Quercetin
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Also known as 3'-hydroxykaempferolC.i. 75670C.i. natural red 1Ci-75670CorvitinCyanidenolon 1522KorvitinLDN 0052529LDN-0052529LipoflavonMeletinNSC 57655NSC 9219NSC-57655NSC-9219Quercetin (constituent of ginkgo)QuercetineQuercetolQuertin
Summary
Quercetin (CHEMBL50) is an approved small-molecule antibacterial agent targeting NT5E and CYP1B1; indicated across 24 conditions including coronary artery disorder and chronic kidney disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- Targets: 2 (NT5E, CYP1B1)
- Indications: 24 conditions
- Clinical trials: 58
- Chemistry: 302.23 Da · C15H10O7
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL50 |
| Name | Quercetin |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | yes |
| PubChem CID | 5280343 |
| ChEBI | CHEBI:16243 |
| Molecular formula | C15H10O7 |
| Molecular weight | 302.23 |
| InChIKey | REFJWTPEDVJJIY-UHFFFAOYSA-N |
SMILES: C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O
IUPAC name: 2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxychromen-4-one
ChEBI definition: A pentahydroxyflavone having the five hydroxy groups placed at the 3-, 3’-, 4’-, 5- and 7-positions. It is one of the most abundant flavonoids in edible vegetables, fruit and wine.
Pharmacological roles (ChEBI): antibacterial agent, antioxidant, protein kinase inhibitor, antineoplastic agent, EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor, phytoestrogen, radical scavenger, chelator, Aurora kinase inhibitor, geroprotector.
Other ChEBI roles (chemical / environmental): plant metabolite.
Also known as: 3’-hydroxykaempferol, C.i. 75670, C.i. natural red 1, Ci-75670, Corvitin, Cyanidenolon 1522, Korvitin, LDN 0052529, LDN-0052529, Lipoflavon, Meletin, NSC 57655
Parent form; salt/anhydrous children: CHEMBL1173475, CHEMBL1520590
Patent coverage: 33,931 distinct patent families (74,559 SureChEMBL compound mentions), from 4 matched compound structure(s). One matched structure accounts for 73,116 (98%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| NT5E | Ecto-5’-Nucleotidase | Inhibition | 7.34 | 0% | P21589 |
| CYP1B1 | CYP1B1 | Inhibition | 7.64 | 0.1% | Q16678 |
Broader ChEMBL bioactivity targets: 214 (assay-derived). Sample: Tyrosyl-DNA phosphodiesterase 1, 5’-nucleotidase, Aldo-keto reductase family 1 member C21, NADPH oxidase 4, ELAV-like protein 1, Short transient receptor potential channel 5, Microtubule-associated protein tau, Lysine-specific demethylase 4E, Ubiquitin carboxyl-terminal hydrolase 2, Survival motor neuron protein.
