gcc-110528
Open Tree Of Life	202544
Observations.org	141959
NCBI Taxonomy	86317
IPNI	180051-1
iNaturalist	158720
GBIF	3120873
EPPO	ARTRU
EOL	489992
Elurikkus	2907
USDA GRIN	4296
Wikipedia	Artemisia_rupestris
CMAUP	NPO12728

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

Enantioselective Synthesis of the Guaipyridine Alkaloid (+)- and (−)-Cananodine

Holliday HM, Bone KI, Sabio R, Vyvyan JR

ACS Omega

07-Feb-2024

PMCID:	PMC10882590
doi:	10.1021/acsomega.3c07735
PMID:	38405498

Novel Tri-Segmented Rhabdoviruses: A Data Mining Expedition Unveils the Cryptic Diversity of Cytorhabdoviruses

Bejerman N, Dietzgen R, Debat H

Viruses

10-Dec-2023

PMCID:	PMC10747219
doi:	10.3390/v15122402
PMID:	38140643

Dietary Artemisia Ordosica Polysaccharide Enhances Spleen and Intestinal Immune Response of Broiler Chickens

Du H, Xing Y, Xu Y, Jin X, Yan S, Shi B

Biology (Basel)

31-Oct-2023

PMCID:	PMC10669473
doi:	10.3390/biology12111390
PMID:	37997990

Synthesis of an aggregation-induced emission-based fluorescent probe based on rupestonic acid

Cui Z, Zhang Y, Zhang Z, Abudurexiti A, Yusuf A

RSC Adv

01-Sep-2023

PMCID:	PMC10472508
doi:	10.1039/d3ra03521b
PMID:	37661955

Antimicrobial activity in Asterceae: The selected genera characterization and against multidrug resistance bacteria

Gou J, Lu Y, Xie M, Tang X, Chen L, Zhao J, Li G, Wang H

Heliyon

31-Mar-2023

PMCID:	PMC10161380
doi:	10.1016/j.heliyon.2023.e14985
PMID:	37151707

Improvement influenza vaccine immune responses with traditional Chinese medicine and its active ingredients

Zhao D, Chen X, Wang L, Zhang J, Lv R, Tan L, Chen Y, Tao R, Li X, Chen Y, He W, He J

Front Microbiol

07-Mar-2023

PMCID:	PMC10027775
doi:	10.3389/fmicb.2023.1111886
PMID:	36960292

Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review

Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK

Int J Mol Sci

01-Jan-2023

PMCID:	PMC9821772
doi:	10.3390/ijms24010739
PMID:	36614181

Development of Foot-and-Mouth Disease Vaccines in Recent Years

Lu Z, Yu S, Wang W, Chen W, Wang X, Wu K, Li X, Fan S, Ding H, Yi L, Chen J

Vaccines (Basel)

28-Oct-2022

PMCID:	PMC9693445
doi:	10.3390/vaccines10111817
PMID:	36366327

Artemisia spp.: An Update on Its Chemical Composition, Pharmacological and Toxicological Profiles

Sharifi-Rad J, Herrera-Bravo J, Semwal P, Painuli S, Badoni H, Ezzat SM, Farid MM, Merghany RM, Aborehab NM, Salem MA, Sen S, Acharya K, Lapava N, Martorell M, Tynybekov B, Calina D, Cho WC

Oxid Med Cell Longev

05-Sep-2022

PMCID:	PMC9467740
doi:	10.1155/2022/5628601
PMID:	36105486

Traditional Use, Phytochemical Profiles and Pharmacological Properties of Artemisia Genus from Central Asia

Nurlybekova A, Kudaibergen A, Kazymbetova A, Amangeldi M, Baiseitova A, Ospanov M, Aisa HA, Ye Y, Ibrahim MA, Jenis J

