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Piper lhotzkyanum

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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 UUID64404a6125080154241212
Scientific name Piper lhotzkyanum
Authority Kunth
First published in Nomencl. Bot. , ed. 2, 2: 341 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Piper damazii C.DC. Bull. Herb. Boissier , sér. 2, 7: 140 (1907)
Piper inversum C.DC. Linnaea 37: 359 (1872)
Artanthe lhotzkyana Miq. Syst. Piperac. : 417 (1844)
Piper carpapatanum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 145 (1936)
Piper ictum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 174 (1936)
Piper incitum Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 175 (1936)
Piper jaculifolium Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 178 (1936)
Piper morator Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 194 (1936)
Piper santabarbaranum Trel. Publ. Field Columb. Mus., Bot. Ser. 22: 11 (1940)
Steffensia lhotzkyana Kunth Linnaea 13: 658 (1840)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Western South America
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001092156
Tropicos 25000691
KEW urn:lsid:ipni.org:names:681969-1
The Plant List tro-25000691
Open Tree Of Life 6030990
IPNI 681969-1
GBIF 4189280

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
Non-polar constituents from leaves of piper lhotzkyanum Davyson de L. Moreira, Elsie F. Guimarães, Maria Auxiliadora C. Kaplan Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00067-3
A C-glucosylflavone from leaves of Piper lhotzkyanum. Moreira DD, Guimarães EF, Kaplan MA Phytochemistry 01-Dec-2000
doi:10.1016/S0031-9422(00)00121-7
PMID:11190396

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
Ethyl 3-(3,4-dimethoxyphenyl)propionate 222974 Click to see CCOC(=O)CCC1=CC(=C(C=C1)OC)OC 238.28 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
Methyl 3-(3,4-dimethoxyphenyl)propanoate 520347 Click to see COC1=C(C=C(C=C1)CCC(=O)OC)OC 224.25 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
> Benzenoids / Phenol ethers / Anisoles
2,4,5-Trimethoxystyrene 152219 Click to see COC1=CC(=C(C=C1C=C)OC)OC 194.23 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
3-(3,7-Dimethylocta-2,6-dienoyl)-4-hydroxybenzoic acid 78127309 Click to see CC(=CCCC(=CC(=O)C1=C(C=CC(=C1)C(=O)O)O)C)C 288.34 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
3-[(2E)-3,7-dimethylocta-2,6-dienoyl]-4-hydroxybenzoic acid 71598393 Click to see CC(=CCCC(=CC(=O)C1=C(C=CC(=C1)C(=O)O)O)C)C 288.34 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
3-[(2Z)-3,7-dimethylocta-2,6-dienoyl]-4-hydroxybenzoic acid 71598392 Click to see CC(=CCCC(=CC(=O)C1=C(C=CC(=C1)C(=O)O)O)C)C 288.34 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Hinesol 10878761 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
CID 24721116 24721116 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
Hinesol 289964 Click to see CC1CCC=C(C12CCC(C2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-[(2R,4aR,8aS)-4a,8-dimethyl-2,3,4,5,6,8a-hexahydro-1H-naphthalen-2-yl]propan-2-ol 12304193 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
7-epi-gamma-Eudesmol 6428429 Click to see CC1=C2CC(CCC2(CCC1)C)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
beta-EUDESMOL 91457 Click to see CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
> 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)00121-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(2R)-2-methyl-2-(4-methylpent-3-enyl)chromene-6-carboxylic acid 162908065 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2)C(=O)O)C)C 272.34 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
2-Methyl-2-(4-methylpent-3-enyl)chromene-6-carboxylic acid 100926543 Click to see CC(=CCCC1(C=CC2=C(O1)C=CC(=C2)C(=O)O)C)C 272.34 unknown https://doi.org/10.1016/S0031-9422(98)00067-3
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 4-hydroxy-3-methoxy-cinnamate 16830 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
Methyl ferulate 5357283 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5-hydroxy-7-methoxy-2-phenyl-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 637836 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3)C4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
5-Hydroxy-7-methoxy-2-phenyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 20979950 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3)C4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
Kaplanin 44257622 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3)C4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 348130 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)00121-7
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-(3,4-Dimethoxyphenyl)propionic acid 75019 Click to see COC1=C(C=C(C=C1)CCC(=O)O)OC 210.23 unknown https://doi.org/10.1016/S0031-9422(00)00121-7

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