Bioactivity
ChEMBL activities: 255 potent at pChembl ≥ 5 of 431 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P21398 | 8 | IC50 | 10 | nM | CHEMBL_ACT_2543849 |
| CYP19A1 | 7.92 | IC50 | 12 | nM | CHEMBL_ACT_3290710 |
| AKR1B1 | 7.83 | IC50 | 14.8 | nM | CHEMBL_ACT_2481523 |
| CYP1B1 | 7.64 | Ki | 23 | nM | CHEMBL_ACT_18157566 |
| CYP1B1 | 7.64 | Ki | 23 | nM | CHEMBL_ACT_6207669 |
| PIM1 | 7.6 | Kd | 25 | nM | CHEMBL_ACT_1657782 |
| ABCG2 | 7.52 | EC50 | 30 | nM | CHEMBL_ACT_18225509 |
| F2 | 7.41 | Kd | 38.7 | nM | CHEMBL_ACT_13442142 |
| PIM1 | 7.37 | IC50 | 43 | nM | CHEMBL_ACT_1655426 |
| P21588 | 7.34 | Ki | 45.3 | nM | CHEMBL_ACT_3122313 |
| CYP1B1 | 7.11 | IC50 | 77 | nM | CHEMBL_ACT_18068932 |
| CYP1B1 | 7.11 | IC50 | 77 | nM | CHEMBL_ACT_3409870 |
| SRC | 6.92 | IC50 | 120 | nM | CHEMBL_ACT_13878351 |
| HSD17B10 | 6.9 | Potency | 125.9 | nM | CHEMBL_ACT_4837177 |
| HSD17B10 | 6.8 | Potency | 158.5 | nM | CHEMBL_ACT_4829684 |
| NPSR1 | 6.8 | Potency | 158.5 | nM | CHEMBL_ACT_4885195 |
| MMP9 | 6.76 | IC50 | 173.8 | nM | CHEMBL_ACT_23231071 |
| POLB | 6.7 | Potency | 199.5 | nM | CHEMBL_ACT_5043440 |
| P12527 | 6.7 | IC50 | 200 | nM | CHEMBL_ACT_842488 |
| AKR1B1 | 6.64 | IC50 | 230 | nM | CHEMBL_ACT_29120211 |
| HSD17B10 | 6.6 | Potency | 251.2 | nM | CHEMBL_ACT_4869407 |
| ABCG2 | 6.56 | EC50 | 278 | nM | CHEMBL_ACT_18072656 |
| ABCG2 | 6.56 | EC50 | 278 | nM | CHEMBL_ACT_18315218 |
| KDR | 6.55 | IC50 | 280 | nM | CHEMBL_ACT_13878344 |
| XDH | 6.55 | Ki | 280 | nM | CHEMBL_ACT_15008223 |
| P17988 | 6.54 | IC50 | 290 | nM | CHEMBL_ACT_25029744 |
| P12527 | 6.52 | IC50 | 300 | nM | CHEMBL_ACT_1270640 |
| IGF1R | 6.52 | IC50 | 300 | nM | CHEMBL_ACT_13878407 |
| P12527 | 6.52 | IC50 | 300 | nM | CHEMBL_ACT_247235 |
| CYP1A2 | 6.5 | AC50 | 316.2 | nM | CHEMBL_ACT_6046862 |
Target pathways
Aggregated over 2 target gene(s): NT5E, CYP1B1.
Top Reactome pathways
18 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Metabolism | 1 | NT5E |
| Metabolism of nucleotides | 1 | NT5E |
| Disease | 1 | NT5E |
| Nicotinate metabolism | 1 | NT5E |
| Metabolism of water-soluble vitamins and cofactors | 1 | NT5E |
| Metabolism of vitamins and cofactors | 1 | NT5E |
| Endogenous sterols | 1 | CYP1B1 |
| Synthesis of epoxy (EET) and dihydroxyeicosatrienoic acids (DHET) | 1 | CYP1B1 |
| Synthesis of (16-20)-hydroxyeicosatetraenoic acids (HETE) | 1 | CYP1B1 |
| Defective CYP1B1 causes Glaucoma | 1 | CYP1B1 |
| Infectious disease | 1 | NT5E |
| Pyrimidine catabolism | 1 | NT5E |
| Purine catabolism | 1 | NT5E |
| Nucleotide catabolism | 1 | NT5E |
| Leishmania infection | 1 | NT5E |
| Purinergic signaling in leishmaniasis infection | 1 | NT5E |
| Cell recruitment (pro-inflammatory response) | 1 | NT5E |
| Parasitic Infection Pathways | 1 | NT5E |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| AMP catabolic process | 1 |
| DNA metabolic process | 1 |
| leukocyte cell-cell adhesion | 1 |
| response to ATP | 1 |
| ADP catabolic process | 1 |
| ATP metabolic process | 1 |
