Scientific name	Authority	First published in
Cinnamosma fragrans var. baillonii	Courchet	Ann. Inst. Colon. Marseille sér. 2, 3: 58. 1905
Cinnamosma fragrans var. perrieri	Courchet	Ann. Inst. Colon. Marseille sér. 2, 3: 58. 1905

Common names Top

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Language	Common/alternative name
Malagasy	mandravasarotra

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

Africa click to expand
- Western Indian Ocean
  - Madagascar

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000605548
Tropicos	5600006
KEW	urn:lsid:ipni.org:names:146027-1
The Plant List	kew-2721726
Open Tree Of Life	5700304
NCBI Taxonomy	1602317
IUCN Red List	128085823
IPNI	146027-1
iNaturalist	429345
GBIF	3877824
Freebase	/m/0125wjjx
EOL	5035546
Wikipedia	Cinnamosma_fragrans

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

“ThermoTRP” Channel Expression in Cancers: Implications for Diagnosis and Prognosis (Practical Approach by a Pathologist)

Szallasi A

Int J Mol Sci

22-May-2023

PMCID:	PMC10219044
doi:	10.3390/ijms24109098
PMID:	37240443

Essential oil of Cymbopogon martini, source of geraniol, as a potential antibacterial agent against Bacillus subtilis, a pathogen of the bakery industry

Santamarta S, Aldavero AC, Rojo MA

F1000Res

24-Mar-2023

PMCID:	PMC9936101
doi:	10.12688/f1000research.54196.1
PMID:	36817513

Bioactive Molecules Derived from Plants in Managing Dengue Vector Aedes aegypti (Linn.)

Priya SS, Vasantha-Srinivasan P, Altemimi AB, Keerthana R, Radhakrishnan N, Senthil-Nathan S, Kalaivani K, Chandrasekar N, Karthi S, Ganesan R, Alkanan ZT, Pal T, Verma OP, Proćków J

Molecules

05-Mar-2023

PMCID:	PMC10005433
doi:	10.3390/molecules28052386
PMID:	36903635

Natural Active Ingredients and TRPV1 Modulation: Focus on Key Chemical Moieties Involved in Ligand–Target Interaction

Andrei C, Zanfirescu A, Nițulescu GM, Olaru OT, Negreș S

Plants (Basel)

11-Jan-2023

PMCID:	PMC9860573
doi:	10.3390/plants12020339
PMID:	36679051

Natural Products as Anticancer Agents: Current Status and Future Perspectives

Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q

Molecules

30-Nov-2022

PMCID:	PMC9737905
doi:	10.3390/molecules27238367
PMID:	36500466

Drimane-Type Sesquiterpenoids Derived from the Tropical Basidiomycetes Perenniporia centrali-africana and Cerrena sp. nov

Pathompong P, Pfütze S, Surup F, Boonpratuang T, Choeyklin R, Matasyoh JC, Decock C, Stadler M, Boonchird C

Molecules

14-Sep-2022

PMCID:	PMC9500820
doi:	10.3390/molecules27185968
PMID:	36144704

Searching for constituents from plants in geographically characterized areas, Egypt, Madagascar, and Okinawa

Sugimoto S

J Nat Med

12-Aug-2022

PMCID:	PMC9411232
doi:	10.1007/s11418-022-01638-x
PMID:	35960490

A Novel Disease (Water Bubble Disease) of the Giant Freshwater Prawn Macrobrachium rosenbergii Caused by Citrobacter freundii: Antibiotic Treatment and Effects on the Antioxidant Enzyme Activity and Immune Responses

Zhao C, Wen H, Huang S, Weng S, He J

Antioxidants (Basel)

29-Jul-2022

PMCID:	PMC9405353
doi:	10.3390/antiox11081491
PMID:	36009210

In vitro efficacy of essential oils against Sarcoptes scabiei

Andriantsoanirina V, Guillot J, Ratsimbason M, Mekhloufi G, Randriamialinoro F, Ranarivelo L, Ariey F, Durand R

Sci Rep

03-May-2022

PMCID:	PMC9065015
doi:	10.1038/s41598-022-11176-x
PMID:	35504935

Anticancer Activity of Natural and Semi-Synthetic Drimane and Coloratane Sesquiterpenoids

Beckmann L, Tretbar US, Kitte R, Tretbar M

Molecules

13-Apr-2022

PMCID:	PMC9031474
doi:	10.3390/molecules27082501
PMID:	35458699

Production, Transmission, Pathogenesis, and Control of Dengue Virus: A Literature-Based Undivided Perspective

Islam MT, Quispe C, Herrera-Bravo J, Sarkar C, Sharma R, Garg N, Fredes LI, Martorell M, Alshehri MM, Sharifi-Rad J, Daştan SD, Calina D, Alsafi R, Alghamdi S, Batiha GE, Cruz-Martins N

Biomed Res Int

15-Dec-2021

PMCID:	PMC8694986
doi:	10.1155/2021/4224816
PMID:	34957305

Activity in MCF-7 Estrogen-Sensitive Breast Cancer Cells of Capsicodendrin from Cinnamosma fragrans

