Artemisia minor

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Details Top

Internal ID	UUID643fd367375c3478249182
Scientific name	Artemisia minor
Authority	Jacquem. ex Besser
First published in	Bull. Soc. Imp. Naturalistes Moscou 9: 22 (1836)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Artemisia tibetica	Hook.f.	Fl. Brit. India 3(8): 329 (1881)
Artemisia sieversiana var. tibetica	C.B.Clarke	Compos. Ind.: 165 (1876)
Artemisia tibetica	(C.B.Clarke) Hook.f. & Thomson	The Flora of British India 3(8): 329 1881

Common names Top

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Language	Common/alternative name
Chinese	垫型蒿
Chinese	小灰蒿
Chinese	那马-甲马
Chinese	那马一甲马

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

Asia-temperate click to expand
- China
  - China North-central
  - Qinghai
  - Tibet
  - Xinjiang

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - West Himalaya

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000131723
Tropicos	2744068
KEW	urn:lsid:ipni.org:names:179813-1
The Plant List	gcc-92588
Open Tree Of Life	12091
Observations.org	291296
NCBI Taxonomy	1227633
IPNI	179813-1
GBIF	3121555
Elurikkus	604877

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

Different feeding strategies can affect growth performance and rumen functions in Gangba sheep as revealed by integrated transcriptome and microbiome analyses

Jize Z, Zhuoga D, Xiaoqing Z, Na T, Jiacuo G, Cuicheng L, Bandan P

Front Microbiol

24-Aug-2022

PMCID:	PMC9449551
doi:	10.3389/fmicb.2022.908326
PMID:	36090079

Isolation and In Silico SARS-CoV-2 Main Protease Inhibition Potential of Jusan Coumarin, a New Dicoumarin from Artemisia glauca

Suleimen YM, Jose RA, Suleimen RN, Ishmuratova MY, Toppet S, Dehaen W, Alsfouk AA, Elkaeed EB, Eissa IH, Metwaly AM

Molecules

31-Mar-2022

PMCID:	PMC9000794
doi:	10.3390/molecules27072281
PMID:	35408682

Antioxidant Activity-guided Phytochemical Investigation of Artemisia aucheri Boiss.: Isolation of Ethyl Caffeate and a Spinacetin Glycoside

Jahanbani P, Nasseri S, Mojarrab M

Iran J Pharm Res

01-Jan-2021

PMCID:	PMC8170746
doi:	10.22037/ijpr.2019.15496.13140
PMID:	34400943

Functionally distinct assembly of vascular plants colonizing alpine cushions suggests their vulnerability to climate change

Dolezal J, Dvorsky M, Kopecky M, Altman J, Mudrak O, Capkova K, Rehakova K, Macek M, Liancourt P

Ann Bot

12-Dec-2018

PMCID:	PMC6417476
doi:	10.1093/aob/mcy207
PMID:	30541052

Chemical Constituents of the Aerial Parts of Artemisia iwayomogi

Xi-Tao Yan, Yan Ding, Wei Li, Ya-Nan Sun, Young Ho Kim

Springer Science and Business Media LLC

09-Nov-2015

doi:	10.1007/S10600-015-1519-X

Testing the Stress-Gradient Hypothesis at the Roof of the World: Effects of the Cushion Plant Thylacospermum caespitosum on Species Assemblages

Dvorský M, Doležal J, Kopecký M, Chlumská Z, Janatková K, Altman J, de Bello F, Řeháková K

PLoS One

10-Jan-2013

PMCID:	PMC3542354
doi:	10.1371/journal.pone.0053514
PMID:	23326446

Natural products possessing protein tyrosine phosphatase 1B (PTP1B) inhibitory activity found in the last decades

Jiang CS, Liang LF, Guo YW

Acta Pharmacol Sin

03-Sep-2012

PMCID:	PMC4002712
doi:	10.1038/aps.2012.90
PMID:	22941286

Chemical constituents from the aerial parts of Artemisia minor.

He ZZ, Yan JF, Song ZJ, Ye F, Liao X, Peng SL, Ding LS

J Nat Prod

01-Jun-2009

doi:	10.1021/NP800643N
PMID:	19476336

Phytochemical Profile Top

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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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methylbenzaldehyde	7725	Click to see CC1=CC=C(C=C1)C=O	120.15	unknown	https://doi.org/10.1021/NP800643N
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxycinnamaldehyde	5280536	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	https://doi.org/10.1007/S10600-015-1519-X
> Lignans, neolignans and related compounds / Coumarinolignans
Cleomiscosin A	442510	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	https://doi.org/10.1007/S10600-015-1519-X
Cleomiscosin C	11464176	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO	416.40	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP800643N
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1007/S10600-015-1519-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496016	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/10.1021/NP800643N
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/10.1007/S10600-015-1519-X
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP800643N
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/10.1007/S10600-015-1519-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	154497544	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1021/NP800643N
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(E)-3-[(2S,3S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]prop-2-enoic acid	162917823	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C=CC(=O)O)CO)O	358.30	unknown	https://doi.org/10.1021/NP800643N
4-[(2R,3R)-3-(hydroxymethyl)-6-[(E)-3-methoxyprop-1-enyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol	101481341	Click to see COCC=CC1=CC2=C(C=C1)OC(C(O2)CO)C3=CC(=C(C=C3)O)O	344.40	unknown	https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl caffeate	5317238	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
Isoferulic acid	736186	Click to see COC1=C(C=C(C=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6,8-dimethoxy-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	163014035	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O	384.30	unknown	https://doi.org/10.1021/NP800643N
6,8-Dimethoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one	12302276	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC3C(C(C(C(O3)CO)O)O)O	384.30	unknown	https://doi.org/10.1007/S10600-015-1519-X
Mandshurin	11740722	Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC3C(C(C(C(O3)CO)O)O)O	384.30	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
Scopolin	439514	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	354.31	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Arteminorin B	44178671	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3=C(C=C4C=C(C(=O)OC4=C3OC)O)OC	412.30	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
Fraxidin	3083616	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC	222.19	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
arteminorin C	44178672	Click to see COC1=C(C(=C2C(=C1)C=C(C(=O)O2)C3=CC4=CC(=C(C=C4OC3=O)O)O)OC)O	398.30	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
4,4'-Biisofraxidin	11259276	Click to see COC1=C(C(=C2C(=C1)C(=CC(=O)O2)C3=CC(=O)OC4=C(C(=C(C=C34)OC)O)OC)OC)O	442.40	unknown	https://doi.org/10.1021/NP800643N
Arteminorin A	44178670	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)OC3=CC4=CC(=C(C(=C4OC3=O)OC)O)OC	442.40	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
Isofraxidin	5318565	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O	222.19	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
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/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N
> 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/10.1007/S10600-015-1519-X
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	284.26	unknown	https://doi.org/10.1021/NP800643N https://doi.org/10.1007/S10600-015-1519-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-7,4'-dimethoxyflavone	15289454	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)O	314.29	unknown	https://doi.org/10.1021/NP800643N
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Tectorigenin	5281811	Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1007/S10600-015-1519-X https://doi.org/10.1021/NP800643N

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Artemisia minor

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