Language	Common/alternative name
English	chinese-plumbago
German	chinesische bleiwurz
Russian	Цератостигма Уилмотта
Chinese	岷江蓝雪花人紫金莲）
Chinese	搬倒甑
Chinese	兴居茹马
Chinese	岷江蓝雪花
Chinese	扳倒甑
Chinese	紫金莲

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  - Tibet

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000596561
UNII	U8O5LNX3QT
USDA Plants	CEWI2
Tropicos	25400543
INPN	90232
KEW	urn:lsid:ipni.org:names:686560-1
The Plant List	kew-2711296
PFAF	Ceratostigma willmottianum
Open Tree Of Life	5143972
NCBI Taxonomy	2054445
IPNI	686560-1
iNaturalist	410981
GBIF	4089798
Freebase	/m/0pd9ht_
EPPO	CEGWL
EOL	2892132
USDA GRIN	9924
Wikipedia	Ceratostigma_willmottianum

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

The complete chloroplast genome of the medicinally important plant Plumbago zeylanica L. (plumbaginaceae) and phylogenetic analysis

Zhou H, Zhang H

Mitochondrial DNA B Resour

03-Apr-2024

PMCID:	PMC10993748
doi:	10.1080/23802359.2024.2333574
PMID:	38586506

Esculetin Alleviates Inflammation, Oxidative Stress and Apoptosis in Intestinal Ischemia/Reperfusion Injury via Targeting SIRT3/AMPK/mTOR Signaling and Regulating Autophagy

Shen X, Shi H, Chen X, Han J, Liu H, Yang J, Shi Y, Ma J

J Inflamm Res

23-Aug-2023

PMCID:	PMC10460583
doi:	10.2147/JIR.S413941
PMID:	37641705

An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta

Yao W, Kong L, Lei D, Zhao B, Tang H, Zhou X, Lin Y, Zhang Y, Wang Y, He W, Li M, Chen Q, Luo Y, Wang X, Tang H, Zhang Y

Front Plant Sci

31-Jul-2023

PMCID:	PMC10425222
doi:	10.3389/fpls.2023.1204267
PMID:	37583592

Epigenetic effects of herbal medicine

Wu YY, Xu YM, Lau AT

Clin Epigenetics

13-May-2023

PMCID:	PMC10183144
doi:	10.1186/s13148-023-01481-1
PMID:	37179342

Synergy, Additivity and Antagonism between Esculetin and Six Commonly Used Chemotherapeutics in Various Malignant Melanoma Cell Lines—An Isobolographic Analysis

Wróblewska-Łuczka P, Góralczyk A, Łuszczki JJ

Molecules

05-May-2023

PMCID:	PMC10180450
doi:	10.3390/molecules28093889
PMID:	37175299

Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health

Sun W, Shahrajabian MH

Molecules

15-Feb-2023

PMCID:	PMC9960276
doi:	10.3390/molecules28041845
PMID:	36838831

Proteomics of Salt Gland–Secreted Sap Indicates a Pivotal Role for Vesicle Transport and Energy Metabolism in Plant Salt Secretion

Lu C, Zhang Y, Mi P, Guo X, Wen Y, Han G, Wang B

Int J Mol Sci

11-Nov-2022

PMCID:	PMC9693062
doi:	10.3390/ijms232213885
PMID:	36430364

RNA-dependent RNA polymerase (RdRp) natural antiviral inhibitors: a review

Leite DR, Mantovani KM, Cordeiro SP, Maia FB, Betim FC, de Bona Sartor E, Montrucchio DP, de Fátima Gaspari Dias J, Miguel OG, Miguel MD

Med Chem Res

29-Sep-2022

PMCID:	PMC9520115
doi:	10.1007/s00044-022-02963-2
PMID:	36193545

Role of Nrf2 in Pancreatic Cancer

Cykowiak M, Krajka-Kuźniak V

Antioxidants (Basel)

30-Dec-2021

PMCID:	PMC8773052
doi:	10.3390/antiox11010098
PMID:	35052602

New Mechanisms of Action of Natural Antioxidants in Health and Disease II

Hrelia S, Angeloni C

Antioxidants (Basel)

27-Jul-2021

PMCID:	PMC8388864
doi:	10.3390/antiox10081200
PMID:	34439447

A Review on Anti-Tumor Mechanisms of Coumarins

Wu Y, Xu J, Liu Y, Zeng Y, Wu G

Front Oncol

04-Dec-2020

PMCID:	PMC7746827
doi:	10.3389/fonc.2020.592853
PMID:	33344242

Esculetin as a Bifunctional Antioxidant Prevents and Counteracts the Oxidative Stress and Neuronal Death Induced by Amyloid Protein in SH-SY5Y Cells

Pruccoli L, Morroni F, Sita G, Hrelia P, Tarozzi A

Antioxidants (Basel)

