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Gonocaryum calleryanum

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 UUID64401e7ad8a9b811926562
Scientific name Gonocaryum calleryanum
Authority (Baill.) Becc.
First published in Malesia 1: 123 (1877)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Gonocaryum diospyrosifolia Hayata Icon. Pl. Formosan. 2: 106 (1912)
Gonocaryum tarlacense S.Vidal Sin. Gen. Pl. Leños. Filip. , Atlas: xx, t. 30, f. C (1883)
Gonocaryum teysmannianum Scheff. Ann. Jard. Bot. Buitenzorg 1: 98 (1876)
Phlebocalymna calleryana Baill. Adansonia 9: 147 (1868)

Common names Top

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Language Common/alternative name
Chinese 台湾琼榄
Chinese 柿葉茶茱萸
Chinese 柿叶茶茱萸

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000706698
Tropicos 50053443
KEW urn:lsid:ipni.org:names:434330-1
The Plant List kew-2829883
Open Tree Of Life 6055605
NCBI Taxonomy 2306983
IPNI 434330-1
iNaturalist 736424
GBIF 3597176
EOL 2888917

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
Secoiridoids from the Seed of Gonocaryum calleryanum and Their Inhibitory Potential on LPS-Induced Tumor Necrosis Factor and Nitric Oxide Production Cheng KC, Chang CI, Lin YC, Liu CI, Zeng YC, Lin YS Molecules 04-Jul-2018
PMCID:PMC6100119
doi:10.3390/molecules23071633
PMID:29973552
In Vitro and In Silico Antidiabetic and Antimicrobial Evaluation of Constituents from Kickxia ramosissima (Nanorrhinum ramosissimum) Amin A, Tuenter E, Foubert K, Iqbal J, Cos P, Maes L, Exarchou V, Apers S, Pieters L Front Pharmacol 01-May-2017
PMCID:PMC5410595
doi:10.3389/fphar.2017.00232
PMID:28507520
A secoiridoid and other constituents of Gonocaryum calleryanum Yu Yi Chan, Yann Lii Leu, Ful Wen Lin, Chia Ying Li, You Cheng Wu, Li Shian Shi, Meei Jen Liou, Tian Shung Wu Elsevier BV 28-Dec-2002
doi:10.1016/S0031-9422(98)80075-7
Secoiridoid and flavonoid glycosides from Gonocaryum calleryanum Tetsuo Kaneko, Mayumi Sakamoto, Kazuhiro Ohtani, Aiko Ito, Ryoji Kasai, Kazuo Yamasaki, William G. Padorina Elsevier BV 26-Jul-2002
doi:10.1016/0031-9422(94)00884-V
A secoiridoid and other constituents of gonocaryum calleryanum Y Yu Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00690-0

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 / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
https://doi.org/10.1016/S0031-9422(98)80075-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-[(2R,3S,4S)-5-methoxycarbonyl-3-[(1S)-1-[(E)-2-methylbut-2-enoyl]oxyethyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetic acid 162904990 Click to see 504.50 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
2-[(2S,3S,4S)-5-methoxycarbonyl-3-[(1S)-1-[(E)-2-methylbut-2-enoyl]oxyethyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetic acid 101756908 Click to see 504.50 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
(3S,4aS,6aR,6aR,6bR,8aR,11R,12S,12aR,14aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,10,11,12,12a,14a-tetradecahydro-1H-picen-3-ol 163023159 Click to see CC1CCC2(CCC3(C(C2C1C)C=CC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 51892422 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 14010964 Click to see 484.80 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
[(3S,6aR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 5318302 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
10-Acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 619165 Click to see 498.70 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
3-O-Acetylerythrodiol 118796402 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C 484.80 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
https://doi.org/10.1016/S0031-9422(98)80075-7
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,4S,5S,8aS,12S,12aS)-4-hydroxy-1,4,5-trimethyl-3,7-dioxo-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,8,8a,12,12a-hexahydropyrano[3,4-g][1,5]dioxecine-9-carboxylic acid 101921661 Click to see 506.50 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
https://doi.org/10.1016/0031-9422(94)00884-V
https://doi.org/10.1016/S0031-9422(98)80075-7
methyl (1S,4S,5S,8aS,12S,12aS)-4-hydroxy-1,4,5-trimethyl-3,7-dioxo-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,8,8a,12,12a-hexahydropyrano[3,4-g][1,5]dioxecine-9-carboxylate 101921660 Click to see CC1C2C(CC(=O)OC(C(C(=O)O1)(C)O)C)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 520.50 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
https://doi.org/10.1016/S0031-9422(98)80075-7
https://doi.org/10.1016/0031-9422(94)00884-V
methyl (1S,8aS,12S,12aS)-4-hydroxy-4-(hydroxymethyl)-1,5-dimethyl-3,7-dioxo-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,8,8a,12,12a-hexahydropyrano[3,4-g][1,5]dioxecine-9-carboxylate 101921662 Click to see 536.50 unknown https://doi.org/10.1016/0031-9422(94)00884-V
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1016/S0031-9422(98)80075-7
https://doi.org/10.1016/S0031-9422(97)00690-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(97)00690-0
> 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/10.1016/0031-9422(94)00884-V
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(94)00884-V
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(94)00884-V
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(94)00884-V
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown https://doi.org/10.1016/0031-9422(94)00884-V

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