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Mezzettia parviflora

Mezzettia parviflora - 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 UUID643ff576a3045116066203
Scientific name Mezzettia parviflora
Authority Becc.
First published in Nuovo Giorn. Bot. Ital. 3: 188 (1871)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lonchomera leptopoda Hook.f. & Thomson Fl. Brit. India 1: 94 (1872)
Mezzettia herveyeana Oliv. Hooker's Icon. Pl. 16: t. 1560 (1887)
Mezzettia curtisii King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 61: 129 (1892)
Mezzettia leptopoda (Hook.f. & Thomson) King J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 61: 129 (1892)
Mezzettia parviflora var. floribunda Boerl. Cat. Pl. Phan. 21 1899
Mezzettia parviflora var. subtetramera Boerl. Cat. Pl. Phan. 21 1899

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
  • Asia-tropical
    • Indo-China
      • Andaman Islands
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Maluku
      • Sulawesi
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000372461
Tropicos 1600930
KEW urn:lsid:ipni.org:names:73910-1
The Plant List kew-2364633
Open Tree Of Life 166065
NCBI Taxonomy 235747
IPNI 73910-1
iNaturalist 427191
GBIF 3156522
EOL 307468
CMAUP NPO25657

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
Hard plant tissues do not contribute meaningfully to dental microwear: evolutionary implications van Casteren A, Strait DS, Swain MV, Michael S, Thai LA, Philip SM, Saji S, Al-Fadhalah K, Almusallam AS, Shekeban A, McGraw WS, Kane EE, Wright BW, Lucas PW Sci Rep 17-Jan-2020
PMCID:PMC6969033
doi:10.1038/s41598-019-57403-w
PMID:31953510
The Feeding Biomechanics and Dietary Ecology of Paranthropus boisei Smith AL, Benazzi S, Ledogar JA, Tamvada K, Pryor Smith LC, Weber GW, Spencer MA, Lucas PW, Michael S, Shekeban A, Al-Fadhalah K, Almusallam AS, Dechow PC, Grosse IR, Ross CF, Madden RH, Richmond BG, Wright BW, Wang Q, Byron C, Slice DE, Wood S, Dzialo C, Berthaume MA, Casteren AV, Strait DS Anat Rec (Hoboken) 01-Jan-2015
PMCID:PMC4420635
doi:10.1002/ar.23073
PMID:25529240
Plant Cuttings Chaffey N Ann Bot 01-Mar-2012
PMCID:PMC3286289
doi:10.1093/aob/mcs035
Evolutionary optimization of material properties of a tropical seed Lucas PW, Gaskins JT, Lowrey TK, Harrison ME, Morrogh-Bernard HC, Cheyne SM, Begley MR J R Soc Interface 25-May-2011
PMCID:PMC3223626
doi:10.1098/rsif.2011.0188
PMID:21613287
Structural characterization, by two-dimensional NMR spectroscopy and fast-atom-bombardment mass spectrometry, of a highly acylated trirhamnoside from <i>Mezzettia</i><i>leptopoda</i> (<i>Annonaceae</i>) Donald A. Powell, William S. York, Herman van Halbeek, Joseph T. Etse, Alexander I. Gray, Peter G. Waterman Canadian Science Publishing 08-May-2006
doi:10.1139/V90-163
Chemistry of the annonaceae, Part 29. Structure of mezzettiaside-2, -4, -5, -6 and -7, new partially esterified 1-O-octyl tri- and tetra-rhamnosyl derivatives from Mezzettia leptopoda Joseph T. Etse, Alexander I. Gray, Catherine Lavaud, Georges Massiot, Jean-Marc Nuzillard, Peter G. Waterman Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19910000861
Novel cytotoxic acylated oligorhamnosides from Mezzettia leptopoda. Cui B, Chai H, Santisuk T, Reutrakul V, Farnsworth NR, Cordell GA, Pezzuto JM, Kinghorn AD J Nat Prod 01-Dec-1998
doi:10.1021/NP980270J
PMID:9868159