Molecules

11-Aug-2022

PMCID:	PMC9415318
doi:	10.3390/molecules27165128
PMID:	36014364

Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine

Chen W, Yang Y, Fu K, Zhang D, Wang Z

Front Pharmacol

28-Jun-2022

PMCID:	PMC9274010
doi:	10.3389/fphar.2022.891273
PMID:	35837276

Integrating Network Pharmacology and In Vivo Model to Investigate the Mechanism of Biheimaer in the Treatment of Functional Dyspepsia

Wang C, Huanbieke N, Cai X, Gao S, Du T, Zhou Z, Wusiman Z, Matturzi M, Aibai S, Li ZJ

Evid Based Complement Alternat Med

27-May-2022

PMCID:	PMC9166952
doi:	10.1155/2022/8773527
PMID:	35668782

Flavonoids as Potential Anti-Inflammatory Molecules: A Review

Al-Khayri JM, Sahana GR, Nagella P, Joseph BV, Alessa FM, Al-Mssallem MQ

Molecules

02-May-2022

PMCID:	PMC9100260
doi:	10.3390/molecules27092901
PMID:	35566252

Quality Assessment of Artemisia rupestris L. Using Quantitative Analysis of Multi-Components by Single Marker and Fingerprint Analysis

Cao X, Li M, Ma L, Wang M, Hou X, Maiwulanjiang M

Molecules

20-Apr-2022

PMCID:	PMC9099709
doi:	10.3390/molecules27092634
PMID:	35565985

Lycium barbarum Polysaccharides as Antibiotic Substitutes Improve Growth Performance, Serum Immunity, Antioxidant Status, and Intestinal Health for Weaned Piglets

