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Xylopia vielana

Xylopia vielana - 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 UUID643ffbaec0d6a344732863
Scientific name Xylopia vielana
Authority Pierre
First published in Fl. Forest. Cochinch. : t. 34 (1881)

Description Top

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Synonyms Top

Scientific name Authority First published in
Xylopicrum vielana Kuntze Revis. Gen. Pl. 1: 8 (1891)

Common names Top

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Language Common/alternative name
Chinese 木瓣树

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-0000428653
Tropicos 1602842
KEW urn:lsid:ipni.org:names:76283-1
The Plant List kew-2467858
Open Tree Of Life 3868013
NCBI Taxonomy 1489966
IPNI 76283-1
GBIF 3157037
EOL 1054086
Wikipedia Xylopia_vielana

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
In-vitro and computational analysis of Urolithin-A for anti-inflammatory activity on Cyclooxygenase 2 (COX-2) Revankar AG, Bagewadi ZK, Shaikh IA, Mannasaheb BA, Ghoneim MM, Khan AA, Asdaq SM Saudi J Biol Sci 06-Sep-2023
PMCID:PMC10505678
doi:10.1016/j.sjbs.2023.103804
PMID:37727526
New Guaiane-Type Sesquiterpenoids Biscogniauxiaols A–G with Anti-Fungal and Anti-Inflammatory Activities from the Endophytic Fungus Biscogniauxia Petrensis Han L, Zheng W, Qian SY, Yang MF, Lu YZ, He ZJ, Kang JC J Fungi (Basel) 23-Mar-2023
PMCID:PMC10144765
doi:10.3390/jof9040393
PMID:37108848
Biosynthesis of anticancer phytochemical compounds and their chemistry Dogra A, Kumar J Front Pharmacol 09-Mar-2023
PMCID:PMC10034375
doi:10.3389/fphar.2023.1136779
PMID:36969868
Synergistic effects of natural compounds and conventional chemotherapeutic agents: recent insights for the development of cancer treatment strategies Castañeda AM, Meléndez CM, Uribe D, Pedroza-Díaz J Heliyon 24-May-2022
PMCID:PMC9163513
doi:10.1016/j.heliyon.2022.e09519
PMID:35669542
A Comprehensive In Silico Exploration of Pharmacological Properties, Bioactivities, Molecular Docking, and Anticancer Potential of Vieloplain F from Xylopia vielana Targeting B-Raf Kinase Hassan SS, Abbas SQ, Ali F, Ishaq M, Bano I, Hassan M, Jin HZ, Bungau SG Molecules 28-Jan-2022
PMCID:PMC8839023
doi:10.3390/molecules27030917
PMID:35164181
Spirocyclic Motifs in Natural Products Chupakhin E, Babich O, Prosekov A, Asyakina L, Krasavin M Molecules 17-Nov-2019
PMCID:PMC6891393
doi:10.3390/molecules24224165
PMID:31744211
Xylopins A–F, six rare guaiane dimers with three different connecting modes from Xylopia vielana Xie YG, Yan R, Zhong X, Piao H, Muhammad I, Ke X, Yan S, Guo Y, Jin HZ, Zhang WD RSC Adv 21-Mar-2019
PMCID:PMC9062023
doi:10.1039/c9ra00347a
PMID:35517671
Xylopidimers A–E, Five New Guaiane Dimers with Various Carbon Skeletons from the Roots of Xylopia vielana Guo YG, Xie YG, Wu GJ, Cheng TF, Zhu SL, Yan SK, Jin HZ, Zhang WD ACS Omega 25-Jan-2019
PMCID:PMC6648509
doi:10.1021/acsomega.8b00828
PMID:31459455
Xyloplains A–F, six new guaiane-type sesquiterpenoid dimers from Xylopia vielana Xie YG, Zhang W, Zhu SL, Cheng TF, Wu GJ, Muhammad I, Yan SK, Zhang Y, Jin HZ, Zhang WD RSC Adv 18-Jul-2018
PMCID:PMC9082531
doi:10.1039/c8ra04356f
PMID:35539790
Effects of logging and recruitment on community phylogenetic structure in 32 permanent forest plots of Kampong Thom, Cambodia Toyama H, Kajisa T, Tagane S, Mase K, Chhang P, Samreth V, Ma V, Sokh H, Ichihashi R, Onoda Y, Mizoue N, Yahara T Philos Trans R Soc Lond B Biol Sci 19-Feb-2015
PMCID:PMC4290422
doi:10.1098/rstb.2014.0008
PMID:25561669
Guaiane dimers from Xylopia vielana. Kamperdick C, Phuong NM, Adam G, Van Sung T Phytochemistry 01-Oct-2003
doi:10.1016/J.PHYTOCHEM.2003.08.003
PMID:14559273
Guaiane dimers from Xylopia vielana. Kamperdick C, Phuong NM, Van Sung T, Adam G Phytochemistry 01-Feb-2001
doi:10.1016/S0031-9422(00)00344-7
PMID:11249097

