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Bursera graveolens

Bursera graveolens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400e50468f1043227724
Scientific name Bursera graveolens
Authority Triana & Planch.
First published in Ann. Sci. Nat., Bot. , sér. 5, 14: 303 (1872)

Description Top

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Synonyms Top

Scientific name Authority First published in
Amyris caranifera Willd. ex Engl. Monogr. Phan. [A.DC. & C.DC.] 4: 49. 1883 [Mar 1883]
Amyris graveolens Spreng. Syst. Veg. 4(2): 148 (1827)
Amyris pubescens Willd. ex Schltdl. Linnaea 16(6): 527. 1843 [Mar 1843]
Bursera anderssonii B.L.Rob. Proc. Amer. Acad. Arts 38: 160 (1902)
Bursera graveolens var. pubescens Engl. Monogr. Phan. 4: 49 (1883)
Bursera graveolens var. villosula Cuatrec. Webbia 12: 431 (1957)
Bursera pubescens (Schltdl.) Standl. Publ. Field Columb. Mus., Bot. Ser. 4: 217. 1929
Bursera tatamaco Triana & Planch. Ann. Sci. Nat., Bot. , sér. 5, 14: 303 (1872)
Elaphrium graveolens Kunth Nov. Gen. Sp. 7: 31 (1824)
Elaphrium pubescens Schltdl. Linnaea 16: 527 (1842)
Elaphrium tatamaco Tul. Ann. Sci. Nat., Bot. , sér. 3, 6: 368 (1846)
Spondias edmonstonei Hook.f. Trans. Linn. Soc. London 20: 230 (1847)
Terebinthus graveolens Rose Contr. U.S. Natl. Herb. 10: 119 (1906)
Terebinthus pubescens Rose Contr. U.S. Natl. Herb. 12: 279 (1909)
Elaphrium tacamaco Tul. Ann. Sci. Nat., Bot. , sér. 3, 6: 368 (1846)

Common names Top

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Language Common/alternative name
Spanish bursera penicillata
Spanish terebinthus graveolens
Spanish spondias edmonstonei
Spanish elaphrium tatamaco
Spanish elaphrium pubescens
Spanish elaphrium graveolens
Spanish bursera tacamaco
Spanish amyris caranifera
Arabic ربد
Arabic ورد الحمار
Croatian sveto drvo
Italian palo santo
Italian palosanto
Polish palo santo
Slovenian palo santo
Chinese 印加聖木
Chinese 帕洛桑托
Chinese 祕魯聖木
Chinese 聖木

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Bursera graveolens subsp. malacophylla (B.L.Rob.) A.Weeks & Tye Bot. J. Linn. Soc. 161: 407 (2009)

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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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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Caribbean
      • Cuba
      • Southwest Caribbean
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000576197
UNII D041Y34RO2
Tropicos 4700223
KEW urn:lsid:ipni.org:names:127138-1
The Plant List kew-2687541
Open Tree Of Life 5146120
NCBI Taxonomy 300214
IUCN Red List 67836767
IPNI 127138-1
iNaturalist 62814
GBIF 7286883
Freebase /m/07jtll
EPPO BUEGR
USDA GRIN 8169
Wikipedia Bursera_graveolens

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
Identification and Genome Characterization of a Novel Virus within the Genus Totivirus from Chinese Bayberry (Myrica rubra) Xu Z, Gao Y, Teng K, Ge H, Zhang X, Wu M, Li R, Wu Z, Zheng L Viruses 12-Feb-2024
PMCID:PMC10893191
doi:10.3390/v16020283
PMID:38400058
Larvicidal Potential of Caribbean Plants Layne-Yarde RN, Sandiford SL Biomed Res Int 26-Aug-2023
PMCID:PMC10474962
doi:10.1155/2023/5518863
PMID:37663786
Therapeutic Applications of Essential Oils from Native and Cultivated Ecuadorian Plants: Cutaneous Candidiasis and Dermal Anti-Inflammatory Activity Sosa L, Espinoza LC, Valarezo E, Bozal N, Calpena A, Fábrega MJ, Baldomà L, Rincón M, Mallandrich M Molecules 05-Aug-2023
PMCID:PMC10420932
doi:10.3390/molecules28155903
PMID:37570874
Adult conspecific density affects Janzen-Connell patterns by modulating the recruitment exclusion zones Bonanomi G, Bobrovskikh A, Cartenì F, Mazzoleni S, Giannino F Front Plant Sci 27-Jun-2023
PMCID:PMC10333542
doi:10.3389/fpls.2023.1079975
PMID:37441185
Biogeographical Relationships and Diversity in the Peruvian Flora Reported by Hipólito Ruiz and José Pavón: Vegetation, Uses and Anthropology Arias-Gámez JM, Linares-Perea E, Vicente-Orellana JA, Galán-de-Mera A Biology (Basel) 13-Feb-2023
PMCID:PMC9953382
doi:10.3390/biology12020294
PMID:36829570
Effects of Microencapsulated Essential Oils on Equine Health: Nutrition, Metabolism and Methane Emission Elghandour MM, Maggiolino A, García EI, Sánchez-Aparicio P, De Palo P, Ponce-Covarrubias JL, Pliego AB, Salem AZ Life (Basel) 06-Feb-2023
PMCID:PMC9963397
doi:10.3390/life13020455
PMID:36836812
Galápagos tortoise stable isotope ecology and the 1850s Floreana Island Chelonoidis niger niger extinction Conrad C, Barceló LP, Scheinberg L, Campbell PD, Wynn A, Gibbs JP, Aguilera WT, Cayot L, Bruner K, Pastron AG, Jones EL Sci Rep 23-Dec-2022
PMCID:PMC9789057
doi:10.1038/s41598-022-26631-y
PMID:36564467
In vitro antiplasmodial activity of selected plants from the Colombian North Coast with low cytotoxicity Vergara S, Diaz F, Diez A, Bautista JM, Moneriz C Trop Parasitol 24-Nov-2022
PMCID:PMC9832501
doi:10.4103/tp.tp_9_22
PMID:36643988
Evaluation of Essential Oils as Sprout Suppressants for Potato (Solanum tuberosum) at Room Temperature Storage Thoma JL, Cantrell CL, Zheljazkov VD Plants (Basel) 11-Nov-2022
PMCID:PMC9696970
doi:10.3390/plants11223055
PMID:36432783
Lignans: a versatile source of anticancer drugs Mukhija M, Joshi BC, Bairy PS, Bhargava A, Sah AN Beni Suef Univ J Basic Appl Sci 04-Jun-2022
PMCID:PMC9166195
doi:10.1186/s43088-022-00256-6
PMID:35694188
Where did the finch go? Insights from radio telemetry of the medium ground finch (Geospiza fortis) Beausoleil M, Camacho C, Rabadán‐González J, Lalla K, Richard R, Carrion‐Avilés P, Hendry AP, Barrett RD Ecol Evol 26-Apr-2022
PMCID:PMC9039628
doi:10.1002/ece3.8768
PMID:35494501
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882
Samarium(ii) iodide-mediated reactions applied to natural product total synthesis Heravi MM, Nazari A RSC Adv 30-Mar-2022
PMCID:PMC8965710
doi:10.1039/d1ra08163b
PMID:35424959
Hedycaryol – Central Intermediates in Sesquiterpene Biosynthesis, Part II Xu H, Dickschat JS Chemistry 21-Mar-2022
PMCID:PMC9310801
doi:10.1002/chem.202200405
PMID:35239190
Machine Learning Analysis of Essential Oils from Cuban Plants: Potential Activity against Protozoa Parasites Barros de Menezes RP, Scotti L, Scotti MT, García J, González R, Monzote L, Setzer WN Molecules 17-Feb-2022
PMCID:PMC8878085
doi:10.3390/molecules27041366
PMID:35209156