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
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(23S)-23-ethoxy-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaene 86310874 Click to see CCOC1C2=C(C=CC3=C2OCO3)C4=C(N1C)C5=CC6=C(C=C5C=C4)OCO6 377.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine 2703 Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5 348.40 unknown via CMAUP database
Sanguinarium 5154 Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6 332.30 unknown via CMAUP database
> Alkaloids and derivatives / Phthalide isoquinolines
(-)-Adlumine 638255 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Adlumine 442155 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
(+)-Corlumine 5316069 Click to see CN1CCC2=CC(=C(C=C2C1C3C4=C(C5=C(C=C4)OCO5)C(=O)O3)OC)OC 383.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(-)-13beta-Hydroxystylopine 6452886 Click to see C1CN2CC3=C(C=CC4=C3OCO4)C(C2C5=CC6=C(C=C51)OCO6)O 339.30 unknown via CMAUP database
(+)-Isocorypalmine 71261649 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Cheilanthifoline 440582 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C5=C(C=C4)OCO5)O 325.40 unknown via CMAUP database
(S)-Tetrahydrocolumbamine 440229 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC 341.40 unknown via CMAUP database
17-Methoxy-5,7-dioxa-1-azoniapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),2,4(8),9,11,14,16,18-octaen-16-ol 45490416 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC5=C(C4=C3)OCO5)O 322.30 unknown via CMAUP database
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown via CMAUP database
Ophiocarpine 12313750 Click to see COC1=C(C2=C(C=C1)C(C3C4=CC5=C(C=C4CCN3C2)OCO5)O)OC 355.40 unknown via CMAUP database
Stylopine 440583 Click to see C1CN2CC3=C(CC2C4=CC5=C(C=C41)OCO5)C=CC6=C3OCO6 323.30 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown via CMAUP database
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Mezzettiaside 11 10394451 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC(=O)C)OC(=O)C)O 646.80 unknown https://doi.org/10.1021/NP980270J
Mezzettiaside 9 10054386 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)O)OC(=O)C)OC(=O)C)O 604.70 unknown https://doi.org/10.1021/NP980270J
Mezzettiasideide 10 10627463 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)O)OC(=O)C)O 604.70 unknown https://doi.org/10.1021/NP980270J
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
6-deoxy-Hex2Ac4Ac(?1-3)6-deoxy-Hex2Ac4Ac(?1-3)[hexanoyl(-4)]6-deoxy-Hex-O-octyl 14861060 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)O)OC(=O)C)OC(=O)C)O 834.90 unknown https://doi.org/10.1021/NP980270J
6-deoxy-Hex4Ac(?1-3)6-deoxy-Hex2Ac4Ac(?1-3)[hexanoyl(-4)]6-deoxy-Hex-O-octyl 14861061 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)O)O)OC(=O)C)O 792.90 unknown https://doi.org/10.1021/NP980270J
Mezzettiaside 2 10102009 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)O)OC(=O)C)OC(=O)C)O 834.90 unknown https://doi.org/10.1039/P19910000861
https://doi.org/10.1021/NP980270J
Mezzettiaside 3 10328148 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)OC(=O)C)O)OC(=O)C)O 834.90 unknown https://doi.org/10.1039/P19910000861
https://doi.org/10.1139/V90-163
https://doi.org/10.1021/NP980270J
Mezzettiaside 4 10350348 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)O)O)OC(=O)C)O 792.90 unknown https://doi.org/10.1021/NP980270J
https://doi.org/10.1039/P19910000861
Mezzettiaside 5 14861063 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)OC4C(C(C(C(O4)C)O)OC(=O)C)O)O)OC(=O)C)O 981.10 unknown https://doi.org/10.1039/P19910000861
Mezzettiaside 8 9987864 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)O)O)OC(=O)C)OC(=O)C)O 792.90 unknown https://doi.org/10.1021/NP980270J
Rha(a1-3)Rha4Ac(a1-3)Rha2Ac4Ac(a1-3)[hexanoyl(-4)]Rha(a)-O-octyl 101884860 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)OC4C(C(C(C(O4)C)O)O)O)O)OC(=O)C)O 939.00 unknown https://doi.org/10.1039/P19910000861
Rha2Ac(a1-3)Rha4Ac(a1-3)Rha2Ac4Ac(a1-3)[hexanoyl(-4)]Rha(a)-O-octyl 14861065 Click to see CCCCCCCCOC1C(C(C(C(O1)C)OC(=O)CCCCC)OC2C(C(C(C(O2)C)OC(=O)C)OC3C(C(C(C(O3)C)OC(=O)C)OC4C(C(C(C(O4)C)O)O)OC(=O)C)O)OC(=O)C)O 981.10 unknown https://doi.org/10.1039/P19910000861
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Noroxyhydrastinine 89047 Click to see C1CNC(=O)C2=CC3=C(C=C21)OCO3 191.18 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
Corypalline 280225 Click to see CN1CCC2=CC(=C(C=C2C1)O)OC 193.24 unknown via CMAUP database

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