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Gardenia thailandica

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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 UUID64403cc4ce5ea649746159
Scientific name Gardenia thailandica
Authority Tirveng.
First published in Nordic J. Bot. 3: 462 (1983)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic غاردينيا تايلندية
Arabic غردينية تايلندية
Thai พุดภูเก็ต

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

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Database ID/link to page
World Flora Online wfo-0000971217
Tropicos 50289333
KEW urn:lsid:ipni.org:names:902087-1
The Plant List kew-88496
Open Tree Of Life 61612
Observations.org 357491
NCBI Taxonomy 1233871
IPNI 902087-1
GBIF 5335018
EOL 1103874
Elurikkus 519140
CMAUP NPO25423

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
Bioactive ZnO Nanoparticles: Biosynthesis, Characterization and Potential Antimicrobial Applications Huq MA, Apu MA, Ashrafudoulla M, Rahman MM, Parvez MA, Balusamy SR, Akter S, Rahman MS Pharmaceutics 16-Nov-2023
PMCID:PMC10675506
doi:10.3390/pharmaceutics15112634
PMID:38004613
Regulation of Staphylococcus aureus Virulence and Application of Nanotherapeutics to Eradicate S. aureus Infection Arunachalam K, Pandurangan P, Shi C, Lagoa R Pharmaceutics 17-Jan-2023
PMCID:PMC9960757
doi:10.3390/pharmaceutics15020310
PMID:36839634
The Use of Medicinal Plant-Derived Metallic Nanoparticles in Theranostics Xulu JH, Ndongwe T, Ezealisiji KM, Tembu VJ, Mncwangi NP, Witika BA, Siwe-Noundou X Pharmaceutics 10-Nov-2022
PMCID:PMC9698412
doi:10.3390/pharmaceutics14112437
PMID:36365255
Biologically Synthesized Silver Nanoparticles and Their Diverse Applications Sampath G, Chen YY, Rameshkumar N, Krishnan M, Nagarajan K, Shyu DJ Nanomaterials (Basel) 09-Sep-2022
PMCID:PMC9500900
doi:10.3390/nano12183126
PMID:36144915
Emerging strategies in nanotechnology to treat respiratory tract infections: realizing current trends for future clinical perspectives Chen M, Shou Z, Jin X, Chen Y Drug Deliv 27-Jul-2022
PMCID:PMC9341380
doi:10.1080/10717544.2022.2089294
PMID:35892224
In Vivo and In Vitro Antimicrobial Activity of Biogenic Silver Nanoparticles against Staphylococcus aureus Clinical Isolates Attallah NG, Elekhnawy E, Negm WA, Hussein IA, Mokhtar FA, Al-Fakhrany OM Pharmaceuticals (Basel) 03-Feb-2022
PMCID:PMC8878289
doi:10.3390/ph15020194
PMID:35215306
Kindia (Pavetteae, Rubiaceae), a new cliff-dwelling genus with chemically profiled colleter exudate from Mt Gangan, Republic of Guinea Cheek M, Magassouba S, Howes MJ, Doré T, Doumbouya S, Molmou D, Grall A, Couch C, Larridon I PeerJ 20-Apr-2018
PMCID:PMC5912204
doi:10.7717/peerj.4666
PMID:29692954
Secondary Metabolites from Rubiaceae Species Martins D, Nunez CV Molecules 22-Jul-2015
PMCID:PMC6331836
doi:10.3390/molecules200713422
PMID:26205062
Cycloartane triterpenes from the exudate of Gardenia thailandica Thanesuan Nuanyai, Reungrit Sappapan, Tirayut Vilaivan, Khanitha Pudhom Elsevier BV 30-Oct-2010
doi:10.1016/J.PHYTOL.2010.10.003
Anti-HIV-1 cycloartanes from leaves and twigs of Gardenia thailandica. Tuchinda P, Saiai A, Pohmakotr M, Yoosook C, Kasisit J, Napaswat C, Santisuk T, Reutrakul V Planta Med 01-Apr-2004
doi:10.1055/S-2004-818951
PMID:15095155
Cytotoxic and anti-HIV-1 constituents from leaves and twigs of Gardenia tubifera Vichai Reutrakul, Chongkon Krachangchaeng, Patoomratana Tuchinda, Manat Pohmakotr, Thaworn Jaipetch, Chalobon Yoosook, Jittra Kasisit, Samaisukh Sophasan, Kulawee Sujarit, Thawatchai Santisuk Elsevier BV 22-Jan-2004
doi:10.1016/J.TET.2003.12.010