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
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(11-Hydroxy-4,8,8,13,16,22-hexamethyl-3,20-dioxo-19-propan-2-yl-9,10-dioxahexacyclo[13.7.1.01,17.02,14.05,14.07,11]tricosa-4,6,16-trien-23-yl) acetate 73802658 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC6(C(=CC5=C(C4=O)C)C(OO6)(C)C)O)C)OC(=O)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
(1S,2S,11R,12R)-1,2,8,15-tetramethyl-5,18-di(propan-2-ylidene)pentacyclo[10.8.0.02,11.03,9.014,20]icosa-3(9),14(20)-diene-6,10,13,17-tetrone 12041176 Click to see CC1CC(=O)C(=C(C)C)CC2=C1C(=O)C3C2(C4(C3C(=O)C5=C4CC(=C(C)C)C(=O)CC5C)C)C 460.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(1S,2S,14R,15R)-9,20-dihydroxy-1,2,6,6,11,18,23,23-octamethyl-7,8,21,22-tetraoxaheptacyclo[13.11.0.02,14.03,12.05,9.017,26.020,24]hexacosa-3(12),4,17(26),24-tetraene-13,16-dione 101093217 Click to see CC1CC2(C(=CC3=C1C(=O)C4C3(C5(C4C(=O)C6=C5C=C7C(OOC7(CC6C)O)(C)C)C)C)C(OO2)(C)C)O 524.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(1S,2S,8S,11R,12R,15R)-1,2,8,15-tetramethyl-5,18-di(propan-2-ylidene)pentacyclo[10.8.0.02,11.03,9.014,20]icosa-3(9),14(20)-diene-6,10,13,17-tetrone 162966120 Click to see CC1CC(=O)C(=C(C)C)CC2=C1C(=O)C3C2(C4(C3C(=O)C5=C4CC(=C(C)C)C(=O)CC5C)C)C 460.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(1S,2S,8S,11R,12R,15S)-1,2,8,15-tetramethyl-5,18-di(propan-2-ylidene)pentacyclo[10.8.0.02,11.03,9.014,20]icosa-3(9),14(20)-diene-6,10,13,17-tetrone 162966119 Click to see CC1CC(=O)C(=C(C)C)CC2=C1C(=O)C3C2(C4(C3C(=O)C5=C4CC(=C(C)C)C(=O)CC5C)C)C 460.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(1S,2S,9S,11S,14R,15R,18R,20S)-9,20-dihydroxy-1,2,6,6,11,18,23,23-octamethyl-7,8,21,22-tetraoxaheptacyclo[13.11.0.02,14.03,12.05,9.017,26.020,24]hexacosa-3(12),4,17(26),24-tetraene-13,16-dione 162975030 Click to see CC1CC2(C(=CC3=C1C(=O)C4C3(C5(C4C(=O)C6=C5C=C7C(OOC7(CC6C)O)(C)C)C)C)C(OO2)(C)C)O 524.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(1S,2S,9S,11S,14R,15R,18S,20S)-9,20-dihydroxy-1,2,6,6,11,18,23,23-octamethyl-7,8,21,22-tetraoxaheptacyclo[13.11.0.02,14.03,12.05,9.017,26.020,24]hexacosa-3(12),4,17(26),24-tetraene-13,16-dione 162975032 Click to see CC1CC2(C(=CC3=C1C(=O)C4C3(C5(C4C(=O)C6=C5C=C7C(OOC7(CC6C)O)(C)C)C)C)C(OO2)(C)C)O 524.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(4,10,13,19-Tetramethyl-3,8,17-trioxo-16-propan-2-yl-7-propan-2-ylidene-20-pentacyclo[10.7.1.01,14.02,11.05,11]icosa-4,13-dienyl) acetate 78200722 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC(=O)C(=C(C)C)CC5=C(C4=O)C)C)OC(=O)C)C)C(C)C 506.70 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
(9-Hydroxy-2,6,6,11,16,22-hexamethyl-13,20-dioxo-19-propan-2-yl-7,8-dioxahexacyclo[13.7.1.01,17.02,14.03,12.05,9]tricosa-3(12),4,16-trien-23-yl) acetate 22298402 Click to see CC1CC(=O)C(CC2=C(C3C4C(=O)C5=C(C4(C12C3OC(=O)C)C)C=C6C(OOC6(CC5C)O)(C)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
[(1R,2R,10R,11S,12R,16R,19S,20R)-4,10,13,19-tetramethyl-3,7,17-trioxo-16-propan-2-yl-6-propan-2-ylidene-20-pentacyclo[10.7.1.01,14.02,11.05,11]icosa-4,13-dienyl] acetate 163104384 Click to see CC1CCC(=O)C(=C(C)C)C2=C(C(=O)C3C12C4C(C35C(CC(=O)C(CC5=C4C)C(C)C)C)OC(=O)C)C 506.70 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
