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Glycosmis trichanthera

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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 UUID64401e300dadc851153894
Scientific name Glycosmis trichanthera
Authority Guillaumin
First published in Bull. Soc. Bot. France 91: 216 (1945)

Description Top

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Synonyms Top

Scientific name Authority First published in
Glycosmis calcicola B.C.Stone Gard. Bull. Singapore 26: 55 (1972)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Glycosmis trichanthera var. kelantanica (B.C.Stone) B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 22 (1985)
Glycosmis trichanthera var. sumatrana B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 22 (1985)

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
  • Asia-tropical
    • Indo-China
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000704606
Tropicos 100343747
KEW urn:lsid:ipni.org:names:773807-1
The Plant List kew-2827680
Open Tree Of Life 755721
NCBI Taxonomy 159052
IPNI 773807-1
GBIF 7268979
EOL 5619596
USDA GRIN 403206

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
Phylogenetic Relationships of Citrus and Its Relatives Based on matK Gene Sequences Penjor T, Yamamoto M, Uehara M, Ide M, Matsumoto N, Matsumoto R, Nagano Y PLoS One 25-Apr-2013
PMCID:PMC3636227
doi:10.1371/journal.pone.0062574
PMID:23638116
High antitrypanosomal activity of plant-derived sulphur-containing amides. Astelbauer F, Obwaller A, Raninger A, Brem B, Greger H, Duchêne M, Wernsdorfer W, Walochnik J Int J Antimicrob Agents 01-Dec-2010
doi:10.1016/J.IJANTIMICAG.2010.07.003
PMID:20851577
Organ-specific chemical differences in Glycosmis trichanthera Srunya Vajrodaya, Markus Bacher, Harald Greger, Otmar Hofer Elsevier BV 23-Apr-2003
doi:10.1016/S0031-9422(97)00986-2
Carbazole alkaloids from roots of Glycosmis arborea Ajit Kumar Chakravarty, Tapas Sarkar, Kazuo Masuda, Kenji Shiojima Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00666-9

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 / Phenol ethers
(e)-3-(Methylsulfonyl)-propenoic acid (e)-4-(3-(5,5-dimethyl-4-oxo-2-oxolen-2-yl)-2-butenyloxy)-phenethyl amide 10741452 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)C2=CC(=O)C(O2)(C)C 433.50 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
(E)-N-[2-[4-[(E)-3-(5,5-dimethyl-4-oxofuran-2-yl)-4-hydroxybut-2-enoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 6520483 Click to see CC1(C(=O)C=C(O1)C(=CCOC2=CC=C(C=C2)CCNC(=O)C=CS(=O)(=O)C)CO)C 449.50 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)-4-hydroxybut-2-enoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 400447 Click to see CC1(C(=O)C=C(O1)C(=CCOC2=CC=C(C=C2)CCNC(=O)C=CS(=O)(=O)C)CO)C 449.50 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)but-2-enoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 85251801 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)C2=CC(=O)C(O2)(C)C 433.50 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
Trichanthin-B 5471616 Click to see CC1(C(=O)C=C(O1)C(=CCOC2=CC=C(C=C2)CCNC(=O)C=CS(=O)(=O)C)CO)C 449.50 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Methylgerambullin 15460080 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)CCN(C)C(=O)C=CS(=O)(=O)C)C)C 419.60 unknown https://doi.org/10.1016/J.IJANTIMICAG.2010.07.003
https://doi.org/10.1016/S0031-9422(97)00986-2
N-[2-[4-(3,7-dimethylocta-2,6-dienoxy)phenyl]ethyl]-N-methyl-3-methylsulfonylprop-2-enamide 163002051 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)CCN(C)C(=O)C=CS(=O)(=O)C)C)C 419.60 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
3,7-Diprenyl indole 400448 Click to see CC(=CCC1=C2C(=CC=C1)C(=CN2)CC=C(C)C)C 253.40 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
Yukocitrine 15286417 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(N3C)C(=CC=C4)O)C 323.30 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
https://doi.org/10.1016/S0031-9422(98)00666-9
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1016/S0031-9422(97)00986-2
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0031-9422(97)00986-2

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