Peumus boldus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Upload a new image!

Details Top

Internal ID UUID64400118af662549469834
Scientific name Peumus boldus
Authority Molina
First published in Sag. Stor. Nat. Chili : 185 (1782)

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
Laurus lingui Bridges ex Nees Syst. Laur. : 672 (1836)
Laurus belloto Miers ex Nees Syst. Laur. : 178 (1836)
Ruizia fragrans Ruiz & Pav. Syst. Veg. Fl. Peruv. Chil. 1: 267. 1798 [late Dec 1798]
Peumus fragrans Pers. Syn. Pl. 2: 629 (1807)
Boldea boldus Looser Revista Univ. (Santiago) 20: 572 (1935)
Boldea fragrans (Pers.) Endl. Cat. Hort. Vindob. 1: 280 (1842)
Boldu boldus (Molina) A.Lyons Pl. Nam. 65. 1900
Boldu chilanum Nees Syst. Laur. 178. 1836
Boldu chilensis Schult. & Schult.f. Syst. Veg. 7: 56 1829

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English boldo
Spanish boldo
Spanish peunbus boldus
Arabic شجرة البلدوة الفاغيه
Arabic بولدو
Arabic شجرة الكبد
Arabic شجرة البولدو
Bulgarian болдо
Catalan boldo
Czech boldovník vonný
German boldoblatt
German boldo
Basque boldo
Persian بولدو
Finnish boldopuu
French boldo
Croatian boldo
Hungarian boldó
Hungarian boldófa
Italian boldo
Japanese ボルド
Korean 볼도
Macedonian Болдо
Dutch boldo
Portuguese boldo-do-chile
Romanian boldo
Russian Пеумус
Russian Болдо
Kinyarwanda boldo
Swedish boldo
Turkish boldo
Chinese 波尔多叶
Chinese 波爾多葉

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-0000474092
UNII 6B03107MP3
USDA Plants PEBO5
Tropicos 21200001
KEW urn:lsid:ipni.org:names:191376-2
The Plant List kew-2547762
Open Tree Of Life 913184
NCBI Taxonomy 63812
IUCN Red List 135682641
IPNI 582202-1
iNaturalist 326673
GBIF 3034108
Freebase /m/07x7fc
EPPO PWUBO
EOL 392758
USDA GRIN 27471
Wikipedia Boldo

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
Exploring In Vitro the Combination of Cistus × incanus L. and Castanea sativa Mill. Extracts as Food Supplement Ingredients against H. pylori Infection Martinelli G, Fumagalli M, Pozzoli C, Nicotra G, Vicentini SF, Maranta N, Sangiovanni E, Dell’Agli M, Piazza S Foods 21-Dec-2023
PMCID:PMC10778332
doi:10.3390/foods13010040
PMID:38201068
Principles of Photocatalysts and Their Different Applications: A Review Hassaan MA, El-Nemr MA, Elkatory MR, Ragab S, Niculescu VC, El Nemr A Top Curr Chem (Cham) 31-Oct-2023
PMCID:PMC10618379
doi:10.1007/s41061-023-00444-7
PMID:37906318
Therapeutic Potential of Myrtenal and Its Derivatives—A Review Dragomanova S, Andonova V, Volcho K, Salakhutdinov N, Kalfin R, Tancheva L Life (Basel) 20-Oct-2023
PMCID:PMC10608190
doi:10.3390/life13102086
PMID:37895468
Exploring the Antioxidant Potential of Talisia esculenta Using In Vitro and In Vivo Approaches da Silva Cordeiro ML, de Queiroz Aquino-Martins VG, da Silva AP, Naliato GF, Silveira ER, Theodoro RC, da Santos DY, Rocha HA, Scortecci KC Nutrients 04-Sep-2023
PMCID:PMC10490396
doi:10.3390/nu15173855
PMID:37686887
Boldine Alters Serum Lipidomic Signatures after Acute Spinal Cord Transection in Male Mice Graham ZA, Siedlik JA, Toro CA, Harlow L, Cardozo CP Int J Environ Res Public Health 17-Aug-2023
PMCID:PMC10454893
doi:10.3390/ijerph20166591
PMID:37623175
Antiproliferative effect of boldine on neural progenitor cells and on glioblastoma cells Jiménez-Madrona E, Morado-Díaz CJ, Talaverón R, Tabernero A, Pastor AM, Sáez JC, Matarredona ER Front Neurosci 16-Aug-2023
PMCID:PMC10467274
doi:10.3389/fnins.2023.1211467
PMID:37655012
The Most Potent Natural Pharmaceuticals, Cosmetics, and Food Ingredients Isolated from Plants with Deep Eutectic Solvents Wawoczny A, Gillner D J Agric Food Chem 11-Jul-2023
PMCID:PMC10375538
doi:10.1021/acs.jafc.3c01656
PMID:37433265
Evolutionary diversity of the endemic genera of the vascular flora of Chile and its implications for conservation Ramírez-Verdugo P, Tapia A, Forest F, Scherson RA PLoS One 05-Jul-2023
PMCID:PMC10321618
doi:10.1371/journal.pone.0287957
PMID:37406022
Phytopharmaceutical practices of traditional health practitioners in Burkina Faso: a cross-sectional study Ouoba K, Lehmann H, Zongo A, Semdé R, Pabst JY BMC Complement Med Ther 30-Jun-2023
PMCID:PMC10311739
doi:10.1186/s12906-023-04055-z
PMID:37391813
Essential Oils for the Conservation of Paper Items Menicucci F, Palagano E, Michelozzi M, Ienco A Molecules 26-Jun-2023
PMCID:PMC10343335
doi:10.3390/molecules28135003
PMID:37446665
Boldine modulates glial transcription and functional recovery in a murine model of contusion spinal cord injury Toro CA, Johnson K, Hansen J, Siddiq MM, Vásquez W, Zhao W, Graham ZA, Sáez JC, Iyengar R, Cardozo CP Front Cell Neurosci 21-Jun-2023
PMCID:PMC10321410
doi:10.3389/fncel.2023.1163436
PMID:37416508
Preliminary Evaluation of Lablab purpureus Phytochemicals for Anti-BoHV-1 Activity Using In Vitro and In Silico Approaches Bhat SS, Pradeep S, Patil SS, Flores-Holguín N, Glossman-Mitnik D, Frau J, Sommano SR, Ali N, Mohany M, Shivamallu C, Prasad SK, Kollur SP ACS Omega 14-Jun-2023
PMCID:PMC10308559
doi:10.1021/acsomega.3c01478
PMID:37396248
Natural Compound Boldine Lessens Myotonic Dystrophy Type 1 Phenotypes in DM1 Drosophila Models, Patient-Derived Cell Lines, and HSALR Mice Álvarez-Abril MC, García-Alcover I, Colonques-Bellmunt J, Garijo R, Pérez-Alonso M, Artero R, López-Castel A Int J Mol Sci 06-Jun-2023
PMCID:PMC10298378
doi:10.3390/ijms24129820
PMID:37372969
Electromagnetic fields disrupt the pollination service by honeybees Molina-Montenegro MA, Acuña-Rodríguez IS, Ballesteros GI, Baldelomar M, Torres-Díaz C, Broitman BR, Vázquez DP Sci Adv 12-May-2023
PMCID:PMC10181175
doi:10.1126/sciadv.adh1455
PMID:37172085
Oxidative stress, free radicals and antioxidants: potential crosstalk in the pathophysiology of human diseases Chaudhary P, Janmeda P, Docea AO, Yeskaliyeva B, Abdull Razis AF, Modu B, Calina D, Sharifi-Rad J Front Chem 10-May-2023
PMCID:PMC10206224
doi:10.3389/fchem.2023.1158198
PMID:37234200

