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Ptychopetalum olacoides

Ptychopetalum olacoides - 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 UUID644053cf82d55440046169
Scientific name Ptychopetalum olacoides
Authority Benth.
First published in London J. Bot. 2: 377 (1843)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
French muira puama
Japanese ムイラプアマ
Japanese プティコペタルム・オラコイデス
Portuguese marapuama
Romanian muira puama
Swedish muira puama
szl muira puama

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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
    • Brazil
      • Brazil North
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001220793
UNII G582QI158H
Tropicos 50005781
INPN 734496
KEW urn:lsid:ipni.org:names:608273-1
The Plant List tro-50005781
Open Tree Of Life 1008642
NCBI Taxonomy 597401
IUCN Red List 174408412
IPNI 608273-1
GBIF 3685538
EOL 5609128
USDA GRIN 402674

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
Network pharmacology-based approach to elucidate the pharmacologic mechanisms of natural compounds from Dictyostelium discoideum for Alzheimer's disease treatment Patil N, Dhariwal R, Mohammed A, Wei LS, Jain M Heliyon 06-Apr-2024
PMCID:PMC11033062
doi:10.1016/j.heliyon.2024.e28852
PMID:38644825
Do índio Passos ao doutor Chernoviz: experiências de cura da lepra no Pará do século XIX Henrique MC Hist Cienc Saude Manguinhos 04-Aug-2023
PMCID:PMC10402912
doi:10.1590/S0104-59702023000100027
PMID:37556716
Binding modes of potential anti-prion phytochemicals to PrPC structures in silico Neupane S, Khadka J, Rayamajhi S, Pandey AS J Ayurveda Integr Med 17-Jul-2023
PMCID:PMC10368899
doi:10.1016/j.jaim.2023.100750
PMID:37453159
Enhanced Production of Nitrogenated Metabolites with Anticancer Potential in Aristolochia manshuriensis Hairy Root Cultures Shkryl YN, Tchernoded GK, Yugay YA, Grigorchuk VP, Sorokina MR, Gorpenchenko TY, Kudinova OD, Degtyarenko AI, Onishchenko MS, Shved NA, Kumeiko VV, Bulgakov VP Int J Mol Sci 08-Jul-2023
PMCID:PMC10379662
doi:10.3390/ijms241411240
PMID:37511000
Determination of Phosphodiesterase Type-5 Inhibitors (PDE-5) in Dietary Supplements Gheorghiu OR, Ciobanu AM, Guțu CM, Chițescu CL, Costea GV, Anghel DM, Vlasceanu AM, Baconi DL Molecules 16-May-2023
PMCID:PMC10221795
doi:10.3390/molecules28104116
PMID:37241857
Phytochemicals: A Promising Alternative for the Prevention of Alzheimer’s Disease Koul B, Farooq U, Yadav D, Song M Life (Basel) 12-Apr-2023
PMCID:PMC10144079
doi:10.3390/life13040999
PMID:37109528
Antidepressant-Like Activity of Solvent Fractions of the Root Bark of Carissa spinarum Linn. (Apocynaceae) in Rodents Involves Multiple Signaling Pathways Ali HS, Engidawork E J Exp Pharmacol 09-Dec-2022
PMCID:PMC9748120
doi:10.2147/JEP.S386015
PMID:36531440
Natural product-based pharmacological studies for neurological disorders Puri V, Kanojia N, Sharma A, Huanbutta K, Dheer D, Sangnim T Front Pharmacol 07-Nov-2022
PMCID:PMC9676372
doi:10.3389/fphar.2022.1011740
PMID:36419628
Natural Products for the Treatment of Post-stroke Depression Fang C, Zhang Z, Xu H, Liu Y, Wang X, Yuan L, Xu Y, Zhu Z, Zhang A, Shao A, Lou M Front Pharmacol 30-May-2022
PMCID:PMC9196125
doi:10.3389/fphar.2022.918531
PMID:35712727
Translational Informatics for Natural Products as Antidepressant Agents Singla RK, Joon S, Shen L, Shen B Front Cell Dev Biol 20-Jan-2022
PMCID:PMC8811306
doi:10.3389/fcell.2021.738838
PMID:35127696
Saracura-Mirá, a Proposed Brazilian Amazonian Adaptogen from Ampelozizyphus amazonicus Leitão SG, Leitão GG, de Oliveira DR Plants (Basel) 12-Jan-2022
PMCID:PMC8781190
doi:10.3390/plants11020191
PMID:35050079
Advantages of Hyaluronic Acid and Its Combination with Other Bioactive Ingredients in Cosmeceuticals Juncan AM, Moisă DG, Santini A, Morgovan C, Rus LL, Vonica-Țincu AL, Loghin F Molecules 22-Jul-2021
PMCID:PMC8347214
doi:10.3390/molecules26154429
PMID:34361586
Alternative medicine and herbal remedies in the treatment of erectile dysfunction: A systematic review Leisegang K, Finelli R Arab J Urol 11-Jun-2021
PMCID:PMC8451697
doi:10.1080/2090598X.2021.1926753
PMID:34552783
Estrogenic Plants: to Prevent Neurodegeneration and Memory Loss and Other Symptoms in Women After Menopause Echeverria V, Echeverria F, Barreto GE, Echeverría J, Mendoza C Front Pharmacol 20-May-2021
PMCID:PMC8172769
doi:10.3389/fphar.2021.644103
PMID:34093183
What’s in a name? Revisiting medicinal and religious plants at an Amazonian market Geertsma IP, Françozo M, van Andel T, Rodríguez MA J Ethnobiol Ethnomed 05-Feb-2021
PMCID:PMC7866673
doi:10.1186/s13002-021-00433-4
PMID:33546714

