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Goniothalamus laoticus

Goniothalamus laoticus - 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 UUID64401e6e4aa11745124884
Scientific name Goniothalamus laoticus
Authority (Finet & Gagnep.) Bân
First published in Bot. Zhurn. (Moscow & Leningrad) 59: 554 (1974)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mitrephora laotica Finet & Gagnep. Bull. Soc. Bot. France 54: 87 (1907)

Common names Top

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Language Common/alternative name
Thai จำปีหิน
Thai ข้าวหลามดง
Chinese 柄芽哥纳香

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-0000706507
Tropicos 100344226
KEW urn:lsid:ipni.org:names:73209-1
The Plant List kew-2829699
Open Tree Of Life 598482
NCBI Taxonomy 306961
IPNI 73209-1
GBIF 3154633
Wikipedia Goniothalamus_laoticus

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
Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU Can J Infect Dis Med Microbiol 28-Oct-2023
PMCID:PMC10625492
doi:10.1155/2023/1860084
PMID:37927532
Traditional Medicinal Plants as a Source of Antituberculosis Drugs: A System Review Xu Y, Liang B, Kong C, Sun Z Biomed Res Int 08-Sep-2021
PMCID:PMC8448615
doi:10.1155/2021/9910365
PMID:34541000
Southeast Asian Medicinal Plants as a Potential Source of Antituberculosis Agent Sanusi SB, Abu Bakar MF, Mohamed M, Sabran SF, Mainasara MM Evid Based Complement Alternat Med 03-Jul-2017
PMCID:PMC5610802
doi:10.1155/2017/7185649
PMID:29081822
Molecular and morphological data supporting phylogenetic reconstruction of the genus Goniothalamus (Annonaceae), including a reassessment of previous infrageneric classifications Tang CC, Thomas DC, Saunders RM Data Brief 09-Jul-2015
PMCID:PMC4532731
doi:10.1016/j.dib.2015.06.021
PMID:26286044
A new cytotoxic 1-azaanthraquinone from the stems of Goniothalamus laoticus. Tip-pyang S, Limpipatwattana Y, Khumkratok S, Siripong P, Sichaem J Fitoterapia 01-Oct-2010
doi:10.1016/J.FITOTE.2010.05.019
PMID:20554005
Bioactive styryllactones and alkaloid from flowers of Goniothalamus laoticus. Lekphrom R, Kanokmedhakul S, Kanokmedhakul K J Ethnopharmacol 17-Aug-2009
doi:10.1016/J.JEP.2009.06.023
PMID:19573585

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 / Aporphines
16,17-Dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14,16,18-hexaene 10041981 Click to see COC1=C(C=C2C(=C1)CC3C4=C2C5=C(C=C4CCN3)OCO5)OC 325.40 unknown https://doi.org/10.1016/J.JEP.2009.06.023
Nordicentrine 168363 Click to see COC1=C(C=C2C(=C1)CC3C4=C2C5=C(C=C4CCN3)OCO5)OC 325.40 unknown https://doi.org/10.1016/J.JEP.2009.06.023
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
9-Deoxygoniopypyrone 126233 Click to see C1C2CC(=O)OC1C(C(O2)C3=CC=CC=C3)O 234.25 unknown https://doi.org/10.1016/J.JEP.2009.06.023
CID 72750925 72750925 Click to see C1C2CC(=O)OC1C(C(O2)C3=CC=CC=C3)O 234.25 unknown https://doi.org/10.1016/J.JEP.2009.06.023
> Organoheterocyclic compounds / Furofurans
3-hydroxy-2-[hydroxy(phenyl)methyl]-3,3a,6,6a-tetrahydro-2H-furo[3,2-b]furan-5-one 14777896 Click to see C1C2C(C(C(O2)C(C3=CC=CC=C3)O)O)OC1=O 250.25 unknown https://doi.org/10.1016/J.JEP.2009.06.023
> Organoheterocyclic compounds / Furopyrans
(+)-8-epi-Altholactone 343590 Click to see C1=CC=C(C=C1)C2C(C3C(O2)C=CC(=O)O3)O 232.23 unknown https://doi.org/10.1016/J.JEP.2009.06.023
(+)-Altholactone 365622 Click to see C1=CC=C(C=C1)C2C(C3C(O2)C=CC(=O)O3)O 232.23 unknown https://doi.org/10.1016/J.JEP.2009.06.023
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
2-(1,2-Dihydroxy-2-phenylethyl)-3-hydroxy-2,3-dihydropyran-6-one 45360156 Click to see C1=CC=C(C=C1)C(C(C2C(C=CC(=O)O2)O)O)O 250.25 unknown https://doi.org/10.1016/J.JEP.2009.06.023
Goniotriol 125950 Click to see C1=CC=C(C=C1)C(C(C2C(C=CC(=O)O2)O)O)O 250.25 unknown https://doi.org/10.1016/J.JEP.2009.06.023
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines
(3R,4S)-3,6-dihydroxy-4-methyl-3,4-dihydro-1H-benzo[g]quinoline-2,5,10-trione 163008371 Click to see CC1C(C(=O)NC2=C1C(=O)C3=C(C2=O)C=CC=C3O)O 273.24 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
3,6-dihydroxy-4-methyl-3,4-dihydro-1H-benzo[g]quinoline-2,5,10-trione 163008370 Click to see CC1C(C(=O)NC2=C1C(=O)C3=C(C2=O)C=CC=C3O)O 273.24 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
CID 85239741 85239741 Click to see CC1C(C(=O)NC2=C1C(=O)C3=CC=CC=C3C2=O)O 257.24 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
Griffithazanone A 10706277 Click to see CC1C(C(=O)NC2=C1C(=O)C3=CC=CC=C3C2=O)O 257.24 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
Marcanine A 10105653 Click to see CC1=CC(=O)NC2=C1C(=O)C3=CC=CC=C3C2=O 239.23 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 159894 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC 238.24 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
Methyl sinapate 5321318 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC 238.24 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
2-(4-Hydroxyphenyl)ethyl 3-(4-hydroxyphenyl)prop-2-enoate 86163337 Click to see C1=CC(=CC=C1CCOC(=O)C=CC2=CC=C(C=C2)O)O 284.31 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester 92203 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019
p-Hydroxyphenylethyl p-coumarate 16119626 Click to see C1=CC(=CC=C1CCOC(=O)C=CC2=CC=C(C=C2)O)O 284.31 unknown https://doi.org/10.1016/J.FITOTE.2010.05.019

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