Scientific name	Authority	First published in
Guarea demerarana	C.DC.	Monogr. Phan. 1: 549 (1878)
Guarea grandiflora	Steud.	Nomencl. Bot. [Steudel], ed. 2. 1: 709. 1840
Guarea perrottetiana	A.Juss.	Bull. Sci. Nat. Geol. 23: 240. 1830 {Nov 1830] , as 'Perrotetiana'
Guarea perrottetii	Griseb.	Fl. Brit. W. I. : 131 (1859)

Common names Top

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Language	Common/alternative name
Portuguese	saco-de-gambá

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Guarea macrophylla subsp. pachycarpa	(C.DC.) T.D.Penn.	Fl. Neotrop. Monogr. 28: 289 (1981)
Guarea macrophylla subsp. pendulispica	(C.DC.) T.D.Penn.	Fl. Neotrop. Monogr. 28: 290 (1981)
Guarea macrophylla subsp. spicaeflora	(A.Juss.) T.D.Penn.	Fl. Neotrop. Monogr. 28: 287 (1981)
Guarea macrophylla subsp. tuberculata	(Vell.) T.D.Penn.	Fl. Neotrop. Monogr. 28: 285 (1981)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Leeward Islands
  - Windward Islands
- Central America
  - Costa Rica
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000710954
Tropicos	20400613
INPN	629789
KEW	urn:lsid:ipni.org:names:578653-1
The Plant List	kew-2834067
Open Tree Of Life	276637
NCBI Taxonomy	155638
IUCN Red List	62968
IPNI	578653-1
iNaturalist	281611
GBIF	7271393

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

Physical Attributes of Tree Holes in the Atlantic Forest Edges: Evaluating Their Association with the Presence and Abundance of Immature Haemagogus leucocelaenus

Tubaki RM, de Menezes RM, David MR, Palasio RG, de Aguiar OT, Baitello JB, Santos VO, Balbino N, Chiaravalloti-Neto F

Trop Med Infect Dis

25-Jun-2023

PMCID:	PMC10383151
doi:	10.3390/tropicalmed8070337
PMID:	37505633

Volatiles as Attractants of Mahogany Shoot Borer, Hypsipyla grandella Zeller (Lepidoptera: Pyralidae)

Díaz-Martínez YC, Malo EA, Alavez-Rosas D, Hernández-Moreno S, Cruz-López L, González-Gómez R

J Chem Ecol

21-Dec-2022

PMCID:	PMC9768390
doi:	10.1007/s10886-022-01398-8
PMID:	36542197

Phytochemistry and Biological Activities of Guarea Genus (Meliaceae)

Safriansyah W, Sinaga SE, Supratman U, Harneti D

Molecules

10-Dec-2022

PMCID:	PMC9786185
doi:	10.3390/molecules27248758
PMID:	36557891

Evaluation of conservation status of plants in Brazil’s Atlantic forest: An ethnoecological approach with Quilombola communities in Serra do Mar State Park

Conde BE, Aragaki S, Ticktin T, Surerus Fonseca A, Yazbek PB, Sauini T, Rodrigues E

PLoS One

18-Sep-2020

PMCID:	PMC7500697
doi:	10.1371/journal.pone.0238914
PMID:	32946472

Structural Elucidation of Malonylcommunol and 6β-Hydroxy-trans-communic Acid, Two Undescribed Diterpenes from Salvia cinnabarina. First Examples of Labdane Diterpenoids from a Mexican Salvia Species

Bustos-Brito C, Nieto-Camacho A, Hernandez-Ortega S, Rivera-Chávez J, Quijano L, Esquivel B

Molecules

15-Apr-2020

PMCID:	PMC7222005
doi:	10.3390/molecules25081808
PMID:	32326502

Yerba Mate (Ilex paraguariensis) Beverage: Nutraceutical Ingredient or Conveyor for the Intake of Medicinal Plants? Evidence from Paraguayan Folk Medicine

Kujawska M

Evid Based Complement Alternat Med

14-Mar-2018

PMCID:	PMC5872613
doi:	10.1155/2018/6849317
PMID:	29725356

Foliar secretory structures in Ekebergia capensis (Meliaceae)

Tilney PM, Nel M, van Wyk AE

Heliyon

01-Mar-2018

PMCID:	PMC5842367
doi:	10.1016/j.heliyon.2018.e00541
PMID:	29527579

The socio-cultural importance of Mauritia flexuosa palm swamps (aguajales) and implications for multi-use management in two Maijuna communities of the Peruvian Amazon

Gilmore MP, Endress BA, Horn CM

J Ethnobiol Ethnomed

22-Apr-2013

PMCID:	PMC3733440
doi:	10.1186/1746-4269-9-29
PMID:	23607601

Chilean Pitavia more closely related to Oceania and Old World Rutaceae than to Neotropical groups: evidence from two cpDNA non-coding regions, with a new subfamilial classification of the family

Groppo M, Kallunki JA, Pirani JR, Antonelli A

PhytoKeys

18-Dec-2012

PMCID:	PMC3597001
doi:	10.3897/phytokeys.19.3912
PMID:	23717188

Evidence for conservation and sustainable use in a fragment of the Atlantic forest in southeastern Brazil by a traditional human group

