Scientific name	Authority	First published in
Osmites camphorina	Thunb.	Fl. Cap. : 700 (1823)
Osmites camphorata	Thunb.	Prodr. Pl. Cap. 2: 163 (1800)
Osmitopsis calva	Gand.	Bull. Soc. Bot. France 65: 46 (1918)
Osmites asteriscoides	P.J.Bergius	Descr. Pl. Cap. 305. 1767 [Sep 1767]
Osmites asteriscoides	L.	Syst. Nat. ed. 12 2: 571 (1767)
Buphthalmum asteriscoides	Baill.	Hist. Pl. 8: 301 (1882)
Osmitopsis camphorina	Less.	Syn. Gen. Compos. : 387 (1832)
Leucanthemum asteriscoides	(L.) Kuntze	Revis. Gen. Pl. (1891) 351.
Osmitopsis asteriscoides	Cass.	Dict. Sci. Nat., ed. 2. 37: 6 (1825)

Common names Top

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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

Africa click to expand
- Southern Africa
  - Cape Provinces

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000019331
KEW	urn:lsid:ipni.org:names:987322-1
The Plant List	gcc-118690
Open Tree Of Life	856824
NCBI Taxonomy	379267
IPNI	987322-1
iNaturalist	447652
GBIF	3110760
EOL	5120497

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

Essential Oils and Supercritical CO2 Extracts of Arctic Angelica (Angelica archangelica L.), Marsh Labrador Tea (Rhododendron tomentosum) and Common Tansy (Tanacetum vulgare)—Chemical Compositions and Antimicrobial Activities

Korpinen RI, Välimaa AL, Liimatainen J, Kunnas S

Molecules

25-Nov-2021

PMCID:	PMC8658896
doi:	10.3390/molecules26237121
PMID:	34885703

The Botanical, Chemical and Ethnobotanical Diversity of Southern African Lamiaceae

Rattray RD, Van Wyk BE

Molecules

18-Jun-2021

PMCID:	PMC8233991
doi:	10.3390/molecules26123712
PMID:	34207006

Anti-SARS-CoV Natural Products With the Potential to Inhibit SARS-CoV-2 (COVID-19)

Verma S, Twilley D, Esmear T, Oosthuizen CB, Reid AM, Nel M, Lall N

Front Pharmacol

25-Sep-2020

PMCID:	PMC7546787
doi:	10.3389/fphar.2020.561334
PMID:	33101023

The traditional use of southern African medicinal plants in the treatment of viral respiratory diseases: A review of the ethnobotany and scientific evaluations

Cock IE, Van Vuuren SF

J Ethnopharmacol

27-Jul-2020

PMCID:	PMC7384428
doi:	10.1016/j.jep.2020.113194
PMID:	32730880

Predicting plant vulnerability to drought in biodiverse regions using functional traits

Skelton RP, West AG, Dawson TE

Proc Natl Acad Sci U S A

20-Apr-2015

PMCID:	PMC4426410
doi:	10.1073/pnas.1503376112
PMID:	25902534

Camphor—A Fumigant during the Black Death and a Coveted Fragrant Wood in Ancient Egypt and Babylon—A Review

Chen W, Vermaak I, Viljoen A

Molecules

10-May-2013

PMCID:	PMC6270224
doi:	10.3390/molecules18055434
PMID:	23666009

Therapeutic Potential of Plants as Anti-microbials for Drug Discovery

Perumal Samy R, Gopalakrishnakone P

Evid Based Complement Alternat Med

24-Jun-2008

PMCID:	PMC2887332
doi:	10.1093/ecam/nen036
PMID:	18955349

cis‐Guajanolide aus Osmitopsis asteriscoides

Ferdinand Bohlmann, Christa Zdero, Jasmin Jakupovic, John P. Rourke

Wiley

19-Jul-2007

doi:	10.1002/JLAC.198519851205

Natürlich vorkommende Terpen‐Derivate, XXXII. Neue Sesquiterpenlactone aus Osmitopsis asteriscoides (L.) Cass.

