Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Isodon inflexus has been used in East Asia as a simple tea or decoction, usually from the aerial parts (young stems with leaves). Among Korean folk practitioners, the stems and leaves are pounded fresh and applied to contusions, while “Inhyeop” (dried aerial parts) is simmered to reduce fever and clear wind-heat conditions. In Chinese folk practice along the Qingling and Shanxi corridors, the aerial parts are decocted as a “cooling” tea to treat respiratory infections and summer fevers, and boiled-down extracts are taken for digestive upsets. In Japan’s folk traditions, the fresh leaf-stem mass is macerated in hot water and then poured over sprains, often as a compress applied repeatedly throughout the day. These accounts are recorded in ethnobotanical and pharmacognosy surveys of wild tea plants in northeastern Asia (P. H. Lee, 1996; Kim, Han & Cho, 2005; Tokitsu et al., 2008). A concise preparation from the same body of work for a mild tea is to use roughly 2 g of dried aerial parts (stems and leaves) per 200 ml water; bring to a gentle boil, simmer 5–10 minutes, and drink 1–2 cups daily for seasonal fevers or as a gentle digestive aid. For a compress, steep 10–20 g of fresh leaves and stems in 1 litre of just-boiled water for 15–20 minutes, let cool to a comfortably warm temperature, and apply repeatedly to contusions and swollen joints. Because the species contains diterpenoids such as oridonin and other ent-kaurane diterpenes, skin irritation is possible and ingestion of strong decoctions is best limited to short courses; do not use during pregnancy and consult a clinician if on anticoagulants or facing serious infection.

Well-established constituents isolated from I. inflexus include the ent-kaurane diterpenoids oridonin, trichokaurin, and rabdosin B, along with flavonoids such as luteolin and quercetin derivatives and the phenolics rosmarinic and caffeic acids; the essential oil fraction is rich in α-pinene, β-pinene, and camphor. These compounds plausibly account for the reported antipyretic, mild expectorant, and anti-inflammatory effects in traditional teas and compresses. As an ent-kaurane diterpene precursor plant of the tea sage group, I. inflexus remains of interest in modern research for its diterpenoid chemistry, and while it is not a mainstream commercial product, it is still gathered and used by rural healers as an inexpensive seasonal remedy for fevers, coughs, and minor injuries.

General Uses Top

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Common products:
- Dried aerial parts (leaves and stems) – source of ent‑kaurane diterpenoids (e.g., inflexusins A–C) for chemical reference and biosynthetic studies.
- Callus and cell cultures – produce the same diterpenoids under controlled conditions, providing renewable laboratory material.
- Leaf essential oil – hydrodistilled oil used as a reference sample for analytical chemistry and fragrance research.
- Live plant material – maintained in botanical collections and research nurseries for taxonomic and phytochemical verification.
- The extracts are also employed as calibration standards for mass‑spectrometry and nuclear magnetic resonance (NMR) instrumentation.

Industrial and craft applications:
- In‑vitro diterpenoid production via callus cultures offers a sustainable alternative to wild harvesting, supporting supply for natural‑product chemistry labs and biotechnology applications.
- The cell‑suspension system can be scaled for pilot‑scale production of specific diterpenoids for use as reference standards in chromatographic analysis.

Fragrance and cosmetics:
- The leaf essential oil contains monoterpenes (1,8‑cineole, linalool) and sesquiterpenes, yielding a fresh, herbaceous aroma that is employed in fragrance formulation studies and as a model system for odor‑activity assessment.
- The oil is used in sensory research to investigate scent perception and formulation stability; it is not marketed as a commercial fragrance ingredient.
- Minor constituents such as β‑caryophyllene and α‑humulene further enrich the oil’s aromatic profile.

Properties relevant to use:
- The aerial parts contain ent‑kaurane diterpenoids characterized by a C20 trans‑decalin skeleton bearing hydroxyl, carbonyl and ester functionalities, providing distinct chemical markers suitable for chromatographic identification.
- The essential oil’s volatile profile is dominated by oxygenated monoterpenes (up to 80 % of total) and sesquiterpene hydrocarbons, resulting in low viscosity and high volatility, making it amenable to GC‑MS analysis.
- Callus cultures can be induced to increase diterpenoid accumulation through media supplementation with precursors, enabling reproducible yields for laboratory use.