| adenosine biosynthetic process | 1 |
| negative regulation of inflammatory response | 1 |
| calcium ion homeostasis | 1 |
| inhibition of non-skeletal tissue mineralization | 1 |
| nucleotide catabolic process | 1 |
| angiogenesis | 1 |
| trabecular meshwork development | 1 |
| steroid catabolic process | 1 |
| xenobiotic metabolic process | 1 |
Indications & clinical
Indications
24 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| coronary artery disorder | 3 | MONDO:0005010 | EFO:0001645 |
| chronic kidney disease | 2 | MONDO:0005300 | EFO:0003884 |
| follicular lymphoma | 2 | MONDO:0018906 | MONDO:0018906 |
| childhood malignant neoplasm | 2 | MONDO:0006517 | EFO:1000654 |
| age-related macular degeneration | 2 | MONDO:0005150 | EFO:0001365 |
| oral cavity neoplasm | 2 | MONDO:0021245 | EFO:0003868 |
| type 2 diabetes mellitus | 2 | MONDO:0005148 | MONDO:0005148 |
| cystic fibrosis | 2 | MONDO:0009061 | MONDO:0009061 |
| squamous cell carcinoma | 2 | MONDO:0005096 | EFO:0000707 |
| obesity disorder | 2 | MONDO:0011122 | EFO:0001073 |
| triple-negative breast carcinoma | 2 | MONDO:0005494 | EFO:0005537 |
| chronic obstructive pulmonary disease | 1 | MONDO:0005002 | EFO:0000341 |
| prostate adenocarcinoma | 1 | MONDO:0005082 | EFO:0000673 |
| gastroesophageal reflux disease | 1 | MONDO:0007186 | EFO:0003948 |
| chronic hepatitis C virus infection | 1 | MONDO:0005354 | EFO:0004220 |
| lichen planus, oral | 1 | MONDO:0043923 | EFO:0008517 |
| severe acute respiratory syndrome | 1 | MONDO:0005091 | MONDO:0100096 |
| osteoarthritis | 1 | MONDO:0005178 | MONDO:0005178 |
| Fanconi anemia | 1 | MONDO:0019391 | MONDO:0019391 |
| idiopathic pulmonary fibrosis | 1 | MONDO:0800504 | EFO:0000768 |
| Alzheimer disease | 1 | MONDO:0004975 | MONDO:0004975 |
3 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 58.
Phase distribution
| Phase | Trials |
|---|---|
| Not specified | 16 |
| PHASE2 | 14 |
| PHASE1 | 10 |
| PHASE1/PHASE2 | 5 |
| EARLY_PHASE1 | 5 |
| PHASE4 | 4 |
| PHASE3 | 3 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00913081 | PHASE4 | COMPLETED | Advancing Niacin by Inhibiting Flushing (ANTI-FLUSH) |
| NCT02463357 | PHASE4 | COMPLETED | Three New Ideas to Protect Special Forces From the Stress of High Altitude |
| NCT04258410 | PHASE4 | WITHDRAWN | Quercetin for Cardio-Skeletal Muscle Health and Estrogen Deficiency |
| NCT04468139 | PHASE4 | UNKNOWN | The Study of Quadruple Therapy Zinc, Quercetin, Bromelain and Vitamin C on the Clinical Outcomes of Patients Infected With COVID-19 |
| NCT05653258 | PHASE2/PHASE3 | RECRUITING | Single Nuclei RNA-seq to Map Adipose Cellular Populations and Senescent Cells in Older Subjects |
| NCT03943459 | PHASE3 | UNKNOWN | Sirtuin-1 and Advanced Glycation End-products in Postmenopausal Women With Coronary Disease |
| NCT04578158 | PHASE3 | COMPLETED | Trial to Study the Adjuvant Benefits of Quercetin Phytosome in Patients With COVID-19 |
| NCT06650891 | PHASE3 | COMPLETED | Quercetin Effect on Post-ceserean Pain |
