Isodon coetsa

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Scientific Literature

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Internal ID	UUID643fdf7c108c9171916576
Scientific name	Isodon coetsa
Authority	(Buch.-Ham. ex D.Don) Kudô
First published in	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 131 (1929)

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Synonyms Top

Scientific name	Authority	First published in
Isodon anisochilus	(C.Y.Wu) H.Hara	J. Jap. Bot. 60: 233 (1985)
Isodon cavaleriei	Kudô	Mem. Fac. Sci. Taihoku Imp. Univ. 2: 130 (1929)
Isodon coetsa var. cavaleriei	(H.Lév.) H.W.Li	J. Arnold Arbor. 69: 371 (1988)
Isodon coetsoides	(C.Y.Wu) H.Hara	J. Jap. Bot. 60: 233 (1985)
Isodon dakglayensis	(Phuong) A.L.Budantzev	Komarovia 1: 25 (1999):.
Isodon javanicus	(Blume) H.W.Li	J. Arnold Arbor. 69: 330 (1988)
Isodon maddenii	(Benth. ex Hook.f.) Murata	Acta Phytotax. Geobot. 22: 21 (1966)
Isodon pluriflorus	(C.Y.Wu & H.W.Li) H.Hara	J. Jap. Bot. 60: 236 (1985)
Isodon polystachys	(Sun ex C.H.Hu) H.Hara	J. Jap. Bot. 60: 236 (1985)
Ocimum coetsa	Spreng.	Syst. Veg. 4(2): 223 (1827)
Plectranthus benthamianus	Miq.	Fl. Ned. Ind. 2: 946 (1858)
Plectranthus cavaleriei	H.Lév.	Repert. Spec. Nov. Regni Veg. 9: 247 (1911)
Plectranthus coetsa	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 117 (1825)
Plectranthus coetsa var. cavaleriei	(Lévl.) McKean	Notes Roy. Bot. Gard. Edinburgh 40: 176 (1982)
Plectranthus coesta var. hookeri	Hook.f.	Fl. Brit. India 4: 620 1885
Plectranthus diffusus	Merr.	Philipp. J. Sci. 1(Suppl.): 235 (1906)
Plectranthus intermedius	Zoll. & Moritzi	Syst. Verz. Java : 55 (1846)
Plectranthus japonicus var. macraei	(Benth.) S.R.Sriniv.	Fl. Tamil Nadu 2: 182 (1987)
Plectranthus javanicus	Benth.	Labiat. Gen. Spec. : 45 (1832)
Plectranthus leptobotrys	Diels	Bot. Jahrb. Syst. 29: 561 (1900)
Plectranthus macraei	Benth.	Labiat. Gen. Spec. : 42 (1832)
Plectranthus maddenii	Benth. ex Hook.f.	Fl. Brit. India 4: 620 (1885)
Plectranthus mairei	H.Lév.	Bull. Soc. Agric. Sarthe 44: 479 (1914)
Plectranthus menthoides	Moritzi	Syst. Verz. Java : 55 (1846)
Plectranthus menthoides	Benth.	Pl. Asiat. Rar. 2: 17 (1830)
Plectranthus polystachys	Y.Z.Sun	Acta Phytotax. Sin. 11(1): 54. 1966 [17 Jan 1966]
Plectranthus rufescens	Benth.	Prodr. 12: 59 (1848)
Rabdosia anisochila	C.Y.Wu	Fl. Reipubl. Popularis Sin. 66: 588 (1977)
Rabdosia coetsa	(Hamilt. ex D.Don) H.Hara	J. Jap. Bot. 47: 194 (1972)
Rabdosia coetsa var. cavaleriei	(Levl.) C.Y.Wu & H.W.Li	Acta Phytotax. Sin. 13(1): 91 (1975)
Rabdosia coesta var. hookeri	(Hook.f.) V.Singh & P.Singh	J. Econ. Taxon. Bot. 15(3): 705. 1992 [1991 publ. 1992]
Rabdosia coetsoides	C.Y.Wu	Fl. Yunnanica 1: 790 (1977)
Rabdosia dakglayensis	Phuong	Bot. Zhurn. (Moscow & Leningrad) 67: 1133 (1982)
Rabdosia javanica	Hassk.	Flora 25(2 Beibl.): 25 (1842)
Rabdosia maddenii	(Benth. ex Hook.f.) H.Hara	J. Jap. Bot. 47: 198 (1972)
Rabdosia megathyrsoides	H.W.Li	Fl. Xizang. 4: 221 (1985)
Rabdosia menthoides	(Benth.) C.Y.Wu & H.W.Li	Fl. Yunnanica 1: 790 (1977)
Rabdosia pluriflora	C.Y.Wu & H.W.Li	Fl. Yunnanica 1: 976 (1977)
Rabdosia polystachys	(Sun ex C.H.Hu) C.Y.Wu & H.W.Li	Acta Phytotax. Sin. 13(1): 92 (1975)
Rabdosia polystachys var. phyllodioides	C.Y.Wu	Fl. Yunnanica 1: 797 (1977)
Plectranthus rugosus var. tomentosus	Benth.	Pl. Asiat. Rar. 2: 17. 1830
Elsholtzia javanica	Blume	Bijdr. Fl. Ned. Ind. : 825 (1826)
Isodon coetsa var. macraei	(Benth.) V.S.Kumar	J. Econ. Taxon. Bot. 36: 511 (2012 publ. 2013)

