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Piper falconeri

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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 UUID644001d74a20c265913686
Scientific name Piper falconeri
Authority C.DC.
First published in Candollea 1: 187 (1923)

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

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-0000479197
Tropicos 100426741
KEW urn:lsid:ipni.org:names:681370-1
Open Tree Of Life 6030723
IPNI 681370-1
GBIF 4191556

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)!
Title Authors Publication Released IDs
ChemInform Abstract: An Insecticidal Amide from Piper falconeri. V. S. PARMAR, R. SINHA, N. A. SHAKIL, O. D. TYAGI, P. M. BOLL, A. WENGEL Wiley 04-Sep-2010
doi:10.1002/CHIN.199325274
Polyphenols and alkaloids from piper species Virinder S Parmar, Subhash C Jain, Sangita Gupta, Sangeeta Talwar, Vivek K Rajwanshi, Rajesh Kumar, Abul Azim, Sanjay Malhotra, Naresh Kumar, Rajni Jain, Nawal K Sharma, Om D Tyagi, Stephen J Lawrie, William Errington, Oliwer W Howarth, Carl E Olsen, Sanjay K.Singh¶andJesper Wengel Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00208-8
Lignans and neolignans from Piper schmidtii Om Dutt Tyagi, Søren Jensen, Per M. Boll, Nawal K. Sharma, Kirpal S. Bisht, Virinder S. Parmar Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)95012-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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
Nerolidol 8888 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00208-8
> 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(00)95012-X
https://doi.org/10.1002/CHIN.199325274
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(00)95012-X
> Organoheterocyclic compounds / Benzodioxoles
(2E,4E)-N-isobutyl-7-(3,4-methylenedioxyphenyl)-hepta-2,4-dienamide 637860 Click to see CC(C)CNC(=O)C=CC=CCCC1=CC2=C(C=C1)OCO2 301.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
7-(1,3-benzodioxol-5-yl)-N-(2-methylpropyl)hepta-2,4-dienamide 78200770 Click to see CC(C)CNC(=O)C=CC=CCCC1=CC2=C(C=C1)OCO2 301.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
https://doi.org/10.1002/CHIN.199325274
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
https://doi.org/10.1002/CHIN.199325274

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