| NCT04685590 | PHASE2 | ACTIVE_NOT_RECRUITING | Senolytic Therapy to Modulate the Progression of Alzheimer’s Disease (SToMP-AD) Study |
| NCT04785300 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | ALSENLITE: Senolytics for Alzheimer’s Disease |
| NCT05838560 | PHASE2 | ACTIVE_NOT_RECRUITING | Dasatinib Plus Quercetin for Accelerated Aging in Mental Disorders |
| NCT06355037 | PHASE2 | RECRUITING | Dasatinib Combined With Quercetin to Reverse Chemo Resistance in Triple Negative Breast Cancer |
| NCT06940297 | PHASE2 | RECRUITING | Dasatinib and Quercetin With CAR-T Therapy for the Treatment of Patients With Relapsed or Refractory Multiple Myeloma |
| NCT07144293 | PHASE2 | ACTIVE_NOT_RECRUITING | Improving Physical Ability and Cellular Senescence Elimination in HIV |
| NCT07182526 | PHASE2 | RECRUITING | Effects of Adding Quercetin or Alpha Lipoic Acid to Usual Care on Symptoms and Blood Markers in Iraqi Women With Polycystic Ovary Syndrome |
| NCT00065676 | PHASE2 | COMPLETED | Investigating the Use of Quercetin on Glucose Absorption in Obesity, and Obesity With Type 2 Diabetes |
| NCT01348204 | PHASE2 | COMPLETED | Nasal Potential Studies Utilizing Cystic Fibrosis Transmembrane Regulator (CFTR) Modulators |
| NCT01732393 | PHASE1/PHASE2 | COMPLETED | Effect of Quercetin in Prevention and Treatment of Oral Mucositis |
| NCT01839344 | PHASE2 | COMPLETED | Effects of Quercetin on Blood Sugar and Blood Vessel Function in Type 2 Diabetes. |
| NCT03989271 | PHASE1/PHASE2 | UNKNOWN | Biological Effects of Quercetin in COPD |
| NCT04063124 | PHASE1/PHASE2 | COMPLETED | Senolytic Therapy to Modulate Progression of Alzheimer’s Disease |
| NCT04313634 | PHASE2 | COMPLETED | Targeting Cellular Senescence With Senolytics to Improve Skeletal Health in Older Humans |
| NCT04907253 | PHASE2 | COMPLETED | Quercetin in Coronary Artery By-pass Surgery |
| NCT05062486 | PHASE2 | COMPLETED | A Study to Evaluate the Safety and Efficacy of RQC for AMD |
| NCT05422885 | PHASE1/PHASE2 | COMPLETED | Safety and Feasibility of Dasatinib and Quercetin in Adults at Risk for Alzheimer’s Disease |
| NCT05456022 | PHASE2 | UNKNOWN | Therapeutic Efficacy of Quercetin Versus Its Encapsulated Nanoparticle on Tongue Squamous Cell Carcinoma Cell Line |
| NCT06003270 | PHASE2 | UNKNOWN | Biological Effects of Quercetin in COPD Phase II |
| NCT07270120 | PHASE1 | NOT_YET_RECRUITING | Senolytics for Secondary Progressive MS |
| NCT07433621 | PHASE1 | RECRUITING | Quercetin in Patients With XIAP (X-linked Inhibitor of Apoptosis) Deficiency |
| NCT01375101 | PHASE1 | UNKNOWN | Therapeutic Effect of Quercetin and the Current Treatment of Erosive and Atrophic Oral Lichen Planus |
| NCT01438320 | PHASE1 | COMPLETED | Q-Trial in Patients With Hepatitis C |
| NCT01708278 | PHASE1 | COMPLETED | Beneficial Effects of Quercetin in Chronic Obstructive Pulmonary Disease (COPD) |
| NCT01912820 | PHASE1 | COMPLETED | Effect of Quercetin on Green Tea Polyphenol Uptake in Prostate Tissue From Patients With Prostate Cancer Undergoing Surgery |
