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Inula hupehensis

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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 UUID643fcee0365c6009718572
Scientific name Inula hupehensis
Authority (Y.Ling) Y.Ling
First published in Acta Phytotax. Sin. 16(3): 82. 1978; et in Fl. Re

Description Top

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Synonyms Top

Scientific name Authority First published in
Inula helianthusaquatilis subsp. hupehensis Ling Acta Phytotaxonomica Sinica 10(2): 178-179 1965

Common names Top

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Language Common/alternative name
Chinese 水朝阳根
Chinese 湖北旋覆花’（湖北朝阳花）
Chinese 湖北旋覆花

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-0000085343
Tropicos 50055855
KEW urn:lsid:ipni.org:names:225932-1
The Plant List gcc-41753
Open Tree Of Life 7051735
NCBI Taxonomy 1805964
IPNI 225932-1
iNaturalist 1123446
GBIF 3148438
CMAUP NPO4280

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
Chloroplast genome analysis and evolutionary insights in the versatile medicinal plant Calendula officinalis L. Zhang N, Huang K, Xie P, Deng A, Tang X, Jiang M, Mo P, Yin H, Huang R, Liang J, He F, Liu Y, Hu H, Wang Y Sci Rep 26-Apr-2024
PMCID:PMC11053094
doi:10.1038/s41598-024-60455-2
PMID:38671173
Lactucin Synthase Inactivation Boosts the Accumulation of Anti-inflammatory 8-Deoxylactucin and Its Derivatives in Chicory (Cichorium intybus L.) Cankar K, Hakkert JC, Sevenier R, Papastolopoulou C, Schipper B, Baixinho JP, Fernández N, Matos MS, Serra AT, Santos CN, Vahabi K, Tissier A, Bundock P, Bosch D J Agric Food Chem 10-Apr-2023
PMCID:PMC10119987
doi:10.1021/acs.jafc.2c08959
PMID:37036799
CRISPR/Cas9 targeted inactivation of the kauniolide synthase in chicory results in accumulation of costunolide and its conjugates in taproots Cankar K, Hakkert JC, Sevenier R, Campo E, Schipper B, Papastolopoulou C, Vahabi K, Tissier A, Bundock P, Bosch D Front Plant Sci 29-Aug-2022
PMCID:PMC9465254
doi:10.3389/fpls.2022.940003
PMID:36105709
Phylogenetic relationship and characterization of the complete chloroplast genome of Laggera crispata, a folk herbal medicine plant in China Zhou Z, Pu T, Duan B, Zhang M Mitochondrial DNA B Resour 28-Jun-2022
PMCID:PMC9246031
doi:10.1080/23802359.2022.2087553
PMID:35783060
Anti-Inflammatory and Immunoregulatory Action of Sesquiterpene Lactones Paço A, Brás T, Santos JO, Sampaio P, Gomes AC, Duarte MF Molecules 08-Feb-2022
PMCID:PMC8839508
doi:10.3390/molecules27031142
PMID:35164406
Retinoid X Receptor: Cellular and Biochemical Roles of Nuclear Receptor with a Focus on Neuropathological Involvement Sharma S, Shen T, Chitranshi N, Gupta V, Basavarajappa D, Sarkar S, Mirzaei M, You Y, Krezel W, Graham SL, Gupta V Mol Neurobiol 11-Jan-2022
PMCID:PMC9015987
doi:10.1007/s12035-021-02709-y
PMID:35015251
Monoterpenes and Their Derivatives—Recent Development in Biological and Medical Applications Zielińska-Błajet M, Feder-Kubis J Int J Mol Sci 25-Sep-2020
PMCID:PMC7582973
doi:10.3390/ijms21197078
PMID:32992914
Mikania micrantha genome provides insights into the molecular mechanism of rapid growth Liu B, Yan J, Li W, Yin L, Li P, Yu H, Xing L, Cai M, Wang H, Zhao M, Zheng J, Sun F, Wang Z, Jiang Z, Ou Q, Li S, Qu L, Zhang Q, Zheng Y, Qiao X, Xi Y, Zhang Y, Jiang F, Huang C, Liu C, Ren Y, Wang S, Liu H, Guo J, Wang H, Dong H, Peng C, Qian W, Fan W, Wan F Nat Commun 17-Jan-2020
PMCID:PMC6969026
doi:10.1038/s41467-019-13926-4
PMID:31953413
Bigelovin inhibits STAT3 signaling by inactivating JAK2 and induces apoptosis in human cancer cells Zhang HH, Kuang S, Wang Y, Sun XX, Gu Y, Hu LH, Yu Q Acta Pharmacol Sin 26-Jan-2015
PMCID:PMC4387296
doi:10.1038/aps.2014.143
PMID:25619393
Pseudoguaianolides and guaianolides from Inula hupehensis as potential anti-inflammatory agents. Qin JJ, Zhu JX, Zeng Q, Cheng XR, Zhu Y, Zhang SD, Shan L, Jin HZ, Zhang WD J Nat Prod 23-Sep-2011
doi:10.1021/NP200319X
PMID:21894898
Antimicrobial activities of some thymol derivatives from the roots of Inula hupehensis Jie Zhao, Ya Li, Quan Liu, Kun Gao Elsevier BV 22-Oct-2009
doi:10.1016/J.FOODCHEM.2009.10.045
Cytotoxicity and NMR spectral assignments of ergolide and bigelovin. Wang Q, Zhou BN, Zhang RW, Lin YY, Lin LZ, Gil RR, Cordell GA Planta Med 01-Apr-1996
doi:10.1055/S-2006-957843
PMID:8657753

