Chrysanthemum lavandulifolium

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643fca48e92b0011550870
Scientific name	Chrysanthemum lavandulifolium
Authority	Makino
First published in	Bot. Mag. (Tokyo) 23: 20, in obs. (1909)

Description Top

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Chrysanthemum lavandulifolium is a perennial flowering plant known for its yellow flowers and belonging to the Asteraceae family. It has 18 chromosomes and is characterized by its erect herb, green oblong leaves, and corymb-style yellow flower heads. It is native to eastern Asia and is commonly found in Korea, Japan, and China. This plant has been used in traditional medicine to treat vertigo and has anti-inflammatory properties. However, it is susceptible to diseases such as black plight and downy mildew, which can cause the plant to wilt and eventually die.

Synonyms Top

Scientific name	Authority	First published in
Chrysanthemum bellum	Grüning	Repert. Spec. Nov. Regni Veg. 12: 311 (1913)
Chrysanthemum boreale	Makino	Bot. Mag. (Tokyo) 23: 20 (1909)
Pyrethrum lavandulifolium	Fisch. ex Trautv.	Trudy Imp. S.-Peterburgsk. Bot. Sada i. (1871-72) 181.
Dendranthema lavandulifolium	(Fisch. ex Trautv.) Y.Ling & C.Shih	Bull. Bot. Lab. N. E. Forest. Inst., Harbin 1980(6): 5 (1980)
Dendranthema seticuspe	(Maxim.) Kitam.	Acta Phytotax. Sin. 38: 380 (1987): (1987)
Chrysanthemum seticuspe f. boreale	(Makino) H.Ohashi & Yonek.	J. Jap. Bot. 79(3): 191 (2004)
Dendranthema boreale	(Makino) Y.Ling ex Kitam.	Acta Phytotax. Geobot. 29(6): 167. 1978 [30 Nov 1978]
Pyrethrum seticuspe	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg xvii. (1872) 423.
Chrysanthemum indicum var. boreale	Makino	Bot. Mag. (Tokyo) 16: 89 (1902)
Dendranthema lavandulifolium var. sianensis	(Kitam.) Kitam.	Acta Phytotax. Geobot. 29: 167 (1978)
Chrysanthemum lavandulifolium var. jucundum	(Nakai & Kitag.) Kitam.	Journal of Japanese Botany 13(3): 166 1937
Chrysanthemum lavandulifolium var. hortense	Makino	J. Jap. Bot. 3: 27 (1926)
Chrysanthemum lavandulifolium var. glabriusculum	(Ling) Kitam.	Journal of Japanese Botany 19: 342 1934
Chrysanthemum seticuspe var. boreale	(Makino) Hand.-Mazz.	Symbolae Sinicae 7(4): 1111 1936
Dendranthema lavandulifolium var. glabriusculum	(Ling) Kitam.	Acta Phytotax. Geobot. 40: 138 (1989)
Chrysanthemum lavandulifolium var. leucanthum	Makino	Bot. Mag. (Tokyo) 25: 11 (1911)
Dendranthema lavandulifolium var. seticuspe	(Maxim.) C.Shih	Bull. Bot. Lab. N. E. Forest. Inst., Harbin 1980(6): 6 (1980)
Chrysanthemum bellum var. jucundum	(Nakai & Kitag.) Hand.-Mazz.	Acta Horti Gothoburgensis 12(9): 260 1938
Chrysanthemum bellum var. glabriusculum	Ling	Contributions from the Institute of Botany, National Academy of Peiping 2: 498 1934
Pyrethrum lavandulifolium var. sianense	Kitam.	Journal of Japanese Botany 20: 197 1919
Chrysanthemum lavandulifolium var. sianense	Kitam.	J. Jap. Bot. 20: 197 (1944)
Chrysanthemum jucundum	Nakai & Kitag.	Rep. Exped. Manchoukuo Sect. IV, Pt. 1, Pl. Nov. Jehol. 58. 1934
Chrysanthemum seticuspe	(Maxim.) Hand.-Mazz.	Symb. Sin. 7: 1111 (1936)
Chrysanthemum wilsonianum	Hand.-Mazz.	Acta Horti Gothob. 12: 258 (1938). (1937-1938 publ. 1938)
Dendranthema lavandulifolium	(fischer ex Trautv.) Kitam.	Acta Phytotax. Geobot. 29(6): 167. 1978 [30 Nov 1978]
Chrysanthemum namikawanum	Kitam.	J. Jap. Bot. 1937, xiii. 162.
Delphinium seticuspe var. tomentellum	(Hand.-Mazz.) Kitan.	Acta Phytotax. Geobot. 41(4–6): 185 1990

