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Gardenia carinata

Gardenia carinata - 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 UUID64403cb0433c3703393559
Scientific name Gardenia carinata
Authority Wall.
First published in Fl. Ind. 2: 560 (1824)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Indonesian cempaka hutan (pohon)
Indonesian cempaka hutan
Malay pokok cempaka hutan
Malay cempaka hutan
Malay jambu batu paya
Malay kepayang air
Malay sempedu burung
Malay randa
Thai พุดน้ำบุษย์
Chinese 龙骨栀子

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-0000970838
Tropicos 100196624
KEW urn:lsid:ipni.org:names:750947-1
The Plant List kew-88143
Open Tree Of Life 241432
NCBI Taxonomy 1233747
IPNI 750947-1
iNaturalist 372063
GBIF 5334934
EOL 1102533
USDA GRIN 71024

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
Bioassay-Guided Fractionation of Erythrostemon yucatanensis (Greenm.) Gagnon & GP Lewis Components with Anti-hemagglutinin Binding Activity against Influenza A/H1N1 Virus Ortiz-López T, Borges-Argáez R, Ayora-Talavera G, Canto-Ramírez E, Cetina-Montejo L, May-May Á, Escalante-Erosa F, Cáceres-Farfán M Molecules 26-Aug-2022
PMCID:PMC9458041
doi:10.3390/molecules27175494
PMID:36080262
Natural Products with Inhibitory Activity against Human Immunodeficiency Virus Type 1 Serna-Arbeláez MS, Florez-Sampedro L, Orozco LP, Ramírez K, Galeano E, Zapata W Adv Virol 29-May-2021
PMCID:PMC8181102
doi:10.1155/2021/5552088
PMID:34194504
Recent advances in natural anti-HIV triterpenoids and analogues Wu HF, Morris-Natschke SL, Xu XD, Yang MH, Cheng YY, Yu SS, Lee KH Med Res Rev 14-Jul-2020
PMCID:PMC7554103
doi:10.1002/med.21708
PMID:32666531
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
Ecological connectivity networks in rapidly expanding cities Nor AN, Corstanje R, Harris JA, Grafius DR, Siriwardena GM Heliyon 23-Jun-2017
PMCID:PMC5486437
doi:10.1016/j.heliyon.2017.e00325
PMID:28706999
Mosquito larvicidal potential of four common medicinal plants of India Rawani A, Ghosh A, Chandra G Indian J Med Res 01-Jul-2014
PMCID:PMC4181141
PMID:25222784
DNA topoisomerase IIα inhibitory and anti-HIV-1 flavones from leaves and twigs of Gardenia carinata. Kongkum N, Tuchinda P, Pohmakotr M, Reutrakul V, Piyachaturawat P, Jariyawat S, Suksen K, Yoosook C, Kasisit J, Napaswad C Fitoterapia 01-Mar-2012
doi:10.1016/J.FITOTE.2011.11.015
PMID:22155186

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
2-(2,5-Dihydroxy-3,4-dimethoxy-phenyl)-5,7-dihydroxy-6-methoxy-chromen-4-one 57336046 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C(=C3O)OC)OC)O)O 376.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
3',5,5',7-Tetrahydroxy-4',6-dimethoxyflavone 10337658 Click to see COC1=C(C=C(C=C1O)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 346.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(2,5-Dihydroxy-3,4-dimethoxy-phenyl)-5-hydroxy-7-methoxy-chromen-4-one 57336045 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3O)OC)OC)O)O 360.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
2-(2,5-Dihydroxy-3,4-dimethoxyphenyl)-5-hydroxy-6,7-dimethoxychromen-4-one 123958045 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3O)OC)OC)O)O)OC 390.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
5-Hydroxy-2-(2-hydroxy-3,4,5-trimethoxy-phenyl)-7-methoxy-chromen-4-one 57336044 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C(=C3O)OC)OC)OC)O 374.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015
5-Hydroxy-2-(3-hydroxy-4,5-dimethoxyphenyl)-6,7-dimethoxychromen-4-one 183329 Click to see COC1=CC(=CC(=C1OC)O)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 374.30 unknown https://doi.org/10.1016/J.FITOTE.2011.11.015

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