Isodon interruptus in Genus Isodon

Details Top

Internal ID	UUID643fdf7e0f8d5919999086
Scientific name	Isodon interruptus
Authority	(C.Y.Wu & H.W.Li) 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
Isodon kunmingensis	(C.Y.Wu & H.W.Li) H.Hara	J. Jap. Bot. 60: 234 (1985)
Rabdosia interrupta	C.Y.Wu & H.W.Li	Fl. Yunnanica 1: 775 (1977)
Rabdosia kunmingensis	C.Y.Wu & H.W.Li	Fl. Yunnanica 1: 776 (1977)

Common names Top

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Language	Common/alternative name
Chinese	昆明香茶菜
Chinese	间断香茶菜

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

Asia-temperate click to expand
- China
  - China South-central

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000217875
Tropicos	17607228
KEW	urn:lsid:ipni.org:names:915132-1
The Plant List	kew-102947
Open Tree Of Life	7054286
Observations.org	451795
NCBI Taxonomy	2494286
IPNI	915132-1
GBIF	5608996
EOL	2898955
Elurikkus	556241

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)!
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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

Antimicrobial Diterpenes: Recent Development From Natural Sources

Saha P, Rahman FI, Hussain F, Rahman SM, Rahman MM

Front Pharmacol

28-Feb-2022

PMCID:	PMC8918777
doi:	10.3389/fphar.2021.820312
PMID:	35295739

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

Diterpenoids from Rabdosia kunmingensis

Zhang Hongjie, Sun Handong

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(89)80357-7

Diterpenoids from Isodon adenoloma

Zhang Rong Ping, Zhang Hongjie, Lin Zhongwen, Zhen Yulin, Sun Handong

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)80450-S

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!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4aR,4bS,7S,10aR)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	44592590	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
1-Phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)-, [1R-(1alpha,4abeta,10aalpha)]-	1201531	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S
1,4a-Dimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-1-carboxylic acid	15618	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S
7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	267302	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5S,9R,10S,12S,13R,16R)-12,16-dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14563760	Click to see CC1(CCCC2(C1CCC34C2CC(C(C3O)C(=C)C4=O)O)C)CO	334.40	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
(2,11,12-Trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14563757	Click to see CC(=O)OC1C2C(C(C3C1(C(CC4C3(CCCC4(C)C)C)O)C(=O)C2=C)O)O	392.50	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S
[(1R,2R,4R,9R,10S,11R,12R,13S,16R)-2,11,12-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162868359	Click to see CC(=O)OC1C2C(C(C3C1(C(CC4C3(CCCC4(C)C)C)O)C(=O)C2=C)O)O	392.50	unknown	https://doi.org/10.1016/S0031-9422(01)00245-X
12,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14563759	Click to see CC1(CCCC2(C1CCC34C2CC(C(C3O)C(=C)C4=O)O)C)CO	334.40	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S
2,11,12,16-Tetrahydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14563775	Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)CO	366.40	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S
2,11,12,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14466845	Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)C	350.40	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
2,11,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14563771	Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)CO	350.40	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
2,12,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14563761	Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)CO	350.40	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
Rabdokunmin A	14563758	Click to see CC(=O)OC1C2C(C(C3C1(C(CC4C3(CCCC4(C)C)C)O)C(=O)C2=C)O)O	392.50	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
rabdokunmin C	14563762	Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)CO	350.40	unknown	https://doi.org/10.1016/S0031-9422(01)00245-X https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7
Rabdokunmin D	45267139	Click to see CC1(CCCC2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)CO	350.40	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/S0031-9422(01)00245-X
Rabdokunmin E	101831556	Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)CO	366.40	unknown	https://doi.org/10.1016/0031-9422(89)80357-7 https://doi.org/10.1016/0031-9422(92)80450-S
Rabdoloxin B	25195035	Click to see CC1(CCCC2(C1CC(C34C2C(C(C(C3O)C(=C)C4=O)O)O)O)C)C	350.40	unknown	https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(89)80357-7

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Isodon interruptus

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top