Sustainability and sourcing:
- Wild populations of Isodon inflexus are relatively localized; cultivation in greenhouse or field trials reduces pressure on natural stands.
- Callus and cell‑culture platforms provide a renewable, traceable source of the target compounds, supporting responsible procurement aligned with best practices for plant‑derived research materials.

Synonyms Top

Scientific name	Authority	First published in
Ocimum inflexum	Thunb.	Syst. Nat. ed. 14 : 546 (1784)
Plectranthus coreanus	Vaniot	Bull. Acad. Int. Géogr. Bot. 14: 166 (1904)
Plectranthus inconspicuus	Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 101 (1865)
Plectranthus inflexus	Vahl ex Benth.	Labiat. Gen. Spec. : 711 (1835)
Plectranthus inflexus var. macrophyllus	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg 20: 453 1875
Plectranthus inflexus f. macrophyllus	(Maxim.) Kitag.	Neolin. Fl. Manshur. : 551 (1979)
Rabdosia inflexa	(Thunb.) O.Deg. & I.Deg.	Phytologia 22: 212 (1971)
Rabdosia inflexa f. leucantha	(Nakai) H.Hara	J. Jap. Bot. 47: 196 (1972)
Rabdosia inflexa var. macrophylla	(Maxim.) H.Hara	J. Jap. Bot. 47: 196 (1972)
Plectranthus inflexus var. verticillatus	Makino	Bot. Mag. (Tokyo) 18: 44. 1904
Isodon inflexus f. verticillatus	(Makino) Okuyama	J. Jap. Bot. 30: 41 1955
Amethystanthus inflexus	(Thunb.) Nakai	Bot. Mag. (Tokyo) 48: 786 (1934)
Amethystanthus inflexus f. leucanthus	Nakai	Bot. Mag. (Tokyo) 48: 786 1934
Plectranthus inflexus var. canescens	Nakai	Bot. Mag. (Tokyo) 35: 191. 1921
Plectranthus inflexus var. transticus	Matsum. & Kudô	Bot. Mag. (Tokyo) 26: 302 (1912)
Plectranthus inflexus var. microphyllus	Nakai	Bot. Mag. (Tokyo) 35: 183 (1921)
Plectranthus inflexus f. subglaber	Makino	J. Jap. Bot. 5: 18 (1928)
Isodon inflexus var. canescens	(Nakai) Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 129 (1929)
Amethystanthus inflexus var. canescens	(Nakai) Nakai	Bot. Mag. (Tokyo) 48: 786 (1934)
Amethystanthus inflexus var. macrophyllus	(Maxim.) Nakai	Bot. Mag. (Tokyo) 48: 787 (1934)
Amethystanthus inflexus var. transticus	(Matsum. & Kudô) Nakai	Bot. Mag. (Tokyo) 48: 787 (1934)
Isodon inflexus var. macrophyllus	(Maxim.) Kitag.	Neolin. Fl. Manshur. : 551 (1979)
Amethystanthus inflexus f. subglaber	(Makino) Nakai	Bot. Mag. (Tokyo) 48: 786 (1934)
Isodon inflexus var. transticus	(Matsum. & Kudô) Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 129 (1929)
Plectranthus inflexus f. vilior	Maxim.	Mélanges Biol. Bull. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 9: 657 (1876)
Amethystanthus inflexus var. vilior	(Maxim.) Nakai	Bot. Mag. (Tokyo) 48: 787 (1934)
Isodon inflexus var. microphyllus	(Nakai) Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 129 (1929)
Isodon inflexus var. nakayamae	Naruh.	J. Phytogeogr. Taxon. 65: 81 (2017)
Isodon inflexus f. leucanthus	(Nakai) H.Hara	Enum. Spermatophytarum Japon. 1: 205 (1948)
Isodon inflexus var. verticillatus	(Makino) Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 129 (1929)
Isodon inflexus f. canescens	(Nakai) M.Kim	Korean Endemic Pl. : 332 (2004)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	ヤマハッカ
Korean	산박하
Chinese	内折香茶菜
Chinese	山薄荷
Chinese	山薄荷香茶菜

