Common products:
No documented commercial products are reported for this species.

Industrial and craft applications:
No industrial or craft applications are documented.

Food and beverages (non-medicinal):
No food or beverage uses are reported.

Colorants and tanning:
No colorant or tanning uses are documented.

Wood and fiber:
No wood or fiber uses are documented.

Fragrance and cosmetics:
No fragrance or cosmetic uses are documented.

Properties relevant to use:
No material properties relevant to commercial applications have been documented for this taxon.

Standards and regulation:
No relevant standards or regulatory frameworks are documented for this species.

Sustainability and sourcing:
No sustainability or sourcing information is documented for commercial use of this species.

Note: Research literature focuses on phytochemical studies of ent-kaurane diterpenoids found in the genus Isodon, but no documented non-medicinal commercial applications for Isodon pharicus have been identified in reliable sources.

Synonyms Top

Scientific name	Authority	First published in
Isodon pseudoirroratus	(C.Y.Wu) H.Hara	J. Jap. Bot. 60: 236 (1985)
Plectranthus pharicus	Prain	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 59: 297 (1890 publ. 1891)
Rabdosia pharica	(Prain) Hara	J. Jap. Bot. 47: 198 (1972)
Rabdosia pseudoirrorata	C.Y.Wu	Fl. Reipubl. Popularis Sin. 66: 587 (1977)
Rabdosia pseudoirrorata var. centellifolia	C.Y.Wu	Fl. Reipubl. Popularis Sin. 66: 588 (1977)

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	川藏香茶菜
Chinese	兴木蒂那布
Chinese	香茶菜
Chinese	香茶菜根

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
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
  - Nepal

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000217935
Tropicos	17607222
KEW	urn:lsid:ipni.org:names:448601-1
The Plant List	kew-103001
Open Tree Of Life	23545
Observations.org	451825
NCBI Taxonomy	204134
IPNI	448601-1
GBIF	5608893
EOL	2898977
Elurikkus	556186
CMAUP	NPO24459

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

A Comprehensive Review of the Classification, Sources, Phytochemistry, and Pharmacology of Norditerpenes

Zeng N, Zhang Q, Yao Q, Fu G, Su W, Wang W, Li B

Molecules

21-Dec-2023

PMCID:	PMC10780140
doi:	10.3390/molecules29010060
PMID:	38202643

川藏香茶菜丙素抑制NLRP3炎症小体活化并缓解小鼠脓毒性休克

N/A

Nan Fang Yi Ke Da Xue Xue Bao

20-Sep-2023

PMCID:	PMC10563096
doi:	10.12122/j.issn.1673-4254.2023.09.04
PMID:	37814861

Cytotoxic Isopentenyl Phloroglucinol Compounds from Garcinia xanthochymus Using LC-MS-Based Metabolomics

Quan F, Luan X, Zhang J, Gao W, Yan J, Li P

Metabolites

10-Feb-2023

PMCID:	PMC9964469
doi:	10.3390/metabo13020258
PMID:	36837877

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

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

Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes

Lautié E, Russo O, Ducrot P, Boutin JA

Front Pharmacol

07-Apr-2020

PMCID:	PMC7154113
doi:	10.3389/fphar.2020.00397
PMID:	32317969

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

2-Bromopalmitate targets retinoic acid receptor alpha and overcomes all-trans retinoic acid resistance of acute promyelocytic leukemia

Lu Y, Yan JS, Xia L, Qin K, Yin QQ, Xu HT, Gao MQ, Qu XN, Sun YT, Chen GQ

Haematologica

01-Jan-2019

PMCID:	PMC6312026
doi:	10.3324/haematol.2018.191916
PMID:	30076181

Phenotype and target-based chemical biology investigations in cancers

Chen GQ, Xu Y, Shen SM, Zhang J

Natl Sci Rev

01-Nov-2018

PMCID:	PMC8291603
doi:	10.1093/nsr/nwy124
PMID:	34691990

Five New ent-Kaurane Diterpenoids from Isodon pharicus

Yong ZHAO, Jian-Xin PU, Li-Mei Li, Wei-Lie XIAO, Li-Bin YANG, Han-Dong SUN

Elsevier BV

02-Dec-2016

doi:	10.1016/S1875-5364(09)60064-9

Oridonin stabilizes retinoic acid receptor alpha through ROS-activated NF-κB signaling

