Protium heptaphyllum

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643ff8216e0ad749564075
Scientific name	Protium heptaphyllum
Authority	Marchand
First published in	Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1873: 55 (1873)

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Synonyms Top

Scientific name	Authority	First published in
Protium multiflorum	Engl.	Fl. Bras. 12(2): 273 (1874)
Protium aromaticum	Engl.	Fl. Bras. 12(2): 273 (1874)
Protium tacamahaca	Marchand	Adansonia 8: 52 (1867)
Tingulonga multiflora	Kuntze	Revis. Gen. Pl. 1: 108 (1891)
Tingulonga heptaphylla	Kuntze	Revis. Gen. Pl. 1: 107 (1891)
Amyris brasiliensis	Willd. ex Engl.	Monogr. Phan. 4: 64 (1883)
Bursera tacahamaca	Baill.	Hist. Pl. 5: 297 (1874)
Icica ambrosiaca	Mart.	Reise Bras. 2: 551 (1828)
Icica heptaphylla	Aubl.	Hist. Pl. Guiane 1: 337 (1775)
Icica salzmannii	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 31(I): 473 (1858)
Icica tacamahaca	Kunth	Nov. Gen. Sp. 7: 33 (1824)
Protium angustifolium	Swart	Recueil Trav. Bot. Néerl. 39: 190 (1942)
Protium octandrum	Swart	Recueil Trav. Bot. Néerl. 39: 198 (1942)
Protium heptaphyllum var. unifoliolatum	Swart	Recueil Trav. Bot. Néerl. 39: 191. 1942
Protium heptaphyllum var. multiflorum	(Engl. ex Mart.) Swart	Recueil Trav. Bot. Néerl. 39: 297. 1942
Protium heptaphyllum var. floribundum	Swart	Recueil Trav. Bot. Néerl. 39: 191. 1942
Protium heptaphyllum var. surinamense	(Miq.) Swart	Recueil Trav. Bot. Néerl. 39: 298 (1942)
Icica surinamensis	Miq.
Protium hostmannii var. brasiliense	Swart	Acta Bot. Neerl. 15: 52 (1966)
Icica guianensis	Triana & Planch.	Ann. Sci. Nat., Bot. , sér. 5, 14: 297 (1872)
Protium heptaphyllum var. angustifolium	Engl.	Fl. Bras. 12(2): 263 (1874)

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Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Protium heptaphyllum subsp. ulei	(Swart) Daly	Fl. Venez. Guayana 3: 716 (1997)

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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Trinidad-Tobago
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Paraguay
- Western South America
  - Bolivia
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000397106
UNII	SU7X243EKX
Tropicos	4700374
INPN	732827
KEW	urn:lsid:ipni.org:names:128338-1
The Plant List	kew-2412252
Open Tree Of Life	645420
NCBI Taxonomy	246847
IUCN Red List	158460267
IPNI	128338-1
iNaturalist	706945
GBIF	7286785
USDA GRIN	438718
Wikipedia	Protium_heptaphyllum

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

New value chain Pentadesma nuts and butter from West Africa to international markets: Biological activities, health benefits, and physicochemical properties

Chabi IB, Aïssi MV, Zannou O, Kpoclou YE, Ayegnon BP, Badoussi ME, Ballogou VY, Goksen G, Mousavi Khaneghah A, Kayodé AP

Food Sci Nutr

20-Nov-2023

PMCID:	PMC10867462
doi:	10.1002/fsn3.3806
PMID:	38370066

Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species

Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q

J Fungi (Basel)

21-Sep-2023

PMCID:	PMC10532644
doi:	10.3390/jof9090953
PMID:	37755061

Snakebite envenomations and access to treatment in communities of two indigenous areas of the Western Brazilian Amazon: A cross-sectional study

de Farias AS, Gomes Filho MR, da Costa Arévalo M, Cristino JS, Farias FR, Sachett A, Silva-Neto AV, de Carvalho FG, Ambrosio SA, da Silva Carvalho E, Lacerda M, Murta F, Machado VA, Wen FH, Monteiro W, Sachett J

PLoS Negl Trop Dis

13-Jul-2023

PMCID:	PMC10368234
doi:	10.1371/journal.pntd.0011485
PMID:	37440596

Identification of Leading Compounds from Euphorbia neriifolia (Dudsor) Extracts as a Potential Inhibitor of SARS-CoV-2 ACE2-RBDS1 Receptor Complex: An Insight from Molecular Docking ADMET Profiling and MD-simulation Studies