Ferdinand Bohlmann, Christa Zdero

Wiley

29-Jun-2007

doi:	10.1002/CBER.19741070501

Polyacetylenverbindungen, 208 Acetylenverbindungen aus Osmitopsis asteriscoides (L.) Cass

Ferdinand Bohlmann, Christa Zdero

Wiley

28-Jun-2007

doi:	10.1002/CBER.19721050615

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 / Fatty Acyls / Fatty alcohol esters
[(2E,8E)-deca-2,8-dien-4,6-diynyl] 3-methylbutanoate	21159440	Click to see CC=CC#CC#CC=CCOC(=O)CC(C)C	230.30	unknown	https://doi.org/10.1002/CBER.19721050615
[(E)-dec-2-en-4,6,8-triynyl] 3-methylbutanoate	14018724	Click to see CC#CC#CC#CC=CCOC(=O)CC(C)C	228.29	unknown	https://doi.org/10.1002/CBER.19721050615
Agn-PC-036due	528757	Click to see CC=CC#CC#CC=CCOC(=O)CC(C)C	230.30	unknown	https://doi.org/10.1002/CBER.19721050615
Dec-2-en-4,6,8-triynyl 3-methylbutanoate	162992466	Click to see CC#CC#CC#CC=CCOC(=O)CC(C)C	228.29	unknown	https://doi.org/10.1002/CBER.19721050615
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1002/JLAC.198519851205
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1002/JLAC.198519851205
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1R,5R)-5-(2-hydroxypropan-2-yl)-2-methylidenecyclohexan-1-ol	101599841	Click to see CC(C)(C1CCC(=C)C(C1)O)O	170.25	unknown	https://doi.org/10.1002/JLAC.198519851205
(1S,5R)-5-(2-hydroxypropan-2-yl)-2-methylidenecyclohexan-1-ol	102376816	Click to see CC(C)(C1CCC(=C)C(C1)O)O	170.25	unknown	https://doi.org/10.1002/JLAC.198519851205
4-Hydroxy-alpha,alpha,4-trimethylcyclohex-2-ene-1-methanol	92632	Click to see CC1(CCC(C=C1)C(C)(C)O)O	170.25	unknown	https://doi.org/10.1002/JLAC.198519851205
5-(2-Hydroxypropan-2-yl)-2-methylidenecyclohexan-1-ol	15600205	Click to see CC(C)(C1CCC(=C)C(C1)O)O	170.25	unknown	https://doi.org/10.1002/JLAC.198519851205
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/JLAC.198519851205
cis-1,8-Dihydroxymenth-2-ene	12618693	Click to see CC1(CCC(C=C1)C(C)(C)O)O	170.25	unknown	https://doi.org/10.1002/JLAC.198519851205
rel-(1S,4S)-4-(2-Hydroxypropan-2-yl)-1-methylcyclohex-2-en-1-ol	20837874	Click to see CC1(CCC(C=C1)C(C)(C)O)O	170.25	unknown	https://doi.org/10.1002/JLAC.198519851205
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
methyl 2-[(1R,4S,5S)-5-methyl-3-oxo-4-(3-oxobutyl)cycloheptyl]prop-2-enoate	162941578	Click to see CC1CCC(CC(=O)C1CCC(=O)C)C(=C)C(=O)OC	280.36	unknown	https://doi.org/10.1002/JLAC.198519851205
Methyl 2-[5-methyl-3-oxo-4-(3-oxobutyl)cycloheptyl]prop-2-enoate	162941577	Click to see CC1CCC(CC(=O)C1CCC(=O)C)C(=C)C(=O)OC	280.36	unknown	https://doi.org/10.1002/JLAC.198519851205
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1R,2S,6R,9R,10R,13R)-9,13-dimethyl-5-methylidene-3,14-dioxatetracyclo[8.4.0.01,13.02,6]tetradecan-4-one	162893872	Click to see CC1CCC2C(C34C1CCC3(O4)C)OC(=O)C2=C	248.32	unknown	https://doi.org/10.1002/CBER.19741070501
(9a-hydroperoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6,6a,7,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate	162904709	Click to see CC1CC(C2C(C3(C1CC=C3C)OO)OC(=O)C2=C)OC(=O)C	322.40	unknown	https://doi.org/10.1002/JLAC.198519851205
(9a-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6,6a,7,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate	163026268	Click to see CC1CC(C2C(C3(C1CC=C3C)O)OC(=O)C2=C)OC(=O)C	306.40	unknown	https://doi.org/10.1002/JLAC.198519851205
[(3aR,4S,6S,6aS,9aS,9bR)-9a-hydroperoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6,6a,7,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] acetate	163195477	Click to see CC1CC(C2C(C3(C1CC=C3C)OO)OC(=O)C2=C)OC(=O)C	322.40	unknown	https://doi.org/10.1002/JLAC.198519851205
