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Calophyllum austroindicum

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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 UUID64400ee2d1c3a735428437
Scientific name Calophyllum austroindicum
Authority Kosterm. ex P.F.Stevens
First published in J. Arnold Arbor. 61: 250 (1980)

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
    • Indo-China
      • Andaman Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000581040
Tropicos 100303655
KEW urn:lsid:ipni.org:names:169541-1
The Plant List kew-2693214
Open Tree Of Life 6098946
IPNI 169541-1
EOL 5710025
Wikipedia Calophyllum_austroindicum

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)!
Title Authors Publication Released IDs
Occurrence of Xanthonolignoids in Guttifereous Plants Munekazu Iinuma, Hideki Tosa, Toshiyuki Tanaka, Tetsuro Ito, Sigetomo Yonemori, Veliah Chelladurai, Mohammad Aquil, Yoshikazu Takahashi, Hiroshi Naganawa The Japan Institute of Heterocyclic Chemistry 31-Mar-2009
doi:10.3987/COM-96-7497
Six xanthones from Calophyllum austroindicum Munekazu Iinuma, Hideki Tosa, Naeko Toriyama, Toshiyuki Tanaka, Tetsuro Ito, V. Chelladurai Elsevier BV 01-May-2003
doi:10.1016/0031-9422(96)00323-8

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
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2R,3R)-10-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-5,8-dimethoxy-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one 101989187 Click to see COC1=CC(=CC2=C1C(=O)C3=CC(=C4C(=C3O2)OC(C(O4)C5=CC(=C(C=C5)O)OC)CO)OC)O 482.40 unknown https://doi.org/10.3987/COM-96-7497
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-7-methoxyxanthone 12214329 Click to see COC1=CC2=C(C=C1)OC3=CC=CC(=C3C2=O)O 242.23 unknown https://doi.org/10.1016/0031-9422(96)00323-8
6-(2,3-Dihydroxy-3-methylbutyl)-1,5-dihydroxyxanthen-9-one 85700963 Click to see CC(C)(C(CC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)O)O)O 330.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
6-(3,3-Dimethylallyl)-1,5-dihydroxyxanthone 5281624 Click to see CC(=CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)O)C 296.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
7-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-c]xanthen-6-one 5464637 Click to see CC(C)(C1CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)O 312.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1016/0031-9422(96)00323-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(3R)-3,8-dihydroxy-2,2,3-trimethyl-4H-pyrano[3,2-c]xanthen-7-one 5464638 Click to see CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)(C)O)C 326.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
3,8-Dihydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 102003040 Click to see CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)O)C 312.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
Dehydrocycloguanandin 5281625 Click to see CC1(C=CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)C 294.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown https://doi.org/10.1016/0031-9422(96)00323-8

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