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Gardenia obtusifolia

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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 UUID64403cbcd3103586179195
Scientific name Gardenia obtusifolia
Authority Roxb.
First published in Fl. Brit. India 3: 116 (1880)

Description Top

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Synonyms Top

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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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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
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000971069
Tropicos 100196780
KEW urn:lsid:ipni.org:names:751162-1
The Plant List kew-88356
Open Tree Of Life 241425
NCBI Taxonomy 1233749
IPNI 751162-1
GBIF 5335148
EOL 1103806

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 plant diversity through soil DNA in Thai national parks for influencing land reform and agriculture planning Osathanunkul M, Sawongta N, Pheera W, Pechlivanis N, Psomopoulos F, Madesis P PeerJ 02-Aug-2021
PMCID:PMC8340909
doi:10.7717/peerj.11753
PMID:34414025
Multiple Myeloma Inhibitory Activity of Plant Natural Products Jöhrer K, Ҫiҫek SS Cancers (Basel) 29-May-2021
PMCID:PMC8198565
doi:10.3390/cancers13112678
PMID:34072312
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
Natural Compounds as Modulators of Cell Cycle Arrest: Application for Anticancer Chemotherapies Bailon-Moscoso N, Cevallos-Solorzano G, Romero-Benavides JC, Orellana MI Curr Genomics 01-Apr-2017
PMCID:PMC5345333
doi:10.2174/1389202917666160808125645
PMID:28367072
Sarothrin from Alkanna orientalis is an antimicrobial agent and efflux pump inhibitor Bame JR, Graf TN, Junio HA, Bussey RO III, Jarmusch SA, El-Elimat T, Falkinham JO III, Oberlies NH, Cech RA, Cech NB Planta Med 06-Mar-2013
PMCID:PMC4527991
doi:10.1055/s-0032-1328259
PMID:23468310
Methoxyflavone derivatives modulate the effect of TRAIL-induced apoptosis in human leukemic cell lines Wudtiwai B, Sripanidkulchai B, Kongtawelert P, Banjerdpongchai R J Hematol Oncol 21-Dec-2011
PMCID:PMC3281787
doi:10.1186/1756-8722-4-52
PMID:22185222
Dihydroxypentamethoxyflavone Down-Regulates Constitutive and Inducible Signal Transducers and Activators of Transcription-3 through the Induction of Tyrosine Phosphatase SHP-1 Phromnoi K, Prasad S, Gupta SC, Kannappan R, Reuter S, Limtrakul P, Aggarwal BB Mol Pharmacol 01-Nov-2011
PMCID:PMC3198920
doi:10.1124/mol.111.073676
PMID:21816954
A Novel Pentamethoxyflavone Down-Regulates Tumor Cell Survival and Proliferative and Angiogenic Gene Products through Inhibition of IκB Kinase Activation and Sensitizes Tumor Cells to Apoptosis by Cytokines and Chemotherapeutic Agents Phromnoi K, Reuter S, Sung B, Prasad S, Kannappan R, Yadav VR, Chanmahasathien W, Limtrakul P, Aggarwal BB Mol Pharmacol 01-Feb-2011
PMCID:PMC3033709
doi:10.1124/mol.110.067512
PMID:20930110
Gardenoins E-H, cycloartane triterpenes from the apical buds of Gardenia obtusifolia. Nuanyai T, Sappapan R, Vilaivan T, Pudhom K Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.385
PMID:21372423
A Dihydroxy-pentamethoxyflavone from Gardenia obtusifolia Suppresses Proliferation and Promotes Apoptosis of Tumor Cells Through Modulation of Multiple Cell Signaling Pathways PHROMNOI K, REUTER S, SUNG B, LIMTRAKUL P, AGGARWAL BB Anticancer Res 01-Sep-2010
PMCID:PMC3142747
PMID:20944143
Biological evaluation of plants of Laos used in the treatment of tuberculosis in Lao traditional medicine Elkington BG, Southavong B, Sydara K, Souliya O, Vanthanouvong M, Nettavong K, Thammachack B, Pak DH, Riley MC, Franzblau SG, Soejarto DD Pharm Biol 01-Jan-2009
PMCID:PMC3071617
doi:10.1080/13880200802398002
PMID:21479105
Cytotoxic and anti-HIV-1 constituents of Gardenia obtusifolia and their modified compounds Patoomratana Tuchinda, Wilart Pompimon, Vichai Reutrakul, Manat Pohmakotr, Chalobon Yoosook, Natedao Kongyai, Samaisukh Sophasan, Kulawee Sujarit, Suchart E Upathum, Thawatchai Santisuk Elsevier BV 25-Mar-2003
doi:10.1016/S0040-4020(02)00999-7

