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Piper hancei

Piper hancei - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64404ad032118816452669
Scientific name Piper hancei
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 31: 94 (1886)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chavica leptostachya Hance J. Bot. 6: 301 (1868)
Piper matthewii Dunn J. Bot. 47: 377 (1909)

Common names Top

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Language Common/alternative name
Chinese 山菊
Chinese 山蒟

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001094105
Tropicos 25004106
KEW urn:lsid:ipni.org:names:681613-1
The Plant List tro-25004106
Open Tree Of Life 911551
NCBI Taxonomy 450286
IPNI 681613-1
iNaturalist 707472
GBIF 4187541
EOL 2871907
CMAUP NPO9078

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
RNA-dependent RNA polymerase (RdRp) natural antiviral inhibitors: a review Leite DR, Mantovani KM, Cordeiro SP, Maia FB, Betim FC, de Bona Sartor E, Montrucchio DP, de Fátima Gaspari Dias J, Miguel OG, Miguel MD Med Chem Res 29-Sep-2022
PMCID:PMC9520115
doi:10.1007/s00044-022-02963-2
PMID:36193545
Complete chloroplast genome sequences of the medicinal plant Piper hancei Zhang L, Hu X, Liu M Mitochondrial DNA B Resour 27-Aug-2021
PMCID:PMC8405093
doi:10.1080/23802359.2021.1967217
PMID:34471701
Optimal nutrition and the ever-changing dietary landscape: a conference report Shao A, Drewnowski A, Willcox DC, Krämer L, Lausted C, Eggersdorfer M, Mathers J, Bell JD, Randolph RK, Witkamp R, Griffiths JC Eur J Nutr 05-May-2017
PMCID:PMC5442251
doi:10.1007/s00394-017-1460-9
PMID:28474121
Ethnobotany of wild plants used for starting fermented beverages in Shui communities of southwest China Hong L, Zhuo J, Lei Q, Zhou J, Ahmed S, Wang C, Long Y, Li F, Long C J Ethnobiol Ethnomed 28-May-2015
PMCID:PMC4458060
doi:10.1186/s13002-015-0028-0
PMID:26017691
Ethnobotanical study on medicinal plants used by Maonan people in China Hong L, Guo Z, Huang K, Wei S, Liu B, Meng S, Long C J Ethnobiol Ethnomed 30-Apr-2015
PMCID:PMC4449599
doi:10.1186/s13002-015-0019-1
PMID:25925830
Caloric Restriction, CR Mimetics, and Healthy Aging in Okinawa: Controversies and Clinical Implications Willcox BJ, Willcox DC Curr Opin Clin Nutr Metab Care 01-Jan-2014
PMCID:PMC5403510
doi:10.1097/MCO.0000000000000019
PMID:24316687
Neolignans from Piper aequale Anderson Maxwell, Darrin Dabideen, William F Reynolds, Stewart McLean Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00545-7

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(4R)-6-(3,4-dimethoxyphenyl)-4-hydroxy-3-methoxy-4,7-dimethyl-1-prop-2-enylbicyclo[3.2.1]oct-2-en-8-one 5317956 Click to see CC1C(C2C(=O)C1(C=C(C2(C)O)OC)CC=C)C3=CC(=C(C=C3)OC)OC 372.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
Burseran 11101102 Click to see COC1=CC(=CC(=C1OC)OC)CC2COCC2CC3=CC4=C(C=C3)OCO4 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Daniellic acid 6955052 Click to see CC12CCCC(C1CCC(=C)C2CCC3=COC=C3)(C)C(=O)O 316.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Hancinone C 6443896 Click to see CC(=CC1=CC(=C(C(=C1)OC)OC)OC)C2(C=C(C(=O)C=C2OC)CC=C)OC 400.50 unknown via CMAUP database
Wallichinine 5315280 Click to see CC(=CC1=CC(=C(C=C1)OC)OC)C2(C=C(C(=O)C=C2OC)CC=C)OC 370.40 unknown via CMAUP database
> 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 via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
8-(3,7-Dimethylocta-2,6-dienyl)-7-hydroxychromen-2-one 78151388 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=O)C=C2)O)C)C 298.40 unknown via CMAUP database
Ostruthin 5281420 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O)C)C 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(9S,11bR,13aR)-3a,5a,8,8,11b,13a-hexamethyl-1-propan-2-yl-1,2,3,4,5,5b,6,9,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 5317958 Click to see CC(C)C1CCC2(C1C3(CCC4(C5CCC(C(C5=CCC4C3(CC2)C)(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
6-(2-Hydroxyethyl)-2,5,7-trimethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroinden-1-one 322489 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O 396.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Futoenone 9819306 Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5 340.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
3-(3-Methyl-2-butenoyl)-1H-indole 11805712 Click to see CC(=CC(=O)C1=CNC2=CC=CC=C21)C 199.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3S,3aR)-2-(2H-1,3-benzodioxol-5-yl)-5-methoxy-3-methyl-3a-(prop-2-en-1-yl)-3,3a-dihydro-1-benzofuran-6(2H)-one 10903924 Click to see CC1C(OC2=CC(=O)C(=CC12CC=C)OC)C3=CC4=C(C=C3)OCO4 340.40 unknown via CMAUP database
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/S0031-9422(98)00545-7
Hancinone 101370414 Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC4=C(C=C3)OCO4 340.40 unknown https://doi.org/10.1016/S0031-9422(98)00545-7
Kadsurenone 122159 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/S0031-9422(98)00545-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Isopimpinellin 68079 Click to see COC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC 246.21 unknown via CMAUP database
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
10-Methoxy-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-8-one 11482357 Click to see CC1(CCC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 260.28 unknown via CMAUP database
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database

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