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Isodon macrocalyx

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 UUID643fdf7f83c3e847861296
Scientific name Isodon macrocalyx
Authority Kudô
First published in Mem. Fac. Sci. Taihoku Imp. Univ. 2: 138 (1929)

Ethnobotanical Use Top

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General Uses Top

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Common products:
None documented.

Industrial and craft applications:
None documented.

Food and beverages (non-medicinal):
None documented.

Colorants and tanning:
None documented.

Wood and fiber:
None documented.

Fragrance and cosmetics:
None documented.

Properties relevant to use:
None documented.

Standards and regulation:
None documented.

Sustainability and sourcing:
None documented.

Synonyms Top

Scientific name Authority First published in
Isodon bifidocalyx (Dunn) H.Hara J. Jap. Bot. 60: 233 (1985)
Isodon taiwanensis (Masam.) S.S.Ying Mem. Coll. Agric. Natl. Taiwan Univ. 31(1): 25 (1991)
Plectranthus bifidocalyx Dunn Bull. Misc. Inform. Kew 1914: 328 (1914)
Plectranthus drosocarpus Hand.-Mazz. Symb. Sin. 7: 940 (1936)
Plectranthus macrocalyx Dunn Notes Roy. Bot. Gard. Edinburgh 8: 157 (1913)
Rabdosia bifidocalyx (Dunn) H.Hara J. Jap. Bot. 47: 194 (1972)
Rabdosia macrocalyx (Dunn) H.Hara J. Jap. Bot. 47: 197 (1972)
Rabdosia taiwanensis (Masam.) H.Hara J. Jap. Bot. 47: 201 (1972)
Amethystanthus taiwanensis Masam. Trans. Nat. Hist. Soc. Formosa 30: 409 (1940)

Common names Top

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Language Common/alternative name
Chinese 大萼香茶菜

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

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-0000217908
Tropicos 17607252
KEW urn:lsid:ipni.org:names:448592-1
The Plant List kew-102978
Open Tree Of Life 6084587
Observations.org 451807
NCBI Taxonomy 2494288
IPNI 448592-1
iNaturalist 707575
GBIF 5608938
EOL 2898966
Elurikkus 556215

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
Acetyl-macrocalin B, an ent-kaurane diterpenoid, initiates apoptosis through the ROS-p38-caspase 9-dependent pathway and induces G2/M phase arrest via the Chk1/2-Cdc25C-Cdc2/cyclin B axis in non-small cell lung cancer Wang JN, Zhang ZR, Che Y, Yuan ZY, Lu ZL, Li Y, Li N, Wan J, Sun HD, Sun N, Puno PT, He J Cancer Biol Ther 08-May-2018
PMCID:PMC5989808
doi:10.1080/15384047.2018.1449613
PMID:29565730
Revised structure of E. coli SSB A.J. Oakley Worldwide Protein Data Bank 17-Dec-2013
doi:10.2210/PDB4MZ9/PDB
Structures of macrocalyxin B, F, G and H, and maoyerabdosin from Isodon macrocalyx Wang Xian-Rong, Wang Hong-Ping, Hu Hui-Ping, Sun Han-Dong, Wang Su-Qing, Shinichi Ueda, Yoshihiro Kuroda, Tetsuro Fujita Elsevier BV 01-May-2003
doi:10.1016/0031-9422(94)00474-8
Enmein type diterpenoids from Isodon japonica. Li B, Tian X Phytochemistry 01-Oct-2001
doi:10.1016/S0031-9422(01)00245-X
PMID:11576594

