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Glycosmis chlorosperma

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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 UUID64401e2987fc9875130921
Scientific name Glycosmis chlorosperma
Authority Spreng.
First published in Syst. Veg. 4(2): 162 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cookia chlorosperma Blume Bijdr. Fl. Ned. Ind. : 135 (1825)
Dioxippe chlorosperma M.Roem. Fam. Nat. Syn. Monogr. 1: 45 (1846)
Glycosmis malayana Ridl. J. Straits Branch Roy. Asiat. Soc. 75: 12 (1917)
Glycosmis monticola Ridl. J. Straits Branch Roy. Asiat. Soc. 75: 14 (1917)

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 chlorosperma var. bidiensis B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 3 (1985)
Glycosmis chlorosperma var. elmeri (Merr.) Tanaka Meded. Rijks-Herb. 69: 3. 1931 (1931)
Glycosmis chlorosperma var. lindleyana (Swingle) B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 3 (1985)
Glycosmis chlorosperma var. macrorachis (King) B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 3 (1985)
Glycosmis chlorosperma var. paraphyllophora B.C.Stone Proc. Acad. Nat. Sci. Philadelphia 137(2): 3 (1985)

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
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000704476
Tropicos 50263458
KEW urn:lsid:ipni.org:names:773818-1
The Plant List kew-2827550
Open Tree Of Life 181645
NCBI Taxonomy 159042
IPNI 773818-1
iNaturalist 427743
GBIF 7269080
EOL 5619491
USDA GRIN 411298

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
Isolation and Characterization of One New Natural Compound with Other Potential Bioactive Secondary Metabolites from Glycosmis cyanocarpa (Blume) Spreng. (Family: Rutaceae) Islam MA, Ashrafi S, Rahman KM, Ahmed S, Molla Jamal AH, Ahsan M Molecules 27-Feb-2023
PMCID:PMC10005784
doi:10.3390/molecules28052207
PMID:36903452
Prenylated flavanones and flavanonols as chemical markers in Glycosmis species (Rutaceae). Lukaseder B, Vajrodaya S, Hehenberger T, Seger C, Nagl M, Lutz-Kutschera G, Robien W, Greger H, Hofer O Phytochemistry 01-May-2009
doi:10.1016/J.PHYTOCHEM.2009.05.007
PMID:19535116
New Sulfur-Containing Amides from<i>Glycosmis</i>Species with Antifungal Activity H. Greger, O. Hofer, G. Zechner, G. Wurz, F. Hadaček Georg Thieme Verlag KG 07-Nov-2008
doi:10.1055/S-2006-961754
Different types of sulphur-containing amides from Glycosmis cf. chlorosperma Harald Greger, Franz Hadacek, Otmar Hofer, Gerald Wurz, Gabriela Zechner Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85232-G
Prenylated sulfonyl amides from Glycosmis species. Hofer O, Greger H, Lukaseder B, Vajrodaya S, Bacher M Phytochemistry 01-May-2000
doi:10.1016/S0031-9422(00)00011-X
PMID:10872212

