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Fagraea blumei

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64401c13e4975521247350
Scientific name Fagraea blumei
Authority G.Don
First published in Gen. Hist. 4: 69 (1837)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Fagraea intermedia Ridl. J. Fed. Malay States Mus. 8(4): 63 (1917)
Fagraea leschenaultii Blume Rumphia 2: 30 (1838)
Fagraea obovata-javana Blume Rumphia 2: 29 (1838)
Fagraea spatiosa S.Moore J. Bot. 63(Suppl.): 69 (1925)
Fagraea vaginata King & Gamble J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 74: 610 (1908)
Fagraea obovata Blume Bijdr. Fl. Ned. Ind. : 1021 (1826)

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

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- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000685529
Tropicos 100336431
KEW urn:lsid:ipni.org:names:546103-1
The Plant List kew-2807375
Open Tree Of Life 6069529
IPNI 546103-1
GBIF 4020459

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
Phytochemical Study of Fagraea spp. Uncovers a New Terpene Alkaloid with Anti-Inflammatory Properties Suciati, Lynette K. Lambert, Benjamin P. Ross, Myrna A. Deseo, Mary J. Garson CSIRO Publishing 17-Apr-2011
doi:10.1071/CH10421
Iridoid Glucosides with Free Radical Scavenging Properties from <i>Fagraea blumei</i> Muriel Cuendet, Kurt Hostettmann, Olivier Potterat, Wahjo Dyatmiko Wiley 28-Dec-2004
doi:10.1002/HLCA.19970800411

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
> Lignans, neolignans and related compounds / Furanoid lignans
(+-)-Pinoresinol 234817 Click to see 358.40 unknown https://doi.org/10.1071/CH10421
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1071/CH10421
> Lignans, neolignans and related compounds / Lignan lactones
(3aR,4S,6aR)-4-(4-hydroxy-3-methoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan-1-one 10955962 Click to see COC1=C(C=CC(=C1)C2C3COC(=O)C3CO2)O 250.25 unknown https://doi.org/10.1071/CH10421
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1R,4aR,7R,7aR)-7-[(4-carboxy-2-hydroxybenzoyl)oxymethyl]-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 162997008 Click to see C1CC2C(C1COC(=O)C3=C(C=C(C=C3)C(=O)O)O)C(OC=C2C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 540.50 unknown https://doi.org/10.1002/HLCA.19970800411
(1R,4aR,7R,7aR)-7-[(4-carboxy-2,5-dihydroxybenzoyl)oxymethyl]-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 163011469 Click to see 556.50 unknown https://doi.org/10.1002/HLCA.19970800411
(1R,4aR,7R,7aR)-7-[[4-[[(1R,4aR,7R,7aR)-4-carboxy-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl]methoxycarbonyl]-2,5-dihydroxybenzoyl]oxymethyl]-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 162997011 Click to see C1CC2C(C1COC(=O)C3=CC(=C(C=C3O)C(=O)OCC4CCC5C4C(OC=C5C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C(OC=C2C(=O)O)OC7C(C(C(C(O7)CO)O)O)O 914.80 unknown https://doi.org/10.1002/HLCA.19970800411
(1R,4aR,7R,7aR)-7-[[4-[[(1R,4aR,7R,7aR)-4-carboxy-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl]methoxycarbonyl]-3-hydroxybenzoyl]oxymethyl]-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 163005924 Click to see C1CC2C(C1COC(=O)C3=CC(=C(C=C3)C(=O)OCC4CCC5C4C(OC=C5C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C(OC=C2C(=O)O)OC7C(C(C(C(O7)CO)O)O)O 898.80 unknown https://doi.org/10.1002/HLCA.19970800411
(1S)-1alpha-(beta-D-Glucopyranosyloxy)-1,4aalpha,5,6,7,7aalpha-hexahydro-7alpha-(hydroxymethyl)cyclopenta[c]pyran-4alpha-carboxylic acid methyl ester 13892715 Click to see COC(=O)C1=COC(C2C1CCC2CO)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown https://doi.org/10.1071/CH10421
7-(Hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 13892716 Click to see 376.36 unknown https://doi.org/10.1071/CH10421
7-[(4-Carboxy-2-hydroxybenzoyl)oxymethyl]-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 73808980 Click to see C1CC2C(C1COC(=O)C3=C(C=C(C=C3)C(=O)O)O)C(OC=C2C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 540.50 unknown https://doi.org/10.1002/HLCA.19970800411
7-[(4-Carboxy-2,5-dihydroxybenzoyl)oxymethyl]-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 73808978 Click to see C1CC2C(C1COC(=O)C3=C(C=C(C(=C3)O)C(=O)O)O)C(OC=C2C(=O)O)OC4C(C(C(C(O4)CO)O)O)O 556.50 unknown https://doi.org/10.1002/HLCA.19970800411
7-[[4-[[4-Carboxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl]methoxycarbonyl]-2,5-dihydroxybenzoyl]oxymethyl]-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 73808979 Click to see 914.80 unknown https://doi.org/10.1002/HLCA.19970800411
7-[[4-[[4-Carboxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-7-yl]methoxycarbonyl]-3-hydroxybenzoyl]oxymethyl]-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 85166099 Click to see C1CC2C(C1COC(=O)C3=CC(=C(C=C3)C(=O)OCC4CCC5C4C(OC=C5C(=O)O)OC6C(C(C(C(O6)CO)O)O)O)O)C(OC=C2C(=O)O)OC7C(C(C(C(O7)CO)O)O)O 898.80 unknown https://doi.org/10.1002/HLCA.19970800411
Adoxoside 11079666 Click to see 390.40 unknown https://doi.org/10.1071/CH10421
Adoxosidic acid 13892717 Click to see C1CC2C(C1CO)C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 376.36 unknown https://doi.org/10.1071/CH10421
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 13965334 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CO 346.33 unknown https://doi.org/10.1071/CH10421
https://doi.org/10.1002/HLCA.19970800411
Di-O-Methylcrenatin 10736338 Click to see 346.33 unknown https://doi.org/10.1071/CH10421
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5-Hydroxy-2-(4-Hydroxyphenyl)-7-Methoxy-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 369636 Click to see 446.40 unknown https://doi.org/10.1002/HLCA.19970800411
Swertisin 124034 Click to see 446.40 unknown https://doi.org/10.1002/HLCA.19970800411

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