PlantaeDB Logo
Login Sign-up

Aspidosperma excelsum

We don't have an image yet. Upload an 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 UUID643fea6155b1b764818953
Scientific name Aspidosperma excelsum
Authority Benth.
First published in J. Bot. (Hooker) 3: 245 (1841)

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
Macaglia excelsa Kuntze Revis. Gen. Pl. 2: 416 (1891)
Aspidosperma aquaticum Ducke Arq. Inst. Biol. Veg. 4: 59 (1938)
Aspidosperma marcgravianum Woodson Ann. Missouri Bot. Gard. 38: 170 (1951)
Aspidosperma nitidum Benth. ex Müll.Arg. Fl. Bras. 6(1): 59 (1860)
Thyroma nitida Miers Apocyn. S. Amer. : 24 (1878)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Dutch wit parelhout
Chinese 桨树
Chinese 桨樹

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000290709
Tropicos 1800114
INPN 732575
KEW urn:lsid:ipni.org:names:77367-1
The Plant List kew-17269
NCBI Taxonomy 2664285
IUCN Red List 145684962
IPNI 77367-1
GBIF 3618555
Freebase /m/02687_z
USDA GRIN 5580
Wikipedia Aspidosperma_excelsum

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
Heavy Metal Bioaccumulation in Peruvian Food and Medicinal Products Tejada-Purizaca TR, Garcia-Chevesich PA, Ticona-Quea J, Martínez G, Martínez K, Morales-Paredes L, Romero-Mariscal G, Arenazas-Rodríguez A, Vanzin G, Sharp JO, McCray JE Foods 29-Feb-2024
PMCID:PMC10931273
doi:10.3390/foods13050762
PMID:38472875
Evaluation of acute and subacute toxicity of ethanolic extract and fraction of alkaloids from bark of Aspidosperma nitidum in mice Brígido HP, Varela EL, Gomes AR, Bastos ML, de Oliveira Feitosa A, do Rosário Marinho AM, Carneiro LA, Coelho-Ferreira MR, Dolabela MF, Percário S Sci Rep 14-Sep-2021
PMCID:PMC8440572
doi:10.1038/s41598-021-97637-1
PMID:34521944
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
Understanding crown shyness from a 3-D perspective van der Zee J, Lau A, Shenkin A Ann Bot 13-Mar-2021
PMCID:PMC8557382
doi:10.1093/aob/mcab035
PMID:33713413
Nigritanine as a New Potential Antimicrobial Alkaloid for the Treatment of Staphylococcus aureus-Induced Infections Casciaro B, Calcaterra A, Cappiello F, Mori M, Loffredo MR, Ghirga F, Mangoni ML, Botta B, Quaglio D Toxins (Basel) 01-Sep-2019
PMCID:PMC6783983
doi:10.3390/toxins11090511
PMID:31480508
Palikur traditional roundwood construction in eastern French Guiana: ethnobotanical and cultural perspectives Ogeron C, Odonne G, Cristinoi A, Engel J, Grenand P, Beauchêne J, Clair B, Davy D J Ethnobiol Ethnomed 24-Apr-2018
PMCID:PMC5916587
doi:10.1186/s13002-018-0226-7
PMID:29690891
Traditional knowledge hiding in plain sight – twenty-first century ethnobotany of the Chácobo in Beni, Bolivia Paniagua Zambrana NY, Bussmann RW, Hart RE, Moya Huanca AL, Ortiz Soria G, Ortiz Vaca M, Ortiz Álvarez D, Soria Morán J, Soria Morán M, Chávez S, Chávez Moreno B, Chávez Moreno G, Roca O, Siripi E J Ethnobiol Ethnomed 10-Oct-2017
PMCID:PMC5634836
doi:10.1186/s13002-017-0179-2
PMID:29017576
Alkaloids of <i>Aspidosperma excelsum Benth</i>. P. R. Benoin, R. H. Burnell, J. D. Medina Canadian Science Publishing 23-Apr-2011
doi:10.1139/V67-118
Alkaloid Studies. XXXIX.<sup>1</sup> The Occurrence of Dihydrocorynantheol and Aricine in Aspidosperma marcgravianum Woodson B. Gilbert, L. D. Antonaccio, Carl Djerassi American Chemical Society (ACS) 29-May-2007
doi:10.1021/JO01059A540
Aspidosperma de Guyane: Alcaloïdes de Aspidosperma marcgravianum G. M. T. Robert, A. Ahond, C. Poupat, P. Potier, C. Jollès, A. Jousselin, H. Jacquemin American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50029A018
Alkaloid studies—LVIII R.R. Arndt, S.H. Brown, N.C. Ling, P. Roller, Carl Djerassi, J.M. Ferreira, F.B. Gilbert, Edson C. Miranda, S.E. Flores, Apparicio P. Duarte, E.P. Carrazzoni Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82898-8