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)-N-[2-[3-hydroxy-4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 101059288 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)O)C 353.40 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
Dambullin 11099800 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)C 337.40 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[3-hydroxy-4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 163076456 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)O)C 353.40 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 85398627 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)C 337.40 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
> Benzenoids / Phenol ethers / Anisoles
(E)-N-[2-[3-methoxy-4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 101059289 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)OC)C 367.50 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[3-methoxy-4-(3-methylbut-2-enoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 162987129 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)OC)C 367.50 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(E)-N-[(2R)-2-[4-[(2E,6E)-3,7-dimethyl-8-oxoocta-2,6-dienoxy]phenyl]-2-hydroxyethyl]-3-methylsulfonylprop-2-enamide 163188630 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CS(=O)(=O)C)O)CCC=C(C)C=O 435.50 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
(E)-N-[(2R)-2-[4-[(2E)-3,7-dimethylocta-2,6-dienoxy]phenyl]-2-hydroxyethyl]-3-methylsulfonylprop-2-enamide 163195468 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CS(=O)(=O)C)O)C)C 421.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
(E)-N-[(2R)-2-hydroxy-2-[4-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 163185097 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CS(=O)(=O)C)O)CCC=C(C)CO 437.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
(E)-N-[2-[3-hydroxy-4-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 101059285 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)O)CCC=C(C)CO 437.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
(E)-N-[2-[4-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]-3-methoxyphenyl]ethyl]-3-methylsulfonylprop-2-enamide 101059286 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)OC)CCC=C(C)CO 451.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
(E)-N-[2-[4-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 101059281 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)CCC=C(C)CO 421.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[3-hydroxy-4-(8-hydroxy-3,7-dimethylocta-2,6-dienoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 162968077 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)O)CCC=C(C)CO 437.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[4-(3,7-dimethyl-8-oxoocta-2,6-dienoxy)phenyl]-2-hydroxyethyl]-3-methylsulfonylprop-2-enamide 163037634 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CS(=O)(=O)C)O)CCC=C(C)C=O 435.50 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[4-(3,7-dimethylocta-2,6-dienoxy)-3-hydroxyphenyl]ethyl]-3-methylsulfonylprop-2-enamide 163018099 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)O)C)C 421.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[4-(3,7-dimethylocta-2,6-dienoxy)phenyl]-2-hydroxyethyl]-3-methylsulfonylprop-2-enamide 163046028 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CS(=O)(=O)C)O)C)C 421.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[4-(8-hydroxy-3,7-dimethylocta-2,6-dienoxy)-3-methoxyphenyl]ethyl]-3-methylsulfonylprop-2-enamide 163084319 Click to see CC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)OC)CCC=C(C)CO 451.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-[4-(8-hydroxy-3,7-dimethylocta-2,6-dienoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 163000564 Click to see CC(=CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)CCC=C(C)CO 421.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
N-[2-hydroxy-2-[4-(8-hydroxy-3,7-dimethylocta-2,6-dienoxy)phenyl]ethyl]-3-methylsulfonylprop-2-enamide 163022708 Click to see CC(=CCOC1=CC=C(C=C1)C(CNC(=O)C=CS(=O)(=O)C)O)CCC=C(C)CO 437.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
Sakerine 101929569 Click to see CC(=CCCC(=CCOC1=C(C=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)O)C)C 421.60 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Naphthalene, 1,2,3,4,4a,7-hexahydro-1,6-dimethyl-4-(1-methylethyl)- 519298 Click to see CC1CCC(C2C1=CCC(=C2)C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,3R,12R,15R,16S,18R)-11,11,15-trimethyl-1,16,18-tris(3-methylbut-2-enyl)-20-oxapentacyclo[16.2.1.03,12.03,15.05,10]henicosa-5,7,9-triene-2,4,19,21-tetrone 102129929 Click to see CC(=CCC1CC2(C(=O)C(C(=O)C34C1(CCC3C(C5=CC=CC=C5C4=O)(C)C)C)(OC2=O)CC=C(C)C)CC=C(C)C)C 584.80 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine-proline anhydride 57275499 Click to see CC(C)CC(C(=O)OC(=O)C1CCCN1)N 228.29 unknown https://doi.org/10.1016/S0031-9422(00)00011-X
> Organic acids and derivatives / Vinylogous thioesters
(Z)-N-methyl-3-methylsulfanylprop-2-enamide 9989310 Click to see CNC(=O)C=CSC 131.20 unknown https://doi.org/10.1016/0031-9422(93)85232-G
https://doi.org/10.1055/S-2006-961754
N-methyl-3-methylsulfanylprop-2-enamide 85085266 Click to see CNC(=O)C=CSC 131.20 unknown https://doi.org/10.1016/0031-9422(93)85232-G
Penangin 10419217 Click to see CNC(=O)C=CSC 131.20 unknown https://doi.org/10.1055/S-2006-961754
https://doi.org/10.1016/0031-9422(93)85232-G
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Chlorospermine 25009582 Click to see C(CCNCCCNCl)CNCCCN 236.78 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(E)-N-methyl-N-(2-methylsulfanylacetyl)-3-phenylprop-2-enamide 10444760 Click to see CN(C(=O)CSC)C(=O)C=CC1=CC=CC=C1 249.33 unknown https://doi.org/10.1016/0031-9422(93)85232-G
(Z)-N-methyl-N-(2-methylsulfanylacetyl)-3-phenylprop-2-enamide 10264083 Click to see CN(C(=O)CSC)C(=O)C=CC1=CC=CC=C1 249.33 unknown https://doi.org/10.1016/0031-9422(93)85232-G
N-methyl-N-(2-methylsulfanylacetyl)-3-phenylprop-2-enamide 163026347 Click to see CN(C(=O)CSC)C(=O)C=CC1=CC=CC=C1 249.33 unknown https://doi.org/10.1016/0031-9422(93)85232-G
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101480799 Click to see CC(=CCC1=C(C=C(C2=C1OC(C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-methoxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162992095 Click to see CC(=CCC1=C(C=C(C2=C1OC(C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
5,4'-Dihydroxy-7-methoxy-8-prenylflavanone 11688951 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)OC)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
7,4'-DI-O-Methyl-8-prenylnaringenin 12072819 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)OC)O)OC)C 368.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
Flowerine 42608075 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)OC)O)OC)C 368.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
Mundulea flavanone B 42608071 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)OC)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
Sophoraflavanone B 509245 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxy-2-[4-(3-methylbut-2-enoxy)phenyl]chroman-4-one 12305191 Click to see CC(=CCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
Archangelenone 71586977 Click to see CC(=CCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 340.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-7-methoxy-2-[4-(3-methylbut-2-enoxy)phenyl]-2,3-dihydrochromen-4-one 101674019 Click to see CC(=CCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007
5-Hydroxy-7-methoxy-4'-prenyloxyflavanone 42608070 Click to see CC(=CCOC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)C 354.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.05.007

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