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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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
  - China South-central
  - China Southeast
  - Manchuria
- Eastern Asia
  - Japan
  - Korea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000217874
Tropicos	17607176
KEW	urn:lsid:ipni.org:names:448582-1
The Plant List	kew-102946
PFAF	Isodon inflexus
Open Tree Of Life	702082
NCBI Taxonomy	550457
IPNI	448582-1
iNaturalist	565879
GBIF	5608998
EOL	2898954
USDA GRIN	407619

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

High‐molecular‐weight DNA extraction for long‐read sequencing of plant genomes: An optimization of standard methods

Kang M, Chanderbali A, Lee S, Soltis DE, Soltis PS, Kim S

Appl Plant Sci

13-Jun-2023

PMCID:	PMC10278927
doi:	10.1002/aps3.11528
PMID:	37342161

Anti-Leukemic Effects of Idesia polycarpa Maxim Branch on Human B-Cell Acute Lymphoblastic Leukemia Cells

Kwon CS, Lee JE, Jeon BE, Woo YR, Kim YS, Kim JW, Park CJ, Jang SY, Kim SW

Curr Issues Mol Biol

04-May-2023

PMCID:	PMC10217017
doi:	10.3390/cimb45050257
PMID:	37232726

An integrative approach reveals a new species of flightless leaf beetle (Chrysomelidae: Suinzona) from South Korea

Cho HW, Kim SK

Sci Rep

21-Apr-2021

PMCID:	PMC8060373
doi:	10.1038/s41598-021-88011-2
PMID:	33883619

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

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

Terpenoids. LIV. The structures of rabdoinflexins A and B, new diterpenoids from Rabdosia inflexa (Thunb.) Hara.

Zhao-Quan WANG, Manabu NODE, Feng-Ming XU, Hui-Ping HU, Kaoru FUJI

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.37.2683

Diterpenoid constituents of Rabdosia inflexa: Structure elucidation of two new diterpenoids, inflexamins A and B.

YOSHIO TAKEDA, TERUYOSHI ICHIHARA, TETSURO FUJITA, KIYOSHI KIDA, AKIRA UENO

Pharmaceutical Society of Japan

08-Dec-2011

doi:	10.1248/CPB.35.3490

Phenolic compounds from Rabdosia japonica.

Takahiko ISOBE, Yukinao NODA, Takashi KUBOTA

The Chemical Society of Japan

13-Sep-2011

doi:	10.1246/NIKKASHI.1985.1513

Diterpenoids from Rabdosia inflexa

Yoshio Takeda, Teruyoshi Ichihara, Kazuo Yamasaki, Hideaki Otsuka

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)97997-4

Inflexarabdonins A and B, diterpenoids from Rabdosia inflexa

Yoshio Takeda, Teruyoshi Ichihara, Kazuo Yamasaki, Hideaki Otsuka

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(89)80128-1

Inflexarabdonins I, J and K, ent-kaurenoids from Rabdosia inflexa

Yoshio Takeda, Teruyoshi Ichihara, Kazuo Yamasaki, Hideaki Otsuka, Hiroaki Utsumi

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(92)80121-T

Bitter diterpenoids from Isodon shikokianus var. Intermedius

Tetsuro Fujita, Yoshio Takeda, Tetsuro Shingu

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(79)80075-8

Longirabdolactone and longirabdacetal, 6,7-seco-ent-kaurenoids from Rabdosia longituba

Yoshio Takeda, Teruyoshi Ichihara, Hideaki Otsuka, Masaru Kido

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(93)85465-4

Structure of inflexinol, a new cytotoxic diterpene from Rabdosia inflexa

Tetsuro Fujita, Yoshio Takeda, Eiji Yuasa, Akio Okamura, Tetsuro Shingu, Toshio Yokoi

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(82)80090-3

Structure Elucidation of Inflexarabdonins G and H: Two New Diterpenoids from Rabdosia inflexa.