Acuña UM, Ezzone N, Rakotondraibe LH, Carcache de Blanco EJ

Anticancer Res

01-Dec-2021

PMCID:	PMC8750382
doi:	10.21873/anticanres.15412
PMID:	34848447

A Review on Medicinal Plants Used in the Management of Headache in Africa

Frimpong EK, Asong JA, Aremu AO

Plants (Basel)

28-Sep-2021

PMCID:	PMC8539318
doi:	10.3390/plants10102038
PMID:	34685845

New Lignanamides with Antioxidant and Anti-Inflammatory Activities Screened Out and Identified from Warburgia ugandensis Combining Affinity Ultrafiltration LC-MS with SOD and XOD Enzymes

Zhuang XC, Chen GL, Liu Y, Zhang YL, Guo MQ

Antioxidants (Basel)

01-Mar-2021

PMCID:	PMC8001783
doi:	10.3390/antiox10030370
PMID:	33804549

Stop the crop: insights into the insecticidal mode of action of cinnamodial against mosquitoes

Kalsi M, Walter A, Lee B, DeLaat A, Trigueros RR, Happel K, Sepesy R, Nguyen B, Manwill PK, Rakotondraibe HL, Piermarini PM

Pestic Biochem Physiol

08-Nov-2020

PMCID:	PMC7770332
doi:	10.1016/j.pestbp.2020.104743
PMID:	33357565

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 / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(2S)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]chroman-6-ol	13988400	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O	396.60	unknown	https://doi.org/10.1021/NP0601298
(c)(1/2)-Tocotrienol pound>>Tocotrienol, delta	53394607	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O	396.60	unknown	https://doi.org/10.1021/NP0601298
delta-Tocotrienol	5282350	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O	396.60	unknown	https://doi.org/10.1021/NP0601298
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(1S,2S,7S,8R,11R,13S,15R)-15-[(1S,4R,4aS,8aS)-4-acetyloxy-1-formyl-1-hydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalen-2-yl]-11-hydroxy-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-8-yl] acetate	163004363	Click to see CC(=O)OC1C=C2C(OC3C2(C4(C1C(CCC4)(C)C)C)OC(O3)C5=CC(C6C(CCCC6(C5(C=O)O)C)(C)C)OC(=O)C)O	616.70	unknown	https://doi.org/10.1021/NP0601298
[(1S,2S,7S,8S,11S,13S,15S)-15-[(1S,4S,4aS,8aS)-4-acetyloxy-1-formyl-1-hydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalen-2-yl]-11-hydroxy-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-8-yl] acetate	163004361	Click to see CC(=O)OC1C=C2C(OC3C2(C4(C1C(CCC4)(C)C)C)OC(O3)C5=CC(C6C(CCCC6(C5(C=O)O)C)(C)C)OC(=O)C)O	616.70	unknown	https://doi.org/10.1021/NP0601298
[(1S,4S,4aS,8aS)-3-[(1S,2S,7S,8S,11S,13S,15S)-8-acetyloxy-11-methoxy-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-15-yl]-4-formyl-4-hydroxy-4a,8,8-trimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-1-yl] acetate	163079970	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C3OC4C5(O3)C(=CC(C6C5(CCCC6(C)C)C)OC(=O)C)C(O4)OC	630.80	unknown	https://doi.org/10.1021/NP0601298
[15-(4-acetyloxy-1-formyl-1-hydroxy-5,5,8a-trimethyl-4a,6,7,8-tetrahydro-4H-naphthalen-2-yl)-11-hydroxy-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-8-yl] acetate	73236904	Click to see CC(=O)OC1C=C2C(OC3C2(C4(C1C(CCC4)(C)C)C)OC(O3)C5=CC(C6C(CCCC6(C5(C=O)O)C)(C)C)OC(=O)C)O	616.70	unknown	https://doi.org/10.1021/NP0601298
Cinnafragrin A	44419503	Click to see CC(=O)OC1C=C2C(OC3C2(C4(C1C(CCC4)(C)C)C)OC(O3)C5=CC(C6C(CCCC6(C5(C=O)O)C)(C)C)OC(=O)C)O	616.70	unknown	https://doi.org/10.1021/NP0601298
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
[(1R,4R,4aR,8aS)-3,4-diformyl-4-hydroxy-4a,8,8-trimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-1-yl] acetate	163040561	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C=O	308.40	unknown	https://doi.org/10.1016/S0040-4039(00)90783-4
Cinnamodial	442354	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C=O	308.40	unknown	https://doi.org/10.1021/NP0601298 https://doi.org/10.1016/S0040-4020(01)82922-7
Cinnamodial B812927K060	321973	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C=O	308.40	unknown	https://doi.org/10.1021/NP0601298 https://doi.org/10.1016/S0040-4039(00)90783-4 https://doi.org/10.1016/S0040-4020(01)82922-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1021/NP0601298
