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Isodon leucophyllus

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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 UUID643fdf7ea10cb200260912
Scientific name Isodon leucophyllus
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 122 (1929)

Description Top

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Synonyms Top

Scientific name Authority First published in
Plectranthus leucophyllus Dunn Notes Roy. Bot. Gard. Edinburgh 8: 157 (1913)
Plectranthus pachythyrsus Hand.-Mazz. Symb. Sin. 7: 937 (1936)
Plectranthus thiothyrsus Hand.-Mazz. Acta Horti Gothob. 9: 94 (1934)
Rabdosia leucophylla (Dunn) H.Hara J. Jap. Bot. 47: 197 (1972)
Rabdosia pachythyrsa (Hand.-Mazz.) H.Hara J. Jap. Bot. 47: 198 (1972)
Rabdosia thiothyrsa (Hand.-Mazz.) H.Hara J. Jap. Bot. 47: 201 (1972)

Common names Top

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Language Common/alternative name
Chinese 香薷
Chinese 白叶香茶菜

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-0000217894
Tropicos 17607201
KEW urn:lsid:ipni.org:names:448589-1
The Plant List kew-102965
Open Tree Of Life 541500
NCBI Taxonomy 662916
IPNI 448589-1
GBIF 5608964
EOL 2898959
CMAUP NPO7527

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
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
Molecular Insight in the Multifunctional Effects of Oridonin Owona BA, Schluesener HJ Drugs R D 20-Aug-2015
PMCID:PMC4561052
doi:10.1007/s40268-015-0102-z
PMID:26290464
Bisleuconins A–D: a pair of epimeric ent-kauranoid dimers and two new asymmetric analogues isolated from Isodon leucophyllus Hai-Bo Zhang, Jian-Xin Pu, Yong Zhao, Fei He, Xiao-Nian Li, Xiao Luo, Li-Guang Lou, Han-Dong Sun Elsevier BV 01-Sep-2011
doi:10.1016/J.TETLET.2011.08.133
Ent-kaurene diterpenoids from Rabdosia leucophylla Xun Liao, Lisheng Ding, Shulin Peng Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00416-0
Enmein type diterpenoids from Isodon japonica. Li B, Tian X Phytochemistry 01-Oct-2001
doi:10.1016/S0031-9422(01)00245-X
PMID:11576594
Diterpenoids from Isodon leucophyllus. Chen SN, Lin ZW, Qin GW, Sun HD, Chen YZ Planta Med 01-Jun-1999
doi:10.1055/S-2006-960818
PMID:17260272

