Details Top

Internal ID UUID68f8f4c3bc2e7275637139
Scientific name Piper lanatum
Authority Roxb.
First published in Fl. Ind. 1: 161 (1820)

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Synonyms Top

Scientific name Authority First published in
Peperomia lanata A.Dietr. Sp. Pl. ed. 6 , 1: 145 (1831)
Piper densibaccum C.DC. Philipp. J. Sci., C 5: 454 (1910)
Piper dagatpanum C.DC. Fragm. Fl. Philipp. 1: 154 (1905)
Piper gelalae C.DC. Philipp. J. Sci., C 11: 260 (1916)
Piper hirsutissimum D.Dietr. Syn. Pl. 1: 122 (1839)
Piper hallieri C.DC. Philipp. J. Sci., C 5: 458 (1910)
Piper haenkeanum Opiz Reliq. Haenk. 1: 159 (1828)
Piper basilanum C.DC. Philipp. J. Sci., C 5: 457 (1910)
Piper cabadbaranum C.DC. Leafl. Philipp. Bot. 6: 2292 (1914)
Piper boerlagei C.DC. Candollea 1: 226 (1923)
Piper bonthainense C.DC. Annuaire Conserv. Jard. Bot. Genève 21: 302 (1920)
Piper acutibaccum C.DC. Philipp. J. Sci., C 5: 459 (1910)
Piper arborisedens C.DC. Philipp. J. Sci., C 11: 223 (1916)
Piper apoanum C.DC. Leafl. Philipp. Bot. 3: 785 (1910)
Piper sablanum Quisumb. Philipp. J. Sci. 43: 15 (1930)
Piper tenuirameum C.DC. Fragm. Fl. Philipp. 1: 159 (1905)
Piper tenuipedunculum C.DC. Philipp. J. Sci., C 5: 460 (1910)
Piper malaganum C.DC. Philipp. J. Sci., C 5: 461 (1910)
Piper marivelesanum C.DC. Fragm. Fl. Philipp. 1: 155 (1905)
Piper lowong Blume Verh. Batav. Genootsch. Kunsten 11: 161 (1826)
Piper javanicum C.DC. Prodr. 16(1): 343 (1869)
Piper kietanum C.DC. Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 89: 527 (1913 publ. 1914)
Piper parcipilum C.DC. Philipp. J. Sci., C 5: 445 (1910)
Piper obovatibracteum C.DC. Leafl. Philipp. Bot. 3: 784 (1910)
Piper perpunctatum C.DC. Philipp. J. Sci., C 11: 219 (1916)
Piper merrittii C.DC. Philipp. J. Sci., C 5: 460 (1910)
Piper viminale Opiz Reliq. Haenk. 1: 150 (1828)
Piper villilimbum C.DC. Leafl. Philipp. Bot. 3: 788 (1910)
Piper pilobracteatum Chaveer. & Sudmoon Acta Phytotax. Sin. 44: 449 (2006)
Chavica haenkeana C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 6: 224 (1851)
Chavica viminalis Miq. Linnaea 20: 131 (1847)
Cubeba canina Miq. Comm. Phytogr. : 33 (1840)
Cubeba lanata Miq. Syst. Piperac. : 298 (1843)
Cubeba lowong Miq. Comm. Phytogr. : 33 (1840)
Piper caninum Blume Verh. Batav. Genootsch. Kunsten 11: 214 (1826)
Piper banksii Miq. Verslagen Meded. Afd. Natuurk. Kon. Akad. Wetensch. ser. 2, 2: 61. 1868
Piper bombycatum Noronha Verh. Batav. Genootsch. Kunst. 5(Art. 4): 23. 1790
Piper negrosense C.DC. Leafl. Philipp. Bot. 3: 786 (1910)
Piper pedunculatum Reinw. ex Miq. Linnaea 21: 484 (1848)
Piper arborescens Thwaites Enum. Pl. Zeyl. : 293 (1860)
Piper caninum var. latibracteum C.DC. Leafl. Philipp. Bot. 3: 787 (1910)
Piper merrittii var. parvifolium C.DC. Philipp. J. Sci., C 11: 224 (1916)
Piper caninum var. thwaitesii (C.DC.) Hook.f. Fl. Brit. India 5: 82 (1886)

