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Gardenia resinifera

Gardenia resinifera - 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 UUID64403cc0a0bab591847327
Scientific name Gardenia resinifera
Authority Roth
First published in Nov. Pl. Sp. : 150 (1821)

Description Top

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Synonyms Top

Scientific name Authority First published in
Gardenia lucida Roxb. Fl. Ind. 2: 553 (1824)
Genipa resinifera Baill. Hist. Pl. 7: 380 (1880)

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
    • Indian Subcontinent
      • Bangladesh
      • India
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000971125
UNII 0W075E2682
Tropicos 50290078
KEW urn:lsid:ipni.org:names:751215-1
The Plant List kew-88409
Open Tree Of Life 583491
NCBI Taxonomy 1288015
IPNI 751215-1
iNaturalist 489316
GBIF 5334965
EOL 1104509
USDA GRIN 103296

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
Drosophila melanogaster as a Translational Model System to Explore the Impact of Phytochemicals on Human Health Lopez-Ortiz C, Gracia-Rodriguez C, Belcher S, Flores-Iga G, Das A, Nimmakayala P, Balagurusamy N, Reddy UK Int J Mol Sci 29-Aug-2023
PMCID:PMC10487418
doi:10.3390/ijms241713365
PMID:37686177
Synergistic and antibiofilm potential of Curcuma aromatica derived silver nanoparticles in combination with antibiotics against multidrug-resistant pathogens Tawre MS, Shiledar A, Satpute SK, Ahire K, Ghosh S, Pardesi K Front Chem 09-Nov-2022
PMCID:PMC9682076
doi:10.3389/fchem.2022.1029056
PMID:36438875
Medicinal and edible plants in the treatment of dyslipidemia: advances and prospects Hu Y, Chen X, Hu M, Zhang D, Yuan S, Li P, Feng L Chin Med 29-Sep-2022
PMCID:PMC9522446
doi:10.1186/s13020-022-00666-9
PMID:36175900
Neuroprotective Drug Discovery From Phytochemicals and Metabolites for CNS Viral Infection: A Systems Biology Approach With Clinical and Imaging Validation Bhattacharjee A, Purohit P, Roy PK Front Neurosci 25-Jul-2022
PMCID:PMC9358258
doi:10.3389/fnins.2022.917867
PMID:35958991
Synthesis of gallotannin capped iron oxide nanoparticles and their broad spectrum biological applications Ahmed B, Syed A, Ali K, Elgorban AM, Khan A, Lee J, AL-Shwaiman HA RSC Adv 08-Mar-2021
PMCID:PMC8695504
doi:10.1039/d1ra00220a
PMID:35423492
GardeninA confers neuroprotection against environmental toxin in a Drosophila model of Parkinson’s disease Maitra U, Harding T, Liang Q, Ciesla L Commun Biol 05-Feb-2021
PMCID:PMC7864937
doi:10.1038/s42003-021-01685-2
PMID:33547411
A green approach for the synthesis of α-Fe2O3 nanoparticles from Gardenia resinifera plant and it's In vitro hyperthermia application Karade VC, Parit SB, Dawkar VV, Devan RS, Choudhary RJ, Kedge VV, Pawar NV, Kim JH, Chougale AD Heliyon 10-Jul-2019
PMCID:PMC6625971
doi:10.1016/j.heliyon.2019.e02044
PMID:31338465
Flavonoids of Ascarina lucida Douglas E. Soltis, Bruce A. Bohm American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50022A009
7-keto-octadec-cis-11-enoic acid from Gardenia lucida seed oil Chirag Mahmood, Jehan D. Daulatabad, Gouse Mohaddin M. Mulla, Abdurrazzaque M. Mirajkar, Kallappa M. Hosamani Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)83659-9

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
9-Octadecenoic acid 965 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1016/0031-9422(91)83659-9
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1016/0031-9422(91)83659-9
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1016/0031-9422(91)83659-9
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1016/0031-9422(91)83659-9
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
7-Keto-11c-octadecenoic acid 14861231 Click to see CCCCCCC=CCCCC(=O)CCCCCC(=O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)83659-9
7-Oxooctadec-11-enoic acid 85700135 Click to see CCCCCCC=CCCCC(=O)CCCCCC(=O)O 296.40 unknown https://doi.org/10.1016/0031-9422(91)83659-9
9,12-Octadecadienoic acid 3931 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/0031-9422(91)83659-9
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1016/0031-9422(91)83659-9
> 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/10.1021/NP50022A009
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP50022A009
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Acerosin 177696 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O 360.30 unknown https://doi.org/10.1021/NP50022A009
Demethoxysudachitin 3083845 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1021/NP50022A009
Gardenin A 261859 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 418.40 unknown https://doi.org/10.1021/NP50022A009
Gardenin B 96539 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O 358.30 unknown https://doi.org/10.1021/NP50022A009
Gardenin E 3084508 Click to see COC1=C(C=C(C=C1O)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O 390.30 unknown https://doi.org/10.1021/NP50022A009
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1021/NP50022A009

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