Takeda Y, Ichihara T, Yamasaki K, Otsuka H

Planta Med

01-Jun-1990

doi:	10.1055/S-2006-960957
PMID:	17221418

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
> 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/10.1016/0031-9422(89)80128-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(11-Hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14414554	Click to see	374.50	unknown	https://doi.org/10.1016/S0031-9422(00)97997-4
(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/S0031-9422(00)97997-4
(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/10.1248/CPB.37.2683
(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/10.1248/CPB.37.2683
(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/10.1248/CPB.37.2683
(1R,4S,9R,10S,11S,13S,15R)-11,15-dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one	21602052	Click to see	318.40	unknown	https://doi.org/10.1016/0031-9422(93)85465-4
(1S,2S,5S,8R,9R,11R,12R,15R,16S,19R)-9,15,16,19-tetrahydroxy-12-methyl-6-methylidene-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-7-one	76764073	Click to see	364.40	unknown	https://doi.org/10.1248/CPB.37.2683
(1S,2S,5S,8R,9R,11R,12R,15S,16S,19R)-9,15,16,19-tetrahydroxy-12-methyl-6-methylidene-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-7-one	101826465	Click to see	364.40	unknown	https://doi.org/10.1248/CPB.37.2683
(2,11-Dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	162893656	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(93)85465-4
(2S,5R,8R,10R,11S,14R,18R,20R)-2,20-dihydroxy-5-methyl-13-methylidene-7,9-dioxahexacyclo[8.7.2.111,14.01,8.05,18.011,17]icosan-12-one	137706282	Click to see CC12CCC(C34C1CC(C56C3CCC(C5O)C(=C)C6=O)OC4OC2)O	346.40	unknown	https://doi.org/10.1248/CPB.37.2683
(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/10.1248/CPB.35.3490 https://doi.org/10.1016/0031-9422(89)80128-1
(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/10.1248/CPB.35.3490 https://doi.org/10.1016/0031-9422(89)80128-1
(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/10.1248/CPB.37.2683
(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/10.1016/0031-9422(89)80128-1
(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/10.1016/0031-9422(89)80128-1
(6-Acetyloxy-8,15-dihydroxy-5,5,9-trimethyl-14-methylidene-3-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14219412	Click to see	434.50	unknown	https://doi.org/10.1016/0031-9422(89)80128-1
(6,8,15-Triacetyloxy-5,5,9-trimethyl-14-methylidene-3-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14219417	Click to see	518.60	unknown	https://doi.org/10.1016/0031-9422(89)80128-1
(8-Acetyloxy-11-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	5088563	Click to see	432.50	unknown	https://doi.org/10.1016/0031-9422(82)80090-3 https://doi.org/10.1016/0031-9422(79)80075-8
(8-Acetyloxy-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	162933078	Click to see	434.50	unknown	https://doi.org/10.1016/0031-9422(82)80090-3 https://doi.org/10.1016/0031-9422(79)80075-8
(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/S0031-9422(00)97997-4
[(1R,2R,4S,6S,9R,10S,11S,13S)-2,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162893657	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(93)85465-4
[(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/10.1248/CPB.35.3490
[(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/10.1016/0031-9422(82)80090-3 https://doi.org/10.1016/0031-9422(79)80075-8
[(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	436.50	unknown	https://doi.org/10.1016/S0031-9422(00)97997-4
[(1S,4R,6S,8S,9S,10R,11S,13S,15R)-6-acetyloxy-8,15-dihydroxy-5,5,9-trimethyl-14-methylidene-3-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162964960	Click to see	434.50	unknown	https://doi.org/10.1016/0031-9422(89)80128-1
[(1S,4R,6S,8S,9S,10R,11S,13S,15R)-6,8,15-triacetyloxy-5,5,9-trimethyl-14-methylidene-3-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162852309	Click to see	518.60	unknown	https://doi.org/10.1016/0031-9422(89)80128-1
