Cratoxylum maingayi - Unknown
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Internal ID UUID644013fca9b92060397773
Scientific name Cratoxylum maingayi
Authority Dyer
First published in Fl. Brit. India 1: 258 (1874)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cratoxylum acuminatum Merr. Pap. Michigan Acad. Sci. 23: 185 (1937 publ. 1938)
Cratoxylum harmandii Pierre Fl. Forest. Cochinch. : t. 53 (1882)
Cratoxylum parvifolium Merr. J. Arnold Arbor. 19: 56 (1938)
Cratoxylum subglaucum Merr. Pap. Michigan Acad. Sci. 23: 186 (1937 publ. 1938)
Cratoxylum thorelii Pierre ex Gagnep. Fl. Indo-Chine , Suppl. 1: 252 (1943)

Common names Top

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Language Common/alternative name
Vietnamese thành ngạnh đỏ

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) 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
    • Indo-China
      • Cambodia
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000625768
Tropicos 100317400
KEW urn:lsid:ipni.org:names:433063-1
The Plant List kew-2742425
Open Tree Of Life 958801
NCBI Taxonomy 271750
IUCN Red List 33937
IPNI 433063-1
iNaturalist 191029
GBIF 3711990
Freebase /m/02w0f4g
Wikipedia Cratoxylum_maingayi
CMAUP NPO7665

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
Characterization of the plastid genome of Cratoxylum species (Hypericaceae) and new insights into phylogenetic relationships Sudmoon R, Kaewdaungdee S, Tanee T, Siripiyasing P, Ameamsri U, Syazwan SA, Lee SY, Chaveerach A Sci Rep 05-Nov-2022
PMCID:PMC9637187
doi:10.1038/s41598-022-23639-2
PMID:36335203
Antiplasmodial activity of some phenolic compounds from Cameroonians Allanblackia Azebaze AG, Teinkela JE, Nguemfo EL, Valentin A, Dongmo AB, Vardamides JC Afr Health Sci 01-Sep-2015
PMCID:PMC4765459
doi:10.4314/ahs.v15i3.18
PMID:26957972
Cratoxylum formosum (Jack) Dyer ssp. pruniflorum (Kurz) Gogel. (Hóng yá mù) extract induces apoptosis in human hepatocellular carcinoma HepG2 cells through caspase-dependent pathways Nonpunya A, Weerapreeyakul N, Barusrux S Chin Med 07-Apr-2014
PMCID:PMC3985586
doi:10.1186/1749-8546-9-12
PMID:24708784
Antiplasmodial Natural Products Nogueira CR, Lopes LM Molecules 04-Mar-2011
PMCID:PMC6259672
doi:10.3390/molecules16032146
Antimalarial and cytotoxic phenolic compounds from Cratoxylum maingayi and Cratoxylum cochinchinense. Laphookhieo S, Maneerat W, Koysomboon S Molecules 30-Mar-2009
PMCID:PMC6254373
doi:10.3390/MOLECULES14041389
PMID:19384270
Antimalarial and Cytotoxic Phenolic Compounds from Cratoxylum maingayi and Cratoxylum cochinchinense Laphookhieo S, Maneerat W, Koysomboon S Molecules 30-Mar-2009
PMCID:PMC6254373
doi:10.3390/molecules14041389
PMID:19384270
Xanthones from Cratoxylum maingayi Maria José, Anake Kijjoa, T.G Gonzalez, Madalena M.M Pinto, Ana M Damas, Ing-on Mondranondra, Artur M.S Silva, Werner Herz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00381-1

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
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
2-[(6,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73323444 Click to see CC1(C(CC2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 348.34 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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 via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Allitol 120700 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,7-Dihydroxy-4-methoxyxanthone 5465785 Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(O2)C=CC(=C3)O 258.23 unknown https://doi.org/10.1016/S0031-9422(98)00381-1
2,8-Dihydroxy-1-methoxyxanthone 5464640 Click to see COC1=C(C=CC2=C1C(=O)C3=C(C=CC=C3O2)O)O 258.23 unknown https://doi.org/10.1016/S0031-9422(98)00381-1
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/S0031-9422(98)00381-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
(2S)-5,9,10-trihydroxy-1,1,2-trimethyl-4-(3-methylbut-2-enyl)-2H-furo[2,3-c]xanthen-6-one 11859088 Click to see CC1C(C2=C(O1)C(=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)CC=C(C)C)(C)C 396.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
gerontoxanthone I 14412270 Click to see CC(=CCC1=C(C2=C(C(=C1O)C(C)(C)C=C)OC3=C(C2=O)C=CC(=C3O)O)O)C 396.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Macluraxanthone 5281646 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C 394.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/

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