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 / Aspidospermatan-type alkaloids
1-[(1R,9R,12R,19R)-6-hydroxy-12-(2-hydroxyethyl)-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5-trien-8-yl]ethanone 162956250 Click to see CC(=O)N1C2CCC3(CCCN4C3C2(CC4)C5=C1C(=CC=C5)O)CCO 356.50 unknown https://doi.org/10.1021/NP50029A018
1-[6-Hydroxy-12-(2-hydroxyethyl)-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2(7),3,5-trien-8-yl]ethanone 162956248 Click to see CC(=O)N1C2CCC3(CCCN4C3C2(CC4)C5=C1C(=CC=C5)O)CCO 356.50 unknown https://doi.org/10.1021/NP50029A018
1-Acetyl-16-methoxy-aspidospermidin-17-ol 12308697 Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=C4C=CC(=C5O)OC)C(=O)C 370.50 unknown https://doi.org/10.1021/NP50029A018
Aspidocarpine 632854 Click to see CCC12CCCN3C1C4(CC3)C(CC2)N(C5=C4C=CC(=C5O)OC)C(=O)C 370.50 unknown https://doi.org/10.1021/NP50029A018
> Alkaloids and derivatives / Cinchona alkaloids
(S)-[(2R,4S)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol 11645562 Click to see CCC1CN2CCC1CC2C(C3=C4C=C(C=CC4=NC=C3)OC)O 326.40 unknown https://doi.org/10.1021/NP50029A018
[(2R,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxy-4-quinolinyl)methanol 24867865 Click to see COC1=CC2=C(C=CN=C2C=C1)C(C3CC4CCN3CC4C=C)O 324.40 unknown https://doi.org/10.1021/NP50029A018
Quinidine 441074 Click to see COC1=CC2=C(C=CN=C2C=C1)C(C3CC4CCN3CC4C=C)O 324.40 unknown https://doi.org/10.1021/NP50029A018
> Alkaloids and derivatives / Corynanthean-type alkaloids
methyl (2R)-2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-hydroxypropanoate 6504264 Click to see CC=C1CN2CCC3=C(C2CC1C(CO)C(=O)OC)NC4=CC=CC=C34 354.40 unknown https://doi.org/10.1021/NP50029A018
> Alkaloids and derivatives / Harmala alkaloids
Ochrolifuanine A 215338 Click to see CCC1CN2CCC3=C(C2CC1CC4C5=C(CCN4)C6=CC=CC=C6N5)NC7=CC=CC=C37 438.60 unknown https://doi.org/10.1021/NP50029A018
Usambarensine 5281413 Click to see CC=C1CN2CCC3=C(C2CC1CC4=NC=CC5=C4NC6=CC=CC=C56)NC7=CC=CC=C37 432.60 unknown https://doi.org/10.1021/NP50029A018
> Alkaloids and derivatives / Yohimbine alkaloids
Anapral 5353923 Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C=CC6=CC(=C(C(=C6)OC)OC)OC 634.70 unknown https://doi.org/10.1021/NP50029A018
Aricine 251575 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=C(C=C5)OC 382.50 unknown https://doi.org/10.1016/S0031-9422(00)82898-8
https://doi.org/10.1021/NP50029A018
beta-Yohimbine 2866 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1021/NP50029A018
CID 5458418 5458418 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1021/NP50029A018
Isoreserpiline 161345 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1021/NP50029A018
methyl (1S,15R,18S,19R,20R)-18-acetyloxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163009240 Click to see CC(=O)OC1CCC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=CC=CC=C45 396.50 unknown https://doi.org/10.1139/V67-118
methyl (1S,15R,18S,19S,20R)-18-hydroxy-7-methoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate 163065731 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3CC5C(C4)CCC(C5C(=O)OC)O 384.50 unknown https://doi.org/10.1139/V67-118
Pubescine 72313 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=CC(=C5)OC 382.50 unknown https://doi.org/10.1021/NP50029A018
Reserpiline 67228 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC 412.50 unknown https://doi.org/10.1021/NP50029A018
Tetrahydroalstonine 72340 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1021/NP50029A018
Yohimbine 8969 Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O 354.40 unknown https://doi.org/10.1021/NP50029A018
> Benzenoids
(R)-Rhazinilam 160263 Click to see CCC12CCCN3C1=C(C=C3)C4=CC=CC=C4NC(=O)CC2 294.40 unknown https://doi.org/10.1021/NP50029A018
