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Piper trichostachyon

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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 UUID644056e8a2fec598762470
Scientific name Piper trichostachyon
Authority (Miq.) C.DC.
First published in Prodr. 16(1): 242 (1869)

Description Top

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Synonyms Top

Scientific name Authority First published in
Muldera trichostachya Miq. London J. Bot. 5: 556 (1846)

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001255555
Tropicos 50179113
KEW urn:lsid:ipni.org:names:683770-1
The Plant List tro-50179113
Open Tree Of Life 6031844
NCBI Taxonomy 1595995
IPNI 683770-1
GBIF 4190789

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
The chloroplast genome of black pepper (Piper nigrum L.) and its comparative analysis with related Piper species Gaikwad AB, Kaila T, Maurya A, Kumari R, Rangan P, Wankhede DP, Bhat KV Front Plant Sci 12-Jan-2023
PMCID:PMC9878596
doi:10.3389/fpls.2022.1095781
PMID:36714762
Comparative Quantification of the Phenolic Compounds, Piperine Content, and Total Polyphenols along with the Antioxidant Activities in the Piper trichostachyon and P. nigrum Al-Khayri JM, Upadhya V, Pai SR, Naik PM, Al-Mssallem MQ, Alessa FM Molecules 13-Sep-2022
PMCID:PMC9503797
doi:10.3390/molecules27185965
PMID:36144701
Genome wide identification and characterization of microsatellite markers in black pepper (Piper nigrum): A valuable resource for boosting genomics applications Kumari R, Wankhede DP, Bajpai A, Maurya A, Prasad K, Gautam D, Rangan P, Latha M, John K. J, A. S, Bhat KV, Gaikwad AB PLoS One 13-Dec-2019
PMCID:PMC6910694
doi:10.1371/journal.pone.0226002
PMID:31834893
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
Pharmacognostic Screening of Piper trichostachyon Fruits and its Comparative Analysis with Piper nigrum Using Chromatographic Techniques Upadhya V, Pai SR, Ankad GM, Hegde HV Pharmacogn Mag 11-May-2016
PMCID:PMC4883072
doi:10.4103/0973-1296.182172
PMID:27279700
Data-mining of potential antitubercular activities from molecular ingredients of traditional Chinese medicines Jamal S, Scaria V PeerJ 17-Jul-2014
PMCID:PMC4106188
doi:10.7717/peerj.476
PMID:25081126
Contributions of vulnerable hydrogeomorphic habitats to endemic plant diversity on the Kas Plateau, Western Ghats Bhattarai U, Tetali P, Kelso S Springerplus 04-Oct-2012
PMCID:PMC3725892
doi:10.1186/2193-1801-1-25
PMID:23961355
Caffeic acid esters and lignans from Piper sanguineispicum. Cabanillas BJ, Le Lamer AC, Castillo D, Arevalo J, Rojas R, Odonne G, Bourdy G, Moukarzel B, Sauvain M, Fabre N J Nat Prod 29-Nov-2010
doi:10.1021/NP1005357
PMID:20954722
Expedient synthesis of unsaturated amide alkaloids from <i>Piper</i> spp: Exploring the scope of recent methodology George M. Strunz, Heather J. Finlay Canadian Science Publishing 09-May-2006
doi:10.1139/V96-046
Potent CYP3A4 inhibitory constituents of Piper cubeba. Usia T, Watabe T, Kadota S, Tezuka Y J Nat Prod 01-Jan-2005
doi:10.1021/NP0401765
PMID:15679319
New amide alkaloids from the roots of Piper nigrum. Wei K, Li W, Koike K, Pei Y, Chen Y, Nikaido T J Nat Prod 01-Jun-2004
doi:10.1021/NP030475E
PMID:15217283
Studies on the genus piper - IX. Structure of trichostachine, an alkaloid from piper trichostachyon Jagdev Singh, K.L Dhar, C.K. Atal Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)88862-6
Lignans of Piper trichostachyon S.K. Koul, S.C. Taneja, P. Pushpangadan, K.L. Dhar Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80219-X
Antifungal amides from Piper hispidum and Piper tuberculatum. Navickiene HM, Alécio AC, Kato MJ, Bolzani VD, Young MC, Cavalheiro AJ, Furlan M Phytochemistry 01-Nov-2000
doi:10.1016/S0031-9422(00)00226-0
PMID:11130674

