Scabiosa comosa

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Distribution

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Scientific Literature

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Details Top

Internal ID	UUID644043c6f03dc378858518
Scientific name	Scabiosa comosa
Authority	Fisch. ex Roem. & Schult.
First published in	Syst. Veg., ed. 15 bis 3: 84 (1818)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Trochocephalus mansenensis	(Nakai) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus hairalensis	(Nakai) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus hopeiensis	(Nakai) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus superbus	(Grüning) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus tschiliensis	(Grüning) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus zuikoensis	(Nakai) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus togashianus	(Hurus.) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Trochocephalus austromongolicus	(Hurus.) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Scabiosa zuikoensis	Nakai	J. Jap. Bot. 19: 274 (1943)
Scabiosa henanensis	Y.K.Yang & J.K.Wu
Scabiosa japonica subsp. tschiliensis	(Grüning) H.Hara
Scabiosa liaoningensis	Y.K.Yang & J.K.Wu
Scabiosa japonica var. acutiloba	H.Hara	J. Jap. Bot. 16(3): 181 1940
Trochocephalus comosus	(Fisch. ex Roem. & Schult.) Á.Löve & D.Löve	Preslia 46: 134 (1974)
Scabiosa fischeri	DC.	Prodr. 4: 658 (1830)
Scabiosa hairalensis	Nakai	J. Jap. Bot. 19: 273 (1943)
Scabiosa austromongolica	Hurus.	Bot. Mag. (Tokyo) 71: 45 (1949)
Scabiosa comosa var. lachnophylla	(Kitag.) Kitag.	Rep. First Sci. Exped. Manchoukuo 4: 113 1940
Scabiosa tschiliensis	Grüning	Repert. Spec. Nov. Regni Veg. 12: 311 (1913)
Scabiosa superba	Grüning	Repert. Spec. Nov. Regni Veg. 12: 310 (1913)
Scabiosa superba f. elatior	Grüning	Repert. Spec. Nov. Regni Veg. 12(325–330): 310–311 1913
Scabiosa fischeri f. breviseta	Hand.-Mazz.	Acta Horti Gothob. 13(6): 230–231 1939
Scabiosa hopeiensis	Nakai	J. Jap. Bot. 16: 69 (1940)
Scabiosa mansenensis	Nakai	J. Jap. Bot. 19: 270 (1943)
Scabiosa tschiliensis var. breviseta	Hurus.	Bot. Mag. (Tokyo) 62: 44 1949
Scabiosa tschiliensis var. longiseta	Hurus.	Bot. Mag. (Tokyo) 62: 45 1949
Scabiosa japonica var. tschiliensis	(Grüning) Hurus.	J. Jap. Bot. 26(3): 90 1951
Scabiosa tschiliensis var. superba	(Grüning) S.Y.He	Fl. Reipubl. Popularis Sin. 73(1): 81 (1986):.
Scabiosa superba f. nana	Grüning	Repert. Spec. Nov. Regni Veg. 12(325–330): 310 1913
Scabiosa togashiana	Hurus.	Bot. Mag. (Tokyo) 62: 43 (1949)
Scabiosa tschiliensis f. alpina	(Nakai) W.Lee	Lineamenta Florae Koreae 1057. 1996
Scabiosa comosa f. albiflora	S.H.Li & S.Z.Liu	Bull. Bot. Res., Harbin 25(2): 135. 2005 [Apr 2005]

Common names Top

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Language	Common/alternative name
Persian	اسکابیوسا کوموسا
Chinese	华北蓝盆花
Chinese	山萝卜
Chinese	窄叶蓝盆花
Chinese	蒙古山萝卜
Chinese	蓝盆花
Chinese	细叶山萝卜

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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 Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Korea
- Mongolia
  - Mongolia
- Siberia
  - Buryatiya
  - Chita
  - Irkutsk

