Scientific name	Authority	First published in
Rubia chinensis var. esquirolii	(H.Lév.) H.Lév.	Cat. Pl. Yun-Nan 248. 1917
Rubia cordifolia var. maillardii	(H.Lév. & Vaniot) H.Lév.	Fl. Kouy-Tcheou 371. 1915
Rubia esquirolii	H.Lév.	Repert. Spec. Nov. Regni Veg. 10: 439 (1912)
Rubia leiocaulis	Diels	Notes Roy. Bot. Gard. Edinburgh 5: 277 (1912)
Rubia maillardii	H.Lév. & Vaniot	Bull. Soc. Bot. France 51: 145 (1907)
Rubia schumanniana var. maillardii	(H.Lév. & Vaniot) Hand.-Mazz.	Sinensia 5: 22. 1934
Rubia cordifolia var. leiocaulis	Franch. ex Diels	Notes Roy. Bot. Gard. Edinburgh 5: 277. 1912

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	大叶茜草
Chinese	小红藤
Chinese	咸洒
Chinese	四能草
Chinese	四轮筋骨草
Chinese	女儿红
Chinese	小红参
Chinese	灯儿草
Chinese	紫脉茜草
Chinese	红血儿
Chinese	茜草

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 South-central

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000298615
Tropicos	50001658
KEW	urn:lsid:ipni.org:names:765350-1
The Plant List	kew-180403
Open Tree Of Life	3872694
NCBI Taxonomy	1650718
IPNI	765350-1
GBIF	2892296
EOL	1107265
CMAUP	NPO14581

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

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

Stewartiacids A–N, C-23 carboxylated triterpenoids from Chinese Stewartia and their inhibitory effects against ATP-citrate lyase and NF-κB

Wan J, Zang Y, Xiao DA, Li N, Li J, Jin ZX, Chen DL, Xiong J, Li J, Hu JF

RSC Adv

21-Jan-2020

PMCID:	PMC9048753
doi:	10.1039/c9ra09542j
PMID:	35497717

Secondary Metabolites from Rubiaceae Species

Martins D, Nunez CV

Molecules

22-Jul-2015

PMCID:	PMC6331836
doi:	10.3390/molecules200713422
PMID:	26205062

Naturally Occurring Anthraquinones: Chemistry and Therapeutic Potential in Autoimmune Diabetes

Chien SC, Wu YC, Chen ZW, Yang WC

Evid Based Complement Alternat Med

18-Mar-2015

PMCID:	PMC4381678
doi:	10.1155/2015/357357
PMID:	25866536

Three new triterpenoids from Rubia schumanniana

Kuang B, Han J, Zeng GZ, Chen XQ, He WJ, Tan NH

Nat Prod Bioprospect

12-Jul-2012

PMCID:	PMC4131627
doi:	10.1007/s13659-012-0038-8

Digiferruginol glycoside from the roots of Rubia schumanniana

Liu Yong-Long, Chen Bi-Zhu, Bai Yi-Li, Helmut Duddeck, Monika Hiegemann

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(91)85285-8

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 / Anthracenes / Anthraquinones
1-hydroxy-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]anthracene-9,10-dione	14890486	Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)COC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O	578.50	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
1-Hydroxy-2-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxymethyl]anthracene-9,10-dione	14890485	Click to see	578.50	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-(7-hydroxy-4-methoxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate	162851261	Click to see	634.60	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
[3,4-Dihydroxy-6-(7-hydroxy-4-methoxy-3-methyl-9,10-dioxoanthracen-2-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate	162851260	Click to see	634.60	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-hydroxy-1-methoxy-2-methylanthracene-9,10-dione	163185819	Click to see	592.50	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-6-hydroxy-1-methoxy-2-methylanthracene-9,10-dione	162986524	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)C(=O)C5=C(C4=O)C=CC(=C5)O)OC)C)CO)O)O)O)O)O	592.50	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-15-(3-methylbut-2-enoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	101618866	Click to see	400.50	unknown	via CMAUP database
(1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-15-(3-methylbutanoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	101618868	Click to see	402.60	unknown	via CMAUP database
(1R,4S,5R,9S,10S,13R,15S)-5,9-dimethyl-15-[(Z)-2-methylbut-2-enoyl]oxy-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	13969122	Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C	400.50	unknown	via CMAUP database
(4R)-15alpha-(Tigloyloxy)-kaura-16-ene-19-oic acid	101618867	Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C	400.50	unknown	via CMAUP database
[(1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-5,9,14-trimethyl-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate	102239831	Click to see	348.50	unknown	via CMAUP database
Ent-Kaurenal	443466	Click to see	286.50	unknown	via CMAUP database
Grandifloric acid	159930	Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O	318.40	unknown	via CMAUP database
Kaurenoic Acid	73062	Click to see	302.50	unknown	via CMAUP database
Kaurenol	443465	Click to see	288.50	unknown	via CMAUP database
Methyl ent-16beta,17-dihydroxy-9(11)-kauren-19-oate	46233508	Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(C4)(CO)O)(C)C(=O)OC	348.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Vicodiol	182938	Click to see	170.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene	12308843	Click to see	204.35	unknown	via CMAUP database
(1E,6Z)-gamma-humulene	24798696	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene	44583886	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Eudesmol	91457	Click to see	222.37	unknown	via CMAUP database
Beta-Selinene	442393	Click to see	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Denudanolide A	10618232	Click to see CC1C(C2C(=O)C(=CC1(OC2=O)OC)CC=C)C3=CC4=C(C=C3)OCO4	356.40	unknown	https://doi.org/10.1016/0031-9422(91)85285-8
> Organoheterocyclic compounds / Oxanes
[(2S,3R)-2-[(E)-non-1-en-3,5,7-triynyl]oxan-3-yl] acetate	11242289	Click to see CC#CC#CC#CC=CC1C(CCCO1)OC(=O)C	256.30	unknown	via CMAUP database
Ichthyothereol acetate	73759958	Click to see CC#CC#CC#CC=CC1CCCOC1OC(=O)C	256.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	5320668	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	via CMAUP database
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	via CMAUP database

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Rubia schumanniana

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top