Scientific name	Authority	First published in
Plectranthus adenanthus	Diels	Notes Roy. Bot. Gard. Edinburgh 5: 228 (1912)
Plectranthus wui	Y.Z.Sun	Acta Phytotax. Sin. 11: 55 (1966)
Rabdosia adenantha	(Diels) H.Hara	J. Jap. Bot. 47: 193 (1972)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	水龙胆草
Chinese	水龙胆草根
Chinese	腺花香茶菜
Chinese	大钮子七
Chinese	路边金
Chinese	铁石元

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000217810
Tropicos	17607261
KEW	urn:lsid:ipni.org:names:448563-1
The Plant List	kew-102888
Open Tree Of Life	1067800
NCBI Taxonomy	662902
IPNI	448563-1
GBIF	5610159
EOL	2898926

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

ent-Kaurane diterpenoids induce apoptosis and ferroptosis through targeting redox resetting to overcome cisplatin resistance

Sun Y, Qiao Y, Liu Y, Zhou J, Wang X, Zheng H, Xu Z, Zhang J, Zhou Y, Qian L, Zhang C, Lou H

Redox Biol

16-Apr-2021

PMCID:	PMC8099784
doi:	10.1016/j.redox.2021.101977
PMID:	33905957

Peroxiredoxin-1 Overexpression Attenuates Doxorubicin-Induced Cardiotoxicity by Inhibiting Oxidative Stress and Cardiomyocyte Apoptosis

Jiang L, Gong Y, Hu Y, You Y, Wang J, Zhang Z, Wei Z, Tang C

Oxid Med Cell Longev

29-Jul-2020

PMCID:	PMC7411498
doi:	10.1155/2020/2405135
PMID:	32802259

Mechanistic Pathways and Molecular Targets of Plant-Derived Anticancer ent-Kaurane Diterpenes

Sarwar MS, Xia YX, Liang ZM, Tsang SW, Zhang HJ

Biomolecules

16-Jan-2020

PMCID:	PMC7023344
doi:	10.3390/biom10010144
PMID:	31963204

Significance of NF-κB as a pivotal therapeutic target in the neurodegenerative pathologies of Alzheimer’s disease and multiple sclerosis

Srinivasan M, Lahiri DK

Expert Opin Ther Targets

04-Feb-2015

PMCID:	PMC5873291
doi:	10.1517/14728222.2014.989834
PMID:	25652642

Oxidative Stress, Redox Regulation and Diseases of Cellular Differentiation

Ye ZW, Zhang J, Townsend DM, Tew KD

Biochim Biophys Acta

15-Nov-2014

PMCID:	PMC4433447
doi:	10.1016/j.bbagen.2014.11.010
PMID:	25445706

Adenanthin targets peroxiredoxin I/II to kill hepatocellular carcinoma cells

Hou JK, Huang Y, He W, Yan ZW, Fan L, Liu MH, Xiao WL, Sun HD, Chen GQ

Cell Death Dis

04-Sep-2014

PMCID:	PMC4540188
doi:	10.1038/cddis.2014.345
PMID:	25188510

Studies on chemical constituents of Rabdosia serra

ZHENG Qin

China Journal of Chinese Materia Medica

22-Sep-2011

doi:	10.4268/CJCMM20111611

Two new ent-kaurane diterpenoids from Isodon excisoides

Ji Xia Zhang, Yong Xue Wang, Zhi An He, Fu Lin Yan, Han Dong Sun

Elsevier BV

31-Dec-2008

doi:	10.1016/J.CCLET.2008.10.040

Adenanthusone, a New Ursane Type Nortriterpenoid from Isodon adenanthus.

Wei Xiang, Qi‐Shi Song, Hong‐Jie Zhang, Rong‐Tao Li, Zhi Na, Han‐Dong Sun

Wiley

22-Mar-2005

doi:	10.1002/CHIN.200516159

Adenanthusone, a New Ursane Type Nortriterpenoid from <i>Isodon adenanthus</i>

Wei Xiang, Qi‐Shi Song, Hong‐Jie Zhang, Rong‐Tao Li, Zhi Na, Han‐Dong Sun

Wiley

24-Nov-2004

doi:	10.1002/HLCA.200490255

ent-Kaurene diterpenoids from Isodon oresbius.

Xiang W, Li RT, Wang ZY, Li SH, Zhao QS, Zhang HJ, Sun HD

Phytochemistry

01-Apr-2004

doi:	10.1016/J.PHYTOCHEM.2004.02.022
PMID:	15110700

Diterpenoids from Isodon adenantha.