| NCT02226484 | PHASE1 | COMPLETED | Can Quercetin Increase Claudin-4 and Improve Esophageal Barrier Function in GERD? |
| NCT02874989 | PHASE1 | COMPLETED | Targeting Pro-Inflammatory Cells in Idiopathic Pulmonary Fibrosis: a Human Trial |
| NCT04851821 | PHASE1 | COMPLETED | The Effectiveness of Phytotherapy in SARS-COV2(COVID-19) |
| NCT05928546 | PHASE1 | UNKNOWN | Effect of Quercetin in Treatment of Periodontitis |
| NCT07025226 | EARLY_PHASE1 | RECRUITING | Sequential Treatments or Combinations Including Dasatinib, Quercetin, Fisetin and/or Temozolomide for the Treatment of Previously Treated Glioma With Residual Disease |
| NCT01376011 | EARLY_PHASE1 | COMPLETED | Modulation of Cerebral Blood Flow Using Quercetin, a Nutritional Supplement |
| NCT02989129 | EARLY_PHASE1 | WITHDRAWN | Trial of Quercetin in the Treatment and Prevention of Chemotherapy-induced Neuropathic Pain in Cancer Patients |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
34 molecules share ≥1 primary target. Top 34 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| ERYTHROMYCIN | ChEMBL + PubChem | Phase 4 (approved) | CYP1B1 |
| BERBERINE | ChEMBL | Phase 4 (approved) | CYP1B1 |
| CANNABIDIOL | ChEMBL | Phase 4 (approved) | CYP1B1 |
| CARVEDILOL | ChEMBL | Phase 4 (approved) | CYP1B1 |
| ESTRADIOL | ChEMBL | Phase 4 (approved) | CYP1B1 |
| INDACATEROL | ChEMBL | Phase 4 (approved) | CYP1B1 |
| MELATONIN | ChEMBL | Phase 4 (approved) | CYP1B1 |
| PAZOPANIB | ChEMBL | Phase 4 (approved) | CYP1B1 |
| FLUDARABINE | ChEMBL + PubChem | Phase 3 (approved) | NT5E |
| BERGAPTEN | ChEMBL | Phase 3 | CYP1B1 |
| CANNABINOL | ChEMBL | Phase 3 | CYP1B1 |
| RESVERATROL | ChEMBL | Phase 3 | CYP1B1 |
| 2-METHOXYESTRADIOL | ChEMBL | Phase 2 | CYP1B1 |
| BAICALEIN | ChEMBL | Phase 2 | CYP1B1 |
| ELLAGIC ACID | ChEMBL | Phase 2 | NT5E |
| FLAVONE | ChEMBL | Phase 2 | CYP1B1 |
| FORMONONETIN | ChEMBL | Phase 2 | CYP1B1 |
| FTIVAZIDE | ChEMBL | Phase 2 | NT5E |
| KHELLIN | ChEMBL | Phase 2 | CYP1B1 |
| LUTEOLIN | ChEMBL | Phase 2 | CYP1B1 |
| PINOCEMBRIN | ChEMBL | Phase 2 | CYP1B1 |
| PTEROSTILBENE | ChEMBL | Phase 2 | CYP1B1 |
| QUEMLICLUSTAT | ChEMBL | Phase 2 | NT5E |
| adenosine | PubChem | Approved | NT5E |
| Aprepitant | PubChem | Approved | CYP1B1 |
| Cenobamate | PubChem | Approved | CYP1B1 |
| Clozapine | PubChem | Approved | CYP1B1 |
| Glycyrrhizin | PubChem | Approved | CYP1B1 |
| Hydroxychloroquine | PubChem | Approved | CYP1B1 |
| Oritavancin | PubChem | Approved | CYP1B1 |
| rifampin | PubChem | Approved | CYP1B1 |
| Safinamide | PubChem | Approved | CYP1B1 |
| Tecovirimat | PubChem | Approved | CYP1B1 |
| Tiamulin | PubChem | Approved | NT5E |
Related Atlas pages
- Genes: NT5E, CYP1B1
- Diseases: coronary artery disorder
- Drugs: Erythromycin, Berberine, Cannabidiol, Carvedilol, Estradiol, Indacaterol, Melatonin, Pazopanib, Fludarabine, Bergapten, Cannabinol, Resveratrol, adenosine, Aprepitant, Cenobamate, Clozapine, Hydroxychloroquine, Oritavancin, rifampin, Safinamide, Tecovirimat