Common names Top

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Language	Common/alternative name
Korean	산국
Chinese	甘菊
Chinese	甘菊人细裂野菊）*
Chinese	岩香菊

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Chrysanthemum lavandulifolium var. discoideum	Hand.-Mazz.	Acta Horti Gothob. 12(9): 259-260 (1938)
Chrysanthemum lavandulifolium var. tomentellum	Hand.-Mazz.	Acta Horti Gothob. 12: 260 (1938)

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
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000037092
Tropicos	2702265
KEW	urn:lsid:ipni.org:names:193550-1
Open Tree Of Life	7211
NCBI Taxonomy	146996
IPNI	193550-1
iNaturalist	840475
GBIF	6064513
Freebase	/m/0jkx7f6
USDA GRIN	410332
Wikipedia	Chrysanthemum_lavandulifolium
CMAUP	NPO28224

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_022545495.1	ASM2254549v1	Chromosome	Beijing Forestry University	2022-03-21	164.0x	2.49 Gb

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

Overexpression of a Fragaria vesca NAM, ATAF, and CUC (NAC) Transcription Factor Gene (FvNAC29) Increases Salt and Cold Tolerance in Arabidopsis thaliana

Li W, Li H, Wei Y, Han J, Wang Y, Li X, Zhang L, Han D

Int J Mol Sci

06-Apr-2024

PMCID:	PMC11012600
doi:	10.3390/ijms25074088
PMID:	38612898

The complete chloroplast genome sequence of a cultivar of Chrysanthemum, Chrysanthemum × morifolium ‘Hangbaiju’ (Asteraceae)

Yao Z, Miao J, Xu W, Lu Q

Mitochondrial DNA B Resour

25-Mar-2024

PMCID:	PMC10967664
doi:	10.1080/23802359.2024.2334014
PMID:	38545568

cla-miR164-NO APICAL MERISTEM (ClNAM) regulates the inflorescence architecture development of Chrysanthemum lavandulifolium

Li J, Wen X, Zhang Q, Tian Y, Pu Y, Wang J, Liu B, Du Y, Dai S

Hortic Res

22-Feb-2024

PMCID:	PMC11017518
doi:	10.1093/hr/uhae039
PMID:	38623074

Genome-wide identification and characterization of TCP gene family in Dendrobium nobile and their role in perianth development

Wei X, Yuan M, Zheng BQ, Zhou L, Wang Y

Front Plant Sci

05-Feb-2024

PMCID:	PMC10875090
doi:	10.3389/fpls.2024.1352119
PMID:	38375086

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

Understanding AP2/ERF Transcription Factor Responses and Tolerance to Various Abiotic Stresses in Plants: A Comprehensive Review

Ma Z, Hu L, Jiang W

Int J Mol Sci

11-Jan-2024

PMCID:	PMC10815832
doi:	10.3390/ijms25020893
PMID:	38255967

Comparative Physiological and Transcriptome Analysis of Crossostephium chinense Reveals Its Molecular Mechanisms of Salt Tolerance

Wang Y, Liu M, Guo Z, Liang Y, Lu Y, Xu Y, Sun M

Int J Mol Sci

27-Nov-2023

PMCID:	PMC10706559
doi:	10.3390/ijms242316812
PMID:	38069143

Morphological Characteristics and Expression Patterns of CmCYC2c of Different Flower Shapes in Chrysanthemum morifolium

Qiu T, Li S, Zhao K, Jia D, Chen F, Ding L

Plants (Basel)

30-Oct-2023

PMCID:	PMC10647454
doi:	10.3390/plants12213728
PMID:	37960083

Editorial: Growth regulation in horticultural plants: new insights in the omics era

Cheng C, Ma N, Zheng Y, Xi L

Front Plant Sci

20-Oct-2023

PMCID:	PMC10623409
doi:	10.3389/fpls.2023.1305520
PMID:	37929172

Genome-wide identification and comprehensive analysis of WRKY transcription factor family in safflower during drought stress