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
1,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,9-diol 248507 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1007/S10637-008-9203-7
1,10-Dimethoxy-6a-alpha-noraporphine-2,9-diol 628557 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1016/0031-9422(93)85226-H
https://doi.org/10.1002/JPS.2600570935
https://doi.org/10.1016/0031-9422(89)80187-6
1,2,10-Trimethoxy-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolin-9-ol 267400 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1002/JPS.2600570935
4,15,16-Trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,13(17),14-hexaen-3-ol 5320211 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown https://doi.org/10.1002/HLCA.19590420317
Boldine 10154 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)O 327.40 unknown https://doi.org/10.1016/S0021-9673(01)93301-1
https://doi.org/10.1007/S10637-008-9203-7
https://doi.org/10.1016/S0021-9673(01)82099-9
https://doi.org/10.1016/0378-4347(93)80179-8
https://doi.org/10.1055/S-2006-960043
https://doi.org/10.1021/NP50033A021
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1002/HLCA.19590420317
https://doi.org/10.1016/S0021-9673(01)82099-9
https://doi.org/10.1016/S0021-9673(01)93301-1
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1016/S0021-9673(01)82099-9
Laurolitsine 22179 Click to see COC1=C(C=C2CC3C4=C(C2=C1)C(=C(C=C4CCN3)O)OC)O 313.30 unknown https://doi.org/10.1002/JPS.2600570935
Laurotetanine 31415 Click to see COC1=C(C2=C3C(CC4=CC(=C(C=C42)OC)O)NCCC3=C1)OC 327.40 unknown https://doi.org/10.1002/JPS.2600570935
N-Methyllaurotetanine; NSC 247506; NSC 247564 631015 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1002/HLCA.19590420317
Norisocorydine 12313549 Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O 327.40 unknown https://doi.org/10.1002/HLCA.19590420317
> Alkaloids and derivatives / Proaporphines
(+)-Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown https://doi.org/10.1021/NP50033A021
> Benzenoids / Phenanthrenes and derivatives
Salutaridine 5408233 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC 327.40 unknown https://doi.org/10.1021/NP50033A021
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.1002/JHRC.1240200910
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1002/JHRC.1240200910
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,2R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-ol 88298 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1002/JHRC.1240200910
trans-Verbenol 89664 Click to see CC1=CC(C2CC1C2(C)C)O 152.23 unknown https://doi.org/10.1002/JHRC.1240200910
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Ascaridole 10545 Click to see CC(C)C12CCC(C=C1)(OO2)C 168.23 unknown https://doi.org/10.1002/JHRC.1240200910
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-[3-(4,5-Dihydroxy-6-methyloxan-2-yl)oxy-4-hydroxyphenyl]-5-hydroxy-7-methoxy-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 162884789 Click to see CC1C(C(CC(O1)OC2=C(C=CC(=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)OC)O)OC5C(C(C(CO5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1007/BF00609278
2-[3-[(2R,4S,5R,6R)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxyphenyl]-5-hydroxy-7-methoxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 162884790 Click to see CC1C(C(CC(O1)OC2=C(C=CC(=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)OC)O)OC5C(C(C(CO5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1007/BF00609278
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-[4-hydroxy-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]-7-methoxychromen-4-one 163039399 Click to see CC1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)OC)O)OC5C(C(C(O5)CO)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/BF00609278
3-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-2-[4-hydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyphenyl]-7-methoxychromen-4-one 163039398 Click to see CC1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=C(C(=O)C4=C(C=C(C=C4O3)OC)O)OC5C(C(C(O5)CO)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1007/BF00609278
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162921504 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00609278
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 12302040 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00609278

Biological Material Top ebay Auctions

Please wait .. loading items ..
Loading...

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.