Common names Top

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Language Common/alternative name
English common pepper
English common piper
Japanese ピペル・カニヌム
Malay pokok sirih hutan
Malay sirih hutan

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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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
Tropicos 50171061
KEW urn:lsid:ipni.org:names:680776-1
The Plant List kew-2557715
Open Tree Of Life 742254
NCBI Taxonomy 130391
IPNI 680776-1
iNaturalist 369557
GBIF 4186275
EPPO PIPCN
CMAUP NPO1782
World Flora Online wfo-0000485935

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
Larvicidal proficiency of volatile compounds present in Commiphora wightii gum extract against Aedes aegypti (Linnaeus, 1762) Patel K, Akbari D, Pandya RV, Trivedi J, Mevada V, Wanale SG, Patel R, Yadav VK, Tank JG, Sahoo DK, Patel A Front Plant Sci 30-Aug-2023
PMCID:PMC10499046
doi:10.3389/fpls.2023.1220339
PMID:37711311
Plant Extracts from the Yucatan Peninsula in the In Vitro Control of Curvularia lunata and Antifungal Effect of Mosannona depressa and Piper neesianum Extracts on Postharvest Fruits of Habanero Pepper Cruz-Cerino P, Cristóbal-Alejo J, Ruiz-Carrera V, Gamboa-Angulo M Plants (Basel) 09-Aug-2023
PMCID:PMC10459550
doi:10.3390/plants12162908
PMID:37631120
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
Natural compounds may contribute in preventing SARS-CoV-2 infection: a narrative review Bizzoca ME, Leuci S, Mignogna MD, Muzio EL, Caponio VC, Muzio LL 02-Jun-2022
PMCID:PMC9160299
doi:10.1016/j.fshw.2022.04.005
Sesquiterpenes and Monoterpenes from the Leaves and Stems of Illicium simonsii and Their Antibacterial Activity Li H, Song X, Li H, Zhu L, Cao S, Liu J Molecules 08-Feb-2022
PMCID:PMC8838251
doi:10.3390/molecules27031115
PMID:35164380
Monoterpenes and Their Derivatives—Recent Development in Biological and Medical Applications Zielińska-Błajet M, Feder-Kubis J Int J Mol Sci 25-Sep-2020
PMCID:PMC7582973
doi:10.3390/ijms21197078
PMID:32992914
Chemical Compositions and Mosquito Larvicidal Activities of Essential Oils from Piper Species Growing Wild in Central Vietnam Huong LT, Hung NH, Dai DN, Tai TA, Hien VT, Satyal P, Setzer WN Molecules 27-Oct-2019
PMCID:PMC6864731
doi:10.3390/molecules24213871
PMID:31717867
Piper Species: A Comprehensive Review on Their Phytochemistry, Biological Activities and Applications Salehi B, Zakaria ZA, Gyawali R, Ibrahim SA, Rajkovic J, Shinwari ZK, Khan T, Sharifi-Rad J, Ozleyen A, Turkdonmez E, Valussi M, Tumer TB, Monzote Fidalgo L, Martorell M, Setzer WN Molecules 07-Apr-2019
PMCID:PMC6479398
doi:10.3390/molecules24071364
PMID:30959974
Pharmacokinetic profile and metabolite identification of bornyl caffeate and caffeic acid in rats by high performance liquid chromatography coupled with mass spectrometry Shi B, Yang L, Gao T, Ma C, Li Q, Nan Y, Wang S, Xiao C, Jia P, Zheng X RSC Adv 30-Jan-2019
PMCID:PMC9060532
doi:10.1039/c8ra07972b
PMID:35518073
Isolation and Purification of Potent Growth Inhibitors from Piper methysticum Root Van TM, Xuan TD, Minh TN, Quan NV Molecules 31-Jul-2018
PMCID:PMC6222926
doi:10.3390/molecules23081907
PMID:30065174
The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates Salomo K, Smith JF, Feild TS, Samain MS, Bond L, Davidson C, Zimmers J, Neinhuis C, Wanke S Syst Bot 18-Dec-2017
PMCID:PMC5792071
doi:10.1600/036364417X696438
PMID:29398773
Application of digital field photographs as documents for tropical plant inventory LaFrankie JV Jr, Chua AI Appl Plant Sci 11-May-2015
PMCID:PMC4435466
doi:10.3732/apps.1400116
PMID:25995976
Bornyl caffeate induces apoptosis in human breast cancer MCF-7 cells via the ROS- and JNK-mediated pathways Yang CB, Pei WJ, Zhao J, Cheng YY, Zheng XH, Rong JH Acta Pharmacol Sin 16-Dec-2013
PMCID:PMC4075736
doi:10.1038/aps.2013.162
PMID:24335836
Chemical Compositions, Antioxidant and Antimicrobial Activities of Essential Oils of Piper caninum Blume Salleh WM, Ahmad F, Yen KH, Sirat HM Int J Mol Sci 08-Nov-2011
PMCID:PMC3233433
doi:10.3390/ijms12117720
PMID:22174627
Cyclic Tetrapyrrolic Photosensitisers from the leaves of Phaeanthus ophthalmicus Tan PJ, Ong CY, Danial A, Yusof HM, Neoh BK, Lee HB Chem Cent J 20-Jun-2011
PMCID:PMC3149563
doi:10.1186/1752-153X-5-32
PMID:21682931

