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Uvaria hamiltonii

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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 UUID644046c883919610804587
Scientific name Uvaria hamiltonii
Authority Hook.f. & Thomson
First published in Fl. Ind. 1: 96 (1855)

Description Top

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Synonyms Top

Scientific name Authority First published in
Uva hamiltonii Kuntze Revis. Gen. Pl. 1: 7 (1891)

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
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001066584
Tropicos 1602923
KEW urn:lsid:ipni.org:names:75726-1
The Plant List tro-1602923
Open Tree Of Life 941820
NCBI Taxonomy 174975
IPNI 75726-1
iNaturalist 362789
GBIF 3154362
EOL 1054029

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
Aurones: A Golden Resource for Active Compounds Mazziotti I, Petrarolo G, La Motta C Molecules 21-Dec-2021
PMCID:PMC8746708
doi:10.3390/molecules27010002
PMID:35011233
An Overview of the Medicinally Important Plant Type III PKS Derived Polyketides Bisht R, Bhattacharyya A, Shrivastava A, Saxena P Front Plant Sci 14-Oct-2021
PMCID:PMC8551677
doi:10.3389/fpls.2021.746908
PMID:34721474
The total synthesis of an aurone isolated from Uvaria hamiltonii: aurones and flavones as anticancer agents. Lawrence NJ, Rennison D, McGown AT, Hadfield JA Bioorg Med Chem Lett 03-Nov-2003
doi:10.1016/J.BMCL.2003.07.003
PMID:14552774
Aristolactams from the stem bark of Uvaria hamiltonii. Hasan CM, Asha KN, Rashid MA Biochem Syst Ecol 01-Feb-2001
doi:10.1016/S0305-1978(00)00035-1
PMID:11106850
New compounds with DNA strand-scission activity from the combined leaf and stem of Uvaria hamiltonii. Huang L, Wall ME, Wani MC, Navarro H, Santisuk T, Reutrakul V, Seo EK, Farnsworth NR, Kinghorn AD J Nat Prod 01-Apr-1998
doi:10.1021/NP9703609
PMID:9584399

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
> Alkaloids and derivatives / Aristolactams
Aristolactam BII 162739 Click to see COC1=C(C2=C3C(=C1)C(=O)NC3=CC4=CC=CC=C42)OC 279.29 unknown https://doi.org/10.1016/S0305-1978(00)00035-1
Goniopedaline 183523 Click to see COC1=C(C(=C2C3=C1C4=CC=CC=C4C=C3NC2=O)OC)O 295.29 unknown https://doi.org/10.1016/S0305-1978(00)00035-1
Griffithinam 5317823 Click to see COC1=CC=CC2=C3C4=C(C=C21)NC(=O)C4=CC(=C3O)OC 295.29 unknown https://doi.org/10.1016/S0305-1978(00)00035-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-5alpha-cycloarta-3beta,21-diol 71716352 Click to see CC(C)C(=C)CCC(CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 456.70 unknown https://doi.org/10.1016/S0305-1978(00)00035-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(2-Benzoyloxy-1,7-dihydroxy-1,2,9,9a-tetrahydroxanthen-4a-yl)methyl benzoate 85227177 Click to see C1C2C(C(C=CC2(OC3=C1C=C(C=C3)O)COC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)O 472.50 unknown https://doi.org/10.1021/NP9703609
[(1S,2R,4aS,9aR)-2-benzoyloxy-1,7-dihydroxy-1,2,9,9a-tetrahydroxanthen-4a-yl]methyl benzoate 162885031 Click to see C1C2C(C(C=CC2(OC3=C1C=C(C=C3)O)COC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)O 472.50 unknown https://doi.org/10.1021/NP9703609
Hemilxanthene 10672110 Click to see C1C2C(C(C=CC2(OC3=C1C=C(C=C3)O)COC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)O 472.50 unknown https://doi.org/10.1021/NP9703609
> Phenylpropanoids and polyketides / Aurone flavonoids
2-[(3,4-Dihydroxyphenyl)methylidene]-4,5,6-trimethoxy-1-benzofuran-3-one 78201133 Click to see COC1=C(C(=C2C(=C1)OC(=CC3=CC(=C(C=C3)O)O)C2=O)OC)OC 344.30 unknown https://doi.org/10.1021/NP9703609
Hamiltrone 642382 Click to see COC1=C(C(=C2C(=C1)OC(=CC3=CC(=C(C=C3)O)O)C2=O)OC)OC 344.30 unknown https://doi.org/10.1021/NP9703609
https://doi.org/10.1016/J.BMCL.2003.07.003
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-2-(3,4-dihydroxyphenyl)-5,6,7-trimethoxy-2,3-dihydrochromen-4-one 163022219 Click to see COC1=C(C(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)OC)OC 346.30 unknown https://doi.org/10.1021/NP9703609
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-2,3-dihydro-4H-chromen-4-one 245874 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC 330.30 unknown https://doi.org/10.1021/NP9703609
Hamiltone a 44566483 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC 330.30 unknown https://doi.org/10.1021/NP9703609
Hamiltone B 9798295 Click to see COC1=C(C(=C2C(=O)CC(OC2=C1)C3=CC(=C(C=C3)O)O)OC)OC 346.30 unknown https://doi.org/10.1021/NP9703609
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Hamilcone 10688914 Click to see COC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC(=C(C=C2)O)O)OC)OC 346.30 unknown https://doi.org/10.1021/NP9703609

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Collections Top

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