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Piper schmidtii

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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 UUID644002abe2054580810641
Scientific name Piper schmidtii
Authority Hook.f.
First published in Fl. Brit. India 5: 89 (1886)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper glabrirhache C.DC. Candollea 1: 193 (1923)
Piper gibsonii C.DC. Candollea 1: 184 (1923)
Piper ovatostemon C.DC. Candollea 1: 196 (1923)
Piper ootacamundense C.DC. Candollea 1: 184 (1923)
Piper opacilimbum C.DC. Candollea 1: 184 (1923)

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-0000485734
Tropicos 25002631
KEW urn:lsid:ipni.org:names:683324-1
Open Tree Of Life 6031622
NCBI Taxonomy 2138340
IPNI 683324-1
GBIF 4190536

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
Manipulating JNK Signaling with (−)-zuonin A Kaoud TS, Park H, Mitra S, Yan C, Tseng CC, Shi Y, Jose J, Taliaferro JM, Lee K, Ren P, Hong J, Dalby KN ACS Chem Biol 30-Aug-2012
PMCID:PMC6459613
doi:10.1021/cb300261e
PMID:22916726
Neolignans from Piper schmidtii and Reassignment of the Structure of Schmiditin. Om Dutt Tyagi, Ashok K. Prasad, Jesper Wengel, Per M. Boll, Carl E. Olsen, Virinder S. Parmar, Nawal K. Sharma, Amitabh Jha, Kirpal S. Bisht Danish Chemical Society 19-Jun-2008
doi:10.3891/ACTA.CHEM.SCAND.49-0142
Chemical Constituents of Piper schmidtii: Structure of a New Neolignan Schmiditirr Neerja Joshi, H. S. Garg, D. S. Bhakuni American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50068A032
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
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Piperenone 36406703 Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC(=C(C=C3)OC)OC 388.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.49-0142
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
5-[5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole 12302263 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
Calopiptin 12302265 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
Galbacin 234441 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
Galgravin 101749 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown https://doi.org/10.1021/NP50068A032
machilin G 10450921 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
Zuihonin A 338287 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol 68972 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 438.80 unknown https://doi.org/10.1021/NP50068A032
> 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/10.3891/ACTA.CHEM.SCAND.49-0142
(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/10.3891/ACTA.CHEM.SCAND.49-0142
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4S)-4-[(2R)-1-(1,3-benzodioxol-5-yl)propan-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 25774968 Click to see CC(CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC 356.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
(4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 101833872 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(00)95012-X
4-[1-(1,3-Benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 182345 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(00)95012-X
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(00)95012-X
Isodihydrofutoquinol A 25774970 Click to see CC(CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC 356.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
Isodihydrofutoquinol B 44715837 Click to see CC(CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC 356.40 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP50068A032
> 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/10.1021/NP50068A032
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/10.1021/NP50068A032
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/10.1021/NP50068A032
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/10.1021/NP50068A032
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see COC1=C2C(=C(C(=C1)CC=C)OC)OCO2 222.24 unknown https://doi.org/10.1016/S0031-9422(00)95012-X
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(00)95012-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/10.3891/ACTA.CHEM.SCAND.49-0142
Methyl piperate 9921021 Click to see COC(=O)C=CC=CC1=CC2=C(C=C1)OCO2 232.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.49-0142
> 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/10.3891/ACTA.CHEM.SCAND.49-0142
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/10.3891/ACTA.CHEM.SCAND.49-0142

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