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Piper argyrophyllum

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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 UUID644001efc7d51632434697
Scientific name Piper argyrophyllum
Authority Miq.
First published in Syst. Piperac. : 330 (1844)

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000479752
KEW urn:lsid:ipni.org:names:680457-1
Open Tree Of Life 993723
NCBI Taxonomy 405317
GBIF 4183896

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
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
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
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
Neolignans and alkaloids from Piper argyrophylum Sanjay K. Singh, Prasad K. Ashok, Carl E. Olsen, Amitabh Jha, Subhash C. Jain, Virinder S. Parmar, Jesper Wenge Elsevier BV 05-Apr-2003
doi:10.1016/S0031-9422(96)00502-X

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
(6aR)-1,2,3-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-6-carbaldehyde 102445436 Click to see COC1=C(C(=C2C3=CC=CC=C3CC4C2=C1CCN4C=O)OC)OC 339.40 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
Cepharadione A 94577 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC5=C4OCO5)C(=O)C1=O 305.30 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Alkaloids and derivatives / Aporphines / 4,5-dioxoaporphines
Cepharadione B 189151 Click to see CN1C2=CC3=CC=CC=C3C4=C2C(=CC(=C4OC)OC)C(=O)C1=O 321.30 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Alkaloids and derivatives / Aristolactams
Aristolactam BII 162739 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)OC 279.29 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
Piperolactam A 3081016 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)O 265.26 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(4R)-4-[(2R)-1-(3,4-dimethoxyphenyl)propan-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 102445641 Click to see CC(CC1=CC(=C(C=C1)OC)OC)C2(C=C(C(=O)C=C2OC)CC=C)OC 372.50 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
(4S)-4-[1-(3,4-dimethoxyphenyl)propan-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 129316665 Click to see CC(CC1=CC(=C(C=C1)OC)OC)C2(C=C(C(=O)C=C2OC)CC=C)OC 372.50 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Futoquinol 5281817 Click to see CC(=CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC 354.40 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-5alpha-cycloarta-3beta,21-diol 71716352 Click to see CC(C)C(=C)CCC(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Organoheterocyclic compounds / Benzodioxoles
Kadsurin A 442885 Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4 372.40 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
Kadsurin B 10022290 Click to see CC1C(OC2(C1(C=C(C(C2)O)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4 374.40 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> 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/S0031-9422(96)00502-X
3-Phenyl-1-(pyrrolidin-1-yl)prop-2-en-1-one 583163 Click to see C1CCN(C1)C(=O)C=CC2=CC=CC=C2 201.26 unknown https://doi.org/10.1016/S0031-9422(96)00502-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
n-cis-Feruloyltyramine 6440659 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1016/S0031-9422(96)00502-X

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