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Glycosmis parva

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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 UUID64401e2dc8c05317263797
Scientific name Glycosmis parva
Authority Craib
First published in Bull. Misc. Inform. Kew 1926: 337 (1926)

Description Top

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Synonyms Top

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Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000704555
Tropicos 100343713
KEW urn:lsid:ipni.org:names:773783-1
The Plant List kew-2827631
Open Tree Of Life 181656
NCBI Taxonomy 159047
IPNI 773783-1
GBIF 3832785
EOL 5619558
USDA GRIN 411354

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
Natural products targeting inflammation-related metabolic disorders: A comprehensive review Nainu F, Frediansyah A, Mamada SS, Permana AD, Salampe M, Chandran D, Emran TB, Simal-Gandara J Heliyon 02-Jun-2023
PMCID:PMC10279840
doi:10.1016/j.heliyon.2023.e16919
PMID:37346355
Histone Demethylase Modulation: Epigenetic Strategy to Combat Cancer Progression Srivastava R, Singh R, Jauhari S, Lodhi N, Srivastava R Epigenomes 17-May-2023
PMCID:PMC10204559
doi:10.3390/epigenomes7020010
PMID:37218871
In vitro and in silico studies of 7′′,8′′-buddlenol D anti-inflammatory lignans from Carallia brachiata as p38 MAP kinase inhibitors Nalinratana N, Suriya U, Laprasert C, Wisidsri N, Poldorn P, Rungrotmongkol T, Limpanasitthikul W, Wu HC, Chang HS, Chansriniyom C Sci Rep 02-Mar-2023
PMCID:PMC9981598
doi:10.1038/s41598-023-30475-5
PMID:36864126
Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH Life (Basel) 11-Nov-2022
PMCID:PMC9696702
doi:10.3390/life12111852
PMID:36430987
Arborinine from Glycosmis parva leaf extract inhibits clear-cell renal cell carcinoma by inhibiting KDM1A/UBE2O signaling Feng C, Gong L, Wang J Food Nutr Res 16-Sep-2022
PMCID:PMC9487452
doi:10.29219/fnr.v66.8714
PMID:36185617
S-deoxydihydroglyparvin from Glycosmis parva inhibits lipopolysaccharide induced murine macrophage activation through inactivating p38 mitogen activated protein kinase Laprasert C, Chansriniyom C, Limpanasithikul W J Adv Pharm Technol Res 09-Jan-2021
PMCID:PMC7832183
doi:10.4103/japtr.JAPTR_64_20
PMID:33532352
Therapeutic Potential of Natural Products in Treatment of Cervical Cancer: A Review Park SH, Kim M, Lee S, Jung W, Kim B Nutrients 05-Jan-2021
PMCID:PMC7824868
doi:10.3390/nu13010154
PMID:33466408
Fermentative N-Methylanthranilate Production by Engineered Corynebacterium glutamicum Walter T, Al Medani N, Burgardt A, Cankar K, Ferrer L, Kerbs A, Lee JH, Mindt M, Risse JM, Wendisch VF Microorganisms 08-Jun-2020
PMCID:PMC7356990
doi:10.3390/microorganisms8060866
PMID:32521697
Crinamine Induces Apoptosis and Inhibits Proliferation, Migration, and Angiogenesis in Cervical Cancer SiHa Cells Khumkhrong P, Piboonprai K, Chaichompoo W, Pimtong W, Khongkow M, Namdee K, Jantimaporn A, Japrung D, Asawapirom U, Suksamrarn A, Iempridee T Biomolecules 16-Sep-2019
PMCID:PMC6770758
doi:10.3390/biom9090494
PMID:31527550
The Chemistry and Pharmacology of Citrus Limonoids Gualdani R, Cavalluzzi MM, Lentini G, Habtemariam S Molecules 13-Nov-2016
PMCID:PMC6273274
doi:10.3390/molecules21111530
PMID:27845763
Aromatase and glycosyl transferase inhibiting acridone alkaloids from fruits of Cameroonian Zanthoxylum species Wouatsa VN, Misra L, Kumar S, Prakash O, Khan F, Tchoumbougnang F, Venkatesh RK Chem Cent J 18-Jul-2013
PMCID:PMC3750308
doi:10.1186/1752-153X-7-125
PMID:23866063
Isolation of acridone alkaloids and N-[(4-monoterpenyloxy)phenylethyl]-substituted sulfur-containing propanamide derivatives from Glycosmis parva and their anti-herpes simplex virus activity. Chansriniyom C, Ruangrungsi N, Lipipun V, Kumamoto T, Ishikawa T Chem Pharm Bull (Tokyo) 01-Nov-2009
doi:10.1248/CPB.57.1246
PMID:19881276
Phenethylamides With an Unusual 4-Oxo-2-oxolenyl Terpenoid Side Chain from Glycosmis Species Otmar Hofer, Srunya Vajrodaya, Harald Greger Springer Science and Business Media LLC 17-Feb-2006
doi:10.1007/PL00010157