Common names Top

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Language	Common/alternative name
Chinese	细锥香茶菜

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
  - China Southeast
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Lesser Sunda Islands
  - Philippines
  - Sulawesi
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000217838
Tropicos	17607236
KEW	urn:lsid:ipni.org:names:448568-1
The Plant List	kew-102913
Open Tree Of Life	634151
NCBI Taxonomy	204131
IPNI	448568-1
iNaturalist	774860
GBIF	7308656
USDA GRIN	317411
CMAUP	NPO17676

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 Rare Cleptoparasitic Bee Tetralonioidella himalayana (Bingham, 1897) (Hymenoptera: Apidae) from India: Review and New Data

Ghosh D, Girish Kumar P, Subramanian KA

Natl Acad Sci Lett

04-Apr-2023

PMCID:	PMC10071265
doi:	10.1007/s40009-023-01243-w
PMID:	37363280

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

Constructing a DNA barcode reference library for southern herbs in China: A resource for authentication of southern Chinese medicine

Gong L, Qiu XH, Huang J, Xu W, Bai JQ, Zhang J, Su H, Xu CM, Huang ZH

PLoS One

25-Jul-2018

PMCID:	PMC6059470
doi:	10.1371/journal.pone.0201240
PMID:	30044868

Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods

Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP

J Ethnobiol Ethnomed

03-May-2016

PMCID:	PMC4855762
doi:	10.1186/s13002-016-0089-8
PMID:	27142597

Tamoxifen induces apoptosis through cancerous inhibitor of protein phosphatase 2A–dependent phospho-Akt inactivation in estrogen receptor–negative human breast cancer cells

Liu CY, Hung MH, Wang DS, Chu PY, Su JC, Teng TH, Huang CT, Chao TT, Wang CY, Shiau CW, Tseng LM, Chen KF

Breast Cancer Res

17-Sep-2014

PMCID:	PMC4303112
doi:	10.1186/s13058-014-0431-9
PMID:	25228280

Erlotinib derivative inhibits hepatocellular carcinoma by targeting CIP2A to reactivate protein phosphatase 2A

Yu HC, Hung MH, Chen YL, Chu PY, Wang CY, Chao TT, Liu CY, Shiau CW, Chen KF

Cell Death Dis

31-Jul-2014

PMCID:	PMC4123111
doi:	10.1038/cddis.2014.325
PMID:	25077545

CIP2A is a target of bortezomib in human triple negative breast cancer cells

Tseng LM, Liu CY, Chang KC, Chu PY, Shiau CW, Chen KF

Breast Cancer Res

26-Apr-2012

PMCID:	PMC3446403
doi:	10.1186/bcr3175
PMID:	22537901

Anti-Viral Activity of Indian Plants

Dhawan BN

Proc Natl Acad Sci India Sect B Biol Sci

18-Jan-2012

PMCID:	PMC7099914
doi:	10.1007/s40011-011-0016-7
PMID:	32226204

Overexpression and Small Molecule-Triggered Downregulation of CIP2A in Lung Cancer

Ma L, Wen ZS, Liu Z, Hu Z, Ma J, Chen XQ, Liu YQ, Pu JX, Xiao WL, Sun HD, Zhou GB

PLoS One

31-May-2011

PMCID:	PMC3105001
doi:	10.1371/journal.pone.0020159
PMID:	21655278

Three angiotensin-converting enzyme inhibitors from Rabdosia coetsa.

