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Gonospermum ferulaceum

Gonospermum ferulaceum - 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 UUID643fc915e6f6d124067213
Scientific name Gonospermum ferulaceum
Authority (Webb) Febles
First published in Conf. Pl. Taxon. 4: 88 (1996)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chrysanthemum ferulaceum (Webb) Sunding Cuad. Bot. Canaria vii. 17 (1969)
Pyrethrum ferulaceum Sch.Bip. Sch. Bip. in Webb & Berthelot, Hist. Nat. Iles Canaries 3(2,2). 1844. 281 1844
Tanacetum ferulaceum Sch.Bip. Tanaceteen : 50 (1844)
Tanacetum ferulaceum var. ferulaceum (Webb) Sch.Bip.
Pyrethrum ferulaceum Webb Hist. Nat. Iles Canaries 3(2; 2): 281 (1844)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Gonospermum ferulaceum var. latipinnum (Svent.) Febles IV Conf. Pl. Taxon. 88. [post 19-22 Sep 1996]

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

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-0000027603
KEW urn:lsid:ipni.org:names:77083690-1
The Plant List gcc-126679
NCBI Taxonomy 127995
IPNI 77083690-1
iNaturalist 768369
GBIF 6063901
Open Tree Of Life 748953

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)!
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Title Authors Publication Released IDs
Cytotoxicity of the Sesquiterpene Lactone Spiciformin and Its Acetyl Derivative against the Human Leukemia Cell Lines U-937 and HL-60 Saavedra E, Estévez-Sarmiento F, Said M, Eiroa JL, Rubio S, Quintana J, Estévez F Int J Mol Sci 16-Apr-2020
PMCID:PMC7215469
doi:10.3390/ijms21082782
PMID:32316340
Sesquiterpene lactones and other constituents of Tanacetum species Antonio G. González, Jaime Bermejo Barrera, Jorge Triana Méndez, Mariana López Sanchez, José L.Eiroa Martínez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)83157-T
Sesquiterpene lactones from Tanacetum ferulaceum Antonio G. Gonzalez, Jaime Bermejo barrera, Jorge Triana Mendez, Mariana Lopez Sanchez, Jose L. Eiroa Martinez Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)83068-C

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
(1S,2S,3R,5S,8Z,11S)-2-hydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-8-en-13-one 101316855 Click to see CC1=CCCC2(C(O2)C(C3C(C1)OC(=O)C3=C)O)C 264.32 unknown https://doi.org/10.1016/0031-9422(90)83068-C
tatridin B 14191260 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1016/0031-9422(90)83068-C
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(5a-Methyl-3,9-dimethylidene-2-oxo-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-4-yl) acetate 162868270 Click to see CC(=O)OC1CC2(CCCC(=C)C2C3C1C(=C)C(=O)O3)C 290.40 unknown https://doi.org/10.1016/0031-9422(92)83157-T
Arbusculin A 160153 Click to see CC12CCCC(C1C3C(CC2)C(=C)C(=O)O3)(C)O 250.33 unknown https://doi.org/10.1016/0031-9422(90)83068-C
Deacetyl-beta-cyclopyrethrosin 21629647 Click to see CC12CC3C(C(C1C(=C)CCC2O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1016/0031-9422(90)83068-C
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,6E,11aR)-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one 133640194 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(90)83068-C
Costunolide 5281437 Click to see CC1=CCCC(=CC2C(CC1)C(=C)C(=O)O2)C 232.32 unknown https://doi.org/10.1016/0031-9422(90)83068-C
tatridin-A 101297649 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1016/0031-9422(90)83068-C
> 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/10.1016/0031-9422(90)83068-C
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/10.1016/0031-9422(90)83068-C
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/10.1016/0031-9422(90)83068-C
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/10.1016/0031-9422(90)83068-C
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/0031-9422(90)83068-C
> 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(90)83068-C
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(90)83068-C
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(90)83068-C

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