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
> Alkaloids and derivatives / Aporphines
Cepharadione A 94577 Click to see 305.30 unknown https://doi.org/10.1021/NP040056X
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1016/J.BMC.2004.05.007
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4S)-4-acetyl-2-chromen-2-ylidene-4-hydroxy-5,5-dimethylcyclopentane-1,3-dione 162902928 Click to see 312.30 unknown https://doi.org/10.1055/S-2006-960855
4-Hydroxy-5-(3-hydroxy-3-methylbutyl)-8,8-dimethyl-3,7-bis(3-methylbut-2-enyl)-1-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione 73113437 Click to see CC(C)C(=O)C12C(=O)C(=C(C(C1=O)(CC(C2(C)C)CC=C(C)C)CCC(C)(C)O)O)CC=C(C)C 486.70 unknown https://doi.org/10.1055/S-2006-960855
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1S,2R,3R,9R,10R,17S)-3-(3,5-dihydroxyphenyl)-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 101103994 Click to see 680.70 unknown via CMAUP database
(1S,2R,3R,9S,10S,17S)-3-[(2S,3S)-3-(3,5-dihydroxyphenyl)-2-(4-hydroxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydro-1-benzofuran-4-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 21606280 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=C8C(C(OC8=CC(=C7)OC9C(C(C(C(O9)CO)O)O)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)C(=C6)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 1069.10 unknown via CMAUP database
(1S,2R,3R,9S,10S,17S)-3-[(2S,3S)-6-hydroxy-2-(4-hydroxyphenyl)-3-[3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydro-1-benzofuran-4-yl]-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 21606279 Click to see 1069.10 unknown via CMAUP database
(1S,4R,5R,11R,12R,15R,16R,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 101053432 Click to see C1=CC(=CC=C1C2C3C(C4=C(C2C5=C3C6=C(C=C5O)OC(C6C7=CC(=CC(=C7)O)O)C8=CC=C(C=C8)O)C9=C(C=C4O)OC(C9C1=CC(=CC(=C1)O)O)C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O 906.90 unknown via CMAUP database
(1S,4R,5R,11R,12R,15R,16S,22S)-4,15-bis(3,5-dihydroxyphenyl)-5,11,16,22-tetrakis(4-hydroxyphenyl)-6,17-dioxahexacyclo[10.9.1.02,10.03,7.013,21.014,18]docosa-2(10),3(7),8,13(21),14(18),19-hexaene-9,20-diol 101103995 Click to see 906.90 unknown via CMAUP database
(2R,9S,10S,11S,12S)-12-(3,5-dihydroxyphenyl)-2-[(R)-[(1S,2R,3R,9S,10S,17S)-3-(3,5-dihydroxyphenyl)-5,13,15-trihydroxy-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaen-6-yl]-(4-hydroxyphenyl)methyl]-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaene-5,7,14,16-tetrol 16149368 Click to see 1361.40 unknown via CMAUP database
