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Piper solmsianum

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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 UUID644002afdbc1e691481503
Scientific name Piper solmsianum
Authority C.DC.
First published in Prodr. 16(1): 291 (1869)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper santosanum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 437 (1917)
Piper leucanthum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 436 (1917)
Artanthe hilariana Miq. Syst. Piperac. : 421 (1844)
Piper hilarianum C.DC. Prodr. 16(1): 321 1869
Piper solmsianum var. hilarianum (C.DC.) Yunck. Bol. Inst. Bot. (São Paulo) 3: 124 (1966)
Schilleria hilariana Kunth Linnaea 13: 711 (1840)

Common names Top

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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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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
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000485816
Tropicos 50217423
KEW urn:lsid:ipni.org:names:683440-1
The Plant List kew-2568593
Open Tree Of Life 390057
NCBI Taxonomy 538350
IPNI 683440-1
GBIF 7305588

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
Occurrence of Alkenylbenzenes in Plants: Flavours and Possibly Toxic Plant Metabolites Götz ME, Eisenreich A, Frenzel J, Sachse B, Schäfer B Plants (Basel) 23-May-2023
PMCID:PMC10255789
doi:10.3390/plants12112075
PMID:37299054
Essential Oils of Aromatic Plant Species from the Atlantic Rainforest Exhibit Extensive Chemical Diversity and Antimicrobial Activity Perigo CV, Haber LL, Facanali R, Vieira MA, Torres RB, Bernacci LC, Guimarães EF, Baitello JB, Sobral ME, Quecini V, Marques MO Antibiotics (Basel) 19-Dec-2022
PMCID:PMC9774909
doi:10.3390/antibiotics11121844
PMID:36551501
Cubeb (Piper cubeba L.f.): A comprehensive review of its botany, phytochemistry, traditional uses, and pharmacological properties Drissi B, Mahdi I, Yassir M, Ben Bakrim W, Bouissane L, Sobeh M Front Nutr 22-Nov-2022
PMCID:PMC9725028
doi:10.3389/fnut.2022.1048520
PMID:36483927
UHPLC-Q-Orbitrap-MS-Based Metabolomics Reveals Chemical Variations of Two Types of Rhizomes of Polygonatum sibiricum Luo G, Lin J, Cheng W, Liu Z, Yu T, Yang B Molecules 22-Jul-2022
PMCID:PMC9331047
doi:10.3390/molecules27154685
PMID:35897876
Piper tectoniifolium Kunth: A New Natural Source of the Bioactive Neolignan (−)-Grandisin Marques AM, da Rocha Queiroz AS, Guimarães EF, Mafud AC, de Sousa Carvalho P, Mascarenhas YP, da Silva Barenco T, Souza PD, Provance DW, do Nascimento JH, Ponte CG, Kaplan MA, de Lima Moreira D, Figueiredo MR Molecules 09-Feb-2022
PMCID:PMC8876808
doi:10.3390/molecules27041151
PMID:35208941
Assessment of antimycobacterial activities of pure compounds extracted from Thai medicinal plants against clarithromycin-resistant Mycobacterium abscessus Sirichoat A, Kham-ngam I, Kaewprasert O, Ananta P, Wisetsai A, Lekphrom R, Faksri K PeerJ 26-Oct-2021
PMCID:PMC8555507
doi:10.7717/peerj.12391
PMID:34760385
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Essential Oil and Major Non-Volatile Secondary Metabolites from the Leaves of Amazonian Piper subscutatum Ramírez J, Andrade MD, Vidari G, Gilardoni G Plants (Basel) 09-Jun-2021
PMCID:PMC8228786
doi:10.3390/plants10061168
PMID:34207495
Ontogenetic Changes in the Chemical Profiles of Piper Species Gaia AM, Yamaguchi LF, Guerrero-Perilla C, Kato MJ Plants (Basel) 28-May-2021
PMCID:PMC8227164
doi:10.3390/plants10061085
PMID:34071315
Evaluation of DNA markers for molecular identification of three Piper species from Brazilian Atlantic Rainforest Egydio Brandão AP, Yamaguchi LF, Tepe EJ, Salatino A, Kato MJ PLoS One 19-Oct-2020
PMCID:PMC7571689
doi:10.1371/journal.pone.0239056
PMID:33075070
Plant Natural Products for the Control of Aedes aegypti: The Main Vector of Important Arboviruses Silvério MR, Espindola LS, Lopes NP, Vieira PC Molecules 31-Jul-2020
PMCID:PMC7435582
doi:10.3390/molecules25153484
PMID:32751878
Metabolite Profiling in Anticancer Drug Development: A Systematic Review Muhamad N, Na-Bangchang K Drug Des Devel Ther 09-Apr-2020
PMCID:PMC7154001
doi:10.2147/DDDT.S221518
PMID:32308372
Phytochemical analysis and broad spectrum antimicrobial activity of ethanolic extract of Jasminum mesnyi Hance leaves and its solventpartitioned fractions Verma R, Balaji BS, Dixit A Bioinformation 31-Aug-2018
PMCID:PMC6166397
doi:10.6026/97320630014430
PMID:30310250
Metabolite profiles of callus and cell suspension cultures of mangosteen Jamil SZ, Rohani ER, Baharum SN, Noor NM 3 Biotech 17-Jul-2018
PMCID:PMC6049810
doi:10.1007/s13205-018-1336-6
PMID:30034986
Dermatophyte Resistance to Antifungal Drugs: Mechanisms and Prospectus Martinez-Rossi NM, Bitencourt TA, Peres NT, Lang EA, Gomes EV, Quaresemin NR, Martins MP, Lopes L, Rossi A Front Microbiol 29-May-2018
PMCID:PMC5986900
doi:10.3389/fmicb.2018.01108
PMID:29896175

