Common products:

Industrial and craft applications:

Food and beverages (non-medicinal):

Colorants and tanning:

Wood and fiber:

Fragrance and cosmetics:

Properties relevant to use:
Oridonin, a diterpenoid present in Isodon excisus, is a crystalline solid with well-characterized physical properties enabling handling in standard chemical laboratories (neutral pH stability in aqueous/organic media at ambient temperature; melting point in the range reported for oridonin; presence of characteristic functional groups allowing standard detection by TLC and HPLC).

Standards and regulation:
Standard chemical-reagent status (catalog-grade) with referenced physical constants and purity specifications in reagent catalogs; disposal according to national chemical waste regulations (e.g., RCRA in the U.S., CLP in the EU); no established monograph in pharmacopoeias for this species or oridonin.

Scientific/model organism use:
Isodon excisus serves as a documented botanical source of oridonin for in vitro assays and chemical standardization. Aerial parts (leaves and stems) are harvested and processed via ethanol extraction followed by purification (e.g., solvent partition and HPLC), yielding oridonin reference material for analytical chemistry, mechanism-of-action studies in cellular systems, and lab protocols. The species is listed in taxonomy databases (e.g., NCBI Taxonomy), and voucher specimens may be maintained to document source authenticity for research datasets and publications.

Sustainability and sourcing:

Synonyms Top

Scientific name	Authority	First published in
Plectranthus excisus	Maxim.	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 213 (1859)
Rabdosia excisa	(Maxim.) H.Hara	J. Jap. Bot. 47: 195 (1972)
Rabdosia excisa f. albiflora	(Sakata) H.Hara	J. Jap. Bot. 47: 195 (1972)
Rabdosia excisa var. chiisanensis	(Nakai) Murata	Acta Phytotax. Geobot. 40: 100 (1989)
Stachys polygonatum	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 449 (1911)
Amethystanthus excisus var. coreanus	Nakai	Bot. Mag. (Tokyo) 48: 788. 1934
Amethystanthus excisus	(Maxim.) Nakai	Bot. Mag. (Tokyo) 48: 787 (1934)
Amethystanthus excisus f. albiflorus	Sakata	Acta Phytotax. Geobot. 7: 16 1938
Amethystanthus excisus var. chiisanensis	Nakai	Bot. Mag. (Tokyo) 48: 788 1934
Rabdosia umbrosa var. coreana	(T.B.Lee) Y.N.Lee	Fl. Korea 1: 696 (1996)
Isodon excisus f. albiflorus	(Sakata) H.Hara	Enum. Spermatophytarum Japon. 1: 205 (1948)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	野苏子
Chinese	尾叶香茶菜
Chinese	高丽花
Chinese	龟叶草

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

Suggest a correction or add new data!

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 North-central
  - Manchuria
- Eastern Asia
  - Korea
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000217853
Tropicos	17607188
KEW	urn:lsid:ipni.org:names:448575-1
The Plant List	kew-102927
Open Tree Of Life	624040
NCBI Taxonomy	705303
IPNI	448575-1
iNaturalist	565880
GBIF	5609026
EOL	2898941
CMAUP	NPO17628

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

Natural Products as Anticancer Agents: Current Status and Future Perspectives

Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q

Molecules

30-Nov-2022

PMCID:	PMC9737905
doi:	10.3390/molecules27238367
PMID:	36500466

Temporal Variation Dominates in Local Carabid Beetle Communities in Korean Mountains

Park Y, Jang T, Kim J, Kim SK, Kim IK, Kim CJ, Takami Y

Insects

12-Nov-2021

PMCID:	PMC8624729
doi:	10.3390/insects12111019
PMID:	34821819

Manipulation of Dietary Intake on Changes in Circulating Testosterone Concentrations

Zamir A, Ben-Zeev T, Hoffman JR

Nutrients

25-Sep-2021

PMCID:	PMC8538516
doi:	10.3390/nu13103375
PMID:	34684376

In Silico Studies of Lamiaceae Diterpenes with Bioinsecticide Potential against Aphis gossypii and Drosophila melanogaster

