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Isodon excisoides

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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 UUID643fdf7c9b31a066990363
Scientific name Isodon excisoides
Authority (Sun ex C.H.Hu) H.Hara
First published in J. Jap. Bot. 60: 234 (1985)

Description Top

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Synonyms Top

Scientific name Authority First published in
Plectranthus excisoides Y.Z.Sun Acta Phytotax. Sin. 11(1): 53. 1966 [17 Jan 1966]
Rabdosia excisoides (Sun ex C.H.Hu) C.Y.Wu & H.W.Li Acta Phytotax. Sin. 13(1): 93 (1975)

Common names Top

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Language Common/alternative name
Chinese 野紫苏
Chinese 拟缺香茶菜

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-0000217852
Tropicos 17607247
KEW urn:lsid:ipni.org:names:915123-1
The Plant List kew-102926
Open Tree Of Life 6084580
NCBI Taxonomy 986861
IPNI 915123-1
GBIF 5609028

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
New Diterpenes with Potential Antitumoral Activity Isolated from Plants in the Years 2017–2022 Forzato C, Nitti P Plants (Basel) 29-Aug-2022
PMCID:PMC9460660
doi:10.3390/plants11172240
PMID:36079622
An In Vitro Evaluation of the Molecular Mechanisms of Action of Medical Plants from the Lamiaceae Family as Effective Sources of Active Compounds against Human Cancer Cell Lines Sitarek P, Merecz-Sadowska A, Śliwiński T, Zajdel R, Kowalczyk T Cancers (Basel) 13-Oct-2020
PMCID:PMC7601952
doi:10.3390/cancers12102957
PMID:33066157
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
Isolation and identification of two pairs of cytotoxic diterpene tautomers and their tautomerization mechanisms Dai LP, Li XF, Feng QM, Zhang LX, Liu QY, Xu EP, Wu H, Wang ZM Sci Rep 29-Jan-2020
PMCID:PMC6989466
doi:10.1038/s41598-020-58260-8
PMID:31996737
Ursolic acid isolated from Isodon excisoides induces apoptosis and inhibits invasion of GBC-SD gallbladder carcinoma cells Chen H, Wu X, Duan Y, Zhi D, Zou M, Zhao Z, Zhang X, Yang X, Zhang J Oncol Lett 27-May-2019
PMCID:PMC6607232
doi:10.3892/ol.2019.10397
PMID:31423212
Three New Cytotoxic ent-Kaurane Diterpenes from Isodon excisoides Dai LP, Li C, Yang HZ, Lu YQ, Yu HY, Gao HM, Wang ZM Molecules 22-Sep-2015
PMCID:PMC6332174
doi:10.3390/molecules200917544
PMID:26402664
Diterpenoids from <i>Isodon excisoides</i> Ji Xia Zhang, Yong Xue Wang, Zhi An He, Fu Lin Yan SAGE Publications 16-Dec-2009
doi:10.3184/030823409X396391
A New <i>ent</i>-Kaurane Deterpenoid from <i>Isodon Excisoides</i> (Sun ex C. H. Hu) C. Y. Wu et H. W. Li Lan Ding, Han Wang, Guoan Liu, Dongjuan Yang SAGE Publications 16-Dec-2009
doi:10.3184/0308234043431898

