PlantaeDB Logo
Login Sign-up

Bursera simaruba

Bursera simaruba - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID64400e55cbc6e729779347
Scientific name Bursera simaruba
Authority Sarg.
First published in Gard. & Forest 3: 260. 1890

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Pistacia simaruba L. Sp. Pl. : 1026 (1753)
Terebinthus simaruba W.Wight ex Rose Contr. U.S. Natl. Herb. x. 122 (1906).
Bursera arborea L.Riley Bull. Misc. Inform. Kew 1923: 167 (1923)
Bursera bonairensis Bold. Fl. Curaçao : 48 (1914)
Bursera gummifera L. Sp. Pl. ed. 2 : 471 (1762)
Bursera gummifera var. glabrata Griseb. Fl. Brit. W. I. : 173 (1859)
Bursera gummifera var. polyphylla DC. Prodr. 2: 78 (1825)
Bursera integerrima Triana & Planch. Ann. Sci. Nat., Bot. , sér. 5, 14: 303 (1872)
Bursera simaruba var. yucatanensis Lundell Wrightia 3: 4 (1961)
Bursera subpubescens Engl. Nat. Pflanzenfam. ed. 2 , 19a: 425 (1931)
Elaphrium arboreum Rose N. Amer. Fl. 25: 247 (1911)
Elaphrium integerrimum Tul. Ann. Sci. Nat., Bot. , sér. 3, 6: 369 (1846)
Elaphrium simaruba Rose N. Amer. Fl. 25: 246 (1911)
Elaphrium subpubescens Rose N. Amer. Fl. 25: 247 (1911)
Icicariba simaruba M.Gómez Fl. Haban. 214; cf. Maza in Maza & Roig, Fl. Cuba (Bol. Secr. Agric. Comerc.Trab., Cuba, No. 22) 66 (1914), in syn.
Terebinthus arborea Rose Contr. U.S. Natl. Herb. 10: 118 (1906)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English gumbo limbo
Spanish chaká
Spanish pistacia simaruba
Spanish palo mulato
Spanish jiñocuajo
Spanish jiñocuabo
Spanish jinocuabo
Spanish indio desnudo
Spanish bursera gummifera
Spanish chaka
Arabic بورسيرا سيماروبا
Czech březule balzámová
German amerikanischer balsam
Estonian turistipuu
Estonian kummibursera
French gommier rouge
Upper Sorbian ameriski balsam
ht gonmye
ht gonmye blan
ht gomye blan
Japanese ガンボリンボ
Malayalam ബർസെറ സിമാരുബ
Chinese 銅木
Chinese 苦木裂欖木
Chinese 裂榄

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000576316
UNII MK9D15R2KB
Florida Plant Atlas 727
USDA Plants BUSI
Tropicos 4700231
INPN 629217
KEW urn:lsid:ipni.org:names:127217-1
The Plant List kew-2687649
Open Tree Of Life 841945
Observations.org 153043
NCBI Taxonomy 80326
Nature Serve 2.145878
IUCN Red List 61987595
IPNI 38669-2
iNaturalist 130734
GBIF 3190450
Freebase /m/0gnt67
EPPO BUESI
EOL 583027
USDA GRIN 310563
Wikipedia Bursera_simaruba
CMAUP NPO27883

