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Iostephane heterophylla

Iostephane heterophylla - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcd5fdb330324114183
Scientific name Iostephane heterophylla
Authority Benth.
First published in Gen. Pl. 2(1): 368 (1873)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ximenesia cavanillesii Spreng. Syst. Veg. 3: 605 (1826)
Iostephane heterophylla var. dicksonii W.M.Sharp Ann. Missouri Bot. Gard. 22: 82 (1935)
Echinacea heterophylla (Cav.) D.Don Brit. Fl. Gard. 4(ser. 2, 1): t. 32 (1830)
Brauneria heterophylla (Cav.) A.Lyons Pl. Nam. : 510 (1907)
Coreopsis heterophylla Cav. Icon. 3(2):34 (-35; t. 268) (1795)
Simsia heterophylla (Cav.) Pers. Syn. Pl. 2(2): 478 (1807)

Common names Top

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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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000071715
Tropicos 2706562
KEW urn:lsid:ipni.org:names:226210-1
The Plant List gcc-2848
Open Tree Of Life 808829
NCBI Taxonomy 1048901
IPNI 30198373-2
iNaturalist 288859
GBIF 3094872
USDA GRIN 408670
Wikipedia Iostephane_heterophylla

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 plastome sequences of invasive weed Parthenium hysterophorus: genome organization, evolutionary significance, structural features, and comparative analysis Lubna, Asaf S, Jan R, Asif S, Bilal S, Khan AL, Al-Rawahi AN, Kim KM, AL-Harrasi A Sci Rep 18-Feb-2024
PMCID:PMC10874969
doi:10.1038/s41598-024-54503-0
PMID:38369569
Comparative Analysis of a Secondary Metabolite Profile from Roots and Leaves of Iostephane heterophylla by UPLC-MS and GC-MS Navarrete-Carriola DV, Paz-González AD, Vázquez-Jiménez LK, De Luna-Santillana E, Cruz-Hernández MA, Bandyopadhyay D, Rivera G ACS Omega 25-Jan-2024
PMCID:PMC10851369
doi:10.1021/acsomega.3c06800
PMID:38343925
Anti-Diabesity Middle Eastern Medicinal Plants and Their Action Mechanisms Saad B, Kmail A, Haq SZ Evid Based Complement Alternat Med 18-Jul-2022
PMCID:PMC9313926
doi:10.1155/2022/2276094
PMID:35899227
Secondary Metabolites of Plants as Modulators of Endothelium Functions Bartáková A, Nováková M Int J Mol Sci 03-Mar-2021
PMCID:PMC7959468
doi:10.3390/ijms22052533
PMID:33802468
Extremely low nucleotide diversity among thirty-six new chloroplast genome sequences from Aldama (Heliantheae, Asteraceae) and comparative chloroplast genomics analyses with closely related genera Loeuille B, Thode V, Siniscalchi C, Andrade S, Rossi M, Pirani JR PeerJ 24-Feb-2021
PMCID:PMC7912680
doi:10.7717/peerj.10886
PMID:33665028
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Antidiabetic Potential of Medicinal Plants and Their Active Components Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J Biomolecules 30-Sep-2019
PMCID:PMC6843349
doi:10.3390/biom9100551
PMID:31575072
A Review of Endothelium-Dependent and -Independent Vasodilation Induced by Phytochemicals in Isolated Rat Aorta Knox M, Vinet R, Fuentes L, Morales B, Martínez JL Animals (Basel) 29-Aug-2019
PMCID:PMC6769919
doi:10.3390/ani9090623
PMID:31470540
Xanthorrhizol: a review of its pharmacological activities and anticancer properties Oon SF, Nallappan M, Tee TT, Shohaimi S, Kassim NK, Sa’ariwijaya MS, Cheah YH Cancer Cell Int 21-Oct-2015
PMCID:PMC4618344
doi:10.1186/s12935-015-0255-4
PMID:26500452
Evolutionary Origins of a Bioactive Peptide Buried within Preproalbumin Elliott AG, Delay C, Liu H, Phua Z, Rosengren KJ, Benfield AH, Panero JL, Colgrave ML, Jayasena AS, Dunse KM, Anderson MA, Schilling EE, Ortiz-Barrientos D, Craik DJ, Mylne JS Plant Cell 28-Mar-2014
PMCID:PMC4001405
doi:10.1105/tpc.114.123620
PMID:24681618
In Vitro Screening of Medicinal Plants Used in Mexico as Antidiabetics with Glucosidase and Lipase Inhibitory Activities Ramírez G, Zavala M, Pérez J, Zamilpa A Evid Based Complement Alternat Med 02-Oct-2012
PMCID:PMC3469274
doi:10.1155/2012/701261
PMID:23082084
An Antimicrobial Compound Isolated from Cinnamomum Iners Leaves with Activity against Methicillin-Resistant Staphylococcus Aureus Mustaffa F, Indurkar J, Ismail S, Shah M, Mansor SM Molecules 08-Apr-2011
PMCID:PMC6260600
doi:10.3390/molecules16043037
PMID:21478819
Chemical Transformation and Biological Studies of Marine Sesquiterpene (S)-(+)-Curcuphenol and Its Analogs Gul W, Hammond NL, Yousaf M, Peng J, Holley A, Hamann MT Biochim Biophys Acta 24-Jul-2007
PMCID:PMC2266081
doi:10.1016/j.bbagen.2007.05.011
PMID:17804167
Novel Bisabolene Glycoside and Other Constituents from the Roots of the Medicinal Plant<i>Iostephane heterophylla</i>(Asteraceae) Maria Isabel Aguilar, Guillermo Delgado Informa UK Limited 07-Jul-2007
doi:10.1080/10575639508043204
Bisabolenes, polycyclic diterpenoids and other constituents from the roots of Iostephane heterophylla María Isabel Aguilar, Guillermo Delgado, Robert Bye, Edelmira Linares Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85041-O