Song X, Hou X, Zeng Y, Jia D, Li Q, Gu Y, Miao H

Sci Rep

07-Oct-2023

PMCID:	PMC10560227
doi:	10.1038/s41598-023-44340-y
PMID:	37805641

Genome-wide identification of the TCP gene family in Chrysanthemum lavandulifolium and its homologs expression patterns during flower development in different Chrysanthemum species

Wu X, Li J, Wen X, Zhang Q, Dai S

Front Plant Sci

29-Sep-2023

PMCID:	PMC10570465
doi:	10.3389/fpls.2023.1276123
PMID:	37841609

Designing of future ornamental crops: a biotechnological driven perspective

Partap M, Verma V, Thakur M, Bhargava B

Hortic Res

25-Sep-2023

PMCID:	PMC10681008
doi:	10.1093/hr/uhad192
PMID:	38023473

Role of methylation in vernalization and photoperiod pathway: a potential flowering regulator?

Shi M, Wang C, Wang P, Yun F, Liu Z, Ye F, Wei L, Liao W

Hortic Res

29-Aug-2023

PMCID:	PMC10569243
doi:	10.1093/hr/uhad174
PMID:	37841501

NACs, generalist in plant life

Han K, Zhao Y, Sun Y, Li Y

Plant Biotechnol J

25-Aug-2023

PMCID:	PMC10651149
doi:	10.1111/pbi.14161
PMID:	37623750

Insights into the Transcriptomics of Crop Wild Relatives to Unravel the Salinity Stress Adaptive Mechanisms