Jiang B, Yang H, Li ML, Hou AJ, Han QB, Wang SJ, Li SH, Sun HD

J Nat Prod

01-Aug-2002

doi:	10.1021/NP020084K
PMID:	12193013

Structure of Adenanthin

Yun-long Xu, Han-dong Sun, De-zu Wang, Takashi Iwashita, Hajime Komura, Mutsuo Kozuka, Keizo Naya, Isao Kubo

Elsevier BV

25-Jul-2002

doi:	10.1016/S0040-4039(00)95765-4

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

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 / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Octacosanoic acid	10470	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	424.70	unknown	https://doi.org/10.4268/CJCMM20111611
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(2S,4S,4aS,4bR,5S,7S,10aR)-4,5-dihydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,1,4a-trimethyl-10-oxo-3,4,4b,5,6,7,8,10a-octahydro-2H-phenanthren-2-yl] acetate	11111974	Click to see CC(=O)OC1CC(C2(C3C(CC(CC3=CC(=O)C2C1(C)C)C(=C)CO)O)C)O	392.50	unknown	https://doi.org/10.1021/NP020084K
[(2S,4S,4aS,5S,7S,10aR)-4,5-dihydroxy-7-(3-hydroxyprop-1-en-2-yl)-1,1,4a-trimethyl-10-oxo-3,4,4b,5,6,7,8,10a-octahydro-2H-phenanthren-2-yl] acetate	101193824	Click to see CC(=O)OC1CC(C2(C3C(CC(CC3=CC(=O)C2C1(C)C)C(=C)CO)O)C)O	392.50	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(2,8-Diacetyloxy-3,6-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	3665870	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)O)(C)C)O)OC(=O)C)C)C(=O)C2=C	492.60	unknown	https://doi.org/10.1016/0031-9422(92)80450-S
(2,8-Diacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	72245809	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3OC(=O)C)C(C(CC4OC(=O)C)O)(C)C)C)C(=O)C2=C	476.60	unknown	https://doi.org/10.1016/0031-9422(92)80450-S
(2,8-Diacetyloxy-6,15-dihydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	85319341	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3OC(=O)C)C(C(CC4OC(=O)C)O)(C)C)C)C(C2=C)O	478.60	unknown	https://doi.org/10.1016/J.CCLET.2008.10.040 https://doi.org/10.1016/S0367-326X(00)00126-X
(6-Acetyloxy-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	73809281	Click to see CC(=O)OC1CC2C(C(CC(C2(C3C14CC(CC3O)C(=C)C4=O)C)O)OC(=O)C)(C)C	434.50	unknown	https://doi.org/10.1016/0031-9422(92)80450-S
[(1R,2R,3R,4R,6S,8S,9R,10S,11S,13S)-2-acetyloxy-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162998611	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)O)OC(=O)C)C(=O)C4=C)O)C)O	450.50	unknown	https://doi.org/10.1021/NP020084K
[(1R,2R,3R,4S,6R,7S,9R,10S,11S,13S)-2,6-diacetyloxy-3,7-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	10505290	Click to see CC(=O)OC1CC2CC3(C1C4(CC(C(C(C4C(C3OC(=O)C)O)(C)C)OC(=O)C)O)C)C(=O)C2=C	492.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022
[(1R,2S,4R,6S,8S,9R,10S,11S,13S,15R)-2,8,15-triacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	11060386	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3OC(=O)C)C(C(CC4OC(=O)C)O)(C)C)C)C(C2=C)OC(=O)C	520.60	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X https://doi.org/10.1021/NP020084K
[(1R,2S,4R,6S,8S,9R,10S,11S,13S)-2-acetyloxy-6,8-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	10950145	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3OC(=O)C)C(C(CC4O)O)(C)C)C)C(=O)C2=C	434.50	unknown	https://doi.org/10.1021/NP020084K https://doi.org/10.1016/S0367-326X(00)00126-X
[(1S,2R,3R,4R,6S,8S,9R,10S,11S,13S,15R)-2,8-diacetyloxy-3,6,15-trihydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	101193825	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)O)(C)C)O)OC(=O)C)C)C(C2=C)O	494.60	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X https://doi.org/10.1021/NP020084K
[(1S,2R,4R,6S,8S,9S,10S,11S,13R,15R)-2,8,15-triacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-3-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163085285	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)O)OC(=O)C)C)C(C2=C)OC(=O)C	534.60	unknown	https://doi.org/10.1021/NP020084K
[(1S,2S,4R,6S,8S,9R,10S,11S,13S,15R)-2,8-diacetyloxy-6,15-dihydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	10928901	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3OC(=O)C)C(C(CC4OC(=O)C)O)(C)C)C)C(C2=C)O	478.60	unknown	https://doi.org/10.1021/NP020084K