[(1R,2S,10R,11S,12R,16R,19S,20R)-4,10,13,19-tetramethyl-3,8,17-trioxo-16-propan-2-yl-7-propan-2-ylidene-20-pentacyclo[10.7.1.01,14.02,11.05,11]icosa-4,13-dienyl] acetate 637104 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC(=O)C(=C(C)C)CC5=C(C4=O)C)C)OC(=O)C)C)C(C)C 506.70 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
[(1R,2S,10R,11S,16R,19S,20R)-4,10,13,19-tetramethyl-3,8,17-trioxo-16-propan-2-yl-7-propan-2-ylidene-20-pentacyclo[10.7.1.01,14.02,11.05,11]icosa-4,13-dienyl] acetate 101093216 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC(=O)C(=C(C)C)CC5=C(C4=O)C)C)OC(=O)C)C)C(C)C 506.70 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
[(1R,2S,11R,13S,14S,15R,19R,22S,23R)-11-hydroxy-4,8,8,13,16,22-hexamethyl-3,20-dioxo-19-propan-2-yl-9,10-dioxahexacyclo[13.7.1.01,17.02,14.05,14.07,11]tricosa-4,6,16-trien-23-yl] acetate 163068988 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC6(C(=CC5=C(C4=O)C)C(OO6)(C)C)O)C)OC(=O)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
[(1R,2S,9R,11R,14R,15R,19S,22R,23S)-9-hydroxy-2,6,6,11,16,22-hexamethyl-13,20-dioxo-19-propan-2-yl-7,8-dioxahexacyclo[13.7.1.01,17.02,14.03,12.05,9]tricosa-3(12),4,16-trien-23-yl] acetate 641709 Click to see CC1CC(=O)C(CC2=C(C3C4C(=O)C5=C(C4(C12C3OC(=O)C)C)C=C6C(OOC6(CC5C)O)(C)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
[(1S,2R,11S,13R,14R,15S,19S,22R,23S)-11-hydroxy-4,8,8,13,16,22-hexamethyl-3,20-dioxo-19-propan-2-yl-9,10-dioxahexacyclo[13.7.1.01,17.02,14.05,14.07,11]tricosa-4,6,16-trien-23-yl] acetate 163068987 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC6(C(=CC5=C(C4=O)C)C(OO6)(C)C)O)C)OC(=O)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
[(1S,2S,11R,14R,15S,19S,22R,23R)-9-hydroxy-2,6,6,11,16,22-hexamethyl-13,20-dioxo-19-propan-2-yl-7,8-dioxahexacyclo[13.7.1.01,17.02,14.03,12.05,9]tricosa-3(12),4,16-trien-23-yl] acetate 101762390 Click to see CC1CC(=O)C(CC2=C(C3C4C(=O)C5=C(C4(C12C3OC(=O)C)C)C=C6C(OOC6(CC5C)O)(C)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
[(2R,13S,15S,19R,23S)-11-hydroxy-4,8,8,13,16,22-hexamethyl-3,20-dioxo-19-propan-2-yl-9,10-dioxahexacyclo[13.7.1.01,17.02,14.05,14.07,11]tricosa-4,6,16-trien-23-yl] acetate 101762391 Click to see CC1CC(=O)C(CC2=C(C3C(C12C4C35C(CC6(C(=CC5=C(C4=O)C)C(OO6)(C)C)O)C)OC(=O)C)C)C(C)C 538.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
1,2,8,15-Tetramethyl-5,18-di(propan-2-ylidene)pentacyclo[10.8.0.02,11.03,9.014,20]icosa-3(9),14(20)-diene-6,10,13,17-tetrone 162966118 Click to see CC1CC(=O)C(=C(C)C)CC2=C1C(=O)C3C2(C4(C3C(=O)C5=C4CC(=C(C)C)C(=O)CC5C)C)C 460.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
9,20-Dihydroxy-1,2,6,6,11,18,23,23-octamethyl-7,8,21,22-tetraoxaheptacyclo[13.11.0.02,14.03,12.05,9.017,26.020,24]hexacosa-3(12),4,17(26),24-tetraene-13,16-dione 162975029 Click to see CC1CC2(C(=CC3=C1C(=O)C4C3(C5(C4C(=O)C6=C5C=C7C(OOC7(CC6C)O)(C)C)C)C)C(OO2)(C)C)O 524.60 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitostenone 60123241 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
Sitostenone 579897 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/S0031-9422(00)00344-7
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.003
https://doi.org/10.1016/S0031-9422(00)00344-7

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