Dysoxylum acutangulum

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Internal ID UUID644018b219a82527563032
Scientific name Dysoxylum acutangulum
Authority Miq.
First published in Fl. Ned. Ind., Eerste Bijv. : 503 (1861)

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Synonyms Top

Scientific name Authority First published in
Alliaria acutangula (Miq.) Kuntze Revis. Gen. Pl. 1: 109. 1891 [5 Nov 1891]

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Dysoxylum acutangulum subsp. foveolatum (Radlk.) Mabb. Blumea 38: 303 (1994)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sumatera
    • Papuasia
      • New Guinea
      • Solomon Islands

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000658461
Tropicos 50285942
KEW urn:lsid:ipni.org:names:578040-1
The Plant List kew-2779850
Open Tree Of Life 5747786
NCBI Taxonomy 1504427
IPNI 578040-1
iNaturalist 427564
GBIF 7271367
Wikipedia Dysoxylum_acutangulum
PFAF Dysoxylum acutangulum

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)!
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Title Authors Publication Released IDs
De novo transcriptome analysis of Dysoxylum binectariferum to unravel the biosynthesis of pharmaceutically relevant specialized metabolites Kumara PM, Varun E, Sanjay JR, Madhushree AH, Thimmappa R Front Plant Sci 09-Aug-2023
PMCID:PMC10450223
doi:10.3389/fpls.2023.1098987
PMID:37636089
Sesquiterpenoids from Meliaceae Family and Their Biological Activities Riyadi SA, Naini AA, Supratman U Molecules 20-Jun-2023
PMCID:PMC10302239
doi:10.3390/molecules28124874
PMID:37375428
Exogenously Applied Rohitukine Inhibits Photosynthetic Processes, Growth and Induces Antioxidant Defense System in Arabidopsis thaliana Ahmed S, Asgher M, Kumar A, Gandhi SG Antioxidants (Basel) 03-Aug-2022
PMCID:PMC9404761
doi:10.3390/antiox11081512
PMID:36009231
Dalmanol biosyntheses require coupling of two separate polyketide gene clusters Zhou ZZ, Zhu HJ, Lin LP, Zhang X, Ge HM, Jiao RH, Tan RX Chem Sci 27-Nov-2018
PMCID:PMC6335865
doi:10.1039/c8sc03697g
PMID:30746075
Chromone and Flavonoid Alkaloids: Occurrence and Bioactivity Khadem S, Marles RJ Molecules 27-Dec-2011
PMCID:PMC6268529
doi:10.3390/molecules17010191
PMID:22202807
5-Hy­droxy-7-meth­oxy-2-methyl-4H-chromen-4-one from Dysoxylum macrocarpum (Meliaceae) Najmuldeen IA, Abdul Hadi AH, Awang K, Mohamad K, Ng SW Acta Crystallogr Sect E Struct Rep Online 03-Jul-2010
PMCID:PMC3007310
doi:10.1107/S1600536810025146
PMID:21588219
Chrotacumines A-D, chromone alkaloids from Dysoxylum acutangulum. Ismail IS, Nagakura Y, Hirasawa Y, Hosoya T, Lazim MI, Lajis NH, Shiro M, Morita H J Nat Prod 01-Oct-2009
doi:10.1021/NP9003849
PMID:19757855
Acutaxylines A and B, two novel triterpenes from Dysoxylum acutangulum Intan Safinar Ismail, Yuta Nagakura, Yusuke Hirasawa, Takahiro Hosoya, Mohd Izwan Mohd Lazim, Nordin Hj Lajis, Hiroshi Morita Elsevier BV 03-Jun-2009
doi:10.1016/J.TETLET.2009.05.110
Total Synthesis of (-)-(7S,10R)-Calamenene and (-)-(7S,10R)- 2-Hydroxycalamenene by Use of a Ring-Closing Metathesis Reaction. A Comparison of the cis- and trans-Isomers Nakashima K, Imoto M, Sono M, Tori M, Nagashima F, Asakawa Y Molecules 31-Jul-2002
PMCID:PMC6146462
doi:10.3390/70700517