Rodrigues GC, dos Santos Maia M, Silva Cavalcanti AB, de Sousa NF, Scotti MT, Scotti L

Molecules

02-Feb-2021

PMCID:	PMC7867283
doi:	10.3390/molecules26030766
PMID:	33540716

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

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

Human Cytochrome P450 Enzymes 5-51 as Targets of Drugs and Natural and Environmental Compounds: Mechanisms, Induction, and Inhibition—Toxic Effects and Benefits

Rendic S, Guengerich FP

Drug Metab Rev

01-Aug-2018

PMCID:	PMC6421578
doi:	10.1080/03602532.2018.1483401
PMID:	30717606

Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus

Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J

Int J Mol Sci

14-May-2018

PMCID:	PMC5983620
doi:	10.3390/ijms19051459
PMID:	29757986

All that glitters is not Ramularia

Videira SI, Groenewald JZ, Braun U, Shin HD, Crous PW

Stud Mycol

29-Jun-2016

PMCID:	PMC4986539
doi:	10.1016/j.simyco.2016.06.001
PMID:	27570325

Elucidating the Ramularia eucalypti species complex

Videira SI, Groenewald JZ, Kolecka A, van Haren L, Boekhout T, Crous PW

Persoonia

20-Nov-2014

PMCID:	PMC4510271
doi:	10.3767/003158515X685670
PMID:	26240445

Dimeric ent-kaurane diterpenoids from Isodon excisus.

Hong SS, Lee SA, Lee C, Han XH, Choe S, Kim N, Lee D, Lee CK, Kim Y, Hong JT, Lee MK, Hwang BY

J Nat Prod

28-Nov-2011

doi:	10.1021/NP200439N
PMID:	22066578

Pyrrolidinone diterpenoid from Isodon excisus and inhibition of nitric oxide production in lipopolysaccharide-induced macrophage RAW264.7 cells.

Hong SS, Lee SA, Kim N, Hwang JS, Han XH, Lee MK, Jung JK, Hong JT, Kim Y, Lee D, Hwang BY

Bioorg Med Chem Lett

15-Feb-2011

doi:	10.1016/J.BMCL.2010.11.095
PMID:	21273070

Inhibitors of Microglial Neurotoxicity: Focus on Natural Products

Choi DK, Koppula S, Suk K

Molecules

25-Jan-2011

PMCID:	PMC6259841
doi:	10.3390/molecules16021021
PMID:	21350391

Phylogenetic lineages in the Capnodiales

Crous PW, Schoch CL, Hyde KD, Wood AR, Gueidan C, de Hoog GS, Groenewald JZ

Stud Mycol

01-Jan-2009

PMCID:	PMC2816965
doi:	10.3114/sim.2009.64.02
PMID:	20169022

Phytochemical Profile Top

Add a new one!

