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Isodon effusus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fdf7c459d6805297083
Scientific name Isodon effusus
Authority (Maxim.) H.Hara
First published in Enum. Spermatophytarum Japon. 1: 204 (1948)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Plectranthus effusus (Maxim.) Honda Bot. Mag. (Tokyo) 46: 419 (1932)
Rabdosia effusa (Maxim.) H.Hara J. Jap. Bot. 47: 195 (1972)
Rabdosia effusa f. leucantha (Honda) H.Hara J. Jap. Bot. 47: 195 (1972)
Amethystanthus effusus (Honda) Honda Bot. Mag. (Tokyo) 54: 2 (1940)
Amethystanthus effusus var. leucanthus Honda Bot. Mag. (Tokyo) 54: 2. 1940
Plectranthus longitubus var. effusus Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 20: 451 (1875)
Isodon longitubus var. effusus (Maxim.) Kudô Mem. Fac. Sci. Taihoku Imp. Univ. 2: 140 (1929)
Amethystanthus longitubus var. effusus (Maxim.) Nakai Bot. Mag. (Tokyo) 48: 791 (1934)
Isodon effusus f. leucanthus (Honda) H.Hara Enum. Spermatophytarum Japon. 1: 205 (1948)

Common names Top

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Language Common/alternative name
Japanese セキヤノアキチョウジ

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000217848
KEW urn:lsid:ipni.org:names:448572-1
The Plant List kew-102922
Open Tree Of Life 567845
NCBI Taxonomy 680379
IPNI 448572-1
iNaturalist 508432
GBIF 5609034
EOL 5380859

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
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Molecular and morphological evidence for a new species of Isodon (Lamiaceae) from southern China Chen YP, Huang CZ, Zhao Y, Xiang CL Plant Divers 14-Jul-2020
PMCID:PMC7987569
doi:10.1016/j.pld.2020.06.004
PMID:33778225
Terpenoids from Rabdosia effusa HARA. Takahiko ISOBE, Yukinao NODA, Kozo SHIBATA, Junko FUJII The Chemical Society of Japan 13-Sep-2011
doi:10.1246/NIKKASHI.1996.754
STRUCTURES OF EFFUSANINS, ANTIBACTERIAL DITERPENOIDS FROM <i>RABDOSIA EFFUSA</i> Tetsuro Fujita, Yoshio Takeda, Tetsuro Shingu, Akira Ueno Oxford University Press (OUP) 25-Jul-2006
doi:10.1246/CL.1980.1635

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 / Diterpenoids / Kaurane diterpenoids
(15-Acetyloxy-9,10-dihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 75052573 Click to see 448.50 unknown https://doi.org/10.1246/CL.1980.1635
(9,10-Dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 10475500 Click to see 390.50 unknown https://doi.org/10.1246/CL.1980.1635
(9,10,15-Trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl)methyl acetate 75052824 Click to see 406.50 unknown https://doi.org/10.1246/CL.1980.1635
[(1S,2S,5R,8S,9S,10S,11R,12R,15S)-9,10,15-trihydroxy-12-methyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-12-yl]methyl acetate 163083341 Click to see 406.50 unknown https://doi.org/10.1246/CL.1980.1635
3,9,10,15-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 12305578 Click to see 364.40 unknown https://doi.org/10.1246/CL.1980.1635
9,10,15-Trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 9997896 Click to see 348.40 unknown https://doi.org/10.1246/CL.1980.1635
CID 34174831 34174831 Click to see 390.50 unknown https://doi.org/10.1246/CL.1980.1635
Effusanin A 34174827 Click to see 348.40 unknown https://doi.org/10.1246/CL.1980.1635
Effusanin D 44585547 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)OC(=O)C)C 448.50 unknown https://doi.org/10.1246/CL.1980.1635
Effusanin E 24721137 Click to see CC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.1246/CL.1980.1635
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,1'R,2'R,5R,6R,9S)-2'-formyl-1'-methyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,3'-cyclohexane]-1'-yl]methyl acetate 101297680 Click to see 388.50 unknown https://doi.org/10.1246/NIKKASHI.1996.754
[(1S,1'R,2'R,5R,6S,7R,9R)-2'-formyl-7-hydroxy-1'-methyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,3'-cyclohexane]-1'-yl]methyl acetate 101670434 Click to see 404.50 unknown https://doi.org/10.1246/NIKKASHI.1996.754
[(1S,1'S,2'R,5R,6S,9R)-2'-formyl-1'-methyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,3'-cyclohexane]-1'-yl]methyl acetate 162909298 Click to see 388.50 unknown https://doi.org/10.1246/CL.1980.1635
[(3R,4a'R,5'S,7'R,9a'R)-2-Formyl-5'-hydroxy-3-methyl-8'-methylene-1',9'-dioxohexahydrospiro[cyclohexane-1,4'-[2]oxa[7,9a]methanocyclohepta[c]pyran]-3-yl]methyl acetate 122739 Click to see CC(=O)OCC1(CCCC2(C1C=O)COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)C 404.50 unknown https://doi.org/10.1246/NIKKASHI.1996.754
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1246/NIKKASHI.1996.754
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1246/NIKKASHI.1996.754
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
Hyptadienic acid 14605533 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)CO)C)C)C2C1(C)O)C)C(=O)O 470.70 unknown https://doi.org/10.1246/NIKKASHI.1996.754

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