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Erycibe obtusifolia

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64402360bdaf7505716421
Scientific name Erycibe obtusifolia
Authority Benth.
First published in Fl. Hongk. : 236 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Erycibe boniana Gagnep. Notul. Syst. (Paris) 3: 137 (1915)
Erycibe versatilihirta C.Y.Ma Acta Bot. Yunnan. 7: 91 (1985)

Common names Top

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Language Common/alternative name
Chinese 丁公藤
Chinese 斑鱼烈
Chinese 麻辣仔藤

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000747936
Tropicos 8502765
KEW urn:lsid:ipni.org:names:267907-1
The Plant List kew-2902014
Open Tree Of Life 5760414
NCBI Taxonomy 1603722
IPNI 267907-1
GBIF 3679474
EOL 2893160
CMAUP NPO29271

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
Quinic acid regulated TMA/TMAO-related lipid metabolism and vascular endothelial function through gut microbiota to inhibit atherosclerotic Jin Q, Zhang C, Chen R, Jiang L, Li H, Wu P, Li L J Transl Med 15-Apr-2024
PMCID:PMC11017595
doi:10.1186/s12967-024-05120-y
PMID:38622667
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
Prevention and Potential Treatment Strategies for Respiratory Syncytial Virus Sun BW, Zhang PP, Wang ZH, Yao X, He ML, Bai RT, Che H, Lin J, Xie T, Hui Z, Ye XY, Wang LW Molecules 25-Jan-2024
PMCID:PMC10856762
doi:10.3390/molecules29030598
PMID:38338343
Toxic Potential of Crude Extract From Cassava Cortex Containing Scopoletin and Cyanide on Wistar Rats and Broilers Njankouo YN, Nyegue MA, Njingou I, Moundipa PF, Mounjouenpou P Dose Response 22-Sep-2023
PMCID:PMC10517615
doi:10.1177/15593258231203587
PMID:37744654
Phytocompounds as a source for the development of new drugs to treat respiratory viral infections Seibert JB, Amparo TR, Almeida TC, de Souza GH, dos Santos OD 23-May-2023
PMCID:PMC10204935
doi:10.1016/B978-0-323-91294-5.00007-5
The genus Porana (Convolvulaceae) - A phytochemical and pharmacological review Peng Y, Li Y, Yang Y, Gao Y, Ren H, Hu J, Cui X, Lu W, Tao H, Chen Z Front Pharmacol 18-Oct-2022
PMCID:PMC9622789
doi:10.3389/fphar.2022.998965
PMID:36330088
Regulatory Effects of Lycium barbarum Extract and Isolated Scopoletin on Atopic Dermatitis-Like Skin Inflammation Bak SG, Lim HJ, Won YS, Lee S, Cheong SH, Lee SJ, Bae EY, Lee SW, Lee SJ, Rho MC Biomed Res Int 15-Sep-2022
PMCID:PMC9499794
doi:10.1155/2022/2475699
PMID:36158872
De novo assembly of the complete mitochondrial genome of sweet potato (Ipomoea batatas [L.] Lam) revealed the existence of homologous conformations generated by the repeat-mediated recombination Yang Z, Ni Y, Lin Z, Yang L, Chen G, Nijiati N, Hu Y, Chen X BMC Plant Biol 10-Jun-2022
PMCID:PMC9185937
doi:10.1186/s12870-022-03665-y
PMID:35681138
DNA Barcoding Medicinal Plant Species from Indonesia Cahyaningsih R, Compton LJ, Rahayu S, Magos Brehm J, Maxted N Plants (Basel) 21-May-2022
PMCID:PMC9147630
doi:10.3390/plants11101375
PMID:35631799
Investigating the anti-inflammatory and analgesic properties of leaves ethanolic extracts of Cedruslibani and Pinusbrutia Karrat L, Abajy MY, Nayal R Heliyon 05-Apr-2022
PMCID:PMC9006851
doi:10.1016/j.heliyon.2022.e09254
PMID:35434396
Investigation of the active ingredients and pharmacological mechanisms of Porana sinensis Hemsl. Against rheumatoid arthritis using network pharmacology and experimental validation Hu J, Zhao L, Li N, Yang Y, Qu T, Ren H, Cui X, Tao H, Chen Z, Peng Y PLoS One 02-Mar-2022
PMCID:PMC8890728
doi:10.1371/journal.pone.0264786
PMID:35235611
The Role of Medicinal and Aromatic Plants against Obesity and Arthritis: A Review Paul AK, Jahan R, Paul A, Mahboob T, Bondhon TA, Jannat K, Hasan A, Nissapatorn V, Wilairatana P, de Lourdes Pereira M, Wiart C, Rahmatullah M Nutrients 25-Feb-2022
PMCID:PMC8912584
doi:10.3390/nu14050985
PMID:35267958
Unprecedented organelle genomic variations in morning glories reveal independent evolutionary scenarios of parasitic plants and the diversification of plant mitochondrial complexes Lin Y, Li P, Zhang Y, Akhter D, Pan R, Fu Z, Huang M, Li X, Feng Y BMC Biol 16-Feb-2022
PMCID:PMC8851834
doi:10.1186/s12915-022-01250-1
PMID:35172831
Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS Molecules 14-Oct-2021
PMCID:PMC8537559
doi:10.3390/molecules26206197
PMID:34684782
Molecular Basis of Prostate Cancer and Natural Products as Potential Chemotherapeutic and Chemopreventive Agents Bai B, Chen Q, Jing R, He X, Wang H, Ban Y, Ye Q, Xu W, Zheng C Front Pharmacol 23-Sep-2021
PMCID:PMC8495205
doi:10.3389/fphar.2021.738235
PMID:34630112

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol 1152279 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O 327.40 unknown via CMAUP database
> Alkaloids and derivatives / Tropane alkaloids
[(1R,5R,6S)-2-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-6-yl] acetate 5317195 Click to see CC(=O)OC1CC2C(CCC1N2C)O 199.25 unknown via CMAUP database
Bao gong teng A 156282 Click to see CC(=O)OC1CC2C(CCC1N2)O 185.22 unknown https://doi.org/10.1358/DOF.1988.013.10.70090
Erycibelline 129917 Click to see C1CC(C2C(CC1N2)O)O 143.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Coumarinolignans
(2S)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-5-methoxy-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one 5315965 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.001
CID 335652 335652 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/10.1016/J.PHYTOCHEM.2007.05.001
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/10.1016/J.PHYTOCHEM.2007.05.001
Cleomiscosin B 156875 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(C=C4C=CC(=O)OC4=C3O2)OC)CO)O 386.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.001
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3,4-Dicaffeoyl quinic acid 10324242 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
4,5-Dicaffeoyl quinic acid 13887346 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
Chlorogenic Acid 1794427 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
Chlorogensaure 12310830 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
cis-Chlorogenic acid 1794425 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
Cryptochlorogenic acid 9798666 Click to see C1C(C(C(CC1(C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O 354.31 unknown via CMAUP database
Isochlorogenic acid A 6474310 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown via CMAUP database
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
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(1R,3R,4R,5R)-3,4-bis[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy]-5-hydroxy-1-methylcyclohexane-1-carboxylic acid 53486249 Click to see CC1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O)C(=O)O 514.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydrochromen-2-one 11953803 Click to see COC1=C(C=C2C(=C1)CCC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 356.32 unknown via CMAUP database
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/10.1016/J.PHYTOCHEM.2007.05.001
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.05.001
https://doi.org/10.1055/S-2005-837789
https://doi.org/10.1111/J.1399-6576.1996.TB04434.X

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