Islam MN, Pramanik ME, Hossain MA, Rahman MH, Hossen MS, Islam MA, Miah MM, Ahmed I, Hossain AM, Haque MJ, Islam AM, Ali MN, Jahan RA, Haque ME, Rahman MM, Hasan MS, Rahman MM, Kabir MM, Basak PM, Sarkar MA, Islam MS, Rahman MR, Prodhan AA, Mosaddik A, Haque H, Fahmin F, Das HS, Islam MM, Emtia C, Gofur MR, Liang A, Akbar SM

Euroasian J Hepatogastroenterol

01-Jul-2023

PMCID:	PMC10785135
doi:	10.5005/jp-journals-10018-1414
PMID:	38222948

Red Yeast Rice for the Improvement of Lipid Profiles in Mild-to-Moderate Hypercholesterolemia: A Narrative Review

Cicero AF, Fogacci F, Stoian AP, Toth PP

Nutrients

12-May-2023

PMCID:	PMC10221652
doi:	10.3390/nu15102288
PMID:	37242171

Health Properties of Plant Bioactive Compounds: Immune, Antioxidant, and Metabolic Effects

Cruz-Chamorro I, Carrillo-Vico A

Int J Mol Sci

26-Apr-2023

PMCID:	PMC10178185
doi:	10.3390/ijms24097916
PMID:	37175623

Preliminary Study on Insecticidal Potential and Chemical Composition of Five Rutaceae Essential Oils against Thrips flavus (Thysanoptera: Thripidae)

Pei TH, Zhao YJ, Wang SY, Li XF, Sun CQ, Shi SS, Xu ML, Gao Y

Molecules

28-Mar-2023

PMCID:	PMC10095842
doi:	10.3390/molecules28072998
PMID:	37049761

The impact of species complexes on tree abundance patterns in Amazonia

Bacon CD, Hill A, ter Steege H, Antonelli A, Damasco G

Am J Bot

04-Oct-2022

PMCID:	PMC9828733
doi:	10.1002/ajb2.16069
PMID:	36193824

Extraction of a Triterpene Solution and Evaluation of the Hypolipidemic Efficacy of the Pleurotus tuber-regium (Fr.) Sing Sclerotium

Wang C, Liu Y, Lan Y, Yuan J

Foods

16-Sep-2022

PMCID:	PMC9498554
doi:	10.3390/foods11182881
PMID:	36141009

In Vitro and In Silico Screening of Anti-Vibrio spp., Antibiofilm, Antioxidant and Anti-Quorum Sensing Activities of Cuminum cyminum L. Volatile Oil

Ghannay S, Aouadi K, Kadri A, Snoussi M

Plants (Basel)

29-Aug-2022

PMCID:	PMC9459890
doi:	10.3390/plants11172236
PMID:	36079620

GC-MS Profiling, Vibriocidal, Antioxidant, Antibiofilm, and Anti-Quorum Sensing Properties of Carum carvi L. Essential Oil: In Vitro and In Silico Approaches

Ghannay S, Aouadi K, Kadri A, Snoussi M

Plants (Basel)

14-Apr-2022

PMCID:	PMC9032858
doi:	10.3390/plants11081072
PMID:	35448799

First report of triterpenes pathway in Calotropis procera revealed to accumulate beta-amyrin

Hassan S, Atef A, Ali HM, Alshamrani R, Ramadan A

Saudi J Biol Sci

05-Mar-2022

PMCID:	PMC9280243
doi:	10.1016/j.sjbs.2022.02.055
PMID:	35844368

Chaetomugilins and Chaetoviridins—Promising Natural Metabolites: Structures, Separation, Characterization, Biosynthesis, Bioactivities, Molecular Docking, and Molecular Dynamics

Omar AM, Mohamed GA, Ibrahim SR

J Fungi (Basel)

27-Jan-2022

PMCID:	PMC8875349
doi:	10.3390/jof8020127
PMID:	35205880

Taste and chemical composition as drives for utilitarian redundancy and equivalence: a case study in local medical systems in Northeastern Brazil