(2R,9S,10S,11S,12S)-12-(3,5-dihydroxyphenyl)-2-[(R)-[(1S,2R,3R,9S,10S,17S)-3-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-5,13,15-trihydroxy-2,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaen-6-yl]-(4-hydroxyphenyl)methyl]-9,11-bis(4-hydroxyphenyl)tetracyclo[8.6.1.03,8.013,17]heptadeca-1(16),3(8),4,6,13(17),14-hexaene-5,7,14,16-tetrol 16151489 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C(C5=C(C=C(C(=C35)C2C6=CC(=CC(=C6)O)O)O)O)C(C7=CC=C(C=C7)O)C8=C(C9=C1C(C(C9C2=C3C(C(OC3=CC(=C2)O)C2=CC=C(C=C2)O)C2=CC(=CC(=C2)O)O)C2=CC=C(C=C2)O)C(C2=C(C=C(C=C2O)O)C2C1=C8OC2C1=CC=C(C=C1)O)C1=CC=C(C=C1)O)O)C1=CC=C(C=C1)O)O 1587.60 unknown via CMAUP database
5-[(2R,3S)-6-hydroxy-2-(4-hydroxyphenyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-3-yl]benzene-1,3-diol 5315234 Click to see 454.50 unknown via CMAUP database
Epsilon-Viniferin 5281728 Click to see 454.50 unknown via CMAUP database
Vaticanol A 44566412 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown via CMAUP database
Vaticanol B 10010985 Click to see 906.90 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
1-Cinnamoylpyrrolidine 765514 Click to see C1CCN(C1)C(=O)C=CC2=CC=CC=C2 201.26 unknown https://doi.org/10.1016/J.BMC.2004.05.007
Cinnamic acid pyrrolidid 583163 Click to see 201.26 unknown https://doi.org/10.1016/J.BMC.2004.05.007
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown https://doi.org/10.1016/J.BMC.2004.05.007
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1016/J.BMC.2004.05.007
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(1,7,7-Trimethyl-2-bicyclo[2.2.1]heptanyl) 3-(3,4-dihydroxyphenyl)prop-2-enoate 432001 Click to see 316.40 unknown https://doi.org/10.1055/S-2006-960855
[(1S,2R,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 101027453 Click to see 316.40 unknown https://doi.org/10.1055/S-2006-960855
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(+)-Bornyl p-coumarate 129317111 Click to see 300.40 unknown https://doi.org/10.1055/S-2006-960855
(1R,4R)-1,7,7-Trimethylbicyclo[2.2.1]heptane-2beta-ol 3-(4-hydroxyphenyl)acrylate 71448949 Click to see CC1(C2CCC1(C(C2)OC(=O)C=CC3=CC=C(C=C3)O)C)C 300.40 unknown https://doi.org/10.1055/S-2006-960855
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
3-Hydroxy-5-(2-(4-hydroxyphenyl)ethenyl)phenyl-beta-D-glucopyranoside 73642 Click to see 390.40 unknown via CMAUP database
Polydatin 5281718 Click to see 390.40 unknown via CMAUP database

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