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 / Prenol lipids / Sesquiterpenoids
methyl (1S,2S,4R,7S,8S,10S,11S,15R,16R)-10-acetyloxy-4-hydroxy-15-[(1S)-3-(2-hydroxypropan-2-yl)-4-oxocyclopent-2-en-1-yl]-2,7,11,16-tetramethyl-5-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-ene-7-carboxylate 162992562 Click to see CC(=O)OC1CC2C(CC(OCC2(C)C(=O)OC)O)(C3C1(C4=CCC(C4(CC3)C)C5CC(=O)C(=C5)C(C)(C)O)C)C 572.70 unknown https://doi.org/10.1016/J.TETLET.2009.05.110
methyl (1S,2S,4R,7S,8S,10S,11S,15R,16R)-4,10-dihydroxy-2,7,11,16-tetramethyl-15-[(1S)-4-oxo-3-propan-2-ylcyclopent-2-en-1-yl]-5-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-ene-7-carboxylate 162898741 Click to see CC(C)C1=CC(CC1=O)C2CC=C3C2(CCC4C3(C(CC5C4(CC(OCC5(C)C(=O)OC)O)C)O)C)C 514.70 unknown https://doi.org/10.1016/J.TETLET.2009.05.110
Methyl 10-acetyloxy-4-hydroxy-15-[3-(2-hydroxypropan-2-yl)-4-oxocyclopent-2-en-1-yl]-2,7,11,16-tetramethyl-5-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-ene-7-carboxylate 74951603 Click to see 572.70 unknown https://doi.org/10.1016/J.TETLET.2009.05.110
Methyl 4,10-dihydroxy-2,7,11,16-tetramethyl-15-(4-oxo-3-propan-2-ylcyclopent-2-en-1-yl)-5-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-ene-7-carboxylate 74951604 Click to see CC(C)C1=CC(CC1=O)C2CC=C3C2(CCC4C3(C(CC5C4(CC(OCC5(C)C(=O)OC)O)C)O)C)C 514.70 unknown https://doi.org/10.1016/J.TETLET.2009.05.110
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
7-Hydroxy-2-methyl-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14524526 Click to see 354.31 unknown https://doi.org/10.1021/NP9003849
Schumanniofioside A 5486897 Click to see 354.31 unknown https://doi.org/10.1021/NP9003849
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Noreugenin 5375252 Click to see 192.17 unknown https://doi.org/10.1021/NP9003849
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(9-Hydroxy-5,14-dimethyl-7-oxo-4,12-dioxa-14-azatetracyclo[11.3.1.02,11.03,8]heptadeca-2(11),3(8),5,9-tetraen-16-yl) benzoate 75068728 Click to see 407.40 unknown https://doi.org/10.1021/NP9003849
[(1R,13R,16S)-9-hydroxy-5,14-dimethyl-7-oxo-4,12-dioxa-14-azatetracyclo[11.3.1.02,11.03,8]heptadeca-2(11),3(8),5,9-tetraen-16-yl] benzoate 44557027 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OC4CC3C(CN4C)OC(=O)C5=CC=CC=C5 407.40 unknown https://doi.org/10.1021/NP9003849
chrotacumine A 46882760 Click to see CC1=CC(=O)C2=C(O1)C3=C(C=C2O)OC4CC3C(CN4C)OC(=O)C5=CC=CC=C5 407.40 unknown https://doi.org/10.1021/NP9003849
> Organoheterocyclic compounds / Piperidines / Phenylpiperidines
[(3S,4R)-4-(5,7-dihydroxy-2-methyl-4-oxochromen-8-yl)-1-methylpiperidin-3-yl] 2-methylbut-2-enoate 162970208 Click to see 387.40 unknown https://doi.org/10.1021/NP9003849
[4-(5,7-Dihydroxy-2-methyl-4-oxochromen-8-yl)-1-methylpiperidin-3-yl] 3,4-dimethoxybenzoate 75068757 Click to see 469.50 unknown https://doi.org/10.1021/NP9003849
[4-(5,7-Dihydroxy-2-methyl-4-oxochromen-8-yl)-1-methylpiperidin-3-yl] 3,4,5-trimethoxybenzoate 75068756 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3CCN(CC3OC(=O)C4=CC(=C(C(=C4)OC)OC)OC)C 499.50 unknown https://doi.org/10.1021/NP9003849
5,7-Dihydroxy-8-(3-hydroxy-1-methyl-4-piperidinyl)-2-methyl-4H-1-benzopyran-4-one 5387431 Click to see 305.32 unknown https://doi.org/10.1021/NP9003849
chrotacumine B 44557028 Click to see CC=C(C)C(=O)OC1CN(CCC1C2=C(C=C(C3=C2OC(=CC3=O)C)O)O)C 387.40 unknown https://doi.org/10.1021/NP9003849
Chrotacumine C 44557091 Click to see 499.50 unknown https://doi.org/10.1021/NP9003849
Chrotacumine D 44557092 Click to see 469.50 unknown https://doi.org/10.1021/NP9003849
Rohitukine 13422573 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3CCN(CC3O)C 305.32 unknown https://doi.org/10.1021/NP9003849

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