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 / Phenols / Cresols / Ortho cresols
2-Methyl-4-(6-methylhept-5-en-2-yl)phenol 21592241 Click to see CC1=C(C=CC(=C1)C(C)CCC=C(C)C)O 218.33 unknown https://doi.org/10.1021/NP010076O
2-methyl-4-[(2R)-6-methylhept-5-en-2-yl]phenol 10353348 Click to see CC1=C(C=CC(=C1)C(C)CCC=C(C)C)O 218.33 unknown https://doi.org/10.1021/NP010076O
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
ent-Beyer-15-en-19-oic acid 101607489 Click to see CC12CCC3C4(CCCC(C4CCC3(C1)C=C2)(C)C(=O)O)C 302.50 unknown https://doi.org/10.1021/NP010076O
https://doi.org/10.1016/0031-9422(93)85041-O
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4R,5S,9R,10S,12S,13S,14R)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid 101713119 Click to see CC12CCCC(C1CCC34C2CC5C(C3)C5(C4)C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
(1R,4S,5R,9S,10S,13R,15S)-15-Hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 159930 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(93)85041-O
(1S,4R,9R,10R,13S,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-en-14-ol 163011342 Click to see CC1(CCCC2(C1CCC34C2C=CC(C3)C(C4)(C)O)C)C 288.50 unknown https://doi.org/10.1021/NP010076O
(1S,4R,9R,10S,13R,14R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 162952054 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
(1S,4S,5R,9R,10R,13S,14R)-14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-5-carboxylic acid 163004419 Click to see CC12CCCC(C1CCC34C2C=CC(C3)C(C4)(C)O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(93)85041-O
(1S,4S,5R,9S,10R,12R,13R,14R)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid 163006936 Click to see CC12CCCC(C1CCC34C2CC5C(C3)C5(C4)C)(C)C(=O)O 302.50 unknown https://doi.org/10.1080/10575630108041265
(1S,4S,5S,9S,10R,12R,13R,14S)-5,9,13-trimethylpentacyclo[11.2.1.01,10.04,9.012,14]hexadecane-5-carboxylic acid 57376411 Click to see CC12CCCC(C1CCC34C2CC5C(C3)C5(C4)C)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP010076O
(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 https://doi.org/10.1016/0031-9422(93)85041-O
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP010076O
https://doi.org/10.1016/0031-9422(93)85041-O
15alpha-(Angeloyloxy)kaura-16-ene-18-oic acid 13969122 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 400.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
19-Trachylobanoic acid 14262763 Click to see CC12CCCC(C1CCC34C2CC5C(C3)C5(C4)C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
https://doi.org/10.1021/NP010076O
5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-en-14-ol 163011341 Click to see CC1(CCCC2(C1CCC34C2C=CC(C3)C(C4)(C)O)C)C 288.50 unknown https://doi.org/10.1021/NP010076O
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP010076O
https://doi.org/10.1016/0031-9422(93)85041-O
5,9-Dimethyl-15-(2-methylbut-2-enoyloxy)-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 434930 Click to see CC=C(C)C(=O)OC1C(=C)C2CCC3C1(C2)CCC4C3(CCCC4(C)C(=O)O)C 400.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
ent-Kauran-16-beta-ol 21593607 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown https://doi.org/10.1021/NP010076O
Ent-trachyloban-19-oic acid 23601154 Click to see CC12CCCC(C1CCC34C2CC5C(C3)C5(C4)C)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
Grandifloric acid 433554 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1016/0031-9422(93)85041-O
Kauran-16-ol 623309 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)C 290.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
https://doi.org/10.1021/NP010076O