Li QL, Li BG, Zhang Y, Gao XP, Li CQ, Zhang GL

Phytomedicine

01-May-2008

doi:	10.1016/J.PHYMED.2007.09.013
PMID:	17977703

SPECIES COMPOSITION, DISTRIBUTION, LIFE FORMS AND FOLK NOMENCLATURE OF FOREST AND COMMON LAND PLANTS OF WESTERN CHITWAN, NEPAL

Dangol DR

J Inst Agric Anim Sci

01-Jan-2005

PMCID:	PMC3434227
PMID:	22962539

Flavonoids from Isodon oresbius

Huang Hao, Sun Handong, Zhao Shouxun

Elsevier BV

30-Apr-2003

doi:	10.1016/0031-9422(96)00084-2

Diterpenoids from Rabdosia coetsoides

Hao Huang, Yunlong Xu, Handong Sun

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)98082-8

Diterpenoid constituents from Rabdosia coetsa

Yunlong Xu, Isao Kubo

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(93)80051-S

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 / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL	5366244	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,2R,4R,6S,9S,10S,13S,16R)-2,6,16-trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	13876276	Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C	350.40	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
(1R,2R,4S,6S,9S,10S,13S,16R)-2,6,16-trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	101915964	Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C	350.40	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8
(1R,2S,3S,5S,8S,9S,11R,15S)-3,9,15-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	44559705	Click to see CC1(CCC(C23C1CC(C45C2C(CC(C4)C(=C)C5=O)O)(OC3)O)O)C	348.40	unknown	via CMAUP database
(1R,2S,5S,8S,9S,10S,11R,13S,16R,18R)-10,13,16,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396787	Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)OC3O)O)O)C	364.40	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
(1R,2S,5S,8S,9S,10S,11R,13S,16S,18R)-10,13,16,18-tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396786	Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)OC3O)O)O)C	364.40	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
(1R,2S,5S,8S,9S,10S,11R,13S,16S,18R)-10,13,18-trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396782	Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)O)C	378.50	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
(1S,2S,5S,8R,9R,11S,13R,18R)-9,13,18-trihydroxy-12,12-dimethyl-6-methylidene-14-oxapentacyclo[11.2.2.15,8.01,11.02,8]octadecan-7-one	13876291	Click to see CC1(C2CC(C34C(C25CCC1(OC5)O)CCC(C3O)C(=C)C4=O)O)C	348.40	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
(1S,2S,5S,8S,9R,11R,13S,16S,18R)-13,18-dihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396780	Click to see CC1(C(CCC23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C	362.50	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
(1S,2S,5S,8S,9R,11R,13S,16S,18R)-16-ethoxy-13,18-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396784	Click to see CCOC1C23CCC(C(C2CC(O1)C45C3CCC(C4O)C(=C)C5=O)(C)C)O	376.50	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
(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 CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C	362.50	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
(9,18-Dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate	85147115	Click to see CC(=O)OC1CCC(C2C13COC(C2)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C	390.50	unknown	https://doi.org/10.1016/0031-9422(93)80051-S https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105001/
[(1R,2S,3S,5S,8S,9S,11R,15S)-9,15-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-3-yl] acetate	44559706	Click to see CC(=O)OC1CC2CC3(C1C45COC3(CC4C(CCC5O)(C)C)O)C(=O)C2=C	390.50	unknown	via CMAUP database
[(1R,2S,5S,8R,9R,11R,15S,18R)-9,18-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate	162964604	Click to see CC(=O)OC1CCC(C2C13COC(C2)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C	390.50	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
[(1S,2S,5S,7R,8S)-10-hydroxy-12,12-dimethyl-6-methylidene-9,16-dioxo-14-oxapentacyclo[11.2.2.15,8.01,11.02,8]octadec-10-en-7-yl] acetate	136018424	Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)C(=O)C(=C4C35COC(C4(C)C)CC5=O)O	386.40	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8
[(2S,5S,9R,11R,15R,18R)-9,18-dihydroxy-12,12-dimethyl-6-methylidene-7-oxo-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl] acetate	101676678	Click to see CC(=O)OC1CCC(C2C13COC(C2)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C	390.50	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