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
(1R,2R,4R,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.0^{1,10.0^{4,9]hexadecan-15-one 13945496 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.3184/0308234043431898
(1R,2R,4S,5S,9R,10S,13S,16R)-2,16-dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 11371473 Click to see CC12CCC(=O)C(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)(C)CO 348.40 unknown https://doi.org/10.3184/0308234043431898
(1R,2R,4S,6R,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 13876282 Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.3184/0308234043431898
(1S,2S,5S,8S,9R,11R,15S,16R,18R)-15,18-dihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 162960861 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C 362.50 unknown https://doi.org/10.3184/0308234043431898
(1S,4S,6R,9R,10S,13R,14S,16R)-5,5,9,14-tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,14,16-triol 163020510 Click to see CC1(C2CCC34CC(C(C3O)CCC4C2(CCC1O)C)(C)O)C 322.50 unknown https://doi.org/10.3184/030823409X396391
(2,16-Dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 13298862 Click to see CC(=O)OC1CCC2(C3CCC4C(C3(C(CC2C1(C)C)O)C(=O)C4=C)O)C 376.50 unknown https://doi.org/10.3184/0308234043431898
(7,9,10,15-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl) acetate 14109082 Click to see CC(=O)OC1CC2CC3(C1C45COC3(C(C4C(CCC5O)(C)C)O)O)C(C2=C)O 408.50 unknown https://doi.org/10.3184/030823409X396391
(7,9,10,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 13919285 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5O)O)(C)C 408.50 unknown https://doi.org/10.3184/030823409X396391
(9,10,18-Trihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 429192 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 406.50 unknown https://doi.org/10.3184/030823409X396391
[(1R,2S,3R,5S,7R,8S,9S,10S,11R,15R)-7,9,10,15-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl] acetate 163092044 Click to see CC(=O)OC1CC2CC3(C1C45COC3(C(C4C(CCC5O)(C)C)O)O)C(C2=C)O 408.50 unknown https://doi.org/10.3184/030823409X396391
[(1S,2S,5S,7R,8R,9S,10S,11R,15S,18R)-7,9,10,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 162966019 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5O)O)(C)C 408.50 unknown https://doi.org/10.3184/030823409X396391
12,12-Dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,9,10,15,18-pentol 73744636 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5O)(OC3)O)O)O)C 366.40 unknown https://doi.org/10.3184/030823409X396391
15,18-Dihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 13945517 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C 362.50 unknown https://doi.org/10.3184/0308234043431898
1alpha,6beta,7beta,14beta,15beta-Pentahydroxy-7alpha,20-epoxy-ent-kaur-16-ene 139078207 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5O)(OC3)O)O)O)C 366.40 unknown https://doi.org/10.3184/030823409X396391
2,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione 72820836 Click to see CC12CCC(=O)C(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)(C)CO 348.40 unknown https://doi.org/10.3184/0308234043431898
2,6,16-Trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one 13876280 Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.3184/0308234043431898
5,5,9,14-Tetramethyltetracyclo[11.2.1.01,10.04,9]hexadecane-6,14,16-triol 163020509 Click to see CC1(C2CCC34CC(C(C3O)CCC4C2(CCC1O)C)(C)O)C 322.50 unknown https://doi.org/10.3184/030823409X396391
CID 101306849 101306849 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/10.3184/030823409X396391
Glaucocalyxin A 10471963 Click to see CC1(C2CC(C34C(C2(CCC1=O)C)CCC(C3O)C(=C)C4=O)O)C 332.40 unknown https://doi.org/10.3184/0308234043431898
Kamebanin 12004580 Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C 334.40 unknown https://doi.org/10.3184/0308234043431898
Kaur-16-en-15-one, 1-(acetyloxy)-7,20-epoxy-6,7,14-trihydroxy-, (1alpha,6beta,7alpha,14R)- 12305580 Click to see CC(=O)OC1CCC(C2C13COC(C2O)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C 406.50 unknown https://doi.org/10.3184/030823409X396391
Lasiodonin 12305578 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/10.3184/030823409X396391
Leukamenin E 45267324 Click to see CC(=O)OC1CCC2(C3CCC4C(C3(C(CC2C1(C)C)O)C(=O)C4=C)O)C 376.50 unknown https://doi.org/10.3184/0308234043431898
LeukaMenin F; Wangzaozin B; Leucamenin F 14193397 Click to see CC1(C2CC(C34C(C2(CCC1=O)C)CCC(C3O)C(=C)C4=O)O)C 332.40 unknown https://doi.org/10.3184/0308234043431898
Oridonin 5321010 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.3184/030823409X396391
Rubescensin A 3576890 Click to see CC1(CCC(C23C1C(C(C45C2CCC(C4O)C(=C)C5=O)(OC3)O)O)O)C 364.40 unknown https://doi.org/10.3184/030823409X396391
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,4S,8R,9S,12S,13S,14S,16S,18R)-9,14,18-trihydroxy-7,7-dimethyl-17-methylidene-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-2-one 162970055 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(C5=C)O)C(=O)O2)O)C 364.40 unknown https://doi.org/10.3184/030823409X396391
(3',7,11-Triacetyloxy-6',6'-dimethyl-10-methylidene-2-oxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl)methyl acetate 13919278 Click to see CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(=C)C4OC(=O)C)OC(=O)C)OC(=O)C)(C)C 534.60 unknown https://doi.org/10.3184/030823409X396391
[(1S,1'R,3'S,5R,6S,7S,9S,10S)-3'-acetyloxy-7-hydroxy-10-(hydroxymethyl)-6',6'-dimethyl-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl]methyl acetate 163188259 Click to see CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(C4=O)CO)O)OC(=O)C)(C)C 466.50 unknown https://doi.org/10.3184/030823409X396391
[(1S,1'S,3'R,5R,6S,7S,9S)-7-hydroxy-3'-(hydroxymethyl)-4',4'-dimethyl-10-methylidene-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl] acetate 13919289 Click to see CC(=O)OC1CCC(C(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)CO)(C)C 406.50 unknown https://doi.org/10.3184/030823409X396391
[3'-Acetyloxy-7-hydroxy-10-(hydroxymethyl)-6',6'-dimethyl-2,11-dioxospiro[3-oxatricyclo[7.2.1.01,6]dodecane-5,2'-cyclohexane]-1'-yl]methyl acetate 162888728 Click to see CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(C4=O)CO)O)OC(=O)C)(C)C 466.50 unknown https://doi.org/10.3184/030823409X396391
1alpha,6,11beta,15beta-Tetraacetoxy-6,7-seco-7,20-olide-ent-kaur-16-ene 13919280 Click to see CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(=C)C4OC(=O)C)OC(=O)C)OC(=O)C)(C)C 534.60 unknown https://doi.org/10.3184/030823409X396391
CID 14109026 14109026 Click to see CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)OC(=O)C)(C)C 448.50 unknown https://doi.org/10.3184/030823409X396391
Enmein, 1-deoxo-13-deoxy-1,5-dihydroxy-, (1alpha,5alpha)- 78178523 Click to see CC1(CCC2C3(C1C(OC3)O)C4C(CC5CC4(C(C5=C)O)C(=O)O2)O)C 364.40 unknown https://doi.org/10.3184/030823409X396391
Maoyecrystal E 13919287 Click to see CC(=O)OC1CCC(C(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)CO)(C)C 406.50 unknown https://doi.org/10.3184/030823409X396391
Rabdosin B 14109027 Click to see CC(=O)OCC1C(CCC(C12COC(=O)C34C2C(CC(C3)C(=C)C4=O)O)OC(=O)C)(C)C 448.50 unknown https://doi.org/10.3184/030823409X396391

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