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(10-Acetyloxy-6,7,9,15-tetrahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl)methyl acetate 155886046 Click to see 468.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(1R,2R,4S,5S,9R,10S,12R,13S,16R)-2,12,16-trihydroxy-5,9-dimethyl-14-methylidene-11,15-dioxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 163010750 Click to see 362.40 unknown https://doi.org/10.1016/S0031-9422(01)00245-X
(1S,2S,8R,9S,11R)-9,10,15,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one 138107787 Click to see 364.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(1S,4R,6S,9R,10R,12S,13S,17S,18R)-10,18-dihydroxy-4-methoxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde 163050128 Click to see 376.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(1S,4R,6S,9R,10R,12S,13S,17S,18S)-4,10,18-trihydroxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde 162983323 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(2S,5S,8R,13R,14S,15R)-13,14,19-trihydroxy-16,16-dimethyl-6-methylidene-10,12-dioxahexacyclo[9.8.0.01,15.02,8.05,9.08,13]nonadecan-7-one 5320676 Click to see CC1(CCC(C23C1C(C4(C56C2CCC(C5OC3O4)C(=C)C6=O)O)O)O)C 362.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(4R,6S,10R,12S,13S,17S,18R)-10,18-dihydroxy-4-methoxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde 101920416 Click to see CC1(CCCC23C1CC(C45C2C(CC(C4O)C(=C)C5=O)(OC3)OC)O)C=O 376.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(6,7,9,10,15-Pentahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl)methyl acetate 162955399 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
(6,7,9,10,18-Pentahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl)methyl acetate 162971809 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
[(1R,2S,5R,6R,7S,8R,9S,10S,11S,18R)-10-acetyloxy-6,7,9,18-tetrahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 134688495 Click to see CC(=O)OCC1(C2CCC3C45CCCC(C4C(C(C3(C2O)C1O)(OC5)O)OC(=O)C)(C)C)O 468.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
[(1R,2S,5R,6S,7S,8R,9S,10S,11R,18R)-10-acetyloxy-6,7,9,18-tetrahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 92855489 Click to see 468.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
[(1R,2S,5R,6S,7S,8R,9S,10S,11R,18R)-6,7,9,10,18-pentahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 101920417 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
[(1R,2S,5R,6S,7S,8R,9S,10S,11R,18S)-6,7,9,10,18-pentahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 162971810 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
[(1S,2S,5R,6S,7S,8S,10S,11R,15R)-10-acetyloxy-6,7,9,15-tetrahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 102004643 Click to see 468.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
https://doi.org/10.2210/PDB4MZ9/PDB
[(1S,2S,5R,6S,7S,8S,9S,10S,11R,15S)-6,7,9,10,15-pentahydroxy-12,12-dimethyl-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-6-yl]methyl acetate 101920418 Click to see 426.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
10,18-Dihydroxy-4-methoxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde 72953470 Click to see 376.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
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/10.1016/0031-9422(94)00474-8
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/10.1016/0031-9422(94)00474-8
2-[(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,9-dimethyl-14-methylidene-11,15-dioxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]acetaldehyde 101402142 Click to see CC1(CCC(C2(C1CC(C34C2C(=O)CC(C3O)C(=C)C4=O)O)C)O)CC=O 376.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
4,10,18-Trihydroxy-13-methyl-7-methylidene-8-oxo-3-oxapentacyclo[7.7.1.16,9.01,12.04,17]octadecane-13-carbaldehyde 72962181 Click to see 362.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
7,12,14-Trihydroxy-15-oxokaur-16-en-18-al 3035527 Click to see 348.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
Macrocalyxin C 14563770 Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)C=O 348.40 unknown https://doi.org/10.1016/0031-9422(94)00474-8
Maoyerabdosin 101920419 Click to see CC(=O)OCC1(C2CCC3C(C2)(C1O)C4(C(C5C3(CO4)C(CCC5(C)C)O)OC(=O)C)O)O 468.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
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/10.1016/0031-9422(94)00474-8
Rabdophyllin H 5320875 Click to see CC(=O)OCC1(C2CCC3C45CCCC(C4C(C(C3(C2O)C1O)(OC5)O)OC(=O)C)(C)C)O 468.50 unknown https://doi.org/10.1016/0031-9422(94)00474-8
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/10.1016/0031-9422(94)00474-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1S,2R,3S,5R,6S)-2-methyl-5-[(1S)-1,2,2-trimethylcyclopentyl]-7-oxabicyclo[4.1.0]heptane-2,3-diol 11076002 Click to see CC1(CCCC1(C)C2CC(C(C3C2O3)(C)O)O)C 254.36 unknown https://doi.org/10.1016/0031-9422(94)00474-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
3-Hydroxy-7a-methyl-10'-methylidenespiro[1,3,3a,5,6,7-hexahydro-2-benzofuran-4,5'-3-oxatricyclo[7.2.1.01,6]dodecane]-2',11'-dione 5318441 Click to see 346.40 unknown https://doi.org/10.1016/S0031-9422(01)00245-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(94)00474-8

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