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Desmos cochinchinensis

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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 UUID6440166e3aae0120558044
Scientific name Desmos cochinchinensis
Authority Lour.
First published in Fl. Cochinch. : 352 (1790)

Description Top

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Synonyms Top

Scientific name Authority First published in
Unona cabog Blanco Fl. Filip. : 466 (1837)
Unona tomentosa Willd. Sp. Pl., ed. 4 , 2: 1271 (1799)
Unona cochinchinensis DC. Syst. Nat. 1: 495 (1817)
Unona velutina Hance J. Bot. 15: 328 (1877)
Desmos cochinchinensis var. fulvescens Bân Bot. Zhurn. (Moscow & Leningrad) 59: 1770 (1974)
Desmos velutinus (Hance) Ast Fl. Indo-Chine , Suppl. 1: 67 (1938)

Common names Top

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Language Common/alternative name
Vietnamese dây chân chim núi

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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No forms added yet.

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000642354
Tropicos 1600921
KEW urn:lsid:ipni.org:names:72773-1
The Plant List kew-2763020
Open Tree Of Life 289107
NCBI Taxonomy 1202408
IPNI 72773-1
iNaturalist 430935
GBIF 3155178
EOL 1054033

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
Anti-diabetic and anti-inflammatory bioactive hits from Coriaria intermedia Matsum. stem and Dracontomelon dao (Blanco) Merr. & Rolfe bark through bioassay-guided fractionation and liquid chromatography-tandem mass spectrometry Fabian MC, Astorga RM, Atis AA, Pilapil LA, Hernandez CC Front Pharmacol 08-Mar-2024
PMCID:PMC10957545
doi:10.3389/fphar.2024.1349725
PMID:38523640
Discovering Potential Compounds for Venous Disease Treatment through Virtual Screening and Network Pharmacology Approach Barrera-Vázquez OS, Escobar-Ramírez JL, Santiago-Mejía J, Carrasco-Ortega OF, Magos-Guerrero GA Molecules 05-Dec-2023
PMCID:PMC10745828
doi:10.3390/molecules28247937
PMID:38138427
Untargeted Metabolomics Analysis of the Orchid Species Oncidium sotoanum Reveals the Presence of Rare Bioactive C-Diglycosylated Chrysin Derivatives Zorzi G, Gambini S, Negri S, Guzzo F, Commisso M Plants (Basel) 02-Feb-2023
PMCID:PMC9920315
doi:10.3390/plants12030655
PMID:36771739
Different compounds against Angiotensin-Converting Enzyme 2 (ACE2) receptor potentially containing the infectivity of SARS-CoV-2: an in silico study Shahbazi B, Mafakher L, Teimoori-Toolabi L J Mol Model 05-Mar-2022
PMCID:PMC8898033
doi:10.1007/s00894-022-05059-1
PMID:35249180
Emerging cellular and molecular mechanisms underlying anticancer indications of chrysin Talebi M, Talebi M, Farkhondeh T, Simal-Gandara J, Kopustinskiene DM, Bernatoniene J, Samarghandian S Cancer Cell Int 15-Apr-2021
PMCID:PMC8050922
doi:10.1186/s12935-021-01906-y
PMID:33858433
Polyoxygenated seco-cyclohexenes derivatives from flower and leaf extracts of Desmos cochinchinensis and their α-glucosidase inhibitory activity Suthiphasilp V, Maneerat T, Duangyod T, Charoensup R, Andersen RJ, Pyne SG, Laphookhieo S Heliyon 23-Dec-2020
PMCID:PMC7772550
doi:10.1016/j.heliyon.2020.e05791
PMID:33385090
Inhibitory effect of chrysin on estrogen biosynthesis by suppression of enzyme aromatase (CYP19): A systematic review Balam FH, Ahmadi ZS, Ghorbani A Heliyon 07-Mar-2020
PMCID:PMC7063143
doi:10.1016/j.heliyon.2020.e03557
PMID:32181408
Phytochemicals in Helicobacter pylori Infections: What Are We Doing Now? Salehi B, Sharopov F, Martorell M, Rajkovic J, Ademiluyi AO, Sharifi-Rad M, Fokou PV, Martins N, Iriti M, Sharifi-Rad J Int J Mol Sci 10-Aug-2018
PMCID:PMC6121492
doi:10.3390/ijms19082361
PMID:30103451
Protective Effects of Chrysin Against Drugs and Toxic Agents Samarghandian S, Farkhondeh T, Azimi-Nezhad M Dose Response 23-Jun-2017
PMCID:PMC5484430
doi:10.1177/1559325817711782
PMID:28694744
Recent Progress in the Discovery of Next Generation Inhibitors of Aromatase from the Structure–Function Perspective Ghosh D, Lo J, Egbuta C J Med Chem 19-Jan-2016
PMCID:PMC4915572
doi:10.1021/acs.jmedchem.5b01281
PMID:26689671
An Overview on Cardamonin Gonçalves LM, Valente IM, Rodrigues JA J Med Food 01-Jun-2014
PMCID:PMC4060836
doi:10.1089/jmf.2013.0061
PMID:24433078
15-Lipoxygenase inhibition of Commelina benghalensis, Tradescantia fluminensis, Tradescantia zebrina Alaba CS, Chichioco-Hernandez CL Asian Pac J Trop Biomed 01-Mar-2014
PMCID:PMC3868787
doi:10.1016/S2221-1691(14)60229-X
PMID:25182435
Hybrid flavan-chalcones, aromatase and lipoxygenase inhibitors, from Desmos cochinchinensis. Bajgai SP, Prachyawarakorn V, Mahidol C, Ruchirawat S, Kittakoop P Phytochemistry 01-Nov-2011
doi:10.1016/J.PHYTOCHEM.2011.07.002
PMID:21802698
New Cytotoxic Fatty Acid from <i>Desmos cochinchinensis</i> (Annonaceae) Nan-Jun Sun, David K. Ho, X. Eric Hu, Jeffrey M. Sneddon, Ralph E. Stephens, John M. Cassady Informa UK Limited 07-Jul-2007
doi:10.1080/10575639508043184
Taxoids from Taxus chinensis. Zhao Y, Wang FS, Peng LY, Li XL, Xu G, Luo XX, Lu Y, Wu L, Zheng QT, Zhao QS J Nat Prod 01-Dec-2006
doi:10.1021/NP060345G
PMID:17190468