[(3aR,4S,6S,6aS,9aS,9bR)-9a-hydroxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6,6a,7,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] acetate	163026269	Click to see CC1CC(C2C(C3(C1CC=C3C)O)OC(=O)C2=C)OC(=O)C	306.40	unknown	https://doi.org/10.1002/JLAC.198519851205
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1R,4R,6R,7R,11R,12S,14S)-4,14-dimethyl-10-methylidene-5,8,15-trioxapentacyclo[10.2.1.01,6.04,6.07,11]pentadecan-9-one	163068161	Click to see CC1CC2C3C(C45C1(O2)CCC4(O5)C)OC(=O)C3=C	262.30	unknown	https://doi.org/10.1002/JLAC.198519851205
(3aR,4S,6S,6aS,9bR)-4-hydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-2-one	163186557	Click to see CC1CC(C2C(C3=C(CCC13)C)OC(=O)C2=C)O	248.32	unknown	https://doi.org/10.1002/JLAC.198519851205
(3aR,6R,6aR,9bS)-6,9-dimethyl-3-methylidene-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-2-one	102239683	Click to see CC1CCC2C(C3=C(CCC13)C)OC(=O)C2=C	232.32	unknown	https://doi.org/10.1002/CBER.19741070501
(6,9-Dimethyl-3-methylidene-2-oxo-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-4-yl) acetate	162867028	Click to see CC1CC(C2C(C3=C(CCC13)C)OC(=O)C2=C)OC(=O)C	290.40	unknown	https://doi.org/10.1002/JLAC.198519851205
(9-hydroperoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl) acetate	162864357	Click to see CC1CC(C2C(C3=C1CCC3(C)OO)OC(=O)C2=C)OC(=O)C	322.40	unknown	https://doi.org/10.1002/JLAC.198519851205
[(3aR,4S,6S,6aS,9bR)-6,9-dimethyl-3-methylidene-2-oxo-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-4-yl] acetate	162867029	Click to see CC1CC(C2C(C3=C(CCC13)C)OC(=O)C2=C)OC(=O)C	290.40	unknown	https://doi.org/10.1002/JLAC.198519851205
[(3aR,4S,6S,9R,9bR)-9-hydroperoxy-6,9-dimethyl-3-methylidene-2-oxo-4,5,6,7,8,9b-hexahydro-3aH-azuleno[4,5-b]furan-4-yl] acetate	162864358	Click to see CC1CC(C2C(C3=C1CCC3(C)OO)OC(=O)C2=C)OC(=O)C	322.40	unknown	https://doi.org/10.1002/JLAC.198519851205
4-Hydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6,6a,7,8,9b-octahydroazuleno[4,5-b]furan-2-one	162956803	Click to see CC1CC(C2C(C3=C(CCC13)C)OC(=O)C2=C)O	248.32	unknown	https://doi.org/10.1002/JLAC.198519851205
4,14-Dimethyl-10-methylidene-5,8,15-trioxapentacyclo[10.2.1.01,6.04,6.07,11]pentadecan-9-one	163068160	Click to see CC1CC2C3C(C45C1(O2)CCC4(O5)C)OC(=O)C3=C	262.30	unknown	https://doi.org/10.1002/JLAC.198519851205
> Organoheterocyclic compounds / Oxanes
(1R,6R,10R,11S,13S)-4,13-dimethyl-9-methylidene-7,14-dioxatetracyclo[9.2.1.01,5.06,10]tetradec-4-en-8-one	162925949	Click to see CC1CC2C3C(C4=C(CCC14O2)C)OC(=O)C3=C	246.30	unknown	https://doi.org/10.1002/JLAC.198519851205
(1S,6S,10S,11R,13R)-4,13-dimethyl-9-methylidene-7,14-dioxatetracyclo[9.2.1.01,5.06,10]tetradec-4-en-8-one	162925948	Click to see CC1CC2C3C(C4=C(CCC14O2)C)OC(=O)C3=C	246.30	unknown	https://doi.org/10.1002/CBER.19741070501
4,13-Dimethyl-9-methylidene-7,14-dioxatetracyclo[9.2.1.01,5.06,10]tetradec-4-en-8-one	74217299	Click to see CC1CC2C3C(C4=C(CCC14O2)C)OC(=O)C3=C	246.30	unknown	https://doi.org/10.1002/JLAC.198519851205
> Organoheterocyclic compounds / Oxepanes
[1,5,5-Trimethyl-6-(3-oxobut-1-enyl)-7-oxabicyclo[4.1.0]heptan-3-yl] tetradecanoate	162856015	Click to see CCCCCCCCCCCCCC(=O)OC1CC(C2(C(C1)(O2)C)C=CC(=O)C)(C)C	434.70	unknown	https://doi.org/10.1002/CBER.19741070501
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(5-Methylthiophen-2-yl)pent-2-en-4-ynyl acetate	162988834	Click to see CC1=CC=C(S1)C#CC=CCOC(=O)C	220.29	unknown	https://doi.org/10.1002/CBER.19741070501

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Osmitopsis asteriscoides

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top