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-Hydroxy-3,5-dimethoxybenzoate	54694262	Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O	197.16	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
(1R,5S,7S)-3-[(3,4-dihydroxyphenyl)-hydroxymethylidene]-6,6-dimethyl-1,7-bis(3-methylbut-3-enyl)-5-[(2,4,4-trimethylcyclohexen-1-yl)methyl]bicyclo[3.3.1]nonane-2,4,9-trione	102283888	Click to see	602.80	unknown	https://doi.org/10.1021/NP060638+
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(16S)-16-hydroxy-9-oxooctadeca-10,12,14-trienoic acid	91478638	Click to see	308.40	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
Corchorifatty Acid B	22956671	Click to see	308.40	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(15-Acetyloxy-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14414556	Click to see	436.50	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	10066480	Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)CO	350.40	unknown	https://doi.org/10.1021/NP030357R
(1R,2R,4R,8S,9R,10S,13R)-2,8,16-trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	146014674	Click to see	350.40	unknown	https://doi.org/10.1021/NP030357R https://doi.org/10.1016/0031-9422(91)83072-S
(1R,2R,4R,8S,9R,10S,13S,14S,16R)-2,8,16-trihydroxy-9,14-bis(hydroxymethyl)-5,5-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	10714063	Click to see	368.50	unknown	https://doi.org/10.1021/NP970155T
(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/10.1021/NP030357R
(1R,2R,4R,8S,9R,10S,13S,16S)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	162871586	Click to see	334.40	unknown	https://doi.org/10.1016/S0031-9422(01)00245-X
(1R,2R,4S,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-9-(hydroxymethyl)-5-methyl-14-methylidene-15-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde	10594940	Click to see CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C=O	364.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.02.022 https://doi.org/10.1021/NP970155T
(1R,2R,4S,6S,9R,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	70691853	Click to see	334.40	unknown	via CMAUP database
(1R,2R,4S,9R,10S,12S,13R,16R)-2,12,16-trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	45271374	Click to see	350.40	unknown	via CMAUP database
(1R,2S,4S,5S,9S,10S,13R)-2-acetyloxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid	102004542	Click to see	360.50	unknown	via CMAUP database
(1R,2S,5S,8R,9S,11R,15S,18R)-9,15,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	10315734	Click to see	348.40	unknown	https://doi.org/10.1021/NP030357R
(1R,4R,9R,10S)-2,8,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	137795540	Click to see	350.40	unknown	https://doi.org/10.1016/0031-9422(91)83072-S https://doi.org/10.1021/NP030357R
(1S,2R,4R,8S,9R,12S,13S,16S)-2,8,12-trihydroxy-5,5-dimethyl-18-methylidene-11-oxapentacyclo[11.3.2.01,12.04,9.09,16]octadecan-17-one	101345678	Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C	348.40	unknown	https://doi.org/10.1021/NP030357R
(1S,2S,5S,8S,9R,11R,15S,16S,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	102371731	Click to see	362.50	unknown	https://doi.org/10.1016/0031-9422(91)83072-S
(2,8,16-Trihydroxy-5,5-dimethyl-14-methylidene-15-oxo-9-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate	3847003	Click to see CC(=O)OCC12C3CCC4C(C3(C(CC1C(CCC2O)(C)C)O)C(=O)C4=C)O	392.50	unknown	https://doi.org/10.1021/NP030357R
(2,8,16-Trihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate	75048976	Click to see	392.50	unknown	https://doi.org/10.1021/NP030357R
(2R,4S,8S,9R,10S,12S,16S)-2,8,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	50987574	Click to see	350.40	unknown	via CMAUP database
(2R,4S,9R,10R)-2,16-dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione	50987570	Click to see	332.40	unknown	via CMAUP database
(3,11-Dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	13874227	Click to see	376.50	unknown	https://doi.org/10.1021/NP060638+
(3,8,11-Trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	13874231	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(=O)C4=C)O)C)O	392.50	unknown	https://doi.org/10.1021/NP060638+
(4R,10S,16R)-2,8,12,16-tetrahydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	5320877	Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)O)C	366.40	unknown	https://doi.org/10.1021/NP030357R