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1S,2S,3R,4aR,8aS)-1-[2-(furan-3-yl)ethyl]-3-hydroxy-2,4a,5-trimethyl-2,3,4,7,8,8a-hexahydronaphthalene-1-carbaldehyde 25135585 Click to see CC1C(CC2(C(C1(CCC3=COC=C3)C=O)CCC=C2C)C)O 316.40 unknown https://doi.org/10.1021/NP8004002
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1055/S-2006-962688
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1055/S-2006-962688
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1055/S-2006-962688
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1055/S-2006-962688
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1055/S-2006-962688
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
1,2,4a,5,6,8a-Hexahydro-1-isopropyl-4,7-dimethylnaphthalene 101708 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
alpha-Guaiene 5317844 Click to see CC1CCC(CC2=C1CCC2C)C(=C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1055/S-2006-962688
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S,2S,12R)-1-[2-(furan-3-yl)ethyl]-6,7,12-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-5-en-11-one 163195063 Click to see CC1C2CC3(C(C1(C(=O)O2)CCC4=COC=C4)CCC=C3C)C 314.40 unknown https://doi.org/10.1021/NP8004002
(1S,2S,7S,9S,12R)-1-[2-(furan-3-yl)ethyl]-6,7,12-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-5-en-11-one 162903366 Click to see CC1C2CC3(C(C1(C(=O)O2)CCC4=COC=C4)CCC=C3C)C 314.40 unknown https://doi.org/10.1021/NP8004002
Ptychonolide 25135583 Click to see CC1C2CC3(C(C1(C(=O)O2)CCC4=COC=C4)CCC=C3C)C 314.40 unknown https://doi.org/10.1021/NP8004002
> Organoheterocyclic compounds / Oxepanes
(1S,2S,7R,9R,11S,12R)-1-[2-(furan-3-yl)ethyl]-11-methoxy-6,7,12-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-5-ene 163030387 Click to see CC1C2CC3(C(C1(C(O2)OC)CCC4=COC=C4)CCC=C3C)C 330.50 unknown https://doi.org/10.1021/NP8004002
(1S,2S,7S,9S,11R,12R)-1-[2-(furan-3-yl)ethyl]-6,7,12-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-5-en-11-ol 163105495 Click to see CC1C2CC3(C(C1(C(O2)O)CCC4=COC=C4)CCC=C3C)C 316.40 unknown https://doi.org/10.1021/NP8004002
1-[2-(Furan-3-yl)ethyl]-6,7,12-trimethyl-10-oxatricyclo[7.2.1.02,7]dodec-5-en-11-ol 74392210 Click to see CC1C2CC3(C(C1(C(O2)O)CCC4=COC=C4)CCC=C3C)C 316.40 unknown https://doi.org/10.1021/NP8004002

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Collections Top

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