Kaurenoic acid 73062 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1021/NP010076O
https://doi.org/10.1016/0031-9422(93)85041-O
methyl (1S,4S,5R,9R,10R,13S,14R)-14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-5-carboxylate 12967808 Click to see CC12CCCC(C1CCC34C2C=CC(C3)C(C4)(C)O)(C)C(=O)OC 332.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
Methyl 14-hydroxy-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadec-11-ene-5-carboxylate 162901408 Click to see CC12CCCC(C1CCC34C2C=CC(C3)C(C4)(C)O)(C)C(=O)OC 332.50 unknown https://doi.org/10.1016/0031-9422(93)85041-O
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6R)-6-(3-hydroxy-4-methylphenyl)-2-methylheptane-2,3-diol 131852964 Click to see CC1=C(C=C(C=C1)C(C)CCC(C(C)(C)O)O)O 252.35 unknown https://doi.org/10.1080/10575630108041265
2-Methyl-5-(6-methylhept-5-en-2-yl)phenol 520468 Click to see CC1=C(C=C(C=C1)C(C)CCC=C(C)C)O 218.33 unknown https://doi.org/10.1021/NP010076O
https://doi.org/10.1016/0031-9422(93)85041-O
5-(5-Hydroxy-6-methylhept-6-en-2-yl)-2-methylphenol 162934727 Click to see CC1=C(C=C(C=C1)C(C)CCC(C(=C)C)O)O 234.33 unknown https://doi.org/10.1016/0031-9422(93)85041-O
5-(6-Hydroxy-6-methylhept-4-en-2-yl)-2-methylphenol 163023193 Click to see CC1=C(C=C(C=C1)C(C)CC=CC(C)(C)O)O 234.33 unknown https://doi.org/10.1016/0031-9422(93)85041-O
5-[(2R,5R)-5-hydroxy-6-methylhept-6-en-2-yl]-2-methylphenol 162934728 Click to see CC1=C(C=C(C=C1)C(C)CCC(C(=C)C)O)O 234.33 unknown https://doi.org/10.1016/0031-9422(93)85041-O
5-[(2R)-4-(3,3-dimethyloxiran-2-yl)butan-2-yl]-2-methylphenol 162859202 Click to see CC1=C(C=C(C=C1)C(C)CCC2C(O2)(C)C)O 234.33 unknown https://doi.org/10.1080/10575630108041265
5-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-2-methylphenol 76285515 Click to see CC1=C(C=C(C=C1)C(C)CC=CC(C)(C)O)O 234.33 unknown https://doi.org/10.1016/0031-9422(93)85041-O
Xanthorrhizol 93135 Click to see CC1=C(C=C(C=C1)C(C)CCC=C(C)C)O 218.33 unknown https://doi.org/10.1016/0031-9422(93)85041-O
https://doi.org/10.1080/10575630108041265
https://doi.org/10.1021/NP010076O
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Arundinol C 71524403 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(C)(COC(=O)C)O 310.40 unknown https://doi.org/10.1016/0031-9422(93)85041-O
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3S,4R,5R)-2-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[(3R,5R)-2-hydroxy-6-(3-hydroxy-4-methylphenyl)-2,5-dimethylheptan-3-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 162928933 Click to see CC1=C(C=C(C=C1)C(C)C(C)CC(C(C)(C)O)OC2C(C(C(C(O2)CO)O)O)OC3C(C(C(CO3)O)O)O)O 560.60 unknown https://doi.org/10.1080/10575630108041265
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/10575639508043204
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/10575639508043204
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1080/10575639508043204
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1080/10575639508043204
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/10575639508043204
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(3R,4S,5S,6R)-2-(2-deuterioethyl)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol 141472729 Click to see CCC1(C(C(C(C(O1)CO)O)O)O)O 209.21 unknown https://doi.org/10.1080/10575639508043204
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
De-O-methylacetovanillochromene 11106833 Click to see CC(=O)C1=CC2=C(C(=C1)O)OC(C=C2)(C)C 218.25 unknown https://doi.org/10.1016/0031-9422(93)85041-O
> 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/10.1016/0031-9422(93)85041-O

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