(6-Acetyloxy-3,8,15-trihydroxy-5,5,9-trimethyl-14-methylidene-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14219410	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(C2=C)O	436.50	unknown	https://doi.org/10.1021/NP060638+
(6-Acetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	163047622	Click to see	418.50	unknown	https://doi.org/10.1021/NP060638+
(6-Acetyloxy-8-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14219409	Click to see	432.50	unknown	https://doi.org/10.1021/NP060638+
(8,11-Dihydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14414558	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(=O)C2C1(C)C)C(=O)C4=C)O)C)O	390.50	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
[(16R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-12-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	367618	Click to see	392.50	unknown	https://doi.org/10.1021/NP030357R https://doi.org/10.1016/0031-9422(91)83072-S
[(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate	44575548	Click to see	392.50	unknown	https://doi.org/10.1016/S0031-9422(96)00738-8 https://doi.org/10.1021/NP030357R
[(1R,2R,4R,5S,8S,9R,10S,13S,16R)-2,8,16-trihydroxy-9-(hydroxymethyl)-5-methyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate	101712256	Click to see	408.50	unknown	via CMAUP database
[(1R,4R,6S,8S,9R,10S,11R,13S)-8,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162870763	Click to see	376.50	unknown	https://doi.org/10.1021/NP060638+
[(1R,4S,5R,6R,9R,10S,11R,13S,15R)-6,11,15-trihydroxy-5,9-dimethyl-14-methylidene-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate	162870761	Click to see	378.50	unknown	https://doi.org/10.1021/NP060638+
[(1R,4S,5R,6S,9R,10S,11R,13S)-11-hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162885244	Click to see CC(=O)OC1CCC2(C(C1(C)CO)CCC34C2C(CC(C3)C(=C)C4=O)O)C	376.50	unknown	https://doi.org/10.1021/NP060638+
[(1R,4S,5R,9R,10S,11R,13S)-11-hydroxy-5,9-dimethyl-14-methylidene-6,15-dioxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate	162946321	Click to see CC(=O)OCC1(C2CCC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)C	374.50	unknown	https://doi.org/10.1021/NP060638+
[(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	via CMAUP database
[(1S,2S,5S,7R,8S,10S,11R,15R)-7-acetyloxy-9,15-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-10-yl] acetate	102004540	Click to see	434.50	unknown	via CMAUP database
[(1S,3S,4R,6S,8R,9R,10S,11R,13S)-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162887309	Click to see	392.50	unknown	https://doi.org/10.1021/NP060638+
[(1S,3S,4R,6S,8R,9R,10S,11R,13S)-8-acetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162933079	Click to see	434.50	unknown	https://doi.org/10.1021/NP060638+
[(1S,3S,4R,6S,8S,9R,10R,11S,13S,15R)-15-acetyloxy-3,8,11-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163030495	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(C4=C)OC(=O)C)O)C)O	436.50	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
[(1S,3S,4R,6S,8S,9R,10S,11R,13S)-3,6,8-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162932886	Click to see	392.50	unknown	https://doi.org/10.1021/NP060638+
[(1S,4S,9S,10R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-12-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	137705109	Click to see	392.50	unknown	https://doi.org/10.1021/NP030357R https://doi.org/10.1016/0031-9422(91)83072-S
[11-Hydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-[(5-oxopyrrolidin-2-yl)oxymethyl]-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	75599925	Click to see CC(=O)OC1CCC2(C(C1(C)COC3CCC(=O)N3)CCC45C2C(CC(C4)C(=C)C5=O)O)C	459.60	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
1,7,12,14-Tetrahydroxykaur-16-en-15-one (1alpha,7alpha,12alpha,14R)	174150	Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C	350.40	unknown	https://doi.org/10.1021/NP030357R https://doi.org/10.1016/0031-9422(91)83072-S
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/10.1021/NP030357R
2,12,16-Trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	73657179	Click to see CC1(CCCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)C	350.40	unknown	https://doi.org/10.1021/NP030357R