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
Piperine 638024 Click to see C1CCN(CC1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3 285.34 unknown https://doi.org/10.1016/S0031-9422(00)00226-0
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(2S,3S)-2-(1,3-benzodioxol-5-ylmethyl)-3-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]butane-1,4-diol 11463373 Click to see COC1=CC(=CC2=C1OCO2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO 388.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
2-(1,3-Benzodioxol-5-ylmethyl)-3-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]butane-1,4-diol 14018795 Click to see COC1=CC(=CC2=C1OCO2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO 388.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
Dihydrocubebin 193042 Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)C(CC3=CC4=C(C=C3)OCO4)CO 358.40 unknown https://doi.org/10.1021/NP1005357
https://doi.org/10.1021/NP0401765
https://doi.org/10.1016/0031-9422(88)80219-X
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactols
(2S,3S,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]oxolan-2-ol 14018790 Click to see COC1=CC(=CC2=C1OCO2)CC3C(COC3O)CC4=CC5=C(C=C4)OCO5 386.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
4-(1,3-Benzodioxol-5-ylmethyl)-3-[(7-methoxy-1,3-benzodioxol-5-yl)methyl]oxolan-2-ol 14018788 Click to see COC1=CC(=CC2=C1OCO2)CC3C(COC3O)CC4=CC5=C(C=C4)OCO5 386.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
Cubebin 117443 Click to see C1C(C(C(O1)O)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 356.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(2S,3S)-2-(5-Methoxy-3,4-methylenedioxybenzyl)-3-(3,4-methylenedioxybenzyl) butyrolactone 11509246 Click to see COC1=CC(=CC2=C1OCO2)CC3C(COC3=O)CC4=CC5=C(C=C4)OCO5 384.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
5-Methoxyhinokinin 14018792 Click to see COC1=CC(=CC2=C1OCO2)CC3C(COC3=O)CC4=CC5=C(C=C4)OCO5 384.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
Hinokinin 442879 Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 354.40 unknown https://doi.org/10.1016/0031-9422(88)80219-X
> Organoheterocyclic compounds / Benzodioxoles
1-[(8E)-9-(3,4-methylenedioxyphenyl)-8-nonenoyl]pyrrolidine 21580214 Click to see C1CCN(C1)C(=O)CCCCCCC=CC2=CC3=C(C=C2)OCO3 329.40 unknown https://doi.org/10.1021/NP030475E
5-(1,3-Benzodioxol-5-yl)-1-pyrrolidin-1-ylpenta-2,4-dien-1-one 117669 Click to see C1CCN(C1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3 271.31 unknown https://doi.org/10.1016/S0040-4039(01)88862-6
Piperyline 636537 Click to see C1CCN(C1)C(=O)C=CC=CC2=CC3=C(C=C2)OCO3 271.31 unknown https://doi.org/10.1016/S0040-4039(01)88862-6
> Organoheterocyclic compounds / Pyrrolidines / N-acylpyrrolidines
N-2,4-Eicosadienoylpyrrolidin 85296773 Click to see CCCCCCCCCCCCCCCC=CC=CC(=O)N1CCCC1 361.60 unknown https://doi.org/10.1139/V96-046
Pyrrolidine, 1-(1-oxo-2,4-eicosadienyl)-, (E,E)- 10872138 Click to see CCCCCCCCCCCCCCCC=CC=CC(=O)N1CCCC1 361.60 unknown https://doi.org/10.1139/V96-046

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