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 / Benzylethers
2-(2-Hydroxy-4-methylphenyl)-2-methoxypropane-1,3-diol 101498009 Click to see CC1=CC(=C(C=C1)C(CO)(CO)OC)O 212.24 unknown https://doi.org/10.1016/J.FOODCHEM.2009.10.045
> Benzenoids / Phenol esters
[(2R)-2-[4-methyl-2-(2-methylpropanoyloxy)phenyl]oxiran-2-yl]methyl 2-methylpropanoate 25837754 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1016/J.FOODCHEM.2009.10.045
Bis(2-methylpropanoyloxy)-9,10-epoxy-p-mentha-1,3,5-triene 11472669 Click to see CC1=CC(=C(C=C1)C2(CO2)COC(=O)C(C)C)OC(=O)C(C)C 320.40 unknown https://doi.org/10.1016/J.FOODCHEM.2009.10.045
> Benzenoids / Phenols / Cresols / Meta cresols
2-(2-Hydroxy-4-methylphenyl)propane-1,2,3-triol 14543617 Click to see CC1=CC(=C(C=C1)C(CO)(CO)O)O 198.22 unknown https://doi.org/10.1016/J.FOODCHEM.2009.10.045
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
(1R,5R,6S,7S,8S,10R,11S)-6-hydroxy-4-oxopseudoguai-2(3)-en-12,8-olide 15558960 Click to see CC1CC2C(C(C(=O)O2)C)C(C3(C1C=CC3=O)C)O 264.32 unknown https://doi.org/10.1021/NP200319X
(1S,2R,5R,6S,7R,8S,10R)-6-acetoxy-2-methoxy-4-oxopseudoguai-11(13)-en-12,8-olide 54669754 Click to see CC1CC2C(C(C3(C1C(CC3=O)OC)C)OC(=O)C)C(=C)C(=O)O2 336.40 unknown https://doi.org/10.1021/NP200319X
(1S,2R,5R,6S,7S,8S,10R)-6-hydroxy-2-ethoxy-4-oxopseudoguai-11(13)-en-12,8-olide 54669753 Click to see CCOC1CC(=O)C2(C1C(CC3C(C2O)C(=C)C(=O)O3)C)C 308.40 unknown https://doi.org/10.1021/NP200319X
(1S,2R,5R,6S,7S,8S,10R)-6-hydroxy-2-methoxy-4-oxopseudoguai-11(13)-en-12,8-olide 54671716 Click to see CC1CC2C(C(C3(C1C(CC3=O)OC)C)O)C(=C)C(=O)O2 294.34 unknown https://doi.org/10.1021/NP200319X
(1S,2S,5R,6S,7R,8S,10R)-6-acetoxy-2-methoxy-4-oxopseudoguai-11(13)-en-12,8-olide 54669755 Click to see CC1CC2C(C(C3(C1C(CC3=O)OC)C)OC(=O)C)C(=C)C(=O)O2 336.40 unknown https://doi.org/10.1021/NP200319X
(1S,5R,6S,7S,8S,10R,11R)-6-hydroxy-4-oxopseudoguai-12,8-olide 54671717 Click to see CC1CC2C(C(C(=O)O2)C)C(C3(C1CCC3=O)C)O 266.33 unknown https://doi.org/10.1021/NP200319X
[(3aS,5S,5aS,8aR,9S,9aS)-8-acetyloxy-9-hydroxy-5,8a-dimethyl-1-methylidene-2-oxo-4,5,5a,6,7,8,9,9a-octahydro-3aH-azuleno[6,5-b]furan-6-yl] acetate 44457222 Click to see CC1CC2C(C(C3(C1C(CC3OC(=O)C)OC(=O)C)C)O)C(=C)C(=O)O2 366.40 unknown https://doi.org/10.1021/NP200319X
8-Epihelenalin 10400473 Click to see CC1CC2C(C(C3(C1C=CC3=O)C)O)C(=C)C(=O)O2 262.30 unknown https://doi.org/10.1021/NP200319X
Bigelovin 3080597 Click to see CC1CC2C(C(C3(C1C=CC3=O)C)OC(=O)C)C(=C)C(=O)O2 304.34 unknown https://doi.org/10.1055/S-2006-957843
https://doi.org/10.1021/NP200319X
Carpesiolin 10015663 Click to see CC1CC2C(C(C3(C1CCC3=O)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/NP200319X
Ergolide 185786 Click to see CC1CC2C(C(C3(C1CCC3=O)C)OC(=O)C)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1055/S-2006-957843
https://doi.org/10.1021/NP200319X