25-Jun-2020

PMCID:	PMC7346165
doi:	10.3390/antiox9060551
PMID:	32630394

Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury

Subramanya SB, Venkataraman B, Meeran MF, Goyal SN, Patil CR, Ojha S

Int J Mol Sci

28-Nov-2018

PMCID:	PMC6321362
doi:	10.3390/ijms19123776
PMID:	30486484

Yao herbal medicinal market during the Dragon Boat Festival in Jianghua County, China

Luo B, Liu Y, Liu B, Liu S, Zhang B, Zhang L, Lin C, Liu Y, Kennelly EJ, Guo Z, Long C

J Ethnobiol Ethnomed

17-Oct-2018

PMCID:	PMC6192344
doi:	10.1186/s13002-018-0260-5
PMID:	30333030

Esculetin induces antiproliferative and apoptotic response in pancreatic cancer cells by directly binding to KEAP1

Arora R, Sawney S, Saini V, Steffi C, Tiwari M, Saluja D

Mol Cancer

18-Oct-2016

PMCID:	PMC5069780
doi:	10.1186/s12943-016-0550-2
PMID:	27756327

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
> 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	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
> Benzenoids / Naphthalenes / Naphthoquinones
Plumbagin	10205	Click to see CC1=CC(=O)C2=C(C1=O)C=CC=C2O	188.18	unknown	https://doi.org/10.1021/NP970044U https://doi.org/10.1007/BF00568230
> Benzenoids / Phenols / Benzenediols / Catechols
(4S,5R)-5-(2,3-dihydroxyphenyl)-4-methyloxolan-2-one	10488568	Click to see CC1CC(=O)OC1C2=C(C(=CC=C2)O)O	208.21	unknown	https://doi.org/10.1021/NP970044U https://doi.org/10.1007/BF00568230
5-(2,3-Dihydroxyphenyl)-4-methyloxolan-2-one	85157427	Click to see CC1CC(=O)OC1C2=C(C(=CC=C2)O)O	208.21	unknown	https://doi.org/10.1021/NP970044U
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine	5280537	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
> Benzenoids / Tetralins
Isoshinanolone	443777	Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O	192.21	unknown	https://doi.org/10.1021/NP970044U https://doi.org/10.1007/BF00568230
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / N-acyl-alpha-hexosamines
Trichaspside C	146683400	Click to see CC1CC(OC2C1CCC(=C2)C)CC(C)OC3C(C(C(C(O3)CO)O)O)NC(=O)C	427.50	unknown	https://doi.org/10.1021/NP970044U
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(3R)-4-(2,3-dihydroxyphenyl)-3-methyl-4-oxobutanoic acid	92468470	Click to see CC(CC(=O)O)C(=O)C1=C(C(=CC=C1)O)O	224.21	unknown	https://doi.org/10.1007/BF00568230
(S)-4-Oxo-3-methyl-4-(2,3-dihydroxyphenyl)butyric acid	92468469	Click to see CC(CC(=O)O)C(=O)C1=C(C(=CC=C1)O)O	224.21	unknown	https://doi.org/10.1021/NP970044U
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
(3R)-3-[(1R,2S)-1,2-dihydroxypropyl]-6-hydroxy-3H-2-benzofuran-1-one	162942001	Click to see CC(C(C1C2=C(C=C(C=C2)O)C(=O)O1)O)O	224.21	unknown	https://doi.org/10.1021/NP970044U
(3S)-3-[(1S,2S)-1,2-dihydroxypropyl]-6-hydroxy-3H-2-benzofuran-1-one	162942000	Click to see CC(C(C1C2=C(C=C(C=C2)O)C(=O)O1)O)O	224.21	unknown	https://doi.org/10.1021/NP970044U
1(3H)-Isobenzofuranone, 3-(1,2-dihydroxypropyl)-6-hydroxy-	10775490	Click to see CC(C(C1C2=C(C=C(C=C2)O)C(=O)O1)O)O	224.21	unknown	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(3,4-Dihydroxyphenyl)-N-[2-(4-hydroxyphenyl)ethyl]prop-2-enamide	54408305	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O	299.32	unknown	https://doi.org/10.1021/NP970044U
N-Caffeoyltyramine	9994897	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O	299.32	unknown	https://doi.org/10.1021/NP970044U https://doi.org/10.1007/BF00568230
N-feruloyltyramine; Moupinamide	125213	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	https://doi.org/10.1021/NP970044U
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1021/NP970044U
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	https://doi.org/10.1021/NP970044U https://doi.org/10.1007/BF00568230
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF00568230 https://doi.org/10.1021/NP970044U
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP970044U
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	26339717	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP970044U
5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one	129010103	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP970044U

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Ceratostigma willmottianum

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