Cao Y, Wei W, Zhang N, Yu Q, Xu WB, Yu WJ, Chen GQ, Wu YL, Yan H

BMC Cancer

10-Apr-2015

PMCID:	PMC4403721
doi:	10.1186/s12885-015-1219-8
PMID:	25886043

Pharicin A, a novel natural ent-kaurene diterpenoid, induces mitotic arrest and mitotic catastrophe of cancer cells by interfering with BubR1 function

Xu HZ, Huang Y, Wu YL, Zhao Y, Xiao WL, Lin QS, Sun HD, Dai W, Chen GQ

Cell Cycle

15-Jul-2010

PMCID:	PMC3233523
doi:	10.4161/cc.9.14.12406
PMID:	20603598

ent-Kaurane diterpenoids from Isodon pharicus.

Zhao Y, Pu JX, Huang SX, Ding LS, Wu YL, Li X, Yang LB, Xiao WL, Chen GQ, Sun HD

J Nat Prod

01-Jun-2009

doi:	10.1021/NP9000366
PMID:	19425589

Diterpenoids from Isodon pharicus

Yong Zhao, Sheng-Xiong Huang, Wei-Lie Xiao, Li-Sheng Ding, Jian-Xin Pu, Xian Li, Li-Bin Yang, Han-Dong Sun

Elsevier BV

22-Feb-2009

doi:	10.1016/J.TETLET.2009.02.102

Cytotoxic ent-kaurane diterpenoids from Isodon henryi.