Sesquiterpene lactone TS-6 325797 Click to see CC1CC2C(C(C3(C1CCC3=O)C)O)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/NP200319X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(1R,5R,6S,7R,8S,10R)-8-hydroxy-4-oxopseudoguai-2(3),11(13)-dien-12,6-olide 54671714 Click to see CC1CC(C2C(C3(C1C=CC3=O)C)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1021/NP200319X
(1S,5S,7R,8S,10R)-14-acetoxy-4-oxopseudoguai-11(13)-en-12,8-olide 54671715 Click to see CC(=O)OCC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1021/NP200319X
Aromaticin 282529 Click to see CC1CC2C(CC3(C1C=CC3=O)C)C(=C)C(=O)O2 246.30 unknown https://doi.org/10.1021/NP200319X
Burrodin 177140 Click to see CC1CC2C(CC3(C1C(CC3=O)O)C)C(=C)C(=O)O2 264.32 unknown https://doi.org/10.1021/NP200319X
Confertin 167852 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown via CMAUP database
Graveolide 11043090 Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1021/NP200319X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,5aS,8S,8aR,9aR)-8-hydroxy-5,8-dimethyl-1-methylidene-5a,6,7,8a,9,9a-hexahydro-3aH-azuleno[6,5-b]furan-2-one 46906382 Click to see CC1=CC2C(CC3C1CCC3(C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1021/NP200319X
2alpha-acetoxy-4alpha,6alpha-dihydroxy-1beta,5alphaH-guai-9(10),11(13)-dien-12,8alpha-olide 54671718 Click to see CC1=CC2C(C(C3C1C(CC3(C)O)OC(=O)C)O)C(=C)C(=O)O2 322.40 unknown https://doi.org/10.1021/NP200319X
4-Epi-Isoinuviscolide 53320574 Click to see CC1=CC2C(CC3C1CCC3(C)O)C(=C)C(=O)O2 248.32 unknown https://doi.org/10.1021/NP200319X
6Alpha-Acetoxyisoinuviscolide 57399052 Click to see CC1=CC2C(C(C3C1CCC3(C)O)OC(=O)C)C(=C)C(=O)O2 306.40 unknown https://doi.org/10.1021/NP200319X
8-Epiinuviscolide 13817985 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1021/NP200319X
Inuviscolide 176489 Click to see CC1(CCC2C1CC3C(CC2=C)OC(=O)C3=C)O 248.32 unknown https://doi.org/10.1021/NP200319X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2S)-2-(2-hydroxy-4-methylphenyl)propoxy]oxane-3,4,5-triol 162847777 Click to see CC1=CC(=C(C=C1)C(C)COC2C(C(C(C(O2)CO)O)O)O)O 328.36 unknown https://doi.org/10.1016/J.FOODCHEM.2009.10.045
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
(2S,3R,4S,5R,6R)-6-[(1R)-1,2-dihydroxyethyl]oxane-2,3,4,5-tetrol 102191387 Click to see C(C(C1C(C(C(C(O1)O)O)O)O)O)O 210.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
alpha-Tyvelopyranose 448819 Click to see CC1C(CC(C(O1)O)O)O 148.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
4beta,10alpha-dihydroxy-5alphaH-guai-1(2),11(13)-dien-12,8alpha-olide 50941544 Click to see CC1(CC=C2C1CC3C(CC2(C)O)OC(=O)C3=C)O 264.32 unknown https://doi.org/10.1021/NP200319X
Inuchinenolide B 57399053 Click to see CC1=C2C(CC3C(C1)OC(=O)C3=C)C(CC2OC(=O)C)(C)O 306.40 unknown https://doi.org/10.1021/NP200319X

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