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 / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,5E,7Z,10Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,9,11a-tetrahydrocyclodeca[b]furan-4-yl] 2-methylpropanoate 10336745 Click to see CC1=CC2C(C(C=C(C=CC1)C=O)OC(=O)C(C)C)C(=C)C(=O)O2 330.40 unknown via CMAUP database
[(3aS,4S,5S,6E,10E,11aR)-6-formyl-10-methyl-3-methylidene-4-(2-methylpropanoyloxy)-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] 2-hydroxy-2-methylpropanoate 21593572 Click to see CC1=CC2C(C(C(C(=CCC1)C=O)OC(=O)C(C)(C)O)OC(=O)C(C)C)C(=C)C(=O)O2 434.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-[(1S,4R,5R,8S,9S,12S,13R)-12-[(2S)-1-hydroxypropan-2-yl]-4,8-dimethyl-5-[(2R)-6-methylhept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 162871925 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(C)CO)C)C 458.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.003
3-[12-(3-Hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-(6-methylhept-5-en-2-yl)-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 92030288 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.003
3-[4,8-Dimethyl-5-(6-methylhept-5-en-2-yl)-12-prop-1-en-2-yl-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 56664437 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.003
Secaubryenol 16099423 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 456.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.003
Sootepin E 44179870 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)C)C)C 440.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.10.003
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
1-Dehydroxy-23-deoxojessic acid 3008861 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C(=O)O)O)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2003.12.010
1H,10H-Cyclopenta[a]cyclopropa[e]phenanthrene-6-carboxylic acid, 1-[(1R)-1,5-dimethyl-3-oxo-4-hexenyl]tetradecahydro-7-hydroxy-3a,6,12a-trimethyl-, (1R,3aS,3bS,5aR,6S,7S,9aR,10aS,12aR)- 3008859 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C(=O)O)O)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2003.12.010
1H,10H-Cyclopenta[a]cyclopropa[e]phenanthrene-6-carboxylic acid, 1-[(1R)-1,5-dimethyl-4-methylenehexyl]tetradecahydro-7-hydroxy-3a,6,12a-trimethyl-9-oxo-, (1R,3aS,3bS,5aR,6S,7S,9aS,10aS,12aR)- 3008860 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(=O)CC(C5(C)C(=O)O)O)C)C 484.70 unknown https://doi.org/10.1055/S-2004-818951
https://doi.org/10.1016/J.TET.2003.12.010
6-(4,6-Dihydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl)-2-methylhept-2-en-4-one 78297375 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C)O)O)C)C 456.70 unknown https://doi.org/10.1016/J.TET.2003.12.010
6-Hydroxy-7,12,16-trimethyl-15-(6-methyl-4-oxohept-5-en-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 78297376 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C(=O)O)O)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2003.12.010
6-Hydroxy-7,12,16-trimethyl-15-(6-methyl-5-methylideneheptan-2-yl)-4-oxopentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 78297377 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(=O)CC(C5(C)C(=O)O)O)C)C 484.70 unknown https://doi.org/10.1016/J.TET.2003.12.010
6-Hydroxy-7,12,16-trimethyl-15-(6-methyl-5-methylideneheptan-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-7-carboxylic acid 75595916 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C(=O)O)O)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2003.12.010
Thailandiol 3008858 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)C(CC(C5(C)C)O)O)C)C 456.70 unknown https://doi.org/10.1055/S-2004-818951
https://doi.org/10.1016/J.TET.2003.12.010
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-2-(2,3,4,5,6-pentamethoxyphenyl)chromen-4-one 5742692 Click to see COC1=C(C(=C(C(=C1OC)OC)OC)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 404.40 unknown https://doi.org/10.1016/J.TET.2003.12.010
5,7-Dihydroxy-2',3',4',5'-tetramethoxyflavone 5742694 Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC)OC)OC 374.30 unknown https://doi.org/10.1016/J.TET.2003.12.010
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone 5352032 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-2-(2,3,4,5-tetramethoxyphenyl)chromen-4-one 5742693 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3OC)OC)OC)OC)O 388.40 unknown https://doi.org/10.1016/J.TET.2003.12.010
5-Hydroxy-7-methoxy-2-(2,3,4,5,6-pentamethoxyphenyl)chromen-4-one 5742691 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=C(C(=C(C(=C3OC)OC)OC)OC)OC)O 418.40 unknown https://doi.org/10.1016/J.TET.2003.12.010

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