Zhao Y, Huang SX, Yang LB, Pu JX, Xiao WL, Li LM, Lei C, Weng ZY, Han QB, Sun HD

Planta Med

01-Jan-2009

doi:	10.1055/S-0028-1088331
PMID:	19031362

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl)methyl acetate	162986868	Click to see	346.50	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
[(1S,4aR,4bS,7S,8S,10aS)-7-ethenyl-8-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl]methyl acetate	102287784	Click to see	346.50	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(11-Acetyloxy-13-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	72245825	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC34C2C(CC(C3)(C(=C)C4=O)O)OC(=O)C)C	418.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
(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 CC1(CCC(C2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C	334.40	unknown	https://doi.org/10.1021/NP9000366
(1R,2R,4S,6R,9R,10S,12S,13R,16S)-2,6,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	162926464	Click to see CC1(C(CCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C	350.40	unknown	https://doi.org/10.1021/NP9000366
(1R,2R,4S,6R,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	13876282	Click to see	334.40	unknown	https://doi.org/10.1021/NP9000366
(1R,2R,4S,6S,9R,10S,13S,16R)-2,6,16-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	45271567	Click to see	334.40	unknown	https://doi.org/10.1021/NP9000366
(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	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
(1R,2R,6R,8S,10R,13R,14S,16S,17R)-10,16-dihydroxy-4,4,9,9,13-pentamethyl-18-methylidene-3,5-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecan-19-one	44179177	Click to see	390.50	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
(1R,4S,10S,11S,13R)-6,11,13-trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	5318552	Click to see CC1(C2CCC34CC(CC(C3C2(CCC1O)C)O)(C(=C)C4=O)O)C	334.40	unknown	via CMAUP database
(2,12,16-Trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	162991676	Click to see	392.50	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
(2,8,15,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidene-12-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	56657519	Click to see	408.50	unknown	via CMAUP database
(2,8,16-Trihydroxy-5,5,9,14-tetramethyl-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	14806016	Click to see	408.50	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9
(6-Acetyloxy-2,16-dihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl acetate	162856659	Click to see	434.50	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
(6,13-Dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl) acetate	72745178	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
[(1R,2R,4R,6S,8R,9S,10S,13S,16R)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162917665	Click to see CC(=O)OC1CC(C2(C3CCC4C(C3(C(CC2C1(C)C)O)C(=O)C4=C)O)C)O	392.50	unknown	https://doi.org/10.1021/NP9000366
[(1R,2R,4R,6S,8S,9R,10S,12S,13R,16R)-2,8,12,16-tetrahydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	44179098	Click to see	408.50	unknown	https://doi.org/10.1021/NP9000366
[(1R,2R,4R,6S,8S,9R,10S,13R,14R,16R)-2,8,16-trihydroxy-5,5,9,14-tetramethyl-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162980922	Click to see CC1C2C(C3(C1=O)C(CC4C(C(CC(C4(C3CC2=O)C)O)OC(=O)C)(C)C)O)O	408.50	unknown	https://doi.org/10.1021/NP9000366
[(1R,2R,4R,6S,8S,9R,10S,13S,16S)-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162882100	Click to see CC(=O)OC1CC(C2(C(C1(C)C)CC(C34C2CC(=O)C(C3O)C(=C)C4=O)O)C)O	406.50	unknown	https://doi.org/10.1021/NP9000366
[(1R,2R,4S,5R,6S,9R,10S,13S,16R)-6-acetyloxy-2,16-dihydroxy-5,9-dimethyl-14-methylidene-15-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate	102287786	Click to see	434.50	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
[(1R,2R,4S,6S,9R,10S,12S,13R,16R)-2,12,16-trihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	102287785	Click to see CC(=O)OC1CCC2(C3CC(C4C(C3(C(CC2C1(C)C)O)C(=O)C4=C)O)O)C	392.50	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
[(1R,2R,4S,6S,9R,10S,13S,16S)-2,16-dihydroxy-5,5,9-trimethyl-14-methylidene-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162882922	Click to see CC(=O)OC1CCC2(C(C1(C)C)CC(C34C2CC(=O)C(C3O)C(=C)C4=O)O)C	390.50	unknown	https://doi.org/10.1021/NP9000366
[(1R,2R,4S,6S,9R,10S,13S,16S)-2,16-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	162997574	Click to see	376.50	unknown	https://doi.org/10.1021/NP9000366
[(1R,4S,5R,6R,9R,10S,11S,13R)-13-hydroxy-5-(hydroxymethyl)-5,6,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	101617536	Click to see	390.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
[(1R,4S,6R,9R,10S,11S,13R)-11-acetyloxy-13-hydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	15109169	Click to see	418.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
[(1R,4S,6R,9R,10S,11S,13R)-6,13-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	15109168	Click to see CC(=O)OC1CC2(CC3(C1C4(CCC(C(C4CC3)(C)C)O)C)C(=O)C2=C)O	376.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
[(1R,4S,6S,9R,10S,12S,13R,15R,16R)-6,12,15-trihydroxy-5,5,9-trimethyl-14-methylidene-16-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	44179096	Click to see	378.50	unknown	https://doi.org/10.1021/NP9000366