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/10.1248/CPB.57.1246
https://doi.org/10.1007/PL00010157
(E)-N-[2-[4-[(3S)-3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]phenyl]ethyl]-3-[(R)-methylsulfinyl]prop-2-enamide 163185331 Click to see CC(CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)C)C2=CC(=O)C(O2)(C)C 419.50 unknown https://doi.org/10.1248/CPB.57.1246
(E)-N-[2-[4-[(3S)-3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 163187074 Click to see CC(CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)C2=CC(=O)C(O2)(C)C 435.50 unknown https://doi.org/10.1007/PL00010157
https://doi.org/10.1248/CPB.57.1246
Isovaleric acid (e)-4-(3-(5,5-dimethyl-4-oxo-2-oxolen-2-yl)-2-butenyloxy)-phenethyl amide 10667811 Click to see CC(C)CC(=O)NCCC1=CC=C(C=C1)OCC=C(C)C2=CC(=O)C(O2)(C)C 385.50 unknown https://doi.org/10.1007/PL00010157
N-[2-[4-[(3S)-3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]phenyl]ethyl]-3-[(R)-methylsulfinyl]propanamide 162934657 Click to see CC(CCOC1=CC=C(C=C1)CCNC(=O)CCS(=O)C)C2=CC(=O)C(O2)(C)C 421.60 unknown https://doi.org/10.1248/CPB.57.1246
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)but-2-enoxy]phenyl]ethyl]-3-methylbut-2-enamide 85216917 Click to see CC(=CC(=O)NCCC1=CC=C(C=C1)OCC=C(C)C2=CC(=O)C(O2)(C)C)C 383.50 unknown https://doi.org/10.1007/PL00010157
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)but-2-enoxy]phenyl]ethyl]-3-methylbutanamide 85225564 Click to see CC(C)CC(=O)NCCC1=CC=C(C=C1)OCC=C(C)C2=CC(=O)C(O2)(C)C 385.50 unknown https://doi.org/10.1007/PL00010157
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/10.1248/CPB.57.1246
https://doi.org/10.1007/PL00010157
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]phenyl]ethyl]-3-methylsulfinylprop-2-enamide 75041436 Click to see CC(CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)C)C2=CC(=O)C(O2)(C)C 419.50 unknown https://doi.org/10.1248/CPB.57.1246
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]phenyl]ethyl]-3-methylsulfinylpropanamide 44521380 Click to see CC(CCOC1=CC=C(C=C1)CCNC(=O)CCS(=O)C)C2=CC(=O)C(O2)(C)C 421.60 unknown https://doi.org/10.1248/CPB.57.1246
N-[2-[4-[3-(5,5-dimethyl-4-oxofuran-2-yl)butoxy]phenyl]ethyl]-3-methylsulfonylprop-2-enamide 85260177 Click to see CC(CCOC1=CC=C(C=C1)CCNC(=O)C=CS(=O)(=O)C)C2=CC(=O)C(O2)(C)C 435.50 unknown https://doi.org/10.1248/CPB.57.1246
https://doi.org/10.1007/PL00010157
Senecioic acid (e)-4-(3-(5,5-dimethyl-4-oxo-2-oxolen-2-yl)-2-butenyloxy)-phenethyl amide 10643693 Click to see CC(=CC(=O)NCCC1=CC=C(C=C1)OCC=C(C)C2=CC(=O)C(O2)(C)C)C 383.50 unknown https://doi.org/10.1007/PL00010157
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,7S,10R,13R,14R,20S)-19-(2-hydroxy-5-oxo-2H-furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 137795622 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(=O)OC7O)C)C)C 502.50 unknown https://doi.org/10.1248/CPB.57.1246
(1S,2R,7S,10R,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 162918695 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1248/CPB.57.1246
Evodia fruit 235284 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1248/CPB.57.1246
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown https://doi.org/10.1248/CPB.57.1246
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
Isolimonexic acid 5321282 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=CC(OC7=O)O)C)C)C 502.50 unknown https://doi.org/10.1248/CPB.57.1246
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Acridines / Acridones
1,3,5-Trihydroxy-2-methoxy-10-methylacridin-9-one 44521378 Click to see CN1C2=CC(=C(C(=C2C(=O)C3=C1C(=CC=C3)O)O)OC)O 287.27 unknown https://doi.org/10.1248/CPB.57.1246
1,6-Dihydroxy-3,4,5-trimethoxy-10-methylacridin-9-one 44626340 Click to see CN1C2=C(C=CC(=C2OC)O)C(=O)C3=C1C(=C(C=C3O)OC)OC 331.32 unknown https://doi.org/10.1248/CPB.57.1246
5,10-Dihydroxy-2,2,11-trimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]acridin-6-one 25141395 Click to see CC(=CCC1=C2C(=C(C3=C1N(C4=C(C3=O)C=CC=C4O)C)O)C=CC(O2)(C)C)C 391.50 unknown https://doi.org/10.1248/CPB.57.1246
Arborinine 5281832 Click to see CN1C2=CC=CC=C2C(=O)C3=C(C(=C(C=C31)OC)OC)O 285.29 unknown https://doi.org/10.1248/CPB.57.1246
Citramine 85583910 Click to see CN1C2=CC(=C(C(=C2C(=O)C3=C1C(=C(C=C3)O)OC)O)OC)O 317.29 unknown https://doi.org/10.1248/CPB.57.1246
N-Methylatalaphylline 15286416 Click to see CC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=C(N2C)C(=CC=C3)O)C 393.50 unknown https://doi.org/10.1248/CPB.57.1246

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