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2-Hydroxy-4-methoxy-6-propylbenzoic acid 15595747 Click to see CCCC1=C(C(=CC(=C1)OC)O)C(=O)O 210.23 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3-[(1S,4R,5R,8S,9S,10R,11S,12R,13R)-10,11-dihydroxy-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2R)-1-(4-methylfuran-2-yl)propan-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 163018804 Click to see CC1=COC(=C1)CC(C)C2CCC3(C2(CCC45C3C(C(C(C4(C5)CCC(=O)O)C(=C)CO)O)O)C)C 500.70 unknown https://doi.org/10.1248/CPB.59.385
3-[(1S,4R,5R,8S,9S,12R,13R)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2R)-1-(4-methylfuran-2-yl)propan-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 102484303 Click to see CC1=COC(=C1)CC(C)C2CCC3(C2(CCC45C3CCC(C4(C5)CCC(=O)O)C(=C)CO)C)C 468.70 unknown https://doi.org/10.1248/CPB.59.385
3-[10,11-Dihydroxy-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[1-(4-methylfuran-2-yl)propan-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 75066722 Click to see CC1=COC(=C1)CC(C)C2CCC3(C2(CCC45C3C(C(C(C4(C5)CCC(=O)O)C(=C)CO)O)O)C)C 500.70 unknown https://doi.org/10.1248/CPB.59.385
3-[12-(3-Hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[1-(4-methylfuran-2-yl)propan-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 162966022 Click to see CC1=COC(=C1)CC(C)C2CCC3(C2(CCC45C3CCC(C4(C5)CCC(=O)O)C(=C)CO)C)C 468.70 unknown https://doi.org/10.1248/CPB.59.385
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-[(1S,4R,5R,8S,9S,12R,13R)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2R)-6-methyl-4-oxohept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 86573098 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 470.70 unknown https://doi.org/10.1248/CPB.59.385
3-[12-(3-Hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-(6-methyl-4-oxohept-5-en-2-yl)-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoic acid 162904626 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)O)C(=C)CO)C)C 470.70 unknown https://doi.org/10.1248/CPB.59.385
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/10.1248/CPB.59.385
methyl 3-[(1S,4R,5R,8S,9S,12R,13R)-12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-[(2R)-6-methyl-4-oxohept-5-en-2-yl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate 101201043 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 484.70 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
Methyl 3-[12-(3-hydroxyprop-1-en-2-yl)-4,8-dimethyl-5-(6-methyl-4-oxohept-5-en-2-yl)-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate 163046776 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC(C3(C4)CCC(=O)OC)C(=C)CO)C)C 484.70 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
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/10.1248/CPB.59.385
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-4-oxohept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 101618850 Click to see CC(CC(=O)C=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
5alpha-Cycloarta-24-ene-3,16,23-trione 11037766 Click to see CC(CC(=O)C=C(C)C)C1C(=O)CC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 452.70 unknown https://doi.org/10.1248/CPB.59.385
https://doi.org/10.1016/S0040-4020(02)00999-7
7,7,12,16-Tetramethyl-15-(6-methyl-4-oxohept-5-en-2-yl)pentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,14-dione 85375877 Click to see CC(CC(=O)C=C(C)C)C1C(=O)CC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 452.70 unknown https://doi.org/10.1248/CPB.59.385
https://doi.org/10.1016/S0040-4020(02)00999-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6,8-trimethoxy- 5386960 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)O 360.30 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 330.29 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
Calycopterin 10429470 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC 374.30 unknown https://doi.org/10.1016/S0040-4020(02)00999-7
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown https://doi.org/10.1016/S0040-4020(02)00999-7

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