Yin Y, Wang F, Yang M, Tan B, Yin Y, Chen J, Yang Z

Front Microbiol

25-Feb-2022

PMCID:	PMC8914510
doi:	10.3389/fmicb.2021.819993
PMID:	35281314

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
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1991.9697991
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1991.9697991
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
7-Hydroxycadalene	608115	Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O	214.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
2-[(5R,8S,8aR)-8-hydroxy-3,8-dimethyl-2-oxo-1,4,5,6,7,8a-hexahydroazulen-5-yl]prop-2-enoic acid	118710989	Click to see CC1=C2CC(CCC(C2CC1=O)(C)O)C(=C)C(=O)O	264.32	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
2-[(5R,8S,8aR)-8a-hydroxy-3,8-dimethyl-2-oxo-1,4,5,6,7,8-hexahydroazulen-5-yl]prop-2-enoic acid	91668306	Click to see CC1CCC(CC2=C(C(=O)CC12O)C)C(=C)C(=O)O	264.32	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
2-[(5S,8S,8aS)-3,8-dimethyl-2-oxo-4,5,6,7,8,8a-hexahydro-1H-azulen-5-yl]prop-2-enoic acid	3081082	Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(=C)C(=O)O	248.32	unknown	via CMAUP database
Aciphyllic acid	171568	Click to see CC1CCC(CC2=C(CCC12)C)C(=C)C(=O)O	234.33	unknown	via CMAUP database
Rupestonic acid	24094149	Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(=C)C(=O)O	248.32	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 2-[(5R,8S,8aS)-3,8-dimethyl-2-oxo-4,5,6,7,8,8a-hexahydro-1H-azulen-5-yl]prop-2-enoate	118710990	Click to see CC1CCC(CC2=C(C(=O)CC12)C)C(=C)C(=O)OC3C(C(C(C(O3)CO)O)O)O	410.50	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-5alpha-hydroxy-7alpha-methylcyclopenta[c]pyran-4-carboxylic acid	102019700	Click to see CC1CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	376.36	unknown	via CMAUP database
(1S)-1-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-5beta-hydroxy-7alpha-methylcyclopenta[c]pyran-4-carboxylic acid	102019699	Click to see CC1CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	376.36	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(5'S,9S,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14,16-diol	24893327	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1	430.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4R,5R)-3,4-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1,5-dihydroxycyclohexane-1-carboxylic acid	118710978	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	516.40	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
methyl (1R,3R,4R,5R)-3,4-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-1,5-dihydroxycyclohexane-1-carboxylate	118710992	Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O	530.50	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
5-hydroxy-2-(4-methoxyphenoxy)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	101552465	Click to see COC1=CC=C(C=C1)OC2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	462.40	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004 https://doi.org/10.1007/S10600-009-9218-0
5-Hydroxy-2-(4-methoxyphenoxy)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162997984	Click to see COC1=CC=C(C=C1)OC2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	462.40	unknown	https://doi.org/10.1007/S10600-009-9218-0
CID 476785	476785	Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O	288.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Isosafrole	637796	Click to see CC=CC1=CC2=C(C=C1)OCO2	162.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
(5S,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-ol	56930757	Click to see CC1CCC(CC2=C1C=CC(=N2)C)O	191.27	unknown	https://doi.org/10.1248/CPB.60.213
1-(2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl)ethanone	162940577	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=O)C	217.31	unknown	https://doi.org/10.1002/HLCA.200900125
1-(2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl)propan-1-one	162951912	Click to see CCC(=O)C1CCC(C2=C(C1)N=C(C=C2)C)C	231.33	unknown	https://doi.org/10.1002/HLCA.200900125
1-[(5R,8R)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]propan-1-one	102165785	Click to see CCC(=O)C1CCC(C2=C(C1)N=C(C=C2)C)C	231.33	unknown	https://doi.org/10.1002/HLCA.200900125
1-[(5R,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]-3-hydroxypropan-1-one	56930753	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=O)CCO	247.33	unknown	https://doi.org/10.1248/CPB.60.213
1-[(5S,8R)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]propan-1-one	102165787	Click to see CCC(=O)C1CCC(C2=C(C1)N=C(C=C2)C)C	231.33	unknown	https://doi.org/10.1002/HLCA.200900125
1-[(5S,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]-2-hydroxyethanone	56930755	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=O)CO	233.31	unknown	https://doi.org/10.1248/CPB.60.213
1-[(5S,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]-3-hydroxypropan-1-one	56930614	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=O)CCO	247.33	unknown	https://doi.org/10.1248/CPB.60.213
1-[(5S,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]ethanone	162940578	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=O)C	217.31	unknown	https://doi.org/10.1002/HLCA.200900125
2-[(5R,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]prop-2-en-1-ol	56930754	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=C)CO	231.33	unknown	https://doi.org/10.1248/CPB.60.213
methyl (5R,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridine-8-carboxylate	56930613	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=O)OC	233.31	unknown	https://doi.org/10.1248/CPB.60.213
methyl 2-[(5S,8S)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]prop-2-enoate	162924213	Click to see CC1CCC(CC2=C1C=CC(=N2)C)C(=C)C(=O)OC	259.34	unknown	https://doi.org/10.1248/CPB.60.213
Rupestine L	56930756	Click to see CC1CCC(CC2=C1C=CC(=N2)C)O	191.27	unknown	https://doi.org/10.1248/CPB.60.213
> Phenylpropanoids and polyketides / Coumarins and derivatives
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-methoxyphenoxy)-	5316512	Click to see COC1=CC=C(C=C1)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O	300.26	unknown	https://doi.org/10.1007/S10600-006-0026-5
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,4',5-Trihydroxy-3',6,7-trimethoxyflavone	6453535	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O)O	360.30	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 5-glucoside	5317471	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dimethoxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	118710991	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC	476.40	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
Linarin	5317025	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O	592.50	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
Tilianin	5321954	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O	446.40	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether	5468749	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC	328.30	unknown	https://doi.org/10.1016/S0305-1978(02)00178-3
Retusin	5352005	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC	358.30	unknown	https://doi.org/10.1016/S0305-1978(02)00178-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Nevadensin	160921	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O	344.30	unknown	https://doi.org/10.1016/J.BMCL.2014.08.004

Biological Material Top

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.

Artemisia rupestris

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top