10,13,16,18-Tetrahydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396785	Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)OC3O)O)O)C	364.40	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
10,13,18-Trihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396781	Click to see CC1(C(CCC23C1C(C(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)O)C	378.50	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
13,18-Dihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396779	Click to see CC1(C(CCC23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C	362.50	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8 https://doi.org/10.1016/0031-9422(96)00084-2
15,18-Dihydroxy-16-methoxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	13945517	Click to see CC1(CCC(C23C1CC(C45C2CCC(C4O)C(=C)C5=O)OC3OC)O)C	362.50	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
16-Ethoxy-13,18-dihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-7-one	14396783	Click to see CCOC1C23CCC(C(C2CC(O1)C45C3CCC(C4O)C(=C)C5=O)(C)C)O	376.50	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
2,6,16-Trihydroxy-9-(hydroxymethyl)-5,5-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-15-one	13876274	Click to see CC1(C(CCC2(C1CC(C34C2CCC(C3O)C(=C)C4=O)O)CO)O)C	350.40	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
9,13,18-Trihydroxy-12,12-dimethyl-6-methylidene-14-oxapentacyclo[11.2.2.15,8.01,11.02,8]octadecan-7-one	13876290	Click to see CC1(C2CC(C34C(C25CCC1(OC5)O)CCC(C3O)C(=C)C4=O)O)C	348.40	unknown	https://doi.org/10.1016/0031-9422(96)00084-2 https://doi.org/10.1016/S0031-9422(00)98082-8
Coestanoic acid	44584281	Click to see CC1C2C(CC3C4(CCCC(C4CC(C3(C2O)C1=O)O)(C)C(=O)O)C)O	366.40	unknown	via CMAUP database
Coetsoidin A	366550	Click to see CC(=O)OC1C(=C)C2CCC3C1(C2)C(=O)C(=C4C35COC(C4(C)C)CC5=O)O	386.40	unknown	https://doi.org/10.1016/S0031-9422(00)98082-8
Gesneroidin C	10602392	Click to see CC(=O)OC1CC2CC3(C1C4(C(CC(C(C4C(C3OC(=O)C)OC(=O)C)(C)C)OC(=O)C)O)C)C(=O)C2=C	534.60	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
Rabdocoetsin B	10452999	Click to see CC(=O)OC1CCC(C2C13COC(C2)(C45C3CCC(C4O)C(=C)C5=O)O)(C)C	390.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Pterodonoic acid	11054003	Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O	248.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
Uvaol	92802	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO	442.70	unknown	https://doi.org/10.1016/0031-9422(93)80051-S
> 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	https://doi.org/10.1016/0031-9422(93)80051-S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Caffeic acid methyl ester	689075	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	https://doi.org/10.1016/J.PHYMED.2007.09.013
Ethyl caffeate	5317238	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	https://doi.org/10.1016/J.PHYMED.2007.09.013
Methyl rosmarinate	6479915	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	unknown	https://doi.org/10.1016/J.PHYMED.2007.09.013
Rosmarinic acid	5281792	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYMED.2007.09.013
Rosmarinic Acid Methyl Ester	3012090	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	unknown	https://doi.org/10.1016/J.PHYMED.2007.09.013
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
Isokaempferide	5280862	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	300.26	unknown	via CMAUP database
Quercetin 3,3'-dimethyl ether	5316900	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone	5352032	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	330.29	unknown	via CMAUP database
Jaceidin	5464461	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,4',5,6,7-Pentamethoxyflavone	521171	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database
4'-Hydroxy-3,5,6,7-tetramethoxyflavone	13983731	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)OC)OC	358.30	unknown	via CMAUP database
Jaranol	5318869	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	314.29	unknown	via CMAUP database
Pachypodol	5281677	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	344.30	unknown	via CMAUP database
Penduletin	5320462	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3-Methoxytangeretin	11741814	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC	402.40	unknown	via CMAUP database

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Isodon coetsa

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