[(1S,2R,4S,6S,9R,10S,13S,14R,15R,16R)-2,15,16-trihydroxy-14-(methoxymethyl)-5,5,9-trimethyl-12-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	45269923	Click to see CC(=O)OC1CCC2(C(C1(C)C)CC(C34C2CC(=O)C(C3O)C(C4O)COC)O)C	424.50	unknown	https://doi.org/10.1021/NP9000366
[(2S,5S,7R,8S,9R,10S,11R)-7,10-diacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl] acetate	5318554	Click to see	476.60	unknown	via CMAUP database
[(4R,6S,8S,9R,10S,13R,14R,16R)-2,8,16-trihydroxy-5,5,9,14-tetramethyl-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163186094	Click to see CC1C2C(C3(C1=O)C(CC4C(C(CC(C4(C3CC2=O)C)O)OC(=O)C)(C)C)O)O	408.50	unknown	https://doi.org/10.1021/NP9000366
[13-Hydroxy-5-(hydroxymethyl)-5,9-dimethyl-14-methylidene-15-oxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	14414481	Click to see	376.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
12-O-Acetylpseurata B	44179018	Click to see CC(=O)OC1CC2C3(CCC(C(C3CC(C24C(C1C(=C)C4=O)O)O)(C)C)O)C	392.50	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
2,6,12,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	14756330	Click to see CC1(C(CCC2(C1CC(C34C2CC(C(C3O)C(=C)C4=O)O)O)C)O)C	350.40	unknown	via CMAUP database
2,6,16-Trihydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	13876280	Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)C)O)C	334.40	unknown	via CMAUP database
2,6,8,16-Tetrahydroxy-5,5,9-trimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	56657353	Click to see CC1(C2CC(C34C(C2(C(CC1O)O)C)CCC(C3O)C(=C)C4=O)O)C	350.40	unknown	https://doi.org/10.1055/S-0028-1088331
3-Epipseurata B	44179017	Click to see	350.40	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
7-O-Acetylpseurata C	44179019	Click to see CC(=O)OC1CCC2(C(C1(C)C)CC(C34C2CC(=O)C(C3O)C(=C)C4=O)OC(=O)C)C	432.50	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
7,14-Dihydroxykaur-16-ene-3,15-dione	127626	Click to see CC1(C2CC(C34C(C2(CCC1=O)C)CCC(C3O)C(=C)C4=O)O)C	332.40	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
CID 196551	196551	Click to see CC(=O)OC1C2CCC3C1(C(CC4C3(CCC(=O)C4(C)C)C)O)C(=O)C2=C	374.50	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
Dihydropseurata F	44179099	Click to see	408.50	unknown	https://doi.org/10.1021/NP9000366
Glaucocalyxin A	10471963	Click to see CC1(C2CC(C34C(C2(CCC1=O)C)CCC(C3O)C(=C)C4=O)O)C	332.40	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
Glaucocalyxin B	14193399	Click to see CC(=O)OC1C2CCC3C1(C(CC4C3(CCC(=O)C4(C)C)C)O)C(=O)C2=C	374.50	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
Isodomedin	442045	Click to see	392.50	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
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/10.1016/S1875-5364(09)60064-9
Leukamenin E	45267324	Click to see CC(=O)OC1CCC2(C3CCC4C(C3(C(CC2C1(C)C)O)C(=O)C4=C)O)C	376.50	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
Minheryin G	45267323	Click to see	350.40	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
Pseurata A	70691855	Click to see	334.40	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP010420H
Pseurata B	45272476	Click to see	350.40	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
Pseurata C	14756333	Click to see	390.50	unknown	https://doi.org/10.1021/NP9000366 https://doi.org/10.1016/S1875-5364(09)60064-9
Pseurata F	45271569	Click to see CC(=O)OC1CC(C2(C(C1(C)C)CC(C34C2CC(=O)C(C3O)C(=C)C4=O)O)C)O	406.50	unknown	https://doi.org/10.1016/S1875-5364(09)60064-9 https://doi.org/10.1021/NP9000366
Rosthornin A	14414480	Click to see CC(=O)OC1CC2(CC3(C1C4(CCCC(C4CC3)(C)CO)C)C(=O)C2=C)O	376.50	unknown	https://doi.org/10.1016/0031-9422(91)80093-G
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Arundinol A	71524401	Click to see CC1=C2CC(CCC2(C(CC1)O)C)C(C)(CO)O	254.36	unknown	via CMAUP database
Arundinol B	71524402	Click to see	250.33	unknown	via CMAUP database
Arundinol C	71524403	Click to see	310.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(1R,4S,10S,11S,13R)-11,13,15-trihydroxy-5,5,9-trimethyl-14-methylidene-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]oxy]oxane-3,4,5-triol	6325426	Click to see CC1(C2CCC34CC(CC(C3C2(CCC1OC5C(C(C(C(O5)CO)O)O)O)C)O)(C(=C)C4O)O)C	498.60	unknown	https://doi.org/10.1016/S0031-9422(01)00245-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(1R,2R,4R,6S,8S,9R,10S,13S,14R,16R)-14-[[(1R,2R,4R,6S,8S,9R,10S,11R,13S,16R)-6-acetyloxy-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-12,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl]-2,8,16-trihydroxy-5,5,9-trimethyl-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	102287783	Click to see	812.90	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
[14-[(6-Acetyloxy-2,8,16-trihydroxy-5,5,9-trimethyl-14-methylidene-12,15-dioxo-11-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methyl]-2,8,16-trihydroxy-5,5,9-trimethyl-12,15-dioxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate	163067620	Click to see	812.90	unknown	https://doi.org/10.1016/J.TETLET.2009.02.102
Npc62469	49867942	Click to see	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 / Benzopyrans / 2-benzopyrans
Arundinone A	71524404	Click to see	264.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Fraxin	5273568	Click to see	370.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	via CMAUP database
Catechin 7-O-apiofuranoside	21676366	Click to see	422.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	124124220	Click to see	482.40	unknown	via CMAUP database

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Isodon pharicus

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