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
Ligand-binding properties of XaffOBP9, a Minus-C odorant-binding protein from Xyleborus affinis (Coleoptera: Curculionidae: Scolytinae) Wang Q, Zhou X, Zhang K, Qin L, Wu Q, Deng L, Xu Z, Guo J Front Physiol 03-Jan-2024
PMCID:PMC10791897
doi:10.3389/fphys.2023.1326099
PMID:38235380
Patterns of shade plant diversity in four agroforestry systems across Central America: a meta-analysis Esquivel MJ, Vilchez-Mendoza S, Harvey CA, Ospina MA, Somarriba E, Deheuvels O, de M. Virginio Filho E, Haggar J, Detlefsen G, Cerdan C, Casanoves F, Ordoñez JC Sci Rep 26-May-2023
PMCID:PMC10219940
doi:10.1038/s41598-023-35578-7
PMID:37237175
Female naturalists and the patterns of suppression of women scientists in history: the example of Maria Sibylla Merian and her contributions about useful plants Mariath F, Baratto LC J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10182609
doi:10.1186/s13002-023-00589-1
PMID:37173737
The Potential Use of Plant Growth Regulators for Modification of the Industrially Valuable Volatile Compounds Synthesis in Hylocreus undatus Stems Jakobina M, Łyczko J, Zydorowicz K, Galek R, Szumny A Molecules 01-May-2023
PMCID:PMC10180215
doi:10.3390/molecules28093843
PMID:37175252
Unveiling the secret of ancient Maya masons: Biomimetic lime plasters with plant extracts Rodriguez-Navarro C, Monasterio-Guillot L, Burgos-Ruiz M, Ruiz-Agudo E, Elert K Sci Adv 19-Apr-2023
PMCID:PMC10115411
doi:10.1126/sciadv.adf6138
PMID:37075113
Integrative taxonomy using the plant core DNA barcodes in Sumatra's Burseraceae Teklemariam DM, Gailing O, Siregar IZ, Amandita FY, Moura CC Ecol Evol 07-Apr-2023
PMCID:PMC10082172
doi:10.1002/ece3.9935
PMID:37038522
Antihypertensive, antidyslipidemic, and renoprotective effects of Bursera simaruba on metabolic syndrome Alejandrina Guzmán Hernández E, Segura Cobos D, González Valle MD, del Carmen Benítez Flores J, Miguel Chávez RS, Mondragón LD, Magos Guerrero GA, Sánchez PL Iran J Basic Med Sci 01-Apr-2023
PMCID:PMC10008388
doi:10.22038/IJBMS.2023.66530.14601
PMID:37009005
Endophytic species of Induratia from coffee and carqueja plants from Brazil and its potential for the biological control of toxicogenic fungi on coffee beans by means of antimicrobial volatiles Gomes AA, Paes SA, Ferreira AP, Pinho DB, de Lourdes Cardeal Z, Menezes HC, Cardoso PG, Pereira OL Braz J Microbiol 04-Jan-2023
PMCID:PMC9944607
doi:10.1007/s42770-022-00887-y
PMID:36598751
Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins Jin L, Song Z, Cai F, Ruan L, Jiang R Molecules 30-Dec-2022
PMCID:PMC9822336
doi:10.3390/molecules28010302
PMID:36615496
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
Acute Toxicity and Anti-Inflammatory Activity of Trattinnickia rhoifolia Willd (Sucuruba) Using the Zebrafish Model de Souza AA, Ortíz BL, Borges SF, Pinto AV, Ramos RD, Pena IC, Rocha Koga RD, Batista CE, de Souza GC, Ferreira AM, Duvoisin Junior S, Tavares Carvalho JC Molecules 10-Nov-2022
PMCID:PMC9699319
doi:10.3390/molecules27227741
PMID:36431841
Birth of a wild black howler monkey (Alouatta pigra) at an anthropogenic site Cárdenas-Navarrete A, Van Belle S Primates 05-Nov-2022
PMCID:PMC9842550
doi:10.1007/s10329-022-01022-z
PMID:36334222
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Electroantennographic Responses of Wild and Laboratory-Reared Females of Xyleborus affinis Eichhoff and Xyleborus ferrugineus (Fabricius) (Coleoptera: Curculionidae: Scolytinae) to Ethanol and Bark Volatiles of Three Host-Plant Species Romero P, Ibarra-Juárez LA, Carrillo D, Guerrero-Analco JA, Kendra PE, Kiel-Martínez AL, Guillén L Insects 21-Jul-2022
PMCID:PMC9320532
doi:10.3390/insects13070655
PMID:35886831
A First Look at the Inhibitory Potential of Urospatha sagittifolia (Araceae) Ethanolic Extract for Bothrops atrox Snakebite Envenomation Vera-Palacios AL, Sacoto-Torres JD, Hernández-Altamirano JA, Moreno A, Peñuela-Mora MC, Salazar-Valenzuela D, Mogollón NG, Almeida JR Toxins (Basel) 17-Jul-2022
PMCID:PMC9315696
doi:10.3390/toxins14070496
PMID:35878234