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic acid 8357 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O 212.20 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
3,4,5-Trimethoxybenzaldehyde 6858 Click to see COC1=CC(=CC(=C1OC)OC)C=O 196.20 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
> Benzenoids / Phenol ethers / Anisoles
1,2,3-Trimethoxy-5-(1E)-1-propen-1-ylbenzene; (E)-Isoelemicin; 1,2,3-Trimethoxy-5-((E)-prop-1-enyl)benzene; 1,2,3-Trimethoxy-5-[(1E)-1-propenyl]benzene 78932 Click to see CC=CC1=CC(=C(C(=C1)OC)OC)OC 208.25 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
https://doi.org/10.1016/S0031-9422(00)00295-8
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
Isoelemicin 5318557 Click to see CC=CC1=CC(=C(C(=C1)OC)OC)OC 208.25 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
https://doi.org/10.1016/S0031-9422(03)00356-X
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(2R,3R,4R,5R)-3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)tetrahydrofuran 10048436 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
https://doi.org/10.1016/S0031-9422(00)00295-8
https://doi.org/10.1016/J.JPBA.2012.08.028
(2S,3R,4R,5S)-3,4-dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 163017716 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
3,4-Dimethyl-2,5-bis(3,4,5-trimethoxyphenyl)oxolane 4485701 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
https://doi.org/10.1016/S0031-9422(03)00356-X
4-Methoxy-6-[5-(7-methoxy-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole 74317763 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC5=C(C(=C4)OC)OCO5)C 400.40 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
6-[(2S,3R,4R,5R)-3,4-dimethyl-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]-4-methoxy-1,3-benzodioxole 637161 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
6-[3,4-Dimethyl-5-(3,4,5-trimethoxyphenyl)oxolan-2-yl]-4-methoxy-1,3-benzodioxole 22297612 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
https://doi.org/10.1016/S0031-9422(03)00356-X
Grandisin 442876 Click to see CC1C(C(OC1C2=CC(=C(C(=C2)OC)OC)OC)C3=CC(=C(C(=C3)OC)OC)OC)C 432.50 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
rel-(7R,8R,7'R,8'R)-3,4,3',4'-dimethylene-dioxy-5,5'-dimethoxy-7,7'-epoxylignan 641713 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC5=C(C(=C4)OC)OCO5)C 400.40 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
rel-(7R,8R,7'R,8'R)-3',4'-methylenedioxy-3,4,5,5'-tetramethoxy-7,7'-epoxylignan 11080226 Click to see CC1C(C(OC1C2=CC3=C(C(=C2)OC)OCO3)C4=CC(=C(C(=C4)OC)OC)OC)C 416.50 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(03)00356-X
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see COC1=C2C(=C(C(=C1)CC=C)OC)OCO2 222.24 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown https://doi.org/10.1016/S0031-9422(00)00295-8
Sarisan 95289 Click to see COC1=CC2=C(C=C1CC=C)OCO2 192.21 unknown https://doi.org/10.1590/S0001-37652001000100004
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-Methoxy-4-[3-methyl-5-(1-propenyl)-2-benzofuranyl]-phenol 193821 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1248/BPB.28.1527
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 70414118 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1248/BPB.28.1527
5-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-1,3-benzodioxole 261729 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1248/BPB.28.1527
5-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-1,3-benzodioxole 6051545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1248/BPB.28.1527
Conocarpan 10999992 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1248/BPB.28.1527
Eupomatenoid 5 6443783 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1248/BPB.28.1527
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/BPB.28.1527
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/BPB.28.1527

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