> Organoheterocyclic compounds / Naphthofurans
(5aR,9aS,9bR)-6,6,9a-trimethyl-5,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzofuran-3-one	163045561	Click to see CC1(CCCC2(C1CC=C3C2COC3=O)C)C	234.33	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
(5aR,9aS)-6,6,9a-trimethyl-1,4,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3,5-dione	163036501	Click to see CC1(CCCC2(C1C(=O)CC3=C2COC3=O)C)C	248.32	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
(5aS,9aR)-6,6,9a-trimethyl-5a,7,8,9-tetrahydro-1H-benzo[e][2]benzofuran-3-one	124356308	Click to see CC1(CCCC2(C1C=CC3=C2COC3=O)C)C	232.32	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
(5aS,9aS)-6,6,9a-trimethyl-1,4,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3,5-dione	15559334	Click to see CC1(CCCC2(C1C(=O)CC3=C2COC3=O)C)C	248.32	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
(5aS)-6,6,9abeta-Trimethyl-5,5aalpha,6,7,8,9,9a,9balpha-octahydronaphtho[1,2-c]furan-3(1H)-one	12303260	Click to see CC1(CCCC2(C1CC=C3C2COC3=O)C)C	234.33	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
(6,6,9a-trimethyl-3-oxo-5,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzofuran-5-yl) acetate	12300029	Click to see CC(=O)OC1C=C2C(COC2=O)C3(C1C(CCC3)(C)C)C	292.40	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
[(1R,4S,4aS,8aS)-3-[(1S,2S,7S,8R,11S,13S,15R)-11-[[(4S,5S,5aS,9aS)-5-acetyloxy-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-4-yl]oxy]-8-acetyloxy-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-15-yl]-4-formyl-4-hydroxy-4a,8,8-trimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-1-yl] acetate	163014139	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C3OC4C5(O3)C(=CC(C6C5(CCCC6(C)C)C)OC(=O)C)C(O4)OC7C(C8C(CCCC8(C9=C7COC9=O)C)(C)C)OC(=O)C	907.10	unknown	https://doi.org/10.1021/NP0601298
[(1S,4S,4aS,8aS)-3-[(1S,2S,7S,8S,11S,13S,15S)-11-[[(4S,5S,5aS,9aS)-5-acetyloxy-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-4-yl]oxy]-8-acetyloxy-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-15-yl]-4-formyl-4-hydroxy-4a,8,8-trimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-1-yl] acetate	163014141	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C3OC4C5(O3)C(=CC(C6C5(CCCC6(C)C)C)OC(=O)C)C(O4)OC7C(C8C(CCCC8(C9=C7COC9=O)C)(C)C)OC(=O)C	907.10	unknown	https://doi.org/10.1021/NP0601298
[(5R,5aR,9aS,9bS)-6,6,9a-trimethyl-3-oxo-5,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzofuran-5-yl] acetate	162950037	Click to see CC(=O)OC1C=C2C(COC2=O)C3(C1C(CCC3)(C)C)C	292.40	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
[(5S,5aS,9aR,9bR)-6,6,9a-trimethyl-3-oxo-5,5a,7,8,9,9b-hexahydro-1H-benzo[e][2]benzofuran-5-yl] acetate	162950038	Click to see CC(=O)OC1C=C2C(COC2=O)C3(C1C(CCC3)(C)C)C	292.40	unknown	https://doi.org/10.1016/S0040-4020(01)82921-5
[3-[8-acetyloxy-11-[(5-acetyloxy-6,6,9a-trimethyl-1-oxo-4,5,5a,7,8,9-hexahydro-3H-benzo[e][2]benzofuran-4-yl)oxy]-2,6,6-trimethyl-12,14,16-trioxatetracyclo[8.6.0.01,13.02,7]hexadec-9-en-15-yl]-4-formyl-4-hydroxy-4a,8,8-trimethyl-5,6,7,8a-tetrahydro-1H-naphthalen-1-yl] acetate	73236907	Click to see CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(C=O)O)C3OC4C5(O3)C(=CC(C6C5(CCCC6(C)C)C)OC(=O)C)C(O4)OC7C(C8C(CCCC8(C9=C7COC9=O)C)(C)C)OC(=O)C	907.10	unknown	https://doi.org/10.1021/NP0601298
6,6,9a-Trimethyl-1,4,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-3,5-dione	15559333	Click to see CC1(CCCC2(C1C(=O)CC3=C2COC3=O)C)C	248.32	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
6,6,9a-trimethyl-5a,7,8,9-tetrahydro-1H-benzo[e][2]benzofuran-3-one	12300027	Click to see CC1(CCCC2(C1C=CC3=C2COC3=O)C)C	232.32	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
Bemadienolide	12300028	Click to see CC1(CCCC2(C1C=CC3=C2COC3=O)C)C	232.32	unknown	https://doi.org/10.1016/S0040-4020(01)82922-7
Cinnamolide	12303261	Click to see CC1(CCCC2(C1CC=C3C2COC3=O)C)C	234.33	unknown	https://doi.org/10.1016/S0040-4039(00)90783-4

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Cinnamosma fragrans

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