[(1S,2S,4R,6S,8S,9R,10S,11S,13S,15R)-8-acetyloxy-6,11,15-trihydroxy-5,5,9-trimethyl-14-methylidene-2-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	10972161	Click to see CC(=O)OC1CC2C(C(CC(C2(C3C14CC(CC3O)C(=C)C4O)C)OC(=O)C)O)(C)C	436.50	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X https://doi.org/10.1021/NP020084K
[(1S,4R,6S,8R,9S,10S,11R,13R,16R)-8,16-diacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163103465	Click to see CC(=O)OC1CC2C(C3(C1C4(C(CC(C(C4C(=O)C3)(C)C)O)OC(=O)C)C)C(=O)C2=C)OC(=O)C	490.50	unknown	https://doi.org/10.1021/NP020084K
[(1S,4R,6S,8R,9S,10S,11R,16R)-8,16-diacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163187541	Click to see CC(=O)OC1CC2C(C3(C1C4(C(CC(C(C4C(=O)C3)(C)C)O)OC(=O)C)C)C(=O)C2=C)OC(=O)C	490.50	unknown	https://doi.org/10.1021/NP020084K
[(2R,4R,6S,8S,9S,10S,11S,13R,15R)-2,8,15-triacetyloxy-6-hydroxy-5,5,9-trimethyl-14-methylidene-3-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163189225	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)O)OC(=O)C)C)C(C2=C)OC(=O)C	534.60	unknown	https://doi.org/10.1021/NP020084K
Adenanthin	15011073	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)O)OC(=O)C)C)C(=O)C2=C	490.50	unknown	https://doi.org/10.1016/S0040-4039(00)95765-4 https://doi.org/10.4268/CJCMM20111611 https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022 https://doi.org/10.1016/S0367-326X(00)00126-X
Adenanthin C	10928875	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC3OC(=O)C)C(C(CC4OC(=O)C)O)(C)C)C)C(=O)C2=C	476.60	unknown	https://doi.org/10.1021/NP020084K https://doi.org/10.1016/S0367-326X(00)00126-X
Adenanthin E	10982976	Click to see CC(=O)OC1CC2C(C(CC(C2(C3C14CC(CC3O)C(=C)C4O)C)O)OC(=O)C)(C)C	436.50	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X https://doi.org/10.1021/NP020084K
Adenanthin F	10873754	Click to see CC(=O)OC1CC2C(C(CC(C2(C3C14CC(CC3O)C(=C)C4=O)C)O)OC(=O)C)(C)C	434.50	unknown	https://doi.org/10.1021/NP020084K https://doi.org/10.1016/S0367-326X(00)00126-X
Adenanthin I	11091621	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(C(C(C2C1(C)C)O)OC(=O)C)C(=O)C4=C)O)C)O	450.50	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X
Adenanthin J	11081505	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)O)OC(=O)C)C)C(C2=C)O	492.60	unknown	https://doi.org/10.1021/NP020084K https://doi.org/10.1016/S0367-326X(00)00126-X
Adenanthin K	11081506	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3O)(C)C)O)OC(=O)C)C)C(C2=C)OC(=O)C	492.60	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X https://doi.org/10.1021/NP020084K
calcicolin B	44577319	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)O)O)C)C(=O)C2=C	448.50	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X https://doi.org/10.1021/NP020084K
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/J.PHYTOCHEM.2004.02.022
Nervosanin	15139218	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3OC(=O)C)(C)C)O)OC(=O)C)C)C(C2=C)OC(=O)C	534.60	unknown	https://doi.org/10.1016/S0367-326X(00)00126-X
Weisiensin A	377386	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)O)(C)C)O)OC(=O)C)C)C(=O)C2=C	492.60	unknown	https://doi.org/10.4268/CJCMM20111611 https://doi.org/10.1016/S0367-326X(00)00126-X
Weisiensin A	14355978	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)O)(C)C)O)OC(=O)C)C)C(=O)C2=C	492.60	unknown	https://doi.org/10.1021/NP020084K
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.4268/CJCMM20111611
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,2S,4S,5R,6S,11R,14R,15S,18S,22R,23R)-9-hydroxy-6,10,14,15,22-pentamethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacos-9-ene-8,25-dione	101136418	Click to see CC1C2C3(CCC1=C)CCC4(C2(C5C(O5)C6C4(CCC7C6(CC(=O)C(=C7C)O)C)C)OC3=O)C	466.60	unknown	https://doi.org/10.1002/HLCA.200490255 https://doi.org/10.1002/CHIN.200516159
9-Hydroxy-6,10,14,15,22-pentamethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacos-9-ene-8,25-dione	162891644	Click to see CC1C2C3(CCC1=C)CCC4(C2(C5C(O5)C6C4(CCC7C6(CC(=O)C(=C7C)O)C)C)OC3=O)C	466.60	unknown	https://doi.org/10.1002/HLCA.200490255

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Isodon adenanthus

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