Heptaptera anisoptera - Unknown
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Internal ID UUID6440202f5472b454434462
Scientific name Heptaptera anisoptera
Authority (DC.) Tutin
First published in Feddes Repert. 74: 33 (1967)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Western Asia
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000719968
Tropicos 1700132
The Plant List kew-2845868
Open Tree Of Life 1091444
NCBI Taxonomy 325718
IPNI 842920-1
iNaturalist 492868
GBIF 3630881

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
Electrochemical Characterization of the Antioxidant Properties of Medicinal Plants and Products: A Review Ziyatdinova G, Kalmykova A Molecules 02-Mar-2023
PMCID:PMC10004803
doi:10.3390/molecules28052308
PMID:36903553
Imperatorin–pharmacological meaning and analytical clues: profound investigation Kozioł E, Skalicka-Woźniak K Phytochem Rev 20-Feb-2016
PMCID:PMC4939159
doi:10.1007/s11101-016-9456-2
PMID:27453708
A Simple Electrochemical Method for the Rapid Estimation of Antioxidant Potentials of Some Selected Medicinal Plants Amidi S, Mojab F, Bayandori Moghaddam A, Tabib K, Kobarfard F Iran J Pharm Res 01-Jan-2012
PMCID:PMC3876568
PMID:25317192
Sesquiterpene coumarin ethers from the genus Heptaptera Giovanni Appendino, Hasan Cetin Özen, Gian Mario Nano, Marco Cisero Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80447-M
Coumarins from Heptaptera anisoptera Giovanni Appendino, Hasan Çetin Özen, Silvia Tagliapietra, Marco Cisero Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83477-G

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[7-[(2E,6E,9S,10R)-9,10-diacetyloxy-11-hydroxy-3,7,11-trimethyldodeca-2,6-dienoxy]-2-oxochromen-5-yl] acetate 162933728 Click to see CC(=CCOC1=CC2=C(C=CC(=O)O2)C(=C1)OC(=O)C)CCC=C(C)CC(C(C(C)(C)O)OC(=O)C)OC(=O)C 558.60 unknown https://doi.org/10.1016/0031-9422(92)80447-M
5-hydroxy-7-[(2E,6E,9S,10R)-9,10,11-trihydroxy-3,7,11-trimethyldodeca-2,6-dienoxy]chromen-2-one 38361715 Click to see CC(=CCOC1=CC(=C2C=CC(=O)OC2=C1)O)CCC=C(C)CC(C(C(C)(C)O)O)O 432.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M
7-[(2E,6E,10R)-10,11-dihydroxy-3,7,11-trimethyldodeca-2,6-dienoxy]-5-hydroxychromen-2-one 101637178 Click to see CC(=CCCC(=CCOC1=CC(=C2C=CC(=O)OC2=C1)O)C)CCC(C(C)(C)O)O 416.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M
7-[(2E,6E,9S,10R)-9,10,11-trihydroxy-3,7,11-trimethyldodeca-2,6-dienoxy]chromen-2-one 38361728 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC=C(C)CC(C(C(C)(C)O)O)O 416.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
> Phenylpropanoids and polyketides / Coumarins and derivatives
[(1R,2R,4aR,5R,8aS)-2-hydroxy-1,4a-dimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 101632341 Click to see CC(=O)OCC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 440.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
[(1R,2S,4aR,5R,8aS)-2-hydroxy-1,4a-dimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 101632342 Click to see CC(=O)OCC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 440.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
[2-hydroxy-1,4a-dimethyl-6-methylidene-5-[(2-oxochromen-7-yl)oxymethyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-1-yl]methyl acetate 162998381 Click to see CC(=O)OCC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 440.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
7-[[(1R,8aR)-5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl]methoxy]chromen-2-one 101793077 Click to see CC1(C2CCC(=C)C(C2(CCC1=O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 380.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
7-[[(1S,4aR,6S,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]chromen-2-one 21627903 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
Colladonin 375430 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)C 382.50 unknown https://doi.org/10.1016/0031-9422(92)83477-G
Conferol 11892267 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M
Feselol 179577 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M
Samarcandin 71587098 Click to see CC1(C2CCC(C(C2(CCC1O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 400.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M
Samarcandone 101285185 Click to see CC1(C2CCC(C(C2(CCC1=O)C)COC3=CC4=C(C=C3)C=CC(=O)O4)(C)O)C 398.50 unknown https://doi.org/10.1016/0031-9422(92)80447-M

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