2,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	72742985	Click to see	334.40	unknown	https://doi.org/10.1016/0031-9422(92)90064-W https://doi.org/10.1016/0031-9422(92)80450-S
2,16-Dihydroxy-5,9-bis(hydroxymethyl)-5-methyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	73657180	Click to see CC1(CCCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)CO	350.40	unknown	https://doi.org/10.1021/NP030357R
2,8,12-Trihydroxy-5,5-dimethyl-18-methylidene-11-oxapentacyclo[11.3.2.01,12.04,9.09,16]octadecan-17-one	73657178	Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C	348.40	unknown	https://doi.org/10.1021/NP030357R
2,8,12,16-Tetrahydroxy-5,5,9-trimethyl-14-methylene-tetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	13193212	Click to see	350.40	unknown	https://doi.org/10.1246/CL.1981.753 https://doi.org/10.1021/NP030357R
2,8,12,16-Tetrahydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14466843	Click to see CC1(CCC(C2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)CO)O)C	366.40	unknown	https://doi.org/10.1021/NP030357R
2,8,16-Trihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	73657181	Click to see	350.40	unknown	https://doi.org/10.1021/NP030357R
2,8,16-Trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	3819	Click to see	350.40	unknown	https://doi.org/10.1021/NP030357R
3,11-Dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-6,15-dione	162843643	Click to see CC1(C2C(CC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)O)C	332.40	unknown	https://doi.org/10.1021/NP060638+
3beta,11beta-Diacetoxy-1alpha-hydroxykaura-16-ene-6,15-dione	442041	Click to see	432.50	unknown	https://doi.org/10.1021/NP060638+ https://doi.org/10.1007/BF02976453
7beta-Hydroxykaur-16-en-19-oic acid	101526595	Click to see	318.40	unknown	via CMAUP database
8,16-Dihydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	56671376	Click to see	334.40	unknown	via CMAUP database
CID 102004538	102004538	Click to see	320.50	unknown	via CMAUP database
Excisanin A	11772488	Click to see	350.40	unknown	https://doi.org/10.1246/CL.1981.753 https://doi.org/10.1021/NP030357R
Excisanin B	13193213	Click to see	392.50	unknown	https://doi.org/10.1246/CL.1981.753 https://doi.org/10.1021/NP030357R
Excisanin C	15011613	Click to see	334.40	unknown	https://doi.org/10.1016/0031-9422(92)90064-W https://doi.org/10.1016/0031-9422(92)80450-S https://doi.org/10.1016/0031-9422(91)83072-S
Excisanin H	10066342	Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C	348.40	unknown	https://doi.org/10.1021/NP030357R
Excisanin I	10360537	Click to see	350.40	unknown	https://doi.org/10.1021/NP030357R
Excisanin J	10405621	Click to see CC1(CCCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)CO	350.40	unknown	https://doi.org/10.1021/NP030357R
Excisanin K	45270538	Click to see	334.40	unknown	https://doi.org/10.1021/NP030357R
Excisusin A	16215553	Click to see	376.50	unknown	https://doi.org/10.1021/NP060638+
Excisusin B	16215554	Click to see	376.50	unknown	https://doi.org/10.1021/NP060638+
excisusin C	16215670	Click to see CC(=O)OCC1(C2CCC34CC(CC(C3C2(CCC1O)C)O)C(=C)C4O)C	378.50	unknown	https://doi.org/10.1021/NP060638+
Excisusin D	16215671	Click to see	392.50	unknown	https://doi.org/10.1021/NP060638+
Excisusin E	16215672	Click to see	374.50	unknown	https://doi.org/10.1021/NP060638+
Excisusin F	53323644	Click to see CC(=O)OC1CCC2(C(C1(C)COC3CCC(=O)N3)CCC45C2C(CC(C4)C(=C)C5=O)O)C	459.60	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
Henryin	11741244	Click to see CC(=O)OCC12C3CCC4C(C3(C(CC1C(CCC2O)(C)C)O)C(=O)C4=C)O	392.50	unknown	https://doi.org/10.1021/NP030357R
Inflexanin A	13874229	Click to see	376.50	unknown	https://doi.org/10.1021/NP060638+
Inflexanin B	44421638	Click to see	392.50	unknown	https://doi.org/10.1021/NP060638+
inflexarabdonin A	44421642	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3)O)(C)C)OC(=O)C)O)C)C(C2=C)O	436.50	unknown	https://doi.org/10.1021/NP060638+
Inflexarabdonin D	53324240	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(C2C1(C)C)O)C(C4=C)OC(=O)C)O)C)O	436.50	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
Inflexarabdonin E	53324930	Click to see CC(=O)OC1CC(C2(C3C(CC4CC3(CC(=O)C2C1(C)C)C(=O)C4=C)O)C)O	390.50	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
