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Piper pedicellatum

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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 UUID64404ad09a39c740964623
Scientific name Piper pedicellatum
Authority C.DC.
First published in J. Bot. 4: 164 (1866)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper clarkei C.DC. Candollea 1: 186 (1923)
Piper subpedicellatum Van Heurck & Müll.Arg. Observ. Bot. Descript. Pl. Nov. Herb. Van Heurckiani 2: 122 (1871)
Piper nigramentum C.DC. Repert. Spec. Nov. Regni Veg. 13: 299 (1914)
Piper curtipedunculum C.DC. Notizbl. Königl. Bot. Gart. Berlin 6: 481 (1917)
Piper pedicellatum var. eglandulatum Chaveer. & Mokkamul Acta Phytotax. Geobot. 58: 35 (2007)

Common names Top

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Language Common/alternative name
Chinese 假山蒟
Chinese 角果胡椒
Chinese 细茎胡椒

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001094114
Tropicos 25004115
KEW urn:lsid:ipni.org:names:682634-1
The Plant List tro-25004115
Open Tree Of Life 5699485
NCBI Taxonomy 1546314
IUCN Red List 50126637
IPNI 682634-1
iNaturalist 362876
GBIF 7305176

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
UHPLC-HRMS/MS Chemical Fingerprinting of the Bioactive Partition from Cultivated Piper aduncum L. de Luna AV, Fagundes TD, Ramos YJ, de Araújo MH, Muzitano MF, Calixto SD, Simão TL, de Queiroz GA, Guimarães EF, Marques AM, Moreira DD Molecules 09-Apr-2024
PMCID:PMC11051932
doi:10.3390/molecules29081690
PMID:38675510
Efficient photocatalytic bactericidal performance of green-synthesised TiO2/reduced graphene oxide using banana peel extracts Utami M, Yenn TW, Alam MW, Ravindran B, Husniati, Purnama I, Salmahaminati, Hidayat H, Dhetaya FN, Salsabilla SN Heliyon 17-Feb-2024
PMCID:PMC10901103
doi:10.1016/j.heliyon.2024.e26636
PMID:38420369
Nutritional Composition and Phytochemical Evaluation of Some Selected Wild Edible Plants in Tach Gaint District, Northwestern Ethiopia Yiblet Y, Adamu E ScientificWorldJournal 16-Oct-2023
PMCID:PMC10593547
doi:10.1155/2023/6670648
PMID:37876588
Nutritional evaluation of some potential wild edible plants of North Eastern region of India Talang H, Yanthan A, Rathi RS, Pradheep K, Longkumer S, Imsong B, Singh LH, Assumi RS, Devi MB, Vanlalruati, Kumar A, Ahlawat SP, Bhatt KC, Bhardwaj R Front Nutr 01-Mar-2023
PMCID:PMC10014872
doi:10.3389/fnut.2023.1052086
PMID:36937351
Plant-Based Synthesis of Gold Nanoparticles and Theranostic Applications: A Review Muddapur UM, Alshehri S, Ghoneim MM, Mahnashi MH, Alshahrani MA, Khan AA, Iqubal SM, Bahafi A, More SS, Shaikh IA, Mannasaheb BA, Othman N, Maqbul MS, Ahmad MZ Molecules 18-Feb-2022
PMCID:PMC8875495
doi:10.3390/molecules27041391
PMID:35209180
A Review on Plant-Mediated Synthesis of Bimetallic Nanoparticles, Characterisation and Their Biological Applications Berta L, Coman NA, Rusu A, Tanase C Materials (Basel) 13-Dec-2021
PMCID:PMC8705710
doi:10.3390/ma14247677
PMID:34947271
Mainstreaming Local Food Species for Nutritional and Livelihood Security: Insights From Traditional Food Systems of Adi Community of Arunachal Pradesh, India Singh RK, Bhardwaj R, Singh A, Payum T, Rai AK, Singh A, Wangchu L, Upadhyay S Front Nutr 16-Aug-2021
PMCID:PMC8415219
doi:10.3389/fnut.2021.590978
PMID:34485354
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Controllable Synthesis of Bimetallic Nanostructures Using Biogenic Reagents: A Green Perspective Ramos RM, Regulacio MD ACS Omega 09-Mar-2021
PMCID:PMC7992060
doi:10.1021/acsomega.1c00692
PMID:33778236
Phytosynthesized nanoparticles as a potential cancer therapeutic agent Jeevanandam J, Kulabhusan PK, Sabbih G, Akram M, Danquah MK 3 Biotech 16-Nov-2020
PMCID:PMC7669941
doi:10.1007/s13205-020-02516-7
PMID:33224704
Green-synthesized nanocatalysts and nanomaterials for water treatment: Current challenges and future perspectives Nasrollahzadeh M, Sajjadi M, Iravani S, Varma RS J Hazard Mater 07-Jul-2020
PMCID:PMC7606836
doi:10.1016/j.jhazmat.2020.123401
PMID:32763697
Elemental Silver Nanoparticles: Biosynthesis and Bio Applications Mikhailov OV, Mikhailova EO Materials (Basel) 27-Sep-2019
PMCID:PMC6803994
doi:10.3390/ma12193177
PMID:31569794
Biogenic synthesis of biopolymer‐based Ag–Au bimetallic nanoparticle constructs and their anti‐proliferative assessment Subbiah KS, Beedu SR IET Nanobiotechnol 22-Aug-2018
PMCID:PMC8675961
doi:10.1049/iet-nbt.2018.5135
PMID:30964012
Synthesis paradigm and applications of silver nanoparticles (AgNPs), a review Beyene HD, Werkneh AA, Bezabh HK, Ambaye TG 24-Aug-2017
PMCID:PMC7148648
doi:10.1016/j.susmat.2017.08.001
Assessment of wild leafy vegetables traditionally consumed by the ethnic communities of Manipur, northeast India Thongam B, Konsam S, Handique AK J Ethnobiol Ethnomed 29-Jan-2016
PMCID:PMC4731935
doi:10.1186/s13002-016-0080-4
PMID:26822996

