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Cratoxylum sumatranum

Cratoxylum sumatranum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644013fcb63fa168552866
Scientific name Cratoxylum sumatranum
Authority (Jack) Blume
First published in Ann. Mus. Bot. Lugduno-Batavi 2: 16 (1856)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cratoxylum hornschuchii Blume Verh. Batav. Genootsch. Kunsten 9: 174. 1823 (1823)
Elodes sumatrana Jack Malayan Misc. 2(n. vII): 22. 1822

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Cratoxylum sumatranum subsp. blancoi (Blume) Gogelein Blumea 15: 463 (1967)
Cratoxylum sumatranum subsp. neriifolium (Kurz) Gogelein Blumea 15: 463 (1967)
Cratoxylum sumatranum subsp. sumatranum Unknown

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000625785
Tropicos 50277009
KEW urn:lsid:ipni.org:names:433074-1
The Plant List kew-2742440
Open Tree Of Life 6101310
NCBI Taxonomy 2516474
IUCN Red List 135803484
IPNI 433074-1
GBIF 3711894
Freebase /m/0hzrb3q
Wikipedia Cratoxylum_sumatranum

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
Water-use characteristics of Syzygium antisepticum and Adinandra integerrima in a secondary forest of Khao Yai National Park in Thailand with implications for environmental management Ampornpitak R, Nathalang A, Tor-ngern P PeerJ 30-Nov-2023
PMCID:PMC10693818
doi:10.7717/peerj.16525
PMID:38050611
Targeting SARS-CoV-2 Non-Structural Proteins Tam D, Lorenzo-Leal AC, Hernández LR, Bach H Int J Mol Sci 20-Aug-2023
PMCID:PMC10455537
doi:10.3390/ijms241613002
PMID:37629182
The history and current epidemiology of malaria in Kalimantan, Indonesia Sugiarto SR, Baird JK, Singh B, Elyazar I, Davis TM Malar J 14-Nov-2022
PMCID:PMC9661770
doi:10.1186/s12936-022-04366-5
PMID:36372877
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
Natural Enantiomers: Occurrence, Biogenesis and Biological Properties Yu JH, Yu ZP, Capon RJ, Zhang H Molecules 14-Feb-2022
PMCID:PMC8880303
doi:10.3390/molecules27041279
PMID:35209066
Ethnobotanical Documentation of Medicinal Plants Used by the Indigenous Panay Bukidnon in Lambunao, Iloilo, Philippines Cordero CS, Meve U, Alejandro GJ Front Pharmacol 10-Jan-2022
PMCID:PMC8784692
doi:10.3389/fphar.2021.790567
PMID:35082673
Antibacterial activities of plant-derived xanthones Liu X, Shen J, Zhu K RSC Med Chem 21-Dec-2021
PMCID:PMC8864485
doi:10.1039/d1md00351h
PMID:35308024
Cytotoxic and Anti-Inflammatory Activities of Dihydroisocoumarin and Xanthone Derivatives from Garcinia picrorhiza Sukandar ER, Kaennakam S, Raab P, Nöst X, Rassamee K, Bauer R, Siripong P, Ersam T, Tip-pyang S, Chavasiri W Molecules 01-Nov-2021
PMCID:PMC8587515
doi:10.3390/molecules26216626
PMID:34771035
Quantitative ethnopharmacological documentation and molecular confirmation of medicinal plants used by the Manobo tribe of Agusan del Sur, Philippines Dapar ML, Alejandro GJ, Meve U, Liede-Schumann S J Ethnobiol Ethnomed 05-Mar-2020
PMCID:PMC7227330
doi:10.1186/s13002-020-00363-7
PMID:32138749
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
New Xanthones from the Barks of Cratoxylum sumatranum ssp. neriifolium Worrapong Phupong, Warraphong Nuangnaowarat, Masahiko Isaka The Japan Institute of Heterocyclic Chemistry 31-Aug-2010
doi:10.3987/COM-10-11994
Engineering Plant Shikimate Pathway for Production of Tocotrienol and Improving Herbicide Resistance Rippert P, Scimemi C, Dubald M, Matringe M Plant Physiol 01-Jan-2004
PMCID:PMC316290
doi:10.1104/pp.103.032441
PMID:14684842
Cytotoxic prenylated xanthones and the unusual compounds anthraquinobenzophenones from Cratoxylum sumatranum. Seo EK, Kim NC, Wani MC, Wall ME, Navarro HA, Burgess JP, Kawanishi K, Kardono LB, Riswan S, Rose WC, Fairchild CR, Farnsworth NR, Kinghorn AD J Nat Prod 01-Mar-2002
doi:10.1021/NP010395F
PMID:11908969

