Hypericum drummondii - Unknown
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Internal ID UUID64405b7fd5ced636976130
Scientific name Hypericum drummondii
Authority (Grev. & Hook.) Torr. & A.Gray
First published in Fl. N. Amer. 1: 165 (1838)

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Synonyms Top

Scientific name Authority First published in
Brathys drummondii (Grev. & Hook.) Spach Ann. Sci. Nat., Bot. , sér. 2, 5: 367 (1836)
Sarothra drummondii Grev. & Hook. Bot. Misc. 3: 236 (1833)

Common names Top

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Language Common/alternative name
English nits and lice

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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
  • Northern America
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Missouri
      • Oklahoma
    • Northeastern U.S.A.
      • Indiana
      • Ohio
      • Pennsylvania
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001295906
Florida Plant Atlas 3806
Flora of Alabama 1558
USDA Plants HYDR
Tropicos 7800708
KEW urn:lsid:ipni.org:names:1219808-2
The Plant List tro-7800708
Open Tree Of Life 295785
Observations.org 330395
NCBI Taxonomy 673924
Nature Serve 2.145690
IPNI 1219808-2
iNaturalist 145368
GBIF 3189500
EPPO HYPDR
EOL 584906
Elurikkus 374098
USDA GRIN 447613

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
Identification of Human Intracellular Targets of the Medicinal Herb St. John’s Wort by Chemical-Genetic Profiling in Yeast McCue PP, Phang JM J Agric Food Chem 26-Nov-2008
PMCID:PMC2645918
doi:10.1021/jf801593a
PMID:18975972
A Utilization of the Selective Inept Experiment for the Structure Elucidation of Oxygenated Chromenes Hiranthi Jayasuriya, N. P. Dhammika Nanayakkara, James D. Mcchesney Informa UK Limited 07-Jul-2007
doi:10.1080/10575639408044038
Subject Index N/A 01-Jan-2005
PMCID:PMC7148952
doi:10.1016/S1572-5995(05)80049-3
Drummondins A–C: three novel rottlerin-type antibiotics from Hypericim drummondii Hiranthi Jayasuriya, James D. McChesney Royal Society of Chemistry (RSC) 30-Mar-2004
doi:10.1039/C39880001592
New antimicrobial filicinic acid derivatives from Hypericum drummondii. Jayasuriya H, Clark AM, McChesney JD J Nat Prod 01-Sep-1991
doi:10.1021/NP50077A013
PMID:1800634
Antimicrobial and cytotoxic activity of rottlerin-type compounds from Hypericum drummondii. Jayasuriya H, McChesney JD, Swanson SM, Pezzuto JM J Nat Prod 01-Mar-1989
doi:10.1021/NP50062A018
PMID:2746258

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
> Organic acids and derivatives / Vinylogous acids
Albaspidin AA 14378646 Click to see CC(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(C(=O)C(=C2O)C(=O)C)(C)C)O)O 404.40 unknown https://doi.org/10.1021/NP50062A018
albaspidin P-P 14378645 Click to see CCC(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(C(=O)C(=C2O)C(=O)CC)(C)C)O)O 432.50 unknown https://doi.org/10.1021/NP50062A018
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Drummondin E 132133 Click to see CC(=CCC1(C(=C(C(=C(C1=O)C(=O)C)O)CC2=C(C=C(C(=C2O)C(=O)C)O)OCC=C(C)C)O)C)C 498.60 unknown https://doi.org/10.1021/NP50077A013
Drummondin F 129595 Click to see CC(=CCC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(C(=O)C(=C2O)C(=O)C)(C)CC=C(C)C)O)O)C 498.60 unknown https://doi.org/10.1021/NP50062A018
https://doi.org/10.1021/NP50077A013
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2-Butanoyl-4-[(8-butanoyl-5,7-dihydroxy-2,2-dimethylchromen-6-yl)methyl]-3,5-dihydroxy-6,6-dimethylcyclohexa-2,4-dien-1-one 441963 Click to see CCCC(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)CCC)O)O 498.60 unknown https://doi.org/10.1021/NP50062A018
https://doi.org/10.1039/C39880001592
Drummondin A 5316970 Click to see CCC(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)CC)O)O 470.50 unknown https://doi.org/10.1021/NP50062A018
https://doi.org/10.1039/C39880001592
drummondin B 10434193 Click to see CCC(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C)O)O 456.50 unknown https://doi.org/10.1021/NP50062A018
https://doi.org/10.1039/C39880001592
Drummondin C 164100 Click to see CC(=O)C1=C(C(=C(C(C1=O)(C)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C)O)O 442.50 unknown https://doi.org/10.1021/NP50062A018
https://doi.org/10.1039/C39880001592
https://doi.org/10.1080/10575639408044038
Drummondin D 132131 Click to see CC(=CCC1(C(=C(C(=C(C1=O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C)O)O)C)C 496.50 unknown https://doi.org/10.1021/NP50077A013
Isodrummondin D 132132 Click to see CC(=CCC1(C(=C(C(=C(C1=O)C(=O)C)O)CC2=C3C(=C(C(=C2O)C(=O)C)O)C=CC(O3)(C)C)O)C)C 496.50 unknown https://doi.org/10.1021/NP50077A013

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