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
3,9-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,10-diol 5290 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O 327.40 unknown https://doi.org/10.1080/10575639508043184
l-Stepholidine 6917970 Click to see COC1=C(C=C2C3CC4=C(CN3CCC2=C1)C(=C(C=C4)O)OC)O 327.40 unknown https://doi.org/10.1080/10575639508043184
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Benzenemethanol, 2-methoxy-, benzoate 3085295 Click to see COC1=CC=CC=C1COC(=O)C2=CC=CC=C2 242.27 unknown https://doi.org/10.1007/BF02977900
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Oleamide 5283387 Click to see CCCCCCCCC=CCCCCCCCC(=O)N 281.50 unknown https://doi.org/10.1080/10575639508043184
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Ethyl Linoleate 5282184 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown https://doi.org/10.1080/10575639508043184
> 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/10.1080/10575639508043184
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/10.1080/10575639508043184
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(1S,3R,7S,8S)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol 129317601 Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O 222.37 unknown https://doi.org/10.1080/10575639508043184
(6S,8S)-2,2,6,8-tetramethyltricyclo[5.3.1.03,8]undecan-3-ol 442384 Click to see CC1CCC2(C(C3CCC2(C1C3)C)(C)C)O 222.37 unknown https://doi.org/10.1080/10575639508043184
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
2H-1-Benzopyran-6-carboxaldehyde, 3,4-dihydro-5,7-dihydroxy-8-methyl-4-oxo-2-phenyl- 597204 Click to see CC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)C=O)O 298.29 unknown https://doi.org/10.1021/NP060345G
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
Demethoxymatteucinol 180550 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)C)O 284.31 unknown https://doi.org/10.1021/NP060345G
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astilbin 119258 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1007/BF02977900
Isoastilbin 316844 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 450.40 unknown https://doi.org/10.1007/BF02977900
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/10.1007/BF02977900
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,4R)-4-[2,6-dihydroxy-4-methoxy-3-(3-phenylprop-2-enoyl)phenyl]-5,7-dihydroxy-2-phenyl-3,4-dihydro-2H-chromene-8-carbaldehyde 162971653 Click to see COC1=C(C(=C(C(=C1)O)C2CC(OC3=C(C(=CC(=C23)O)O)C=O)C4=CC=CC=C4)O)C(=O)C=CC5=CC=CC=C5 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
(2S,4R)-4-[2,6-dihydroxy-4-methoxy-3-[(E)-3-phenylprop-2-enoyl]phenyl]-5,7-dihydroxy-2-phenyl-3,4-dihydro-2H-chromene-8-carbaldehyde 54597384 Click to see COC1=C(C(=C(C(=C1)O)C2CC(OC3=C(C(=CC(=C23)O)O)C=O)C4=CC=CC=C4)O)C(=O)C=CC5=CC=CC=C5 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
(2S,4S)-4-[2,6-dihydroxy-4-methoxy-3-(3-phenylprop-2-enoyl)phenyl]-5,7-dihydroxy-2-phenyl-3,4-dihydro-2H-chromene-8-carbaldehyde 162971652 Click to see COC1=C(C(=C(C(=C1)O)C2CC(OC3=C(C(=CC(=C23)O)O)C=O)C4=CC=CC=C4)O)C(=O)C=CC5=CC=CC=C5 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
Desmosflavan A 54597383 Click to see COC1=C(C(=C(C(=C1)O)C2CC(OC3=C(C(=CC(=C23)O)O)C=O)C4=CC=CC=C4)O)C(=O)C=CC5=CC=CC=C5 538.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Negletein 471719 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown https://doi.org/10.1007/BF02977900
https://doi.org/10.1021/NP060345G
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxy-6-methoxyphenyl)-3-phenylprop-2-en-1-one 154102 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.07.002

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