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
> Lignans, neolignans and related compounds / Lignan lactones
(5aR,8aR,9S)-9-(1,3-benzodioxol-4-yl)-4-methoxy-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one 163106153 Click to see COC1=C2CC3COC(=O)C3C(C2=CC4=C1OCO4)C5=C6C(=CC=C5)OCO6 382.40 unknown https://doi.org/10.1248/CPB.53.229
(5R,5aR,8aR)-5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 156202 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1248/CPB.53.229
(5R,5aS,8aR)-5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 10338061 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1002/CHIN.200533271
https://doi.org/10.1248/CPB.53.229
5-(1,3-benzodioxol-5-yl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one 5199318 Click to see C1C2COC(=O)C2C(C3=CC4=C(C=C31)OCO4)C5=CC6=C(C=C5)OCO6 352.30 unknown https://doi.org/10.1248/CPB.53.229
9-(1,3-benzodioxol-5-yl)-4-methoxy-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one 72762427 Click to see COC1=C2CC3COC(=O)C3C(C2=CC4=C1OCO4)C5=CC6=C(C=C5)OCO6 382.40 unknown https://doi.org/10.1248/CPB.53.229
Burseranin 11234404 Click to see COC1=C2CC3COC(=O)C3C(C2=CC4=C1OCO4)C5=CC6=C(C=C5)OCO6 382.40 unknown https://doi.org/10.1002/CHIN.200533271
https://doi.org/10.1248/CPB.53.229
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 10550384 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/10.1248/CPB.53.229
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/10.3987/COM-03-9822
Epilupeol 5270628 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/10.1002/CHIN.200533271
https://doi.org/10.1248/CPB.53.229
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/10.1248/CPB.53.229
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/10.1248/CPB.53.229
https://doi.org/10.1002/CHIN.200533271
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(1R,2S,4aS,4bR,6aR,10aR,12aR)-1-(carboxymethyl)-2-(2-carboxypropan-2-yl)-1,4a,4b,9,9-pentamethyl-3,4,5,6,7,8,10,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 163188569 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)O)C)C2C1)C)C(=O)O)C 502.70 unknown https://doi.org/10.1039/JR9640004254
1-(carboxymethyl)-2-(2-carboxypropan-2-yl)-1,4a,4b,9,9-pentamethyl-3,4,5,6,7,8,10,10a,12,12a-decahydro-2H-chrysene-6a-carboxylic acid 75067116 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)O)C)C2C1)C)C(=O)O)C 502.70 unknown https://doi.org/10.1039/JR9640004254
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.3987/COM-03-9822
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/10.3987/COM-03-9822
> Organoheterocyclic compounds / Benzofurans
3,6-Dimethyl-7a-hydroxy-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 156203 Click to see CC1CCC2=C(C(=O)OC2(C1)O)C 182.22 unknown https://doi.org/10.1039/JR9640004254
Schizonepetin 86575555 Click to see CC1CCC2=C(C(=O)OC2(C1)O)C 182.22 unknown https://doi.org/10.1039/JR9640004254
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.3987/COM-03-9822
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.3987/COM-03-9822
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.3987/COM-03-9822
kaempferol 3-O-beta-D-xyloside 21310440 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown https://doi.org/10.3987/COM-03-9822

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