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001046403
Tropicos	11200175
KEW	urn:lsid:ipni.org:names:319797-1
The Plant List	tro-11200175
Open Tree Of Life	984352
Observations.org	121929
NCBI Taxonomy	1161150
IPNI	319797-1
iNaturalist	503001
GBIF	7301113
EOL	5234698
Elurikkus	7080
USDA GRIN	402939
CMAUP	NPO14327

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

Luteolin Alleviates Liver Fibrosis in Rat Hepatic Stellate Cell HSC-T6: A Proteomic Analysis

Batudeligen, Han Z, Chen H, Narisu, Xu Y, Anda, Han G

Drug Des Devel Ther

17-Jun-2023

PMCID:	PMC10285022
doi:	10.2147/DDDT.S402864
PMID:	37360572

Inhibitory Effects of Mongolian Medicine Yihe-Tang on Continuous Darkness Induced Liver Steatosis in Zebrafish

Sa R, Feng C, Bai H, Yin X, Song L, Hu X, Xu R, Li X, Dong W, Yang J

Evid Based Complement Alternat Med

20-May-2022

PMCID:	PMC9142287
doi:	10.1155/2022/5794655
PMID:	35646144

Treatment of Liver Cancer: Role of the Traditional Mongolian Medicine

Bao X, Chen L, Liu Y, Sheng H, Wang K, Luo Y, Qin T, Liu Y, Qiu Y

Evid Based Complement Alternat Med

14-Feb-2022

PMCID:	PMC8860509
doi:	10.1155/2022/6535977
PMID:	35198036

Potential Mechanisms Involved in the Protective Effect of Dicaffeoylquinic Acids from Artemisia annua L. Leaves against Diabetes and Its Complications

El-Askary H, Salem HH, Abdel Motaal A

Molecules

27-Jan-2022

PMCID:	PMC8839821
doi:	10.3390/molecules27030857
PMID:	35164118

Lineage-Specific Variation in IR Boundary Shift Events, Inversions, and Substitution Rates among Caprifoliaceae s.l. (Dipsacales) Plastomes

Park S, Jun M, Park S, Park S

Int J Mol Sci

28-Sep-2021

PMCID:	PMC8508905
doi:	10.3390/ijms221910485
PMID:	34638831

Chemical compositions by using LC–MS/MS and GC–MS and antioxidant activities of methanolic extracts from leaf and flower parts of Scabiosa columbaria subsp. columbaria var. columbaria L.

Akar Z

Saudi J Biol Sci

17-Jul-2021

PMCID:	PMC8568819
doi:	10.1016/j.sjbs.2021.07.039
PMID:	34764779

Network-based modeling of herb combinations in traditional Chinese medicine

Wang Y, Yang H, Chen L, Jafari M, Tang J

Brief Bioinform

08-Apr-2021

PMCID:	PMC8425426
doi:	10.1093/bib/bbab106
PMID:	33834186

Systematic profiling of the effective ingredients and mechanism of Scabiosa comosa and S. tschilliensis against hepatic fibrosis combined with network pharmacology

Chen Q, Wang Y, Ma F, Han M, Wang Z, Xue P, Lu J

Sci Rep

28-Jan-2021

PMCID:	PMC7843997
doi:	10.1038/s41598-021-81399-x
PMID:	33510287

Botanical and Genetic Identification Followed by Investigation of Chemical Composition and Biological Activities on the Scabiosa atropurpurea L. Stem from Tunisian Flora

Hrichi S, Chaabane-Banaoues R, Bayar S, Flamini G, Oulad El Majdoub Y, Mangraviti D, Mondello L, El Mzoughi R, Babba H, Mighri Z, Cacciola F

Molecules

29-Oct-2020

PMCID:	PMC7684468
doi:	10.3390/molecules25215032
PMID:	33138334

Scabiosa Genus: A Rich Source of Bioactive Metabolites

Pinto DC, Rahmouni N, Beghidja N, Silva AM

Medicines (Basel)

