quercetin 3-sambubioside: isolated from Actinidia arguta [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
quercetin 3-O-[beta-D-xylosyl-(1->2)-beta-D-glucoside] : A quercetin O-glucoside that is quercetin attached to a beta-D-sambubiosyl residue at position 3 via a glycosidc linkage. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]
| Flora | Rank | Flora Definition | Family | Family Definition |
|---|---|---|---|---|
| Actinidia | genus | A plant species of the family ACTINIDIACEAE, order ERICALES.[MeSH] | Actinidiaceae | A plant family of the order Theales, subclass Dilleniidae, class Magnoliopsida. It is best known for Kiwi fruit (ACTINIDIA).[MeSH] |
| Actinidia arguta | species | [no description available] | Actinidiaceae | A plant family of the order Theales, subclass Dilleniidae, class Magnoliopsida. It is best known for Kiwi fruit (ACTINIDIA).[MeSH] |
| ID Source | ID |
|---|---|
| PubMed CID | 5487635 |
| CHEMBL ID | 455758 |
| CHEBI ID | 32081 |
| MeSH ID | M0194786 |
| Synonym |
|---|
| 4h-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2-o-beta-d-xylopyranosyl-beta-d-glucopyranosyl)oxy)- |
| quercetin 3-o-beta-xylopyranosyl-(1-2)-o-beta-glucopyranoside |
| 83048-35-5 |
| quercetin 3-o-[beta-d-xylosyl-(1->2)-beta-d-glucoside] |
| C12637 , |
| quercetin 3-sambubioside |
| chebi:32081 , |
| CHEMBL455758 , |
| quercetin 3-o-sambubioside |
| AC1NUPP6 , |
| 3-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2s,3r,4s,5r)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one |
| 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4h-chromen-3-yl 2-o-beta-d-xylopyranosyl-beta-d-glucopyranoside |
| 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2-o-beta-d-xylopyranosyl-beta-d-glucopyranosyl)oxy)-4h-1-benzopyran-4-one |
| DTXSID40232141 |
| 3-[(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2s,3r,4s,5r)-3,4,5-trihydroxytetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-chromen-4-one |
| Q27114776 |
| D85015 |
| MS-30578 |
| 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2-o-|a-d-xylopyranosyl-|a-d-glucopyranosyl)oxy]-4h-1-benzopyran-4-one |
| CS-0139004 |
| HY-N8028 |
| AKOS040760777 |
| Role | Description |
|---|---|
| antioxidant | A substance that opposes oxidation or inhibits reactions brought about by dioxygen or peroxides. |
| plant metabolite | Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. |
| [role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] | |
| Class | Description |
|---|---|
| quercetin O-glucoside | A quercetin O-glycoside that is an O-glucosylated derivative of quercetin. |
| disaccharide derivative | A carbohydrate derivative that is formally obtained from a disaccharide. |
| tetrahydroxyflavone | Any hydroxyflavone carrying four hydroxy substituents. |
| [compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] | |
| Assay ID | Title | Year | Journal | Article |
|---|---|---|---|---|
| AID377795 | Cytotoxicity against dog RBC | 2005 | Journal of natural products, Apr, Volume: 68, Issue:4 | Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri. |
| AID401229 | Antiviral activity against influenza virus type A H1N1 in MDCK cells assessed as inhibition of virus-induced cytopathic effect | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID377796 | Cytotoxicity against human RBC | 2005 | Journal of natural products, Apr, Volume: 68, Issue:4 | Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri. |
| AID401226 | Selectivity index, ratio of CC50 for MDCK cells to IC50 for RSV Long | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID401228 | Selectivity index, ratio of CC50 for MDCK cells to IC50 for PIV3 | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID377793 | Antibabesial activity against Babesia gibsoni in dog erythrocytes after 72 hrs | 2005 | Journal of natural products, Apr, Volume: 68, Issue:4 | Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri. |
| AID401224 | Antiviral activity against RSV Long in MDCK cells assessed as inhibition of virus-induced cytopathic effect | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID501209 | Antiviral activity against HSV1 infected african green monkey Vero cells assessed as reduction of plaque formation after 3 days by using crystal violet stain | 2010 | Journal of natural products, Feb-26, Volume: 73, Issue:2 | Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni. |
| AID377794 | Antiplasmodial activity against chloroquine-susceptible Plasmodium falciparum FCR3 in human erythrocytes after 24 hrs | 2005 | Journal of natural products, Apr, Volume: 68, Issue:4 | Anti-babesial and anti-plasmodial compounds from Phyllanthus niruri. |
| AID401227 | Antiviral activity against PIV3 in MDCK cells assessed as inhibition of virus-induced cytopathic effect | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID401225 | Cytotoxicity against MDCK cells | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID401230 | Selectivity index, ratio of CC50 for MDCK cells to IC50 for influenza virus type A H1N1 | 2004 | Journal of natural products, Apr, Volume: 67, Issue:4 | Antiviral flavonoids from the seeds of Aesculus chinensis. |
| AID501210 | Cytotoxicity against african green monkey Vero cells after 3 days by MTT assay | 2010 | Journal of natural products, Feb-26, Volume: 73, Issue:2 | Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni. |
| [information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||||
| Timeframe | Studies, This Drug (%) | All Drugs % |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (12.50) | 18.2507 |
| 2000's | 3 (37.50) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.68) All Compounds (24.57) |
| Publication Type | This drug (%) | All Drugs (%) |
|---|---|---|
| Trials | 0 (0.00%) | 5.53% |
| Reviews | 0 (0.00%) | 6.00% |
| Case Studies | 0 (0.00%) | 4.05% |
| Observational | 0 (0.00%) | 0.25% |
| Other | 8 (100.00%) | 84.16% |
| [information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] | ||