Calophyllum membranaceum - Unknown
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Internal ID UUID64400eebcb967559700209
Scientific name Calophyllum membranaceum
Authority Gardner & Champ.
First published in Hooker's J. Bot. Kew Gard. Misc. 1: 309 (1849)

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Synonyms Top

Scientific name Authority First published in
Calophyllum bonii Pit. Fl. Indo-Chine 1: 317 (1910)
Calophyllum spectabile Hook. & Arn. Bot. Beechey Voy. 174. 1833 [Oct 1833]
Calophyllum tonkinense Pit. Fl. Indo-Chine 1: 317 (1910)

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Language Common/alternative name
Chinese 横经席
Chinese 横经席叶
Chinese 薄叶红厚壳
Chinese 薄叶红厚壳(薄叶胡桐)
Chinese 小果海棠木
Chinese 独筋猪尾
Chinese 薄叶胡桐
Chinese 跌打将军
Chinese 一种维管植物

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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-0000581228
Tropicos 7801602
KEW urn:lsid:ipni.org:names:427222-1
The Plant List kew-2693390
Open Tree Of Life 847646
NCBI Taxonomy 1009336
IPNI 427222-1
iNaturalist 740813
GBIF 8374262

Genomes (via NCBI) Top

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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
Inhibition of Seizure-Like Paroxysms and Toxicity Effects of Securidaca longepedunculata Extracts and Constituents in Zebrafish Danio rerio Moussavi N, van der Ent W, Diallo D, Sanogo R, Malterud KE, Esguerra CV, Wangensteen H ACS Chem Neurosci 25-Jan-2024
PMCID:PMC10853935
doi:10.1021/acschemneuro.3c00642
PMID:38270158
Biphenyls in Clusiaceae: Isolation, structure diversity, synthesis and bioactivity Wang Y, Huang Q, Zhang L, Zheng C, Xu H Front Chem 01-Dec-2022
PMCID:PMC9751493
doi:10.3389/fchem.2022.987009
PMID:36531325
Recent Advances on Natural Aryl-C-glycoside Scaffolds: Structure, Bioactivities, and Synthesis—A Comprehensive Review Liu CF Molecules 01-Nov-2022
PMCID:PMC9654268
doi:10.3390/molecules27217439
PMID:36364266
Naturally Occurring Calanolides: Occurrence, Biosynthesis, and Pharmacological Properties Including Therapeutic Potential Nahar L, Talukdar AD, Nath D, Nath S, Mehan A, Ismail FM, Sarker SD Molecules 28-Oct-2020
PMCID:PMC7663239
doi:10.3390/molecules25214983
PMID:33126458
Seasonal variations in group leaf characteristics in species with red young leaves Zhang TJ, Tian XS, Liu XT, Huang XD, Peng CL Sci Rep 11-Nov-2019
PMCID:PMC6848096
doi:10.1038/s41598-019-52753-x
PMID:31712569
A Review on the Phytochemistry, Pharmacology, and Pharmacokinetics of Amentoflavone, a Naturally-Occurring Biflavonoid Yu S, Yan H, Zhang L, Shan M, Chen P, Ding A, Li SF Molecules 16-Feb-2017
PMCID:PMC6155574
doi:10.3390/molecules22020299
PMID:28212342
Comparative Proteomic Analyses Provide New Insights into Low Phosphorus Stress Responses in Maize Leaves Zhang K, Liu H, Tao P, Chen H PLoS One 23-May-2014
PMCID:PMC4032345
doi:10.1371/journal.pone.0098215
PMID:24858307
2-Hydr­oxy-1-methoxyxanthen-9-one monohydrate Chen G, Zhao J, Cen C, Han C, Song X Acta Crystallogr Sect E Struct Rep Online 23-Oct-2009
PMCID:PMC2971388
doi:10.1107/S1600536809039348
PMID:21578390
Inhibition of HIV-1 entry by extracts derived from traditional Chinese medicinal herbal plants Park IW, Han C, Song X, Green LA, Wang T, Liu Y, Cen C, Song X, Yang B, Chen G, He JJ BMC Complement Altern Med 05-Aug-2009
PMCID:PMC2736925
doi:10.1186/1472-6882-9-29
PMID:19656383
Selective cyclooxygenase-2 inhibitors from Calophyllum membranaceum. Zou J, Jin D, Chen W, Wang J, Liu Q, Zhu X, Zhao W J Nat Prod 01-Oct-2005
doi:10.1021/NP0502342
PMID:16252917

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 / Benzopyrans / 1-benzopyrans / Pyranochromenes
(3R)-3-[(2S,3R)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]hexanoic acid 162932865 Click to see CCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1021/NP0502342
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 23250748 Click to see CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1021/NP0502342
(3R)-3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]octanoic acid 163030896 Click to see CCCCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 416.50 unknown https://doi.org/10.1021/NP0502342
(3R)-3-[(7S,8R)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]-3-phenylpropanoic acid 38349892 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)O)C4=CC=CC=C4)(C)C)O)C 422.50 unknown https://doi.org/10.1021/NP0502342
3-[(2R,3S)-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-f]chromen-6-yl]hexanoic acid 16077644 Click to see CCCC(CC(=O)O)C1=C2C(=C3C(=C1)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 372.50 unknown https://doi.org/10.1021/NP0502342
3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 3012916 Click to see CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1021/NP0502342
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,8-Dimethoxy-2-hydroxyxanthone 493307 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C=CC(=C3OC)O 272.25 unknown https://doi.org/10.1021/NP0502342
2-Hydroxyxanthone 74708 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C=CC(=C3)O 212.20 unknown https://doi.org/10.1021/NP0502342
2-Methoxy-9H-xanthen-9-one 71034 Click to see COC1=CC2=C(C=C1)OC3=CC=CC=C3C2=O 226.23 unknown https://doi.org/10.1021/NP0502342
2,7-Dihydroxy-1,8-dimethoxyxanthen-9-one 101992985 Click to see COC1=C(C=CC2=C1C(=O)C3=C(O2)C=CC(=C3OC)O)O 288.25 unknown https://doi.org/10.1021/NP0502342
3-Hydroxy-4-methoxyxanthen-9-one 5464639 Click to see COC1=C(C=CC2=C1OC3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1021/NP0502342
3,4-Dihydroxyxanthone 5748382 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C(=C(C=C3)O)O 228.20 unknown https://doi.org/10.1021/NP0502342
4-Hydroxyxanthone 611428 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O 212.20 unknown https://doi.org/10.1021/NP0502342
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(10S)-5-hydroxy-6-[(2S,3S)-3-hydroxy-2-methylbutanoyl]-2,2-dimethyl-10-propan-2-yl-9,10-dihydropyrano[2,3-f]chromen-8-one 154496288 Click to see CC(C)C1CC(=O)OC2=C(C(=C3C=CC(OC3=C12)(C)C)O)C(=O)C(C)C(C)O 388.50 unknown https://doi.org/10.1021/NP0502342

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