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
> Alkaloids and derivatives / Aporphines
(+)-Isodomesticine 15690954 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC5=C(C=C43)OCO5)OC)O 325.40 unknown via CMAUP database
(6aS)-1,2,9,10-Tetramethoxy-4,5,6,6aalpha-tetrahydro-7H-dibenzo[de,g]quinoline-6-carboxylic acid methyl ester 44207164 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)OC)N(CCC3=C1)C(=O)OC)OC 399.40 unknown via CMAUP database
(6aS)-9-Hydroxy-1,2,10-trimethoxy-4,5,6,6aalpha-tetrahydro-7H-dibenzo[de,g]quinoline-6-carboxylic acid methyl ester 44206920 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)N(CCC3=C1)C(=O)OC)OC 385.40 unknown via CMAUP database
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown via CMAUP database
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown via CMAUP database
CID 91884708 91884708 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O 327.40 unknown via CMAUP database
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown via CMAUP database
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown via CMAUP database
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown via CMAUP database
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown via CMAUP database
Norisocorydine 12313549 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown via CMAUP database
Oxonantenine 3084224 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC5=C(C=C42)OCO5)OC 335.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Litebamine 196885 Click to see CN1CCC2=C3C=CC4=CC(=C(C=C4C3=C(C(=C2C1)O)OC)OC)O 339.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3~{S},4~{S})-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one 10476098 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
(3S,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 15941633 Click to see COC1=C(C=C(C=C1)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
2(3H)-Furanone, 4-(1,3-benzodioxol-5-ylmethyl)dihydro-3-((3,4,5-trimethoxyphenyl)methyl)- 2988 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
2(3H)-Furanone, dihydro-3,4-dipiperonyl-, trans-(-)- 11002708 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
3,4-Bis(1,3-benzodioxol-5-ylmethyl)tetrahydrofuran-2-one 327062 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one 13916162 Click to see COC1=C(C=C(C=C1)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
Bursehernin 94504 Click to see COC1=C(C=C(C=C1)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
Yatein 442835 Click to see COC1=CC(=CC(=C1OC)OC)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4 400.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
> Lignans, neolignans and related compounds / Lignan glycosides
(5aR,8aS,9R)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one 132553617 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O)COC3=O 576.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
beta-Peltatin-beta-D-glucoside 6325789 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)OC6C(C(C(C(O6)CO)O)O)O)COC3=O 576.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
Picraquassioside C 10077272 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C(=C2)OC)OC3C(C(C(C(O3)CO)O)O)O)OC)O)OC)C=CCO 598.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
> Lignans, neolignans and related compounds / Lignan lactones
(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/10.1021/NP50090A009
(8aR)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 5320458 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=C(C5=C(C=C24)OCO5)O)COC3=O 414.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(Z)-4-Decenoic acid 5312351 Click to see CCCCCC=CCCC(=O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> 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 via CMAUP database
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
(1R,2R,5S)-5-Methyl-2-(1-methylethenyl)cyclohexanol 7057942 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Menthoglycol 19100 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[4,5-Dihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl] 11-hydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162943369 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4)C)(CCC7C6(CC(C(C7(C)CO)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)O 1121.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/NP50116A019
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/NP50116A019
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/10.1021/NP50116A019
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/NP50116A019
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
Litseacubebic acid 76312534 Click to see CC(=CC=CC(C)(C)O)C(=O)O 170.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-2-(2-hydroxypropan-2-yl)-5-methyl-3,4-dihydro-2H-oxepin-7-one 76319759 Click to see CC1=CC(=O)OC(CC1)C(C)(C)O 184.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6R)-2-(3-hydroxy-5-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 162998585 Click to see COC1=CC(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl hydrogen sulfate 101470870 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O 426.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methyl hydrogen sulfate 101470872 Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O)O 396.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
[(2R,3S,4S,5R,6S)-6-(3,4-dimethoxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl hydrogen sulfate 101470871 Click to see COC1=C(C=C(C=C1)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O)OC 396.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
[3,4,5-Trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl hydrogen sulfate 163091823 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O 426.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
[3,4,5-Trihydroxy-6-[2-hydroxy-5-(2-hydroxyethyl)phenoxy]oxan-2-yl]methyl hydrogen sulfate 163047588 Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O)O 396.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
[6-(3,4-Dimethoxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl hydrogen sulfate 163021160 Click to see COC1=C(C=C(C=C1)OC2C(C(C(C(O2)COS(=O)(=O)O)O)O)O)OC 396.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
1-[2,6-Dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 74155556 Click to see CC(=O)C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 330.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
1-[4-[[2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]ethanone 44726258 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C(C(=C3)O)C(=O)C)O)CO)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
1-[4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,6-dihydroxyphenyl]ethanone 4192933 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C(C(=C3)O)C(=O)C)O)CO)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
3-methoxy-5-hydroxyphenol-1-O-beta-d-glucopyranoside 91378659 Click to see COC1=CC(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
Phloracetophenone 4'-O-glucoside 23928130 Click to see CC(=O)C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)O 330.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
Picraquassioside D 56776291 Click to see COC1=CC(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.02.009
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown via CMAUP database
> 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/J.PHYTOCHEM.2009.02.009

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.