09-Oct-2018

PMCID:	PMC6313729
doi:	10.3390/medicines5040110
PMID:	30304864

Variation of active constituents and antioxidant activity in Scabiosa tschiliensis Grunning from different stages

Wang J, Liu K, Li X, Bi K, Zhang Y, Huang J, Zhang R

J Food Sci Technol

12-Jun-2017

PMCID:	PMC5502020
doi:	10.1007/s13197-017-2666-9
PMID:	28740285

Hepato-protective effects and chemical constituents of a bioactive fraction of the traditional compound medicine-Gurigumu-7

Xu H, Ma Q, Ma J, Wu Z, Wang Y, Ma C

BMC Complement Altern Med

13-Jun-2016

PMCID:	PMC4906903
doi:	10.1186/s12906-016-1156-3
PMID:	27296281

Coumarins of the epigeal part of Scabiosa comosa

T. D. Dargaeva, L. I. Brutko

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00567814

Hentriacontane fromScabiosa comosa

T. D. Dargaeva, L. I. Brutko

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00564813

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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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	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	436.80	unknown	https://doi.org/10.1007/BF00564813
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin	91458	Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O	346.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Umbelliprenin	1781413	Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C	366.50	unknown	https://doi.org/10.1007/BF00567814 https://doi.org/10.1007/BF00564813
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aS,6bR,8aR,10S,12aR,12bR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carboxylic acid	7163172	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
alpha-Amyrin palmitate	10394654	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C	665.10	unknown	via CMAUP database
Neochlorogenin	12303066	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1	432.60	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate	3698251	Click to see C(C(=O)[O-])[OH2+]	76.05	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)Glc(b1-2b)Fruf	44420456	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O	504.40	unknown	via CMAUP database
Stachyose	439531	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O	666.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine	190	Click to see C1=NC2=NC=NC(=C2N1)N	135.13	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-[(E)-3-(beta-D-glucopyranosyloxy)-1-propenyl]-7-methoxy-2,3-dihydrobenzofuran-3beta-methanol	11027727	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CCOC4C(C(C(C(O4)CO)O)O)O	520.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3R,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate	110062419	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
Calceolarioside A	5273566	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O	478.40	unknown	via CMAUP database
Calceolarioside B	5273567	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
Hellicoside	5281778	Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(OC(C(C2OC3C(C(C(C(O3)CO)O)O)O)O)OCC(C4=CC(=C(C=C4)O)O)O)CO)O)O	656.60	unknown	via CMAUP database
Isoacteoside	6476333	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
Isomartynoside	91895373	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)OC)O)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)O	652.60	unknown	via CMAUP database
Leucosceptoside A	10394343	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	638.60	unknown	via CMAUP database
Martynoside	5319292	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O	652.60	unknown	via CMAUP database
Plantainoside A	5320625	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	478.40	unknown	via CMAUP database
Plantainoside B	9847922	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O	478.40	unknown	via CMAUP database
Plantamajoside	5281788	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	640.60	unknown	via CMAUP database
Plantasioside	44423103	Click to see C1C(OC2C(C(C(OC2O1)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)C4=CC(=C(C=C4)O)O	476.40	unknown	via CMAUP database
Sanangoside	6915840	Click to see C1=CC(=C(C=C1CCOC2C(C(C(C(O2)CO)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O	478.40	unknown	via CMAUP database
Scroside B	9831187	Click to see COC1=C(C=C(C=C1)CCOC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	668.60	unknown	via CMAUP database
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin	323	Click to see C1=CC=C2C(=C1)C=CC(=O)O2	146.14	unknown	https://doi.org/10.1007/BF00564813
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1007/BF00564813 https://doi.org/10.1007/BF00567814
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Plantagoside	174157	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O	466.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	53384378	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)O	608.50	unknown	via CMAUP database
Homoplantaginin	5318083	Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	462.40	unknown	via CMAUP database
Plantaginin	5320623	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database

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Scabiosa comosa

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