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/10.1002/CHIN.200447158
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Crotepoxide 161314 Click to see CC(=O)OC1C2C(O2)C3C(C1OC(=O)C)(O3)COC(=O)C4=CC=CC=C4 362.30 unknown https://doi.org/10.1016/0031-9422(92)80212-W
Piperenol A 14890277 Click to see C1=CC=C(C=C1)C(=O)OCC2=CC(C(C(C2O)OC(=O)C3=CC=CC=C3)O)O 384.40 unknown https://doi.org/10.1016/0031-9422(91)85269-6
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
3-(4-Hydroxyphenyl)propyl tetracosanoate 15736296 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCCC1=CC=C(C=C1)O 502.80 unknown https://doi.org/10.1016/0031-9422(92)80212-W
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Pellitorine 5318516 Click to see CCCCCC=CC=CC(=O)NCC(C)C 223.35 unknown https://doi.org/10.1002/CHIN.200447158
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10-(hydroxymethyl)-6,10,14,15,21,21-hexamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 56671304 Click to see CC1(CCC23CCC4(C5(CCC6C(C5C7C(C4(C2C1)OC3=O)O7)(CCC(C6(C)CO)OC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)C 780.90 unknown https://doi.org/10.1002/CHIN.200447158
> 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/10.1016/0031-9422(92)80212-W
https://doi.org/10.1002/CHIN.200447158
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/10.1002/CHIN.200447158
https://doi.org/10.1016/0031-9422(92)80212-W
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CHIN.200447158
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CHIN.200447158
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1002/CHIN.200447158
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1002/CHIN.200447158
> Organoheterocyclic compounds / Benzodioxoles
Pipernonaline 9974595 Click to see C1CCN(CC1)C(=O)C=CCCCCC=CC2=CC3=C(C=C2)OCO3 341.40 unknown https://doi.org/10.1002/CHIN.200447158
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Denudatin B 442834 Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC 356.40 unknown https://doi.org/10.1016/0031-9422(95)00036-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/S0031-9422(00)89819-2

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