Scientific name	Authority	First published in
Helichrysum roulingi	De Wild.	Ann. Mus. Congo Belge, Bot. , sér. 5, 3(2): 310 (1910)
Helichrysum engleri	O.Hoffm.	Bot. Jahrb. Syst. 20(1-2): 232 (1894)
Achyrocline hochstetteri	Sch.Bip. ex A.Rich.	Tent. Fl. Abyss. 1: 428 (1848)
Gnaphalium aureofulvum	P.J.Bergius	Descr. Pl. Cap. : 257 (1767)
Gnaphalium odoratissimum	L.	Sp. Pl. : 855 (1753)
Gnaphalium undulifolium	Rchb. ex DC.	Prodr. 6: 202 (1838)
Gnaphalium maritimum	Schrank	Denkschr. Königl. Akad. Wiss. München viii. (1824) 153
Gnaphalium adnatum	Willd. ex Spreng.	Syst. Veg. 3: 469 (1826)
Helichrysum odoratissimum var. odoratissimum	(L.) Sweet
Gnaphalium strigosum	Thunb.	Prodr. Pl. Cap. 2: 150 (1800)
Gnaphalium odorum	Salisb.	Prodr. Stirp. Chap. Allerton : 192 (1796)
Helichrysum rosmarinum	Mattf.	Bot. Jahrb. Syst. 59(4, Beibl. 133): 13 (1924)
Helichrysum butaguense	De Wild.	Pl. Bequaert. v. 46 (1929).

Common names Top

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Filter by language:

Language	Common/alternative name
Afrikaans	kooigoed

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Helichrysum odoratissimum var. scabrum	Moeser

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

Africa click to expand
- East Tropical Africa
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Sudan
- South Tropical Africa
  - Angola
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Free State
  - Kwazulu-Natal
  - Lesotho
  - Northern Provinces
  - Swaziland
- West Tropical Africa
  - Nigeria
- West-central Tropical Africa
  - Cameroon
  - Gulf Of Guinea Islands
  - Zaïre

Europe click to expand
- Northern Europe
  - Great Britain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000025613
Tropicos	2719408
KEW	urn:lsid:ipni.org:names:213115-1
The Plant List	gcc-124749
Open Tree Of Life	803657
NCBI Taxonomy	112363
NBN Atlas	NBNSYS0200002302
IPNI	213115-1
iNaturalist	586984
GBIF	3131161
EPPO	HECOD
USDA GRIN	470501

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

Zn nutrients-loaded chitosan nanocomposites and their efficacy as nanopriming agents for maize (Zea mays) seeds

Zungu B, Kamdem Paumo H, Gaorongwe JL, Tsuene GN, Ruzvidzo O, Katata-Seru L

Front Chem

11-Aug-2023

PMCID:	PMC10457009
doi:	10.3389/fchem.2023.1243884
PMID:	37638104

Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments

Mohanta YK, Mishra AK, Nongbet A, Chakrabartty I, Mahanta S, Sarma B, Panda J, Panda SK

Front Pharmacol

03-Aug-2023

PMCID:	PMC10441548
doi:	10.3389/fphar.2023.1153600
PMID:	37608892

Helichrysum stoechas (L.) Moench Inflorescence Extract for Tomato Disease Management

Sánchez-Hernández E, Álvarez-Martínez J, González-García V, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P

Molecules

03-Aug-2023

PMCID:	PMC10421166
doi:	10.3390/molecules28155861
PMID:	37570830

The updates and implications of cutaneous microbiota in acne

Huang C, Zhuo F, Han B, Li W, Jiang B, Zhang K, Jian X, Chen Z, Li H, Huang H, Dou X, Yu B

Cell Biosci

21-Jun-2023

PMCID:	PMC10283232
doi:	10.1186/s13578-023-01072-w
PMID:	37344849

Anticancer Potential of Natural Chalcones: In Vitro and In Vivo Evidence

Michalkova R, Mirossay L, Kello M, Mojzisova G, Baloghova J, Podracka A, Mojzis J

Int J Mol Sci

19-Jun-2023

PMCID:	PMC10299153
doi:	10.3390/ijms241210354
PMID:	37373500

Anti-Inflammatory and Anti-Quorum Sensing Effect of Camellia sinensis Callus Lysate for Treatment of Acne

Cañellas-Santos M, Rosell-Vives E, Montell L, Bilbao A, Goñi-de-Cerio F, Fernandez-Campos F

Curr Issues Mol Biol

04-May-2023

PMCID:	PMC10217533
doi:	10.3390/cimb45050255
PMID:	37232724

Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches

Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF

Plants (Basel)

02-Mar-2023

PMCID:	PMC10005506
doi:	10.3390/plants12051145
PMID:	36904005

Bioprospecting of Helichrysum Species: Chemical Profile, Phytochemical Properties, and Antifungal Efficacy against Botrytis cinerea

Matrose NA, Belay ZA, Obikeze K, Mokwena L, Caleb OJ

Plants (Basel)