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 / Anthracenes / Anthraquinones
2-[(1R)-1-[3-benzoyl-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-2,4-dihydroxyphenyl]-3-methylbutyl]-1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione 636862 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C(CC(C)C)C4=C(C=C(C(=C4O)C(=O)C5=CC=CC=C5)O)OCC=C(C)CCC=C(C)C)O 718.80 unknown https://doi.org/10.1021/NP010395F
2-[(1S,3S)-1-[3-benzoyl-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-2,4-dihydroxyphenyl]-3,7-dimethyloct-6-enyl]-1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione 162970467 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C(CC(C)CCC=C(C)C)C4=C(C=C(C(=C4O)C(=O)C5=CC=CC=C5)O)OCC=C(C)CCC=C(C)C)O 786.90 unknown https://doi.org/10.1021/NP010395F
Cratoxyarborequinone B 11967184 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)C(CC(C)CCC=C(C)C)C4=C(C=C(C(=C4O)C(=O)C5=CC=CC=C5)O)OCC=C(C)CCC=C(C)C)O 786.90 unknown https://doi.org/10.1021/NP010395F
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
1-Dehydroxybaccatin IV 21679297 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 636.70 unknown https://doi.org/10.1021/NP010395F
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
delta-Tocotrienol 5282350 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O 396.60 unknown https://doi.org/10.1021/NP010395F
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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 https://doi.org/10.1021/NP010395F
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2R)-5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-1,2-dihydrofuro[2,3-c]xanthen-6-one 163191216 Click to see CC(C)(C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC=C4O)O)O 328.30 unknown https://doi.org/10.3987/COM-10-11994
(2R)-5,9-dihydroxy-10-methoxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 102414484 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4OC)O)O)(C)C 342.30 unknown https://doi.org/10.3987/COM-10-11994
(2S)-5,10-dihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 162995704 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC=C4O)O)(C)C 312.30 unknown https://doi.org/10.3987/COM-10-11994
1,3,6-Trihydroxy-5-methoxy-4-(2-methylbut-3-en-2-yl)xanthen-9-one 102042409 Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3OC)O)O)O 342.30 unknown https://doi.org/10.3987/COM-10-11994
5,10-Dihydroxy-2-(2-hydroxypropan-2-yl)-1,2-dihydrofuro[2,3-c]xanthen-6-one 15705039 Click to see CC(C)(C1CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC=C4O)O)O 328.30 unknown https://doi.org/10.3987/COM-10-11994
5,9-Dihydroxy-10-methoxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 10641036 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4OC)O)O)(C)C 342.30 unknown https://doi.org/10.3987/COM-10-11994
Cratoxyarborenone F 10061042 Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(O2)C=C(C=C3)O 258.23 unknown https://doi.org/10.1021/NP010395F
isocudraniaxanthone A 10687703 Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)O 328.30 unknown https://doi.org/10.3987/COM-10-11994
Pancixanthone A 10852567 Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC=C3O)O)O 312.30 unknown https://doi.org/10.3987/COM-10-11994
Pancixanthone B 10519161 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC=C4O)O)(C)C 312.30 unknown https://doi.org/10.3987/COM-10-11994
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
5-O-Methylxanthone V1 12178329 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC(=C4OC)O)O)C=CC(O2)(C)C)C 408.40 unknown https://doi.org/10.3987/COM-10-11994
Cratoxyarborenone E 5323543 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=CC(=C(C(=C3O2)CC=C(C)C)OC)O)C 410.50 unknown https://doi.org/10.1021/NP010395F
Trapezifolixanthone 188341 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C 378.40 unknown https://doi.org/10.3987/COM-10-11994
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2R)-4,7,8,9-tetrahydroxy-6-(3-methylbut-2-enyl)-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-b]xanthen-5-one 162899667 Click to see CC(=CCC1=C2C(=C(C(=C1O)O)O)OC3=CC4=C(CC(O4)C(=C)C)C(=C3C2=O)O)C 410.40 unknown https://doi.org/10.1021/NP010395F
8-(3,7-Dimethylocta-2,6-dienyl)-1,3,5,7-tetrahydroxy-2-(3-methylbut-2-enyl)xanthen-9-one 85122962 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C)C 464.50 unknown https://doi.org/10.1021/NP010395F
Beta-Mangostin 5495925 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)OC)O)OC)C 424.50 unknown https://doi.org/10.3987/COM-10-11994
Cratoxyarborenone A 10367180 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C)C 464.50 unknown https://doi.org/10.1021/NP010395F
Cratoxyarborenone B 10475842 Click to see CC(=CCC1=C2C(=C(C=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)C 396.40 unknown https://doi.org/10.1021/NP010395F
Cratoxyarborenone C 10342293 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C=C(C(=C3C2=O)CC=C(C)C)OC)OC)O)C 424.50 unknown https://doi.org/10.1021/NP010395F
Cratoxyarborenone D 10092969 Click to see CC(=CCC1=C2C(=C(C(=C1O)O)O)OC3=CC4=C(CC(O4)C(=C)C)C(=C3C2=O)O)C 410.40 unknown https://doi.org/10.1021/NP010395F
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6,10-dihydroxy-11-methoxy-1,1-dimethyl-2H-pyrano[2,3-c]xanthene-3,7-dione 78319182 Click to see CC1(CC(=O)OC2=C1C3=C(C(=C2)O)C(=O)C4=C(O3)C(=C(C=C4)O)OC)C 356.30 unknown https://doi.org/10.3987/COM-10-11994
> Organoheterocyclic compounds / Naphthopyrans
(9R)-9,12-dihydroxy-5-methoxy-2,2,9-trimethyl-8,10-dihydronaphtho[6,7-h]chromen-11-one 154497676 Click to see CC1(C=CC2=C(O1)C3=C(C4=C(CC(CC4=O)(C)O)C=C3C=C2OC)O)C 354.40 unknown https://doi.org/10.1021/NP010395F
Vismione B 10247551 Click to see CC1(C=CC2=C(O1)C3=C(C4=C(CC(CC4=O)(C)O)C=C3C=C2OC)O)C 354.40 unknown https://doi.org/10.1021/NP010395F

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