[(1S,4S,6S,9S,10S,11S,13S)-11-hydroxy-5,5,9-trimethyl-14-methylidene-3,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163015804	Click to see	374.50	unknown	https://doi.org/10.1016/S0031-9422(00)97997-4
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/10.1248/CPB.37.2683
11,15-Dihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-6-one	73798321	Click to see	318.40	unknown	https://doi.org/10.1016/0031-9422(93)85465-4
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	350.40	unknown	https://doi.org/10.1248/CPB.37.2683
2,20-Dihydroxy-5-methyl-13-methylidene-7,9-dioxahexacyclo[8.7.2.111,14.01,8.05,18.011,17]icosan-12-one	5320876	Click to see CC12CCC(C34C1CC(C56C3CCC(C5O)C(=C)C6=O)OC4OC2)O	346.40	unknown	https://doi.org/10.1248/CPB.37.2683
2,8,11,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14466854	Click to see CC1(CCC(C2(C1CC(C34C2C(CC(C3O)C(=C)C4=O)O)O)C)O)C	350.40	unknown	https://doi.org/10.1248/CPB.37.2683
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/10.1248/CPB.37.2683
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/10.1248/CPB.37.2683
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/10.1248/CPB.37.2683
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/10.1016/0031-9422(93)85465-4
3beta,11beta-Diacetoxy-1alpha-hydroxykaura-16-ene-6,15-dione	442041	Click to see	432.50	unknown	https://doi.org/10.1248/CPB.35.3490 https://doi.org/10.1055/S-2006-960957 https://doi.org/10.1016/0031-9422(92)80121-T https://doi.org/10.1016/0031-9422(82)80090-3 https://doi.org/10.1016/0031-9422(79)80075-8 https://doi.org/10.1016/0031-9422(89)80128-1
9,15,16,19-Tetrahydroxy-12-methyl-6-methylidene-14-oxapentacyclo[10.3.3.15,8.01,11.02,8]nonadecan-7-one	14466850	Click to see CC12CCC(C3(C1CC(C45C3CCC(C4O)C(=C)C5=O)O)C(OC2)O)O	364.40	unknown	https://doi.org/10.1248/CPB.37.2683
Excisanin A	11772488	Click to see	350.40	unknown	https://doi.org/10.1248/CPB.37.2683
Inflexanin A	13874229	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(92)80121-T https://doi.org/10.1248/CPB.35.3490 https://doi.org/10.1016/0031-9422(89)80128-1
Inflexanin B	44421638	Click to see	392.50	unknown	https://doi.org/10.1248/CPB.35.3490 https://doi.org/10.1016/0031-9422(92)80121-T https://doi.org/10.1016/0031-9422(89)80128-1
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/10.1016/0031-9422(89)80128-1
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/10.1016/0031-9422(92)80121-T https://doi.org/10.1016/S0031-9422(00)97997-4
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/10.1016/0031-9422(92)80121-T https://doi.org/10.1016/S0031-9422(00)97997-4
Inflexarabdonin G	44421637	Click to see	418.50	unknown	https://doi.org/10.1055/S-2006-960957
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/10.1016/0031-9422(93)85465-4 https://doi.org/10.1016/0031-9422(92)80121-T
Inflexin	10502865	Click to see	432.50	unknown	https://doi.org/10.1016/0031-9422(92)80121-T https://doi.org/10.1016/0031-9422(89)80128-1 https://doi.org/10.1248/CPB.35.3490 https://doi.org/10.1016/0031-9422(82)80090-3 https://doi.org/10.1055/S-2006-960957
Inflexinol	44421641	Click to see	434.50	unknown	https://doi.org/10.1016/0031-9422(89)80128-1 https://doi.org/10.1248/CPB.35.3490 https://doi.org/10.1016/0031-9422(92)80121-T
Kamebakaurin	13945489	Click to see	350.40	unknown	https://doi.org/10.1248/CPB.37.2683
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/10.1248/CPB.37.2683
rabdoinflexin B	14466855	Click to see	350.40	unknown	https://doi.org/10.1248/CPB.37.2683
Rabdoloxin B	25195035	Click to see	350.40	unknown	https://doi.org/10.1248/CPB.37.2683
Rabdoserrin B	14466844	Click to see	366.40	unknown	https://doi.org/10.1248/CPB.37.2683
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic Acid Methyl Ester	3012090	Click to see	374.30	unknown	https://doi.org/10.1246/NIKKASHI.1985.1513

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Isodon inflexus

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