Christo AG, Guedes-Bruni RR, Sobrinho F, da Silva AG, Peixoto AL

Springerplus

28-Sep-2012

PMCID:	PMC3725884
doi:	10.1186/2193-1801-1-21
PMID:	23961351

Checklist of vascular plants of the Department of Ñeembucú, Paraguay

Egea JD, Peña-Chocarro M, Espada C, Knapp S

PhytoKeys

30-Jan-2012

PMCID:	PMC3281576
doi:	10.3897/phytokeys.9.2279
PMID:	22371688

Barking up the same tree: a comparison of ethnomedicine and canine ethnoveterinary medicine among the Aguaruna

Jernigan KA

J Ethnobiol Ethnomed

10-Nov-2009

PMCID:	PMC2777850
doi:	10.1186/1746-4269-5-33
PMID:	19903346

The importance of chemosensory clues in Aguaruna tree classification and identification

Jernigan KA

J Ethnobiol Ethnomed

03-May-2008

PMCID:	PMC2412849
doi:	10.1186/1746-4269-4-12
PMID:	18454871

Phylogenetic Variation in the Silicon Composition of Plants

HODSON MJ, WHITE PJ, MEAD A, BROADLEY MR

Ann Bot

21-Sep-2005

PMCID:	PMC4247092
doi:	10.1093/aob/mci255
PMID:	16176944

Cycloartane triterpenoids from Guarea macrophylla.

Lago JH, Roque NF

Phytochemistry

01-Jun-2002

doi:	10.1016/S0031-9422(02)00123-1
PMID:	12031420

Phytochemical Profile Top

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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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2-Hydroxy-4-methoxy-6-propylbenzoic acid	15595747	Click to see CCCC1=C(C(=CC(=C1)OC)O)C(=O)O	210.23	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3S,4aS,4bS,7S,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-3-ol	101716771	Click to see CC1(CC(CC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C	288.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
(E)-5-[(4aS,8aS)-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-ol	12109350	Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(=CCO)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
5-(2,5,5,8a-Tetramethyl-3,4,4a,6,7,8-hexahydronaphthalen-1-yl)-3-methylpent-2-en-1-ol	162868057	Click to see CC1=C(C2(CCCC(C2CC1)(C)C)C)CCC(=CCO)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-3-ol	74034790	Click to see CC1(CC(CC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C	288.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Isopimara-7,15-dien-3beta-ol	15541537	Click to see CC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C	288.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Pimara-7,15-dien-3-ol	620519	Click to see CC1(C(CCC2(C1CC=C3C2CCC(C3)(C)C=C)C)O)C	288.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol	443162	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aS,7R,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4,5,6,7,7a,7b-octahydro-1aH-cyclopropa[h]azulen-4a-ol	129416164	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	97032059	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	5321422	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
1,1,7-Trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol	522266	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Globulol	101716	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Ledol	92812	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Ledum camphor	22297324	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Palustrol	110745	Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1S,3aS,4S,8aR)-1,4-dimethyl-7-propan-2-yl-2,3,3a,5,6,8a-hexahydro-1H-azulen-4-ol	15541534	Click to see CC1CCC2C1C=C(CCC2(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
cis-Guai-6-en-10-ol	91747157	Click to see CC1CCC2C1C=C(CCC2(C)O)C(C)C	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-ethenyl-3,4a,7,7,10a-pentamethyl-2,5,6,6a,8,9,10,10b-octahydro-1H-benzo[f]chromene	518574	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
Labd-14-ene, 8,13-epoxy-, (13S)-	6432025	Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C	290.50	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2S,3S)-3-hydroxy-6-methyl-5-methylideneheptan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	163043715	Click to see CC(C)C(=C)CC(C(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3.0^{3,8.0^{12,16]octadecan-6-ol	496638	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	162950932	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-15-[(2R)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	131848483	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-15-[(E,2S,3S)-3,6-dihydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	162852225	Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C)C(C=CC(C)(C)O)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R,4E)-6-methylhepta-4,6-dien-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	22297599	Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	422.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-4-oxohept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	101618850	Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	438.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2S,4E)-6-methylhepta-4,6-dien-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	163191428	Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	422.70	unknown	https://doi.org/10.1016/S0031-9422(00)00302-2
(6R)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-en-4-one	101637203	Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
15-(3-Hydroxy-6-methyl-5-methylideneheptan-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	163043714	Click to see CC(C)C(=C)CC(C(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
15-(3,6-Dihydroxy-6-methylhept-4-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	73880611	Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C)C(C=CC(C)(C)O)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
15-(4-Hydroxy-6-methylhept-5-en-2-yl)-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	162950930	Click to see CC(CC(C=C(C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
25-Hydroxycycloart-23-en-3-one	44423578	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
6-(6-Hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl)-2-methylhept-2-en-4-one	163015474	Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
7,7,12,16-Tetramethyl-15-(6-methylhepta-4,6-dien-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	73880678	Click to see CC(CC=CC(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	422.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1 https://doi.org/10.1016/S0031-9422(00)00302-2
Cycloart-23-ene-3beta,25-diol	5470009	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(02)00123-1
> 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/S0031-9422(00)00302-2
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/S0031-9422(00)00302-2
Beta-Sitosterol	222284	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/S0031-9422(00)00302-2

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Guarea macrophylla

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