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Internal ID UUID643fcc45b831e831296235
Scientific name Brachylaena ramiflora
Authority Humbert
First published in Compos. Madagascar 54, in clavi. (1923)

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Synonyms Top

Scientific name Authority First published in
Vernonia piptocarphoides Baker J. Linn. Soc., Bot. 20: 177 (1883)
Synchodendron ramiflorum DC. Prodr. 5: 93 (1836)
Cacalia piptocarphodes Kuntze Revis. Gen. Pl. 1: 324 (1891)

Common names Top

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Language Common/alternative name
Malagasy merana

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Varieties (abbr. var.) Top

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Name Authority First published in
Brachylaena ramiflora var. bernieri (Baill.) Humbert Mém. Soc. Linn. Normandie, Bot. 25: 54 (1923)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000060728
Tropicos 2703758
KEW urn:lsid:ipni.org:names:186104-1
The Plant List gcc-17770
Open Tree Of Life 5784835
NCBI Taxonomy 1542379
IUCN Red List 61990371
IPNI 186104-1
iNaturalist 471644
GBIF 3140969
CMAUP NPO12713

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
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Natural products targeting the p53-MDM2 pathway and mutant p53: Recent advances and implications in cancer medicine Qin JJ, Li X, Hunt C, Wang W, Wang H, Zhang R Genes Dis 20-Jul-2018
PMCID:PMC6176154
doi:10.1016/j.gendis.2018.07.002
PMID:30320185
Antimalarial Activity of Plant Metabolites Pan WH, Xu XY, Shi N, Tsang SW, Zhang HJ Int J Mol Sci 06-May-2018
PMCID:PMC5983777
doi:10.3390/ijms19051382
PMID:29734792
Medicinal plants sold in the markets of Antananarivo, Madagascar Randriamiharisoa MN, Kuhlman AR, Jeannoda V, Rabarison H, Rakotoarivelo N, Randrianarivony T, Raktoarivony F, Randrianasolo A, Bussmann RW J Ethnobiol Ethnomed 28-Jul-2015
PMCID:PMC4517502
doi:10.1186/s13002-015-0046-y
PMID:26216098
Nutraceuticals as potential therapeutic agents for colon cancer: a review Kuppusamy P, Yusoff MM, Maniam GP, Ichwan SJ, Soundharrajan I, Govindan N Acta Pharm Sin B 03-May-2014
PMCID:PMC4629076
doi:10.1016/j.apsb.2014.04.002
PMID:26579381
Two new triterpene esters from the twigs of Brachylaena ramiflora from the Madagascar rainforest. Chaturvedula VS, Schilling JK, Miller JS, Andriantsiferana R, Rasamison VE, Kingston DG J Nat Prod 01-Aug-2002
doi:10.1021/NP0201220
PMID:12193040

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown via CMAUP database
Arctigenin, (+)- 28125531 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Matairesinol monoglucoside 23757184 Click to see COC1=C(C=CC(=C1)CC2C(COC2=O)CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(4,4,6a,6b,8a,9,9,14b-Octamethyl-1,2,3,4a,5,6,7,8,10,11,12,12a,14,14a-tetradecahydropicen-3-yl) hexadecanoate 73093635 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CCCC5(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
Kairatenyl Palmitate 636841 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CCCC5(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(5a,5b,8,8,11a,13b-Hexamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-yl) hexadecanoate 75049124 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5(CCC(C5CCC4(C3(CCC2C1(C)C)C)C)C(=C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
[(3S,3As,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-hexamethyl-3-prop-1-en-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysen-9-yl] hexadecanoate 11136108 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5(CCC(C5CCC4(C3(CCC2C1(C)C)C)C)C(=C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
Hopenyl Palmitate 44575981 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5(CCC(C5CCC4(C3(CCC2C1(C)C)C)C)C(=C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
11,12,13-Trihydroxy-4(15),8-eudesmadiene-9-one 639678 Click to see CC12CCCC(=C)C1CC(=CC2=O)C(CO)(CO)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Encelin 72540 Click to see CC12CC3C(CC1C(=C)C(=O)C=C2)C(=C)C(=O)O3 244.28 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1021/NP0201220
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) hexadecanoate 13915598 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
[(3S,4aR,6aR,6bS,8aS,11R,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] hexadecanoate 44575982 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
[(3S,6aR,8aR,12S,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] hexadecanoate 5318360 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
[(3S,6aR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 5318302 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1021/NP0201220
[(3S,6aR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] hexadecanoate 5318370 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1021/NP0201220
alpha-Amyrin palmitate 10394654 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1021/NP0201220
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1021/NP0201220
Beta-Amyrin Palmitate 13915599 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
CID 15599867 15599867 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP0201220
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1021/NP0201220
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1021/NP0201220
Lupeol Acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1021/NP0201220
Octadecanoic acid 1beta-hydroxyurs-9(11),12-diene-3beta-yl ester 12085701 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1CC(C2(C(C1(C)C)CCC3(C2=CC=C4C3(CCC5(C4C(C(CC5)C)C)C)C)C)C)O 707.20 unknown via CMAUP database
Sambuculin a 14486636 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4C5C(CCC5(CCC4(C3(CCC2C1(C)C)C)C)C)C(=C)C)C 665.10 unknown https://doi.org/10.1021/NP0201220
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
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

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