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Chromolaena subscandens

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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 UUID643fd18f91044440193480
Scientific name Chromolaena subscandens
Authority (Hieron.) R.M.King & H.Rob.
First published in Phytologia 20(3): 206 (1970)

Description Top

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Synonyms Top

Scientific name Authority First published in
Eupatorium suratense B.L.Rob. Contr. Gray Herb. 80: 29 (1928)
Chromolaena suratensis (B.L.Rob.) R.M.King & H.Rob. Phytologia 20(3): 206 (1970)
Eupatorium tequendamense Hieron. ex Sodiro Bot. Jahrb. Syst. 29(1): 6. 1900 [22 May 1900]
Eupatorium elongatum Willd. ex Hieron. 6 1900
Eupatorium subscandens Hieron. Bot. Jahrb. Syst. 22(4-5): 742 (1897)

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Northern South America
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000116364
Tropicos 2713108
KEW urn:lsid:ipni.org:names:57495-2
The Plant List gcc-77770
Open Tree Of Life 7603099
IPNI 57495-2
iNaturalist 551465
GBIF 3087821

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)!
Title Authors Publication Released IDs
Flavonoids from the Leaves of Chromolaena subscandens J. Manuel Amaro-Luis, Paulino Delgado-Méndez American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50094A023

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 / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.1021/NP50094A023
> 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/10.1021/NP50094A023
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/10.1021/NP50094A023
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1021/NP50094A023
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258935 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1021/NP50094A023
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1021/NP50094A023
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5,7-Dihydroxy-8,4'-dimethoxyflavanone 42608108 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(O2)C(=C(C=C3O)O)OC 316.30 unknown https://doi.org/10.1021/NP50094A023

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