Reinaldo RC, Santoro FR, Albuquerque UP, de Medeiros PM

J Ethnobiol Ethnomed

25-Jan-2022

PMCID:	PMC8787910
doi:	10.1186/s13002-022-00503-1
PMID:	35078497

The Role of Cyclodextrins in the Design and Development of Triterpene-Based Therapeutic Agents

Prodea A, Mioc A, Banciu C, Trandafirescu C, Milan A, Racoviceanu R, Ghiulai R, Mioc M, Soica C

Int J Mol Sci

10-Jan-2022

PMCID:	PMC8775686
doi:	10.3390/ijms23020736
PMID:	35054925

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
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lignans, neolignans and related compounds / Coumarinolignans
2-(4-Hydroxy-3-methoxyphenyl)-5-methoxy-3-methyl-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-9-one	15608272	Click to see CC1C(OC2=C3C(=CC(=C2O1)OC)C=CC(=O)O3)C4=CC(=C(C=C4)O)OC	370.40	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
CID 335652	335652	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
Cleomiscosin A	442510	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)OC)C=CC(=O)O4)CO)O	386.40	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Hexadecanal	984	Click to see CCCCCCCCCCCCCCCC=O	240.42	unknown	https://doi.org/10.1080/10412905.1995.9698581
Pentadecanal	17697	Click to see CCCCCCCCCCCCCCC=O	226.40	unknown	https://doi.org/10.1080/10412905.1995.9698581
Tetradecanal	31291	Click to see CCCCCCCCCCCCCC=O	212.37	unknown	https://doi.org/10.1080/10412905.1995.9698581
> 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/10.1080/10412905.1995.9698581
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1080/10412905.1995.9698581
> 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/10.1080/10412905.1995.9698581
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698581
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698581
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
(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/10.1080/10412905.1995.9698581
(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/10.1080/10412905.1995.9698581
(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/10.1080/10412905.1995.9698581
alpha-Cubebene	442359	Click to see CC1CCC(C2C13C2C(=CC3)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Alpha-Farnesene	5281516	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-	89316	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	https://doi.org/10.1080/10412905.1995.9698581
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
beta-EUDESMOL	91457	Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O	222.37	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(-)-Germacrene A	9548706	Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
(1Z,5Z,8S)-1,5-dimethyl-8-prop-1-en-2-ylcyclodeca-1,5-diene	6440527	Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,4aS,6aR,6aR,6bR,8aR,10S,12aR,14aR,14bR)-1,2,4a,6a,6b,9,9,12a-octamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14,14a,14b-hexadecahydropicene-2,10-diol	162934031	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)O)C	444.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
(3S,4S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	162999807	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
(4aR,6aR,6aR,6bR,8aS,11S,12S,12aR,14aR,14bR)-11-hydroxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-tetradecahydro-1H-picen-3-one	162959926	Click to see CC1C2C3CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
(4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picene-3,3-diol	162968551	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)(O)O)C)C)C2C1)C)C)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
4,4,6a,6b,8a,11,11,14b-octamethyl-2,4a,5,6,7,8,9,10,12,12a,14,14a-dodecahydro-1H-picene-3,3-diol	162968550	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)(O)O)C)C)C2C1)C)C)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
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/10.1016/S0367-326X(01)00289-1
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/10.1016/S0367-326X(01)00289-1
Brein	9803424	Click to see CC1CCC2(C(CC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)O)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
Friedelan-3-one	244297	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
gamma-Taraxastane-3,20-diol	14313597	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)O)C	444.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
gamma-Taraxastanonol	14357350	Click to see CC1C2C3CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CCC1(C)O)C)C)C)(C)C)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
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/10.1016/S0305-1978(01)00130-2
Maniladiol	397934	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C)C	442.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
Olean-12-en-3beta-ol	225689	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/10.1016/S0367-326X(01)00289-1
Urs-12-en-3beta-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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/S0305-1978(01)00130-2
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/S0305-1978(01)00130-2
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
> Organoheterocyclic compounds / Benzodioxoles
Dillapiol	10231	Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC	222.24	unknown	https://doi.org/10.1080/10412905.1995.9698581
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Fraxetin	5273569	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O	208.17	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	https://doi.org/10.1016/S0305-1978(01)00130-2
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
5,7-Dihydroxy-6,8-bis(3-methylbut-2-enyl)-3-(2,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one	10478410	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(CO2)C3=CC(=C(C=C3O)O)O)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1016/S0367-326X(01)00289-1

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Protium heptaphyllum

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