22-Dec-2022

PMCID:	PMC9824591
doi:	10.3390/plants12010058
PMID:	36616185

Comparing Crop Yield, Secondary Metabolite Contents, and Antifungal Activity of Extracts of Helichrysum odoratissimum Cultivated in Aquaponic, Hydroponic, and Field Systems

Zantanta N, Kambizi L, Etsassala NG, Nchu F

Plants (Basel)

13-Oct-2022

PMCID:	PMC9611307
doi:	10.3390/plants11202696
PMID:	36297720

Multiple Mycotoxin Contamination in Medicinal Plants Frequently Sold in the Free State Province, South Africa Detected Using UPLC-ESI-MS/MS

Ndoro J, Manduna IT, Nyoni M, de Smidt O

Toxins (Basel)

08-Oct-2022

PMCID:	PMC9607566
doi:	10.3390/toxins14100690
PMID:	36287959

Chemical Study and Comparison of the Biological Activities of the Essential Oils of Helichrysum petiolare, H. cymosum, and H. odoratissimum

Adewinogo SO, Sharma R, Africa CW, Marnewick JL, Hussein AA

Plants (Basel)

03-Oct-2022

PMCID:	PMC9573642
doi:	10.3390/plants11192606
PMID:	36235472

Editorial: Nanomaterials for targeted delivery of therapeutic and imaging agents

Chockalingam S, Packirisamy G, Paulmurugan R

Front Cell Dev Biol

05-Aug-2022

PMCID:	PMC9397375
doi:	10.3389/fcell.2022.978690
PMID:	36016653

Helichrysum Genus and Compound Activities in the Management of Diabetes Mellitus

Akinfenwa AO, Sagbo IJ, Makhaba M, Mabusela WT, Hussein AA

Plants (Basel)

23-May-2022

PMCID:	PMC9143910
doi:	10.3390/plants11101386
PMID:	35631811

Traditional uses of wild and tended plants in maintaining ecosystem services in agricultural landscapes of the Eastern Cape Province in South Africa

Maroyi A

J Ethnobiol Ethnomed

15-Mar-2022

PMCID:	PMC8925170
doi:	10.1186/s13002-022-00512-0
PMID:	35292046

Medicinal Plants for Mitigating Pain and Inflammatory-Related Conditions: An Appraisal of Ethnobotanical Uses and Patterns in South Africa