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
(8S,11bS)-7,11-dihydroxy-3,4,8,11b-tetramethyl-1,2,8,9-tetrahydronaphtho[2,1-f][1]benzofuran-6-one 11174780 Click to see CC1COC2=C(C3=C(C(=O)C=C4C3(CCC(=C4C)C)C)C(=C12)O)O 326.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(16S)-1alpha,11alpha-Diacetoxy-17-ethoxy-7alpha,20-epoxy-6beta,7-dihydroxykaurane-15-one 100937099 Click to see CCOCC1C2CC(C3C(C2)(C1=O)C4(C(C5C3(CO4)C(CCC5(C)C)OC(=O)C)O)O)OC(=O)C 494.60 unknown https://doi.org/10.1055/S-2006-960818
(1alpha,4alpha,6beta,7alpha,11alpha)-1,11,18-Tris(acetyloxy)-7,20-epoxy-6,7-dihydroxykaur-16-en-15-one 100937100 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)OC(=O)C)(OC3)O)O)OC(=O)C)C 506.50 unknown https://doi.org/10.1055/S-2006-960818
(2-Acetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72245811 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(=O)C2C1(C)C)OC(=O)C)C(=O)C4=C)O)C)O 448.50 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
(2-Acetyloxy-8,11,15-trihydroxy-5,5,9-trimethyl-14-methylidene-3-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 162999506 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C4=C)O)C(C(=O)C2C1(C)C)OC(=O)C)O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
(2,6-Diacetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72245826 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)OC(=O)C)O)C)C(=O)C2=C 490.50 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
(2,8-Diacetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate 72245819 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)O)OC(=O)C)C(=O)C4=C)O)C)OC(=O)C 492.60 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
(3,15-Diacetyloxy-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 163023369 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2C(CC(C4)C(=C)C5=O)OC(=O)C)(OC3)O)O)OC(=O)C)C 506.50 unknown https://doi.org/10.1055/S-2006-960818
[(1R,2S,3R,5S,6R,8S,9S,10S,11R,15S)-3-acetyloxy-6-(ethoxymethyl)-9,10-dihydroxy-12,12-dimethyl-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 100937097 Click to see CCOCC1C2CC(C3C(C2)(C1=O)C4(C(C5C3(CO4)C(CCC5(C)C)OC(=O)C)O)O)OC(=O)C 494.60 unknown https://doi.org/10.1055/S-2006-960818
[3-Acetyloxy-6-(ethoxymethyl)-9,10-dihydroxy-12,12-dimethyl-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate 163041809 Click to see CCOCC1C2CC(C3C(C2)(C1=O)C4(C(C5C3(CO4)C(CCC5(C)C)OC(=O)C)O)O)OC(=O)C 494.60 unknown https://doi.org/10.1055/S-2006-960818
2,12,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-11,15-dione 14807615 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)CO 364.40 unknown https://doi.org/10.1016/J.TETLET.2011.08.133
Leucophyllin A 101938881 Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)OC(=O)C)O)C)C(=O)C2=C 490.50 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
Leucophyllin B 101938882 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(=O)C2C1(C)C)OC(=O)C)C(=O)C4=C)O)C)O 448.50 unknown https://doi.org/10.1016/S0031-9422(01)00245-X
https://doi.org/10.1016/S0031-9422(97)00416-0
Leucophyllin C 101938883 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C4=C)O)C(C(=O)C2C1(C)C)OC(=O)C)O)C)O 450.50 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
https://doi.org/10.1016/S0031-9422(01)00245-X
Leucophyllin D 101938884 Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)O)OC(=O)C)C(=O)C4=C)O)C)OC(=O)C 492.60 unknown https://doi.org/10.1016/S0031-9422(97)00416-0
https://doi.org/10.1016/S0031-9422(01)00245-X
rabdoloxin A 45271373 Click to see CC1(CCCC2(C1CC(C34C2C(=O)C(C(C3O)C(=C)C4=O)O)O)C)CO 364.40 unknown https://doi.org/10.1016/J.TETLET.2011.08.133
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(14,18-Dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-9-yl) acetate 162904647 Click to see CC(=O)OC1C2C(CCC3C2(CO1)C4C(CC5CC4(C(C5=C)O)C(=O)O3)O)(C)C 406.50 unknown https://doi.org/10.1055/S-2006-960818
[(1S,4S,8R,9S,12S,13S,14S,16S,18R)-14,18-dihydroxy-7,7-dimethyl-17-methylidene-2-oxo-3,10-dioxapentacyclo[14.2.1.01,13.04,12.08,12]nonadecan-9-yl] acetate 100937098 Click to see CC(=O)OC1C2C(CCC3C2(CO1)C4C(CC5CC4(C(C5=C)O)C(=O)O3)O)(C)C 406.50 unknown https://doi.org/10.1055/S-2006-960818
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-O-Acetyloleanolic acid 151202 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown via CMAUP database
O-Acetyloleanolic aldehyde 14829106 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C 482.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
22-Dehydroclerosterol 15608667 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
4-Hydroxy-4-(2-hydroxyethyl)cyclohexan-1-one 184824 Click to see C1CC(CCC1=O)(CCO)O 158.19 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Cleroindicin C 10975728 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown via CMAUP database
Cleroindicin E 11744892 Click to see C1CC2(CCOC2CC1O)O 158.19 unknown via CMAUP database
epi-Cleroindicin D 10749706 Click to see C1COC2C1(C(CC(=O)C2)O)O 172.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Scutellarein 5281697 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5318059 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 476.40 unknown via CMAUP database
beta-D-Glucopyranosiduronic acid, 2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-1-benzopyran-7-yl 158227 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 492.40 unknown via CMAUP database
Scutellarin 185617 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',6,7-tetramethoxyflavone 152430 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown via CMAUP database

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