Abdul Aziz M, Masmoudi K

Int J Mol Sci

06-Jun-2023

PMCID:	PMC10298703
doi:	10.3390/ijms24129813
PMID:	37372961

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(2-Hexa-2,4-diynylidene-4-hydroxy-1,10-dioxaspiro[4.5]decan-3-yl) 3-methylbutanoate	318603	Click to see CC#CC#CC=C1C(C(C2(O1)CCCCO2)O)OC(=O)CC(C)C	332.40	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
(8-Acetyloxy-2-hexa-2,4-diynylidene-4-hydroxy-1,10-dioxaspiro[4.5]decan-3-yl) 3-methylbutanoate	73825125	Click to see CC#CC#CC=C1C(C(C2(O1)CCC(CO2)OC(=O)C)O)OC(=O)CC(C)C	390.40	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
Hkcljbndomxpcy-ctjdijsbsa-	21726157	Click to see CC#CC#CC=C1C(C(C2(O1)CCC(CO2)OC(=O)C)O)OC(=O)CC(C)C	390.40	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
Leoznwwipmvkhh-nfnysahwsa-	21726158	Click to see CC#CC#CC=C1C(C(C2(O1)CCCCO2)O)OC(=O)CC(C)C	332.40	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Thujone	12304612	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1246/NIKKASHI1948.81.9_1470
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1246/NIKKASHI1948.81.9_1470
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Thujopsadiene	6428961	Click to see CC1=CCC2(CC=CC(C23C1C3)(C)C)C	202.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Handelin	90474153	Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3	552.70	unknown	https://doi.org/10.1021/NP4009877
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3R,3aS,7R,9S,10Z,11aS)-7-hydroperoxy-9-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one	21726161	Click to see CC1C2CCC(=C)C(CC(C(=CC2OC1=O)C)O)OO	282.33	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
(3R,3aS,7R,9S,10Z,11aS)-7,9-dihydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one	21726160	Click to see CC1C2CCC(=C)C(CC(C(=CC2OC1=O)C)O)O	266.33	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
7-Hydroperoxy-9-hydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one	73825127	Click to see CC1C2CCC(=C)C(CC(C(=CC2OC1=O)C)O)OO	282.33	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
7,9-Dihydroxy-3,10-dimethyl-6-methylidene-3,3a,4,5,7,8,9,11a-octahydrocyclodeca[b]furan-2-one	73825126	Click to see CC1C2CCC(=C)C(CC(C(=CC2OC1=O)C)O)O	266.33	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(6-acetyloxy-7-methoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate	85134494	Click to see CC1=CC(C2C1C3C(C(CC2(C)OC(=O)C)OC(=O)C)C(=C)C(=O)O3)OC	378.40	unknown	https://doi.org/10.1055/S-2001-16477
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) 2-methylbut-2-enoate	5255772	Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O	346.40	unknown	https://doi.org/10.1007/BF02975380 https://doi.org/10.1055/S-2001-16477
(6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate	3809323	Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C(=C)C(=O)O3	306.40	unknown	https://doi.org/10.1055/S-2001-16477
(6-hydroxy-7-methoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate	85080006	Click to see CC1=CC(C2C1C3C(C(CC2(C)O)OC(=O)C)C(=C)C(=O)O3)OC	336.40	unknown	https://doi.org/10.1055/S-2001-16477
(6,8-Dihydroxy-6-methyl-3,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) acetate	85087082	Click to see CC(=O)OC1CC(C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O)(C)O	322.40	unknown	https://doi.org/10.1055/S-2001-16477
[(3aR,4S,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (E)-2-methylbut-2-enoate	10450323	Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O	346.40	unknown	https://doi.org/10.1055/S-2001-16477
[(3aR,4S,6R,6aR,9aR,9bR)-6-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate	10450322	Click to see CC=C(C)C(=O)OC1CC(C2CC=C(C2C3C1C(=C)C(=O)O3)C)(C)O	346.40	unknown	https://doi.org/10.1055/S-2001-16477
[(3aR,4S,6R,6aS,7S,9aR,9bR)-6-acetyloxy-7-methoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] acetate	162967239	Click to see CC1=CC(C2C1C3C(C(CC2(C)OC(=O)C)OC(=O)C)C(=C)C(=O)O3)OC	378.40	unknown	https://doi.org/10.1055/S-2001-16477
[(3aR,4S,6R,6aS,7S,9aR,9bR)-6-hydroxy-7-methoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] acetate	163012955	Click to see CC1=CC(C2C1C3C(C(CC2(C)O)OC(=O)C)C(=C)C(=O)O3)OC	336.40	unknown	https://doi.org/10.1055/S-2001-16477
4,6-Dihydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6,6a,7,9a,9b-octahydroazuleno[4,5-b]furan-2(3h)-one	99115	Click to see CC1=CCC2C1C3C(C(CC2(C)O)O)C(=C)C(=O)O3	264.32	unknown	https://doi.org/10.1055/S-2001-16477
Borenolide	9996231	Click to see CC(=O)OC1CC(C2CC(C(=C)C2C3C1C(=C)C(=O)O3)O)(C)O	322.40	unknown	https://doi.org/10.1055/S-2001-16477 https://doi.org/10.1055/S-2003-43221
cumambrin A	174867	Click to see CC1=CCC2C1C3C(C(CC2(C)O)OC(=O)C)C(=C)C(=O)O3	306.40	unknown	https://doi.org/10.1055/S-2001-16477 https://doi.org/10.1007/BF02975380
Cumambrin B	9992975	Click to see CC1=CCC2C1C3C(C(CC2(C)O)O)C(=C)C(=O)O3	264.32	unknown	https://doi.org/10.1007/BF02975380 https://doi.org/10.1055/S-2001-16477
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(4-Acetyloxy-2-hexa-2,4-diynylidene-1,10-dioxaspiro[4.5]decan-3-yl) acetate	318602	Click to see CC#CC#CC=C1C(C(C2(O1)CCCCO2)OC(=O)C)OC(=O)C	332.30	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
[(2E,3S,4S,5R)-4-acetyloxy-2-hexa-2,4-diynylidene-1,10-dioxaspiro[4.5]decan-3-yl] acetate	21726159	Click to see CC#CC#CC=C1C(C(C2(O1)CCCCO2)OC(=O)C)OC(=O)C	332.30	unknown	https://doi.org/10.1016/S0040-4020(01)87880-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Dehydroisostebenone	15558821	Click to see CC(=CC(=O)C1=CC(=CC2=C1OC(CC2=O)(C)C)C(=O)C)C	300.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxanes
Eucalyptol	2758	Click to see CC1(C2CCC(O1)(CC2)C)C	154.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> 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/BF02979135
Apigenin-7-olate	25200950	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)[O-])O	269.23	unknown	via CMAUP database
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/BF02979135
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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/10.1007/BF02979135
> 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/10.1007/BF02979135

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Chrysanthemum lavandulifolium

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

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