Aremu AO, Pendota SC

Front Pharmacol

22-Oct-2021

PMCID:	PMC8569556
doi:	10.3389/fphar.2021.758583
PMID:	34744737

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 / Phenanthrenes and derivatives / Hydrophenanthrenes
2,4b-Dimethyl-8-methylene-2-vinyl-1,2,3,4,4a,4b,5,6,7,8,8a,9-dodecahydrophenanthrene	560947	Click to see CC1(CCC2C(=CCC3C2(CCCC3=C)C)C1)C=C	256.40	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Cyclohexane	8078	Click to see C1CCCCC1	84.16	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Acoradiene	90351	Click to see CC1CCC(C12CCC(=CC2)C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
10-Nonadecanol	85611	Click to see CCCCCCCCCC(CCCCCCCCC)O	284.50	unknown	https://doi.org/10.1080/10412905.1993.9698178
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235 https://doi.org/10.1080/10412905.1993.9698178
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
Citronellal	7794	Click to see CC(CCC=C(C)C)CC=O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698178
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698178
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698235
Linalyl acetate	8294	Click to see CC(=CCCC(C)(C=C)OC(=O)C)C	196.29	unknown	https://doi.org/10.1080/10412905.1993.9698178
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698178 https://doi.org/10.1080/10412905.1993.9698235
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698178
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1080/10412905.1993.9698178
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1993.9698235 https://doi.org/10.1080/10412905.1993.9698178
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Isoborneol	6973640	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698235
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
(1R)-endo-(+)-Fenchyl alcohol	6997371	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698235
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199903/04)14:2<82::AID-FFJ780>3.0.CO;2-Z https://doi.org/10.1080/10412905.1993.9698178 https://doi.org/10.1080/10412905.1993.9698235
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698178 https://doi.org/10.1080/10412905.1993.9698235
Fenchol	15406	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698235
Pinocarveol	102667	Click to see CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
trans-beta-Bergamotene	12300069	Click to see CC(=CCCC1(C2CCC(=C)C1C2)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698235
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698235
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1080/10412905.1993.9698235
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698178 https://doi.org/10.1080/10412905.1993.9698235
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1080/10412905.1993.9698178 https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-alpha-Curcumene	442360	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	https://doi.org/10.1002/(SICI)1099-1026(199903/04)14:2<82::AID-FFJ780>3.0.CO;2-Z
(-)-beta-Curcumene	14014430	Click to see CC1=CCC(=CC1)C(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
(+)-Gamma-cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315594	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol	5315592	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
(1S,5R,7S,10R)-4,10-dimethyl-7-propan-2-yltricyclo[4.4.0.01,5]dec-3-ene	134779875	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol	6506009	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
(E,E)-1,4,4-Trimethyl-8-methylene-1,5-cycloundecadiene	5318102	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
1-(6,10-Dimethylundeca-5,9-dien-2-yl)-4-methylbenzene	53942264	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CCC=C(C)C	270.50	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
1-[(2R,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-4-methylbenzene	163186428	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)CCC=C(C)C	270.50	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
1-[(2S,5E)-6,10-dimethylundeca-5,9-dien-2-yl]-4-methylcyclohexa-1,3-diene	163034181	Click to see CC1=CC=C(CC1)C(C)CCC=C(C)CCC=C(C)C	272.50	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
1-Methyl-4-(6-methylhept-6-en-2-yl)cyclohexa-1,4-diene	5316213	Click to see CC1=CCC(=CC1)C(C)CCCC(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene	101708	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
1,4,4-Trimethyl-8-methylenecycloundeca-1,5-diene	24798692	Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
3-[(2S)-6-methylhept-5-en-2-yl]-6-methylidenecyclohexene	5321277	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
alpha-Curcumene	92139	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	https://doi.org/10.1080/10412905.1993.9698235 https://doi.org/10.1002/(SICI)1099-1026(199903/04)14:2<82::AID-FFJ780>3.0.CO;2-Z
alpha-Muurolene	12306047	Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Beta-Sesquiphellandrene	12315492	Click to see CC(CCC=C(C)C)C1CCC(=C)C=C1	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235 https://doi.org/10.1080/10412905.1993.9698178
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
Delta-Guaiene	94275	Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Humuladienone	101297706	Click to see CC1CC=CC(CC=C(CCC1=O)C)(C)C	220.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235 https://doi.org/10.1080/10412905.1993.9698178
Zingiberene	92776	Click to see CC1=CCC(C=C1)C(C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
alpha-Gurjunene	15560276	Click to see CC1CCC2C(C2(C)C)C3=C(CCC13)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
beta-Gurjunene	6450812	Click to see CC1CCC2C(C2(C)C)C3C1CCC3=C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Viridiflorene	10910653	Click to see CC1CCC2=C(CCC3C(C12)C3(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Cedrane and isocedrane sesquiterpenoids
beta-Cedrene	11106485	Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Cedr-8(15)-ene	102432	Click to see CC1CCC2C13CCC(=C)C(C3)C2(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Cedrol	65575	Click to see CC1CCC2C13CCC(C(C3)C2(C)C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698178
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-ol	547972	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
Elemol	92138	Click to see CC(=C)C1CC(CCC1(C)C=C)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene	288227	Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
Valencene	9855795	Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Himachalane and lippifoliane sesquiterpenoids
3,5,5,9-tetramethyl-2,4a,5,6,7,8-hexahydro-1H-benzo[7]annulene	15095	Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
beta-Himachalene	11586487	Click to see CC1=CC2C(=C(CCCC2(C)C)C)CC1	204.35	unknown	https://doi.org/10.1080/10412905.1993.9698235
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1080/10412905.1993.9698178
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2-methyl-1-[2,4,6-trihydroxy-3-(3-methylbut-2-enyl)phenyl]butan-1-one	162965167	Click to see CCC(C)C(=O)C1=C(C=C(C(=C1O)CC=C(C)C)O)O	278.34	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
2-Methyl-1-[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)phenyl]-1-propanone	13411738	Click to see CC(C)C(=O)C1=C(C=C(C(=C1O)CC=C(C)C)O)O	264.32	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
2-Methyl-1-[2,4,6-trihydroxy-3-(3-methylbut-2-en-1-yl)phenyl]butan-1-one	14282623	Click to see CCC(C)C(=O)C1=C(C=C(C(=C1O)CC=C(C)C)O)O	278.34	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
6-Ethyl-4-hydroxy-5-methyl-3-[[2,4,6-trihydroxy-3-(2-methylbutanoyl)-5-(3-methylbut-2-enyl)phenyl]methyl]pyran-2-one	101538377	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)CC)O)O)C	444.50	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
6-Ethyl-4-hydroxy-5-methyl-3-[[2,4,6-trihydroxy-3-(3-methyl-2-butenyl)-5-(2-methyl-1-oxopropyl)phenyl]methyl]-2 h-pyran-2-one	129835966	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)C)O)O)C	430.50	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
6-ethyl-4-hydroxy-5-methyl-3-[[2,4,6-trihydroxy-3-[(2R)-2-methylbutanoyl]-5-(3-methylbut-2-enyl)phenyl]methyl]pyran-2-one	162939050	Click to see CCC1=C(C(=C(C(=O)O1)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C(C)CC)O)O)C	444.50	unknown	https://doi.org/10.1016/0031-9422(80)85038-2
> 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	https://doi.org/10.1021/NP50063A025

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Helichrysum odoratissimum

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