Inflexarabdonin G	44421637	Click to see	418.50	unknown	https://doi.org/10.1021/NP060638+
inflexarabdonin I	44421635	Click to see CC1(C2C(CC34CC(CC(C3C2(CCC1=O)C)O)C(=C)C4=O)O)C	332.40	unknown	https://doi.org/10.1021/NP060638+
Inflexin	10502865	Click to see	432.50	unknown	https://doi.org/10.1021/NP060638+ https://doi.org/10.1007/BF02976453
Inflexinol	44421641	Click to see	434.50	unknown	https://doi.org/10.1021/NP060638+
Kamebakaurin	13945489	Click to see	350.40	unknown	https://doi.org/10.1021/NP030357R
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/10.1021/NP030357R https://doi.org/10.1016/0031-9422(91)83072-S
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/10.1021/NP030357R
Rabdoserrin B	14466844	Click to see	366.40	unknown	https://doi.org/10.1021/NP030357R
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
1-O-(2,3,19,23-Tetrahydroxy-28-oxours-12-en-28-yl)hexopyranose	44566341	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	666.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1S,2R,5S,8S,9R,11R,15S,18R)-15,18-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecane-7,16-dione	44575567	Click to see	346.40	unknown	https://doi.org/10.1021/NP030357R
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1007/BF02976453
(4aS,6aS,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	11887403	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Arjunolic acid	73641	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Asiatic Acid	119034	Click to see	488.70	unknown	via CMAUP database
Biexcisusin A, (rel)-	57393032	Click to see	903.10	unknown	https://doi.org/10.1021/NP200439N
Biexcisusin B, (rel)-	57398302	Click to see	869.00	unknown	https://doi.org/10.1021/NP200439N
Biexcisusin C, (rel)-	57399961	Click to see	901.00	unknown	https://doi.org/10.1021/NP200439N
Biexcisusin D, (rel)-	57403476	Click to see	899.00	unknown	https://doi.org/10.1021/NP200439N
Biexcisusin E, (rel)-	57403477	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(=O)C3)(C)C)OC(=O)C)O)C)C(=O)OC5(CCC2=O)C6CC(C7C8(C(CC(C(C8C(CC7(C6)C5=O)O)(C)C)OC(=O)C)O)C)OC(=O)C	899.00	unknown	https://doi.org/10.1021/NP200439N
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	via CMAUP database
Npc62469	49867942	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
Solasodine	442985	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1	413.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	52940117	Click to see	576.80	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
Eustifoline C	14635307	Click to see CC1=CC2=C(C=C1)NC3=C2C(=C(C=C3)O)CC=C(C)CCC=C(C)C	333.50	unknown	https://doi.org/10.1246/CL.1981.753 https://doi.org/10.1021/NP030357R
> Organoheterocyclic compounds / Oxepanes
6-(3-Hydroxybut-1-enyl)-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol	539381	Click to see	226.31	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
Corchoionol A	10656857	Click to see CC(C=CC12C(CC(CC1(O2)C)O)(C)C)O	226.31	unknown	https://doi.org/10.1016/J.BMCL.2010.11.095
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-(4-Hydroxy-3-Methoxyphenyl)-N-(2-(4-Hydroxyphenyl)-2-Methoxyethyl)Acrylamide	643362	Click to see	343.40	unknown	https://doi.org/10.1021/NP000604G
3-(4-hydroxy-3-methoxyphenyl)-N-[2-(4-hydroxyphenyl)-2-methoxyethyl]prop-2-enamide	68977241	Click to see	343.40	unknown	https://doi.org/10.1021/NP000604G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3-(3,4-Dihydroxyphenyl) acrylic acid 1-(3,4-dihydroxyphenyl)-2-methoxycarbonylethyl ester	73809375	Click to see	374.30	unknown	https://doi.org/10.1021/NP000604G
methyl (3S)-3-(3,4-dihydroxyphenyl)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxypropanoate	10452024	Click to see	374.30	unknown	https://doi.org/10.1021/NP000604G
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)prop-2-enoate	54710367	Click to see	179.15	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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one	53399169	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	24211973	Click to see	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Pedalitin	31161	Click to see	316.26	unknown	via CMAUP database

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Isodon excisus

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