Rhazinilam 11312435 Click to see CCC12CCCN3C1=C(C=C3)C4=CC=CC=C4NC(=O)CC2 294.40 unknown https://doi.org/10.1021/NP50029A018
> Lignans, neolignans and related compounds / Furanoid lignans
1,4-Bis(3,4,5-trimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 99091 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1016/S0031-9422(00)82898-8
Syringaresinol 100067 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown https://doi.org/10.1016/S0031-9422(00)82898-8
> Organoheterocyclic compounds / Indoles and derivatives
2,3-Diethyl-2-(3-ethylpiperidin-1-yl)indole 163192617 Click to see CCC1CCCN(C1)C2(C(=C3C=CC=CC3=N2)CC)CC 284.40 unknown https://doi.org/10.1021/NP50029A018
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1R,4R,12R,16S)-5-acetyl-7-hydroxy-17-oxa-5,15-diazahexacyclo[13.4.3.01,16.04,12.06,11.012,16]docosa-6(11),7,9-trien-18-one 163104195 Click to see CC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=C1C(=CC=C6)O)OC(=O)C4 368.40 unknown https://doi.org/10.1021/NP50029A018
1-(19,21-Epoxy-17-hydroxy-16-methoxyaspidospermidin-1-yl)ethanone 12308698 Click to see CC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=C1C(=C(C=C6)OC)O)OCC4 384.50 unknown https://doi.org/10.1021/NP50029A018
1-[(1R,4R,12R,16S)-7-hydroxy-17-oxa-5,15-diazahexacyclo[13.4.3.01,16.04,12.06,11.012,16]docosa-6(11),7,9-trien-5-yl]ethanone 15559624 Click to see CC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=C1C(=CC=C6)O)OCC4 354.40 unknown https://doi.org/10.1021/NP50029A018
5-Acetyl-7-hydroxy-17-oxa-5,15-diazahexacyclo[13.4.3.01,16.04,12.06,11.012,16]docosa-6(11),7,9-trien-18-one 163104194 Click to see CC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=C1C(=CC=C6)O)OC(=O)C4 368.40 unknown https://doi.org/10.1021/NP50029A018
Aspidolimidine 630961 Click to see CC(=O)N1C2CCC34CCCN5C3(C2(CC5)C6=C1C(=C(C=C6)OC)O)OCC4 384.50 unknown https://doi.org/10.1021/NP50029A018
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
methyl (2R)-2-[3-[2-[(3S)-3-ethylpiperidin-1-yl]ethyl]-1H-indol-2-yl]propanoate 162891111 Click to see CCC1CCCN(C1)CCC2=C(NC3=CC=CC=C32)C(C)C(=O)OC 342.50 unknown https://doi.org/10.1021/NP50029A018
methyl 2-[3-[2-(3-ethylpiperidin-1-yl)ethyl]-1H-indol-2-yl]propanoate 162891110 Click to see CCC1CCCN(C1)CCC2=C(NC3=CC=CC=C32)C(C)C(=O)OC 342.50 unknown https://doi.org/10.1021/NP50029A018
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3E)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizine 5386990 Click to see CC=C1CCC2C3=C(CCN2C1)C4=CC=CC=C4N3 252.35 unknown https://doi.org/10.1021/NP50029A018
10-Methoxycorynan-17-ol 14488056 Click to see CCC1CN2CCC3=C(C2CC1CCO)NC4=C3C=C(C=C4)OC 328.40 unknown https://doi.org/10.1016/S0031-9422(00)82898-8
2-[(2R,3Z,12bS)-3-ethylidene-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 21595545 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1021/NP50029A018
2-[(2R,3Z,12bS)-3-ethylidene-9-methoxy-2,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]ethanol 101630448 Click to see CC=C1CN2CCC3=C(C2CC1CCO)NC4=C3C=C(C=C4)OC 326.40 unknown https://doi.org/10.1021/NP50029A018
Antirhine 5462421 Click to see C=CC(CO)C1CCN2CCC3=C(C2C1)NC4=CC=CC=C34 296.40 unknown https://doi.org/10.1021/NP50029A018
Corynan-17-ol 164952 Click to see CCC1CN2CCC3=C(C2CC1CCO)NC4=CC=CC=C34 298.40 unknown https://doi.org/10.1021/JO01059A540
https://doi.org/10.1021/NP50029A018
> Organoheterocyclic compounds / Indoles and derivatives / Tryptamines and derivatives
1-{1-[2-(2-Ethyl-1H-indol-3-yl)ethyl]piperidin-3-yl}ethan-1-one 71319091 Click to see CCC1=C(C2=CC=CC=C2N1)CCN3CCCC(C3)C(=O)C 298.40 unknown https://doi.org/10.1021/NP50029A018

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.